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用于光催化的0D/2D石墨烯量子点-二硫化钼混合范德华异质结的第一性原理计算:从I型到II型的转变

First-principles calculations of 0D/2D GQDs-MoS mixed van der Waals heterojunctions for photocatalysis: a transition from type I to type II.

作者信息

Luo Li-Long, Wang Ping-Xia, Geng Xiang-Yan, Liu Ying-Tao, Eglitis Roberts I, Xia Hong-Qiang, Lai Xiao-Yong, Wang Xin

机构信息

State Key Laboratory of High-Efficiency Utilization of Coal and Green Chemical Engineering, National Demonstration Center for Experimental Chemistry Education, College of Chemistry and Chemical Engineering, Ningxia University, Yinchuan 750021, China.

Institute of Solid State Physics, University of Latvia, 8 Kengaraga Str., Riga LV1067, Latvia.

出版信息

Phys Chem Chem Phys. 2022 Apr 6;24(14):8529-8536. doi: 10.1039/d1cp05448a.

Abstract

The fabrication of type II heterojunctions is an efficient strategy to facilitate charge separation in photocatalysis. Here, mixed dimensional 0D/2D van der Waals (vdW) heterostructures (graphene quantum dots (GQDs)-MoS) for generating hydrogen from water splitting are investigated based on density functional theory (DFT). The electronic and photocatalytic properties of three heterostructures, namely, CH-MoS, CH-MoS and CH-MoS are estimated by analyzing the density of states, charge density difference, work function, Bader charge, absorption spectra and band alignment. The results indicated that the built-in electric fields from GQDs to MoS boost charge separation. Meanwhile, all the GQDs-MoS exhibit strong absorption in the visible light region. Surprisingly, the transition of heterojunctions from type I to type II is realized by tuning the size of GQDs. In particular, CH-MoS with enhanced visible-light absorption and an appropriate band edge position, as a type II heterostructure, may be a promising photocatalyst for generating hydrogen from water splitting. Thus, in this work a novel type II 0D/2D nanocomposite as a photocatalyst is constructed that provides a strategy to regulate the type of heterostructure from the perspective of theoretical calculation.

摘要

II型异质结的制备是促进光催化中电荷分离的有效策略。在此,基于密度泛函理论(DFT)研究了用于水分解产氢的混合维度0D/2D范德华(vdW)异质结构(石墨烯量子点(GQDs)-MoS)。通过分析态密度、电荷密度差、功函数、巴德电荷、吸收光谱和能带排列,估算了三种异质结构CH-MoS、CH-MoS和CH-MoS的电子和光催化性能。结果表明,从GQDs到MoS的内建电场促进了电荷分离。同时,所有的GQDs-MoS在可见光区域都表现出强烈的吸收。令人惊讶的是,通过调节GQDs的尺寸实现了异质结从I型到II型的转变。特别地,作为II型异质结构的具有增强可见光吸收和合适带边位置的CH-MoS,可能是一种有前途的用于水分解产氢 的光催化剂。因此,在这项工作中构建了一种新型的II型0D/2D纳米复合材料作为光催化剂,从理论计算的角度提供了一种调节异质结构类型的策略。

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