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Noble Metal-Free Photocatalysts Consisting of Graphitic Carbon Nitride, Nickel Complex, and Nickel Oxide Nanoparticles for Efficient Hydrogen Generation

A facile and simple synthetic route is developed to prepare earth-abundant and noble metal-free hybrid photocatalysts, which are composed of graphitic carbon nitride (CN), nickel complex, and NiO x nanoparticles. Bimolecular nucleophilic substitution reaction was employed to attach a nickel complex...

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Bibliographic Details
Published in:ACS applied materials & interfaces 2019-04, Vol.11 (16), p.14986-14996
Main Authors: Zhang, Yun-Xiao, Tang, Shuang, Zhang, Wei-De, Yu, Yu-Xiang
Format: Article
Language:English
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Summary:A facile and simple synthetic route is developed to prepare earth-abundant and noble metal-free hybrid photocatalysts, which are composed of graphitic carbon nitride (CN), nickel complex, and NiO x nanoparticles. Bimolecular nucleophilic substitution reaction was employed to attach a nickel complex onto a graphitic CN framework through covalent bonds to support its high loading and dispersion. NiO x nanoparticles were further incorporated into the catalysts to serve as a hole-transporting medium to improve the separation of photogenerated carriers for higher photocatalytic activity. Both yNiL/CN and yNiL/NiO x /CN exhibit superb H2 evolution activity. The optimum H2 evolution rate of the binary photocatalysts yNiL/CN reaches 303.3 μmol·h–1·g–1, whereas that of the ternary photocatalysts yNiL/NiO x /CN reaches 524.1 μmol·h–1·g–1, and the apparent quantum efficiency reaches 1.46% at 450 nm. This finding reveals that coordination of a nickel complex is significant in promoting photocatalytic performance, and the incorporation of NiO x nanoparticles as a hole-transporting medium is beneficial for separation of the photogenerated charge carriers. The novel hybrid system offers a new horizon for designing transition-metal complex-modified graphitic CN as noble metal-free and highly active photocatalysts for efficient visible light-driven hydrogen generation.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.9b01704