Sonochemical Fabrication of s-Scheme Hierarchical CdS/BiOBr Heterojunction Photocatalyst with High Performance for Carbon Dioxide Reduction

被引:10
|
作者
Xiao, Yunxue [1 ]
Maimaitizi, Hujiabudula [1 ]
Okitsu, Kenji [2 ]
Tursun, Yalkunjan [1 ]
Abulizi, Abulikemu [1 ]
机构
[1] Xinjiang Univ Urumqi, Coll Chem Engn, Xinjiang Key Lab Coal Clean Convers & Chem Engn, Urumqi 830017, Peoples R China
[2] Osaka Prefecture Univ, Grad Sch Humanities & Sustainable Syst Sci, Osaka 5998531, Japan
基金
美国国家科学基金会;
关键词
BiOBr microspheres; CdS; CO; (2) reduction; hydrolysis-ultrasonic method; photocatalysis; s-scheme heterostructures; CO2; REDUCTION; HOLLOW MICROSPHERES; CDS NANOPARTICLES; BIOBR NANOSHEETS; OXYGEN VACANCIES; HETEROSTRUCTURE; COMPOSITE; CERIA; TIO2;
D O I
10.1002/ppsc.202200019
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
CO2 conversion to methanol becomes a promising strategy by using semiconductor-based photocatalyst for environmental remediation and converting solar energy. In this study, a series of CdS-modified BiOBr (CdS/BiOBr) microspheres are fabricated by mild hydrolysis-ultrasonic method and the effect of CdS growing on the photocatalytic CO2 reduction activities of BiOBr are systematically investigated. Among all CdS/BiOBr composite photocatalysis, the highest value of CH3OH yields (876 mu mol g(cat)(-1), 4 h) is achieved with 15% CdS/BiOBr, which is nearly double higher than alone BiOBr (435 mu mol g(cat)(-1)). Comparatively, the CdS/BiOBr microspheres with s-scheme heterostructure exhibit the surprising photocatalytic performance and CH3OH selectivity, which are attributed to the enhanced light absorption, as well as effective separation and migration of the photoinduced electron-hole pairs induced by the s-scheme heterojunction between BiOBr and CdS. This study provides a mild hydrolysis-ultrasonic method for environmental remediation and converting energy using cost-effective semiconductor materials.
引用
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页数:9
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