This disclosure generally relates to forming an interconnect structure in a semiconductor device, such as a transistor device. Certain aspects of this disclosure pertain to forming an ohmic contact by depositing an interfacial dielectric between a metal and semiconductor in the source and drain regions of the semiconductor device.
In integrated circuit (IC) manufacturing, semiconductor devices such as the transistors are fabricated on a silicon substrate and then connected together to perform the desired circuit functions. This connection process is generally called “metallization”, and can be performed using a number of photolithographic patterning, etching, and deposition steps.
To form the connections, metallization layers include vias and interconnect structures that function as electrical pathways to interconnect the semiconductor devices. In the metallization layers, the interconnect structures and vias form a contact with the substrate to form a metal-semiconductor contact. However, direct metal to semiconductor contact may be highly resistive. As devices scale smaller and smaller, such resistivity can be highly undesirable.
This disclosure pertains to a method and apparatus for manufacturing an interconnect structure in a semiconductor device. The method can include providing the semiconductor device, such as a transistor. The semiconductor device includes a substrate, a gate dielectric over the substrate, a gate electrode over the gate dielectric, and source and drain regions in the substrate and on laterally opposite sides of the gate electrode. In certain implementations, a method can proceed by depositing by chemical vapor deposition (CVD) an interfacial dielectric over the source and drain regions of the substrate, depositing a pre-metal dielectric over the interfacial dielectric, forming one or more vias through the pre-metal dielectric over the source and drain regions of the substrate, and depositing by CVD a metal over the interfacial dielectric. In other implementations, a method can proceed by depositing a pre-metal dielectric over the substrate, forming one or more vias through the pre-metal dielectric over the source and drain regions of the substrate, depositing by CVD an interfacial dielectric over the source and drain regions of the substrate, and depositing by CVD a metal over the interfacial dielectric. In some embodiments, the method can further include depositing a barrier, adhesion, or nucleation layer by CVD between the metal and the interfacial dielectric.
This disclosure also pertains to an apparatus, such as an integrated process tool, with a controller configured with instructions for performing the aforementioned operations. In some aspects, the apparatus can include a wafer stepper. In some aspects, the apparatus can include modules for cleaning as well as modules for performing deposition steps, including deposition by CVD of the metal and/or interfacial dielectric. The deposition by CVD steps and/or the cleaning steps may be performed in an integrated process tool without introducing a vacuum break. In some embodiments, the cleaning step can be a chemical oxide removal step prior to depositing the interfacial dielectric.
In some embodiments, the interfacial dielectric is configured to unpin the metal Fermi level from the source or drain regions of the substrate. In some embodiments, the interfacial dielectric has a thickness between about 3 Å and about 20 Å. In some embodiments, the interfacial dielectric can include at least one of titanium oxide, strontium titanium oxide, zinc oxide, tantalum oxide, lanthanum oxide, zinc sulfide, zinc selenide, germanium oxide, cadmium oxide, and tin oxide. In some embodiments, the interfacial dielectric has an energy bandgap of greater than about 2.0 eV.
In the following description, numerous specific details are set forth in order to provide a thorough understanding of the presented concepts. The presented concepts may be practiced without some or all of these specific details. In other instances, well known process operations have not been described in detail so as to not unnecessarily obscure the described concepts. While some concepts will be described in conjunction with the specific embodiments, it will be understood that these embodiments are not intended to be limiting.
Introduction
Although the present invention may be used in a variety of applications, one very useful application is in transistors, such as metal oxide semiconductor (MOS) field-effect transistors. MOS transistors can include two types: negative channel metal oxide semiconductor (NMOS) transistors and positive channel metal oxide semiconductor (PMOS) transistors. The transistors and other devices may be interconnected using interconnect structures to form. ICs.
The metal-semiconductor junction between the electrical contacts 150 and the source and drain regions 104a and 104b of the substrate 102 create a Schottky barrier. The Schottky barrier enables high switching speeds and low voltage drops compared to a p-n junction. A Schottky barrier contact that does not rectify current may be referred to as an ohmic contact. Electrical resistance in an ohmic contact can be reduced by forming a silicide or germanide at the metal-semiconductor interface of the Schottky barrier.
Forming a silicide or germanide between the metal and the semiconductor can require several steps. First, the surface of the substrate 102 may be pre-cleaned prior to deposition of any metals to form the silicide or germanide. Next, a metal may be deposited over the source and drain regions 104a and 104b of the substrate 102. The metals can include any metal that is capable of reacting with silicon or germanium to form a silicide or germanide layer 105, respectively. Examples of such metals include titanium (Ti), tantalum (Ta), tungsten (W), cobalt (Co), nickel (Ni), platinum (Pt), palladium (Pd), and alloys thereof. Deposition of the metals can be achieved using conventional deposition techniques, such as chemical vapor deposition (CVD), physical vapor deposition (PVD), sputtering, evaporation, plating, and the like. Then, the metal may be annealed to form the silicide or germanide layers 105 using annealing techniques such as rapid thermal processing (RTP) anneal or laser anneal. The annealing can be performed at a temperature between about 300° C. and about 3000° C. Upon formation of the silicide after annealing, unreacted metal portions may be etched away using conventional etching techniques. Any of these steps may be repeated to form the silicide or germanide layers 105.
The aforementioned steps can significantly add to the cost and complexity of processing in forming an interconnect structure. Moreover, as semiconductor devices get smaller and smaller, there is less semiconductor material available to form a silicide and germanide. It is also possible for the formation of a silicide and germanide to impart strain on the semiconductor device.
When a metal is electrically in contact with a semiconductor, the work required to go from the metal Fermi level to the carrier band edge of the semiconductor can describe the Schottky barrier height ΦB. The Schottky barrier height ΦB is directly proportional with the contact resistance at the metal-semiconductor interface.
Introduction of a silicide or germanide layer is one approach that can reduce the Schottky barrier height ΦB. However, the Schottky barrier height ΦB can be reduced only to a certain extent because of the effect of Fermi level pinning
The interfacial dielectric layer 320 may be formed of any insulating material, such as a dielectric material. The dielectric material can include at least one of hafnium oxide (HfO2), aluminum oxide (Al2O3), zirconium oxide (ZrO2), silicon nitride (Si3N4), silicon oxide (SiO2), silicon oxynitride (SiON), titanium oxide (TiO2), strontium titanium oxide (SrTiO3), zinc oxide (ZnO), tantalum oxide (Ta2O5), lanthanum oxide (La2O3), zinc sulfide (ZnS), zinc selenide (ZnSe), germanium oxide (GeO2), cadmium oxide (CdO), tin oxide (SnO2), and other suitable insulating dielectric materials. The choice of the dielectric material may have a sufficiently high energy bandgap so that the insulator itself does not pin the metal Fermi level. For example, the dielectric material can have an energy bandgap that is greater than about 2.0 eV. In addition, the choice of the dielectric material may have a sufficiently high dielectric constant. For example, the dielectric material can have a dielectric constant greater than about 5, such as between about 5 and 300. In some embodiments, the dielectric material may be selected so that an electron effective mass is relatively low. For example, the dielectric material can have an electron effective mass of less than about 0.7.
The thickness of the interfacial dielectric layer 320 may be chosen to unpin the metal Fermi level from the source/drain regions 304 of the substrate 302. As a result, the thickness of the insulating layer 320 may be very thin. For example, the thickness of the interfacial dielectric layer 320 may be less than about 50 Å, such as between about 3 Å and about 20 Å, or such as between about 5 Å and about 10 Å. Without being limited by theory, the thickness of the interfacial dielectric layer may be tuned to balance the effects of resistance associated with the Schottky barrier and the resistance associated with electron tunneling.
Therefore, the composition and thickness of the interfacial dielectric layer 320 may be tuned to control the Schottky barrier height ΦB of a metal-semiconductor interface. By controlling the Schottky barrier height ΦB, transistor performance may be controlled. The interconnect structure as described with respect to
Process
A method of manufacturing an interconnect structure to provide an ohmic contact at a metal-semiconductor interface for a semiconductor device is provided. The method includes providing a semiconductor device, such as a transistor, that includes a gate dielectric, a gate electrode, and source and drain regions in a substrate. The substrate can include a semiconducting material, such as silicon. An interfacial dielectric may be deposited by CVD over the source and drain regions. As used herein, CVD can include any number of CVD processes practiced in a variety of different formats as is known in the art. For example, deposition by CVD can include a metal organic chemical vapor deposition (MOCVD) process in which the CVD process is based on metal organic precursors. As used herein, CVD can also refer to processes in which one or more vapor phase reactants are introduced into a deposition chamber for reaction or decomposition. For the purposes of this document, this includes CVD processes in which reactants are introduced simultaneously to the chamber and/or are in the vapor phase simultaneously in the chamber, as well as surface-mediated processes in which reactants are introduced sequentially. The latter may include atomic layer deposition (ALL)) and conformal film deposition (CFD) reactions. According to various implementations, the CVD processes may be thermal or plasma-enhanced, and can include plasma-enhanced CVD (PECVD) and plasma-enhanced ALD (PEALD) processes. Examples of CFD processes for depositing dielectric material can be described in U.S. application Ser. No. 13/084,399, U.S. application Ser. No. 13/084,305, and U.S. application Ser. No. 13/242,084, each incorporated by reference in its entirety and for all purposes.
The interfacial dielectric may have a thickness and composition that unpins the metal Fermi level from the source and drain regions of the substrate. Other materials and layers may be deposited also by CVD in manufacturing the interconnect structure, including depositing by CVD a pre-metal dielectric (PMD) layer and/or a metal layer. For example, the interfacial dielectric and the metal layer may be deposited without a vacuum break (e.g., air break). An air break can introduce oxidation into the semiconductor device, which can lead to higher electrical resistance and decreased transistor performance. In some embodiments, the interconnect structure may be manufactured in an integrated process tool, described in more detail below.
In
The semiconductor device 500 also includes a gate dielectric 506 over the substrate 502, and a gate electrode 508 over the gate dielectric 506. Source and drain regions 504a and 504b may be formed in the substrate 502 and on laterally opposite sides of the gate dielectric 506. In some embodiments, the source and drain regions 504a and 504b may be n-doped or p-doped, using doping processes as is known in the art. Spacers 510 may be formed on laterally opposite sides of the gate dielectric 506 and over the substrate 502.
The process 400 continues with step 410 where an interfacial dielectric is deposited by CND over the source and drain regions of the substrate. The interfacial dielectric may be conformally deposited over the semiconductor device and form a relatively thin layer of dielectric material. The interfacial dielectric may be selected to have a thickness and a composition to unpin a metal Fermi level from the source and drain regions of the substrate.
In some implementations, step 410 may include additional process operations. For example, prior to depositing the interfacial dielectric, the substrate surface may be cleaned. A wet cleaning or a dry plasma process may be used to remove unwanted contaminants and residue. Such processes may be used alone or in combination with each other. Afterwards, the interfacial dielectric may be deposited over a surface of the substrate that is substantially clean. Deposition of the interfacial dielectric and the cleaning step may be performed in an integrated apparatus without introducing a vacuum break.
In some implementations, the cleaning of the substrate surface may be accomplished using a chemical oxide removal. One exemplary process can include introducing hydrofluoric acid (HF) and ammonia (NH3) to interact with a native oxide (such as SiO2) and form a solid reaction product (such as ammonium hexafluorosilicate). As the reaction proceeds, the native oxide is consumed and the solid reaction product increases in thickness to form a diffusion barrier against the HF and the NH3. Thus, the chemical oxide removal process is a self-limiting process even as the time is increased.
After consuming the native oxide and forming the solid reaction product, the solid reaction product is sublimated at elevated temperatures. The substrate can be heated to an elevated temperature, such as between about 80° C. and about 150° C. to sublimate the solid reaction product. The chemical oxide removal process reduces edge roughness and provides substantially uniform “etching” on the substrate surface.
Returning to
Returning to
Returning to
The vias 540 are formed through the PMD layer 530 up to the interfacial dielectric 520. In some embodiments, the interfacial dielectric 520 serves as an etch stop layer. Instead of depositing a separate etch stop layer over the substrate 502 or using the substrate 502 itself as an etch stop, the interfacial dielectric 520 may function as an etch stop during formation of the vias 540 since many dielectric materials typically have highly selective etch chemistries.
Returning to
In some implementations, prior to depositing the metal over the interfacial dielectric, additional layers may be deposited over the interfacial dielectric. Such layers may include barrier, nucleation, and/or seed layers. Each of these layers may be formed using a conventional deposition method known in the art, such as CVD, and may each serve multiple functions. In some embodiments, the barrier layer may limit the diffusion of metal atoms into the interfacial dielectric and the PMD layer. In some embodiments, the adhesive layer may serve to promote the adhesion of metal onto the interfacial dielectric. In some embodiments, the nucleation layer may promote the nucleation of bulk metal over the interfacial dielectric.
The thickness of the adhesive, barrier, or nucleation layer may be relatively thin, such as less than about 500 Å. Materials for the adhesive, barrier, or nucleation layer can include but is not limited to ruthenium (Ru), rhodium (Rh), Pd, Ni, Co, Pt, Ti, Ta, W, titanium nitride (TiN), tantalum nitride (TaN), tungsten nitride (WN), zirconium (Zr), and hafnium (Hf). For example, a barrier layer over the interfacial dielectric can include TiN or WN. In some embodiments, the adhesive, barrier, or nucleation layer can include multiple layers of materials, such as combinations of some of the materials listed above.
In
In some implementations, the metal 550 includes W and forms a tungsten plug as an electrical contact. Formation of a tungsten plug may provide a low resistivity electrical contact. In some instances, the tungsten plug may be formed by depositing a thin barrier layer of WN, and then depositing bulk W to fill the via 540. The thin barrier layer of WN may be deposited using a pulsed nucleation layer (PNL) technique, and the bulk W may be deposited using CVD or a combination of PNL deposition and CVD. A description of depositing WN by a PNL process is described in U.S. Pat. No. 7,005,372, which is herein incorporated by reference for all purposes. In some instances, the tungsten plug may be formed by depositing bulk W into the via 540 without a nucleation layer. A description of depositing bulk W by CVD without a nucleation layer is described in U.S. patent application Ser. No. 13/560,688, which is herein incorporated by reference for all purposes. In some instances, the tungsten plug can be formed using a deposition-etch-deposition process to at least substantially fill the via 540 with W. A description of such a technique is described in U.S. Patent Publication No. 2012/0009785, which is herein incorporated by reference for all purposes.
In
The process 600 continues with step 610, where a PMD layer is deposited over the semiconductor device. Hence, deposition of the PMD layer may occur prior to the deposition of an interfacial dielectric. In some instances, an etch stop may be formed over the substrate prior to the deposition of the PMD layer. Step 610 may be similar to step 415 in the process 400.
The process 600 continues with step 615, where one or more vias are formed through the PMD layer over the source and drain regions of the substrate. Step 615 may be similar to step 425 in the process 400. In some embodiments, the removal of material from the PMD layer to form the one or more vias may require an etch stop over the substrate. In some embodiments, the substrate may not require an etch stop, such as in instances where the etchant is sufficiently selective to the PMD material over the substrate material.
Returning to
Returning to
Returning to
In
Apparatus
The methods presented herein may be carried out in various types of deposition apparatuses available from various vendors. Examples of a suitable apparatus include a Novellus Concept-1 ALTUS™, a Concept 2 ALTUS™, a Concept-2 ALTUS-S™, Concept 3 ALTUS™ deposition system, and ALTUS Max™ or any of a variety of other commercially available CVD tools. In some cases, the process can be performed on multiple deposition stations sequentially. A description can be found in, for example, U.S. Pat. No. 6,143,082, which is incorporated herein by reference for all purposes.
In some embodiments, each of the CVD processes occurring at different steps may be performed in a single chamber, or within a single chamber having multiple deposition stations. Thus, each of the deposition steps for a PMD layer, an interfacial dielectric, a barrier layer, an adhesion layer, a nucleation layer, and/or a metal may be performed in a single chamber or integrated process tool. Such an arrangement can avoid having to introduce a vacuum break or otherwise transfer the substrate to another chamber or process tool.
In some embodiments, where a soaking or cleaning step occurs before any one of the CVD processes, chemical solvents, reducing agents, acids, and other liquids or gases relevant to the soaking or cleaning step can be first introduced to the surface of the substrate at a first station. Then a second station may be used to complete a CVD process, such as for depositing tungsten. In such embodiments, a tungsten-containing precursor and hydrogen gas at a high partial pressure are introduced to the surface of the feature using an individual gas supply system that creates a localized atmosphere at the substrate surface. Alternatively, the soaking or cleaning treatment step as well as the CVD process can occur in the same chamber or same station, and the apparatus may be configured to change the relevant chemical species introduced into the chamber or station.
In some embodiments, where a plasma treatment step occurs before any one of the CVD processes, an inert gas containing plasma, corresponding carrier gases, and other gases are introduced to the surface of the substrate at a first station. Then the substrate may be optionally transferred to a CVD station or chamber to complete a CVD process. For example, to complete a CVD process for depositing metal, a tungsten-containing precursor, hydrogen gas, and potentially other carrier gases are introduced to the surface of the feature using an individual gas supply system that creates a localized atmosphere at the substrate surface.
In some embodiments, a downstream plasma apparatus including a plasma generator may be used. A showerhead or other gas inlet can separate the plasma generator and an exposure area of a treatment chamber. Sources of gas provide a flow of gas into the plasma generator. In some embodiments, the plasma generator includes induction coils connected to a power source. During operation, gas mixtures are introduced into the plasma generator, with induction coils energized, and plasma is generated in the plasma generator. In embodiments in which a showerhead assembly is used, the assembly may have an applied voltage. The assembly may terminate the flow of some or substantially all ions and allow the flow of neutral species such as radicals into the treatment chamber. In some embodiments, the plasma is created by flowing gas through an inductively coupled source in which the plasma acts as the secondary in a transformer. An example of this type of remote plasma source is the Astron®, manufactured by MKS Instruments of Wilmington, Mass. Reactive species can be produced within the plasma and transported to a chamber which contains the substrate. In some embodiments, ionic species are not introduced from the remote plasma source.
In some embodiments, each CVD process may be performed in one of two, four, five, or even more deposition stations positioned within a single chamber or apparatus. Process gases for each of the CVD processes may be introduced to the surface of the substrate at a station using an individual gas supply system that creates a localized atmosphere at the substrate surface.
The processing system 800 includes a transfer module 803. The transfer module 803 provides a clean, pressurized environment to minimize the risk of contamination of substrates being processed as they are moved between the various reactor modules. Mounted on the transfer module 803 is a multi-station chamber 809 capable of performing substrate soaking/cleaning, plasma treatment, liner layer deposition if desired, and CVD, according to some embodiments. Chambers 809a and 809b may include multiple stations 811a, 813a, 815a, 817a, 811b, 813b, 813c, and 813d that may sequentially perform these operations. For example, chamber 809a could be configured such that station 811a performs soaking, station 813a performs liner layer deposition, and stations 815a and 817a perform CVD, such as CVD of an interfacial dielectric layer. Chamber 809b could be configured such that station 811b performs soaking, station 813b performs liner layer deposition, and stations 815b and 817b perform CVD, such as CVD of a metal. In some implementations, deposition by CVD of the interfacial dielectric and the metal may occur together in the same chamber, such as either chamber 809a or 809b. Each deposition station may include a heated substrate pedestal and a showerhead, dispersion plate or other gas inlet. An example of a deposition station 900 is depicted in
Also mounted on the transfer module 803 may be one or more single or multi-station modules 807a or 807b capable of performing a cleaning step, such as a chemical oxide removal. The module 807a or 807b may also be used for various other treatments, e.g., WN or other liner layer deposition or post-liner WN CVD. The processing system 800 also includes one or more (in this case, two) substrate source modules 801 where substrates are stored before and after processing. An atmospheric robot 823 in the atmospheric transfer chamber 819 first removes substrates from the source modules 801 to load locks 821. A substrate transfer device 825, such as a robot arm unit, in the transfer module 803 moves the substrates from the load locks 821 to and among the modules 807a and 807b mounted on the transfer module 803. Thus, the processing system 800 may perform the aforementioned processes, including cleaning, deposition by CVD of the interfacial dielectric, and deposition by CVD of the metal, in the same tool without introducing a vacuum break.
In certain embodiments, a system controller 829 is employed to control process conditions during deposition. The controller will typically include one or more memory devices and one or more processors. The processor may include a CPU or computer, analog and/or digital input/output connections, stepper motor controller boards, etc.
The controller 829 may control all of the activities of the deposition apparatus. The system controller executes system control software including sets of instructions for controlling the timing, mixture of gases, chamber pressure, chamber temperature, wafer temperature, RF power levels, wafer chuck or pedestal position, and other parameters of a particular process. Other computer programs stored on memory devices associated with the controller may be employed in some embodiments.
Typically there will be a user interface associated with the controller. The user interface may include a display screen, graphical software displays of the apparatus and/or process conditions, and user input devices such as pointing devices, keyboards, touch screens, microphones, etc.
The computer program code for controlling the deposition and other processes in a process sequence can be written in any conventional computer readable programming language: for example, assembly language, C, C++, Pascal, Fortran or others. Compiled object code or script is executed by the processor to perform the tasks identified in the program.
The controller parameters relate to process conditions such as, for example, process gas composition and flow rates, temperature, pressure, plasma conditions, such as RF power levels and the low frequency RF frequency, cooling gas pressure, and chamber wall temperature. These parameters are provided to the user in the form of a recipe, and may be entered utilizing the user interface.
Signals for monitoring the process may be provided by analog and/or digital input connections of the system controller. The signals for controlling the process are output on the analog and digital output connections of the deposition apparatus.
The system software may be designed or configured in many different ways. For example, various chamber component subroutines or control objects may be written to control operation of the chamber components necessary to carry out the deposition processes. Examples of programs or sections of programs for this purpose include substrate positioning code, process gas control code, pressure control code, heater control code, and plasma control code.
A substrate positioning program may include program code for controlling chamber components that are used to load the substrate onto a pedestal or chuck and to control the spacing between the substrate and other parts of the chamber such as a gas inlet and/or target. A process gas control program may include code for controlling gas composition and flow rates and optionally for flowing gas into the chamber prior to deposition in order to stabilize the pressure in the chamber. A pressure control program may include code for controlling the pressure in the chamber by regulating, e.g., a throttle valve in the exhaust system of the chamber. A heater control program may include code for controlling the current to a heating unit that is used to heat the substrate. Alternatively, the heater control program may control delivery of a heat transfer gas such as helium to the wafer chuck.
Examples of chamber sensors that may be monitored during deposition include mass flow controllers, pressure sensors such as manometers, and thermocouples located in pedestal or chuck. Appropriately programmed feedback and control algorithms may be used with data from these sensors to maintain desired process conditions. The foregoing describes implementation of some embodiments in a single or multi-chamber semiconductor processing tool.
In some embodiments, the controller 829 may be configured with instructions for performing the operations described earlier herein. The controller 829 may include instructions for receiving a semiconductor device, wherein the semiconductor device includes a substrate, a gate dielectric over the substrate, a gate electrode over the dielectric, and source and drain regions in the substrate and on laterally opposite sides of the gate electrode. The controller 829 also includes instructions for depositing by CVD an interfacial dielectric over the source and drain regions of the substrate, depositing a PMD layer over the semiconductor device, forming one or more vias through the PMD layer over the source and drain regions of the substrate, and depositing by CVD a metal over the interfacial dielectric. In some implementations, some of the deposition steps by CVD can occur in at least one or a plurality of deposition stations.
In some embodiments, the controller 829 includes instructions for depositing the interfacial dielectric before depositing the PMD layer and before forming the one or more vias through the PMD layer. In some embodiments, the controller 829 includes instructions for depositing the interfacial dielectric after forming the one or more vias through the PMD layer. In some embodiments, the controller 829 includes instructions for depositing a barrier, adhesion, or nucleation layer by CVD between the metal and the interfacial dielectric. For example, a barrier layer can include at least one of WN and TiN. In some embodiments, the interfacial dielectric is configured to unpin the metal Fermi level from the source and drain regions of the substrate.
The apparatus/process described herein above may be used in conjunction with lithographic patterning tools or processes, for example, for the fabrication or manufacture of semiconductor devices, displays, LEDs, photovoltaic panels and the like. Typically, though not necessarily, such tools/processes will be used or conducted together in a common fabrication facility. Lithographic patterning of a film typically includes some or all of the following operations, each operation enabled with a number of possible tools: (1) application of photoresist on a workpiece, i.e., substrate, using a spin-on or spray-on tool; (2) curing of photoresist using a hot plate or furnace or UV curing tool; (3) exposing the photoresist to visible or UV or x-ray light with a tool such as a wafer stepper; (4) developing the resist so as to selectively remove resist and thereby pattern it using a tool such as a wet bench; (5) transferring the resist pattern into an underlying film or workpiece by using a dry or plasma-assisted etching tool; and (6) removing the resist using a tool such as an RF or microwave plasma resist stripper.
Other Embodiments
Although the foregoing has been described in some detail for purposes of clarity and understanding, it will be apparent that certain changes and modifications may be practiced within the scope of the appended claims. It should be noted that there are many alternative ways of implementing the processes, systems, and apparatus described. Accordingly, the described embodiments are to be considered as illustrative and not restrictive.
Number | Name | Date | Kind |
---|---|---|---|
4746375 | Iacovangelo | May 1988 | A |
4804560 | Shioya et al. | Feb 1989 | A |
4874719 | Kurosawa | Oct 1989 | A |
4962063 | Maydan et al. | Oct 1990 | A |
5028565 | Chang et al. | Jul 1991 | A |
5227329 | Kobayashi et al. | Jul 1993 | A |
5250329 | Miracky et al. | Oct 1993 | A |
5250467 | Somekh et al. | Oct 1993 | A |
5308655 | Eichman et al. | May 1994 | A |
5326723 | Petro et al. | Jul 1994 | A |
5370739 | Foster et al. | Dec 1994 | A |
5391394 | Hansen | Feb 1995 | A |
5567583 | Wang et al. | Oct 1996 | A |
5661080 | Hwang et al. | Aug 1997 | A |
5726096 | Jung | Mar 1998 | A |
5795824 | Hancock | Aug 1998 | A |
5804249 | Sukharev et al. | Sep 1998 | A |
5817576 | Tseng et al. | Oct 1998 | A |
5833817 | Tsai et al. | Nov 1998 | A |
5913145 | Lu et al. | Jun 1999 | A |
5926720 | Zhao et al. | Jul 1999 | A |
5956609 | Lee et al. | Sep 1999 | A |
5963833 | Thakur | Oct 1999 | A |
5994749 | Oda | Nov 1999 | A |
6001729 | Shinriki et al. | Dec 1999 | A |
6017818 | Lu | Jan 2000 | A |
6034419 | Nicholls et al. | Mar 2000 | A |
6037263 | Chang | Mar 2000 | A |
6066366 | Berenbaum et al. | May 2000 | A |
6099904 | Mak et al. | Aug 2000 | A |
6107200 | Takagi et al. | Aug 2000 | A |
6143082 | McInerney et al. | Nov 2000 | A |
6174812 | Hsiung et al. | Jan 2001 | B1 |
6206967 | Mak et al. | Mar 2001 | B1 |
6245654 | Shih et al. | Jun 2001 | B1 |
6265312 | Sidhwa et al. | Jul 2001 | B1 |
6277744 | Yuan et al. | Aug 2001 | B1 |
6294468 | Gould-Choquette et al. | Sep 2001 | B1 |
6297152 | Itoh et al. | Oct 2001 | B1 |
6306211 | Takahashi et al. | Oct 2001 | B1 |
6309966 | Govindarajan et al. | Oct 2001 | B1 |
6310300 | Cooney et al. | Oct 2001 | B1 |
6355558 | Dixit et al. | Mar 2002 | B1 |
6404054 | Oh et al. | Jun 2002 | B1 |
6429126 | Herner et al. | Aug 2002 | B1 |
6465347 | Ishizuka et al. | Oct 2002 | B2 |
6491978 | Kalyanam | Dec 2002 | B1 |
6551929 | Kori et al. | Apr 2003 | B1 |
6566250 | Tu et al. | May 2003 | B1 |
6566262 | Rissman et al. | May 2003 | B1 |
6581258 | Yoneda et al. | Jun 2003 | B2 |
6593233 | Miyazaki et al. | Jul 2003 | B1 |
6607976 | Chen et al. | Aug 2003 | B2 |
6635965 | Lee et al. | Oct 2003 | B1 |
6706625 | Sudijono et al. | Mar 2004 | B1 |
6720261 | Anderson et al. | Apr 2004 | B1 |
6740585 | Yoon et al. | May 2004 | B2 |
6777331 | Nguyen | Aug 2004 | B2 |
6797340 | Fang et al. | Sep 2004 | B2 |
6844258 | Fair et al. | Jan 2005 | B1 |
6861356 | Matsuse et al. | Mar 2005 | B2 |
6902763 | Elers et al. | Jun 2005 | B1 |
6903016 | Cohen | Jun 2005 | B2 |
6905543 | Fair et al. | Jun 2005 | B1 |
6908848 | Koo | Jun 2005 | B2 |
6936538 | Byun | Aug 2005 | B2 |
6939804 | Lai et al. | Sep 2005 | B2 |
6962873 | Park | Nov 2005 | B1 |
7005372 | Levy et al. | Feb 2006 | B2 |
7141494 | Lee et al. | Nov 2006 | B2 |
7157798 | Fair et al. | Jan 2007 | B1 |
7211144 | Lu et al. | May 2007 | B2 |
7220671 | Simka et al. | May 2007 | B2 |
7235486 | Kori et al. | Jun 2007 | B2 |
7262125 | Wongsenakhum et al. | Aug 2007 | B2 |
7355254 | Datta et al. | Apr 2008 | B2 |
7416979 | Yoon et al. | Aug 2008 | B2 |
7419904 | Kato | Sep 2008 | B2 |
7429402 | Gandikota et al. | Sep 2008 | B2 |
7465665 | Xi et al. | Dec 2008 | B2 |
7465666 | Kori et al. | Dec 2008 | B2 |
7501343 | Byun et al. | Mar 2009 | B2 |
7501344 | Byun et al. | Mar 2009 | B2 |
7563718 | Kim | Jul 2009 | B2 |
7589017 | Chan et al. | Sep 2009 | B2 |
7595263 | Chung et al. | Sep 2009 | B2 |
7605083 | Lai et al. | Oct 2009 | B2 |
7611990 | Yoon et al. | Nov 2009 | B2 |
7655567 | Gao et al. | Feb 2010 | B1 |
7674715 | Kori et al. | Mar 2010 | B2 |
7675119 | Taguwa | Mar 2010 | B2 |
7691749 | Levy et al. | Apr 2010 | B2 |
7695563 | Lu et al. | Apr 2010 | B2 |
7709385 | Xi et al. | May 2010 | B2 |
7732327 | Lee et al. | Jun 2010 | B2 |
7745329 | Wang et al. | Jun 2010 | B2 |
7745333 | Lai et al. | Jun 2010 | B2 |
7749815 | Byun | Jul 2010 | B2 |
7754604 | Wongsenakhum et al. | Jul 2010 | B2 |
7772114 | Chan et al. | Aug 2010 | B2 |
7955972 | Chan et al. | Jun 2011 | B2 |
7964505 | Khandelwal et al. | Jun 2011 | B2 |
7977243 | Sakamoto et al. | Jul 2011 | B2 |
8048805 | Chan et al. | Nov 2011 | B2 |
8053365 | Humayun et al. | Nov 2011 | B2 |
8058170 | Chandrashekar et al. | Nov 2011 | B2 |
8062977 | Ashtiani et al. | Nov 2011 | B1 |
8087966 | Hebbinghaus et al. | Jan 2012 | B2 |
8101521 | Gao et al. | Jan 2012 | B1 |
8110877 | Mukherjee et al. | Feb 2012 | B2 |
8207062 | Gao et al. | Jun 2012 | B2 |
8258057 | Kuhn et al. | Sep 2012 | B2 |
8329576 | Chan et al. | Dec 2012 | B2 |
8367546 | Humayun et al. | Feb 2013 | B2 |
8409985 | Chan et al. | Apr 2013 | B2 |
8409987 | Chandrashekar et al. | Apr 2013 | B2 |
8551885 | Chen et al. | Oct 2013 | B2 |
8623733 | Chen et al. | Jan 2014 | B2 |
8709948 | Danek et al. | Apr 2014 | B2 |
8853080 | Guan et al. | Oct 2014 | B2 |
20010008808 | Gonzalez | Jul 2001 | A1 |
20010014533 | Sun | Aug 2001 | A1 |
20010015494 | Ahn | Aug 2001 | A1 |
20010044041 | Badding et al. | Nov 2001 | A1 |
20020037630 | Agarwal et al. | Mar 2002 | A1 |
20020090796 | Desai et al. | Jul 2002 | A1 |
20020117399 | Chen et al. | Aug 2002 | A1 |
20020132472 | Park | Sep 2002 | A1 |
20020155722 | Satta et al. | Oct 2002 | A1 |
20020168840 | Hong et al. | Nov 2002 | A1 |
20020177316 | Miller et al. | Nov 2002 | A1 |
20030059980 | Chen et al. | Mar 2003 | A1 |
20030091870 | Bhowmik et al. | May 2003 | A1 |
20030104126 | Fang et al. | Jun 2003 | A1 |
20030123216 | Yoon et al. | Jul 2003 | A1 |
20030127043 | Lu et al. | Jul 2003 | A1 |
20030129828 | Cohen et al. | Jul 2003 | A1 |
20030190802 | Wang et al. | Oct 2003 | A1 |
20040014315 | Lai et al. | Jan 2004 | A1 |
20040044127 | Okubo et al. | Mar 2004 | A1 |
20040142557 | Levy et al. | Jul 2004 | A1 |
20040151845 | Nguyen et al. | Aug 2004 | A1 |
20040202786 | Wongsenakhum et al. | Oct 2004 | A1 |
20040206267 | Sambasivan et al. | Oct 2004 | A1 |
20050031786 | Lee et al. | Feb 2005 | A1 |
20050059236 | Nishida et al. | Mar 2005 | A1 |
20050136594 | Kim | Jun 2005 | A1 |
20050179141 | Yun et al. | Aug 2005 | A1 |
20050191803 | Matsuse et al. | Sep 2005 | A1 |
20060003581 | Johnston et al. | Jan 2006 | A1 |
20060075966 | Chen et al. | Apr 2006 | A1 |
20060094238 | Levy et al. | May 2006 | A1 |
20060145190 | Salzman et al. | Jul 2006 | A1 |
20060211244 | Deshpande et al. | Sep 2006 | A1 |
20060284317 | Ito et al. | Dec 2006 | A1 |
20070087560 | Kwak et al. | Apr 2007 | A1 |
20070099420 | Dominquez et al. | May 2007 | A1 |
20070190780 | Chung et al. | Aug 2007 | A1 |
20080045010 | Wongsenakhum et al. | Feb 2008 | A1 |
20080081127 | Thompson et al. | Apr 2008 | A1 |
20080081453 | Kim et al. | Apr 2008 | A1 |
20080124926 | Chan et al. | May 2008 | A1 |
20080254619 | Lin et al. | Oct 2008 | A1 |
20080254623 | Chan et al. | Oct 2008 | A1 |
20080280438 | Lai et al. | Nov 2008 | A1 |
20090045517 | Sugiura et al. | Feb 2009 | A1 |
20090053893 | Khandelwal et al. | Feb 2009 | A1 |
20090149022 | Chan et al. | Jun 2009 | A1 |
20090160030 | Tuttle | Jun 2009 | A1 |
20090163025 | Humayun et al. | Jun 2009 | A1 |
20090315154 | Kirby et al. | Dec 2009 | A1 |
20100035427 | Chan et al. | Feb 2010 | A1 |
20100055904 | Chen et al. | Mar 2010 | A1 |
20100130002 | Dao et al. | May 2010 | A1 |
20100130003 | Lin et al. | May 2010 | A1 |
20100155846 | Mukherjee et al. | Jun 2010 | A1 |
20100159694 | Chandrashekar et al. | Jun 2010 | A1 |
20100244141 | Beyer et al. | Sep 2010 | A1 |
20100267230 | Chandrashekar et al. | Oct 2010 | A1 |
20100267235 | Chen et al. | Oct 2010 | A1 |
20100273327 | Chan et al. | Oct 2010 | A1 |
20100330800 | Ivanov et al. | Dec 2010 | A1 |
20110059608 | Gao et al. | Mar 2011 | A1 |
20110156154 | Hoentschel et al. | Jun 2011 | A1 |
20110221044 | Danek et al. | Sep 2011 | A1 |
20110223763 | Chan et al. | Sep 2011 | A1 |
20110233778 | Lee et al. | Sep 2011 | A1 |
20110236594 | Haverkamp et al. | Sep 2011 | A1 |
20120009785 | Chandrashekar et al. | Jan 2012 | A1 |
20120015518 | Chandrashekar et al. | Jan 2012 | A1 |
20120040530 | Humayun et al. | Feb 2012 | A1 |
20120199887 | Chan et al. | Aug 2012 | A1 |
20120231626 | Lee et al. | Sep 2012 | A1 |
20120244699 | Khandelwal et al. | Sep 2012 | A1 |
20120294874 | Macary et al. | Nov 2012 | A1 |
20130062677 | Li et al. | Mar 2013 | A1 |
20130109172 | Collins et al. | May 2013 | A1 |
20130168864 | Lee et al. | Jul 2013 | A1 |
20130171822 | Chandrashekar et al. | Jul 2013 | A1 |
20130302980 | Chandrashekar et al. | Nov 2013 | A1 |
20140011358 | Chen et al. | Jan 2014 | A1 |
20140027664 | Wei et al. | Jan 2014 | A1 |
20140030889 | Chen et al. | Jan 2014 | A1 |
20140061931 | Kang | Mar 2014 | A1 |
20140073135 | Guan et al. | Mar 2014 | A1 |
20140154883 | Humayun et al. | Jun 2014 | A1 |
20140162451 | Chen et al. | Jun 2014 | A1 |
Number | Date | Country |
---|---|---|
0 437 110 | Jul 1991 | EP |
1 156 132 | Nov 2001 | EP |
1 179 838 | Feb 2002 | EP |
08-115984 | May 1996 | JP |
09-027596 | Jan 1997 | JP |
H10-144688 | May 1998 | JP |
11-330006 | Nov 1999 | JP |
2000-208516 | Jul 2000 | JP |
2000-235962 | Aug 2000 | JP |
2001-525889 | Dec 2001 | JP |
2002-124488 | Apr 2002 | JP |
2004-235456 | Aug 2004 | JP |
2004-273764 | Sep 2004 | JP |
2005-029821 | Feb 2005 | JP |
2005-518088 | Jun 2005 | JP |
2007-009298 | Jan 2007 | JP |
2007-027627 | Feb 2007 | JP |
2007-027680 | Feb 2007 | JP |
2007-507892 | Mar 2007 | JP |
2007-520052 | Jul 2007 | JP |
2007-250907 | Sep 2007 | JP |
2007-251164 | Sep 2007 | JP |
2008-016803 | Jan 2008 | JP |
2008-060603 | Mar 2008 | JP |
2008-091844 | Apr 2008 | JP |
2008-283220 | Nov 2008 | JP |
2009-024252 | Feb 2009 | JP |
2009-144242 | Jul 2009 | JP |
2009-540123 | Nov 2009 | JP |
10-2002-0049730 | Jun 2002 | KR |
10-2005-0022261 | Mar 2005 | KR |
10-2005-0087428 | Aug 2005 | KR |
10-2006-0087844 | Aug 2006 | KR |
705936 | Apr 2007 | KR |
10-2008-0036679 | Apr 2008 | KR |
10-2008-0110897 | Dec 2008 | KR |
10-2009-0103815 | Oct 2009 | KR |
WO 9851838 | Nov 1998 | WO |
WO 0127347 | Apr 2001 | WO |
WO 0129893 | Apr 2001 | WO |
WO 0241379 | May 2002 | WO |
WO 03029515 | Apr 2003 | WO |
WO 2005027211 | Mar 2005 | WO |
WO 2007121249 | Oct 2007 | WO |
WO 2007146537 | Dec 2007 | WO |
WO 2010025357 | Mar 2010 | WO |
WO 2011119293 | Sep 2011 | WO |
WO 2013148444 | Oct 2013 | WO |
WO 2013148880 | Oct 2013 | WO |
Entry |
---|
Manik. P, et al. Fermi-level unpinning and low resistivity in contacts to n-type Ge with a thin ZnO interfacial layer, App. Phys. Lett. 101, 182105 (2012). |
U.S. Appl. No. 14/135,375, filed Dec. 19, 2013, entitled “Method for Depositing Extremely Low Resistivity Tungsten.” |
U.S. Appl. No. 13/758,928, filed Feb. 4, 2013, entitled “Methods for Forming All Tungsten Contacts and Lines.” [NOVLP244C2/NVLS003350C2]. |
US Office Action, dated Apr. 7, 2014, issued in U.S. Appl. No. 13/633,502. |
US Office Action, dated Jul. 17, 2002, issued in U.S. Appl. No. 09/975,074. |
US Notice of Allowance, dated Mar. 12, 2003, issued in U.S. Appl. No. 09/975,074. |
US Office Action, dated Feb. 8, 2005, issued in U.S. Appl. No. 10/649,351. |
US Final Office Action, dated Jul. 14, 2005, issued in U.S. Appl. No. 10/649,351. |
US Office Action, dated Dec. 30, 2005, issued in U.S. Appl. No. 10/649,351. |
US Notice of Allowance, dated Jul. 21, 2006, issued in U.S. Appl. No. 10/649,351. |
US Office Action, dated Jun. 22, 2004, issued in U.S. Appl. No. 10/435,010. |
US Notice of Allowance, dated Oct. 7, 2004, issued in U.S. Appl. No. 10/435,010. |
US Notice of Allowance, dated Jan. 19, 2005, issued in U.S. Appl. No. 10/435,010. |
US Office Action, dated Nov. 23, 2005, issued in U.S. Appl. No. 10/984,126. |
US Final Office Action, dated May 17, 2006, issued in U.S. Appl. No. 10/984,126. |
US Notice of Allowance, dated Aug. 25, 2006, issued in U.S. Appl. No. 10/984,126. |
US Office Action, dated Mar. 23, 2005, issued in U.S. Appl. No. 10/690,492. |
US Notice of Allowance, dated Sep. 14, 2005, issued in U.S. Appl. No. 10/690,492. |
US Office Action, dated Jun. 27, 2008, issued in U.S. Appl. No. 11/305,368. |
US Office Action, dated Apr. 3, 2009, issued in U.S. Appl. No. 11/305,368. |
US Notice of Allowance, dated Nov. 17, 2009, issued in U.S. Appl. No. 11/305,368. |
US Office Action, dated Jul. 12, 2005, issued in U.S. Appl. No. 10/815,560. |
US Final Office Action, dated Dec. 28, 2005, issued in U.S. Appl. No. 10/815,560. |
US Office Action, dated Apr. 17, 2006, issued in U.S. Appl. No. 10/815,560. |
US Office Action, dated Sep. 28, 2006, issued in U.S. Appl. No. 10/815,560. |
US Notice of Allowance dated Apr. 24, 2007, issued in U.S. Appl. No. 10/815,560. |
US Office Action, dated Aug. 21, 2008, issued in U.S. Appl. No. 11/265,531. |
US Final Office Action, dated Feb. 26, 2009, issued in U.S. Appl. No. 11/265,531. |
US Notice of Allowance, dated May 4, 2009, issued in U.S. Appl. No. 11/265,531. |
US Office Action, dated Nov. 23, 2010, issued in U.S. Appl. No. 12/538,770. |
US Notice of Allowance, dated Jun. 30, 2011, issued in U.S. Appl. No. 12/538,770. |
US Office Action, dated Oct. 16, 2008, issued in U.S. Appl. No. 11/349,035. |
US Final Office Action, dated Feb. 25, 2009, issued in U.S. Appl. No. 11/349,035. |
US Office Action, dated Jun. 4, 2009, issued in U.S. Appl. No. 11/349,035. |
US Final Office Action, dated Nov. 20, 2009, issued in U.S. Appl. No. 11/349,035. |
US Notice of Allowance, dated Mar. 2, 2010, issued in U.S. Appl. No. 11/349,035. |
US Office Action, dated Sep. 29, 2008, issued in U.S. Appl. No. 11/782,570. |
US Final Office Action, dated Apr. 28, 2009, issued in U.S. Appl. No. 11/782,570. |
US Notice of Allowance, dated Sep. 17, 2009, issued in U.S. Appl. No. 11/782,570. |
US Office Action, dated Jan. 25, 2011, issued in U.S. Appl. No. 12/636,616. |
US Final Office Action, dated Jun. 15, 2011, issued in U.S. Appl. No. 12/636,616. |
US Notice of Allowance, dated Sep. 30, 2011, issued in U.S. Appl. No. 12/636,616. |
US Office Action, dated Jun. 24, 2009, issued in U.S. Appl. No. 12/030,645. |
US Final Office Action, dated Jan. 13, 2010, issued in U.S. Appl. No. 12/030,645. |
US Final Office Action, dated Jul. 23, 2010, issued in U.S. Appl. No. 12/030,645. |
US Notice of Allowance and Fee Due, dated Jan. 24, 2011, issued in U.S. Appl. No. 12/030,645. |
US Office Action, dated Aug. 6, 2012, issued in U.S. Appl. No. 13/095,734. |
Notice of Allowance dated Dec. 3, 2012, issued in U.S. Appl. No. 13/095,734. |
US Office Action, dated Aug. 5, 2009, issued in U.S. Appl. No. 11/951,236. |
US Final Office Action, dated Jan. 26, 2010 from U.S. Appl. No. 11/951,236. |
US Notice of Allowance, dated Apr. 6, 2010, issued in U.S. Appl. No. 11/951,236. |
US Office Action, dated Jun. 30, 2011, issued in U.S. Appl. No. 12/829,119. |
US Final Office Action, dated Nov. 17, 2011, issued in U.S. Appl. No. 12/829,119. |
US Office Action, dated Apr. 19, 2012, issued in U.S. Appl. No. 12/829,119. |
US Notice of Allowance, dated Aug. 7, 2012, issued in U.S. Appl. No. 12/829,119. |
US Office Action, dated Jun. 11, 2009, issued in U.S. Appl. No. 11/963,698. |
US Final Office Action, dated Dec. 9, 2009, issued in U.S. Appl. No. 11/963,698. |
US Office Action, dated Jun. 11, 2010, issued in U.S. Appl. No. 11/963,698. |
US Final Office Action, dated Dec. 30, 2010, issued in U.S. Appl. No. 11/963,698. |
US Notice of Allowance, dated Sep. 2, 2011, issued in U.S. Appl. No. 11/963,698. |
US Office Action, dated Apr. 16, 2012, issued in U.S. Appl. No. 13/276,170. |
US Notice of Allowance, dated Oct. 4, 2012, issued in U.S. Appl. No. 13/276,170. |
US Notice of Allowance, dated Jul. 25, 2011, issued in U.S. Appl. No. 12/363,330. |
US Office Action dated Oct. 21, 2009, issued in U.S. Appl. No. 12/202,126. |
US Final Office Action, dated May 7, 2010, issued in U.S. Appl. No. 12/202,126. |
US Office Action, dated Jul. 26, 2010 issued in U.S. Appl. No. 12/202,126. |
US Final Office Action, dated Feb. 7, 2011, issued in U.S. Appl. No. 12/202,126. |
US Office Action, dated Jan. 7, 2013, issued in U.S. Appl. No. 12/202,126. |
US Notice of Allowance, dated Jun. 7, 2013, issued in U.S. Appl. No. 12/202,126. |
US Office Action, dated May 3, 2010, issued in U.S. Appl. No. 12/407,541. |
US Final Office Action, dated Oct. 19, 2010, issued in U.S. Appl. No. 12/407,541. |
US Office Action, dated May 2, 2011, issued in U.S. Appl. No. 12/407,541. |
US Notice of Allowance, dated Sep. 19, 2011, issued in U.S. Appl. No. 12/407,541. |
US Office Action, dated Mar. 6, 2012, issued in U.S. Appl. No. 13/244,016. |
US Notice of Allowance dated Nov. 29, 2012, issued in U.S. Appl. No. 13/244,016. |
US Office Action, dated Jun. 14, 2011, issued in U.S. Appl. No. 12/556,490. |
US Notice of Allowance, dated Mar. 2, 2012, issued in U.S. Appl. No. 12/556,490. |
US Office Action, dated May 13, 2011, issued in U.S. Appl. No. 12/755,248. |
US Office Action, dated Oct. 28, 2011, issued in U.S. Appl. No. 12/755,248. |
US Final Office Action, dated Apr. 30, 2012, issued in U.S. Appl. No. 12/755,248. |
US Office Action, dated Feb. 15, 2013, issued in U.S. Appl. No. 12/755,248. |
US Office Action dated Dec. 18, 2012, issued in U.S. Appl. No. 12/723,532. |
US Office Action dated Jul. 18, 2013, issued in U.S. Appl. No. 12/723,532. |
US Notice of Allowance dated Dec. 24, 2013, issued in U.S. Appl. No. 12/723,532. |
US Office Action, dated Feb. 16, 2012, issued in U.S. Appl. No. 12/755,259. |
US Final Office Action, dated Sep. 12, 2012, issued in U.S. Appl. No. 12/755,259. |
US Notice of Allowance, dated Jul. 10, 2013, issued in U.S. Appl. No. 12/755,259. |
US Notice of Allowance dated Sep. 4, 2013 issued in U.S. Appl. No. 12/755,259. |
US Office Action, dated May 10, 2012, issued in U.S. Appl. No. 13/020,748. |
US Final Office Action, dated Nov. 16, 2012, issued in U.S. Appl. No. 13/020,748. |
US Office Action, dated Feb. 24, 2014, issued in U.S. Appl. No. 13/020,748. |
US Final Office Action, dated Jul. 2, 2014, issued in U.S. Appl. No. 13/020,748. |
US Office Action, dated Jun. 20, 2013, issued in U.S. Appl. No. 13/560,688. |
US Final Office Action, dated Feb. 14, 2014, issued in U.S. Appl. No. 13/560,688. |
US Office Action, dated Jun. 14, 2013, issued in U.S. Appl. No. 13/633,798. |
US Final Office Action, dated Nov. 26, 2013, issued in U.S. Appl. No. 13/633,798. |
US Notice of Allowance, dated May 23, 2014, issued in U.S. Appl. No. 13/633,798. |
PCT Search Report and Written Opinion, dated Jan. 19, 2005, issued in PCT/US2004/006940. |
Korean First Notification of Provisional Rejection, dated Dec. 8, 2010, issued in Application No. 2004-0036346. |
Korean Office Action, dated Jun. 13, 2011, issued in Application No. 2011-0032098. |
Korean Office Action, dated Nov. 24, 2010, issued in Application No. KR 10-2004-0013210. |
Korean Office Action, dated Mar. 28, 2013, issued in Application No. KR 10-2007-0012027. |
Japanese Office Action dated May 7, 2013, issued in Application No. JP 2008-310322. |
Japanese Office Action dated Sep. 3, 2013, issued in Application No. JP 2008-325333. |
PCT International Search Report and Written Opinion, dated Apr. 12, 2010, issued in PCT/US2009/055349. |
PCT International Preliminary Report on Patentability and Written Opinion, dated Mar. 10, 2011, issued in PCT/US2009/055349. |
Chinese First Office Action dated Sep. 18, 2012 issued in Application No. 200980133560.1. |
Chinese Second Office Action dated Aug. 7, 2013 issued in Application No. 200980133560.1. |
Chinese Third Office Action dated Apr. 22, 2014 issued in Application No. 200980133560.1. |
Japanese Office Action dated Dec. 3, 2013 issued in Application No. 2011-525228. |
Korean Office Action dated Sep. 6, 2012 issued in Application No. 2011-7004322. |
Korean Office Action dated Jul. 19, 2013 issued in Application No. 2011-7004322. |
Korean Office Action dated Nov. 4, 2013 issued in Application No. 10-2013-7027117. |
Korean Office Action dated Jun. 17, 2014 issued in Application No. 10-2013-7027117. |
Japanese Office Action dated Jun. 17, 2014 issued in Application No. JP 2010-055163. |
Korean Office Action dated Mar. 21, 2013 issued in KR Application No. 10-2010-0024905. |
Korean Notification of Provisional Rejection dated Jul. 17, 2012, issued in Application No. 2010-0087997. |
Japanese Office Action dated Mar. 4, 2014 issued in JP 2010-093522. |
Korean Office Action dated Mar. 4, 2013 in KR Application No. 2010-0035449. |
Japanese Office Action dated Jul. 29, 2014 issued in JP 2010-093544. |
Korean Second Office Action dated Jan. 25, 2014 in KR Application No. 10-2010-0035453. |
PCT International Search Report and Written Opinion, dated Jun. 28, 2013, issued in PCT/US2013/033174. |
PCT International Search Report and Written Opinion, dated Jul. 26, 2013, issued in PCT/US2013/034167. |
Becker, Jill (Apr. 7, 2003) “Diffusion barrier properties of tungsten nitride films grown by atomic layer deposition from bis(tert-butylimido)bis(dimethylamido)tungsten and ammonia,” Applied Physics Letters, 82(14):2239-2241, [Retrieved online Dec. 13, 2013 at http://dx.doi.org/10.1063/1.1565699]. |
Bell et al. (Jan. 1996) “Batch Reactor Kinetic Studies of Tungsten LPCVD from Silane and Tungsten Hexafluoride”, J. Electrochem. Soc., 143(1):296-302. |
Collins et al. (Jan. 21, 2003) “Pulsed Deposition of Ultra Thin Tungsten for Plugfill of High Aspect Ratio Contacts,” Presentation made at Semicon Korea, 9 pages. |
Collins et al. (Jan. 21, 2003) “Pulsed Deposition of Ultra Thin Tungsten for Plugfill of High Aspect Ratio Contacts,” Semiconductor Equipment and Materials International, Semicon Korea, 3 pages. |
Diawara, Y. et al. (1993) “Rapid thermal annealing for reducing stress in tungsten x-ray mask absorber,” http://dx.doi.org/10.1116/1.586673, Journal of Vacuum Science & Technology B 11:296-300 (per table of contents of journal). |
Elam et al. (2001) “Nucleation and Growth During Tungsten Atomic Layer Deposition on SiO2 Surfaces,” Thin Solid Films, 13pp. |
Fair, James A. (1983) Presentation by Inventor “Chemical Vapor Deposition of Refractory Metal Silicides,” GENUS Incorporated, 27 pp. |
George et al. (1996) “Surface Chemistry for atomic Layer Growth”, J. Phys. Chem, 100(31):13121-13131. |
Gonohe, Narishi (2002) “Tungsten Nitride Deposition by Thermal Chemical Vapor Deposition as Barrier Metal for Cu Interconnection,” [http://www.jim.co.jp/journal/e/pdf3/43/07/1585.pdf], Materials Transactions, 43(7): 1585-1592. |
Hoover, Cynthia (Jul. 2007) “Enabling Materials for Contact Metallization,” Praxair Electronic Materials R&D, pp. 1-16. |
Klaus et al. (2000) “Atomic layer deposition of tungsten using sequential surface chemistry with a sacrificial stripping reaction,” Thin Solid Films 360:145-153. |
Klaus et al. (2000) “Atomically Controlled Growth of Tungsten and Tungsten Nitride Using Sequential Surface Reactions,” Applied Surface Science, pp. 162-163, 479-491. |
Lai, Ken et al. (Jul. 17, 2000) “Tungsten chemical vapor deposition using tungsten hexacarbonyl: microstructure of as-deposited and annealed films,” [http://dx.doi.org/10.1016/S0040-6090(00)00943-3], Thin Solid Films, 370:114-121. |
Lai, Ken K. and Lamb, H. Henry (1995) “Precursors for Organometallic Chemical Vapor Deposition of Tungsten Carbide Films,” Chemistry Material, 7(12):2284-2292. |
Lee et al. (Jan. 21, 2003) “Pulsed Deposition of Ultra Thin Tungsten and its Application for Plugfill of High Aspect Ratio Contacts,” Abstract, 1 page. |
Li et al. (2002) “Deposition of WNxCy Thin Films by ALCVD™ Method for Diffusion Barriers in Metallization,” IITC Conference Report, 3 pp. |
Saito et al. (2001) “A Novel Copper Interconnection Technology Using Self Aligned Metal Capping Method,” IEEE, 3pp. |
Shioya, Yoshimi et al. (Dec. 1, 1985) “Analysis of stress in chemical vapor deposition tungsten silicide film,” [Retrieved online Dec. 18, 2013 at http://dx.doi.org/10.1063/1.335552], Journal of Applied Physics, 58(11):4194-4199. |
U.S. Appl. No. 14/502,817, filed Sep. 30, 2014, entitled “Tungsten Feature Fill”. |
US Final Office Action, dated Nov. 5, 2014, issued in U.S. Appl. No. 13/633,502. |
US Office Action, dated Dec. 11, 2014, issued in U.S. Appl. No. 14/173,733. |
US Office Action, dated Jan. 15, 2015, issued in U.S. Appl. No. 13/774,350. |
US Office Action, dated Dec. 23, 2014, issued in U.S. Appl. No. 13/851,885. |
US Office Action, dated Dec. 18, 2014, issued in U.S. Appl. No. 14/502,817. |
US Office Action, dated Sep. 18, 2014, issued in U.S. Appl. No. 13/928,216. |
US Notice of Allowance, dated Nov. 4, 2014, issued in U.S. Appl. No. 13/560,688. |
Chinese Fourth Office Action dated Jan. 5, 2015 issued in Application No. 200980133560.1. |
PCT International Premliminary Report on Patentability and Written Opinion, dated Oct. 9, 2014, issued in PCT/US2013/033174. |
PCT International Premliminary Report on Patentability and Written Opinion, dated Oct. 9, 2014, issued in PCT/US2013/034167. |
Number | Date | Country | |
---|---|---|---|
20140308812 A1 | Oct 2014 | US |