Efficient Charge Separation from F- Selective Etching and Doping of Anatase-TiO2{001} for Enhanced Photocatalytic Hydrogen Production.
Yurong YangKe YeDianxue CaoPeng GaoMin QiuLi LiuPiaoping YangPublished in: ACS applied materials & interfaces (2018)
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 H2 evolution is up to 18270 μ mol h-1 g-1 and its quantum efficiency is up to 21.6% at λ = 420 nm. As an innovative exploration, this study provides a direct spatial charge separation strategy for developing highly efficient photocatalysts.
Keyphrases
- visible light
- highly efficient
- liquid chromatography
- quantum dots
- electron transfer
- solar cells
- magnetic resonance imaging
- photodynamic therapy
- computed tomography
- molecular dynamics
- magnetic resonance
- high resolution
- radiation therapy
- mass spectrometry
- density functional theory
- blood brain barrier
- simultaneous determination
- oxide nanoparticles