journal article·2023-06-12

Investigation of Self-Assembled Dual-Phase Cathodes with Triple Conductivity for Protonic Ceramic Fuel Cells

Caiyue Xie, Jun Li, Yifei Wang, Haowei Li, Haibo Hu, Xinghong Zhou, Xiaoyu Wang, Xifeng Ding

ACS Applied Energy Materials· Volume 6· Issue 11
Publisher page

Abstract

Efficient cathodes with high catalytic activity and stability are crucial for the development of protonic ceramic fuel cells (PCFCs). Single-phase cathode is difficult to meet multiple requirements, such as high electrochemical performance, oxygen reducing activity, stability, and CO 2 -resistance. In this regard, we report self-assembled dual-phase perovskite cathodes Ba(Co 0.7 Fe 0.3 ) x (Ce 0.8 Y 0.2 ) 1- x O 3-δ (BCFCY, x = 0.6, 0.7, 0.8) prepared by a one-pot method for PCFCs. The cathode displays a triple O 2– /e – /H + conducting behavior, which consists of a cubic phase ( C-BCFCY, Co-rich) and a rhombohedral phase ( R–BCFCY, Ce-rich) in this perovskite. The C-BCFCY has high O 2– /e – conductivity and low basicity, while the latter R–BCFCY exhibited excellent hydration performance, which synergistically results in cathode with high electrochemical activity and CO 2 -resistance. Owing to its appropriate dual phase composition, the Ba(Co 0.7 Fe 0.3 ) 0.7 (Ce 0.8 Y 0.2 ) 0.3 O 3-δ (BCFCY73) electrode demonstrates low polarization resistance (0.065 Ω cm 2 ) at 700 °C in 5 vol % water steam. The peak power density of anode-supported single cells BZCYYb | BCFCY73 | BZCYYb is 545.3 mW cm –2 at 700 °C. This result proves that regulating the content of two phases (proton conductors and ionic conductors, respectively) of perovskite oxide by the one-pot method is an effective strategy to design PCFC cathode materials with high activity, and this method can also be applied in other energy transfer materials fields.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advancements in Solid Oxide Fuel Cells · Fuel Cells and Related Materials · Advanced battery technologies research

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

Affiliations

School of Materials Science and Engineering, Nanjing University of Science and Technology, Nanjing, Jiangsu 210094, China

Funding

Fundamental Research Funds for the Central Universities · National Natural Science Foundation of China

References (47)

Show source-provided references
1. 10.1126/science.120409010.1126/science.1204090 ↗
2. 10.1115/1.400375010.1115/1.4003750 ↗
3. 10.1016/j.ijhydene.2010.11.05310.1016/j.ijhydene.2010.11.053 ↗
4. 10.1016/j.elecom.2011.12.02310.1016/j.elecom.2011.12.023 ↗
5. 10.1038/nmat283710.1038/nmat2837 ↗
6. 10.1016/j.ssi.2007.11.03110.1016/j.ssi.2007.11.031 ↗
7. 10.1039/c0jm00350f10.1039/c0jm00350f ↗
8. 10.1126/science.aab398710.1126/science.aab3987 ↗
9. 10.1149/2.0121710jes10.1149/2.0121710jes ↗
10. 10.1039/d0ta03899g10.1039/d0ta03899g ↗
11. 10.1016/j.jpowsour.2009.07.05710.1016/j.jpowsour.2009.07.057 ↗
12. 10.1021/acsaem.8b0161710.1021/acsaem.8b01617 ↗
13. 10.1016/j.ceramint.2021.02.12310.1016/j.ceramint.2021.02.123 ↗
14. 10.1016/j.jpowsour.2012.01.03310.1016/j.jpowsour.2012.01.033 ↗
15. 10.1002/adma.20190697910.1002/adma.201906979 ↗
16. 10.1016/j.jpowsour.2019.22760910.1016/j.jpowsour.2019.227609 ↗
17. 10.1016/j.ijhydene.2015.07.10410.1016/j.ijhydene.2015.07.104 ↗
18. Maleki B. · Acta Chim. Slov. · 2012 · 59 · 814
19. 10.1007/s11814-014-0265-210.1007/s11814-014-0265-2 ↗
20. 10.1021/acs.biochem.9b0061310.1021/acs.biochem.9b00613 ↗
21. 10.1016/j.ijhydene.2021.11.25010.1016/j.ijhydene.2021.11.250 ↗
22. 10.1021/acsenergylett.6b0061710.1021/acsenergylett.6b00617 ↗
23. 10.1016/0167-2738(92)90097-910.1016/0167-2738(92)90097-9 ↗
24. 10.1016/j.ijhydene.2020.08.14710.1016/j.ijhydene.2020.08.147 ↗
25. 10.1016/j.jpowsour.2009.06.07110.1016/j.jpowsour.2009.06.071 ↗
26. 10.1016/s0167-2738(00)00771-210.1016/s0167-2738(00)00771-2 ↗
27. 10.1016/j.jpowsour.2014.11.12310.1016/j.jpowsour.2014.11.123 ↗
28. 10.1039/c9ta04335g10.1039/c9ta04335g ↗
29. 10.1039/c8ee01140k10.1039/c8ee01140k ↗
30. 10.1002/adma.20210637910.1002/adma.202106379 ↗
31. 10.1016/j.electacta.2015.09.09710.1016/j.electacta.2015.09.097 ↗
32. 10.1002/smtd.20180027910.1002/smtd.201800279 ↗
33. 10.1149/1.183855710.1149/1.1838557 ↗
34. 10.1016/s0167-2738(99)00188-510.1016/s0167-2738(99)00188-5 ↗
35. 10.1039/c5ta10090a10.1039/c5ta10090a ↗
36. 10.1021/ic503006u10.1021/ic503006u ↗
37. 10.1016/j.ssi.2015.05.01410.1016/j.ssi.2015.05.014 ↗
38. 10.1039/d0ee03283b10.1039/d0ee03283b ↗
39. 10.1021/acsaem.0c0048610.1021/acsaem.0c00486 ↗
40. 10.1021/acscatal.1c0480710.1021/acscatal.1c04807 ↗
41. 10.1016/j.joule.2018.02.00810.1016/j.joule.2018.02.008 ↗
42. 10.1149/1.298102410.1149/1.2981024 ↗
43. 10.1016/j.ssi.2011.06.01110.1016/j.ssi.2011.06.011 ↗
44. 10.1016/j.memsci.2011.10.03010.1016/j.memsci.2011.10.030 ↗
45. 10.1016/0022-3115(89)90418-210.1016/0022-3115(89)90418-2 ↗
46. 10.1002/anie.20080383710.1002/anie.200803837 ↗
47. 10.1016/j.ssi.2005.09.04010.1016/j.ssi.2005.09.040 ↗