4.7 Article

Uniform Pt quantum dots-decorated porous g-C3N4 nanosheets for efficient separation of electron-hole and enhanced solar-driven photocatalytic performance

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 531, Issue -, Pages 119-125

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2018.07.047

Keywords

g-C3N4; Pt quantum dot; Porous structure; Solar-driven photocatalysis

Funding

  1. National Basic Research Program of China (973Program) [2013CB933104]
  2. Natural Science Foundation of Heilongjiang Province [B2018010]
  3. Heilongjiang Postdoctoral Startup Fund [LBH-Q14135]
  4. University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province [UNPYSCT-2016018]

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Uniform Pt quantum dots-decorated porous g-C3N4 nanosheets (Pt/CN) are fabricated by a facile impregnation-ultrasonic-calcination method, using melamine as precursor. The as-prepared samples are evidently investigated by X-ray diffraction, UV-vis diffuse reflection spectra, N-2 adsorption, transmission electron microscope, surface photovoltage spectroscopy and photoluminescence. The deposited Pt quantum dots with particle size of similar to 5 nm are decorated on the surface of porous g-C3N4 nanosheets uniformly. The Pt/CN nanosheets show conspicuous solar-driven photocatalytic activity for splitting water to produce H-2. The solar-driven photocatalytic hydrogen production rate of Pt/CN is up to similar to 107 mu mol h(-1) g(-1), which is about 5 times higher than that of pristine g-C3N4. The enhancement can be attributed to the porous structure offering adequate surface active sites and the efficient decoration of uniform Pt quantum dots on g-C3N4 nanosheets facilitating the separation of photogenerated electron-hole pairs, which is confirmed by surface photovoltage spectroscopy and photoluminescence. The strategy for fabricating Pt quantum dots-decorated g-C3N4 nanosheets offers new insights for constructing other high-performance quantum dot-semiconductor photocatalytic materials. (C) 2018 Elsevier Inc. All rights reserved.

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