期刊
APPLIED SURFACE SCIENCE
卷 557, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.apsusc.2021.149797
关键词
Photoreduction; Adsorption; Heterostructure; SnS2
类别
资金
- National Natural Science Foundation of China [U1601214]
- Science and Technology Program of Guangzhou [2019050001]
- Scientific and Technological Plan of Guangdong Province [2018B050502010, 2019B090905005]
- The third batch of Zhaoqing Xijiang Talent Innovation Team project (2019)
- National Natural Science Foundation of Guangdong Province [U1601214]
In this study, a PANI@SnS2@Cs heterostructure composite was prepared to improve the photoreduction performance and adsorption capability by reducing the rapid recombination of photogenerated carriers. The composite demonstrated efficient purification of Cr(VI) contaminated water under solar light within a short period of time. Characterizations were conducted to confirm the heterostructure and optical performance of the composite, while the mechanism of charge transfer between PANI and SnS2 was also investigated.
Tin sulfide (SnS2) is an excellent photocatalyst, which is widely used in reduction of heavy metal pollutants. However, its application is hindered by the rapid recombination of photogenerated carriers. In this study, a heterostructure composite composed of PANI, SnS2 and carbon sphere (PANI@SnS2@Cs) was prepared by a hydrothermal approach combined with in-situ oxidative polymerization to release the fast recombination of photogenerated carriers and improve the photoreduction performance. Compared with bare SnS2 and SnS2@Cs, PANI@SnS2@Cs not only provides more efficient photoreduction performance, but also possesses stronger adsorption capability. In neutral solution, 60 mg PANI@SnS2@Cs is capable of reducing 60 mL contaminated water with a concentration of 100 mg/L Cr(VI) within 30 min of solar light. Characterizations including transmission electron microscope and UV-Vis-NIR diffusive reflectance spectra were applied to provide evidences to confirm the heterostructure and the excellent optical performance of PANI@SnS2@Cs. Besides, the mechanism behind PANI@SnS2@Cs was investigated that the photogenerated e- in the lowest unoccupied molecular orbital (LUMO) of PANI can be transferred into the conduction band of SnS2 while h+ in valence band of SnS2 can be transferred into the highest occupied molecular orbital (HOMO) of PANI.
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