Janus Chromium Dichalcogenide Monolayers with Low Carrier Recombination for Photocatalytic Overall Water-Splitting under Infrared Light

被引:63
作者
Zhao, Pei [1 ]
Liang, Yan [1 ]
Ma, Yandong [1 ]
Huang, Baibiao [1 ]
Dai, Ying [1 ]
机构
[1] Shandong Univ, Sch Phys, State Key Lab Crystal Mat, Shandanan Str 27, Jinan 250100, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSITION-METAL DICHALCOGENIDES; NONADIABATIC MOLECULAR-DYNAMICS; HYDROGEN EVOLUTION; OPTICAL-PROPERTIES; PYXAID PROGRAM; BAND-GAP; Z-SCHEME; ENERGY; INSULATORS; MOLYBDENUM;
D O I
10.1021/acs.jpcc.8b11240
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
Photocatalytic overall water-splitting is known as one of most promising methods to alleviate energy crisis. Searching for stable and efficient photocatalysts plays a critical role in this process. Here, we propose a novel class of Janus chromium dichalcogenide (CrXY, X/Y = S, Se, and Te) monolayers serving as efficient photocatalysts for overall water-splitting under infrared light irradiation. We reveal that these Janus monolayers harbor an intrinsic dipole, which promotes the spatial separation of photogenerated carriers. More significantly, these systems exhibit suitable band gaps as well as band edge positions, enabling preeminent infrared optical absorption and high carrier mobility. Furthermore, the nonradiative recombination of photo induced charge carriers in CrXY monolayers is evaluated based on time domain density functional theory. The obtained long-lived excited carriers ns) are even comparable with that in transition-metal dichalcogenide heterostructures, which benefits for the photocatalytic reaction with high efficiency. Our results provide a new guidance for designing brand new photocatalytic systems with broad optical absorption and low carrier recombination.
引用
收藏
页码:4186 / 4192
页数:7
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