材料科学
技术
复合数
氧化物
质子
阴极
燃料电池
化学工程
复合材料
纳米技术
物理化学
冶金
核物理学
电离层
化学
物理
天文
工程类
作者
Yang Gao,Min Fu,Shuang Zhao,Zhongyu Hou,Kechen Liu,Xiangbo Deng,Zetian Tao
标识
DOI:10.1002/adfm.202416625
摘要
Abstract One of the key challenges for high‐performance proton‐conducting solid oxide fuel cells (H‐SOFCs) is the mismatch in thermal expansion coefficients (TEC) between the cathode and electrolyte. While incorporating negative thermal expansion (NTE) materials can mitigate this issue, mechanical mixing often weakens cathode strength. To address this, a TEC gradient cathode is proposed and successfully implemented by co‐sintering PrBa(Co 0.7 Fe 0.3 ) 2 O 5‐δ (PBCF) with Y 2 W 3 O 12 (YWO) in this work. In this work, Ba atoms at the A‐site of PBCF migrated from the lattice, generating A‐site defects. The resulting BaWO 4 and Y 10 W 8 O 21 phases, which have low TEC, are uniformly distributed between PBCF and YWO, forming a TEC gradient composite cathode. In addition, the transition phase captures the A‐site element Ba in the electrolyte layer, optimizing the electrolyte‐cathode interface. The composite cathode exhibits a reduced TEC, closely matching that of the electrolyte, significantly enhancing interface bonding, thereby providing a lower ohmic resistance of 0.051 Ω cm 2 and a higher power density of 1.88 W cm −2 at 700 °C. Remarkably, thermal cycling tests conducted under temperature switching conditions demonstrate the composite cathode's long‐term thermal and chemical stability.
科研通智能强力驱动
Strongly Powered by AbleSci AI