TY - JOUR
T1 - Improved redox cycling durability in alternative Ni alloy-based SOFC anodes
AU - Ishibashi, Yusuke
AU - Matsumoto, Kohei
AU - Futamura, Shotaro
AU - Tachikawa, Yuya
AU - Matsuda, Junko
AU - Lyth, Stephen M.
AU - Shiratori, Yusuke
AU - Taniguchi, Shunsuke
AU - Sasaki, Kazunari
N1 - Funding Information: This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives 4.0 License (CC BY-NC-ND, ), which permits non-commercial reuse, distribution, and reproduction in any medium, provided the original work is not changed in any way and is properly cited. For permission for commercial reuse, please email: [email protected]. Japan Science and Technology Agency (JST) COI Program Grant No. JPMJCE1318 yes 2020 The Author(s). Published on behalf of The Electrochemical Society by IOP Publishing Limited http://creativecommons.org/licenses/by-nc-nd/4.0/
Publisher Copyright: © 2020 The Author(s). Published on behalf of The Electrochemical Society by IOP Publishing Limited.
Yusuke Ishibashi et al 2020 J. Electrochem. Soc. 167 124517 DOI 10.1149/1945-7111/abac87
PY - 2020/8/19
Y1 - 2020/8/19
N2 - Repeated reduction and oxidation of metallic nickel in the anodes of solid oxide fuel cell (SOFC) causes volume changes and agglomeration. This disrupts the electron conducting network, resulting in deterioration of the electrochemical performance. It is therefore desirable to develop more robust anodes with high redox stability. Here, new cermet anodes are developed, based on nickel alloyed with Co, Fe, and/or Cr. The stable phases of these different alloys are calculated for oxidizing and reducing conditions, and their electrochemical characteristics are evaluated. Whilst alloying causes a slight decrease in power generation efficiency, the Ni-alloy based anodes have significantly improved redox cycle durability. Microstructural observation reveals that alloying results in the formation of a dense oxide film on the surface of the catalyst particle (e.g. Co-oxide or a complex Fe-Ni-Cr oxide). These oxide layers help suppress oxidation of the underlying nickel catalyst particles, preventing oxidation-induced volume changes/agglomeration, and thereby preserving the electron conducting pathways. As such, the use of these alternative Ni-alloy based cermets significantly improves the redox stability of SOFC anodes.
AB - Repeated reduction and oxidation of metallic nickel in the anodes of solid oxide fuel cell (SOFC) causes volume changes and agglomeration. This disrupts the electron conducting network, resulting in deterioration of the electrochemical performance. It is therefore desirable to develop more robust anodes with high redox stability. Here, new cermet anodes are developed, based on nickel alloyed with Co, Fe, and/or Cr. The stable phases of these different alloys are calculated for oxidizing and reducing conditions, and their electrochemical characteristics are evaluated. Whilst alloying causes a slight decrease in power generation efficiency, the Ni-alloy based anodes have significantly improved redox cycle durability. Microstructural observation reveals that alloying results in the formation of a dense oxide film on the surface of the catalyst particle (e.g. Co-oxide or a complex Fe-Ni-Cr oxide). These oxide layers help suppress oxidation of the underlying nickel catalyst particles, preventing oxidation-induced volume changes/agglomeration, and thereby preserving the electron conducting pathways. As such, the use of these alternative Ni-alloy based cermets significantly improves the redox stability of SOFC anodes.
KW - redox cycling durability
KW - anodes
KW - catalysts
KW - chromium alloys
KW - redox reactions
KW - solid oxide fuel cells (SOFC)
KW - electrochemical characteristics
UR - http://www.scopus.com/inward/record.url?scp=85090110497&partnerID=8YFLogxK
U2 - 10.1149/1945-7111/abac87
DO - 10.1149/1945-7111/abac87
M3 - Article
AN - SCOPUS:85090110497
SN - 0013-4651
VL - 167
SP - 1
EP - 17
JO - Journal of the Electrochemical Society
JF - Journal of the Electrochemical Society
IS - 12
M1 - 124517
ER -