Direct Z-scheme GaSe/ZrS2 heterojunction for overall water splitting

被引:47
作者
Ge, Chuanpeng [1 ]
Wang, Biyi [2 ]
Yang, Hongdong [3 ]
Feng, Qingyi [1 ]
Huang, Sizhao [1 ]
Zu, Xiaotao [1 ]
Li, Li [1 ]
Deng, Hongxiang [1 ]
机构
[1] Univ Elect Sci & Technol China, Sch Phys, 2006 XiYuan Ave, Chengdu 611731, Peoples R China
[2] Sci & Technol Electroopt Informat Secur Control La, Tianjin 300308, Peoples R China
[3] Shanghai Inst Space Power Sources, 2965 Dongchuan Rd, Shanghai 200245, Peoples R China
基金
中国国家自然科学基金;
关键词
Direct Z-scheme heterojunction; Overall water splitting; Photocatalysts; Hydrogen energy; DER-WAALS HETEROSTRUCTURE; LAYER; PHOTOCATALYST; HYDROGEN; PERFORMANCE;
D O I
10.1016/j.ijhydene.2022.12.247
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
In this paper, a novel GaSe/ZrS2 heterojunction is designed and systematically studied. The monolayers in this heterojunction can be easily fabricated and the heterojunction has good density and the built-in electric field show that it is a direct Z-scheme photocatalyst that can not only effectively separate photogenerated carriers but also improve the redox ability of carriers. The mobility of the electrons in this heterostructure is as large as 1450.38 cm2V-1s-1 (same magnitude order of black phosphorene) along the zigzag direction, which is beneficial to photocatalytic performance. The band alignment shows that GaSe/ZrS2 is suitable for overall water splitting and the splitting can happen spontaneously. Moreover, GaSe/ZrS2 heterojunction has excellent absorption coefficients (higher than 105cm-1) in both visible and ultraviolet ranges which is very beneficial to photocatalytic overall water splitting. The study of electric field and biaxial strain effects on GaSe/ZrS2 heterojunction show that the light absorption coefficients of GaSe/ZrS2 heterojunction can be obviously further improved by applying biaxial strain. Our work shows that GaSe/ZrS2 heterojunction is a promising photocatalysts for overall water splitting. (c) 2022 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:13460 / 13469
页数:10
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