Synergistic effect of adsorption and photocatalysis of BiOBr/lignin-biochar composites with oxygen vacancies under visible light irradiation

生物炭 光催化 木质素 吸附 可见光谱 材料科学 氧气 光化学 化学工程 带隙 吸光度 辐照 化学 热解 催化作用 有机化学 物理 工程类 核物理学 光电子学 色谱法
作者
Qiang Yang,Xiang Li,Qingwen Tian,Aixiang Pan,Xingjian Liu,Hang Yin,Yingqiao Shi,Guigan Fang
出处
期刊:Journal of Industrial and Engineering Chemistry [Elsevier BV]
卷期号:117: 117-129 被引量:58
标识
DOI:10.1016/j.jiec.2022.09.044
摘要

Effective utilization solar energy through photocatalysis is an ideal way to solve environmental problems and achieve sustainable development. Herein, a novel BiOBr/Lignin-Biochar photocatalyst has been successfully synthesized by a simple hydrothermal method. The number of oxygen vacancies of BiOBr increased after C doping, which improves visible-light absorbance, reduces the recombination of photo-generated carriers and promotes O2 activation to produce O2−. UV–vis DRS result demonstrated that the visible-light absorption capacity of BiOBr improved significantly with the addition of lignin. Compared with BiOBr, the adsorption and photocatalytic ability of BiOBr/Lignin-Biochar composites were greatly enhanced due to enriched oxygen vacancies and the congenerous effect between BiOBr and lignin-biochar. The RhB removal with pure BiOBr and BiOBr/Lignin-Biochar under visible-light irradiation at 60 min was 54.5% and 99.2%, respectively, owing to the interface interaction between BiOBr and lignin-biochar promoted the separation between electron and holes and the enrichment of RhB around the photocatalysts. Notably, the bandgap of BiOBr/Lignin-Biochar composites decreased from 2.65 eV to 2.56 eV after C doping, useful for visible-light-driven photocatalysis. The superoxide radical anions (O2−) were the main active species, as demonstrated by free radical capture experiments and ESR characterization results. Hence, the present work provides new insights into constructing cost-effective, high-efficiency composite materials for environmental remediation.
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