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Strain engineering of type-II C2N/WS2 van der Waals heterojunction for highly enhanced photocatalytic hydrogen evolution
被引:3
|作者:
Li, Quan
[1
]
Pan, Cong
[1
]
Huang, Hao
[1
]
Wang, Ling-Ling
[2
]
Zhu, Xiaojun
[3
]
机构:
[1] Jiangxi Univ Sci & Technol, Sch Energy & Mech Engn, Nanchang 330013, Peoples R China
[2] Hunan Univ, Sch Phys & Elect, Changsha 410082, Peoples R China
[3] Jiangxi Univ Sci & Technol, Sch Software Engn, Nanchang 330013, Peoples R China
关键词:
Van der Waals heterojunctions;
Strain engineering;
Photocatalyst;
Hydrogen evolution reaction First-principles calculations;
ELECTRONIC-STRUCTURES;
OPTICAL-ABSORPTION;
WATER;
HETEROSTRUCTURE;
ENERGY;
GAP;
C2N;
D O I:
10.1016/j.ijhydene.2023.03.158
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:
The first-principles calculations demonstrate that the photocatalytic performance of type II C2N/WS2 van der Waals heterobilayer can be improved to a new and high level by applying weak biaxial strain, with desired band structure, tunable interface charge transfer, superior visible-light absorption, and ideal hydrogen evolution reaction (HER) activity. Tensile strains can largely reduce the energy gap, strengthen the interfacial interactions, and promote the visible-light absorption of C2N/WS2 heterostructure, and even induce a direct band gap of 1.70 eV for overall water splitting at 2% strain. Compressive strains like-2% can upshift the valence band and conduction band positions of the C2N/WS2 bilayer to acquire outstanding redox abilities, and enhance the interface charge transfer and separation by increasing the electrostatic potential drop. More importantly, the cycle between spontaneous H* adsorption and energetically favorable H2 release may be realized by dynamic strains between & PLUSMN;2%, maximizing the HER activities of C2N/WS2 heterostructure. & COPY; 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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页码:26119 / 26132
页数:14
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