4.6 Article

Synthesis and Visible Light Catalytic Performance of BiOI/Carbon Nanofibers Heterojunction

期刊

CATALYSTS
卷 12, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/catal12121548

关键词

BiOI; carbon nanofibers; photocatalysts; electrospinning

资金

  1. National Natural Science Foundation of China [11905096]
  2. Natural Science Foundation of Henan Province [19A430020, 212102210312, 222300420241, 22A430030, 222300420240, 21A140017, 21A140016, 222102240114, 23B140015]

向作者/读者索取更多资源

Semiconductor materials have great potential as photocatalysts. In this study, a synthesis method combining electrospinning technique and SILAR reaction was used to prepare BiOI/CNFs photocatalytic material. The results showed that BiOI/CNFs had a much higher degradation rate of methyl orange under visible light compared to pure BiOI, due to the conductive CNFs improving the separation and transformation of photogenerated charges. Moreover, the fabricated BiOI/CNFs could be easily recycled due to their ultra-long one-dimensional nano-structural property.
Semiconductor materials as photocatalysts hold great prospects for renewable energy substitutes and environmental protection. Nanostructured BiOX (X=Cl, Br, I) with favorable features of a unique layered crystal structure and suitable band gaps has been demonstrated to be a promising photocatalytic material. In this paper, a two-step synthesis route combining an electrospinning technique and SILAR reaction has been accepted as a straightforward protocol for the exploitation of BiOI/carbon nanofibers' (CNFs) hierarchical heterostructures. As expected, the BiOI/CNFs presented a much higher degradation rate of methyl orange than that of the pure BiOI under visible light. The degradation rate of methyl orange reaches 85% within 210 min. The enhanced photocatalytic activity could be attributed to the fact that conductive CNFs as substrate could effectively improve the separation and transformation of photogenerated charges. Moreover, the fabricated BiOI/CNFs after five cycles could be easily recycled without a decrease in photocatalytic activity due to their ultra-long one-dimensional nano-structural property.

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