磷化物
过电位
制氢
分解水
电解
材料科学
阳极
无机化学
催化作用
析氧
电化学
钴
化学
化学工程
物理化学
光催化
电极
电解质
生物化学
工程类
作者
Wenzhi Yuan,Tengfei Jiang,Xueqing Fang,Yu Fan,Sheng Qian,Yingying Gao,Ningyan Cheng,Huaiguo Xue,Jingqi Tian
标识
DOI:10.1016/j.cej.2022.135743
摘要
Electrochemical hydrogen production is largely limited by the sluggish anodic oxygen evolution reaction (OER). Urea-assisted energy-saving alkaline hydrogen production has been promising alternative pathway. Herein, we demonstrate an ion-exchange strategy to fabricate cobalt phosphide nanowire decorated with nickel phosphide nanosheets [email protected] heterostructured arrays with sulfur doping at the interface (S-Co2[email protected]2P) for both hydrogen evolution reaction (HER) and urea oxidation reaction (UOR). Interfacial S-doping induces charge transfer from S-Co2P to Ni2P in the heterostructure, generating electron-rich Ni centers and electron-deficient Co centers to be active sites for HER and UOR, respectively, with optimized absorption/desorption energies of reactants/products to accelerate the catalytic kinetics of HER and UOR. As a result, S-Co2[email protected]2P requires an overpotential of 103 mV and potential of 1.36 V (vs. RHE) to achieve 100 mA cm−2 for HER and UOR, respectively, and drives the full urea electrolysis at 1.43 V to deliver current density of 10 mA cm−2.
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