h2D-C2N/C3B Two-Dimensional Heterostructures: A Direct Z-Scheme Photocatalyst for Overall Water Splitting

被引:1
|
作者
Ding, Chang-Chun [1 ]
Sun, Yu-Jie [1 ]
Liu, Tong [1 ]
Li, Hui-Dong [1 ]
Fan, Qun-Chao [1 ]
机构
[1] Xihua Univ, Sch Sci, Key Lab High Performance Sci Computat, Chengdu 610039, Peoples R China
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2024年 / 128卷 / 08期
关键词
TOTAL-ENERGY CALCULATIONS; CHARGE SEPARATION; BAND ALIGNMENT; SEMICONDUCTORS; EFFICIENCY; HYDROGEN;
D O I
10.1021/acs.jpcc.3c07825
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
A research hotspot in the clean-energy field has been the two-dimensional (2D) heterostructure (HTS)-boosted mechanisms for photocatalytic water splitting. In this work, a direct Z-scheme photocatalyst based on holey 2D C2N (h2D-C2N) and C3B composites is put forward. Through density functional theory (DFT), the band structures, partial charge density, and optical properties of h2D-C2N/C3B HTSs are explored. The band-edge locations can be effectively adjusted by strain. During the process of photocatalytic water splitting, the charge-transfer path of electrons is determined. The conduction band (CB) of h2D-C2N and the valence band (VB) of C3B maintain their respective oxidation and reduction capabilities. The composite electrons are provided by the CB of C3B, while the composite holes are provided by the VB of h2D-C2N. Based on this, h2D-C2N/C3B HTSs are determined as Z-scheme photocatalysts. Meanwhile, A-B and A-C HTSs, under specific strain, which have close to the ideal potential requirements for the HER and the OER, are predicted. Our findings suggest that h2D-C2N/C3B HTSs are promising candidates for future optoelectronic and nanoelectronic applications, which also provide a precious reference for future experimental investigations.
引用
收藏
页码:3377 / 3383
页数:7
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