TY - JOUR
T1 - High-Performance and Durable Fuel Cells using Co/Sr-Free Fluorite-Based Mixed Conducting (Pr,Ce)O2-δ Cathode
AU - Seo, Han Gil
AU - Kim, Dong Hwan
AU - Seo, Jongsu
AU - Jeong, Seung Jin
AU - Kim, Jinwook
AU - Tuller, Harry L.
AU - Son, Ji Won
AU - Jung, Woo Chul
N1 - Funding Information:
This work was supported by a National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (2021M3H4A1A01002695). J.‐W.S. and D.H.K. also appreciate financial support from Korea Institute of Energy Technology Evaluation and Planning (KETEP), the Ministry of Trade, Industry & Energy, Republic of Korea (No. 20213030030040). H.L.T. acknowledges support from U.S. Department of Energy (DOE), National Energy Technology Laboratory (NETL), Office of Fossil Energy under Award no. DE‐FE0031668.
Publisher Copyright:
© 2022 The Authors. Advanced Energy Materials published by Wiley-VCH GmbH.
PY - 2022/11/17
Y1 - 2022/11/17
N2 - A major challenge to overcome in demonstrating solid oxide fuel cells (SOFCs) to be suitable as efficient and environmentally friendly energy conversion devices capable of addressing pressing clean energy and environmental needs is to surmount chemical and thermo-mechanical instabilities in their operational phase. To date, perovskite-based mixed conducting cathodes, which include inherent Co and Sr elements for enhanced reactivity and conductivity, have been intensively studied. These Co/Sr-based oxides, however, exhibit severe thermochemical expansion and suffer from Sr surface segregation, ultimately degrading the electrode performance. Here, high-performance and durable SOFCs are demonstrated by employing a Co/Sr-free fluorite-based mixed conducting (Pr,Ce)O2-δ (PCO) cathode eminently compatible with fluorite-based solid electrolytes. The nanocolumnar PCO electrode developed in this study provides not only a remarkable low level of electrode resistance (e.g., ≈0.05 Ω cm2 at 600 °C) but also exceptional long-term stability (e.g., a degradation rate 15 times slower compared to the state-of-the-art La0.6Sr0.4CoO3-δ perovskite). The competitive peak power densities of an anode-supported single cell with the PCO cathode are also successively achieved, recording a value of 0.92 W cm−2 at 600 °C. These findings herald the development of new Co/Sr-free electrodes for SOFCs at intermediate temperatures.
AB - A major challenge to overcome in demonstrating solid oxide fuel cells (SOFCs) to be suitable as efficient and environmentally friendly energy conversion devices capable of addressing pressing clean energy and environmental needs is to surmount chemical and thermo-mechanical instabilities in their operational phase. To date, perovskite-based mixed conducting cathodes, which include inherent Co and Sr elements for enhanced reactivity and conductivity, have been intensively studied. These Co/Sr-based oxides, however, exhibit severe thermochemical expansion and suffer from Sr surface segregation, ultimately degrading the electrode performance. Here, high-performance and durable SOFCs are demonstrated by employing a Co/Sr-free fluorite-based mixed conducting (Pr,Ce)O2-δ (PCO) cathode eminently compatible with fluorite-based solid electrolytes. The nanocolumnar PCO electrode developed in this study provides not only a remarkable low level of electrode resistance (e.g., ≈0.05 Ω cm2 at 600 °C) but also exceptional long-term stability (e.g., a degradation rate 15 times slower compared to the state-of-the-art La0.6Sr0.4CoO3-δ perovskite). The competitive peak power densities of an anode-supported single cell with the PCO cathode are also successively achieved, recording a value of 0.92 W cm−2 at 600 °C. These findings herald the development of new Co/Sr-free electrodes for SOFCs at intermediate temperatures.
KW - (Pr,Ce)O
KW - Co/Sr-free mixed conducting oxides
KW - nanocolumnar structures
KW - oxygen reduction reaction
KW - solid oxide fuel cells
UR - http://www.scopus.com/inward/record.url?scp=85137537089&partnerID=8YFLogxK
U2 - 10.1002/aenm.202202101
DO - 10.1002/aenm.202202101
M3 - Article
AN - SCOPUS:85137537089
SN - 1614-6832
VL - 12
JO - Advanced Energy Materials
JF - Advanced Energy Materials
IS - 43
M1 - 2202101
ER -