材料科学
过电位
夹
纳米片
析氧
分解水
塔菲尔方程
电催化剂
化学工程
磷化物
钴
成核
电化学
氢氧化物
纳米技术
催化作用
电极
金属
光催化
物理化学
复合材料
工程类
有机化学
化学
冶金
作者
Mingxing Chen,Huijie Li,Cailing Wu,Yubo Liang,Jing Qi,Jing Li,Enbo Shangguan,Wei Zhang,Rui Cao
标识
DOI:10.1002/adfm.202206407
摘要
Abstract The oxygen evolution reaction (OER) remains a bottleneck for the overall water splitting. Electrocatalysts with superior activity and stability are still highly desired. Herein, a stepwise electrochemical strategy is developed to prepare Co(OH) 2 /NiP x nanosheet arrays with intimate and abundant heterostructures. The Co(OH) 2 nanosheets, which are first electrodeposited on a blank carbon cloth electrode, serve as the substrate for the nucleation and growth of NiP x . The resultant heterointerfaces are well regulated by altering the loading of NiP x . The heterostructured Co(OH) 2 /NiP x with optimal NiP x loading demonstrate significantly enhanced conductivity and hydrophilicity, which greatly facilitate electron and mass transfer. In addition, strong electronic interaction between Co(OH) 2 and NiP x is observed, favoring the generation of high‐valence cobalt center, thus the electrocatalytic performances toward OER are remarkably improved. The heterostructured Co(OH) 2 /NiP x nanosheets achieve the current density of 10 mA cm −2 at an overpotential of 236 mV, while the corresponding values for Co(OH) 2 and the benchmark Ir/C are 292 and 262 mV, respectively. This study provides a facile and effective strategy to fabricate transition metal hydroxide/phosphide composite nanomaterials with intimate heterostructures, enhanced conductivity, and improved wettability, which opens a new direction for the design of highly active electrocatalysts.
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