Affiliation:
1. School of Environment and Energy South China University of Technology 382 East Road, Higher Education Mega Center Guangzhou 510006 P. R. China
2. School of Material Science and Engineering Georgia Institute of Technology Atlanta GA 30318 USA
3. State Key Laboratory of Materials‐Oriented Chemical Engineering College of Chemical Engineering Nanjing Tech University Nanjing 211816 P. R. China
Abstract
AbstractReversible protonic ceramic electrochemical cells (R‐PCECs) are emerging as ideal devices for highly efficient energy conversion (generating electricity) and storage (producing H2) at intermediate temperatures (400–700 °C). However, their commercialization is largely hindered by the development of highly efficient air electrodes for oxygen reduction and water‐splitting reactions. Here, the findings in the design of a highly active and durable air electrode are reported: high‐entropy Pr0.2Ba0.2Sr0.2La0.2Ca0.2CoO3−δ (HE‐PBSLCC), which exhibits impressive activity and stability for oxygen reduction and water‐splitting reactions, as confirmed by electrochemical characterizations and structural analysis. When used as an air electrode of R‐PCEC, the HE‐PBSLCC achieves encouraging performances in dual modes of fuel cells (FCs) and electrolysis cells (ECs) at 650 °C, demonstrating a maximum power density of 1.51 W cm−2 in FC mode, and a current density of −2.68 A cm−2 at 1.3 V in EC mode. Furthermore, the cells display good operational durabilities in FC and EC modes for over 270 and 500 h, respectively, and promising cycling durability for 70 h with reasonable Faradaic efficiencies. This study offers an effective strategy for the design of active and durable air electrodes for efficient oxygen reduction and water splitting.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Guangdong Province
Subject
Mechanical Engineering,Mechanics of Materials,General Materials Science
Cited by
74 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献