Electrochemical and Catalytic Behaviors of Ni–YSZ Anode for the Direct Utilization of Ammonia Fuel in Solid Oxide Fuel Cells
Source abstract
Abstract
In this study the electrochemical performances of Ni–YSZ anode in humidified H 2 , NH 3 and CH 4 fuels were compared under almost the same partial pressure of oxygen at 500–800°C. The cell performance was significantly affected by fuel species and operating temperature. The single cell exhibited higher performance in wet NH 3 as compared with that in CH 4 , which was caused by the difference in the catalytic activity of anode for the hydrogen production in wet NH 3 and CH 4 . Thus, it was clarified that NH 3 is a preferable fuel rather than CH 4 for the direct use in SOFCs. Furthermore, the kinetics study on ammonia decomposition over Ni–YSZ anode was conducted at 600°C. Although the ammonia decomposition increased with increasing ammonia concentration, the decomposition reduced in the presence of hydrogen in the reactant gas. Such a behavior was not confirmed at 850°C. These results indicated the inhibition effect of hydrogen for ammonia decomposition, which will be the key factor for the design of anode and the operating condition setting.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Electronic and Structural Properties of Oxides · Ammonia Synthesis and Nitrogen Reduction
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (31)
Show source-provided references
1. 10.1016/j.electacta.2014.08.12010.1016/j.electacta.2014.08.120 ↗
2. 10.1016/S0167-2738(00)00452-510.1016/S0167-2738(00)00452-5 ↗
3. 10.1016/j.jpowsour.2004.06.04010.1016/j.jpowsour.2004.06.040 ↗
4. 10.1016/j.fuproc.2009.02.00410.1016/j.fuproc.2009.02.004 ↗
5. 10.1016/S0926-860X(01)00941-310.1016/S0926-860X(01)00941-3 ↗
6. 10.1016/j.ces.2005.05.03010.1016/j.ces.2005.05.030 ↗
7. 10.1016/j.jcat.2012.03.01210.1016/j.jcat.2012.03.012 ↗
8. 10.1126/science.112587710.1126/science.1125877 ↗
9. 10.1016/j.ijhydene.2012.01.11910.1016/j.ijhydene.2012.01.119 ↗
10. 10.1016/j.jpowsour.2013.04.01410.1016/j.jpowsour.2013.04.014 ↗
11. 10.1039/C3TA12766D10.1039/C3TA12766D ↗
12. 10.1016/j.ijhydene.2009.04.06010.1016/j.ijhydene.2009.04.060 ↗
13. 10.1016/S1872-2067(07)60062-X10.1016/S1872-2067(07)60062-X ↗
14. 10.1016/j.jpowsour.2008.02.09710.1016/j.jpowsour.2008.02.097 ↗
15. 10.1002/fuce.20130027610.1002/fuce.201300276 ↗
16. 10.1016/j.cattod.2005.10.01110.1016/j.cattod.2005.10.011 ↗
17. 10.1016/j.jpowsour.2011.10.14210.1016/j.jpowsour.2011.10.142 ↗
18. 10.1016/S0378-7753(03)00083-110.1016/S0378-7753(03)00083-1 ↗
19. 10.1016/j.jpowsour.2006.06.04710.1016/j.jpowsour.2006.06.047 ↗
20. 10.1016/j.jpowsour.2006.09.09310.1016/j.jpowsour.2006.09.093 ↗
21. 10.1016/j.ijhydene.2012.04.10110.1016/j.ijhydene.2012.04.101 ↗
22. 10.1016/j.jpowsour.2005.02.04010.1016/j.jpowsour.2005.02.040 ↗
23. 10.1016/j.jpowsour.2004.08.02010.1016/j.jpowsour.2004.08.020 ↗
24. 10.1016/j.jpowsour.2006.06.05610.1016/j.jpowsour.2006.06.056 ↗
25. 10.1016/j.jpowsour.2007.09.04010.1016/j.jpowsour.2007.09.040 ↗
26. 10.1016/j.jpowsour.2006.04.09910.1016/j.jpowsour.2006.04.099 ↗
27. 10.1016/j.jpowsour.2008.11.03710.1016/j.jpowsour.2008.11.037 ↗
28. 10.1002/fuce.20140013510.1002/fuce.201400135 ↗
29. 10.1149/06801.2751ecst10.1149/06801.2751ecst ↗
30. 10.1149/1.333683010.1149/1.3336830 ↗
31. 10.1021/acsami.5b0104810.1021/acsami.5b01048 ↗