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Quasi zero-dimensional MoS2 quantum dots decorated 2D Ti3C2Tx MXene as advanced electrocatalysts for hydrogen evolution reaction
被引:24
|作者:
Chen, Long
[1
]
Liang, Junmei
[1
,3
]
Zhang, Qicheng
[1
]
Hu, Xuewen
[1
]
Peng, Wenchao
[1
,2
]
Li, Yang
[1
,2
]
Zhang, Fengbao
[1
]
Fan, Xiaobin
[1
,2
]
机构:
[1] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn, State Key Lab Chem Engn, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
[2] Chem & Chem Engn Guangdong Lab, Shantou 515031, Peoples R China
[3] Beijing Inst Metrol, Beijing 100029, Peoples R China
基金:
中国国家自然科学基金;
关键词:
MoS2 quantum dots;
Ti3C2Tx MXene;
High-percentage;
1T-phase;
Hydrogen evolution reaction;
ACTIVE EDGE SITES;
TITANIUM CARBIDE;
NANOSHEETS;
EFFICIENT;
ALKALINE;
HETEROSTRUCTURES;
PERFORMANCE;
GRAPHENE;
CATALYST;
CARBON;
D O I:
10.1016/j.ijhydene.2021.12.185
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 advanced noble-metal-free electrocatalysts for the hydrogen evolution reaction (HER) is still a great challenge. Herein, a novel HER catalyst with quasi zero-dimensional (0D) MoS2 quantum dots (QDs) supported on two-dimensional (2D) Ti3C2Tx MXene nanosheets is facilely synthesized. The MoS2 QDs/Ti3C2Tx nanohybrid retains the unique layer structure, and the MoS2 QDs are in situ formed and distributed uniformly. The obtained MoS2 QDs/Ti3C2Tx catalyst exhibits superior electrocatalytic activity due to its excellent conductivity, abundant of active sites exposed and a high percentage of 1T metallic phase (~76%) of MoS2 QDs. Remarkably, an early HER overpotential of 220 mV at 10 mA cm(-2) and a small Tafel slope of 72 mV dec(-1) of MoS2 QDs/Ti3C2Tx are achieved in 0.5 M H2SO4 solution. In addition, the exchange current density of MoS2 QDs/Ti3C2Tx is ~5 times larger compared with pure MoS2, thus demonstrating an accelerated charge transfer during the electrocatalytic process. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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页码:10583 / 10593
页数:11
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