4.6 Article

The visible-light photocatalytic activity for enhancing RhB degradation and hydrogen evolution from SrTiO3 nanoparticles decorated red phosphorus nanorods as photocatalysts

期刊

出版社

IOP PUBLISHING LTD
DOI: 10.1088/1361-6463/ab58df

关键词

strontium titanaterutile; red phosphorus nanorods; heterostructure; photodegradation; hydrogen evolution

资金

  1. National Natural Science Foundation of China [51672031]
  2. Natural Science Foundation of Chongqing, China [cstc-2019jcyj-msxmX0572]
  3. Fundamental Research Funds for the Central Universities [2018CDJDWL0011, 2019CDXZWL002]
  4. sharing fund of large-scale equipment of Chongqing University

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Visible-light-sensitive crystalline red phosphorus (P) nanorod composited with SrTiO3 (STO) particles have been successfully assembled via a solid-state reaction routine, wherein STO nanoparticles were immobilized on the surface of P nanorods. The obtained crystalline P/STO heterostructured composites with an intimate interfacial contact facilitate efficient charge separation and transfer of photogenerated electron-hole pairs, and the P nanorods with a large exposed surface exhibit strong Vis-light absorption. Therefore, by adjusting different molar ratio and calcination temperature, the P-2.0/STO-700 degrees C composites presented the best photocatalytic activities of RhB degradation and hydrogen evolution (169.95 mu molh(-1) g(-1)) and possessed high stability during three cycling experiments. The reaction rate constant (k(app)) of the optimum P-2.0/STO-700 degrees C composites is about 215 times and 11.3 times as high as that of pristine STO and P, respectively. In this paper, the crystalline, morphologies and optical properties of the as-prepared photocatalysts were sufficiently studied via various characterization techniques. Meanwhile, a reasonable charge transfer mechanism on P/STO composites was brought up and a trapping experiment was analysized in detail. This research provides some perspectives for the future development of P-based photocatalytic materials.

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