Nanostructure and stoichiometry tailoring of CoS2 for high performance hydrogen evolution reaction

被引:9
|
作者
Hu, Yingfei [1 ,2 ]
Qi, Yujia [1 ]
Pi, Mingyu [2 ,3 ]
Qiao, Yi [2 ,3 ]
Hao, Lingyun [1 ]
Wang, Yuanyuan [1 ]
Guan, Hangmin [1 ]
Feng, Jianyong [2 ,3 ]
机构
[1] Jinling Inst Technol, Sch Mat Engn, Nanjing 211169, Peoples R China
[2] Nanjing Univ, Collaborat Innovat Ctr Adv Microstruct, Sch Phys, Natl Lab Solid State Microstruct, Nanjing 210093, Peoples R China
[3] Nanjing Univ, Coll Engn & Appl Sci, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
CoS2; Transition metal dichalcogenides; Electrocatalysis; Hydrogen evolution reaction; EFFICIENT; NANOSHEETS; CATALYSTS; ARRAY; FOAM;
D O I
10.1016/j.ijhydene.2023.01.127
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
Developing efficient and low-cost electrocatalysts for hydrogen evolution reaction (HER) is important for hydrogen fuel production. In this study, we synthesized two different types of CoS2 under low sulfur (LS) and high sulfur concentration (HS) conditions. Structural analysis results show that CoS impurity phase forms easily when the concentration of sulfur is low, while at high sulfur concentration the growth of CoS impurity phase is inhibited and leads to phase-pure CoS2. Electrochemical investigation of HER performance reveals that the onset potential of CoS2 (HS) electrode (ca. -0.11 V vs. the reversible hydrogen electrode, RHE) is 30 mV anodic of the CoS2 (LS) one (ca. -0.14 V vs. RHE). At a specific current density of 10 mA cm-2 the required overpotential on CoS2 (HS) electrode is only 163 mV, which is 40 mV less than the CoS2 (LS) electrode. Electrochemical impedance spectroscopy (EIS) data further demonstrate that the charge transfer rate of CoS2 (HS) electrode is faster than that of CoS2 (LS) electrode towards HER.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:16279 / 16285
页数:7
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