退火(玻璃)
材料科学
超亲水性
过电位
催化作用
化学工程
电化学
电催化剂
多孔性
电解质
纳米技术
原位
氢气储存
电极
化学
复合材料
物理化学
有机化学
润湿
工程类
合金
作者
Xibang Chen,Lang Sheng,Shuangxiao Li,Yu Cui,Tingrui Lin,Xueyan Que,Zhonghe Du,Zeyu Zhang,Jing Peng,Hui-Ling Ma,Jiuqiang Li,Jingyi Qiu,Maolin Zhai
标识
DOI:10.1016/j.cej.2021.131029
摘要
Transition metal phosphides (TMPs) have drawn considerable attention as a result of their high catalytic activities for the hydrogen evolution reaction (HER). In this work, a three-dimensional (3D) porous CoxP ordered nanoarray structure was successfully deposited on nickel foam (denoted as [email protected]xP, 1 ≦ x ≦ 2) via a strategy involving facile gamma ray irradiation and annealing without the use of reducing agent. By modulating the annealing temperature in the synthetic process for [email protected]xP, 3D porous ordered nanoarray composites exhibiting inherently superhydrophilic and superaerophobic properties were produced, the physical properties were confirmed with the use of various in-situ test techniques. The superhydrophilic properties of [email protected]xP help to increase the rate of ion transfer between the CoxP and the electrolyte. Additionally, in-situ verification of the superaerophobic properties showed that they are beneficial for quick release of the generated H2 bubbles from the surface of [email protected]xP electrode, which was analyzed by coupling a 3D confocal microscope with an electrochemical workstation for the first time. As expected, when the resulting [email protected]xP composites were employed as catalyst electrodes for the HER in a 1 M KOH electrolyte, the 3D porous ordered nanoarray structure exhibited an overpotential of 272 mV at the current density of 200 mA cm−2, which was much higher than those of commercial 20%Pt/C catalysts. Therefore, the synthetic strategy for producing [email protected]xP composites with 3D porous ordered nanoarray structures showed high potential for application in the HER.
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