过电位
析氧
镍
氢氧化物
电子转移
催化作用
碳纳米管
材料科学
化学工程
氧化还原
纳米技术
无机化学
化学
光化学
电化学
冶金
物理化学
电极
工程类
生物化学
作者
Yi Wang,Zheng Yan-tao,Jinhao Xie,Minchang Lv,Jun Luo,Fan Yang,Yanxia Yu,Xihong Lu
标识
DOI:10.1016/j.cej.2022.139369
摘要
The practical potential of nickel hydroxide for oxygen evolution reaction (OER) is hindered by its low electron transport efficiency and weak coupling between hydroxyl groups and active sites. Here, we introduce iron into the nickel hydroxide to effectively adjust the local coordination environment and electron structure. This conception is realized by a facile surface-redox-etching method to grow Fe-decorated nickel hydroxide nanoparticles on the three-dimensional (3D) carbon nanotube networks (Fe-Ni(OH)2/CNT). It is surprising that the Fe-Ni(OH)2/CNT catalyst displays extraordinary OER performance with a low overpotential of 63 mV and 228 mV at 10 mA cm−2 and 100 mA cm−2, respectively, outstripping most OER electrocatalysts. The superior OER performance is ascribed to the 3D CNT networks and synergistic interaction between Ni and Fe in the lattice, which not only accelerate electron transfer but also induce strong electron coupling with OH*, boosting the reaction kinetics of OER.
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