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Greatly increased visible-light photocatalytic activity of SnS2/carbon nanotube composite for Cr(VI) reduction: Insights into effects of solid acid structure

•p-π bond was successfully fabricated in SnS2/CNT composite by ball-milling method.•p-π bond and persistent radical sites make the composite has a solid acid structure.•Solid acid structure is conducive to the proton-coupled electron transfer reaction.•SnS2/CNT composite shows 800% higher photocatal...

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Bibliographic Details
Published in:Journal of materials science & technology 2023-10, Vol.161, p.233-244
Main Authors: Wan, Zhen, Mao, Qihang, Xiang, Jingjing, Ma, Dongge, Tang, Heqing
Format: Article
Language:English
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Summary:•p-π bond was successfully fabricated in SnS2/CNT composite by ball-milling method.•p-π bond and persistent radical sites make the composite has a solid acid structure.•Solid acid structure is conducive to the proton-coupled electron transfer reaction.•SnS2/CNT composite shows 800% higher photocatalytic activities compared with SnS2.•Structure-activity relationship in Cr(VI) reduction by the composite is proposed. A composite of SnS2 and carbon nanotube (CNT) was successfully synthesized as a visible-light-driven photocatalyst with a mechanochemical method. In comparing with SnS2, the SnS2/CNT composite improved much the photocatalytic removal of Cr(VI) in acidic condition, which was confirmed to its special solid acid structure. During the synthesis of the SnS2/CNT composite by ball milling, S-C p-π bonding was formed between sulfur atoms in SnS2 and carbon atoms in CNT. The generated S-C p-π bonding enhanced the transfer of photo-induced electrons in the bulk phase of the composite photocatalyst under visible light irradiation. Moreover, the persistent radical sites on CNT were able to trap photo-induced electrons and served as conjugated acid sites in the photocatalysis, which increased surface concentration of protons through their association with H+. These made the catalyst have a solid acid structure with plentiful surface protons, promoting the interfacial electron transfer between the catalysts and Cr(VI) and increasing the source of H+ for the reduction of Cr(VI). As a result, the photocatalytic reduction rate of Cr(VI) on the SnS2/CNT composite were dramatically enhanced, being about 800% that on SnS2. On the basis of various characterizations and probe experiments, we confirmed the significance of the solid acid structure of the photocatalyst and clarified the catalytic mechanism of the new photocatalyst. Our finding may provide a new strategy to prepare highly active photocatalysts for proton-involved reactions.
ISSN:1005-0302
1941-1162
DOI:10.1016/j.jmst.2023.03.028