Synergistic effect between Ru cluster and Co3O4 nanowires assisted by B-O bonding for hydrogen evolution

被引:6
|
作者
Liu, Bin [1 ]
Wang, Feng-Ge [1 ]
Liu, Xin [1 ]
Luan, Ren-Ni [1 ]
Li, Wen-Jing [1 ]
Xu, Na [1 ]
Zhang, Zhi-Jie [1 ]
Chai, Yong-Ming [1 ]
Dong, Bin [1 ]
机构
[1] China Univ Petr East China, Coll Chem & Chem Engn, State Key Lab Heavy Oil Proc, Qingdao 266580, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-support interaction; Ru nanoclusters; Electronic structure; B -O bond; Hydrogen evolution reaction; EFFICIENT; ELECTROCATALYSTS; PH; CATALYST;
D O I
10.1016/j.jallcom.2023.169826
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Anchoring noble metal nanoclusters (NCs) on appropriate supports through structural engineering is an effective strategy for reducing the noble metal loading and improving catalytic activity for alkali hydrogen evolution reaction (HER). Generally, the local coordination environment of the active sites is key factor to regulate the interaction between the metal atoms and support. Here, a simple boronation method is proposed for preparing ruthenium nanoclusters anchored on B-doped Co3O4 nanowires supported on Ni foam (denoted as Ru/B-Co3O4) for alkaline HER. B embedded into Co3O4 nanoarrays through B-O bonding can change the electronic structure between Ru active sites and Co3O4. After optimizing electronic structure of Ru and Co sites, Ru/B-Co3O4 showed remarkable activity for HER, with current density of 100 and 500 mA cm-2 at overpotential of 143 and 233 mV, respectively. The experimental and theoretical studies display that the embedding of B into Co3O4 effectively induces the electron transfer from Co to Ru atoms by bridging O atom, leading to the formation of electron-deficient Co sites. The charge redistribution of Ru accelerates the cleavage of H-OH, which optimizes H* adsorption energy and finally promotes HER. This study provides further insight into the regulation of metal-support interaction for HER electrocatalysts.(c) 2023 Published by Elsevier B.V.
引用
收藏
页数:8
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