Copper residue chamber clean

Information

  • Patent Grant
  • 9114438
  • Patent Number
    9,114,438
  • Date Filed
    Wednesday, August 21, 2013
    11 years ago
  • Date Issued
    Tuesday, August 25, 2015
    9 years ago
Abstract
Methods of removing copper residue from interior surfaces of an etch process chamber are described. A plasma treatment using halogen-containing precursors transforms the copper residue into halogen-copper complexes. Plasma-excited inert gases are used to desorb the halogen-copper complexes. In this way, the copper residue is removed from the interior surfaces of the etch process chamber.
Description
FIELD

The present invention relates to substrate processing.


BACKGROUND

The use of copper as a conductive interconnect material is favored in semiconductor devices because of the high conductivities and circuit speeds copper enables. On the other hand, copper is difficult to pattern and copper interconnect leads have predominantly heretofore been formed using damascene and dual damascene processing technology whereby openings are formed in a dielectric layer on a substrate such as a semiconductor substrate used to form semiconductor devices. Copper is deposited over the dielectric layer and within the openings. Polishing/planarization removes copper from over the dielectric leaving the copper inlaid within the openings. In this way, the burden on photolithography is shifted from copper to the more manageable dielectric layer. The inlaid copper includes an upper surface that is essentially co-planar with the top surface of the patterned dielectric layer in which the copper is formed.


Subtractive copper etching is the alternative to a damascene process flow. A layer of copper is deposited and then patterned to form horizontal electrical interconnections. Early attempts to investigate subtractive copper etching used plasma excited halides which were found to provide many advantages but degraded the physical integrity of the copper near grain boundaries and other seams. There is renewed interest in subtractive copper etching since progress has been made in addressing these shortcomings. This renewed interest in subtractive copper etching brings renewed interest in associated properties of such a process. Thus, there is a need in the art to develop maintenance procedures unique to subtractive copper etching.


SUMMARY

Methods of removing copper residue from interior surfaces of an etch process chamber are described. A plasma treatment using halogen-containing precursors transforms the copper residue into halogen-copper complexes. Plasma-excited inert gases are used to desorb the halogen-copper complexes. In this way, the copper residue is removed from the interior surfaces of the etch process chamber.


Embodiments of the invention include methods of cleaning a dielectric window of a substrate processing chamber having a substrate processing region. The method includes flowing a halogen-containing precursor into the substrate processing region while forming a first local plasma in the substrate processing region having a first local plasma power to form excited halogen-containing species. The method further includes flowing an inert gas into the substrate processing region while forming a second local plasma in the substrate processing region having a second local plasma power. The copper residue on interior surfaces of the dielectric window is transformed into a copper halogen layer during the first local plasma. The copper halogen layer is desorbed as desorbed species from the dielectric window during the second local plasma which occurs after the first local plasma.


Embodiments of the invention include methods of cleaning a dielectric window of a substrate processing chamber. The methods include flowing a halogen-free precursor into the substrate processing region while forming a subtractive etch local plasma in the substrate processing region having a subtractive etch local plasma power to form excited halogen-free species. The subtractive etch removes copper from a substrate and leaves a copper residue on the interior surfaces of the dielectric window. The substrate processing region is devoid of halogens during the subtractive etch local plasma. The methods further include removing the substrate from the substrate processing region. The methods further include flowing a halogen-containing precursor into the substrate processing region while forming a halogen local plasma in a substrate processing region having a halogen local plasma power to form excited halogen-containing species. The halogen local plasma transforms the copper residue on interior surfaces of the dielectric window into a copper halogen layer. The methods further include flowing an inert gas into the substrate processing region while forming an inert gas local plasma in the substrate processing region having an inert gas local plasma power. The copper halogen layer is desorbed as desorbed species from the dielectric window. The inert gas local plasma occurs after the halogen local plasma.


Additional embodiments and features are set forth in part in the description that follows, and in part will become apparent to those skilled in the art upon examination of the specification or may be learned by the practice of the embodiments. The features and advantages of the embodiments may be realized and attained by means of the instrumentalities, combinations, and methods described in the specification.





BRIEF DESCRIPTION OF THE DRAWINGS

A further understanding of the nature and advantages of the embodiments may be realized by reference to the remaining portions of the specification and the drawings.



FIG. 1 is a flow chart of a residual copper removal process according to embodiments.



FIG. 2 is a schematic of a etch process chamber which can be cleaned according to a residual copper removal process according to embodiments.



FIG. 3 is a schematic diagram of an etch process chamber which can be used to carry out processes according to embodiments.



FIG. 4 is a schematic top-view diagram of an exemplary multi-chamber substrate processing system which can be used to carry out processes according to embodiments.





In the appended figures, similar components and/or features may have the same reference label. Further, various components of the same type may be distinguished by following the reference label by a dash and a second label that distinguishes among the similar components. If only the first reference label is used in the specification, the description is applicable to any one of the similar components having the same first reference label irrespective of the second reference label.


DETAILED DESCRIPTION

Methods of removing copper residue from interior surfaces of an etch process chamber are described. A plasma treatment using halogen-containing precursors transforms the copper residue into halogen-copper complexes. Plasma-excited inert gases are used to desorb the halogen-copper complexes. In this way, the copper residue is removed from the interior surfaces of the etch process chamber.


The processes disclosed herein remove remnants from interior surfaces of an etch process chamber. The interior surface is on a dielectric window which can be used to pass electromagnetic energy from inductive coils positioned outside the etch process chamber. Accumulation of copper residue has been found to absorb electromagnetic energy and may even cause heat buildup on the dielectric window during plasma excitation. Previously, methods of etching copper avoided forming copper residue by including halogen-containing precursors during the subtractive copper etch process and also by subtractive copper etching at high substrate/chamber temperatures. Inclusion of halogen-containing precursors and maintaining high substrate/chamber temperatures increased the volatility of etch by-products and increased the probability that etch by-products would be evacuated through a vacuum pump. Recent subtractive etch process development activity involves using halogen-free precursors and/or lower substrate/chamber temperatures. As a result, remnants of the copper etch (referred to herein as “copper residue”) may now be a problem which needs to be addressed. Copper residue accumulates on interior surfaces of the dielectric window during these more recent subtractive copper etch processes. Removing the copper residue, as taught herein, involves treating the interior surface of the etch process chamber to remove the copper residue after the previous substrate is removed and before a subsequent substrate arrives into the etch process chamber. Removing the copper residue enables plasma power to be efficiently transferred into the etch process chamber, facilitating processing of the subsequent substrate.


In order to better understand and appreciate the invention, reference is now made to FIG. 1 which is a flow chart of an exemplary residual copper removal process 100 according to embodiments. Reference will concurrently be made to FIG. 2 which shows a schematic of an exemplary etch process chamber 200 which may be used to perform exemplary copper residue removal processes. A wide variety of substrate processing chambers may also benefit from exemplary residual copper removal process 100. The first two operations are optional and represent one method of producing the undesirable copper residue on an interior surface of the etch process chamber 200. The exemplary substrate 206 is coated with a layer of copper and a patterned mask positioned atop the copper layer. The copper layer is etched (operation 110) to transfer the pattern of the mask into the copper and etch effluents are pumped out of substrate processing region 210 through vacuum pump 202. This pattern transfer etch may be referred to herein as a subtractive copper etch process.


During the subtractive copper etch process, the etch precursors are delivered through precursor/gas inlets 250 into substrate processing region 210. The etch precursors are excited by an inductively coupled plasma created by applying alternating current (AC) power 241 to inductive coils 240. The plasma may be referred to herein as a subtractive etch local plasma and is applied with a subtractive etch local plasma power. Electromagnetic radiation passes through dielectric window 220 which may also be referred to as a lid or a dielectric lid herein. Dielectric window 220 mates with metal chamber portion 201 to form the bulk of the etch process chamber 200. The etch precursor may be halogen-free and may include one or more of methanol (CH3OH), ethane (C2H4), oxygen (O2), hydrogen (H2), carbon monoxide (CO), helium (He) or argon (Ar). Subtractive plasma excited halogen-free species etch copper from substrate 206 and leave a copper residue on the interior surfaces of the etch process chamber 200. Substrate processing region 210 may be devoid of halogens during operation 110 in embodiments. During this etch, residual copper accumulates on dielectric window 220 and metal chamber portion 201. The etched substrate 206 is removed from substrate pedestal 205 in operation 120.


Once substrate 206 is removed from substrate processing region 210, a plasma-excited halogen may be used to process the residual copper without damage to the seams and grain boundaries of the patterned copper layer. The substrate has been removed which makes it safe to introduce a halogen at this stage. Chlorine gas (Cl2) is flowed into substrate processing region 210 through precursor/gas inlets 250 and excited in a first local plasma using inductive coils 240 (operation 130) in embodiments. Alternatively (or in combination) the chlorine gas may be excited in a first local capacitively-coupled plasma within substrate processing region 210 if the etch process chamber 200 is configured with the appropriate hardware. The substrate processing region 210 may contain other elements, for example, the substrate processing region 210 may contain chlorine and argon or may consist essentially of chlorine and argon in embodiments. The inclusion of the term “essentially” allows for unavoidable elemental concentrations and low concentrations which do not adversely affect the formation of a copper-halogen layer. The treatment using chlorine occurs during the first local plasma and subsequent processing occurs in operation 140 described below. The treatment operation 130 transforms adsorbed copper into adsorbed copper chloride on the surface of the dielectric window 220 and possibly the metal chamber portion 201 and other components as well.


In general, a halogen-containing precursor may be flowed (operation 130) into substrate processing region and the halogen-containing precursor comprises a halogen or may comprise at least one element from chlorine, bromine, and iodine. In embodiments, the substrate processing region may consist essentially of chlorine and an inert gas, halogen and an inert gas or chlorine and argon. Other components may reduce the ability of the halogen to form copper-halogen complexes in a copper halogen layer on the interior surfaces of the etch process chamber 200. The inclusion of the term “essentially” allows for other elemental concentrations which may be unavoidably present in a typical processing system as well as low concentrations which do not adversely affect the formation of the copper-halogen layer.


A flow of helium is then introduced into substrate processing region 210 (operation 140) where the helium is excited in a second local plasma struck within the substrate processing region 210. The second plasma may be created by the same excitation source and in the same rough location as the first plasma had been. In general the helium may be one or more inert gases, where inert gases include any gases which do not ultimately form covalent bonds within the copper or copper chloride on the interior surfaces of substrate processing region 210. The substrate processing region may consist essentially of inert gases, associated ions and desorbed species during operation 140 in some embodiments. The inert gas may include one or more of neon, helium, argon, xenon and the like. The second local plasma may consist essentially of inert gases. The substrate processing region may comprise helium and may consist essentially of helium during operation 140 in embodiments. In embodiments, the inert gas or the substrate processing region consists essentially of argon, consists essentially of neon or consists essentially of xenon. The inert gas or substrate processing region consists essentially of helium, argon, neon and/or xenon in embodiments of the invention.


Operation 140 is effective if a flow of one or more of hydrogen (H2), HCl, HBr, and HI are also flowed into the substrate processing region in addition to the inert gases already mentioned. As such, the substrate processing region consists essentially of hydrogen (H), halogens, inert elements and desorbed species during operation 140 in embodiments. Other components may reduce the ability of the inert gas (and possibly HCl, HBr or HI) to desorb the copper-halogen complexes in a copper halogen layer on the interior surfaces of the etch process chamber 200. The inclusion of the term “essentially” allows for other elemental concentrations which may be unavoidably present in a typical processing system as well as low concentrations which do not adversely affect the desorption of the copper-halogen layer.


Operation 140 selectively removes copper chloride from substrate processing region 219 and may do so without removing copper or other metals from the chamber walls in embodiments. Generally speaking, operation 140 desorbs copper-halogen material from the chamber walls. The substrate processing region may be devoid of halogens during operation 140 aside from the desorbed species in embodiments. Desorbed species of the copper halogen layer are exhausted from the substrate processing region during or after operation 140 in embodiments.


The method includes applying energy to the halogen-containing precursor in the first local plasma and to the inert gas (e.g. helium) in the second local plasma while in the substrate processing region to generate the radicals used to treat and etch the interior surfaces of the substrate processing chamber. The plasma may be generated using known techniques (e.g., radio frequency excitations, capacitively-coupled power, inductively coupled power, and the like). In an embodiment, the energy is applied using an inductively-coupled plasma power supply unit 241. The AC power is supplied to the inductive coils 240 shown in cross-section in FIG. 2. The first local plasma power may have a first local plasma power which is less than a second local plasma power of the second local plasma. The first local plasma power may be between about 50 watts and about 2500 watts, between about 100 watts and about 2000 watts, between about 150 watts and about 1500 watts, or between about 250 watts and about 1000 watts in embodiments of the invention. The second local plasma power may be between about 100 watts and about 5000 watts, between about 200 watts and about 4000 watts, between about 300 watts and about 3000 watts, or between about 500 watts and about 2000 watts in embodiments of the invention. In embodiments, no DC accelerating voltage may be applied between substrate pedestal 205 and metal chamber portion 201 in order to ensure effective reaction of first local plasma and second local plasma with interior chamber walls. The pressure in the substrate processing region may be between about 0.5 mTorr and about 500 mTorr, between about 2 mTorr and about 200 mTorr or between about 5 mTorr and about 100 mTorr in embodiments, during either the operation 130 or operation 140.


The RF frequency applied for either the local or remote plasmas described herein may be low RF frequencies less than about 200 kHz, high RF frequencies between about 10 MHz and about 15 MHz, or microwave frequencies greater than or about 1 GHz in embodiments.


The flow of the halogen-containing precursor may further include one or more relatively inert gases such as He, N2, Ar. The inert gas can be used to improve plasma stability, process uniformity and the like. Argon is helpful, as an additive, to promote the formation of a stable plasma. Process uniformity is generally increased when helium is included. These additives are present in embodiments throughout this specification. Flow rates and ratios of the different gases may be used to control etch rates and etch selectivity.


In embodiments, the halogen-containing precursor (e.g. Cl2) is supplied at a flow rate of between about 5 sccm (standard cubic centimeters per minute) and 400 sccm, and argon at a flow rate of between about 0 slm and 1 slm. One of ordinary skill in the art would recognize that other gases and/or flows may be used depending on a number of factors including processing chamber configuration, substrate size, geometry and layout of features being etched, and the like. With regard to operation 140, the inert gas (e.g. helium) is supplied at a flow rate of between about 50 sccm (standard cubic centimeters per minute) and 2 slm in embodiments of the invention. The temperature of the substrate may be between about −20° C. and about 200° C. during both the halogen treatment operation (operation 130) and the residual copper removal operation (operation 140).


Additional considerations will be presented in the course of presenting an alternative exemplary substrate processing chamber as well as an exemplary substrate processing system which may be used to perform residual copper removal process 100.


Exemplary Processing Equipment



FIG. 3 depicts a schematic diagram of an etch process chamber 1001 which can be incorporated into a substrate processing system 1101 described later with reference to FIG. 4. Exemplary etch process chamber 1001 may also be referred to as a decoupled-plasma source chamber or DPS chamber. Etch process chamber 1001 includes inductive coils 1012, positioned exterior to a dielectric, dome-shaped ceiling 1020 (referred to herein as the dome 1020). Other chambers may have other types of ceilings, e.g., a flat ceiling. Inductive coil 1012 can be coupled to a radio-frequency (RF) source 1018 (that is generally capable of producing an RF signal having a tunable frequency). RF source 1018 is coupled to inductive coil 1012 through a matching network 1019. Etch process chamber 1001 can include a substrate support pedestal (cathode) 1016 that is coupled to a second RF source 1022 that is generally capable of producing an RF signal. RF source 1022 can be coupled to pedestal 1016 through a matching network 1024. Etch process chamber 1001 may also contain a conductive chamber wall 1030 that is connected to an electrical ground 1034. A controller 1040 including a central processing unit (CPU) 1044, a memory 1042, and support circuits 1046 for a CPU 1044 is coupled to various components of etch process chamber 1001 to facilitate control of the etch process.


In operation, a semiconductor substrate 1014 is placed on pedestal 1016 and gaseous components are supplied from a gas handling system 1038 to etch process chamber 1001 through entry port(s) 1026 to form a gaseous mixture 1050. Gaseous mixture 1050 is ignited into a plasma 1052 in etch process chamber 1001 by applying RF power from RF sources 1018 and 1022 respectively to inductive coil 1012 and pedestal 1016. The pressure within the interior of etch process chamber 1001 is controlled using a throttle valve 1027 situated between etch process chamber 1001 and a vacuum pump 1036. The temperature at the surface of chamber wall 1030 is controlled using liquid-containing conduits (not shown) that are located in chamber wall 1030 of etch process chamber 1001.


The temperature of substrate 1014 is controlled by stabilizing the temperature of pedestal 1016 and flowing helium gas from a helium source 1048 to channels formed by the back of substrate 1014 and grooves (not shown) on the pedestal surface. The helium gas is used to facilitate heat transfer between pedestal 1016 and substrate 1014. During the etch process, substrate 1014 is heated by a resistive heater within the pedestal to a steady state temperature and the helium facilitates uniform heating of substrate 1014. Using thermal control of both dome 1020 and pedestal 1016, substrate 1014 is maintained at a temperature of between about 100° C. and about 500° C.



FIG. 4 is a schematic top-view diagram of an illustrative multi-chamber processing system 1101. The processing system 1101 can include one or more load lock chambers 1102, 1104 for transferring of substrates into and out of the processing system 1101. Typically, since the processing system 1101 is under vacuum, the load lock chambers 1102, 1104 may “pump down” the substrates introduced into the processing system 1101. A first robot 1110 may transfer the substrates between the load lock chambers 1102, 1104, and a first set of one or more substrate processing chambers 1112, 1114, 1116, 1118 (four are shown). Each processing chamber 1112, 1114, 1116, 1118, can be outfitted to perform a number of substrate processing operations including the dry etch processes described herein in addition to cyclical layer deposition (CLD), atomic layer deposition (ALD), chemical vapor deposition (CVD), physical vapor deposition (PVD), etch, pre-clean, degas, orientation and other substrate processes.


The first robot 1110 can also transfer substrates to/from one or more transfer chambers 1122, 1124. The transfer chambers 1122, 1124 can be used to maintain ultrahigh vacuum conditions while allowing substrates to be transferred within the processing system 1101. A second robot 1130 can transfer the substrates between the transfer chambers 1122, 1124 and a second set of one or more processing chambers 1132, 1134, 1136, 1138. Similar to processing chambers 1112, 1114, 1116, 1118, the processing chambers 1132, 1134, 1136, 1138 can be outfitted to perform a variety of substrate processing operations including the dry etch processes described herein in addition to cyclical layer deposition (CLD), atomic layer deposition (ALD), chemical vapor deposition (CVD), physical vapor deposition (PVD), etch, pre-clean, degas, and orientation, for example. Any of the substrate processing chambers 1112, 1114, 1116, 1118, 1132, 1134, 1136, 1138 may be removed from the processing system 1101 if not necessary for a particular process to be performed by the processing system 1101. A copper etch processing chamber for carrying out the methods described and claimed herein may be installed in any one or more of substrate processing chamber locations.


System controller 1157 is used to control motors, valves, flow controllers, power supplies and other functions required to carry out process recipes described herein. System controller 1157 may rely on feedback from optical sensors to determine and adjust the position of movable mechanical assemblies. Mechanical assemblies may include the robot, throttle valves and susceptors which are moved by motors under the control of system controller 1157. A gas handling system 1155 is used to deliver halogen-containing precursors and inert species at various stages during the methods described herein.


In an exemplary embodiment, system controller 1157 includes a hard disk drive (memory), USB ports, a floppy disk drive and a processor. System controller 1157 includes analog and digital input/output boards, interface boards and stepper motor controller boards. Various parts of multi-chamber processing system 1101 which contains processing chamber 400 are controlled by system controller 1157. The system controller executes system control software in the form of a computer program stored on computer-readable medium such as a hard disk, a floppy disk or a flash memory thumb drive. Other types of memory can also be used. The computer program includes sets of instructions that dictate the timing, mixture of gases, chamber pressure, chamber temperature, RF power levels, susceptor position, and other parameters of a particular process.


A process for etching, depositing or otherwise processing a film on a substrate or a process for cleaning chamber can be implemented using a computer program product that is executed by the controller. The computer program code can be written in any conventional computer readable programming language: for example, 68000 assembly language, C, C++, Pascal, Fortran or others. Suitable program code is entered into a single file, or multiple files, using a conventional text editor, and stored or embodied in a computer usable medium, such as a memory system of the computer. If the entered code text is in a high level language, the code is compiled, and the resultant compiler code is then linked with an object code of precompiled Microsoft Windows® library routines. To execute the linked, compiled object code the system user invokes the object code, causing the computer system to load the code in memory. The CPU then reads and executes the code to perform the tasks identified in the program.


The interface between a user and the controller may be via a touch-sensitive monitor and may also include a mouse and keyboard. In one embodiment two monitors are used, one mounted in the clean room wall for the operators and the other behind the wall for the service technicians. The two monitors may simultaneously display the same information, in which case only one is configured to accept input at a time. To select a particular screen or function, the operator touches a designated area on the display screen with a finger or the mouse. The touched area changes its highlighted color, or a new menu or screen is displayed, confirming the operator's selection.


Having disclosed several embodiments, it will be recognized by those of skill in the art that various modifications, alternative constructions, and equivalents may be used without departing from the spirit of the disclosed embodiments. Additionally, a number of well known processes and elements have not been described to avoid unnecessarily obscuring the present invention. Accordingly, the above description should not be taken as limiting the scope of the invention.


Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limits of that range is also specifically disclosed. Each smaller range between any stated value or intervening value in a stated range and any other stated or intervening value in that stated range is encompassed. The upper and lower limits of these smaller ranges may independently be included or excluded in the range, and each range where either, neither or both limits are included in the smaller ranges is also encompassed within the invention, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included.


As used herein and in the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to “a process” includes a plurality of such processes and reference to “the dielectric material” includes reference to one or more dielectric materials and equivalents thereof known to those skilled in the art, and so forth.


Also, the words “comprise,” “comprising,” “include,” “including,” and “includes” when used in this specification and in the following claims are intended to specify the presence of stated features, integers, components, or steps, but they do not preclude the presence or addition of one or more other features, integers, components, steps, acts, or groups.

Claims
  • 1. A method of cleaning a dielectric window comprising: flowing a halogen-containing precursor into a substrate processing region while forming a first local plasma in the substrate processing region having a first local plasma power to form excited halogen-containing species, wherein a copper residue on interior surfaces of the dielectric window is transformed into a copper halogen layer on the dielectric window;flowing an inert gas into the substrate processing region while forming a second local plasma in the substrate processing region having a second local plasma power, wherein the copper halogen layer is desorbed as desorbed species from the dielectric window and wherein the second local plasma occurs after the first local plasma, wherein the substrate processing region is devoid of halogens during the second local plasma aside from the desorbed species.
  • 2. The method of claim 1 wherein the desorbed species of the copper halogen layer are exhausted from the substrate processing region during or after the second local plasma.
  • 3. The method of claim 1 wherein the halogen-containing precursor comprises chlorine.
  • 4. The method of claim 1 wherein the halogen-containing precursor comprises at least one of bromine or iodine.
  • 5. The method of claim 1 wherein the inert gas comprises helium.
  • 6. The method of claim 1 wherein the substrate processing region consists essentially of one or more of hydrogen, the inert gas, and the desorbed species during the second local plasma.
  • 7. The method of claim 1 wherein the substrate processing region consists essentially of the inert gas and the desorbed species during the second local plasma.
  • 8. The method of claim 1 wherein the first local plasma and the second local plasma are each attained using inductively-coupled power.
  • 9. The method of claim 1 wherein the first local plasma power is between about 50 watts and about 2500 watts.
  • 10. The method of claim 1 wherein the second local plasma power is between about 100 watts and about 5000 watts.
  • 11. The method of claim 1 wherein a pressure within the substrate processing region is between about 0.5 mTorr and about 500 mTorr during the first local plasma.
  • 12. The method of claim 1 wherein a pressure within the substrate processing region is between about 0.5 mTorr and about 500 mTorr during the second local plasma.
  • 13. A method of cleaning a dielectric window comprising: flowing a halogen-free precursor into a substrate processing region while forming a subtractive etch local plasma in the substrate processing region having a subtractive etch local plasma power to form excited halogen-free species, wherein the subtractive etch local plasma etches copper from a substrate and leaves a copper residue on the interior surfaces of the dielectric window;removing the substrate from the substrate processing region;flowing a halogen-containing precursor into the substrate processing region while forming a halogen local plasma in the substrate processing region having a halogen local plasma power to form excited halogen-containing species, wherein the halogen local plasma transforms a copper residue on the interior surfaces of the dielectric window into a copper halogen layer; andflowing an inert gas into the substrate processing region while forming an inert gas local plasma in the substrate processing region having an inert gas local plasma power, wherein the copper halogen layer is desorbed as desorbed species from the dielectric window and wherein the inert gas local plasma occurs after the halogen local plasma, wherein the substrate processing region is devoid of halogens during the inert as local plasma aside from the desorbed species.
CROSS-REFERENCES TO RELATED APPLICATIONS

This application claims the benefit of U.S. Prov. Pat. App. No. 61/825,834 filed May 21, 2013, and titled “COPPER RESIDUE CHAMBER CLEAN” by Hoinkis et al., which is hereby incorporated herein in its entirety by reference for all purposes.

US Referenced Citations (654)
Number Name Date Kind
2369620 Sullivan et al. Feb 1945 A
3451840 Hough Jun 1969 A
3937857 Brummett et al. Feb 1976 A
4006047 Brummett et al. Feb 1977 A
4209357 Gorin et al. Jun 1980 A
4214946 Forget et al. Jul 1980 A
4232060 Mallory, Jr. Nov 1980 A
4234628 DuRose Nov 1980 A
4265943 Goldstein et al. May 1981 A
4364803 Nidola et al. Dec 1982 A
4368223 Kobayashi et al. Jan 1983 A
4397812 Mallory, Jr. Aug 1983 A
4468413 Bachmann Aug 1984 A
4565601 Kakehi et al. Jan 1986 A
4571819 Rogers et al. Feb 1986 A
4579618 Celestino et al. Apr 1986 A
4585920 Hoog et al. Apr 1986 A
4625678 Shioya et al. Dec 1986 A
4632857 Mallory, Jr. Dec 1986 A
4656052 Satou et al. Apr 1987 A
4690746 McInerney et al. Sep 1987 A
4714520 Gwozdz Dec 1987 A
4749440 Blackwood et al. Jun 1988 A
4753898 Parrillo et al. Jun 1988 A
4793897 Dunfield et al. Dec 1988 A
4807016 Douglas Feb 1989 A
4810520 Wu Mar 1989 A
4816638 Ukai et al. Mar 1989 A
4851370 Doklan et al. Jul 1989 A
4865685 Palmour Sep 1989 A
4872947 Wang et al. Oct 1989 A
4878994 Jucha et al. Nov 1989 A
4886570 Davis et al. Dec 1989 A
4892753 Wang et al. Jan 1990 A
4894352 Lane et al. Jan 1990 A
4904341 Blaugher et al. Feb 1990 A
4951601 Maydan et al. Aug 1990 A
4960488 Law et al. Oct 1990 A
4980018 Mu et al. Dec 1990 A
4981551 Palmour Jan 1991 A
4985372 Narita et al. Jan 1991 A
4994404 Sheng et al. Feb 1991 A
5000113 Wang et al. Mar 1991 A
5013691 Lory et al. May 1991 A
5030319 Nishino et al. Jul 1991 A
5061838 Lane et al. Oct 1991 A
5089441 Moslehi Feb 1992 A
5089442 Olmer Feb 1992 A
5147692 Bengston Sep 1992 A
5156881 Okano et al. Oct 1992 A
5186718 Tepman et al. Feb 1993 A
5198034 deBoer et al. Mar 1993 A
5203911 Sricharoenchaikit et al. Apr 1993 A
5215787 Homma Jun 1993 A
5228501 Tepman et al. Jul 1993 A
5231690 Soma et al. Jul 1993 A
5235139 Bengston et al. Aug 1993 A
5238499 van de Ven et al. Aug 1993 A
5240497 Shacham et al. Aug 1993 A
5248527 Uchida et al. Sep 1993 A
5252178 Moslehi Oct 1993 A
5266157 Kadomura Nov 1993 A
5270125 America et al. Dec 1993 A
5271972 Kwok et al. Dec 1993 A
5275977 Otsubo et al. Jan 1994 A
5279865 Chebi et al. Jan 1994 A
5288518 Homma Feb 1994 A
5290382 Zarowin et al. Mar 1994 A
5300463 Cathey et al. Apr 1994 A
5302233 Kim et al. Apr 1994 A
5306530 Strongin et al. Apr 1994 A
5314724 Tsukune et al. May 1994 A
5316804 Tomikawa et al. May 1994 A
5319247 Matsuura Jun 1994 A
5326427 Jerbic Jul 1994 A
5328558 Kawamura et al. Jul 1994 A
5328810 Lowrey et al. Jul 1994 A
5334552 Homma Aug 1994 A
5345999 Hosokawa Sep 1994 A
5352636 Beinglass Oct 1994 A
5356478 Chen et al. Oct 1994 A
5362526 Wang et al. Nov 1994 A
5368897 Kurihara et al. Nov 1994 A
5380560 Kaja et al. Jan 1995 A
5382311 Ishikawa et al. Jan 1995 A
5384284 Doan et al. Jan 1995 A
5385763 Okano et al. Jan 1995 A
5399529 Homma Mar 1995 A
5403434 Moslehi Apr 1995 A
5413967 Matsuda et al. May 1995 A
5415890 Kloiber et al. May 1995 A
5416048 Blalock et al. May 1995 A
5420075 Homma et al. May 1995 A
5429995 Nishiyama et al. Jul 1995 A
5439553 Grant et al. Aug 1995 A
5451259 Krogh Sep 1995 A
5468342 Nulty et al. Nov 1995 A
5474589 Ohga et al. Dec 1995 A
5478403 Shinagawa et al. Dec 1995 A
5478462 Walsh Dec 1995 A
5483920 Pryor Jan 1996 A
5500249 Telford et al. Mar 1996 A
5505816 Barnes et al. Apr 1996 A
5510216 Calabrese et al. Apr 1996 A
5516367 Lei et al. May 1996 A
5531835 Fodor et al. Jul 1996 A
5534070 Okamura et al. Jul 1996 A
5536360 Nguyen et al. Jul 1996 A
5549780 Koinuma et al. Aug 1996 A
5558717 Zhao et al. Sep 1996 A
5560779 Knowles et al. Oct 1996 A
5563105 Dobuzinsky et al. Oct 1996 A
5571576 Qian et al. Nov 1996 A
5578130 Hayashi et al. Nov 1996 A
5591269 Arami et al. Jan 1997 A
5599740 Jang et al. Feb 1997 A
5624582 Cain Apr 1997 A
5626922 Miyanaga et al. May 1997 A
5635086 Warren, Jr. Jun 1997 A
5645645 Zhang et al. Jul 1997 A
5648125 Cane Jul 1997 A
5648175 Russell et al. Jul 1997 A
5656093 Burkhart et al. Aug 1997 A
5661093 Ravi et al. Aug 1997 A
5674787 Zhao et al. Oct 1997 A
5679606 Wang et al. Oct 1997 A
5688331 Aruga et al. Nov 1997 A
5695810 Dubin et al. Dec 1997 A
5712185 Tsai et al. Jan 1998 A
5716500 Bardos et al. Feb 1998 A
5716506 Maclay et al. Feb 1998 A
5719085 Moon et al. Feb 1998 A
5733816 Iyer et al. Mar 1998 A
5747373 Yu May 1998 A
5755859 Brusic et al. May 1998 A
5756400 Ye et al. May 1998 A
5756402 Jimbo et al. May 1998 A
5781693 Ballance et al. Jul 1998 A
5786276 Brooks et al. Jul 1998 A
5789300 Fulford Aug 1998 A
5800686 Littau et al. Sep 1998 A
5804259 Robles Sep 1998 A
5812403 Fong et al. Sep 1998 A
5820723 Benjamin et al. Oct 1998 A
5824599 Schacham-Diamand et al. Oct 1998 A
5830805 Shacham-Diamand et al. Nov 1998 A
5838055 Kleinhenz et al. Nov 1998 A
5843538 Ehrsam et al. Dec 1998 A
5844195 Fairbairn et al. Dec 1998 A
5846332 Zhao et al. Dec 1998 A
5846375 Gilchrist et al. Dec 1998 A
5846598 Semkow et al. Dec 1998 A
5849639 Molloy et al. Dec 1998 A
5850105 Dawson et al. Dec 1998 A
5855681 Maydan et al. Jan 1999 A
5856240 Sinha et al. Jan 1999 A
5858876 Chew Jan 1999 A
5872052 Iyer Feb 1999 A
5872058 Van Cleemput et al. Feb 1999 A
5882786 Nassau et al. Mar 1999 A
5885404 Kim et al. Mar 1999 A
5885749 Huggins et al. Mar 1999 A
5888906 Sandhu et al. Mar 1999 A
5891349 Tobe et al. Apr 1999 A
5891513 Dubin et al. Apr 1999 A
5897751 Makowiecki Apr 1999 A
5899752 Hey et al. May 1999 A
5904827 Reynolds May 1999 A
5907790 Kellam May 1999 A
5910340 Uchida et al. Jun 1999 A
5913140 Roche et al. Jun 1999 A
5913147 Dubin et al. Jun 1999 A
5915190 Pirkle Jun 1999 A
5920792 Lin Jul 1999 A
5932077 Reynolds Aug 1999 A
5933757 Yoshikawa et al. Aug 1999 A
5935334 Fong et al. Aug 1999 A
5937323 Orczyk et al. Aug 1999 A
5939831 Fong et al. Aug 1999 A
5942075 Nagahata et al. Aug 1999 A
5944902 Redeker et al. Aug 1999 A
5951601 Lesinski et al. Sep 1999 A
5951776 Selyutin et al. Sep 1999 A
5953635 Andideh Sep 1999 A
5968610 Liu et al. Oct 1999 A
5969422 Ting et al. Oct 1999 A
5976327 Tanaka Nov 1999 A
5990000 Hong et al. Nov 1999 A
5990013 Berenguer et al. Nov 1999 A
5993916 Zhao et al. Nov 1999 A
6004884 Abraham Dec 1999 A
6010962 Liu et al. Jan 2000 A
6013191 Nasser-Faili et al. Jan 2000 A
6013584 M'Saad Jan 2000 A
6015724 Yamazaki et al. Jan 2000 A
6015747 Lopatin et al. Jan 2000 A
6020271 Yanagida Feb 2000 A
6030666 Lam et al. Feb 2000 A
6030881 Papasouliotis et al. Feb 2000 A
6035101 Sajoto et al. Mar 2000 A
6037018 Jang et al. Mar 2000 A
6037266 Tao et al. Mar 2000 A
6039851 Iyer Mar 2000 A
6053982 Halpin et al. Apr 2000 A
6059643 Hu et al. May 2000 A
6063683 Wu et al. May 2000 A
6063712 Gilton et al. May 2000 A
6065424 Shacham-Diamand et al. May 2000 A
6072227 Yau et al. Jun 2000 A
6077780 Dubin Jun 2000 A
6080529 Ye et al. Jun 2000 A
6083344 Hanawa et al. Jul 2000 A
6086677 Umotoy et al. Jul 2000 A
6087278 Kim et al. Jul 2000 A
6093594 Yeap et al. Jul 2000 A
6099697 Hausmann Aug 2000 A
6107199 Allen et al. Aug 2000 A
6110530 Chen et al. Aug 2000 A
6110836 Cohen et al. Aug 2000 A
6110838 Loewenstein Aug 2000 A
6113771 Landau et al. Sep 2000 A
6117245 Mandrekar et al. Sep 2000 A
6136163 Cheung et al. Oct 2000 A
6136685 Narwankar et al. Oct 2000 A
6136693 Chan et al. Oct 2000 A
6140234 Uzoh et al. Oct 2000 A
6144099 Lopatin et al. Nov 2000 A
6147009 Grill et al. Nov 2000 A
6149828 Vaartstra Nov 2000 A
6150628 Smith et al. Nov 2000 A
6153935 Edelstein et al. Nov 2000 A
6165912 McConnell et al. Dec 2000 A
6167834 Wang et al. Jan 2001 B1
6169021 Akram et al. Jan 2001 B1
6170428 Redeker et al. Jan 2001 B1
6171661 Zheng et al. Jan 2001 B1
6174812 Hsiung et al. Jan 2001 B1
6176198 Kao et al. Jan 2001 B1
6177245 Ward et al. Jan 2001 B1
6179924 Zhao et al. Jan 2001 B1
6180523 Lee et al. Jan 2001 B1
6182602 Redeker et al. Feb 2001 B1
6189483 Ishikawa et al. Feb 2001 B1
6190233 Hong et al. Feb 2001 B1
6191026 Rana et al. Feb 2001 B1
6194038 Rossman Feb 2001 B1
6197181 Chen Mar 2001 B1
6197364 Paunovic et al. Mar 2001 B1
6197680 Lin et al. Mar 2001 B1
6197688 Simpson Mar 2001 B1
6197705 Vassiliev Mar 2001 B1
6203863 Liu et al. Mar 2001 B1
6204200 Shieh et al. Mar 2001 B1
6217658 Orczyk et al. Apr 2001 B1
6228233 Lakshmikanthan et al. May 2001 B1
6228751 Yamazaki et al. May 2001 B1
6228758 Pellerin et al. May 2001 B1
6235643 Mui et al. May 2001 B1
6238513 Arnold et al. May 2001 B1
6238582 Williams et al. May 2001 B1
6241845 Gadgil et al. Jun 2001 B1
6242349 Nogami et al. Jun 2001 B1
6245670 Cheung et al. Jun 2001 B1
6251236 Stevens Jun 2001 B1
6251802 Moore et al. Jun 2001 B1
6258220 Dordi et al. Jul 2001 B1
6258223 Cheung et al. Jul 2001 B1
6258270 Hilgendorff et al. Jul 2001 B1
6261637 Oberle Jul 2001 B1
6277752 Chen Aug 2001 B1
6277763 Kugimiya et al. Aug 2001 B1
6281135 Han et al. Aug 2001 B1
6291282 Wilk et al. Sep 2001 B1
6291348 Lopatin et al. Sep 2001 B1
6303418 Cha et al. Oct 2001 B1
6312995 Yu Nov 2001 B1
6313035 Sandhu et al. Nov 2001 B1
6319387 Krishnamoorthy et al. Nov 2001 B1
6323128 Sambucetti et al. Nov 2001 B1
6335261 Natzle et al. Jan 2002 B1
6335288 Kwan et al. Jan 2002 B1
6340435 Bjorkman et al. Jan 2002 B1
6342733 Hu et al. Jan 2002 B1
6344410 Lopatin et al. Feb 2002 B1
6350320 Sherstinsky et al. Feb 2002 B1
6351013 Luning et al. Feb 2002 B1
6352081 Lu et al. Mar 2002 B1
6364949 Or et al. Apr 2002 B1
6364954 Umotoy et al. Apr 2002 B2
6364957 Schneider et al. Apr 2002 B1
6372657 Hineman et al. Apr 2002 B1
6375748 Yudovsky et al. Apr 2002 B1
6379575 Yin et al. Apr 2002 B1
6383951 Li May 2002 B1
6387207 Janakiraman et al. May 2002 B1
6395150 Van Cleemput et al. May 2002 B1
6403491 Liu et al. Jun 2002 B1
6416647 Dordi et al. Jul 2002 B1
6432819 Pavate et al. Aug 2002 B1
6436816 Lee et al. Aug 2002 B1
6440863 Tsai et al. Aug 2002 B1
6441492 Cunningham Aug 2002 B1
6446572 Brcka Sep 2002 B1
6448537 Nering Sep 2002 B1
6458718 Todd Oct 2002 B1
6462371 Weimer et al. Oct 2002 B1
6465366 Nemani et al. Oct 2002 B1
6477980 White et al. Nov 2002 B1
6479373 Dreybrodt et al. Nov 2002 B2
6488984 Wada et al. Dec 2002 B1
6494959 Dreybrodt et al. Dec 2002 B1
6500728 Wang Dec 2002 B1
6503843 Xia et al. Jan 2003 B1
6506291 Tsai et al. Jan 2003 B2
6516815 Stevens et al. Feb 2003 B1
6518548 Sugaya et al. Feb 2003 B2
6527968 Wang et al. Mar 2003 B1
6528409 Lopatin et al. Mar 2003 B1
6531377 Knorr et al. Mar 2003 B2
6537733 Campana et al. Mar 2003 B2
6541397 Bencher Apr 2003 B1
6541671 Martinez et al. Apr 2003 B1
6544340 Yudovsky Apr 2003 B2
6547977 Yan et al. Apr 2003 B1
6551924 Dalton et al. Apr 2003 B1
6565729 Chen et al. May 2003 B2
6569773 Gellrich et al. May 2003 B1
6573030 Fairbairn et al. Jun 2003 B1
6573606 Sambucetti et al. Jun 2003 B2
6596602 Iizuka et al. Jul 2003 B2
6596654 Bayman et al. Jul 2003 B1
6602434 Hung et al. Aug 2003 B1
6603269 Vo et al. Aug 2003 B1
6605874 Leu et al. Aug 2003 B2
6616967 Test Sep 2003 B1
6627532 Gaillard et al. Sep 2003 B1
6635578 Xu et al. Oct 2003 B1
6638810 Bakli et al. Oct 2003 B2
6645301 Sainty et al. Nov 2003 B2
6645550 Cheung et al. Nov 2003 B1
6656831 Lee et al. Dec 2003 B1
6656837 Xu et al. Dec 2003 B2
6677242 Liu et al. Jan 2004 B1
6677247 Yuan et al. Jan 2004 B2
6679981 Pan et al. Jan 2004 B1
6717189 Inoue et al. Apr 2004 B2
6720213 Gambino et al. Apr 2004 B1
6740585 Yoon et al. May 2004 B2
6743473 Parkhe et al. Jun 2004 B1
6743732 Lin et al. Jun 2004 B1
6759261 Shimokohbe et al. Jul 2004 B2
6762127 Boiteux et al. Jul 2004 B2
6762435 Towle Jul 2004 B2
6764958 Nemani et al. Jul 2004 B1
6765273 Chau et al. Jul 2004 B1
6772827 Keller et al. Aug 2004 B2
6794290 Papasouliotis et al. Sep 2004 B1
6794311 Huang et al. Sep 2004 B2
6796314 Graff et al. Sep 2004 B1
6797189 Hung et al. Sep 2004 B2
6800830 Mahawili Oct 2004 B2
6802944 Ahmad et al. Oct 2004 B2
6808564 Dietze Oct 2004 B2
6808748 Kapoor et al. Oct 2004 B2
6821571 Huang Nov 2004 B2
6823589 White et al. Nov 2004 B2
6830624 Janakiraman et al. Dec 2004 B2
6835995 Li Dec 2004 B2
6846745 Papasouliotis et al. Jan 2005 B1
6858153 Bjorkman et al. Feb 2005 B2
6867141 Jung et al. Mar 2005 B2
6869880 Krishnaraj et al. Mar 2005 B2
6878206 Tzu et al. Apr 2005 B2
6879981 Rothschild et al. Apr 2005 B2
6893967 Wright et al. May 2005 B1
6903031 Karim et al. Jun 2005 B2
6903511 Chistyakov Jun 2005 B2
6908862 Li et al. Jun 2005 B2
6911112 An Jun 2005 B2
6911401 Khandan et al. Jun 2005 B2
6921556 Shimizu et al. Jul 2005 B2
6924191 Liu et al. Aug 2005 B2
6942753 Choi et al. Sep 2005 B2
6951821 Hamelin et al. Oct 2005 B2
6958175 Sakamoto et al. Oct 2005 B2
6958286 Chen et al. Oct 2005 B2
6974780 Schuegraf Dec 2005 B2
7017269 White et al. Mar 2006 B2
7030034 Fucsko et al. Apr 2006 B2
7049200 Arghavani et al. May 2006 B2
7078312 Sutanto et al. Jul 2006 B1
7081414 Zhang et al. Jul 2006 B2
7084070 Lee et al. Aug 2006 B1
7115525 Abatchev et al. Oct 2006 B2
7122949 Strikovski Oct 2006 B2
7148155 Tarafdar et al. Dec 2006 B1
7166233 Johnson et al. Jan 2007 B2
7183214 Nam et al. Feb 2007 B2
7196342 Ershov et al. Mar 2007 B2
7205240 Karim et al. Apr 2007 B2
7223701 Min et al. May 2007 B2
7226805 Hallin et al. Jun 2007 B2
7253123 Arghavani et al. Aug 2007 B2
7256370 Guiver Aug 2007 B2
7288482 Panda et al. Oct 2007 B2
7341633 Lubomirsky et al. Mar 2008 B2
7390710 Derderian et al. Jun 2008 B2
7396480 Kao et al. Jul 2008 B2
7465358 Weidman et al. Dec 2008 B2
7484473 Keller et al. Feb 2009 B2
7488688 Chung et al. Feb 2009 B2
7494545 Lam et al. Feb 2009 B2
7581511 Mardian et al. Sep 2009 B2
7628897 Mungekar et al. Dec 2009 B2
7709396 Bencher et al. May 2010 B2
7722925 White et al. May 2010 B2
7785672 Choi et al. Aug 2010 B2
7807578 Bencher et al. Oct 2010 B2
7871926 Xia et al. Jan 2011 B2
7910491 Soo Kwon et al. Mar 2011 B2
7915139 Lang et al. Mar 2011 B1
7939422 Ingle et al. May 2011 B2
7968441 Xu Jun 2011 B2
7981806 Jung Jul 2011 B2
8008166 Sanchez et al. Aug 2011 B2
8058179 Draeger et al. Nov 2011 B1
8071482 Kawada Dec 2011 B2
8074599 Choi et al. Dec 2011 B2
8083853 Choi et al. Dec 2011 B2
8133349 Panagopoulos Mar 2012 B1
8187486 Liu et al. May 2012 B1
8211808 Sapre et al. Jul 2012 B2
8309440 Sanchez et al. Nov 2012 B2
8328939 Choi et al. Dec 2012 B2
8435902 Tang et al. May 2013 B2
8491805 Kushibiki et al. Jul 2013 B2
8642481 Wang et al. Feb 2014 B2
20010008803 Takamatsu et al. Jul 2001 A1
20010015261 Kobayashi et al. Aug 2001 A1
20010028922 Sandhu Oct 2001 A1
20010030366 Nakano et al. Oct 2001 A1
20010034121 Fu et al. Oct 2001 A1
20010041444 Shields et al. Nov 2001 A1
20010055842 Uh et al. Dec 2001 A1
20020011210 Satoh et al. Jan 2002 A1
20020016080 Khan et al. Feb 2002 A1
20020016085 Huang et al. Feb 2002 A1
20020028585 Chung et al. Mar 2002 A1
20020029747 Powell et al. Mar 2002 A1
20020033233 Savas Mar 2002 A1
20020036143 Segawa et al. Mar 2002 A1
20020045966 Lee et al. Apr 2002 A1
20020054962 Huang May 2002 A1
20020069820 Yudovsky Jun 2002 A1
20020098681 Hu et al. Jul 2002 A1
20020124867 Kim et al. Sep 2002 A1
20020177322 Li et al. Nov 2002 A1
20020187655 Tan et al. Dec 2002 A1
20020197823 Yoo et al. Dec 2002 A1
20030010645 Ting et al. Jan 2003 A1
20030019428 Ku et al. Jan 2003 A1
20030029566 Roth Feb 2003 A1
20030029715 Yu et al. Feb 2003 A1
20030032284 Enomoto et al. Feb 2003 A1
20030038127 Liu et al. Feb 2003 A1
20030038305 Wasshuber Feb 2003 A1
20030072639 White et al. Apr 2003 A1
20030075808 Inoue et al. Apr 2003 A1
20030077909 Jiwari Apr 2003 A1
20030079686 Chen et al. May 2003 A1
20030087531 Kang et al. May 2003 A1
20030091938 Fairbairn et al. May 2003 A1
20030098125 An May 2003 A1
20030109143 Hsieh et al. Jun 2003 A1
20030116087 Nguyen et al. Jun 2003 A1
20030116439 Seo et al. Jun 2003 A1
20030121608 Chen et al. Jul 2003 A1
20030124465 Lee et al. Jul 2003 A1
20030124842 Hytros et al. Jul 2003 A1
20030129106 Sorensen et al. Jul 2003 A1
20030129827 Lee et al. Jul 2003 A1
20030132319 Hytros et al. Jul 2003 A1
20030148035 Lingampalli Aug 2003 A1
20030173333 Wang et al. Sep 2003 A1
20030173347 Guiver Sep 2003 A1
20030181040 Ivanov et al. Sep 2003 A1
20030183244 Rossman Oct 2003 A1
20030190426 Padhi et al. Oct 2003 A1
20030199170 Li Oct 2003 A1
20030221780 Lei et al. Dec 2003 A1
20030224217 Byun et al. Dec 2003 A1
20030224617 Baek et al. Dec 2003 A1
20040005726 Huang Jan 2004 A1
20040033678 Arghavani et al. Feb 2004 A1
20040069225 Fairbairn et al. Apr 2004 A1
20040070346 Choi Apr 2004 A1
20040072446 Liu et al. Apr 2004 A1
20040101667 O'Loughlin et al. May 2004 A1
20040110354 Natzle et al. Jun 2004 A1
20040115876 Goundar et al. Jun 2004 A1
20040129224 Yamazaki Jul 2004 A1
20040137161 Segawa et al. Jul 2004 A1
20040154535 Chen et al. Aug 2004 A1
20040175929 Schmitt et al. Sep 2004 A1
20040182315 Laflamme et al. Sep 2004 A1
20040192032 Ohmori et al. Sep 2004 A1
20040194799 Kim et al. Oct 2004 A1
20040211357 Gadgil et al. Oct 2004 A1
20040219789 Wood et al. Nov 2004 A1
20040245091 Karim et al. Dec 2004 A1
20050001276 Gao et al. Jan 2005 A1
20050003676 Ho et al. Jan 2005 A1
20050009358 Choi et al. Jan 2005 A1
20050026430 Kim et al. Feb 2005 A1
20050026431 Kazumi et al. Feb 2005 A1
20050035455 Hu et al. Feb 2005 A1
20050048801 Karim et al. Mar 2005 A1
20050090120 Hasegawa et al. Apr 2005 A1
20050098111 Shimizu et al. May 2005 A1
20050112901 Ji et al. May 2005 A1
20050121750 Chan et al. Jun 2005 A1
20050181588 Kim Aug 2005 A1
20050199489 Stevens et al. Sep 2005 A1
20050205110 Kao et al. Sep 2005 A1
20050218507 Kao et al. Oct 2005 A1
20050221552 Kao et al. Oct 2005 A1
20050230350 Kao et al. Oct 2005 A1
20050236694 Wu et al. Oct 2005 A1
20050266622 Arghavani et al. Dec 2005 A1
20050266691 Gu et al. Dec 2005 A1
20050287771 Seamons et al. Dec 2005 A1
20060000805 Todorow et al. Jan 2006 A1
20060019456 Bu et al. Jan 2006 A1
20060019486 Yu et al. Jan 2006 A1
20060024954 Wu et al. Feb 2006 A1
20060024956 Zhijian et al. Feb 2006 A1
20060033678 Lubomirsky et al. Feb 2006 A1
20060046419 Sandhu et al. Mar 2006 A1
20060046484 Abatchev et al. Mar 2006 A1
20060051966 Or et al. Mar 2006 A1
20060051968 Joshi et al. Mar 2006 A1
20060054184 Mozetic et al. Mar 2006 A1
20060093756 Rajagopalan et al. May 2006 A1
20060102076 Smith et al. May 2006 A1
20060130971 Chang et al. Jun 2006 A1
20060166107 Chen et al. Jul 2006 A1
20060166515 Karim et al. Jul 2006 A1
20060178008 Yeh et al. Aug 2006 A1
20060185592 Matsuura Aug 2006 A1
20060207504 Hasebe et al. Sep 2006 A1
20060211260 Tran et al. Sep 2006 A1
20060216923 Tran et al. Sep 2006 A1
20060226121 Aoi Oct 2006 A1
20060240661 Annapragada et al. Oct 2006 A1
20060246217 Weidman et al. Nov 2006 A1
20060251800 Weidman et al. Nov 2006 A1
20060251801 Weidman et al. Nov 2006 A1
20060252252 Zhu et al. Nov 2006 A1
20060261490 Su et al. Nov 2006 A1
20060264003 Eun Nov 2006 A1
20060264043 Stewart et al. Nov 2006 A1
20070071888 Shanmugasundram et al. Mar 2007 A1
20070072408 Enomoto et al. Mar 2007 A1
20070090325 Hwang et al. Apr 2007 A1
20070099428 Shamiryan et al. May 2007 A1
20070099431 Li May 2007 A1
20070099438 Ye et al. May 2007 A1
20070107750 Sawin et al. May 2007 A1
20070108404 Stewart et al. May 2007 A1
20070111519 Lubomirsky et al. May 2007 A1
20070117396 Wu et al. May 2007 A1
20070123051 Arghavani et al. May 2007 A1
20070181057 Lam et al. Aug 2007 A1
20070197028 Byun et al. Aug 2007 A1
20070232071 Balseanu et al. Oct 2007 A1
20070238321 Futase et al. Oct 2007 A1
20070269976 Futase et al. Nov 2007 A1
20070281106 Lubomirsky et al. Dec 2007 A1
20080044990 Lee Feb 2008 A1
20080081483 Wu Apr 2008 A1
20080085604 Hoshino et al. Apr 2008 A1
20080099431 Kumar et al. May 2008 A1
20080115726 Ingle et al. May 2008 A1
20080124919 Huang et al. May 2008 A1
20080124937 Xu et al. May 2008 A1
20080142483 Hua et al. Jun 2008 A1
20080160210 Yang et al. Jul 2008 A1
20080162781 Haller et al. Jul 2008 A1
20080182381 Kiyotoshi Jul 2008 A1
20080182382 Ingle et al. Jul 2008 A1
20080230519 Takahashi Sep 2008 A1
20080233709 Conti et al. Sep 2008 A1
20080261404 Kozuka et al. Oct 2008 A1
20080268645 Kao et al. Oct 2008 A1
20080292798 Huh et al. Nov 2008 A1
20090004849 Eun Jan 2009 A1
20090017227 Fu et al. Jan 2009 A1
20090045167 Maruyama Feb 2009 A1
20090104738 Ring et al. Apr 2009 A1
20090104764 Xia et al. Apr 2009 A1
20090104782 Lu et al. Apr 2009 A1
20090189246 Wu et al. Jul 2009 A1
20090255902 Satoh et al. Oct 2009 A1
20090275205 Kiehlbauch et al. Nov 2009 A1
20090275206 Katz et al. Nov 2009 A1
20090280650 Lubomirsky et al. Nov 2009 A1
20100059889 Gosset et al. Mar 2010 A1
20100075503 Bencher et al. Mar 2010 A1
20100093151 Arghavani et al. Apr 2010 A1
20100098884 Balseanu et al. Apr 2010 A1
20100099236 Kwon et al. Apr 2010 A1
20100099263 Kao et al. Apr 2010 A1
20100105209 Winniczek et al. Apr 2010 A1
20100144140 Chandrashekar et al. Jun 2010 A1
20100173499 Tao et al. Jul 2010 A1
20100187534 Nishi et al. Jul 2010 A1
20100187588 Kim et al. Jul 2010 A1
20100330814 Yokota et al. Dec 2010 A1
20110008950 Xu Jan 2011 A1
20110034035 Liang et al. Feb 2011 A1
20110053380 Sapre et al. Mar 2011 A1
20110081782 Liang et al. Apr 2011 A1
20110143542 Feurprier et al. Jun 2011 A1
20110151674 Tang et al. Jun 2011 A1
20110151676 Ingle et al. Jun 2011 A1
20110151677 Wang et al. Jun 2011 A1
20110151678 Ashtiani et al. Jun 2011 A1
20110159690 Chandrashekar et al. Jun 2011 A1
20110165771 Ring et al. Jul 2011 A1
20110195575 Wang Aug 2011 A1
20110226734 Sumiya et al. Sep 2011 A1
20110230052 Tang et al. Sep 2011 A1
20110266252 Thadani et al. Nov 2011 A1
20110294300 Zhang et al. Dec 2011 A1
20120003782 Byun et al. Jan 2012 A1
20120009796 Cui et al. Jan 2012 A1
20120068242 Shin et al. Mar 2012 A1
20120135576 Lee et al. May 2012 A1
20120164839 Nishimura Jun 2012 A1
20120196447 Yang et al. Aug 2012 A1
20120211462 Zhang et al. Aug 2012 A1
20120238102 Zhang et al. Sep 2012 A1
20120238103 Zhang et al. Sep 2012 A1
20120285621 Tan Nov 2012 A1
20120292664 Kanike Nov 2012 A1
20120309204 Kang et al. Dec 2012 A1
20130034968 Zhang et al. Feb 2013 A1
20130045605 Wang et al. Feb 2013 A1
20130052827 Wang et al. Feb 2013 A1
20130052833 Ranjan et al. Feb 2013 A1
20130059440 Wang et al. Mar 2013 A1
20130089988 Wang et al. Apr 2013 A1
20130119483 Alptekin et al. May 2013 A1
20130260533 Sapre et al. Oct 2013 A1
Foreign Referenced Citations (90)
Number Date Country
1375575 Oct 2002 CN
1412861 Apr 2003 CN
101465386 Jun 2009 CN
0329406 Aug 1989 EP
0376252 Jul 1990 EP
0475567 Mar 1992 EP
0 496 543 Jul 1992 EP
0 658 928 Jun 1995 EP
0697467 Feb 1996 EP
0913498 May 1999 EP
1099776 May 2001 EP
1107288 Jun 2001 EP
1496542 Jan 2005 EP
1568797 Aug 2005 EP
2285174 Jun 1995 GB
61-276977 Dec 1986 JP
2058836 Feb 1990 JP
02-121330 May 1990 JP
02256235 Oct 1990 JP
4-239750 Jul 1992 JP
4-341568 Nov 1992 JP
07-130713 May 1995 JP
7-161703 Jun 1995 JP
7297543 Nov 1995 JP
08-306671 Nov 1996 JP
09153481 Jun 1997 JP
09-205140 Aug 1997 JP
10-178004 Jun 1998 JP
2010-154699 Jun 1998 JP
11124682 May 1999 JP
H11-204442 Jul 1999 JP
2000-012514 Jan 2000 JP
2001-308023 Nov 2001 JP
2002-100578 Apr 2002 JP
2002-141349 May 2002 JP
2002-222861 Aug 2002 JP
2002-256235 Sep 2002 JP
2003-019433 Jan 2003 JP
2003-059914 Feb 2003 JP
2003-179038 Jun 2003 JP
2003-217898 Jul 2003 JP
2003-318158 Nov 2003 JP
2003-347278 Dec 2003 JP
2004-047956 Feb 2004 JP
2004-156143 Jun 2004 JP
04-239723 Aug 2004 JP
2005-033023 Feb 2005 JP
2007-173383 Jul 2007 JP
08-148470 Jun 2008 JP
10-0155601 Dec 1998 KR
10-0236219 Dec 1999 KR
1020000008278 Feb 2000 KR
2000-0044928 Jul 2000 KR
2001-0014064 Feb 2001 KR
10-2001-0049274 Jun 2001 KR
10-2001-0058774 Jul 2001 KR
10-1050454 Jul 2001 KR
10-2001-0082109 Aug 2001 KR
1020030081177 Oct 2003 KR
10-2004-0049739 Jun 2004 KR
10-2004-0096365 Nov 2004 KR
1020050042701 May 2005 KR
10-0681390 Sep 2006 KR
1020080063988 Jul 2008 KR
10-2010-0013980 Feb 2010 KR
10-2010-0074508 Jul 2010 KR
1020110126675 Nov 2011 KR
1020120082640 Jul 2012 KR
9220833 Nov 1992 WO
9926277 May 1999 WO
9954920 Oct 1999 WO
9954920 Oct 1999 WO
9962108 Dec 1999 WO
0013225 Mar 2000 WO
0022671 Apr 2000 WO
0022671 Apr 2000 WO
0194719 Dec 2001 WO
02083981 Oct 2002 WO
03014416 Feb 2003 WO
2004006303 Jan 2004 WO
2004074932 Sep 2004 WO
2004114366 Dec 2004 WO
2005036615 Apr 2005 WO
2006069085 Jun 2006 WO
2009071627 Jun 2009 WO
2011087580 Jul 2011 WO
2011115761 Sep 2011 WO
2011139435 Nov 2011 WO
2012018449 Feb 2012 WO
2012125654 Sep 2012 WO
Non-Patent Literature Citations (67)
Entry
C.K. Hu, et al. “Reduced Electromigration of Cu Wires by Surface Coating” Applied Physics Letters, vol. 81, No. 10, Sep. 2, 2002—pp. 1782-1784.
European Search Report dated May 23, 2006 for EP Application No. 05251143.3.
European Examination Report dated Nov. 13, 2007 for EP Application No. 05251143.3.
EP Partial Search Report, Application No. 08150111.601235/1944796, dated Aug. 22, 2008.
Eze, F. C., “Electroless deposition of CoO thin films,” J. Phys. D: Appl. Phys. 32 (1999), pp. 533-540.
Galiano et al. “Stress-Temperature Behavior of Oxide Films Used for Intermetal Dielectric Applications”, VMIC Conference, Jun. 9-10, 1992, pp. 100-106.
Iijima, et al., “Highly Selective SiO2 Etch Employing Inductively Coupled Hydro-Fluorocarbon Plasma Chemistry for Self Aligned Contact Etch”, Jpn. J. Appl. Phys., Sep. 1997, pp. 5498-5501, vol. 36, Part 1, No. 9A.
International Search Report of PCT/US2009/059743 mailed on Apr. 26, 2010, 4 pages.
International Search Report of PCT/US2012/061726 mailed on May 16, 2013, 3 pages.
International Search Report of PCT/2013/052039 mailed on Nov. 8, 2013, 9 pages.
International Search Report of PCT/2013/037202 mailed on Aug. 23, 2013, 11 pages.
Lin, et al., “Manufacturing of Cu Electroless Nickel/Sn—Pb Flip Chip Solder Bumps”, IEEE Transactions on Advanced Packaging, vol. 22, No. 4 (Nov. 1999), pp. 575-579.
Lopatin, et al., “Thin Electroless barrier for copper films”, Part of the SPIE Conference of Multilevel Interconnect technology II, SPIE vol. 3508 (1998), pp. 65-77.
Musaka, “Single Step Gap Filling Technology fo Subhalf Micron Metal Spacings on Plasma Enhanced TEOS/O2 Chemical Vapor Deposition System,” Extended Abstracts of the 1993 International Conference on Solid State Devices and Materials pages, 1993, 510-512.
Pearlstein, Fred. “Electroless Plating,” J. Res. Natl. Bur. Stan., Ch. 31 (1974), pp. 710-747.
Saito, et al., “Electroless deposition of Ni—B, Co—B and Ni—Co—B alloys using dimethylamineborane as a reducing agent,” Journal of Applied Electrochemistry 28 (1998), pp. 559-563.
Schacham-Diamond, et al., “Electrochemically deposited thin film alloys for ULSI and MEMS applications,” Microelectronic Engineering 50 (2000), pp. 525-531.
Schacham-Diamond, et al. “Material properties of electroless 100-200 nm thick CoWP films,” Electrochemical Society Proceedings, vol. 99-34, pp. 102-110.
Smayling, et al., “APF® Pitch-Halving for 2nm Logic Cells using Gridded Design Rules”, proceedings of the SPIE, 2008, 8 pages.
Vassiliev, et al., “Trends in void-free pre-metal CVD dielectrics,” Solid State Technology, Mar. 2001, pp. 129-136.
Weston, et al., “Ammonium Compounds,” Kirk-Othmer Encyclopedia of Chemical Technology, 2003,30 pages see pp. 717-718, John Wiley & Sons, Inc.
Yosi Shacham-Diamond, et al. “High Aspect Ratio Quarter-Micron Electroless Copper Integrated Technology”, Microelectronic Engineering 37/38 (1997) pp. 77-88.
Abraham, “Reactive Facet Tapering of Plasma Oxide for Multilevel Interconnect Applications”, IEEE, V-MIC Conference, Jun. 15-16, 1987, pp. 115-121.
Applied Materials, Inc., “Applied Siconi™ Preclean,” printed on Aug. 7, 2009, 8 pages.
Carlson, et al., “A Negative Spacer Lithography Process for Sub-100nm Contact Holes and Vias”, University of California at Berkeley, Jun. 19, 2007, 4 pp.
Chang et al. “Frequency Effects and Properties of Plasma Deposited Fluorinated Silicon Nitride”, J. Vac Sci Technol B 6(2), Mar./Apr. 1988, pp. 524-532.
Cheng, et al., “New Test Structure to Identify Step Coverage Mechanisms in Chemical Vapor Deposition of Silicon Dioxide,” Appl. Phys. Lett., 58 (19), May 13, 1991, p. 2147-2149.
Examination Report dated Jun. 28, 2010 for European Patent Application No. 05251143.3.
Fukada et al., “Preparation of SiOF Films with Low Dielectric Constant by ECR Plasma CVD,” ISMIC, DUMIC Conference, Feb. 21-22, 1995, pp. 43-49.
Hashim et al., “Characterization of thin oxide removal by RTA Treatment,” ICSE 1998 Proc. Nov. 1998, Rangi, Malaysia, pp. 213-216.
Hausmann, et al., “Rapid Vapor Deposition of Highly Conformal Silica Nanolaminates,” Science, Oct. 11, 2002, p. 402-406, vol. 298.
Hayasaka, N. et al. “High Quality Low Dielectric Constant SiO2 CVD Using High Density Plasma,” Proceedings of the Dry Process Symposium, 1993, pp. 163-168.
Hwang et al., “Smallest Bit-Line Contact of 76nm pitch on NAND Flash Cell by using Reversal PR (Photo Resist) and SADP (Self-Align Double Patterning) Process,” IEEE/SEMI Advanced Semiconductor Manufacturing Conference, 2007, 3 pages.
International Search Report and Written Opinion of the International Searching Authority mailed Jul. 3, 2008.
International Search Report and Written Opinion for PCT Application No. PCT/US2011/027221, mailed on Nov. 1, 2011, 8 pages.
International Search Report and Written Opinion of PCT/US2010/057676 mailed on Jun. 27, 2011, 9 pages.
International Search Report and Written Opinion of PCT/US2011/030582 mailed Dec. 7, 2011, 9 pages.
International Search Report and Written Opinion of PCT/US2011/064724 mailed on Oct. 12, 2012, 8 pages.
International Search Report and Written Opinion of PCT/US2012/028952 mailed on Oct. 29, 2012, 9 pages.
International Search Report and Written Opinion of PCT/US2012/048842 mailed on Nov. 28, 2012, 10 pages.
International Search Report and Written Opinion of PCT/US2012/053329 mailed on Feb. 15, 2013, 8 pages.
International Search Report and Written Opinion of PCT/US2012/057294 mailed on Mar. 18, 2013, 12 pages.
International Search Report and Written Opinion of PCT/US2012/057358 mailed on Mar. 25, 2013, 10 pages.
International Search Report and Written Opinion of PCT/US2012/058818 mailed on Apr. 1, 2013, 9 pages.
International Search Report and Written Opinion of the International Searching Authority for PCT Application No. PCT/US2012/028957, mailed on Oct. 18, 2012, 9 pages.
International Search report and Written Opinion of PCT/CN2010/000932 dated Mar. 31, 2011, 8 pages.
Japanese Patent Office, Official Action for Application No. 2007-317207 mailed on Dec. 21, 2011, 2 pages.
International Search Report and Written Opinion of PCT/US2013/076217 mailed on Apr. 28, 2014, 11 pages.
Jung, et al., “Patterning with amorphous carbon spacer for expanding the resolution limit of current lithography tool”, Proc. SPIE , 2007, 9 pages, vol. 6520, 65201C.
Laxman, “Low ε Dielectrics: CVD Fluorinated Silicon Dioxides”, Semiconductor International, May 1995, pp. 71-74.
Lee, et al., “Dielectric Planarization Techniques for Narrow Pitch Multilevel Interconnects,” IEEE, V-MIC Conference Jun. 15-16, 1987, pp. 85-92 (1987).
Matsuda, et al. “Dual Frequency Plasma CVD Fluorosilicate Glass Deposition for 0.25 um Interlevel Dielectrics”, ISMIC, DUMIC Conference Feb. 21-22, 1995, pp. 22-28.
Meeks, Ellen et al., “Modeling of SiO2 deposition in high density plasma reactors and comparisons of model predictions with experimental measurements,” J. Vac. Sci. Technol. A, Mar./Apr. 1998, pp. 544-563, vol. 16(2).
Mukai, et al., “A Study of CD Budget in Spacer Patterning Process”, Toshiba, SPIE 2008, Feb. 26, 2008, 12 pages.
Nishino, et al.; Damage-Free Selective Etching of SI Native Oxides Using NH3/NF3 and SF6/H20 Down-Flow Etching, The Japanese Society of Applied Physics, vol. 74, No. 2, pp. 1345-1348, XP-002491959, Jul. 15, 1993.
Ogawa, et al., “Dry Cleaning Technology for Removal of Silicon Native Oxide Employing Hot NH3/NF3 Exposure”, Japanese Journal of Applied Physics, pp. 5349-5358, Aug. 2002, vol. 41 Part 1, No. 8.
Ota, et al., “Stress Controlled Shallow Trench Isolation Technology to Suppress the Novel Anti-Isotropic Impurity Diffusion for 45nm-Node High Performance CMOSFETs,” Symposium on VLSI Technology Digest of Technical Papers, 2005, pp. 138-139.
Qian, et al., “High Density Plasma Deposition and Deep Submicron Gap Fill with Low Dielectric Constant SiOF Films,” ISMIC, DUMIC Conference Feb. 21-22, 1995, 1995, pp. 50-56.
Robles, et al. “Effects of RF Frequency and Deposition Rates on the Moisture Resistance of PECVD TEOS-Based Oxide Films”, ECS Extended Abstracts, Abstract No. 129, May 1992, pp. 215-216, vol. 92-1.
Shapiro, et al. “Dual Frequency Plasma CVD Fluorosilicate Glass: Water Absorption and Stability”, ISMIC, DUMIC Conference Feb. 21-22, 1995, 1995. pp. 118-123.
S.M. Sze, VLSI Technology, McGraw-Hill Book Company, pp. 107, 108.
C.C. Tang and D. W. Hess, Tungsten Etching in CF4 and SF6 Discharges, J. Electrochem. Soc., 1984, 131 (1984) p. 115-120.
Usami, et al., “Low Dielectric Constant Interlayer Using Fluorine-Doped Silicon Oxide”, Jpn. J. Appl. Phys., Jan. 19, 1994. pp. 408-412, vol. 33 Part 1, No. 1B.
Wang et al.; Ultra High-selectivity silicon nitride etch process using an inductively coupled plasma source; J. Vac. Sci. Techno!. A 16(3),May/Jun. 1998, pp. 1582-1587.
Wolf et al.; Silicon Processing for the VLSI Era; vol. 1; 1986; Lattice Press, pp. 546, 547, 618, 619.
Yu, et al., “Step Coverage Study of Peteos Deposition for Intermetal Dielectric Applications,” abstract, VMIC conference, Jun. 12-13, 1990, 7 pages, No. 82.
Yutaka, et al., “Selective Etching of Silicon Native Oxide with Remote-Plasma-Excited Anhydrous Hydrogen Fluoride,” Japanese Journal of Applied Physics, 1998, vol. 37, pp. L536-L538.
Related Publications (1)
Number Date Country
20140345645 A1 Nov 2014 US
Provisional Applications (1)
Number Date Country
61825834 May 2013 US