纳米片
电催化剂
过电位
材料科学
介孔材料
硒化物
镍
钴
催化作用
化学工程
硫化钴
二硒醚
分解水
无机化学
纳米技术
物理化学
电化学
化学
电极
冶金
有机化学
工程类
光催化
硒
作者
Bin Liu,Yufei Zhao,Hui‐Qing Peng,Zhenyu Zhang,Chun Kit Sit,Muk‐Fung Yuen,Tierui Zhang,Chun‐Sing Lee,Wenjun Zhang
标识
DOI:10.1002/adma.201606521
摘要
Novel 3D Ni 1− x Co x Se 2 mesoporous nanosheet networks with tunable stoichiometry are successfully synthesized on Ni foam (Ni 1− x Co x Se 2 MNSN/NF with x ranging from 0 to 0.35). The collective effects of special morphological design and electronic structure engineering enable the integrated electrocatalyst to have very high activity for hydrogen evolution reaction (HER) and excellent stability in a wide pH range. Ni 0.89 Co 0.11 Se 2 MNSN/NF is revealed to exhibit an overpotential (η 10 ) of 85 mV at −10 mA cm −2 in alkaline medium (pH 14) and η 10 of 52 mV in acidic solution (pH 0), which are the best among all selenide‐based electrocatalysts reported thus far. In particular, it is shown for the first time that the catalyst can work efficiently in neutral solution (pH 7) with a record η 10 of 82 mV for all noble metal‐free electrocatalysts ever reported. Based on theoretical calculations, it is further verified that the advanced all‐pH HER activity of Ni 0.89 Co 0.11 Se 2 is originated from the enhanced adsorption of both H + and H 2 O induced by the substitutional doping of cobalt at an optimal level. It is believed that the present work provides a valuable route for the design and synthesis of inexpensive and efficient all‐pH HER electrocatalysts.
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