过电位
电催化剂
材料科学
二硒醚
催化作用
正交晶系
钴
电解质
钌
化学工程
化学物理
电化学
无机化学
电极
化学
晶体结构
物理化学
结晶学
硒
有机化学
冶金
工程类
作者
Xiaolong Zhang,Shao‐Jin Hu,Ya‐Rong Zheng,Rui Wu,Fei‐Yue Gao,Peng‐Peng Yang,Zhuang‐Zhuang Niu,Chao Gu,Xingxing Yu,Xusheng Zheng,Cheng Ma,Xiao Zheng,Junfa Zhu,Min‐Rui Gao,Shu‐Hong Yu
标识
DOI:10.1038/s41467-019-12992-y
摘要
Abstract Many platinum group metal-free inorganic catalysts have demonstrated high intrinsic activity for diverse important electrode reactions, but their practical use often suffers from undesirable structural degradation and hence poor stability, especially in acidic media. We report here an alkali-heating synthesis to achieve phase-mixed cobalt diselenide material with nearly homogeneous distribution of cubic and orthorhombic phases. Using water electroreduction as a model reaction, we observe that the phase-mixed cobalt diselenide reaches the current density of 10 milliamperes per square centimeter at overpotential of mere 124 millivolts in acidic electrolyte. The catalyst shows no sign of deactivation after more than 400 h of continuous operation and the polarization curve is well retained after 50,000 potential cycles. Experimental and computational investigations uncover a boosted covalency between Co and Se atoms resulting from the phase mixture, which substantially enhances the lattice robustness and thereby the material stability. The findings provide promising design strategy for long-lived catalysts in acid through crystal phase engineering.
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