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2D PtS nanorectangles/g-C3N4 nanosheets with a metal sulfide-support interaction effect for high-efficiency photocatalytic H2 evolution.
Lin, Bo; Zhou, Yao; Xu, Baorong; Zhu, Chao; Tang, Wu; Niu, Yingchun; Di, Jun; Song, Pin; Zhou, Jiadong; Luo, Xiao; Kang, Lixing; Duan, Ruihuan; Fu, Qundong; Liu, Haishi; Jin, Ronghua; Xue, Chao; Chen, Qiang; Yang, Guidong; Varga, Kalman; Xu, Quan; Li, Yonghui; Liu, Zheng; Liu, Fucai.
Affiliation
  • Lin B; School of Optoelectronic Science and Engineering, University of Electronic Science and Technology of China, Chengdu 611731, China. fucailiu@uestc.edu.cn.
Mater Horiz ; 8(2): 612-618, 2021 Feb 01.
Article in En | MEDLINE | ID: mdl-34821278
ABSTRACT
Cocatalyst design is a key approach to acquire high solar-energy conversion efficiency for photocatalytic hydrogen evolution. Here a new in situ vapor-phase (ISVP) growth method is developed to construct the cocatalyst of 2D PtS nanorectangles (a length of ∼7 nm, a width of ∼5 nm) on the surface of g-C3N4 nanosheets. The 2D PtS nanorectangles/g-C3N4 nanosheets (PtS/CN) show an unusual metal sulfide-support interaction (MSSI), which is evidenced by atomic resolution HAADF-STEM, synchrotron-based GIXRD, XPS and DFT calculations. The effect of MSSI contributes to the optimization of geometrical structure and energy-band structure, acceleration of charge transfer, and reduction of hydrogen adsorption free energy of PtS/CN, thus yielding excellent stability and an ultrahigh photocatalytic H2 evolution rate of 1072.6 µmol h-1 (an apparent quantum efficiency of 45.7% at 420 nm), up to 13.3 and 1532.3 times by contrast with that of Pt nanoparticles/g-C3N4 nanosheets and g-C3N4 nanosheets, respectively. This work will provide a new platform for designing high-efficiency photocatalysts for sunlight-driven hydrogen generation.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mater Horiz Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mater Horiz Year: 2021 Document type: Article