Double self-aligned phase change memory device structure

Information

  • Patent Grant
  • 9640757
  • Patent Number
    9,640,757
  • Date Filed
    Monday, October 28, 2013
    10 years ago
  • Date Issued
    Tuesday, May 2, 2017
    7 years ago
  • Inventors
  • Original Assignees
  • Examiners
    • Yushina; Galina
    Agents
    • Entegris, Inc. Legal Dept.
    • Kissoon; Nidhi G.
    • Pillion; John E.
Abstract
A double self-aligned phase change memory device structure, comprising spaced-apart facing phase change memory film members symmetrically arranged with respect to one another, each of the phase change memory film members at an upper portion thereof being in contact with a separate conductive element, and each of the phase change memory film members being in a range of from 5 nm to 25 nm in thickness. Also described are various methods of making such phase change memory device structure.
Description
FIELD

The present disclosure relates to double self-aligned phase change memory device structures and methods of making the same.


DESCRIPTION OF THE RELATED ART

Phase change memory (PCM) is a type of non-volatile computer memory that utilizes differences in the electrical resistivity of the crystalline and amorphous phase states of memory materials. Devices that incorporate PCM typically comprise substrates on which a particular memory material (e.g., a chalcogenide) is deposited.


The memory material is characteristically deposited within structures (such as holes, trenches, or the like) in or on the surfaces of the substrate. Patterned electrodes are also deposited on the substrate to allow for the conduction of current. The conduction of current is effected through the deposited memory material, with the level of current being dependent on the resistivity and heating efficiency of such memory material and its alloy properties on phase change.


Memory materials used in the manufacture of PCM devices include germanium antimony telluride (GST) and germanium-telluride (GeTe). The GST materials can function in principle very effectively as phase change material for a volume, v, having characteristic dimensions as small as 5 nm. The trend is to make PCM devices based on GST with characteristic dimensions in the regime of 30 to 10 nm or less in future generations of devices.


To confine the heat for phase change, PCM material-containing structures may be fabricated with surrounding or otherwise associated dielectric material, and the structure may embody aspect ratios or dimensional characteristics that facilitate heating efficiency. The deposition of the phase change memory material can be carried out by vapor deposition processes, e.g., chemical vapor deposition (CVD) or atomic layer deposition (ALD), to produce films of useful character for phase change memory applications inside a cavity, e.g., a hole or trench in a substrate.


In addition to the deposition of phase change memory materials into existing substrate surface structures such as cavities, e.g., holes or trenches, phase change memory device structures can also be fabricated as confined cell equivalent structures by initially forming the phase change memory material, and then surrounding the phase change memory material with dielectric material. The phase change memory material in such applications may be in a very small cell structure having correspondingly small top and bottom contact areas, e.g., areas on the order of 5-10 nm×50-100 nm (thickness of contact metal x width of contact metal) permitted by current lithography capability, with the phase change memory material extended at a height of 30 nm or more. In such cell structures, the phase change memory material is surrounded by thermally and electrically insulating materials.


SUMMARY

The present disclosure relates to double self-aligned phase change memory device structures and methods of making the same.


In one aspect, the disclosure relates to a double self-aligned phase change memory device structure, comprising spaced-apart facing phase change memory film members symmetrically arranged with respect to one another, each of the phase change memory film members at an upper portion thereof being in contact with a separate conductive element, and each of the phase change memory film members being in a range of from 5 nm to 25 nm in thickness.


In another aspect, the disclosure relates to a method of forming a memory device structure of the disclosure, comprising the process flow illustrated in FIGS. 1-4 herein.


In a further aspect, the disclosure relates to a method of forming a memory device structure of the disclosure, comprising the process flow illustrated in FIGS. 10-23 herein.


Other aspects, features and embodiments of the disclosure will be more fully apparent from the ensuing description and appended claims.





BRIEF DESCRIPTION OF THE DRAWINGS


FIGS. 1-4 show a process flow for fabricating a phase change memory device sidewall line cell structure.



FIG. 5 is a front elevation view of a phase change memory device cell structure, as fabricated by a process flow sequence as shown in FIGS. 1-4.



FIG. 6 is a perspective view of the phase change memory device cell structure.



FIGS. 7-9 show perspective schematic views of different cell structures and their respective contact areas.



FIGS. 10-23 illustrate a schematic process flow for forming a double self-aligned phase change memory device structure.



FIG. 24 is a schematic cross-sectional elevation view of a double self-aligned phase change memory device structure.



FIG. 25 is an enlarged portion of the phase change memory device structure of FIG. 24, showing the details of the phase change film member and associated TiN layer.



FIG. 26 is a schematic cross-sectional elevation view of a double self-aligned phase change memory device structure of a general type shown in FIG. 24, but wherein the transitional segment of the multi-segmented phase change memory film element has been removed by etch processing.





DETAILED DESCRIPTION

The present disclosure relates to double self-aligned phase change memory device structures and methods of making the same.


In one aspect, the disclosure relates to a double self-aligned phase change memory device structure, comprising spaced-apart facing phase change memory film members symmetrically arranged with respect to one another, each of the phase change memory film members at an upper portion thereof being in contact with a separate conductive element, and each of the phase change memory film members being in a range of from 5 nm to 25 nm in thickness.


Such memory device structure may be fabricated with a protecting layer disposed on facing surfaces of said phase change memory film members. The protecting layer may extend downwardly from an upper end of each phase change memory film member over the facing surface thereof to a lower portion of the phase change memory film member. In various embodiments, the structure may be fabricated, with a dielectric material between the protecting layers of the phase change memory film members.


In the memory device structure, each of the phase change memory film members may be of any suitable thickness, e.g., a thickness in a range of from 8 to 20 nm, a thickness in a range of from 10 to 15 nm, a thickness in a range of from 5 to 15 nm, or any other suitable thickness effective for performance of the memory device structure in a phase change memory implementation.


In various embodiments, each phase change memory film member may have a height appropriate to the phase change memory implementation of the structure, e.g., in a range of from 20 to 80 nm, in a range of from 30 to 75 nm, or any other suitable range of height values.


The phase change memory material itself may comprise any suitable material, e.g., a chalcogenide, such as a germanium-antimony-tellurium alloy, or a germanium telluride alloy.


In some embodiments of the memory device structure of the disclosure, the phase change memory material film members may be arranged in a confined cell arrangement comprising a cross-spacer structure wherein the phase change memory material film members are positioned transversely to and reposed on titanium nitride members. In such cross-spacer structure, the contact area of each phase change memory film member and the titanium nitride member on which it is reposed may be in a range of for example from 50 to 150 nm2, a range of from 80 to 120 nm2, or any other suitable contact area range.


The memory device structure of the disclosure may include arrangements in which each phase change memory material film member comprises an upper planar segment, an intermediate angular transition segment, and a lower planar segment, arranged so that the upper planar segment and lower planar segment of each phase change memory material film member are generally parallel to one another and to respective upper planar and lower planar segments of the other phase change memory material film member facing it, wherein transverse spacing distance between upper planar segments of the respective phase change memory material film members is greater than transverse spacing distance between lower planar segments of the respective phase change memory film members. In such structural arrangements, the intermediate angular transition segment may be of a generally planar character, or may be in a curvate or other non-planar conformation.


In other embodiments of the every device structure of the present disclosure, each phase change memory material film member may comprise an upper planar segment and a lower planar segment, elevationally spaced apart from one another, and arranged so that the upper planar segment and lower planar segment of each phase change memory material film member are generally parallel to one another and to respective upper planar and lower planar segments of the other phase change memory material film member facing it, wherein transverse spacing distance between upper planar segments of the respective phase change memory material film members is greater than transverse spacing distance between lower planar segments of the respective phase change memory film members.


The present disclosure further contemplates various methods of forming memory device structures of the disclosure, as hereinafter more fully described, and including the process flow illustrated in FIGS. 1-4 herein, as well as the process flow illustrated in FIGS. 10-23 herein.


The features, aspects, and advantages of the double self-aligned phase change memory device structures of the present disclosure, and methods of making the same, are more fully illustrated with respect to the ensuing description of FIGS. 1-26.



FIGS. 1-4 show a process flow for fabricating a phase change memory device sidewall line cell structure.



FIG. 1 illustrates a trench in a substrate on which a phase change material, e.g., an alloy such as germanium-antimony-tellurium (GST) or germanium telluride (GeTe) is conformally deposited by a vapor deposition process, e.g., MOCVD process, to form a phase change memory material film on wall surface of the trench. Such conformal deposition yields a central open core region in the interior volume of the trench that is bounded by the phase change memory material film on wall surface of the trench.



FIG. 2 shows the structure of FIG. 1 in which a conformal protecting layer of suitable material is deposited over the phase change memory material film. Next, a vertical anisotropic spacer etch is carried out, yielding the structure shown in FIG. 3. Thereafter, the gap in the central open core of the structure is filled with suitable material, e.g., dielectric material, followed by chemical mechanical planarization, and formation of the top electrode members, yielding the structure as shown in FIG. 4, in which the vertically extending phase change memory film members have a thickness of 10 nm.



FIG. 5 is a front elevation view of a phase change memory device cell structure, as fabricated by a process flow sequence as shown in FIGS. 1-4. The vertically extending phase change memory film member has a thickness of 10 nm, and the height of the phase change memory film may be in a range of from 30 to 75 nm, as illustrated.



FIG. 6 is a perspective view of the phase change memory device cell structure, showing two GST members in a cross-spacer structure on respective TiN members.



FIGS. 7-9 show perspective schematic views of different cell structures and their respective contact areas.



FIG. 7 shows a self-aligned wall storage arrangement including a GST member having a transverse dimension of about 45 nm and a height of 30 nm or more, reposed on a TiN member having a corresponding transverse dimension of about 45 nm and a thickness of 10 nm. The contact area of the GST member with the TiN member in such arrangement is 450 nm2, and the arrangement exhibits a reset current of approximately 0.2 mA.



FIG. 8 shows a dashboard cell structure in which the GST member has a height of 30 nm and a thickness of approximately 7.5 nm. Each of the GST member and the TiN member has a width dimension on the order of 25 nm. The contact area of the GST member with the TiN member in such arrangement is approximately 200 nm2, and the arrangement exhibits a reset current of approximately 0.08 mA.



FIG. 9 shows a cross-spacer structure in which the GST member has a height of 30 nm, and is positioned transversely to the TiN member. The contact area of the GST member with the TiN member in such arrangement is approximately 100 nm2.



FIGS. 10-23 illustrate a schematic process flow for forming a double self-aligned phase change memory device structure.



FIG. 10 is a perspective view of a trench structure in a SiO2 substrate. As shown in FIG. 11, a TiN film is deposited on the trench structure, e.g., at a thickness on the order of 10 nm. FIG. 12 shows a protective insulating material being deposited over the TiN film. An anisotropic etch with over-etching is next carried out, to form the structure shown in FIG. 13. Conformal deposition of GST is thereafter carried out, to form the structure shown in FIG. 14. A protective insulating layer then is deposited on the GST, to form the structure shown in FIG. 15.


An anisotropic etch of the GST next is conducted to yield the structure shown in FIG. 16, following which SiO2 is filled in the trench, as illustrated in FIG. 17. Next, chemical mechanical planarization (CMP) is carried out to remove excess SiO2, yielding the structure as shown in FIG. 18. A top metal layer then is deposited, to form the structure shown in FIG. 19. A resist then is applied to the metal layer to define the self-alignment structure, as shown in FIG. 20, and the resist is developed to form the structure shown in FIG. 21. Next, metal is selectively removed to isolate the top electrode members as illustrated in FIG. 22.



FIG. 23 shows the resulting structure of a double isolated PCM arrangement. The GST region 1 is identified in FIG. 23 as an upper portion of the GST film, and is the active region of the device. The GST region 2 is identified in FIG. 23 as a lower portion of the GST film, and is an inactive portion of the device, since electrical field at such lower portion is zero.



FIG. 24 is a schematic cross-sectional elevation view of a double self-aligned phase change memory device structure 100 of the present disclosure, according to one embodiment thereof. The device structure 100 comprises silicon dioxide (SiO2) 102 bounding the double self-aligned phase change memory film members 104, 106, which may be formed of GST, GT, or other phase change material.


Each of the phase change memory film members 104, 106 comprises a bottom upwardly extending segment 116 that is coupled to a top upwardly extending segment 112 by an angled transitional segment 114 therebetween. The transitional segment 114 may have any suitable angle in relation to the top and bottom segments 112, 116 of the phase change memory film members, e.g., 45°. Layers 108, 110, 122 and 124 comprise titanium nitride (TiN), and layers 118 and 120 are layers of protective material for the TiN in the double self-aligned phase change memory device structure.


In the FIG. 24 structure, the upper phase change memory segment 112 in region “A” is active. The lower phase change memory segment 116 and transition segment 114 in region “B” are inactive, although the transition segment 114 effects some heat loss (heat dissipation) in the operation of the device structure.



FIG. 25 is an enlarged portion of the phase change memory device structure 100 of FIG. 24, showing the details of the phase change film member and associated TiN layer. In the FIG. 25 drawing, the components of the structure are numbered correspondingly with respect to the reference numerals in FIG. 24.


In the FIG. 24 phase change memory device structure, the phase change memory material in transition segment 114 may be selectively removed, e.g., by over-etching during the anisotropic etching step (FIG. 16) for removal of the transition segment. By such modification, the upper segment 112 of phase change memory material is not electrically or thermally associated with the lower segment 116, and, as discussed, only the upper segment of phase change memory material constitutes the active phase change memory material in the structure.


Such a modified phase change memory device structure is shown in FIG. 26, which is a schematic illustration of the double self-aligned phase change memory device structure corresponding to that shown in FIG. 24, but wherein the transition segment has been selectively removed so that the upper segment 112 of phase change memory material is physically isolated from the lower segment 116 of such material.


While the disclosure has been set out herein in reference to specific aspects, features and illustrative embodiments, it will be appreciated that the utility of the disclosure is not thus limited, but rather extends to and encompasses numerous other variations, modifications and alternative embodiments, as will suggest themselves to those of ordinary skill in the field of the present disclosure, based on the description herein. Correspondingly, the invention as hereinafter claimed is intended to be broadly construed and interpreted, as including all such variations, modifications and alternative embodiments, within its spirit and scope.

Claims
  • 1. A double self-aligned phase change memory device structure, comprising spaced-apart facing phase change memory film members symmetrically arranged with respect to one another, each of the phase change memory film members at an upper portion thereof being in contact with a separate conductive element, and each of the phase change memory film members being in a range of from 5 nm to 25 nm in thickness.
  • 2. The memory device structure of claim 1, wherein a protecting layer is disposed on facing surfaces of said phase change memory film members.
  • 3. The memory device structure of claim 2, wherein the protecting layer extends downwardly from an upper end of each phase change memory film member over the facing surface thereof to a lower portion of the phase change memory film member.
  • 4. The memory device structure of claim 3, further comprising a dielectric material between the phase change memory film members.
  • 5. The memory device structure of claim 1, wherein each of the phase change memory film members has a thickness in a range of from 8 nm to 20 nm.
  • 6. The memory device structure of claim 1, wherein each of the phase change memory film members has a thickness in a range of from 10 to 15 nm.
  • 7. The memory device structure of claim 1, wherein each of the phase change memory film members has a thickness in a range of from 5 to 15 nm.
  • 8. The memory device structure of claim 1, wherein each phase change memory film member has a height in a range of from 20 to 80 nm.
  • 9. The memory device structure of claim 1, wherein each phase change memory film member has a height in a range of from 30 to 75 nm.
  • 10. The memory device structure of claim 1, wherein each of the phase change memory film members comprises a chalcogenide.
  • 11. The memory device structure of claim 1, wherein each of the phase change memory film members comprises a germanium-antimony-telluride alloy.
  • 12. The memory device structure of claim 1, wherein each of the phase change memory film members comprises a germanium telluride alloy.
  • 13. The memory device structure of claim 1, wherein the phase change memory film members are arranged in a confined cell arrangement comprising a cross-spacer structure wherein the phase change memory film members are reposed on titanium nitride members.
  • 14. The memory device structure of claim 13, wherein a contact area of each phase change memory film member and the titanium nitride member on which it is reposed is in a range of from 50 to 150 nm2.
  • 15. The memory device structure of claim 13, wherein a contact area of each phase change memory film member and the titanium nitride member on which it is reposed is in a range of from 80 to 120 nm2.
  • 16. A double self-aligned phase change memory device structure, comprising spaced-apart facing phase change memory film members symmetrically arranged with respect to one another, each of the phase change memory film members at an upper portion thereof being in contact with a separate conductive element, and each of the phase change memory film members being in a range of from 5 nm to 25 nm in thickness, wherein each phase change memory film member comprises an upper planar segment, an intermediate angular transition segment, and a lower planar segment, arranged so that the upper planar segment and lower planar segment of each phase change memory film member are generally parallel to one another and to respective upper planar and lower planar segments of the other phase change memory film member facing it, wherein spacing distance between upper planar segments of the respective phase change memory film members is greater than spacing distance between lower planar segments of the respective phase change memory film members.
  • 17. The memory device structure of claim 16, wherein the intermediate angular transition segment is generally planar.
  • 18. A double self-aligned phase change memory device structure, comprising spaced-apart facing phase change memory film members symmetrically arranged with respect to one another, each of the phase change memory film members at an upper portion thereof being in contact with a separate conductive element, and each of the phase change memory film members being in a range of from 5 nm to 25 nm in thickness, wherein each phase change memory film member comprises an upper planar segment and a lower planar segment, elevationally spaced apart from one another, and arranged so that the upper planar segment and lower planar segment of each phase change memory material film member are generally parallel to one another and to respective upper planar and lower planar segments of the other phase change memory material film member facing it, wherein spacing distance between upper planar segments of the respective phase change memory material film members is greater than spacing distance between lower planar segments of the respective phase change memory film members.
  • 19. A method of forming a double self-aligned memory device structure of claim 1, comprising: depositing a phase change material to form spaced-apart facing phase change memory film members symmetrically arranged with respect to one another, wherein each of the phase change memory film members is in a range of from 5 nm to 25 nm in thickness; andforming conductive elements so that each of the phase change memory film members at an upper portion thereof is in contact with a separate conductive element.
  • 20. The method of claim 19, wherein the spaced-apart facing phase change memory film members are formed so that they are physically isolated from one another in the memory device structure.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a U.S. national phase under the provisions of 35 U.S.C. §371 of International Patent Application No. PCT/US13/67145 filed Oct. 28, 2013, which in turn claims the benefit of priority under 35 USC 119 of U.S. Provisional Patent Application No. 61/720,283 filed Oct. 30, 2012 in the name of Jun-Fei Zheng for DOUBLE SELF-ALIGNED PHASE CHANGE MEMORY DEVICE STRUCTURE. The disclosures of such International Patent Application No. PCT/US 13/67,145 and U.S. Provisional Patent Application No. 61/720,283 are hereby incorporated herein by reference, in their respective entireties, for all purposes.

PCT Information
Filing Document Filing Date Country Kind
PCT/US2013/067145 10/28/2013 WO 00
Publishing Document Publishing Date Country Kind
WO2014/070682 5/8/2014 WO A
US Referenced Citations (228)
Number Name Date Kind
3467686 Creamer Sep 1969 A
4383119 Pullukat et al. May 1983 A
4491669 Arkles et al. Jan 1985 A
4499198 Pullukat et al. Feb 1985 A
4895709 Laine Jan 1990 A
4927670 Erbil May 1990 A
4948623 Beach et al. Aug 1990 A
4960916 Pazik Oct 1990 A
4962214 Villacorta et al. Oct 1990 A
5003092 Beachley, Jr. Mar 1991 A
5008422 Blum et al. Apr 1991 A
5084588 Ocheltree et al. Jan 1992 A
5139825 Gordon et al. Aug 1992 A
5178911 Gordon et al. Jan 1993 A
5210254 Ritscher et al. May 1993 A
5225561 Kirlin et al. Jul 1993 A
5268496 Geisberger Dec 1993 A
5312983 Brown et al. May 1994 A
5417823 Narula et al. May 1995 A
5442200 Tischler Aug 1995 A
5453494 Kirlin et al. Sep 1995 A
5566045 Summerfelt et al. Oct 1996 A
5576928 Summerfelt et al. Nov 1996 A
5583205 Rees, Jr. Dec 1996 A
5596522 Ovshinsky et al. Jan 1997 A
5653806 Van Buskirk Aug 1997 A
5687112 Ovshinsky Nov 1997 A
5698726 Rauleder et al. Dec 1997 A
5719417 Roeder et al. Feb 1998 A
5726294 Rees, Jr. Mar 1998 A
5820664 Gardiner et al. Oct 1998 A
5919522 Baum et al. Jul 1999 A
5976991 Laxman et al. Nov 1999 A
5980265 Tischler Nov 1999 A
5998236 Roeder et al. Dec 1999 A
6005127 Todd et al. Dec 1999 A
6015917 Bhandari et al. Jan 2000 A
6086779 Bishop et al. Jul 2000 A
6133051 Hintermaier et al. Oct 2000 A
6146608 Todd et al. Nov 2000 A
6269979 Dumont Aug 2001 B1
6281022 Li et al. Aug 2001 B1
6319565 Todd et al. Nov 2001 B1
6399208 Baum et al. Jun 2002 B1
6506666 Marsh Jan 2003 B2
6511718 Paz de Araujo et al. Jan 2003 B1
6646122 Nuhlen et al. Nov 2003 B1
6716271 Arno et al. Apr 2004 B1
6750079 Lowrey et al. Jun 2004 B2
6767830 Wang et al. Jul 2004 B2
6787186 Hintermaier Sep 2004 B1
6861559 Odom Mar 2005 B2
6869638 Baum et al. Mar 2005 B2
6872963 Kostylev et al. Mar 2005 B2
6908812 Lowrey Jun 2005 B2
6916944 Furukawa et al. Jul 2005 B2
6984591 Buchanan et al. Jan 2006 B1
6998289 Hudgens et al. Feb 2006 B2
7005303 Hintermaier et al. Feb 2006 B2
7029978 Dodge Apr 2006 B2
7087482 Yeo et al. Aug 2006 B2
7114517 Sund et al. Oct 2006 B2
7115927 Hideki et al. Oct 2006 B2
7312165 Jursich et al. Dec 2007 B2
7332735 Campbell Feb 2008 B2
7371429 Lee et al. May 2008 B2
7397060 Lung Jul 2008 B2
7399666 Ahn et al. Jul 2008 B2
7402851 Hideki et al. Jul 2008 B2
7419698 Jones Sep 2008 B2
7425735 Park et al. Sep 2008 B2
7439536 Pellizzer et al. Oct 2008 B2
7462900 Hideki et al. Dec 2008 B2
7473921 Lam et al. Jan 2009 B2
7476917 Hideki et al. Jan 2009 B2
7488967 Burr et al. Feb 2009 B2
7525117 Kostylev et al. Apr 2009 B2
7569417 Lee et al. Aug 2009 B2
7615401 Park et al. Nov 2009 B2
7615439 Schricker et al. Nov 2009 B1
7632456 Cheong et al. Dec 2009 B2
7704787 Hideki et al. Apr 2010 B2
7728172 Lee et al. Jun 2010 B2
7732801 Chen Jun 2010 B2
7791932 Kuh et al. Sep 2010 B2
7838329 Hunks et al. Nov 2010 B2
7851253 Chen Dec 2010 B2
7935564 Breitwisch et al. May 2011 B2
7935594 Schricker et al. May 2011 B2
7943502 Park et al. May 2011 B2
7943923 Gidon May 2011 B2
7969011 Sekar et al. Jun 2011 B2
7989795 Chen et al. Aug 2011 B2
7989796 Lam et al. Aug 2011 B2
8008117 Hunks et al. Aug 2011 B2
8192592 Kim et al. Jun 2012 B2
8272347 Nasman et al. Sep 2012 B2
8330136 Zheng et al. Dec 2012 B2
8410468 Zheng Apr 2013 B2
8445354 Ha et al. May 2013 B2
8617972 Zheng Dec 2013 B2
9012876 Zheng Apr 2015 B2
9070875 Zheng Jun 2015 B2
20020004266 Hashimoto et al. Jan 2002 A1
20020090815 Koike et al. Jul 2002 A1
20030073295 Xu Apr 2003 A1
20030135061 Norman et al. Jul 2003 A1
20040012009 Casagrande et al. Jan 2004 A1
20040038808 Hampden-Smith et al. Feb 2004 A1
20040087074 Hwang et al. May 2004 A1
20040197945 Woelk et al. Oct 2004 A1
20040215030 Norman Oct 2004 A1
20050029502 Hudgens Feb 2005 A1
20050064334 Hirotsune et al. Mar 2005 A1
20050082624 Gousev et al. Apr 2005 A1
20050208699 Furkay et al. Sep 2005 A1
20050267345 Korgel et al. Dec 2005 A1
20050283012 Xu et al. Dec 2005 A1
20050287747 Chakravarti et al. Dec 2005 A1
20060006449 Jeong et al. Jan 2006 A1
20060024429 Horii Feb 2006 A1
20060027451 Park et al. Feb 2006 A1
20060035462 Millward Feb 2006 A1
20060040485 Lee et al. Feb 2006 A1
20060046521 Vaartstra et al. Mar 2006 A1
20060049447 Lee et al. Mar 2006 A1
20060054878 Lowrey Mar 2006 A1
20060105556 Matsui et al. May 2006 A1
20060113520 Yamamoto et al. Jun 2006 A1
20060115595 Shenai-Khatkhate et al. Jun 2006 A1
20060138393 Seo et al. Jun 2006 A1
20060141155 Gordon et al. Jun 2006 A1
20060141710 Yoon et al. Jun 2006 A1
20060172067 Ovshinsky et al. Aug 2006 A1
20060172083 Lee et al. Aug 2006 A1
20060180811 Lee et al. Aug 2006 A1
20060249369 Marangon et al. Nov 2006 A1
20070025226 Park et al. Feb 2007 A1
20070090336 Asano et al. Apr 2007 A1
20070120104 Ahn et al. May 2007 A1
20070121363 Lung May 2007 A1
20070152205 Chen Jul 2007 A1
20070154637 Shenai-Khatkhate et al. Jul 2007 A1
20070160760 Shin et al. Jul 2007 A1
20070246748 Breitwisch et al. Oct 2007 A1
20070252127 Arnold et al. Nov 2007 A1
20070272950 Kim et al. Nov 2007 A1
20080003359 Gordon et al. Jan 2008 A1
20080017841 Lee et al. Jan 2008 A1
20080035906 Park et al. Feb 2008 A1
20080035961 Chen et al. Feb 2008 A1
20080067490 Hayakawa Mar 2008 A1
20080078984 Park et al. Apr 2008 A1
20080096386 Park et al. Apr 2008 A1
20080099791 Lung et al. May 2008 A1
20080118636 Shin et al. May 2008 A1
20080164453 Breitwisch et al. Jul 2008 A1
20080169457 Hideki et al. Jul 2008 A1
20080191187 Lung et al. Aug 2008 A1
20080210163 Carlson et al. Sep 2008 A1
20080254218 Lei et al. Oct 2008 A1
20080254232 Gordon et al. Oct 2008 A1
20080258127 Lee et al. Oct 2008 A1
20080265236 Lee et al. Oct 2008 A1
20080272355 Cho et al. Nov 2008 A1
20080290335 Lin et al. Nov 2008 A1
20090020738 Happ et al. Jan 2009 A1
20090057643 Chen Mar 2009 A1
20090065761 Chen Mar 2009 A1
20090075420 Bae et al. Mar 2009 A1
20090087561 Chen et al. Apr 2009 A1
20090097305 Bae et al. Apr 2009 A1
20090101883 Lai et al. Apr 2009 A1
20090112009 Chen et al. Apr 2009 A1
20090124039 Roeder et al. May 2009 A1
20090184309 Mathew et al. Jul 2009 A1
20090215225 Stender et al. Aug 2009 A1
20090227066 Joseph et al. Sep 2009 A1
20090242865 Lung Oct 2009 A1
20090250682 Park et al. Oct 2009 A1
20090275164 Chen et al. Nov 2009 A1
20090291208 Gordon et al. Nov 2009 A1
20090298223 Cheek et al. Dec 2009 A1
20090302297 Park et al. Dec 2009 A1
20090305458 Hunks et al. Dec 2009 A1
20090321706 Happ Dec 2009 A1
20090321733 Gatineau et al. Dec 2009 A1
20100012917 Takaura et al. Jan 2010 A1
20100018439 Cameron et al. Jan 2010 A1
20100054029 Happ et al. Mar 2010 A1
20100059731 Chang Mar 2010 A1
20100081263 Horii et al. Apr 2010 A1
20100096610 Wang et al. Apr 2010 A1
20100112211 Xu et al. May 2010 A1
20100112795 Kaim et al. May 2010 A1
20100116990 Xu et al. May 2010 A1
20100130013 Liu et al. May 2010 A1
20100164057 Hunks et al. Jul 2010 A1
20100190341 Park et al. Jul 2010 A1
20100209610 Cameron et al. Aug 2010 A1
20100243981 Kang et al. Sep 2010 A1
20100264396 Lung et al. Oct 2010 A1
20100270527 Sawamura Oct 2010 A1
20100270529 Lung Oct 2010 A1
20100317150 Hunks et al. Dec 2010 A1
20110001107 Zheng Jan 2011 A1
20110006279 Chen Jan 2011 A1
20110060165 Cameron et al. Mar 2011 A1
20110065252 Nakamura Mar 2011 A1
20110111556 Chen et al. May 2011 A1
20110124182 Zheng May 2011 A1
20110136316 Chang Jun 2011 A1
20110155989 Park Jun 2011 A1
20110198555 Kikuchi et al. Aug 2011 A1
20110212568 Shin Sep 2011 A1
20110227021 Schrott et al. Sep 2011 A1
20110227029 Liu Sep 2011 A1
20110260132 Zheng et al. Oct 2011 A1
20110260290 Kalra Oct 2011 A1
20110263100 Hunks et al. Oct 2011 A1
20120032135 Kuh et al. Feb 2012 A1
20120115315 Zheng et al. May 2012 A1
20120134204 Happ et al. May 2012 A1
20120171812 Marsh Jul 2012 A1
20130078475 Zheng Mar 2013 A1
20130112933 Zheng May 2013 A1
20130241037 Jeong et al. Sep 2013 A1
20130284999 Zheng Oct 2013 A1
Foreign Referenced Citations (55)
Number Date Country
1466918 Oct 2004 EP
1675194 Jun 2006 EP
1806427 Jul 2007 EP
1710807 Nov 2008 EP
58-38296 Mar 1983 JP
5-311423 Nov 1993 JP
6-80413 Mar 1994 JP
6-293778 Oct 1994 JP
7-263431 Oct 1995 JP
8-74055 Mar 1996 JP
2000-215510 Aug 2000 JP
2001-67720 Mar 2001 JP
2002-211924 Jul 2002 JP
2002-220658 Aug 2002 JP
2006-511716 Apr 2006 JP
2006-124262 May 2006 JP
2006-182781 Jul 2006 JP
2008-252088 Oct 2008 JP
2011-66135 Mar 2011 JP
10-2004-0076225 Aug 2004 KR
10-2005-0048891 May 2005 KR
10-2006-0001089 Jan 2006 KR
10-0585175 May 2006 KR
10-2006-0091160 Aug 2006 KR
10-2007-0025612 Mar 2007 KR
10-0695168 Mar 2007 KR
10-2007-0105752 Oct 2007 KR
10-2008-0052362 Jun 2008 KR
10-2008-0080273 Sep 2008 KR
10-2009-0008799 Jan 2009 KR
10-2009-0029488 Mar 2009 KR
10-2009-0036771 Apr 2009 KR
10-2009-0045132 May 2009 KR
10-2011-0076394 Jul 2011 KR
10-1067969 Sep 2011 KR
768457 Oct 1980 SU
200625543 Jul 2006 TW
200822356 May 2008 TW
0015865 Mar 2000 WO
0067300 Nov 2000 WO
2004046417 Jun 2004 WO
2004076712 Sep 2004 WO
2005084231 Sep 2005 WO
2006012052 Feb 2006 WO
2007070218 Jun 2007 WO
2007126690 Nov 2007 WO
2007140813 Dec 2007 WO
2008002546 Jan 2008 WO
2008057616 May 2008 WO
2009006272 Jan 2009 WO
2009020888 Feb 2009 WO
2009034775 Mar 2009 WO
2009059237 May 2009 WO
2011002705 Jan 2011 WO
2011146913 Nov 2011 WO
Non-Patent Literature Citations (95)
Entry
Bochmann, M. et al., “Synthesis of Some Alkyl Metal Selenolato Complexes of Zinc, Cadmium and Mercury, X-Ray Crystal Structure of Me, Hg, Se(2,4,6-Pr13C6H2)”, “Polyhedron”, 1992, pp. 507-512, vol. 11, No. 5.
Bradley, D., et al., “Metallo-organic compounds containing metal-nitrogen bonds. Part I. Some dialkylamino-derivatives of titanium and Zirconium”, “Journal of the Chemical Society”, Oct. 1960, pp. 3857-3861.
Bradley, D., et al., “Metallo-organic compounds containing metal-nitrogen bonds: Part III. Dialkylamino compounds of tantalum”, “Canadian Journal of Chemistry”, Jul. 1962, pp. 1355-1360, vol. 40, No. 7.
Bwembya, G., et al., “Phosphinochalcogenoic Amidato Complexes of Zinc and Cadmium as Novel Single-Source Precursors for the Deposition of Metal Selenide and Telluride Films”, “Chemical Vapor Deposition”, 1995, pp. 78-80, vol. 1, No. 3.
Carmalt, C., et al., “Synthesis of titanium(IV) guanidinate complexes and the formation of titanium carbonitride via low-pressure chemical vapor deposition”, “Inorganic Chemistry”, Jan. 7, 2005, pp. 615-619, vol. 44, No. 3.
Chen, T., et al., “Low temperature Deposition of Ge Thin Films with a Ge(II) Silylamido Source”, “ECS Transactions”, 2007, pp. 269-278, vol. 11, No. 7.
Cheng, H., et al., “Wet Etching of Ge2Sb2Te5 Films and Switching Properties of Resultant Phase Change Memory Cells”, “Semiconductor Science and Technology”, Sep. 26, 2005, pp. 1111-1115, vol. 20, No. 11.
Chiu, H., et al., “Deposition of tantalum nitride thin films from ethylimidotantalum complex”, “Journal of Materials Science Letters”, Jan. 1992, pp. 96-98, vol. 11, No. 2.
Cho, K., et al., “Designing PbSe Nanowires and Nanorings through Oriented Attachment of Nanoparticles”, “J. Am. Chem. Soc.”, Apr. 23, 2005, pp. 7140-7147, vol. 127.
Choi, B.,et al., “Combined Atomic Layer and Chemical Vapor Deposition, and Selective Growth of Ge2Sb2Te5 Films on TiN/W Contact Plug”, “Chem. Mater.”, Aug. 14, 2007, pp. 4387-4389, vol. 19.
Choi, B., et al., “Cyclic PECVD of Ge2Sb2Te5 Films Using Metallorganic Sources”, “Journal of the Electrochemical Society”, Feb. 22, 2007, pp. H318-H324, vol. 154, No. 4.
Chorley, R., et al., “Subvalent Group 14 metal compounds XIV. The X-ray crystal structures of two monomeric Group 14 metal bisamides, Ge[N(SiMe3)2]2 and Sn[NC(Me)2(CH2)3CMe2]2”, “Inorganica Chimica Acta”, Aug.-Oct. 1992, pp. 203-209, vol. 198-200.
Cole-Hamilton, D., “MOVPE Mechanisms from studies of specially designed and labelled precursors”, “Chem. Commun.”, 1999, pp. 759-765.
Cummins, C., et al., “Synthesis of Terminal Vanadium(V) Imido, Oxo, Sulfido, Selenido, and Tellurido Complexes by Imido Group or or Chalcogen Atom Transfer to Trigonal Monopyramidal V[N3N] (N3N=[(Me3SiNCH2CH2)3N]3-”, “Inorganic Chemistry”, Mar. 30, 1994, pp. 1448-1457, vol. 33, No. 7.
Drake, J., et al., “Studies of Silyl and Germyl Group 6 Species. 5. Silyl and Germyl Derivatives of Methane- and Benzenetellurols”, “Inorg. Chem.”, 1980, pp. 1879-1883, vol. 19.
Foley, S., et al., “Facile Formation of Rare Terminal Chalcogenido Germanium Complexes with Alkylamidinates as Supporting Ligands”, “J. Am. Chem. Soc.”, Oct. 29, 1997, pp. 10359-10363, vol. 119, No. 43.
Foley, S., et al., “Synthesis and structural characterization of the first trialylguanidinate and hexahydropyramidinate complexes of tin”, “Polyhedron”, 2002, pp. 619-627, vol. 21.
Gehrhus, B., et al., “New Reactions of a Silylene: Insertion into M—N Bonds of M[N(SiMe3)2]2 (M=Ge, Sn, or Pb)”, “Angew. Chem. Int. Ed. Engl.”, 1997, pp. 2514-2516, vol. 36, No. 22.
Gordon, R., et al., “Silicon dimethylamido complexes and ammonia as precursors for the atmospheric pressure chemical vapor deposition of Silicon Nitride thin films”, “Chem. Mater.”, Sep. 1990, pp. 480-482, vol. 2, No. 5.
Note: For the non-patent literature citations that no month of publication is indicated, the year of publication is more than 1 year prior to the effective filing date of the present application.
Green, S., et al., “Synthetic, structural and theoretical studies of amidinate and guanidinate stabilised germanium(I) dimers”, “Chem. Commun.”, Sep. 8, 2006, pp. 3978-3980.
Green, S., et al., “Complexes of an Anionic Gallium(I) N-Heterocyclic Carbene Analogue with Group 14 Element(II) Fragments: Synthetic, Structural and Theoretical Studies”, “Inorganic Chem.”, Aug. 3, 2006, pp. 7242-7251, vol. 45, No. 18.
Gumrukcu, I., et al., “Electron Spin Resonance of t-Alkyl-, Silyl-, and Germyl-aminyl Radicals and some Observations on the Amides MBr{N(SiMe3)2}3 (M=Ge,Sn, or Pb)”, “J.C.S. Chem. Comm.”, 1980, pp. 776-777.
Gupta, A., et al., “Triorganoantimony(V) complexes with internally functionallized oximes: synthetic, spectroscopic and structural aspects of [R3Sb(Br)L], [R3Sb(OH)L] and [R3SbL2], crystal and molecular structures of [Me3Sb{ON=C(Me)C4H3O}2], [Me3Sb{ON=C(Me)C4H3S}2] 2-OC4H3C(Me)=NOH and 2-SC4H3C(Me)=NOH”, “Journal of Organometallic Chemistry”, 2002, pp. 118-126, vol. 645.
Gynane, M., et al., “Subvalent Group 4B Metal Alkyls and Amides. Part 5. The Synthesis and Physical Properties of Thermally Stable Amides of Germanium(II), Tin(II), and Lead(II)”, “J. Chem. Soc., Dalton Transactions”, 1977, pp. 2004-2009.
Han, L., et al., “Extremely Facile Oxidative Addition of Silyl, Germyl, and Stannyl Tellurides and Other Chalcogenides to Platinum(0) Complexes, X-ray Structure of trans-Pt(4-PhC6H4Te)(SiMe3)(PEt3)2”, “J. Am. Chem. Soc.”, 1997, pp. 8133-8134, vol. 119.
Harris, D., et al., “Monomeric, Volatile Bivalent Amides of Group IVB Elements, M(NR12)2 and M(NR1R2)2 (M=Ge, Sn, or Pb; R1=Me3Si, R2=Me3C)”, “J.C.S. Chem. Comm.”, 1974, pp. 895-896.
Hatanpaa, T., et al., “Synthesis and characterisation of cyclopentadienyl complexes of barium: precursors for atomic layer deposition of BaTiO3”, “Dalton Trans.”, Mar. 22, 2004, pp. 1181-1188, vol. 8.
Herrmann, W., et al., “Stable Cyclic Germanediyls (‘Cyclogermylenes’): Synthesis, Structure, Metal Complexes, and Thermolyses”, “Angew. Chem. Int. Ed. Engl.”, 1992, pp. 1485-1488, vol. 31, No. 11.
Herrmann, W., et al., “Volatile Metal Alkoxides according to the Concept of Donor Functionalization”, “Angew. Chem. Int. Ed. Engl.”, 1995, pp. 2187-2206, vol. 34.
Hitchcock, P., et al., “Subvalent Group 14 Metal Compounds-XIII. Oxidative Addition Reactions of Germanium and Tin Amides M(NR2)2 (R=SiMe3, M=Ge or Sn) With Sulphur, Selenium, Tellurium or MeOOCC==CCOOMe; X-Ray Structures of [Ge(NR2)2(mu-Te)]2 and Sn(NR2)2CC(OMe)OSn(NR2)2CC(OMe)O”, “Polyhedron”, 1991, pp. 1203-1213, vol. 10, No. 117.
Hitchcock, P., et al., “Synthesis and Structures of Bis[bis(trimethylsilyl)amido]-tin(iv) Cyclic Chalcogenides [{Sn[ N (Si Me3)2]2(mu-E)}2] and a Heterobimetallic Analogue [{(Me3Si)2N}2Ge(mu-Te)2Sn—{N(SiMe3)2}2] (E=S, Se or Te)”, “J. Chem Soc. Dalton Trans.”, 1995, pp. 3179-3187.
Hor, Y., et al., “Superconducting NbSe2 nanowires and nanoribbons converted from NbSe3 nanostructures”, “Applied Physics Letters”, Sep. 27, 2005, pp. 1-3, vol. 87, No. 142506.
Horii, H., et al., “A Novel Cell Technology Using N-Doped GeSbTe Films for Phase Change RAM”, “Symposium on VLSI Technology Digest of Technical Papers”, Jun. 10-12, 2003, pp. 177-178.
Hudgens, S., et al., “Overview of Phase Change Chalcogenide Nonvolatile Memory Technology”, “MRS Bulletin”, Nov. 2004, pp. 1-5.
George, T., et al., “Amino-derivatives of Metals and Metalloids. Part II. Amino-stannylation of Unsaturated Substrates, and the Infrared Spectra and Structures of Carbamato- and Dithiocarbamato-trimethylstannanes and Related Compounds”, “J. Chemical Society”, 1965, pp. 2157-2165, No. 385.
Just, O., et al., “Synthesis and Single-Crystal X-ray Diffraction Examination of a Structurally Homologous Series of TetracoordinateHeteroleptic Anionic Lanthanide Complexes: Ln{N[Si(CH3)2CH2CH2Si(CH3)2]}3(I—CI)Li(L)3 [Ln=Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb; (L)3=(THF)3, (Et2O)3, (THF)2(Et2O)]”, “Inorg. Chem.”, Mar. 9, 2001, pp. 1751-1755, vol. 40, No. 8.
Kapoor, P., et al., “High surface area homogeneous nanocrystalline bimetallic oxides obtained by hydrolysis of bimetallic mu-oxo alkoxides”, “J. Mater. Chem.”, Jan. 14, 2003, pp. 410-414, vol. 13.
Karsch, H., et al., “Bis(amidinate) Complexes of Silicon and Germanium”, “Eur. J. Inorg. Chemistry”, Apr. 1998, pp. 433-436, vol. 4.
Kim, R., et al., “Structural properties of Ge2Sb2Te5 thin films by metal organic chemical vapor deposition for phase change memory applications”, “Applied Physics Letters”, Sep. 6, 2006, pp. 102107-1-102107-3, vol. 89.
Ritch, J., et al., “The single molecular precursor approach to metal telluride thin films: imino-bis (diisopropylphosphine tellurides) as examples”, “Chem. Soc. Rev.”, Jun. 27, 2007, pp. 1622-1631, vol. 36.
Kim, S., et al., “Electrical Properties and Crystal Structures of Nitrogen-Doped Ge2Sb2Te5 Thin Film for Phase Change Memory”, “Thin Solid Films”, Dec. 22, 2004, pp. 322-326, vol. 469-470.
Kuchta, M., et al., “Multiple Bonding Between Germanium and the Chalcogens: The Syntheses and Structures of the Terminal Chalogenido Complexes (n4-Me8taa)GeE (E=S, Se, Te)”, “J. Chem. Soc. Chem. Commun.”, 1994, pp. 1351-1352.
Kuchta, M., et al., “Comparison of the reactivity of germanium and tin terminal chalcogenido complexes: the syntheses of chalcogenolate and dichalcogenidostannacyclopentane derivatives”, “Chem. Commun.”, 1996, pp. 1669-1670.
Kuehl, O., “N-heterocyclic germylenes and related compounds”, “Coordination Chemistry Reviews”, 2004, pp. 411-427, vol. 248.
Lappert, M., et al., “Monomeric Bivalent Group 4B Metal Dialkylamides M[NCMe2(CH2)3CMe2] (M=Ge or Sn), and the Structure of a Gaseous Disilylamide, Sn[N(SiMe3)2]2, by Gas Electron Diffraction”, “J.C.S. Chem. Comm.”, 1979, pp. 369-370, vol. 8.
Lappert, M., et al., “Monomeric, Coloured Germanium(II) and Tin(II) Di-t-Butylamides, and the Crystal and Molecular Structure of Ge(NCMe2[CH2]3CMe2)2”, “J.C.S. Chem. Comm.”, 1980, pp. 621-622, vol. 13.
Lee, J., et al., “GeSbTe deposition for the PRAM application”, “Applied Surface Science”, Feb. 2007, pp. 3969-3976, vol. 253, No. 8.
Leskela, M., et al., “Atomic layer deposition chemistry: recent developments and future challenges”, “Angew. Chem. Int. Ed.”, Nov. 24, 2003, pp. 5548-5554, vol. 42, No. 45.
Macomber, D., et al., “(n5-Cyclopentadienyl)- and (n5-Pentamethylcyclopentadienyl)copper Compounds Containing Phosphine, Carbonyl, and n2-Acetylenic Ligands”, “J. Am. Chem. Soc.”, 1983, pp. 5325-5329, vol. 105.
Maruyama, T., et al., “Silicon dioxide thin films prepared by chemical vapor deposition from tetrakis(diethylamino) silane and ozone”, “Appl. Phys. Letters”, May 23, 1994, pp. 2800-2802, vol. 64, No. 21.
Maruyama, T., “Electrical Characterization of Silicon Dioxide Thin Films Prepared by Chemical Vapor Deposition from Tetrakis(diethylamino)silane and Ozone”, “Jpn. J. Appl. Phys.”, Jul. 15, 1997, pp. L922-L925, vol. 36, Part 2, No. 7B.
Mathur, S., et al., “Germanium Nanowires and Core-Shell Nanostructures by Chemical Vapor Deposition of [Ge(C5H5)2]”, “Chem. Mater.”, May 15, 2004, pp. 2449-2456, vol. 16, No. 12.
Matsuda, I., et al., “Reactions of Group IV Organometallic Compounds: XXVIII. The Insertion Reactions of Benzoyl-Tert-Butylcarbodiimide With Group IV Trimethylmetallylamines and the Perparation of Trimethyl-Silyl- and -Germyl-tert-Butyl-Carbodiimide”, “Journal of Organometallic Chemistry”, 1974, pp. 353-359, vol. 69.
Meller, A., et al., “Synthesis and Isolation of New Germanium(II) Compounds and of Free Germylenes”, “Chem. Ber.”, May 1985, pp. 2020-2029 (English Abstract), vol. 118, No. 5.
Metzler, N., et al., “Synthesis of a silylene-borane adduct and its slow conversion to a silylborane”, “Chem. Commun.”, 1996, pp. 2657-2658.
Neumann, W., “Germylenes and Stannylenes”, “Chem. Rev.”, 1991, pp. 311-334, vol. 91, Publisher: American Chemical Society.
Oakley, S., et al., “Structural consequences of the prohibition of hydrogen bonding in copper-guanidine systems”, “Inorg. Chem.”, Jul. 13, 2004, pp. 5168-5172, vol. 43, No. 16 (Abstract).
O'Brien, P., et al., “Single-molecule Precursor Chemistry for the Deposition of Chalcogenide(S or Se)-containing Compound Semiconductors by MOCVD and Related Methods”, “J. Mater. Chem.”, 1995, pp. 1761-1773, vol. 5, No. 11.
Ovshinsky, S., “Reversible Electrical Switching Phenomena in Disordered Structures”, “Physical Review Letters”, Nov. 11, 1968, pp. 1450-1455, vol. 21, No. 20.
Pickett, N., et al., “Gas-phase formation of zinc/cadmium chalcogenide cluster complexes and their solid-state thermal decomposition to form II-VI nanoparticulate material”, “J. Mater. Chem.”, 1998, pp. 2769-2776, vol. 8.
Privitera, S., et al., “Phase change mechanisms in Ge2Sb2Te5”, “Journal of Applied Physics”, Jul. 9, 2007, pp. 1-5, vol. 102, No. 013516.
Raj, P., et al., “Synthesis and characterization of the complex triorganoantimony (V) cations, R3SbL'2+ and R3Sb(L-L)2+”, “Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry”, 1992, pp. 543-557 (Abstract), vol. 22, No. 5.
Raj, P., et al., “Synthesis and geometry of complex triorganoantimony(V) cations”, “Synthesis and Reactivity in Inorganic and Metal-Organic Chemistry”, 1992, pp. 1471-1494 (Abstract), vol. 22, No. 10.
Raoux, S., et al., “Influence of Dopants on the Crystallization Temperature, Crystal Structure, Resistance, and Threshold Field for Ge2Sb2Te5 and GeTe Phase Change Materials”, “European/Phase Change and Ovonics Symposium”, Sep. 4-6, 2011, pp. 1-8, Published in: Zuerich, Switzerland.
Raoux, S., et al., “Materials Engineering for Phase Change Random Access Memory”, “11th Annual Non-Volatile Memory Technology Symposium (NVMTS)”, Nov. 7-9, 2011, pp. 1-5.
Ren, H., et al., “Synthesis and structures of cyclopentadienyl N-heterocyclic carbene copper(I) complexes”, “Journal of Organometallic Chemistry”, Jun. 21, 2006, pp. 4109-4113, vol. 691.
Richardson, M., et al., “Volatile rare earth chelates of 1,1,1,5,5,5-hexafluoro-2,4-pentanedione and 1,1,1,2,2,3,3,7,7,7-decafluoro-4,6-heptanedione”, “Inorganic Chemistry”, 1971, pp. 498-504, vol. 10, No. 3.
Note: For the non-patent literature citations that no month of publication is indicated, the year of publication is more than 1 year prior to the effective date of the present application.
Schlecht, S., et al., “Direct Synthesis of (PhSe)4Ge and (PhTe)4Ge from Activated Hydrogenated Germanium—Crystal Structure and Twinning of (PhTe)4Ge”, “Eur. J. Inorg. Chem.”, 2003, pp. 1411-1415.
Shenai, D., et al., “Safer alternative liquid germanium precursors for relaxed graded SiGe layers and strained silicon by MOVPE”, “Journal of Crystal Growth”, Jan. 8, 2007, pp. 172-175, vol. 298.
Shi, Y., et al., “Titanium dipyrrolylmethane derivatives: rapid intermolecular alkyne hydroamination”, “Chem. Comm.”, Mar. 7, 2003, pp. 586-587, No. 5.
Stauf, G., et al., “Low Temperature ALD of Germanium for Phase Change Memory Thin Films”, “AVS 7th International Conference on Atomic Layer Deposition—ALD 2007”, Jun. 24, 2007, pp. 1-8.
Steigerwald, M., et al., “Organometallic Synthesis of II-VI Semiconductors. 1. Formation and Decomposition of Bis(organotelluro)mercury and Bis(organotelluro)cadmium Compounds”, “J. Am. Chem. Soc.”, 1987, pp. 7200-7201, vol. 109.
Sun, S., et al., “Performance of MOCVD tantalum nitride diffusion barrier for copper metallization”, “1995 Symposium on VLSI Technology Digest of Technical Papers”, Jun. 1995, pp. 29-30.
Tsai, M., et al., “Metalorganic chemical vapor deposition of tantalum nitride by tertbutylimidotris(diethylamido) tantalum for advanced metallization”, “Appl. Phys. Lett.”, Aug. 21, 1995, pp. 1128-1130, vol. 67, No. 8.
Tsai, M., et al., “Metal-organic chemical vapor deposition of tantalum nitride barrier layers for ULSI applications”, “Thin Solid Films”, Dec. 1, 1995, pp. 531-536, vol. 270, No. 1-2.
Tsumuraya, T., et al., “Telluradigermiranes. A Novel Three-membered Ring System Containing Tellurium”, “J. Chem. Soc. Chem. Commun.”, 1990, pp. 1159-1160.
Vehkamaki, M., et al., “Atomic Layer Deposition of SrTiO3 Thin Films from a Novel Strontium Precursor-Strontium-bis(tri-isopropylcyclopentadienyl)”, “Chemical Vapor Deposition”, Mar. 2001, pp. 75-80, vol. 7, No. 2.
Veith, M., et al., “Additionsreaktionen an intramolekular basenstabilisierte Ge=N- und Ge=S-Doppelbindungen”, “Chem. Ber.”, 1991, pp. 1135-1141 (English Abstract), vol. 124.
Veith, M., et al., “New perspectives in the tailoring of hetero (bi and tri-) metallic alkoxide derivatives”, “Polyhedron”, 1998, pp. 1005-1034, vol. 17, No. 5-6.
Veith, M., et al., “Molecular precursors for (nano) materials—a one step strategy”, “J. Chem. Soc. Dalton. Trans.”, May 20, 2002, pp. 2405-2412.
Veprek, S., et al., “Organometallic chemical vapor deposition of germanium from a cyclic germylene, 1,3-Di-tert-butyl-1,3,2-diazagermolidin-2-ylidine”, “Chem. Mater.”, 1996, pp. 825-831, vol. 8.
Weller, H., “Colloidal Semiconductor Q-Particles: Chemistry in the Transition Region Between Solid State and Molecules”, “Angew. Chem. Int. Ed. Engl.”, 1993, pp. 41-53, vol. 32.
Weller, H., “Self-organized Superlattices of Nanoparticles”, “Angew. Chem. Int. Ed. Engl.”, 1996, pp. 1079-1081, vol. 35, No. 10.
Sasamori, T., et al., “Reactions of a Germacyclopropabenzene with Elemental Chalcogens: Syntheses and Structures of a Series of Stable 2H-Benzo[c][1,2]chalcogenagermetes”, “Organometallics”, Jan. 14, 2005, pp. 612-618, vol. 24.
Abrutis, A., et al., “Hot-Wire Chemical Vapor Deposition of Chalcogenide Materials for Phase Change Memory Applications”, “Chem. Mater.”, May 2008, pp. 3557-3559, vol. 20, No. 11.
Allen, F., et al., “Tables of Bond Lengths Determined by X-ray and Neutron Diffraction. Part 1. Bond Lengths in Organic Compounds”, “J. Chem. Soc. Perkin Tran. II”, 1987, pp. S1-S19.
Anderson, H., “Dialkylaminogermanes and Dialkylaminosilanes”, “J. Amer. Chem. Soc.”, Mar. 20, 1952, pp. 1421-1423, vol. 74, No. 6.
Anderson, Q., et al., “Synthesis and Characterization of the First Pentaphenylcyclopentadienyl Copper(I) Complex, (Ph5Cp)Cu(PPh3)”, “Organometallics”, 1998, pp. 4917-4920, vol. 17.
Artaud-Gillet, M., et al., “Evaluation of copper organometallic sources for CuGaSe2 photovoltaic applications”, “Journal of Crystal Growth”, 2003, pp. 163-168, vol. 248.
Auner, N., et al., “Organosilicon Chemistry IV: From Molecules to Materials”, Mar. 2000, p. 291 (Abstract), Publisher: Wiley-Vch.
Baines, K., et al., “A Facile Digermene-to-germylgermylene Rearrangement; Bulky Germylene Insertion into the Si—H Bond”, “J. Chem. Soc. Chem. Commun.”, 1992, pp. 1484-1485.
Baxter, D., et al., “Low Pressure Chemical Vapor Deposition of Metallic Films of Iron, Manganese, Cobalt, Copper, Germanium and Tin Employing Bis(trimethyl)silylamido Complexes, M(N(SiMe3)2)n”, “Chemical Vapor Deposition”, 1995, pp. 49-51, vol. 1, No. 2.
Behrens, S., et al., “Synthesis and Structure of the Nanoclusters [Hg32Se14(SePh)36], [Cd32Se14(SePh) 36″(PPh3)4], [P(Et)2(Ph)C4H8OSiMe3]5[Cd18I17(PSiMe3)12]”, “Angew. Chem. Int. Ed. Engl.”, 1996, pp. 2215-2218, vol. 35, No. 19.
Related Publications (1)
Number Date Country
20150280115 A1 Oct 2015 US
Provisional Applications (1)
Number Date Country
61720283 Oct 2012 US