材料科学
阴极
纳米复合材料
氧化物
钙钛矿(结构)
电化学
化学工程
催化作用
固体氧化物燃料电池
极限抗拉强度
电极
纳米技术
复合材料
阳极
冶金
物理化学
有机化学
化学
工程类
作者
Zhihong Du,Leyu Shen,Yue Gong,Min Zhang,Jingyan Zhang,Jiangyuan Feng,Keyun Li,Konrad Świerczek,Hailei Zhao
标识
DOI:10.1002/adfm.202310790
摘要
Abstract The sluggish kinetics of oxygen reduction reaction (ORR) at low temperatures and the fast degradation of the cathode are the main obstacles to the commercialization of solid oxide fuel cells (SOFCs). However, it is still very challenging to achieve both high catalytic activity and favorable stability for single‐phase materials. Herein, a highly active and durable nanocomposite cathode (Ba 0.5 Sr 0.5 ) 0.75 Pr 0.25 Co 0.575 Fe 0.3 W 0.125 O 3‐δ (BSPCFW) for low‐temperature SOFC (≤650 °C) is presented, which self‐assembles into two cubic perovskites: the simple perovskite Pr 0.38 Ba 0.25 Sr 0.37 Co 0.62 Fe 0.38 O 3‐δ (PBSCF‐ c ) and the B‐site cations ordered double perovskite Ba 1.30 Sr 0.70 Co 1.0 Fe 0.25 W 0.75 O 6‐δ (BSCFW‐ c ). The former PBSCF‐ c serves as the highly conductive and active catalyst for ORR, while the latter BSCFW‐ c with a large lattice parameter introduces a key beneficial lattice tensile strain into the PBSCF‐ c phase through a coherent interface, which significantly promotes the ORR activity at low temperatures with the area specific resistance of 0.034 Ω cm 2 at 650 °C, and the long‐term stability of 2 years storage and 1280 h operation in symmetrical cell. The introduction of the beneficial lattice tensile strain in self‐assembled composite catalysts is an effective way to synergistically enhance the electrochemical activity and durability of the electrode materials for electrochemical devices.
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