Investigation of Electrochemical Reaction Mechanism at the Fuel Electrode Surface in Proton-Conducting Oxide Cells
Jinwook Kim a, Seongwoo Nam a, Sejong Ahn a, Hyunseung Kim a, Jun Hyuk Kim b, Byeom Gyun Jeong c, Di Chen d, WooChul Jung a
a Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon 34141, Korea, Korea, Republic of
b Sungkyunkwan University, South Korea, 300 Cheoncheon-dong, Jangan-gu, Suwon, 440, Korea, Republic of
c Korea Basic Science Institute (KBSI), Daejeon, Republic of Korea
d Tsinghua University, Yifu Building Room 2422, Tsinghua University,Haidian District, Beijing, 100084, China
Proceedings of 24th International Conference on Solid State Ionics (SSI24)
Fundamentals: Experiment and simulation
London, United Kingdom, 2024 July 14th - 19th
Organizers: John Kilner and Stephen Skinner
Oral, Jinwook Kim, presentation 345
Publication date: 10th April 2024

 Proton-conducting ceramic cells are emerging as promising alternatives to conventional oxygen ion-conducting devices, offering the potential for low-temperature operation in next-generation energy technologies [1-3]. Despite their promise, a detailed understanding of the electrochemical reactions at the electrodes of proton-conducting ceramic cells remains elusive, impeded by the complex nature of these reactions and a gap in knowledge concerning electrode materials. Notably, the use of model electrodes for in-depth mechanistic studies [4-6]—commonplace in the research of traditional oxygen ion-conducting fuel cells—is scarce for proton-conducting counterparts.

 This study focuses on fundamental research of the electrochemical reactions occurring at the fuel electrode surface in proton-conducting cells. Metal patterned BaZr0.4Ce0.4Y0.1Yb0.1O3−δ model composite electrodes are utilized to investigate the electrode reactions. Impedance analysis is conducted under various hydrogen partial pressures and applied voltages to analyze the electrochemical activity. Additionally, in-operando X-ray photoelectron spectroscopy is employed to perform real-time surface chemical analysis under high-temperature with hydrogen exposure conditions and over-potentials. This comprehensive analysis lead to the identification of triple phase boundaries as the dominant active sites and the charge transfer step of protons to metal as the RDS for the hydrogen incorporation reaction among 45 candidate steps. The findings contribute to a comprehensive understanding of the electrochemical processes in proton-conducting ceramic fuel cells, providing valuable insights for the design of fuel electrode materials.

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