US20030020169A1 - Copper technology for ULSI metallization - Google Patents
Copper technology for ULSI metallization Download PDFInfo
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- US20030020169A1 US20030020169A1 US10/109,713 US10971302A US2003020169A1 US 20030020169 A1 US20030020169 A1 US 20030020169A1 US 10971302 A US10971302 A US 10971302A US 2003020169 A1 US2003020169 A1 US 2003020169A1
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- methylsilsequiazane
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- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76843—Barrier, adhesion or liner layers formed in openings in a dielectric
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- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
- H01L21/28506—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers
- H01L21/28512—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table
- H01L21/28556—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table by chemical means, e.g. CVD, LPCVD, PECVD, laser CVD
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/285—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation
- H01L21/28506—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers
- H01L21/28512—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table
- H01L21/28556—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table by chemical means, e.g. CVD, LPCVD, PECVD, laser CVD
- H01L21/28562—Selective deposition
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- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/28—Manufacture of electrodes on semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/268
- H01L21/283—Deposition of conductive or insulating materials for electrodes conducting electric current
- H01L21/288—Deposition of conductive or insulating materials for electrodes conducting electric current from a liquid, e.g. electrolytic deposition
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3205—Deposition of non-insulating-, e.g. conductive- or resistive-, layers on insulating layers; After-treatment of these layers
- H01L21/321—After treatment
- H01L21/32115—Planarisation
- H01L21/3212—Planarisation by chemical mechanical polishing [CMP]
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- H—ELECTRICITY
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- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76801—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
- H01L21/76802—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing by forming openings in dielectrics
- H01L21/76807—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing by forming openings in dielectrics for dual damascene structures
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- H—ELECTRICITY
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- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/70—Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
- H01L21/71—Manufacture of specific parts of devices defined in group H01L21/70
- H01L21/768—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
- H01L21/76838—Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the conductors
- H01L21/76841—Barrier, adhesion or liner layers
- H01L21/76871—Layers specifically deposited to enhance or enable the nucleation of further layers, i.e. seed layers
- H01L21/76874—Layers specifically deposited to enhance or enable the nucleation of further layers, i.e. seed layers for electroless plating
Definitions
- the present invention relates to the field of semiconductors and, in particular, to a method of forming damascene structures in semiconductor devices.
- Advanced copper dual damascene processes include a two-step sequential mask/etch process to form a two-level structure, such as a via connected to a metal line situated above the via.
- a known copper dual damascene process as applied to interconnect formation begins with the deposition of a first insulating layer 14 over a first level interconnect copper layer 12 , which in turn is formed over or within a semiconductor substrate 10 .
- a second insulating layer 16 is next formed over the first insulating layer 14 .
- An etch stop layer 15 is typically formed between the first and second insulating layers 14 , 16 .
- the second insulating layer 16 is patterned by photolithography with a first mask (not shown) to form a trench 17 corresponding to a copper line of a second level interconnect.
- the etch stop layer 15 prevents the upper level trench pattern 17 from being etched through the first insulating layer 14 .
- a second masking step followed by an etch step are applied to form a via 18 through the etch stop layer 15 and the first insulating layer 14 .
- both the trench 17 and the via 18 are filled with copper material 20 , as illustrated in FIG. 3.
- the copper material 20 undergoes a chemical mechanical polishing (CMP) step to remove any copper material from above the second insulating layer 16 and to form, therefore, a copper damascene structure as illustrated in FIG. 4.
- CMP chemical mechanical polishing
- a second etch stop layer (not shown) may be formed between the substrate 10 and the first insulating layer 14 during the formation of the copper damascene structure 25 .
- the via and the trench are simultaneously filled with metal.
- Another disadvantage is that copper deposition methods for conventional damascene processes employ a large amount of high-purity copper material, of which a considerable amount is removed and wasted by the CMP process described above with reference to FIGS. 3 - 4 .
- the dual damascene processing is very expensive and entails a large number of processing steps.
- the present invention provides a method for fabricating a copper interconnect structure in a semiconductor device which requires fewer processing steps and reduces the diffusion of copper atoms to underlying damascene layers.
- trenches and vias are formed by direct patterning of a low-dielectric constant material, subsequent to which a thin tungsten nitride (WN 2 ) diffusion barrier layer is formed by an atomic layer deposition using sequential surface reactions inside the trenches and vias.
- a selective copper CVD process is used to fill in the trenches and vias with copper.
- an electroless deposition technique is employed in lieu of the selective copper CVD process. This way, the sequential photoresist/mask/etch steps and the etch-stop layers are eliminated, while the diffusion of copper atoms into adjacent interconnect layers is suppressed.
- FIG. 1 is a cross-sectional view of a conventional semiconductor device at a preliminary stage of production.
- FIG. 2 is a cross-sectional view of the semiconductor device of FIG. 1 at a subsequent stage of production.
- FIG. 3 is a cross-sectional view of the semiconductor device of FIG. 2 at a subsequent stage of production.
- FIG. 4 is a cross-sectional view of the semiconductor device of FIG. 3 at a subsequent stage of production.
- FIG. 5 is a cross-sectional view of a semiconductor device at a preliminary stage of production and in accordance with a first embodiment of the present invention.
- FIG. 6 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 7 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 8 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 9 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 10 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 11 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 12 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 13 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 14 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 15 is a cross-sectional view of a semiconductor device constructed in accordance with a second embodiment of the present invention.
- FIG. 16 is a cross-sectional view of the semiconductor device of FIG. 15 at a subsequent stage of production.
- FIG. 17 is a cross-sectional view of a semiconductor device constructed in accordance with a third embodiment of the present invention.
- FIG. 18 illustrates a computer system having a memory cell with a copper damascene structure according to the present invention.
- substrate used in the following description may include any semiconductor-based structure that has a semiconductor surface.
- the term should be understood to include silicon, silicon-on insulator (SOI), silicon-on sapphire (SOS), doped and undoped semiconductors, epitaxial layers of silicon supported by a base semiconductor foundation, and other semiconductor structures.
- the semiconductor need not be silicon-based.
- the semiconductor could be silicon-germanium, germanium, or gallium arsenide.
- copper is intended to include not only elemental copper, but also copper with other trace metals or in various alloyed combinations with other metals as known in the art, as long as such alloy retains the physical and chemical properties of copper.
- copper is also intended to include conductive oxides of copper.
- FIGS. 5 - 17 illustrate the formation of copper damascene structures 100 , 200 , 300 (FIGS. 14, 16, 17 ) formed in accordance with exemplary embodiments of the present invention.
- FIG. 5 depicts a portion of an insulating layer 51 formed over a semiconductor substrate 50 , on or within which a metal layer 52 has been formed.
- the metal layer 52 represents a lower metal interconnect layer which is to be later interconnected with an upper copper interconnect layer.
- the metal layer 52 may be formed of copper (Cu), but other conductive materials, such as tungsten (W) or aluminum (Al) and their alloys, may be used also.
- an intermetal dielectric layer 55 is formed overlying the insulating layer 51 and the metal layer 52 .
- the intermetal dielectric layer 55 is formed of a low-dielectric constant material to a thickness of about 2,000 Angstroms to 50,000 Angstroms, more preferably of about 5,000 Angstroms to 20,000 Angstroms.
- a low-dielectric constant material is a material with a dielectric constant of less than about 4.
- the intermetal dielectric layer 55 is a low-dielectric constant material which can be directly patterned, without using a photoresist material, and which may be formed by a method described by Kikkawa in Current and Future Low - k Dielectrics for Cu Interconnects, Technical Digests of IEDM, pp. 253-56 (2000), the disclosure of which is incorporated by reference herein. Kikkawa has demonstrated that fabrication of photo-resistive low-dielectric constant films, such as methylsilsesquiazane (MSZ) films, can eliminate photoresist coating, dry etching and etch stop layers.
- MSZ methylsilsesquiazane
- vias and/or holes are formed in methylsilsesquiazane (MSZ) films by direct patterning, such as direct EB (electron beam) or UV (ultra violet) lithography, without using photoresist or dry etching.
- direct patterning such as direct EB (electron beam) or UV (ultra violet) lithography, without using photoresist or dry etching.
- a methylsilsesquiazane (MSZ) film precursor is deposited on a silicon substrate by spin-coating at 2700 rpm and pre-baked at about 90° C. for about 10 minutes.
- EB lithography is subsequently carried out with doses of about 3 ⁇ C/cm 2 to about 123 ⁇ C/cm 2 .
- UV (I-line) lithography is carried out with doses of about 45 mJ/cm 2 to about 315 mJ/cm 2 .
- moisture absorption is conducted at 25° C. and 50% relative humidity for about 10 minutes.
- Development of the methylsilsesquiazane (MSZ) film is then carried out in a tetra-methyl-ammonium hydroxide (TMAH) solution.
- TMAH tetra-methyl-ammonium hydroxide
- the methylsilsesquiazane (MSZ) film undergoes curing at 400° C. in a nitrogen ambient to be subsequently transformed into a methylsilsesquioxane (MSQ) film.
- Kikkawa et al. have observed that, during curing at 400° C. in the nitrogen ambient, the methylsilsesquiazane (MSZ) film undergoes photochemical reactions so that the resulting methylsilsesquioxane (MSQ) film comprises no Si—N bonds and only Si—O and Si—CH 3 bonds.
- the intermetal dielectric layer 55 may be also formed of a conventional insulating oxide, such as silicon oxide (SiO 2 ), or other low-dielectric constant materials such as, for example, polyimide, spin-on-polymers (SOP), parylene, flare, polyarylethers, polytetrafluoroethylene, benzocyclobutene (BCB), SILK, fluorinated silicon oxide (FSG), NANOGLASS or hydrogen silsesquioxane, which have dielectric constants of less than about 4.
- a conventional insulating oxide such as silicon oxide (SiO 2 )
- other low-dielectric constant materials such as, for example, polyimide, spin-on-polymers (SOP), parylene, flare, polyarylethers, polytetrafluoroethylene, benzocyclobutene (BCB), SILK, fluorinated silicon oxide (FSG), NANOGLASS or hydrogen silsesquioxane, which have dielectric constants
- a first mask layer 58 having images of a via pattern 59 is formed over the intermetal dielectric layer 55 for direct patterning.
- a via 65 may be formed by etching through the intermetal dielectric layer 55 with an etchant.
- the etchant (not shown) may be selected in accordance with the characteristics of the intermetal dielectric layer 55 , so that the dielectric material is selectively etched until the etchant reaches the metal layer 52 .
- the etchant is a tetra-methyl-ammonium hydroxide (TMAH) solution.
- a trench 67 (FIG. 10) is formed by employing a second mask layer 62 (FIG. 9) having images of a trench pattern 63 (FIG. 9) over the intermetal dielectric layer 55 .
- the trench pattern 63 is then etched into the intermetal dielectric layer 55 using the mask layer 62 to form trench 67 , as shown in FIG. 10.
- the etching of the trench 67 may be accomplished using the same etchant employed to form the via 65 (FIG. 8), which according to a preferred embodiment of the invention is a tetra-methyl-ammonium hydroxide (TMAH) solution.
- TMAH tetra-methyl-ammonium hydroxide
- the intermetal dielectric layer 55 is formed of methylsilsesquiazane material and if UV lithography is employed, the methylsilsesquiazane (MSZ) material undergoes curing at 400° C. in a nitrogen ambient to be subsequently transformed into a methylsilsesquioxane (MSQ) film.
- MSZ methylsilsesquiazane
- a diffusion barrier layer 72 (FIG. 11) is formed on the via 65 and the trench 67 to a thickness of about 50 Angstroms to about 200 Angstroms, more preferably of about 100 Angstroms.
- the diffusion barrier layer 72 is formed of tungsten nitride (WN 2 ) by a method described by Klaus et al. in Atomic Layer Deposition of Tungsten Nitride Films Using Sequential Surface Reactions, J. of Electrochemical Soc., Vol. 147(3), pp. 1175-1181 (2000), the disclosure of which is incorporated by reference herein. Klaus et al. have demonstrated that tungsten nitride films deposited with atomic layer control using sequential surface reactions have a stoichiometry with low carbon (C) and oxygen (O) impurity concentrations which prevent the diffusion of copper at elevated temperatures.
- C carbon
- O oxygen
- tungsten nitride films are deposited at a temperature of about 600-800K using an initial treatment of 10 mTorr Si 2 H 6 at 600K for about 5 minutes on a hydroxilated SiO 2 surface.
- tungsten nitride film growth can be conducted at reactions temperatures between about 550-800K by employing, for example, cycles of WVF 6 and NH 3 to transform the SiO 2 surface to a tungsten nitride surface.
- the tungsten nitride films formed by the above-described atomic layer control using sequential surface reactions technique have a microcrystalline structure and a remarkably flat surface indicating smooth film growth.
- the tungsten nitride diffusion barrier layer 72 is simultaneously deposited in both the via 65 and the trench 67 (FIG. 11), the invention is not limited to this embodiment.
- the tungsten-nitride diffusion barrier layer 72 may be deposited first in the via 65 before the formation of the trench 67 , and then in the trench 67 after its respective formation.
- horizontal portions of the tungsten nitride material formed above the surface of the intermetal dielectric layer 55 are removed by a light polishing technique to form the structure illustrated in FIG. 12.
- a fight chemical mechanical polishing is used to polish away excess tungsten-nitride material above the intermetal dielectric layer 55 and the trench level. This way, the intermetal dielectric layer 55 acts as a polishing stop layer when light CMP is used.
- a conductive material 80 comprising copper (Cu) is next deposited to fill in both the via 65 and the trench 67 .
- the copper is selectively deposited by CVD as described by Kaloyeros et al. in Blanket And Selective Copper CVD From Cu ( fod ) 2 For Multilevel Metallization, Mat. Res. Soc. Symp. Proc., Vol. 181 (1990), the disclosure of which is incorporated by reference herein.
- LTMOCVD blanket and selective low-temperature metal-organic chemical vapor deposition
- the reactor is first pumped down to a base pressure of less than 5 ⁇ 10 ⁇ 7 torr. Subsequently, the source compound is introduced into the sublimator which is heated to 40-75° C. A mass flow controller is employed to control the flow of the mixed gas/precursor into the reactor.
- Copper deposition is carried out using argon (Ar) and hydrogen (H 2 ) as the carrier gases.
- the substrate 50 is heated to about 300-400° C., while the pressure during deposition ranges from about 1 torr to about 10 torr, at a gas flow range of about 30 sccm to about 55 sccm.
- CMP chemical mechanical polishing
- the selective deposition of copper by CVD that was described above is not the only method that could be employed for forming the conductive material 80 .
- copper can be selectively deposited by an electroless plating technique, which is more attractive than conventional electroplating methods.
- electroless plating According to studies done by Shacham-Diamand et al. printed in Copper electroless deposition technology for ultra - large - scale - integration ( ULSI ) metallization, Microelectronic Engineering, Vol. 33, pp. 47-58 (1997), the disclosure of which is incorporated by reference herein, elecroless plating has a very high selectivity, excellent step coverage and good via/trench filling because of the very thin seed layers formed by this method. Electroless plating is also more advantageous than electroplating because of the low cost of tools and materials.
- contact displacement copper deposition is used to first selectively activate the tungsten nitride diffusion barrier layer 72 , after which selective electroless copper deposition is employed to obtain a copper layer 81 (FIG. 15). Copper deposition by contact displacement offers the advantage of room temperature, which in turn allows many low dielectric constant organic and/or inorganic materials to be used as the material of choice for interlayer dielectrics, such as the intermetal dielectric layer 55 .
- excess copper formed above the surface of the intermetal dielectric layer 55 may be removed by either an etching or a polishing technique to form a copper dual damascene structure 200 illustrated in FIG. 16.
- CMP chemical mechanical polishing
- FIG. 14 and FIG. 16 respectively, it must be readily apparent to those skilled in the art that in fact any number of such copper dual damascene structures may be formed on the substrate 50 .
- the exemplary embodiments described above refer to the formation of a copper dual damascene structure 100 , 200
- the invention is further applicable to other types of damascene structures, for example triple damascene structures, as long as they include a tungsten nitride diffusion barrier layer and copper selectively deposited by the methods described in detail above.
- FIG. 17 illustrates a triple damascene structure 300 formed within the intermetal dielectric layer 55 and over the substrate 50 , and in which vias and trenches are filled simultaneously with the selectively deposited copper by the methods described above.
- the interconnect structure of the invention may be used in the upper layer metallization patterns of many integrated circuit devices including, but not limited to, memory devices and processors.
- FIG. 18 illustrates a typical processor-based system 400 which includes a memory circuit 448 , for example a DRAM memory circuit employing a plurality of DRAM memory devices.
- memory circuit 448 for example a DRAM memory circuit employing a plurality of DRAM memory devices.
- CPU central processing unit
- DRAM memory device may contain damascene structures, such as the copper damascene structures 100 , 200 , 300 fabricated according to the present invention.
- a processor system such as a computer system, generally comprises the central processing unit (CPU) 444 , such as a microprocessor, a digital signal processor, or other programmable digital logic devices, which communicates with an input/output (I/O) device 446 over a bus 452 .
- the memory 448 communicates with the system over bus 452 .
- the processor system may include peripheral devices such as a floppy disk drive 454 and a compact disk (CD) ROM drive 456 which also communicate with CPU 444 over the bus 452 .
- Memory 448 is preferably constructed as an integrated circuit, which includes one or more copper damascene structures 100 , 200 , 300 . If desired, the memory 448 may be combined with the processor, for example CPU 444 , in a single integrated circuit.
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Abstract
A copper damascene structure formed by direct patterning of a low-dielectric constant material is disclosed. The copper damascene structure includes a tungsten nitride barrier layer formed by atomic layer deposition using sequential deposition reactions. Copper is selectively deposited by a CVD process and/or by an electroless deposition technique.
Description
- The present invention relates to the field of semiconductors and, in particular, to a method of forming damascene structures in semiconductor devices.
- In an attempt to improve the performance, reliability and density of filly integrated ULSI (ultra-large scale integration) interconnects, the microelectronics industry has recently begun migrating away from the use of aluminum (Al) and/or its alloys for the ULSI interconnects. As such, advanced dual damascene processes have begun using copper (Cu) as the material of choice because copper has high conductivity, extremely low resistivity (about 1.7 μΩcm) and good resistance to electromigration. Unfortunately, copper diffuses rapidly through silicon dioxide (SiO2) or other interlayer dielectrics, such as polyimides and parylenes, and copper diffusion can destroy active devices, such as transistors and capacitors, formed in the IC substrate. In addition, metal adhesion to the underlying substrate materials must be excellent to form reliable interconnect structures but the adhesion of copper to interlayer dielectrics, particularly to SiO2, is generally poor.
- Another problem associated with dual damascene processing is the cost and complexity of the process. Advanced copper dual damascene processes include a two-step sequential mask/etch process to form a two-level structure, such as a via connected to a metal line situated above the via. As illustrated in FIG. 1, a known copper dual damascene process as applied to interconnect formation begins with the deposition of a first
insulating layer 14 over a first levelinterconnect copper layer 12, which in turn is formed over or within asemiconductor substrate 10. A secondinsulating layer 16 is next formed over the first insulatinglayer 14. Anetch stop layer 15 is typically formed between the first and secondinsulating layers insulating layer 16 is patterned by photolithography with a first mask (not shown) to form atrench 17 corresponding to a copper line of a second level interconnect. Theetch stop layer 15 prevents the upperlevel trench pattern 17 from being etched through the firstinsulating layer 14. - As illustrated in FIG. 2, a second masking step followed by an etch step are applied to form a via18 through the
etch stop layer 15 and thefirst insulating layer 14. After the etching is completed, both thetrench 17 and thevia 18 are filled withcopper material 20, as illustrated in FIG. 3. Typically, thecopper material 20 undergoes a chemical mechanical polishing (CMP) step to remove any copper material from above the secondinsulating layer 16 and to form, therefore, a copper damascene structure as illustrated in FIG. 4. The CMP step leaves thecopper damascene structure 25 with a copper planarized surface for subsequent metallization to build multi-level interconnects. - If desired, a second etch stop layer (not shown) may be formed between the
substrate 10 and the firstinsulating layer 14 during the formation of thecopper damascene structure 25. In any event, and in contrast to a single damascene process, the via and the trench are simultaneously filled with metal. Thus, although copper dual damascene process is more advantageous over the copper single damascene process, one big disadvantage remains the high number of sequential photoresist/mask/etch steps and etch-stop layers which, as described above, are conventionally used in damascene processing and which increase the fabrication cost and reduce the production yield. Another disadvantage is that copper deposition methods for conventional damascene processes employ a large amount of high-purity copper material, of which a considerable amount is removed and wasted by the CMP process described above with reference to FIGS. 3-4. Thus, even the dual damascene processing is very expensive and entails a large number of processing steps. - Accordingly, there is a need for an improved and simplified copper damascene process which reduces production costs and increases productivity. There is also a need for a method of increasing the adhesion of copper to underlying damascene layers as well as a method of decreasing copper diffusion in such layers.
- The present invention provides a method for fabricating a copper interconnect structure in a semiconductor device which requires fewer processing steps and reduces the diffusion of copper atoms to underlying damascene layers.
- In an exemplary embodiment, trenches and vias are formed by direct patterning of a low-dielectric constant material, subsequent to which a thin tungsten nitride (WN2) diffusion barrier layer is formed by an atomic layer deposition using sequential surface reactions inside the trenches and vias. A selective copper CVD process is used to fill in the trenches and vias with copper. In another exemplary embodiment, an electroless deposition technique is employed in lieu of the selective copper CVD process. This way, the sequential photoresist/mask/etch steps and the etch-stop layers are eliminated, while the diffusion of copper atoms into adjacent interconnect layers is suppressed.
- Additional advantages of the present invention will be more apparent from the detailed description and accompanying drawings, which illustrate preferred embodiments of the invention.
- FIG. 1 is a cross-sectional view of a conventional semiconductor device at a preliminary stage of production.
- FIG. 2 is a cross-sectional view of the semiconductor device of FIG. 1 at a subsequent stage of production.
- FIG. 3 is a cross-sectional view of the semiconductor device of FIG. 2 at a subsequent stage of production.
- FIG. 4 is a cross-sectional view of the semiconductor device of FIG. 3 at a subsequent stage of production.
- FIG. 5 is a cross-sectional view of a semiconductor device at a preliminary stage of production and in accordance with a first embodiment of the present invention.
- FIG. 6 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 7 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 8 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 9 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 10 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 11 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 12 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 13 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 14 is a cross-sectional view of the semiconductor device of FIG. 5 at a subsequent stage of production.
- FIG. 15 is a cross-sectional view of a semiconductor device constructed in accordance with a second embodiment of the present invention.
- FIG. 16 is a cross-sectional view of the semiconductor device of FIG. 15 at a subsequent stage of production.
- FIG. 17 is a cross-sectional view of a semiconductor device constructed in accordance with a third embodiment of the present invention.
- FIG. 18 illustrates a computer system having a memory cell with a copper damascene structure according to the present invention.
- In the following detailed description, reference is made to various specific embodiments in which the invention may be practiced. These embodiments are described with sufficient detail to enable those skilled in the art to practice the invention, and it is to be understood that other embodiments may be employed, and that structural, electrical and process changes may be made without departing from the spirit or scope of the present invention.
- The term “substrate” used in the following description may include any semiconductor-based structure that has a semiconductor surface. The term should be understood to include silicon, silicon-on insulator (SOI), silicon-on sapphire (SOS), doped and undoped semiconductors, epitaxial layers of silicon supported by a base semiconductor foundation, and other semiconductor structures. The semiconductor need not be silicon-based. The semiconductor could be silicon-germanium, germanium, or gallium arsenide. When reference is made to a “substrate” in the following description, previous process steps may have been utilized to form regions or junctions in or on the base semiconductor or foundation.
- The term “copper” is intended to include not only elemental copper, but also copper with other trace metals or in various alloyed combinations with other metals as known in the art, as long as such alloy retains the physical and chemical properties of copper. The term “copper” is also intended to include conductive oxides of copper.
- Referring now to the drawings, where like elements are designated by like reference numerals, FIGS.5-17 illustrate the formation of copper
damascene structures insulating layer 51 formed over asemiconductor substrate 50, on or within which ametal layer 52 has been formed. Themetal layer 52 represents a lower metal interconnect layer which is to be later interconnected with an upper copper interconnect layer. Themetal layer 52 may be formed of copper (Cu), but other conductive materials, such as tungsten (W) or aluminum (Al) and their alloys, may be used also. - Referring now to FIG. 6, an
intermetal dielectric layer 55 is formed overlying the insulatinglayer 51 and themetal layer 52. In an exemplary embodiment of the present invention, theintermetal dielectric layer 55 is formed of a low-dielectric constant material to a thickness of about 2,000 Angstroms to 50,000 Angstroms, more preferably of about 5,000 Angstroms to 20,000 Angstroms. For the purposes of the present invention, a low-dielectric constant material is a material with a dielectric constant of less than about 4. - In a preferred embodiment of the invention, the
intermetal dielectric layer 55 is a low-dielectric constant material which can be directly patterned, without using a photoresist material, and which may be formed by a method described by Kikkawa in Current and Future Low-k Dielectrics for Cu Interconnects, Technical Digests of IEDM, pp. 253-56 (2000), the disclosure of which is incorporated by reference herein. Kikkawa has demonstrated that fabrication of photo-resistive low-dielectric constant films, such as methylsilsesquiazane (MSZ) films, can eliminate photoresist coating, dry etching and etch stop layers. According to recent experiments conducted by Kikkawa, vias and/or holes are formed in methylsilsesquiazane (MSZ) films by direct patterning, such as direct EB (electron beam) or UV (ultra violet) lithography, without using photoresist or dry etching. - According to the experiments conducted by Kikkawa, a methylsilsesquiazane (MSZ) film precursor is deposited on a silicon substrate by spin-coating at 2700 rpm and pre-baked at about 90° C. for about 10 minutes. EB lithography is subsequently carried out with doses of about 3 μC/cm2 to about 123 μC/cm2. Alternatively, UV (I-line) lithography is carried out with doses of about 45 mJ/cm2 to about 315 mJ/cm2. For either the UV or the EB lithography, moisture absorption is conducted at 25° C. and 50% relative humidity for about 10 minutes. Development of the methylsilsesquiazane (MSZ) film is then carried out in a tetra-methyl-ammonium hydroxide (TMAH) solution.
- If UV lithography is employed, the methylsilsesquiazane (MSZ) film undergoes curing at 400° C. in a nitrogen ambient to be subsequently transformed into a methylsilsesquioxane (MSQ) film. Kikkawa et al. have observed that, during curing at 400° C. in the nitrogen ambient, the methylsilsesquiazane (MSZ) film undergoes photochemical reactions so that the resulting methylsilsesquioxane (MSQ) film comprises no Si—N bonds and only Si—O and Si—CH3 bonds.
- Although low-dielectric constant materials such as the methylsilsesquiazane (MSZ) films are preferred, the present invention is not limited to these materials. Thus, the
intermetal dielectric layer 55 may be also formed of a conventional insulating oxide, such as silicon oxide (SiO2), or other low-dielectric constant materials such as, for example, polyimide, spin-on-polymers (SOP), parylene, flare, polyarylethers, polytetrafluoroethylene, benzocyclobutene (BCB), SILK, fluorinated silicon oxide (FSG), NANOGLASS or hydrogen silsesquioxane, which have dielectric constants of less than about 4. - Next, as illustrated in FIG. 7, a
first mask layer 58 having images of a viapattern 59 is formed over theintermetal dielectric layer 55 for direct patterning. Thus, as shown in FIG. 8, a via 65 may be formed by etching through theintermetal dielectric layer 55 with an etchant. The etchant (not shown) may be selected in accordance with the characteristics of theintermetal dielectric layer 55, so that the dielectric material is selectively etched until the etchant reaches themetal layer 52. As noted above, and according to a preferred embodiment, the etchant is a tetra-methyl-ammonium hydroxide (TMAH) solution. - After the formation of the via65 through the
intermetal dielectric layer 55, a trench 67 (FIG. 10) is formed by employing a second mask layer 62 (FIG. 9) having images of a trench pattern 63 (FIG. 9) over theintermetal dielectric layer 55. Thetrench pattern 63 is then etched into theintermetal dielectric layer 55 using themask layer 62 to formtrench 67, as shown in FIG. 10. The etching of thetrench 67 may be accomplished using the same etchant employed to form the via 65 (FIG. 8), which according to a preferred embodiment of the invention is a tetra-methyl-ammonium hydroxide (TMAH) solution. - As noted above, if the
intermetal dielectric layer 55 is formed of methylsilsesquiazane material and if UV lithography is employed, the methylsilsesquiazane (MSZ) material undergoes curing at 400° C. in a nitrogen ambient to be subsequently transformed into a methylsilsesquioxane (MSQ) film. - Subsequent to the formation of
trench 67, thesecond mask layer 62 is removed so that further steps to create the copper dual damascene structure 100 (FIG. 14) may be carried out. As such, a diffusion barrier layer 72 (FIG. 11) is formed on the via 65 and thetrench 67 to a thickness of about 50 Angstroms to about 200 Angstroms, more preferably of about 100 Angstroms. - In a preferred embodiment, the
diffusion barrier layer 72 is formed of tungsten nitride (WN2) by a method described by Klaus et al. in Atomic Layer Deposition of Tungsten Nitride Films Using Sequential Surface Reactions, J. of Electrochemical Soc., Vol. 147(3), pp. 1175-1181 (2000), the disclosure of which is incorporated by reference herein. Klaus et al. have demonstrated that tungsten nitride films deposited with atomic layer control using sequential surface reactions have a stoichiometry with low carbon (C) and oxygen (O) impurity concentrations which prevent the diffusion of copper at elevated temperatures. According to the atomic layer control using sequential surface reactions technique described by Klaus et al., tungsten nitride films are deposited at a temperature of about 600-800K using an initial treatment of 10 mTorr Si2H6 at 600K for about 5 minutes on a hydroxilated SiO2 surface. After the initial Si2H6 treatment, tungsten nitride film growth can be conducted at reactions temperatures between about 550-800K by employing, for example, cycles of WVF6 and NH3 to transform the SiO2 surface to a tungsten nitride surface. The tungsten nitride films formed by the above-described atomic layer control using sequential surface reactions technique have a microcrystalline structure and a remarkably flat surface indicating smooth film growth. - Although in a preferred embodiment of the invention the tungsten nitride
diffusion barrier layer 72 is simultaneously deposited in both the via 65 and the trench 67 (FIG. 11), the invention is not limited to this embodiment. Thus, the tungsten-nitridediffusion barrier layer 72 may be deposited first in the via 65 before the formation of thetrench 67, and then in thetrench 67 after its respective formation. In any event, after the formation of thediffusion barrier layer 72, horizontal portions of the tungsten nitride material formed above the surface of theintermetal dielectric layer 55 are removed by a light polishing technique to form the structure illustrated in FIG. 12. In a preferred embodiment of the present invention, a fight chemical mechanical polishing (CMP) is used to polish away excess tungsten-nitride material above theintermetal dielectric layer 55 and the trench level. This way, theintermetal dielectric layer 55 acts as a polishing stop layer when light CMP is used. - As illustrated in FIG. 13, a
conductive material 80 comprising copper (Cu) is next deposited to fill in both the via 65 and thetrench 67. In an exemplary embodiment, the copper is selectively deposited by CVD as described by Kaloyeros et al. in Blanket And Selective Copper CVD From Cu(fod)2 For Multilevel Metallization, Mat. Res. Soc. Symp. Proc., Vol. 181 (1990), the disclosure of which is incorporated by reference herein. Studies of blanket and selective low-temperature metal-organic chemical vapor deposition (LTMOCVD) of copper have been conducted by Kaloyeros et al. at 300-400° C. in an atmosphere of pure H2 or Ar from the β-diketonate precursor bis(6,6,7,8,8,8-heptafluoro-2,2-dimetyl 1-3,5-octanedino) copper (II), Cu (fod)2. According to one selective LTMOCVD technique proposed by Kaloyeros et al., the reactor is first pumped down to a base pressure of less than 5×10−7 torr. Subsequently, the source compound is introduced into the sublimator which is heated to 40-75° C. A mass flow controller is employed to control the flow of the mixed gas/precursor into the reactor. Copper deposition is carried out using argon (Ar) and hydrogen (H2) as the carrier gases. Thesubstrate 50 is heated to about 300-400° C., while the pressure during deposition ranges from about 1 torr to about 10 torr, at a gas flow range of about 30 sccm to about 55 sccm. - After the deposition of the
copper material 80, excess copper formed above the surface of theintermetal dielectric layer 55 may be removed by either an etching or a polishing technique to form the copperdual damascene structure 100 illustrated in FIG. 14. In a preferred embodiment of the present invention, chemical mechanical polishing (CMP) is used to polish away excess copper above theintermetal dielectric layer 55 and the trench level. This way, theintermetal dielectric layer 55 acts as a polishing stop layer when CMP is used. - The selective deposition of copper by CVD that was described above is not the only method that could be employed for forming the
conductive material 80. For example, according to another embodiment of the invention, copper can be selectively deposited by an electroless plating technique, which is more attractive than conventional electroplating methods. According to studies done by Shacham-Diamand et al. printed in Copper electroless deposition technology for ultra-large-scale-integration (ULSI) metallization, Microelectronic Engineering, Vol. 33, pp. 47-58 (1997), the disclosure of which is incorporated by reference herein, elecroless plating has a very high selectivity, excellent step coverage and good via/trench filling because of the very thin seed layers formed by this method. Electroless plating is also more advantageous than electroplating because of the low cost of tools and materials. - According to Shacham-Diamand et al., three practical seeding methods for the electroless deposition of copper could be used: (1) noble metal seeding, typically on gold, palladium or platinum; (2) copper seeding using an aluminum sacrificial layer; and (3) wet activation of surfaces using a contact displacement method. Shacham-Diamand et al. have successfully used the third method to deposit copper on Ti/TiN or TiN/AlCu at room temperature. Accordingly, in an exemplary embodiment of the present invention, contact displacement copper deposition is used to first selectively activate the tungsten nitride
diffusion barrier layer 72, after which selective electroless copper deposition is employed to obtain a copper layer 81 (FIG. 15). Copper deposition by contact displacement offers the advantage of room temperature, which in turn allows many low dielectric constant organic and/or inorganic materials to be used as the material of choice for interlayer dielectrics, such as theintermetal dielectric layer 55. - After the deposition of the copper material81 (FIG. 15), excess copper formed above the surface of the
intermetal dielectric layer 55 may be removed by either an etching or a polishing technique to form a copperdual damascene structure 200 illustrated in FIG. 16. In a preferred embodiment of the present invention, chemical mechanical polishing (CMP) is used to polish away excess copper above theintermetal dielectric layer 55 and the trench level. This way, theintermetal dielectric layer 55 acts as a polishing stop layer when CMP is used. - Although only one copper
dual damascene structure substrate 50. Also, although the exemplary embodiments described above refer to the formation of a copperdual damascene structure damascene structure 300 formed within theintermetal dielectric layer 55 and over thesubstrate 50, and in which vias and trenches are filled simultaneously with the selectively deposited copper by the methods described above. - In addition, further steps to create a functional semiconductor circuit structure may be carried out. Thus, additional multilevel interconnect layers and associated dielectric layers could be formed to create operative electrical paths from any of the
copper damascene structures substrate 50. - The interconnect structure of the invention may be used in the upper layer metallization patterns of many integrated circuit devices including, but not limited to, memory devices and processors. FIG. 18 illustrates a typical processor-based
system 400 which includes amemory circuit 448, for example a DRAM memory circuit employing a plurality of DRAM memory devices. One or both of central processing unit (CPU) 444 and the DRAM memory device may contain damascene structures, such as thecopper damascene structures device 446 over abus 452. Thememory 448 communicates with the system overbus 452. - In the case of a computer system, the processor system may include peripheral devices such as a
floppy disk drive 454 and a compact disk (CD)ROM drive 456 which also communicate withCPU 444 over thebus 452.Memory 448 is preferably constructed as an integrated circuit, which includes one or morecopper damascene structures memory 448 may be combined with the processor, forexample CPU 444, in a single integrated circuit. - The above description and drawings are only to be considered illustrative of exemplary embodiments which achieve the features and advantages of the present invention. Modification and substitutions to specific process conditions and structures can be made without departing from the spirit and scope of the present invention. Accordingly, the invention is not to be considered as being limited by the foregoing description and drawings, but is only limited by the scope of the appended claims.
Claims (45)
1. A method of forming a copper damascene structure, said method comprising the steps of:
directly patterning a low-dielectric constant layer to form at least one opening through said low-dielectric constant layer;
forming a tungsten nitride layer by atomic-layer deposition using sequential surface reactions, said tungsten nitride layer being in contact with said at least one opening; and
providing a copper layer in said at least one opening.
2. The method of claim 1 , wherein said low-dielectric constant layer includes a material selected from the group consisting of methylsilsequiazane, polyimide, spin-on-polymers, flare, polyarylethers, parylene, polytetrafluoroethylene, benzocyclobutene, SILK, fluorinated silicon oxide, hydrogen silsesquioxane and NANOGLASS.
3. The method of claim 1 , wherein said low-dielectric constant layer comprises methylsilsequiazane.
4. The method of claim 3 , wherein said step of forming said at least one opening further comprises patterning said low-dielectric constant layer.
5. The method of claim 4 , wherein said step of patterning said low-dielectric constant layer further comprises exposing said low-dielectric constant layer to an electron beam or ultra violet light.
6. The method of claim 5 , wherein said step of forming said at least one opening further comprises etching said low-dielectric constant layer with a tetramethyl-ammonium hydroxide solution.
7. The method of claim 3 , wherein said low-dielectric constant layer is formed by spin coating to a thickness of about 2,000 to 50,000 Angstroms.
8. The method of claim 7 , wherein said low-dielectric constant layer is formed by spin coating to a thickness of about 5,000 to 20,000 Angstroms.
9. The method of claim 1 , wherein said tungsten nitride layer is formed at a temperature of about 550-800K.
10. The method of claim 1 , wherein said copper layer is selectively deposited by chemical vapor deposition.
11. The method of claim 10 , wherein said copper layer is selectively deposited at a temperature of about 300° C. to about 400° C.
12. The method of claim 11 , wherein said copper layer is selectively deposited in an atmosphere of pure hydrogen from the β-diketonate precursor bis(6,6,7,8,8,8-heptafluoro-2,2-dimetyl 1-3,5-octanedino) copper (II).
13. The method of claim 11 , wherein said copper layer is selectively deposited in an atmosphere of pure argon from the β-diketonate precursor bis(6,6,7,8,8,8-heptafluoro-2,2-dimetyl 1-3,5-octanedino) copper (II).
14. The method of claim 1 , wherein said copper layer is formed by electroless deposition.
15. The method of claim 1 further comprising the act of chemical mechanical polishing said tungsten nitride layer.
16. The method of claim 1 further comprising the act of chemical mechanical polishing said copper layer.
17. A method of forming a copper damascene structure, said method comprising the steps of:
forming a material layer of methylsilsequiazane over a substrate;
forming at least one opening through said methylsilsequiazane layer;
forming a tungsten nitride layer by atomic-layer deposition using sequential surface reactions, said tungsten nitride layer being in contact with said at least one opening; and
providing a copper layer in said at least one opening.
18. The method of claim 17 , wherein said step of forming said at least one opening further comprises directly patterning said methylsilsequiazane layer with a mask to form said at least one opening.
19. The method of claim 18 , wherein said step of directly patterning said methylsilsequiazane layer further comprises exposing said methylsilsequiazane layer to an electron beam or ultra violet light.
20. The method of claim 19 , wherein said step of forming said at least one opening further comprises etching said methylsilsequiazane layer with a tetramethyl-ammonium hydroxide solution.
21. The method of claim 17 , wherein said methylsilsequiazane layer is formed by spin coating to a thickness of about 21,000 to 50,000 Angstroms.
22. The method of claim 21 , wherein said methylsilsequiazane layer is formed by spin coating to a thickness of about 5,000 to 20,000 Angstroms.
23. The method of claim 17 , wherein said tungsten nitride layer is formed at a temperature of about 550-800K.
24. The method of claim 17 , wherein said copper layer is selectively deposited by chemical vapor deposition.
25. The method of claim 24 , wherein said copper layer is selectively deposited at a temperature of about 300° C. to about 400° C.
26. The method of claim 25 , wherein said copper layer is selectively deposited in an atmosphere of pure hydrogen from the β-diketonate precursor bis(6,6,7,8,8,8-heptafluoro-2,2-dimetyl 1-3,5-octanedino) copper (II).
27. The method of claim 25 , wherein said copper layer is selectively deposited in an atmosphere of pure argon from the β-diketonate precursor bis(6,6,7,8,8,8-heptafluoro-2,2-dimetyl 1-3,5-octanedino) copper (II).
28. The method of claim 17 , wherein said copper layer is formed by electroless deposition.
29. The method of claim 17 further comprising the act of chemical mechanical polishing said tungsten nitride layer.
30. The method of claim 17 further comprising the act of chemical mechanical polishing said copper layer.
31. A dual damascene structure comprising:
a substrate;
a metal layer provided within said substrate;
a methylsilsequiazane layer located over said substrate;
a via situated within said methylsilsequiazane layer and extending to at least a portion of said metal layer, said via being lined with a tungsten nitride layer and filled with a copper material; and
a trench situated within said methylsilsequiazane layer and extending to said via, said trench being lined with said tungsten nitride layer and filled with said copper material.
32. The dual damascene structure of claim 31 , wherein said methylsilsequiazane layer has a thickness of about 2,000 to 50,000 Angstroms.
33. The dual damascene structure of claim 31 , wherein said tungsten nitride layer has a thickness of about 50 to 200 Angstroms.
34. The dual damascene structure of claim 31 , wherein said tungsten nitride layer is a sequential atomic layer deposition tungsten nitride layer.
35. The dual damascene structure of claim 31 , wherein said substrate is a semiconductor substrate.
36. The dual damascene structure of claim 31 , wherein said substrate is a silicon substrate.
37. A damascene structure comprising:
a substrate;
a metal layer provided within said substrate;
a methylsilsequiazane layer located over said substrate; and
at least one opening situated within said methylsilsequiazane layer and extending to at least a portion of said metal layer, said opening being lined with a tungsten nitride layer and filled with a copper material.
38. The damascene structure of claim 37 , wherein said methylsilsequiazane layer has a thickness of about 2,000 to 50,000 Angstroms.
39. The damascene structure of claim 37 , wherein said tungsten nitride layer has a thickness of about 50 Angstroms to about 200 Angstroms.
40. The damascene structure of claim 37 , wherein said tungsten nitride layer is a sequential atomic layer deposition tungsten nitride layer.
41. The damascene structure of claim 37 , wherein said copper material includes copper or a copper alloy.
42. The damascene structure of claim 37 , wherein said substrate is a semiconductor substrate.
43. The damascene structure of claim 37 , wherein said substrate is a silicon substrate.
44. A processor-based system comprising:
a processor; and
an integrated circuit coupled to said processor, at least one of said processor and integrated circuit including a damascene structure, said damascene structure comprising a metal layer over a substrate, a methylsilsequiazane layer over said metal layer, and at least one opening situated within said methylsilsequiazane layer and extending to at least a portion of said metal layer, said opening being lined with a tungsten nitride layer and filled with copper.
45. The processor-based system of claim 44 , wherein said processor and said integrated circuit are integrated on same chip.
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US6673698B1 (en) | 2002-01-19 | 2004-01-06 | Megic Corporation | Thin film semiconductor package utilizing a glass substrate with composite polymer/metal interconnect layers |
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TW503496B (en) | 2001-12-31 | 2002-09-21 | Megic Corp | Chip packaging structure and manufacturing process of the same |
US6716741B2 (en) * | 2002-04-09 | 2004-04-06 | United Microelectronics Corp. | Method of patterning dielectric layer with low dielectric constant |
US7221017B2 (en) | 2002-07-08 | 2007-05-22 | Micron Technology, Inc. | Memory utilizing oxide-conductor nanolaminates |
US6884739B2 (en) | 2002-08-15 | 2005-04-26 | Micron Technology Inc. | Lanthanide doped TiOx dielectric films by plasma oxidation |
US7199023B2 (en) | 2002-08-28 | 2007-04-03 | Micron Technology, Inc. | Atomic layer deposited HfSiON dielectric films wherein each precursor is independendently pulsed |
US7084078B2 (en) | 2002-08-29 | 2006-08-01 | Micron Technology, Inc. | Atomic layer deposited lanthanide doped TiOx dielectric films |
JP2004146691A (en) * | 2002-10-25 | 2004-05-20 | Chi Mei Electronics Corp | Method for forming microcrystalline thin film, method for manufacturing thin film transistor, thin film transistor, and image display device using thin film transistor |
FR2858876B1 (en) * | 2003-08-12 | 2006-03-03 | St Microelectronics Sa | METHOD FOR FORMATION UNDER A THIN LAYER OF A FIRST MATERIAL OF PORTIONS OF ANOTHER MATERIAL AND / OR VACUUM ZONES |
US7208837B2 (en) * | 2004-02-10 | 2007-04-24 | United Microelectronics Corp. | Semiconductor chip capable of implementing wire bonding over active circuits |
US6900541B1 (en) * | 2004-02-10 | 2005-05-31 | United Microelectronics Corp. | Semiconductor chip capable of implementing wire bonding over active circuits |
US7601649B2 (en) | 2004-08-02 | 2009-10-13 | Micron Technology, Inc. | Zirconium-doped tantalum oxide films |
US7081421B2 (en) | 2004-08-26 | 2006-07-25 | Micron Technology, Inc. | Lanthanide oxide dielectric layer |
US7378342B2 (en) * | 2004-08-27 | 2008-05-27 | Micron Technology, Inc. | Methods for forming vias varying lateral dimensions |
US7494939B2 (en) | 2004-08-31 | 2009-02-24 | Micron Technology, Inc. | Methods for forming a lanthanum-metal oxide dielectric layer |
US7235501B2 (en) | 2004-12-13 | 2007-06-26 | Micron Technology, Inc. | Lanthanum hafnium oxide dielectrics |
US7560395B2 (en) | 2005-01-05 | 2009-07-14 | Micron Technology, Inc. | Atomic layer deposited hafnium tantalum oxide dielectrics |
US7374964B2 (en) | 2005-02-10 | 2008-05-20 | Micron Technology, Inc. | Atomic layer deposition of CeO2/Al2O3 films as gate dielectrics |
US7687409B2 (en) | 2005-03-29 | 2010-03-30 | Micron Technology, Inc. | Atomic layer deposited titanium silicon oxide films |
US7160802B2 (en) * | 2005-06-06 | 2007-01-09 | Novellus Systems, Inc. | Adhesion of tungsten nitride films to a silicon surface |
US8110469B2 (en) | 2005-08-30 | 2012-02-07 | Micron Technology, Inc. | Graded dielectric layers |
US8071476B2 (en) | 2005-08-31 | 2011-12-06 | Micron Technology, Inc. | Cobalt titanium oxide dielectric films |
US8368220B2 (en) * | 2005-10-18 | 2013-02-05 | Taiwan Semiconductor Manufacturing Co. Ltd. | Anchored damascene structures |
US7709402B2 (en) | 2006-02-16 | 2010-05-04 | Micron Technology, Inc. | Conductive layers for hafnium silicon oxynitride films |
TWI299896B (en) * | 2006-03-16 | 2008-08-11 | Advanced Semiconductor Eng | Method for forming metal bumps |
JP2008085175A (en) * | 2006-09-28 | 2008-04-10 | Tokyo Electron Ltd | Semiconductor device manufacturing method, semiconductor device, substrate processing system, program, and storage medium |
US7601604B2 (en) * | 2006-10-12 | 2009-10-13 | Atmel Corporation | Method for fabricating conducting plates for a high-Q MIM capacitor |
US10199267B2 (en) * | 2017-06-30 | 2019-02-05 | Lam Research Corporation | Tungsten nitride barrier layer deposition |
CN114203557A (en) * | 2021-11-23 | 2022-03-18 | 江苏东海半导体科技有限公司 | Semiconductor device manufacturing method, semiconductor device manufacturing apparatus and storage medium |
Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5451551A (en) * | 1993-06-09 | 1995-09-19 | Krishnan; Ajay | Multilevel metallization process using polishing |
US6010962A (en) * | 1999-02-12 | 2000-01-04 | Taiwan Semiconductor Manufacturing Company | Copper chemical-mechanical-polishing (CMP) dishing |
US6040243A (en) * | 1999-09-20 | 2000-03-21 | Chartered Semiconductor Manufacturing Ltd. | Method to form copper damascene interconnects using a reverse barrier metal scheme to eliminate copper diffusion |
US6110648A (en) * | 1998-09-17 | 2000-08-29 | Taiwan Semiconductor Manufacturing Company | Method of enclosing copper conductor in a dual damascene process |
US6297158B1 (en) * | 2000-05-31 | 2001-10-02 | Taiwan Semiconductor Manufacturing Company | Stress management of barrier metal for resolving CU line corrosion |
US20010036739A1 (en) * | 1999-05-13 | 2001-11-01 | Robert Cook | Interim oxidation of silsesquioxane dielectric for dual damascene process |
US6313028B2 (en) * | 1999-03-05 | 2001-11-06 | United Microelectronics Corp. | Method of fabricating dual damascene structure |
US20020009880A1 (en) * | 1999-08-27 | 2002-01-24 | Qing-Tang Jiang | Metal barrier for copper interconnects that incorporates silicon in the metal barrier or at the copper/metal barrier interface |
US6352938B2 (en) * | 1999-12-09 | 2002-03-05 | United Microelectronics Corp. | Method of removing photoresist and reducing native oxide in dual damascene copper process |
US6368954B1 (en) * | 2000-07-28 | 2002-04-09 | Advanced Micro Devices, Inc. | Method of copper interconnect formation using atomic layer copper deposition |
US20020048931A1 (en) * | 2000-08-28 | 2002-04-25 | Farrar Paul A. | Damascene structure and method of making |
US6380083B1 (en) * | 1998-08-28 | 2002-04-30 | Agere Systems Guardian Corp. | Process for semiconductor device fabrication having copper interconnects |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001217242A (en) | 2000-02-03 | 2001-08-10 | Seiko Epson Corp | Semiconductor device and method of manufacturing the same |
US6531777B1 (en) | 2000-06-22 | 2003-03-11 | Advanced Micro Devices, Inc. | Barrier metal integrity testing using a dual level line to line leakage testing pattern and partial CMP |
US6395632B1 (en) | 2000-08-31 | 2002-05-28 | Micron Technology, Inc. | Etch stop in damascene interconnect structure and method of making |
-
2001
- 2001-07-24 US US09/910,914 patent/US6919266B2/en not_active Expired - Fee Related
-
2002
- 2002-04-01 US US10/109,713 patent/US20030020169A1/en not_active Abandoned
Patent Citations (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5451551A (en) * | 1993-06-09 | 1995-09-19 | Krishnan; Ajay | Multilevel metallization process using polishing |
US6380083B1 (en) * | 1998-08-28 | 2002-04-30 | Agere Systems Guardian Corp. | Process for semiconductor device fabrication having copper interconnects |
US6110648A (en) * | 1998-09-17 | 2000-08-29 | Taiwan Semiconductor Manufacturing Company | Method of enclosing copper conductor in a dual damascene process |
US6010962A (en) * | 1999-02-12 | 2000-01-04 | Taiwan Semiconductor Manufacturing Company | Copper chemical-mechanical-polishing (CMP) dishing |
US6313028B2 (en) * | 1999-03-05 | 2001-11-06 | United Microelectronics Corp. | Method of fabricating dual damascene structure |
US20010036739A1 (en) * | 1999-05-13 | 2001-11-01 | Robert Cook | Interim oxidation of silsesquioxane dielectric for dual damascene process |
US20020009880A1 (en) * | 1999-08-27 | 2002-01-24 | Qing-Tang Jiang | Metal barrier for copper interconnects that incorporates silicon in the metal barrier or at the copper/metal barrier interface |
US6040243A (en) * | 1999-09-20 | 2000-03-21 | Chartered Semiconductor Manufacturing Ltd. | Method to form copper damascene interconnects using a reverse barrier metal scheme to eliminate copper diffusion |
US6352938B2 (en) * | 1999-12-09 | 2002-03-05 | United Microelectronics Corp. | Method of removing photoresist and reducing native oxide in dual damascene copper process |
US6297158B1 (en) * | 2000-05-31 | 2001-10-02 | Taiwan Semiconductor Manufacturing Company | Stress management of barrier metal for resolving CU line corrosion |
US6368954B1 (en) * | 2000-07-28 | 2002-04-09 | Advanced Micro Devices, Inc. | Method of copper interconnect formation using atomic layer copper deposition |
US20020048931A1 (en) * | 2000-08-28 | 2002-04-25 | Farrar Paul A. | Damascene structure and method of making |
Cited By (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6852167B2 (en) | 2001-03-01 | 2005-02-08 | Micron Technology, Inc. | Methods, systems, and apparatus for uniform chemical-vapor depositions |
US7410668B2 (en) | 2001-03-01 | 2008-08-12 | Micron Technology, Inc. | Methods, systems, and apparatus for uniform chemical-vapor depositions |
US20050087134A1 (en) * | 2001-03-01 | 2005-04-28 | Micron Technology, Inc. | Methods, systems, and apparatus for uniform chemical-vapor depositions |
US20020122885A1 (en) * | 2001-03-01 | 2002-09-05 | Micron Technology, Inc. | Methods, systems, and apparatus for uniform chemical-vapor depositions |
US20060000412A1 (en) * | 2002-05-02 | 2006-01-05 | Micron Technology, Inc. | Systems and apparatus for atomic-layer deposition |
US20030207032A1 (en) * | 2002-05-02 | 2003-11-06 | Micron Technology, Inc. | Methods, systems, and apparatus for atomic-layer deposition of aluminum oxides in integrated circuits |
US7670646B2 (en) | 2002-05-02 | 2010-03-02 | Micron Technology, Inc. | Methods for atomic-layer deposition |
US20050023584A1 (en) * | 2002-05-02 | 2005-02-03 | Micron Technology, Inc. | Atomic layer deposition and conversion |
US7160577B2 (en) | 2002-05-02 | 2007-01-09 | Micron Technology, Inc. | Methods for atomic-layer deposition of aluminum oxides in integrated circuits |
US7560793B2 (en) | 2002-05-02 | 2009-07-14 | Micron Technology, Inc. | Atomic layer deposition and conversion |
US7589029B2 (en) | 2002-05-02 | 2009-09-15 | Micron Technology, Inc. | Atomic layer deposition and conversion |
US8093638B2 (en) | 2002-06-05 | 2012-01-10 | Micron Technology, Inc. | Systems with a gate dielectric having multiple lanthanide oxide layers |
US20050023624A1 (en) * | 2002-06-05 | 2005-02-03 | Micron Technology, Inc. | Atomic layer-deposited HfAlO3 films for gate dielectrics |
US20050023594A1 (en) * | 2002-06-05 | 2005-02-03 | Micron Technology, Inc. | Pr2O3-based la-oxide gate dielectrics |
US20030227033A1 (en) * | 2002-06-05 | 2003-12-11 | Micron Technology, Inc. | Atomic layer-deposited HfA1O3 films for gate dielectrics |
US7554161B2 (en) | 2002-06-05 | 2009-06-30 | Micron Technology, Inc. | HfAlO3 films for gate dielectrics |
US7205218B2 (en) | 2002-06-05 | 2007-04-17 | Micron Technology, Inc. | Method including forming gate dielectrics having multiple lanthanide oxide layers |
US8228725B2 (en) | 2002-07-08 | 2012-07-24 | Micron Technology, Inc. | Memory utilizing oxide nanolaminates |
US20100244122A1 (en) * | 2002-07-08 | 2010-09-30 | Leonard Forbes | Memory utilizing oxide nanolaminates |
US7728626B2 (en) | 2002-07-08 | 2010-06-01 | Micron Technology, Inc. | Memory utilizing oxide nanolaminates |
US8125038B2 (en) | 2002-07-30 | 2012-02-28 | Micron Technology, Inc. | Nanolaminates of hafnium oxide and zirconium oxide |
US20050277256A1 (en) * | 2002-07-30 | 2005-12-15 | Micron Technology, Inc. | Nanolaminates of hafnium oxide and zirconium oxide |
US7405454B2 (en) | 2003-03-04 | 2008-07-29 | Micron Technology, Inc. | Electronic apparatus with deposited dielectric layers |
US20070059881A1 (en) * | 2003-03-31 | 2007-03-15 | Micron Technology, Inc. | Atomic layer deposited zirconium aluminum oxide |
US7625794B2 (en) | 2003-03-31 | 2009-12-01 | Micron Technology, Inc. | Methods of forming zirconium aluminum oxide |
US20060261397A1 (en) * | 2003-06-24 | 2006-11-23 | Micron Technology, Inc. | Lanthanide oxide/hafnium oxide dielectric layers |
US7312494B2 (en) | 2003-06-24 | 2007-12-25 | Micron Technology, Inc. | Lanthanide oxide / hafnium oxide dielectric layers |
US7129553B2 (en) | 2003-06-24 | 2006-10-31 | Micron Technology, Inc. | Lanthanide oxide/hafnium oxide dielectrics |
US20050029547A1 (en) * | 2003-06-24 | 2005-02-10 | Micron Technology, Inc. | Lanthanide oxide / hafnium oxide dielectric layers |
US20050023626A1 (en) * | 2003-06-24 | 2005-02-03 | Micron Technology, Inc. | Lanthanide oxide / hafnium oxide dielectrics |
US7588988B2 (en) | 2004-08-31 | 2009-09-15 | Micron Technology, Inc. | Method of forming apparatus having oxide films formed using atomic layer deposition |
US8541276B2 (en) | 2004-08-31 | 2013-09-24 | Micron Technology, Inc. | Methods of forming an insulating metal oxide |
US20070090441A1 (en) * | 2004-08-31 | 2007-04-26 | Micron Technology, Inc. | Titanium aluminum oxide films |
US20060043504A1 (en) * | 2004-08-31 | 2006-03-02 | Micron Technology, Inc. | Atomic layer deposited titanium aluminum oxide films |
US8154066B2 (en) | 2004-08-31 | 2012-04-10 | Micron Technology, Inc. | Titanium aluminum oxide films |
US20060141777A1 (en) * | 2004-12-23 | 2006-06-29 | Yeong-Sil Kim | Methods for patterning a layer of a semiconductor device |
US20060244082A1 (en) * | 2005-04-28 | 2006-11-02 | Micron Technology, Inc. | Atomic layer desposition of a ruthenium layer to a lanthanide oxide dielectric layer |
US7662729B2 (en) | 2005-04-28 | 2010-02-16 | Micron Technology, Inc. | Atomic layer deposition of a ruthenium layer to a lanthanide oxide dielectric layer |
US7572695B2 (en) | 2005-05-27 | 2009-08-11 | Micron Technology, Inc. | Hafnium titanium oxide films |
US20070090439A1 (en) * | 2005-05-27 | 2007-04-26 | Micron Technology, Inc. | Hafnium titanium oxide films |
US7700989B2 (en) | 2005-05-27 | 2010-04-20 | Micron Technology, Inc. | Hafnium titanium oxide films |
US20060270147A1 (en) * | 2005-05-27 | 2006-11-30 | Micron Technology, Inc. | Hafnium titanium oxide films |
US8501563B2 (en) | 2005-07-20 | 2013-08-06 | Micron Technology, Inc. | Devices with nanocrystals and methods of formation |
US8921914B2 (en) | 2005-07-20 | 2014-12-30 | Micron Technology, Inc. | Devices with nanocrystals and methods of formation |
US20070049023A1 (en) * | 2005-08-29 | 2007-03-01 | Micron Technology, Inc. | Zirconium-doped gadolinium oxide films |
US20070048926A1 (en) * | 2005-08-31 | 2007-03-01 | Micron Technology, Inc. | Lanthanum aluminum oxynitride dielectric films |
US20070090440A1 (en) * | 2005-08-31 | 2007-04-26 | Micron Technology, Inc. | Lanthanum aluminum oxynitride dielectric films |
US7531869B2 (en) | 2005-08-31 | 2009-05-12 | Micron Technology, Inc. | Lanthanum aluminum oxynitride dielectric films |
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