磷化物
过电位
硫化镍
硫化物
镍
析氧
无定形固体
材料科学
化学工程
分解水
吸附
水溶液
冶金
无机化学
化学
催化作用
电化学
电极
物理化学
有机化学
工程类
光催化
作者
Chao Wang,Yili Wu,Zixiang Zhou,Jinlian Wang,Shaotong Pei,Shuling Liu
标识
DOI:10.1016/j.ijhydene.2022.09.200
摘要
The preparation of inexpensive and efficient electrocatalysts for oxygen evolution reaction (OER) is crucial in the widespread application of water electrolyzers. A simple one-step aqueous electrodeposition method is utilized to prepare amorphous nickel-iron sulfide (Ni–Fe–S) and phosphide (Ni–Fe–P) films on Ni foam. The deposited films are highly porous, and can convert to active electrocatalysts for OER. In 1 M KOH, the Ni–Fe–S shows the highest OER activity, and requires only 230 mV overpotential to reach 0.05 A cm−2 OER current densities. The Fe–Ni–S also sustains the 30 h 0.05 A cm−2 galvanostatic OER test. Ex-situ characterizations show that sulfur in the Fe–Ni–S is oxidized and leached into the solution during OER, and that (oxy)hydroxide layer is formed at the surface. The adsorption energy of the hydroxyl group, an OER intermediate, is tuned by the electron interaction between the Ni and Fe, and the Ni–Fe–S exhibits the optimum hydroxyl group adsorption energy and the most facile OER kinetics. Also, higher intrinsic OER activity is observed for the electrodeposited amorphous nickel phosphide-derived film than the amorphous nickel sulfide-derived film.
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