4.8 Article

Efficient Charge Separation from F- Selective Etching and Doping of Anatase-TiO2{001} for Enhanced Photocatalytic Hydrogen Production

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 10, Issue 23, Pages 19633-19638

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b02804

Keywords

TiO2; photogenerated carrier; {001} facets; photocatalytic hydrogen production; visible light

Funding

  1. Program for National Natural Science Foundation of China [51672056]
  2. Natural Science Foundation of Heilongjiang Province of China [LC2015004]
  3. Pandeng Plan Foundation of Hangzhou Normal University for youth scholars of materials
  4. Natural Science Foundation of Heilongjiang Province [B201603, E2017058]
  5. Nature Science Foundation of Zhejiang Provincial [LY18E020010]
  6. Heilongjiang Province Department of Education [18KYYWFC-XY06]
  7. Heihe University [KJY201702]

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TiO2 nanomaterials with coexposed {001} and {101} facets have aroused much interest owing to their outstanding photocatalytic performance. In this study, on the basis of its unique characteristics of photoinduced electron and hole transfer to different lattice planes, we synthesized F- selective etching and doping on {001} facets of anatase TiO2 nanosheets using TiO2 nanosheets with coexposed {001} and {101} facets as a precursor. Through a series of measurements, such as photoluminescence, transient photocurrent response, electrochemical impedance spectra, and Mott-Schottky measurements, it is proved that F- selective etching and doping on {001} facets of TiO2 can extremely accelerate the separation of photogenerated carriers by shortening the transfer pathway of holes and introducing Ti3+ and oxygen vacancies in {001} facets. Therefore, the as-obtained sample shows excellent photocatalytic properties under the visible-light irradiation; the highest rate of photocatalytic H-2 evolution is up to 18270 mu mol h(-1) g(-1) and its quantum efficiency is up to 21.6% at lambda = 420 nm. As an innovative exploration, this study provides a direct spatial charge separation strategy for developing highly efficient photocatalysts.

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