Heterogeneous CoS2/MS2 microspheres for an efficient oxygen evolution reaction

被引:4
|
作者
Wang, Xiaoqu [1 ,4 ]
Wang, Limin [1 ]
Rani, Karuppasamy Kohila [2 ,3 ]
Peng, Xinglan [1 ]
Ning, Yu [1 ]
Liu, Xiaotian [1 ]
Fan, Youjun [1 ]
Chen, Du-Hong [1 ]
Chen, Wei [1 ]
机构
[1] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, Guangxi Key Lab Low Carbon Energy Mat, Guilin 541004, Peoples R China
[2] Nanjing Tech Univ NanjingTech, Key Lab Flexible Elect KLOFE, Nanjing 211816, Peoples R China
[3] Nanjing Tech Univ NanjingTech, Inst Adv Mat IAM, Nanjing 211816, Peoples R China
[4] Yunnan Univ, Inst Energy Storage Technol, Sch Mat & Energy, Kunming 650091, Peoples R China
基金
中国国家自然科学基金;
关键词
TOTAL-ENERGY CALCULATIONS; DEEP EUTECTIC SOLVENT; COBALT SULFIDE; ELECTROCATALYSTS; SHELL; CONVERSION; GRAPHENE; DERIVATIVES; ARRAYS; ZIF-8;
D O I
10.1039/d3qi01878d
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Delicately fabricating efficient electro-catalysts to boost the catalytic kinetics of the oxygen evolution reaction (OER) is essential for realizing the efficient performance of water splitting into hydrogen to alleviate environmental issues and the energy crisis. Here, heterogeneous and hollow microspheres (denoted as CoS2/MS2-HPMS, M = Fe, FeCo) were obtained by the sulfurization of Fe3+-decorated ZIF-67 hollow microspheres (ZIF-67-HMS). At a current density of 10 mA cm(-2), the prepared CoS2/MS2-HPMS showed an overpotential of 217 mV for the OER, which is lower than that of commercial RuO2 (336 mV). Density functional theory calculations demonstrated low reaction free energies of the intermediates of the OER and significant charge accumulation at the heterojunction interface between CoS2 and FeCoS2. This work establishes a method for the assembly of nanoparticles and the construction of heterojunctions.
引用
收藏
页码:98 / 106
页数:9
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