4.7 Article

Optical and photocatalytic properties of S doped BiOCl nanosheets with tunable exposed {001} facets and band gap

期刊

APPLIED SURFACE SCIENCE
卷 600, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.apsusc.2022.154020

关键词

BiOCl nanosheets; S doping; Visible light; Tunable surface facet; Photocatalytic mechanism

资金

  1. National Natural Science Foundation of China [51472205, 51302218]
  2. Natural Science Basic Research Plan in Shaanxi Province of China [2018JM5039, 2021JQ-257]
  3. Fundamental Research Funds for the Central Universities of China [3102016ZY033]
  4. Fundamental Research Funds for the Central Universities [.300102120305]

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In this study, S-doped BiOCl nanosheets were successfully synthesized via a facial hydrothermal reaction, leading to improved optical and photochemical properties. The S-doped BiOCl nanosheets with dominant {001} facets exhibited longer lifespans of photo-induced carriers and enhanced absorption of visible light, resulting in higher photocatalytic efficiency.
Element doping and crystal facet engineering are considered effective methods to improve the optical and photochemical properties of semiconductor materials. In this study, we successfully produced S-doped BiOCl nanosheets with a controllable band gap and exposure ratio of {001} facets via a facial hydrothermal reaction wherein thioacetamide served as an S donor and played a vital role in regulating the growth of the (0 01) plane of BiOCl. The PL and UV results suggested that S-doped BiOCl nanosheets with dominant {001} facets possessed photo-induced carriers with longer lifespans and enhanced absorption of visible light compared to undoped BiOCl. The photocatalytic results showed that S-doped BiOCl with a Bi/S molar ratio of 100:3 exhibited the highest photodegradation efficiency, which was 2.6 times that of the undoped BiOCl nanosheets. The improved photocatalytic efficiency could be explained by the synergistic effect of the enhanced exposure ratio of the {0 0 1} facets and the reduced bandgap, leading to broadened light absorption and enhanced separation of photoexcited carriers. The possible mechanism of the separation and transfer of electron-hole pairs was analyzed and dis-cussed. This work provides useful information for the synthesis of efficient semiconductor photocatalysts, combining the merits of non-metal doping and crystal engineering.

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