Interfacial engineering of heterostructured carbon-supported molybdenum cobalt sulfides for efficient overall water splitting

被引:0
|
作者
Ming-Yue Ma [1 ]
Han-Zhi Yu [1 ]
Li-Ming Deng [1 ]
Lu-Qi Wang [1 ]
Shu-Yi Liu [1 ]
Hui Pan [2 ]
Jian-Wei Ren [3 ]
Maxim Yu.Maximov [4 ]
Feng Hu [1 ]
Sheng-Jie Peng [1 ]
机构
[1] College of Materials Science and Technology ,Nanjing University of Aeronautics and Astronautics
[2] Institute of Applied Physics and Materials Engineering ,University of Macau
[3] Department of Mechanical Engineering Science ,University of Johannesburg
[4] Peter the Great Saint-Petersburg Polytechnic University
基金
中央高校基本科研业务费专项资金资助; 中国博士后科学基金; 中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
TQ116.2 [氢气]; TQ426 [催化剂(触媒)];
学科分类号
080502 ; 0817 ; 081705 ;
摘要
Constructing hetero-structured catalyst is promising but still challenging to achieve overall water splitting for hydrogen production with high efficiency.Herein,we developed a sulfide-based MoS2/Col-xS@C hetero-structure for highly efficient electrochemical hydrogen evolution reaction(HER) and oxygen evolution reaction(OER).The carbon derived from the filter paper acts as a conducting carrier to ensure adequate exposure of the active sites guaranteed with improved catalytic stability.The unique hierarchical nano-sheets facilitate the charge and ion transfer by shortening the diffusion path during electro-catalysis.Meanwhile,the robust hetero-interfaces in MoS2/Co1-xS@C can expose rich electrochemical active sites and facilitate the charge transfer,which further cooperates synergistically toward electro-catalytic reactions.Consequently,the optimal MoS2/Co1-xS@C hetero-structures present small over-potentials toward HER(135 mV@10 mA·cm-2) and OER(230 mV@10 mA·cm-2).The MoS2/Co1-xS@C electrolyzer requires an ultralow voltage of 1.6 V at the current density of 10 mA·cm-2with excellent durability,outperforming the state-of-the-art electro-catalysts.This work sheds light on the design of the hetero-structured catalysts with interfacial engineering toward large-scale water splitting.
引用
收藏
页码:589 / 597
页数:9
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