4.7 Article

MoS2 decorated CdS hybrid heterojunction for enhanced photoelectrocatalytic performance under visible light irradiation

Journal

JOURNAL OF COLLOID AND INTERFACE SCIENCE
Volume 533, Issue -, Pages 561-568

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2018.08.078

Keywords

Hybrid, metal sulphide; Electrodeposition; Photocatalytic; Visible light

Funding

  1. project of China Postdoctoral Science Foundation [2016M602483]
  2. PhD Start-up Fund of Natural Science Foundation of Guangdong Province, China [2017A030310420]
  3. Science Technology Office of Guangzhou [201607010276]
  4. National Science and Technology Major Projects [2017ZX07202004]
  5. Special Project of Applicable Science and Technology of Guangdong Province [2016B020240008]

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Pervious photocatalysis application of nanostructured suspensions reveals high recombination rates of photogenerated electron-hole pairs, low recycling efficiency and secondary pollution problems. Herein, MoS2@CdS nanocomposites thin films on FTO (fluorine-doped tin oxide) substrates are fabricated using facile electrodeposition by decorating a layer of highly-active MoS2 cocatalyst on CdS film to optimize the interface modification. The hybrid film exhibits enhanced photoelectrocatalytic activity compared to pristine CdS film. The synthesized CdS exhibits a bandgap of 2.42 eV with the conduct band at ca. -0.25 V vs. RHE, while MoS2 reveals a bandgap of 1.73 eV with the valance band at ca. 1.59 V vs. RHE. The appropriate band alignment between the hybrid films favours the electrons transfer thus the charge recombination are suppressed. The MoS2@CdS film yields a highest photocurrent of 15.2 mA/cm(2) at 0 V vs. Ag/AgCl under visible light illumination (lambda >= 420 nm), exhibiting a 5.2 times enhancement as compared to that of CdS film (2.9 mA/cm(2)). The structural integration of MoS2 with CdS will be a promising strategy to develop a high-efficient and low-cost non-noble metal cocatalyst for solar energy conversion. (C) 2018 Elsevier Inc. All rights reserved.

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