Dynamic hydrogen bubble template electrodeposition of Ru on amorphous Co support for electrochemical hydrogen evolution

过电位 无定形固体 电催化剂 电化学 材料科学 化学工程 离解(化学) 吸附 催化作用 无机化学 纳米技术 化学 电极 物理化学 冶金 结晶学 有机化学 工程类
作者
Hongwei� Jiang,Ning Cong,Hucheng Jiang,Miaojie Tian,Zhiqiang Xie,Hua Fang,Juanjuan Han,Zhandong Ren,Yuchan Zhu
出处
期刊:International Journal of Hydrogen Energy [Elsevier BV]
卷期号:48 (57): 21599-21609 被引量:19
标识
DOI:10.1016/j.ijhydene.2023.03.077
摘要

Electrolyzing water is an environmentally friendly and renewable way to obtain high purity hydrogen. Ruthenium has strong water dissociation ability and suitable hydrogen adsorption energy, so it is considered as one of the candidates of excellent electrocatalysts for hydrogen evolution in alkaline solution. The dynamic hydrogen bubble template (DHBT) is a good electrodeposition technology, which can obtain the 3D metal foams. However, as far as we know, there is no report on the preparation of Ru electrocatalyst by the DBHT method. In this work, the trumpet-shaped Ru on amorphous cobalt support (T-Ru/a-Co) is prepared by the DHBT electrodeposition for the first time. The defect locations are uniformly distributed on the surface of amorphous cobalt (a-Co), which can effectively lead to the formation of nano-bubble template in the DHBT process. However, this special morphology cannot be obtained on the surface of crystalline Co (c-Co). In addition, the electronic structure of T-Ru/a-Co has also been obviously modified, in which the proportion of Ru4+/Ru0 in T-Ru/a-Co has increased, accompanied by the change of binding energy of Ru. It only needs an overpotential of 49 mV to obtain a current density of 10 mA cm−2 for the T-Ru/a-Co. The specific activity (SA), turnover frequency (TOF) and mass activity (MA) of T-Ru/a-Co are 0.23 mA cm−2, 0.48 s−1 and 0.24 A mg−1, which are both higher than those of Pt/C, the disk-shaped Ru on the c-Co support (D-Ru/c-Co) and Ru/C, respectively.
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