电催化剂
材料科学
过电位
协调数
配位几何学
过渡金属
无机化学
电化学
结晶学
催化作用
氢键
化学
物理化学
电极
离子
分子
有机化学
生物化学
作者
Zhiping Lin,Beibei Xiao,Zongpeng Wang,Weiying Tao,Shijie Shen,Liangai Huang,Jitang Zhang,Fanqi Meng,Qinghua Zhang,Lin Gu,Wenwu Zhong
标识
DOI:10.1002/adfm.202102321
摘要
Abstract The coordination environment is crucial for the activity of an electrocatalyst, which defines the interaction between the central and adjacent atoms. In traditional 2D MX 2 (M = Mo, W, etc., X = S, Se), M is usually coordinated with 6 X atoms in either trigonal prismatic (2H) or octahedral (1T) polyhedrons. With such a coordination configuration, only the edge X sites exhibit activity for hydrogen evolution reaction (HER). Here, a planar‐coordination transition metal chalcogenide, PdSe 2 is reported, as an efficient electrocatalyst for the HER in an alkaline electrolyte. By reducing the spatial polyhedron coordination to planar polygon coordination, the M sites in PdSe 2 can be efficiently activated to interact with the adsorptive intermediates. As a result, both Pd and Se atoms act as active sites for hydrogen evolution with neutral adsorption ability. With an overpotential of 138 mV at 10 mA cm −2 , this work advances the exploration of planar‐coordination HER electrocatalysts.
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