A tube-like dual Z-scheme indium oxide@indium phosphide/cuprous oxide photocatalyst based on metal-organic framework for efficient CO2 reduction with water

被引:28
|
作者
Wang, Yi [1 ,2 ]
Xu, Jixiang [1 ,3 ]
Wan, Jun [1 ,2 ]
Wang, Jing [3 ]
Wang, Lei [1 ,2 ,3 ]
机构
[1] Qingdao Univ Sci & Technol, Key Lab Ecochem Engn, Taishan Scholar Advantage & Characterist Disciplin, Qingdao 266042, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Environm & Safety Engn, Qingdao 266042, Shandong, Peoples R China
[3] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
Photocatalytic CO2 reduction; tube In2O3; Phosphidation; Cu2O; dual Z-scheme; GRAPHITIC CARBON NITRIDE; HYDROGEN EVOLUTION; OXIDATION; PHOTOREDUCTION; CATALYST;
D O I
10.1016/j.jcis.2022.02.101
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
Developing a photocatalyst for efficient reduction of carbon dioxide (CO2) is a long-term goal to address global climate change. In this work, a tube-like indium oxide@indium phosphide/cuprous oxide (In2O3@InP/Cu2O) photocatalyst was prepared by annealing-phosphidation of In-Materials of Institute Lavoisier-68 (In-MIL-68) followed by electrodeposition of Cu2O, which was used to reduce CO2 with water under light irradiation. Partial phosphidation of In2O3 endowed In2O3@InP/Cu2O with strong light-harvesting ability. The In2O3@InP heterojunction combined with in situ loaded Cu2O provided a dual Z-scheme heterojunction for efficient electrons-holes separation. Under the synergisms of each component, the optimized In2O3@InP60/Cu2O-1 exhibited strong adsorption of CO2 and excellent photocatalytic performance in CO2 reduction. The yields of CO and CH4 were 13.7 and 38.8 mu mol g1, respectively, after 5 h simulated light illumination, higher than the corresponding yields with In2O3 (CO: 7.2 mu mol g1, CH4: 13.2 mu mol g1). This study may provide some insights into the design of specific ternary photocatalysts with dual Z-scheme charge transfer mode for CO2 reduction. (c) 2022 Elsevier Inc. All rights reserved.
引用
收藏
页码:532 / 539
页数:8
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