期刊
JOURNAL OF ALLOYS AND COMPOUNDS
卷 893, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2021.162289
关键词
BiOBr; (001)-TiO2; Ti3C2Tx; 2D/2D/2D; Photocatalytic activity
资金
- Natural Science Basic Research Plan in Shaanxi Province [2020JM-482]
- National Natural Science Foundation of China [62004155]
- Independent Research and Development project of State Key Laboratory of Green Building in Western China [LSZZ202117, LSZZ202118]
- State Key Laboratory of Advanced Refractories [SKLAR202107, SKLAR202004]
Coupling a semiconductor with exposed high-activity crystal facets and a suitable co-catalyst to form a heterojunction is an effective way to enhance photocatalytic activity. The novel BiOBr/(001)-TiO2/Ti3C2Tx (BTT-y) shows remarkable Rhodamine B (RhB) degradation performance due to better synergy among the three substances. The improvement of RhB degradation performance is mainly attributed to the perfect matching of BiOBr and (001)-TiO2 band structure positions, which promotes the formation of heterojunction, extends visible-light absorption range, and inhibits carrier recombination.
Coupling a semiconductor with exposed high-activity crystal facets and a suitable co-catalyst to form a heterojunction is considered to be a feasible measure to improve photocatalytic activity. Therefore, the novel BiOBr/(001)-TiO2/Ti3C2Tx (BTT-y) were synthesized by in-situ construction. The BTT-y possess a remarkable Rhodamine B (RhB) degradation performance due to there is a better synergy among the three substances. The improvement of RhB degradation performance is mainly attributed to the perfect matching of BiOBr and (001)-TiO2 band structure positions, which is conductive to the formation of heterojunction and thus could expand visible-light absorption range and inhibit the recombination of photo-generated carriers. Furthermore, Ti3C2Tx in the heterojunction would further separate the photo-generated carriers. This study provided reference insights for improving photocatalytic performance with 2D/2D/2D structure. (C) 2021 Elsevier B.V. All rights reserved.
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