MOF-derived synthesis of MnS/In2S3 p-n heterojunctions with hierarchical structures for efficient photocatalytic CO2 reduction

被引:71
作者
Tan, Jun [1 ]
Yu, Mengshi [1 ]
Cai, Zhenzhi [1 ]
Lou, Xiaodan [1 ]
Wang, Jin [1 ]
Li, Zhengquan [1 ]
机构
[1] Zhejiang Normal Univ, Minist Educ Adv Catalysis Mat, Key Lab, Jinhua 321004, Zhejiang, Peoples R China
关键词
Photocatalysts; Metal-organic frameworks; P-n heterojunction; CO2; photoreduction; METAL-ORGANIC FRAMEWORK; HYDROGEN EVOLUTION; CARBON NITRIDE; COMPOSITE; SEMICONDUCTOR; DESIGN; FABRICATION; CONVERSION; JUNCTION; TIO2;
D O I
10.1016/j.jcis.2020.12.110
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
Photoreduction of CO2 to valuable fuels with semiconductor photocatalysts is a good solution to the problems of global warming and energy crisis. Creation of hybrid nanomaterials with hierarchical and/or heterojunction structures is beneficial to develop efficient photocatalysts for CO2 reduction. Herein we present a convenient method to obtain a hybrid photocatalyst consisting of MnS and In2S3 nanosheets with assembled hierarchical structures through using Mn2+-Ioaded MIL-68(In) submicro-rods as templates. Owing to the dispersive Mn2+ and In3+ ions in templates, numerous small p-n heterojunctions of MnS/In2S3 could be simultaneously produced in each hierarchical particle. The p-type MnS and ntype In2S3 with an original type II band alignment can create a stronger built-in electric field after the formation of p-n heterojunctions, which is favorable for charge separation and migration to catalyst surface. The prepared MnS/In2S3 heterojunctions show an 4-fold higher photocatalytic activity toward CO2 reduction than pristine MnS and In2S3. The MnS/In2S3 hierarchical structures were well characterized and their working mechanism was explored. This work demonstrates a facile strategy to create efficient hybrid photocatalysts with both hierarchical structures and p-n heterojunctions for photocatalytic applications. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页码:547 / 556
页数:10
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