Understanding the Coarsening and Degradation in a Nanoscale Nickel Gadolinia-Doped-Ceria Electrode for High-Temperature Applications
Source abstract
Abstract
Nanostructure engineering is an effective approach to enhance the electrochemical performance of energy devices. While the high surface area of nanoparticles greatly enlarges the density of reaction sites, it often also leads to relatively rapid degradation as the particles tend to coarsen to reduce their high surface energy. Therefore, a nickel/gadolinia-doped-ceria (CGO) cermet electrode is studied, with a novel porous nanostructure consisting of nanoscale Ni (100 nm) and CGO (50 nm) crystallites, cosintered from nanocomposite precursor agglomerate particles. This electrode combines both high performance and excellent durability, with a total area-specific resistance (ASR) of 0.11 Ω cm2 at 800 °C and a stable ASR with up to 170 h ageing in humidified 5% H2–N2. Post-test analysis by 3D tomography shows that nickel coarsens and is responsible for the initial increase in ASR. However, the subsequent electrochemical performance is stable because reaction at the double phase boundaries (DPBs) on the surfaces of nanoscale CGO becomes dominant and is resistant to ageing. At this stage, the coarsened Ni network is also stabilized by the surrounding nanostructure. The dominant role of the DPB reaction is supported quantitatively using a continuum model with geometrical parameters obtained from 3D tomography.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Catalytic Processes in Materials Science · Electronic and Structural Properties of Oxides
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Materials, Imperial College, London SW7 2AZ, U.K.
Dyson School of Design Engineering, Imperial College, London SW7 2AZ, U.K.
Department of Earth Science and Engineering, Imperial College, London SW7 2AZ, U.K.
Faculty of Engineering, Imperial College, London SW7 2AZ, U.K.
Funding
Engineering and Physical Sciences Research Council · China Scholarship Council · H2FC SUPERGEN
References (46)
Show source-provided references
1. 10.1021/am301978810.1021/am3019788 ↗
2. 10.1016/s1359-6462(97)00435-110.1016/s1359-6462(97)00435-1 ↗
3. 10.1016/j.jcat.2017.06.00510.1016/j.jcat.2017.06.005 ↗
4. 10.1126/science.120409010.1126/science.1204090 ↗
5. 10.1149/1.139175810.1149/1.1391758 ↗
6. 10.1021/ef050053810.1021/ef0500538 ↗
7. 10.1016/j.actamat.2007.09.02310.1016/j.actamat.2007.09.023 ↗
8. 10.1016/j.jpowsour.2014.05.03810.1016/j.jpowsour.2014.05.038 ↗
9. 10.1016/j.ssi.2007.10.00210.1016/j.ssi.2007.10.002 ↗
10. 10.1016/j.jpowsour.2010.04.05910.1016/j.jpowsour.2010.04.059 ↗
11. 10.1149/1.320574310.1149/1.3205743 ↗
12. 10.1002/fuce.20160022010.1002/fuce.201600220 ↗
13. 10.1016/j.ijhydene.2011.09.00710.1016/j.ijhydene.2011.09.007 ↗
14. 10.1016/j.jpowsour.2010.08.01710.1016/j.jpowsour.2010.08.017 ↗
15. 10.1016/j.jpowsour.2010.05.04710.1016/j.jpowsour.2010.05.047 ↗
16. 10.1016/j.ijhydene.2013.11.08610.1016/j.ijhydene.2013.11.086 ↗
17. 10.1039/c3ta10439g10.1039/c3ta10439g ↗
18. 10.1038/nmat318410.1038/nmat3184 ↗
19. 10.1016/j.jpowsour.2006.09.01510.1016/j.jpowsour.2006.09.015 ↗
20. 10.1016/j.ssi.2010.04.01410.1016/j.ssi.2010.04.014 ↗
21. 10.1016/j.electacta.2015.09.09710.1016/j.electacta.2015.09.097 ↗
22. 10.3390/catal712036810.3390/catal7120368 ↗
23. 10.1016/j.ssi.2014.02.01210.1016/j.ssi.2014.02.012 ↗
24. 10.1016/j.ceramint.2014.05.01010.1016/j.ceramint.2014.05.010 ↗
25. 10.1016/j.jpowsour.2010.11.11710.1016/j.jpowsour.2010.11.117 ↗
26. 10.1016/j.jpowsour.2012.07.03110.1016/j.jpowsour.2012.07.031 ↗
27. 10.1111/j.1551-2916.2005.00740.x10.1111/j.1551-2916.2005.00740.x ↗
28. 10.1149/2.0501409jes10.1149/2.0501409jes ↗
29. 10.1149/1.323149010.1149/1.3231490 ↗
30. 10.1149/2.0821709jes10.1149/2.0821709jes ↗
31. 10.1039/c9nr06740j10.1039/c9nr06740j ↗
32. 10.1149/1.183725210.1149/1.1837252 ↗
33. 10.1039/tf956520078610.1039/tf9565200786 ↗
34. 10.1016/s0167-2738(96)00588-710.1016/s0167-2738(96)00588-7 ↗
35. 10.1149/1.183813910.1149/1.1838139 ↗
36. 10.1016/s0167-2738(00)00530-010.1016/s0167-2738(00)00530-0 ↗
37. 10.1016/S0167-2738(97)00345-710.1016/S0167-2738(97)00345-7 ↗
38. 10.1016/s0167-2738(02)00500-310.1016/s0167-2738(02)00500-3 ↗
39. 10.1039/c3ta13404k10.1039/c3ta13404k ↗
40. 10.1016/s0167-2738(00)00462-810.1016/s0167-2738(00)00462-8 ↗
41. 10.1016/j.electacta.2015.12.04410.1016/j.electacta.2015.12.044 ↗
42. 10.1016/j.jpowsour.2007.11.08310.1016/j.jpowsour.2007.11.083 ↗
43. 10.1016/j.nanoen.2017.06.02810.1016/j.nanoen.2017.06.028 ↗
44. 10.1016/j.jpowsour.2016.09.00610.1016/j.jpowsour.2016.09.006 ↗
45. 10.1016/j.jpowsour.2010.08.04710.1016/j.jpowsour.2010.08.047 ↗
46. 10.1149/1.333683010.1149/1.3336830 ↗