MXene Hybrid Nanosheet of WS2/Ti3C2 for Electrocatalytic Hydrogen Evolution Reaction

被引:4
|
作者
Tekalgne, Mahider Asmare [1 ]
Do, Ha Huu [2 ]
Nguyen, Tuan Van [1 ]
Le, Quyet Van [1 ]
Hong, Sung Hyun [1 ]
Ahn, Sang Hyun [3 ]
Kim, Soo Young [1 ]
机构
[1] Korea Univ, Inst Green Mfg Technol, Dept Mat Sci & Engn, Seoul 02841, South Korea
[2] Nguyen Tat Thanh Univ, NTT Hitech Inst, VKTech Res Ctr, Ho Chi Minh City 700000, Vietnam
[3] Chung Ang Univ, Sch Chem Engn & Mat Sci, Seoul 06974, South Korea
来源
ACS OMEGA | 2023年 / 8卷 / 44期
基金
新加坡国家研究基金会;
关键词
EFFICIENT ELECTROCATALYST; HIGH-PERFORMANCE; HETEROSTRUCTURE; EXFOLIATION; CATALYSTS; COBALT;
D O I
10.1021/acsomega.3c06403
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Designing low-cost hybrid electrocatalysts for hydrogen production is of significant importance. Recently, MXene-based materials are being increasingly employed in energy storage devices owing to their layered structure and high electrical conductivity. In this study, we propose a facile hydrothermal strategy for producing WS2/Ti3C2 nanosheets that function as electrocatalysts in the hydrogen evolution reaction (HER). WS2 provides a high surface area and active sites for electrocatalytic activity, whereas MXene Ti3C2 facilitates charge transfer. As a result, the synthesized WS2/Ti3C2 offers an increased surface area and exhibits an enhanced electrocatalytic activity in acidic media. The WS2/Ti3C2 (10%) catalyst exhibited a low onset potential of -150 mV versus RHE for the HER and a low Tafel slope of similar to 62 mV dec(-1). Moreover, WS2/Ti3C2 (10%) exhibited a double-layer capacitance of 1.2 mF/cm(-2), which is 3 and 6 times greater than those of bare WS2 and Ti3C2, respectively. This catalyst also maintained a steady catalytic activity for the HER for over 1000 cycles.
引用
收藏
页码:41802 / 41808
页数:7
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