过电位
塔菲尔方程
纳米片
电催化剂
硒
材料科学
催化作用
制氢
硒化物
过渡金属
分解水
硫化镍
无机化学
氢
镍
化学工程
化学
电化学
电极
纳米技术
物理化学
冶金
光催化
有机化学
工程类
生物化学
作者
Fengmei Wang,Yuanchang Li,Tofik Ahmed Shifa,Kaili Liu,Feng Wang,Zhenxing Wang,Peng Xu,Qisheng Wang,Jun He
标识
DOI:10.1002/anie.201602802
摘要
Abstract To address the urgent need for clean and sustainable energy, the rapid development of hydrogen‐based technologies has started to revolutionize the use of earth‐abundant noble‐metal‐free catalysts for the hydrogen evolution reaction (HER). Like the active sites of hydrogenases, the cation sites of pyrite‐type transition‐metal dichalcogenides have been suggested to be active in the HER. Herein, we synthesized electrodes based on a Se‐enriched NiSe 2 nanosheet array and explored the relationship between the anion sites and the improved hydrogen evolution activity through theoretical and experimental studies. The free energy for atomic hydrogen adsorption is much lower on the Se sites (0.13 eV) than on the Ni sites (0.87 eV). Notably, this electrode benefits from remarkable kinetic properties, with a small overpotential of 117 mV at 10 mA cm −2 , a low Tafel slope of 32 mV per decade, and excellent stability. Control experiments showed that the efficient conversion of H + into H 2 is due to the presence of an excess of selenium in the NiSe 2 nanosheet surface.
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