4.7 Article

Red Phosphorus Nanodot-Decorated Polymeric Carbon Nitride Nanotubes for Visible-Light-Driven Photocatalytic Bacterial Inactivation

Journal

ACS APPLIED NANO MATERIALS
Volume 5, Issue 1, Pages 862-870

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.1c03567

Keywords

red phosphorus; carbon nitride; heterostructure; bacterial inactivation; photocatalysis

Funding

  1. National Natural Science Foundation of China [51672143, 51808303, 52102362]
  2. Taishan Scholar Program of Shandong Province [ts201712030]
  3. Outstanding Youth of Natural Science in Shandong Province [JQ201713]
  4. Applied Basic Research of Qingdao City (Special Youth Project) [19-6-2-74-cg]
  5. State Key Laboratory of BioFibers and Eco-Textiles (Qingdao University) [ZKT-25, ZKT26, ZKT-30, KF2020103]
  6. Science and Technology Support Plan for Youth Innovation of Colleges in Shandong Province [DC2000000961]

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This study synthesized a superior visible-light-driven photocatalyst comprising a red phosphorus nanodot-modified carbon nitride nanotube heterostructure for bacterial inactivation. The optimized photocatalyst rapidly and completely destroyed Escherichia coli and Staphylococcus aureus under white LED irradiation. The efficient photocatalytic activity was attributed to the unique heterojunction structure and broad absorption spectra.
Pathogenic microorganisms related to infectious diseases severely threaten human health, and visible-light-driven (VLD) photocatalysis is a promising strategy for mitigating microbial-induced health crises. In this work, a superior and effective VLD photocatalyst comprising a red phosphorus nanodot-modified one-dimensional carbon nitride nanotube (RP-CN) heterostructure was synthesized with a simple chemical vapor deposition method and used for bacterial inactivation. The optimized RP (40)-CN rapidly and completely destroyed Escherichia coli and Staphylococcus aureus (10(7) CFU mL(-1)) within 25 and 30 min under irradiation with a white LED, respectively. The efficient photocatalytic activity was attributed to the fact that the matching work function in the CN-RP heterojunction promotes the charge migration/separation that occurs at the CN and RP interface and the broad absorption spectra by RP loading. Additional unpaired photoelectrons reacted with water to generate O-center dot(2)- radicals and H2O2 for efficient bacterial cell inactivation. The present study highlights the design of nanostructured photocatalysts with wide spectral responses for efficient energy conversion and wide antibacterial scope.

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