Supramolecular Macrocycle Regulated Single-Atom MoS2@Co Catalysts for Enhanced Oxygen Evolution Reaction

被引:5
|
作者
Cao, Shuai [1 ]
Wu, Wenzhuo [2 ]
Liu, Chaozhong [2 ]
Song, Leqian [1 ]
Xu, Qun [2 ,3 ]
Zhang, Huacheng [1 ,4 ]
Zhao, Yanli [4 ]
机构
[1] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, Xian 710049, Peoples R China
[2] Zhengzhou Univ, Henan Inst Adv Technol, Zhengzhou 450052, Peoples R China
[3] Zhengzhou Univ, Dept Mat Sci & Engn, Zhengzhou 450001, Peoples R China
[4] Nanyang Technol Univ, Sch Chem Chem Engn & Biotechnol, 21 Nanyang Link, Singapore 637371, Singapore
关键词
electrocatalysis; oxygen evolution reaction; pillar[4]arene[1]quinone; single atoms; transition-metal dichalcogenides; ELECTROCATALYSTS; MOS2; HYDROXIDE; MECHANISM; NANOCUBES; PHASE; STATE; OER;
D O I
10.1002/eem2.12702
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The development of active water oxidation catalysts for water splitting has stimulated considerable interest. Herein, the design and building of single atom Co sites using a supramolecular tailoring strategy are reported, that is, the introduction of pillar[4]arene[1]quinone (P4A1Q) permits mononuclear Co species stereoelectronically assembled on MoS2 matrix to construct an atomically dispersed MoS2@Co catalyst with modulated local electronic structure, definite chemical environment and enhanced oxygen evolution reaction performance. Theoretical calculations indicate that immsobilized single-Co sites exhibit an optimized adsorption capability of oxygen-containing intermediates, endowing the catalyst an excellent electrocatalytic oxygen evolution reaction activity, with a low overpotential of 370 mV at 10 mA cm(-2) and a small Tafel slope of 90 mV dec(-1). The extendable potential of this strategy to other electrocatalysts such as MoS2@Ni and MoS2@Zn, and other applications such as the hydrogen evolution reaction was also demonstrated. This study affords new insights into the rational design of single metal atom systems with enhanced electrocatalytic performance.
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页数:9
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