journal article·2016-07-20

Aluminum Nitride Hydrolysis Enabled by Hydroxyl-Mediated Surface Proton Hopping

Christopher J. Bartel, Christopher L. Muhich, Alan W. Weimer, Charles B. Musgrave

Publisher page

Abstract

Aluminum nitride (AlN) is used extensively in the semiconductor industry as a high-thermal-conductivity insulator, but its manufacture is encumbered by a tendency to degrade in the presence of water. The propensity for AlN to hydrolyze has led to its consideration as a redox material for solar thermochemical ammonia (NH3) synthesis applications where AlN would be intentionally hydrolyzed to produce NH3 and aluminum oxide (Al2O3), which could be subsequently reduced in nitrogen (N2) to reform AlN and reinitiate the NH3 synthesis cycle. No quantitative, atomistic mechanism by which AlN, and more generally, metal nitrides react with water to become oxidized and generate NH3 yet exists. In this work, we used density-functional theory (DFT) to examine the reaction mechanisms of the initial stages of AlN hydrolysis, which include: water adsorption, hydroxyl-mediated proton diffusion to form NH3, and NH3 desorption. We found activation barriers (Ea) for hydrolysis of 330 and 359 kJ/mol for the cases of minimal adsorbed water and additional adsorbed water, respectively, corroborating the high observed temperatures for the onset of steam AlN hydrolysis. We predict AlN hydrolysis to be kinetically limited by the dissociation of strong Al-N bonds required to accumulate protons on surface N atoms to form NH3. The hydrolysis mechanism we elucidate is enabled by the diffusion of protons across the AlN surface by a hydroxyl-mediated Grotthuss mechanism. A comparison between intrinsic (Ea = 331 kJ/mol) and mediated proton diffusion (Ea = 89 kJ/mol) shows that hydroxyl-mediated proton diffusion is the predominant mechanism in AlN hydrolysis. The large activation barrier for NH3 generation from AlN (Ea = 330 or 359 kJ/mol, depending on water coverage) suggests that in the design of materials for solar thermochemical ammonia synthesis, emphasis should be placed on metal nitrides with less covalent metal-nitrogen bonds and, thus, more-facile NH3 liberation.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Semiconductor materials and devices · Hydrogen Storage and Materials · Boron and Carbon Nanomaterials Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Mechanical and Process Engineering, ETH Zurich, 8092 Zurich, Switzerland

Funding

Division of Graduate Education · Division of Chemical, Bioengineering, Environmental, and Transport Systems

References (70)

Show source-provided references
1. 10.1016/0022-3697(87)90153-310.1016/0022-3697(87)90153-3 ↗
2. Mohammed, A. C.; Corbett, S. J.Thick Film Metallizations and Performance of a Power Hybrid Module on Aluminum Nitride Substrates.InProceedings of the International Symposium on Microelectronics, International Society of Hybrid Microelectronics, Anaheim, CA, November 11–14, 1985;International Society for Hybrid Microelectronics:Reston, VA, 1985; 218.
3. 10.1557/JMR.1999.019110.1557/JMR.1999.0191 ↗
4. Weimer, A. W.Carbide, Nitride and Boride Materials Synthesis and Processing;Springer:The Netherlands, 1997; p696.10.1007/978-94-009-0071-4 ↗
5. 10.1109/TCHMT.1984.113638010.1109/TCHMT.1984.1136380 ↗
6. Kuramoto, N.; Taniguchi, H.Fine Powder of Aluminum Nitride, Composition and Sintered Body Thereof and Processes for Their Production. U.S. Patent 4,618,592, Oct 21, 1986.
7. 10.1111/j.1151-2916.1994.tb06951.x10.1111/j.1151-2916.1994.tb06951.x ↗
8. Katila, P.UV and Industrial LED Applications Require Efficient Thermal Substrates.LEDs Magazine, March 23, 2015.
9. Harris, J.Cost-Reduced AlN Delivers Thermals Needed in HBLED Packages.LEDs Magazine, September 2013, 2013.
10. 10.1016/j.mattod.2014.04.00310.1016/j.mattod.2014.04.003 ↗
11. Bardsely, N.; Bland, S.; Chwastyk, D.; Pattison, L.; Pattison, M.; Stober, K.; Yamada, M.Manufacturing Roadmap: Solid-State Lighting Research and Development;United States Department of Energy: Energy Efficiency & Renewable Energy:Washington, DC, 2014; pp1–127.
12. 10.1111/j.1151-2916.2000.tb01633.x10.1111/j.1151-2916.2000.tb01633.x ↗
13. 10.1111/j.1151-2916.1994.tb07060.x10.1111/j.1151-2916.1994.tb07060.x ↗
14. 10.1111/j.1151-2916.1989.tb07684.x10.1111/j.1151-2916.1989.tb07684.x ↗
15. 10.1016/0022-3697(73)90092-910.1016/0022-3697(73)90092-9 ↗
16. 10.1111/j.1151-2916.1989.tb06027.x10.1111/j.1151-2916.1989.tb06027.x ↗
17. 10.1016/j.jeurceramsoc.2008.02.02510.1016/j.jeurceramsoc.2008.02.025 ↗
18. 10.2109/jcersj2.122.21110.2109/jcersj2.122.211 ↗
19. 10.1007/BF0072182410.1007/BF00721824 ↗
20. 10.1111/j.1744-7402.2004.tb00188.x10.1111/j.1744-7402.2004.tb00188.x ↗
21. 10.1016/S0021-9797(03)00065-110.1016/S0021-9797(03)00065-1 ↗
22. 10.1021/jp056982h10.1021/jp056982h ↗
23. 10.1016/j.energy.2004.03.03610.1016/j.energy.2004.03.036 ↗
24. Ritter, S. K.The Haber-Bosch Reaction: An Early Chemical Impact on Sustainability.Chem. Eng. NewsAug 18, 2008; 86 (33).10.1021/cen-v086n015.p011a ↗
25. 10.1002/wene.17410.1002/wene.174 ↗
26. 10.1021/ie061551m10.1021/ie061551m ↗
27. 10.1039/C5SC00789E10.1039/C5SC00789E ↗
28. 10.1016/j.energy.2012.03.06210.1016/j.energy.2012.03.062 ↗
29. 10.1021/jp307382r10.1021/jp307382r ↗
30. 10.1002/aic.1371710.1002/aic.13717 ↗
31. 10.1098/rsfs.2014.008410.1098/rsfs.2014.0084 ↗
32. 10.1016/j.solener.2011.08.00510.1016/j.solener.2011.08.005 ↗
33. 10.1023/A:100471832900310.1023/A:1004718329003 ↗
34. 10.1006/jssc.1997.767210.1006/jssc.1997.7672 ↗
35. 10.1111/j.1151-2916.1990.tb06579.x10.1111/j.1151-2916.1990.tb06579.x ↗
36. 10.1186/1556-276X-8-23210.1186/1556-276X-8-232 ↗
37. 10.1038/nature0100910.1038/nature01009 ↗
38. 10.1016/0021-9517(85)90343-410.1016/0021-9517(85)90343-4 ↗
39. 10.1039/b807618a10.1039/b807618a ↗
40. 10.1021/am403946z10.1021/am403946z ↗
41. 10.1126/science.118832810.1126/science.1188328 ↗
42. 10.1021/ja801282510.1021/ja8012825 ↗
43. 10.1103/PhysRevLett.96.06610710.1103/PhysRevLett.96.066107 ↗
44. 10.1126/science.121946810.1126/science.1219468 ↗
45. 10.1021/ja306480910.1021/ja3064809 ↗
46. 10.1021/jp300081210.1021/jp3000812 ↗
47. 10.1016/S0009-2614(02)00720-010.1016/S0009-2614(02)00720-0 ↗
48. 10.1021/jp200309d10.1021/jp200309d ↗
49. 10.1021/ja510131a10.1021/ja510131a ↗
50. 10.1021/acs.jpclett.5b0182710.1021/acs.jpclett.5b01827 ↗
51. 10.1063/1.142072910.1063/1.1420729 ↗
52. 10.1021/jp507872d10.1021/jp507872d ↗
53. 10.1038/ncomms753910.1038/ncomms7539 ↗
54. Caldararu M. · Prog. Catal · 2005 · 14 · 9
55. 10.1016/S0254-0584(00)00473-910.1016/S0254-0584(00)00473-9 ↗
56. Oijerholm J. · 2007
57. 10.1016/0927-0256(96)00008-010.1016/0927-0256(96)00008-0 ↗
58. 10.1103/PhysRevB.54.1116910.1103/PhysRevB.54.11169 ↗
59. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
60. 10.1103/PhysRevB.59.175810.1103/PhysRevB.59.1758 ↗
61. 10.1103/PhysRevB.89.06410910.1103/PhysRevB.89.064109 ↗
62. 10.1016/j.scriptamat.2012.07.02710.1016/j.scriptamat.2012.07.027 ↗
63. 10.1016/j.commatsci.2005.04.01010.1016/j.commatsci.2005.04.010 ↗
64. 10.1002/jcc.2057510.1002/jcc.20575 ↗
65. 10.1088/0953-8984/21/8/08420410.1088/0953-8984/21/8/084204 ↗
66. Jonsson H. · 1998
67. 10.1063/1.132967210.1063/1.1329672 ↗
68. 10.1063/1.48009710.1063/1.480097 ↗
69. 10.1103/PhysRevB.74.10411610.1103/PhysRevB.74.104116 ↗
70. Madelung O. · 2004 · 810.1007/978-3-642-18865-7 ↗