دورية أكاديمية

Investigation of Cathodic Reaction Mechanism in Solid Oxide Fuel Cells by Operando X-Ray Absorption Spectroscopy

التفاصيل البيبلوغرافية
العنوان: Investigation of Cathodic Reaction Mechanism in Solid Oxide Fuel Cells by Operando X-Ray Absorption Spectroscopy
المؤلفون: Yoichiro TSUJI, Koji AMEZAWA, Takayuki NAKAO, Toshiaki INA, Tatsuya KAWADA, Kentaro YAMAMOTO, Yoshiharu UCHIMOTO, Yuki ORIKASA
المصدر: Electrochemistry, Vol 88, Iss 6, Pp 560-565 (2020)
بيانات النشر: The Electrochemical Society of Japan, 2020.
سنة النشر: 2020
المجموعة: LCC:Technology
LCC:Physical and theoretical chemistry
مصطلحات موضوعية: oxygen chemical potential, sofc, cathode, operando x-ray absorption, Technology, Physical and theoretical chemistry, QD450-801
الوصف: The oxygen chemical potential is an essential indicator for the rate-limiting step of the oxygen reduction reaction in high-temperature electrochemical devices such as solid oxide fuel cells (SOFCs). However, standard electrochemical measurements cannot successfully analyze the oxygen potential profile. Herein, the relationship between oxygen deficiencies and the valence state was determined directly through operando X-ray absorption spectroscopy. To compare the rate-limiting reactions in SOFC cathodes, dense thin-film electrodes of La0.6Sr0.4CoO3−δ (LSC) on a Ce0.9Gd0.1O1.95 (GDC) electrolyte, La0.6Sr0.4Co0.8Fe0.2O3−δ (LSCF) on a Y0.1Ce0.9O1.95 (YDC) electrolyte, and La0.9Sr0.1MnO3±δ (LSM) on a Zr0.92Y0.08O1.96 (YSZ) electrolyte were examined as model SOFC cathodes. Variations in the oxygen chemical potential of the electrodes with and without cathodic polarization were experimentally evaluated from the energy shift of the transition metal (Co, Fe, and Mn) K-edge X-ray absorption. It was found that the oxygen chemical potential of the LSC and LSCF electrodes was reduced by applying a cathodic potential and that this change in the oxygen chemical potential occurred mainly on the electrode surface. This result directly demonstrates that the electrochemical oxygen reduction at the cathode is rate-controlled by surface reactions. By contrast, the oxygen potential of LSM changes not at the electrode surface but inside the electrode, which demonstrates that oxide ion diffusion is the rate-determining step for the LSM/YSZ model electrode. This study directly reveals the different rate-determining steps of the electrode reaction for various SOFC cathodes.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2186-2451
Relation: https://www.jstage.jst.go.jp/article/electrochemistry/88/6/88_20-00108/_pdf/-char/en; https://doaj.org/toc/2186-2451
DOI: 10.5796/electrochemistry.20-00108
URL الوصول: https://doaj.org/article/c134e27630a047d1bc230decf004840c
رقم الأكسشن: edsdoj.134e27630a047d1bc230decf004840c
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:21862451
DOI:10.5796/electrochemistry.20-00108