4.8 Article

WS2/Graphitic Carbon Nitride Heterojunction Nanosheets Decorated with CdS Quantum Dots for Photocatalytic Hydrogen Production

期刊

CHEMSUSCHEM
卷 11, 期 7, 页码 1187-1197

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.201800053

关键词

interfaces; photochemistry; quantum dots; semiconductors; water splitting

资金

  1. National Natural Science Fund Committee-Baosteel Group Corporation Steel Joint Research Fund, China [U1460105]
  2. National Science Foundation of China [51521065]
  3. State Key Laboratory of Crystal Materials, Shandong University, China [KF1710]
  4. State Key Laboratory of Electrical Insulation and Power Equipment (Xi'an Jiaotong University) [EIPE18311]

向作者/读者索取更多资源

Two-dimensional/two-dimensional (2D/2D) stacking heterostructures are highly desirable in fabricating efficient photocatalysts because face-to-face contact can provide a maximized interfacial region between the two semiconductors; this largely facilitates the migration of charge carriers. Herein, a WS2/graphitic carbon nitride (CN) 2D/2D nanosheet heterostructure decorated with CdS quantum dots (QDs) has been designed, for the first time. Optimized CdS/WS2/CN without another cocatalyst exhibits a significantly enhanced photocatalytic H-2 evolution rate of 1174.5 mu molh(-1)g(-1) under visible-light irradiation (lambda > 420 nm), which is nearly 67 times higher than that of the pure CN nanosheets. The improved photocatalytic activity can be primarily attributed to the highly efficient charge-transfer pathways built among the three components, which effectively accelerate the separation and transfer of photogenerated electrons and holes, and thus, inhibit their recombination. Moreover, the extended light-absorption range also contributes to excellent photocatalytic efficiency. In addition, the CdS/WS2/CN photocatalyst shows excellent stability and reusability without apparent decay in the photocatalytic H-2 evolution within 4 cycles in 20 h. It is believed that this work may shed light on specifically designed 2D/2D nanosheet heterostructures for more efficient visible-light-driven photocatalysts.

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