Constructing Heterogeneous Interface by Growth of Carbon Nanotubes on the Surface of MoB2 for Boosting Hydrogen Evolution Reaction in a Wide pH Range

被引:21
|
作者
Sun, Jianhang [1 ]
Guo, Feifan [1 ]
Ai, Xuan [2 ]
Tian, Yuyang [1 ]
Yang, Jin [1 ]
Zou, Xiaoxin [3 ]
Zhu, Guangshan [1 ]
机构
[1] Northeast Normal Univ, Fac Chem, Key Lab Polyoxometalate & Reticular Mat Chem, Minist Educ, Changchun 130024, Peoples R China
[2] Shaanxi Normal Univ, Sch Mat Sci & Engn, Xian 710062, Peoples R China
[3] Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
carbon nanotubes; heterogeneous interface engineering; hydrogen evolution reaction; metal boride; wide pH range; HETEROSTRUCTURES; CATALYSTS; EFFICIENT;
D O I
10.1002/smll.202304573
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition metal diborides represented by MoB2 have attracted widespread attention for their excellent acidic hydrogen evolution reaction (HER). Nevertheless, their electrocatalytic performance is generally unsatisfactory in high-pH electrolytes. Heterogeneous interface engineering is one of the most promising methods for optimizing the composition and structure of electrocatalysts, thereby greatly affecting their electrochemical performance. Herein, a heterostructure, composed of MoB2 and carbon nanotubes (CNTs), is rationally constructed by boronizing precursors including (NH4)(4)[NiH6Mo6O24]center dot 5H(2)O (NiMo6) and Co complexes on the carbon cloth (Co,Ni-MoB2@CNT/CC). In this method, NiMo6 is boronized to form MoB2 by a modified molten-salt-assisted borothermal reduction. Meanwhile, Co catalyzes extra carbon sources to grow CNTs on the surface of MoB2. Thanks to the successful production of the heterostructure, Co,Ni-MoB2@CNT/CC exhibits remarkable HER performance with a low overpotential of 98.6, 113.0, and 73.9 mV at 10 mA cm(-2) in acidic, neutral, and alkaline electrolytes, respectively. Notably, even at 500 mA cm(-2), the electrochemical activity of Co,Ni-MoB2@CNT/CC exceeds that of Pt/C/CC in an alkaline solution and maintains over 50 h. Theoretical calculations reveal that the construction of the heterostructure is beneficial to both water dissociation and reactive intermediate adsorption, resulting in superior alkaline HER performance.
引用
收藏
页数:11
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