过电位
材料科学
中心(范畴论)
结晶学
D波段
析氧
电负性
催化作用
物理化学
物理
有机化学
化学
电极
拉曼光谱
光学
电化学
作者
Zongpeng Wang,Zhiping Lin,Jun Deng,Shijie Shen,Fanqi Meng,Jitang Zhang,Qinghua Zhang,Wenwu Zhong,Lin Gu
标识
DOI:10.1002/aenm.202003023
摘要
Abstract Significant efforts have been dedicated to boosting the electrocatalytic activity of Co 9 S 8 for the oxygen evolution reaction (OER); however, with limited improvement in its intrinsic activity, which relies on careful band engineering. Fe possesses one less 3d electron and lower electronegativity than Co, suggesting a higher d‐band center when forming polyhedron with S anions. Here, to improve the intrinsic activity by elevating the d‐band center, the six‐coordinated octahedrons in Co 9 S 8 are redesigned utilizing an Fe‐incorporated topochemical deintercalation method. Through substituting partial Co octahedrons by Fe octahedrons with higher d‐band, the overall d‐band center is regulated to achieve optimized adsorption and thus superior OER activity. With a reduction of 95 mV on the overpotential (at 10 mA cm −2 ), this work sheds lights on the design of OER catalysts through polyhedron engineering using topochemical deintercalation.
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