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Graphene and g-C3N4Nanosheets Cowrapped Elemental α-Sulfur As a Novel Metal-Free Heterojunction Photocatalyst for Bacterial Inactivation under Visible-Light

Wang, Wanjun, Yu, Jimmy C., Xia, Dehua, Wong, Po Keung, Li, Yecheng·2013·Environmental Science & Technology

Abstract

A new class of metal-free heterojunction photocatalysts was prepared by wrapping reduced graphene oxide (RGO) and g-C3N4 (CN) sheets on crystals of cyclooctasulfur (α-S8). Two distinctive structures were fabricated by wrapping RGO and CN sheets in different orders. The first was RGO sheets sandwiched in heterojunction of CN sheets and α-S8 (i.e., CNRGOS8), while the second structure was the other way around (i.e., RGOCNS8). Both structures exhibited antibacterial activity under visible-light irradiation. CNRGOS8 showed stronger bacterial inactivation than RGOCNS8 in aerobic conditions. However, RGOCNS8 was more active than CNRGOS8 under anaerobic condition. A possible mechanism was proposed to explain the differences between photocatalytic oxidative inactivation and reductive inactivation. As a proof-of-concept, this work could offer new inroads into exploration and utilization of graphene sheets and g-C3N4 sheets cowrapped nanocomposites for environmental applications.

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Metadata

Authors
Wang, W., Yu, J. C., Xia, D., Wong, P. K., & Li, Y.
Venue
Environmental Science & Technology
Published
2013-07-29
Volume
47
Issue
15
Pages
8724-8732
ISSN
  • 0013-936X (ISSN-L)
  • 1520-5851
OpenAlex
W2330845752
Cited by
418
References
0
FWCI
11.90
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Graphene and g-C3N4Nanosheets Cowrapped Elemental α-Sulfur As a Novel Metal-Free Heterojunction Photocatalyst for Bacterial Inactivation under Visible-Light. https://app.cochat.ai/papers/10.1021/es4013504
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Wang, W., Yu, J. C., Xia, D., Wong, P. K., & Li, Y. (2013). Graphene and g-C3N4Nanosheets Cowrapped Elemental α-Sulfur As a Novel Metal-Free Heterojunction Photocatalyst for Bacterial Inactivation under Visible-Light. Environmental Science & Technology. https://doi.org/10.1021/es4013504

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