4.6 Article

Modification of g-C3N4 Photocatalyst with Flower-like ReS2 for Highly Efficient Photocatalytic Hydrogen Evolution

期刊

CHEMCATCHEM
卷 12, 期 24, 页码 6385-6392

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.202001330

关键词

Graphitic carbon nitride; Nanocomposite; Noble-metal-free; Photocatalysis; Rhenium sulfide

资金

  1. National Natural Science Foundation of China [91233108, 21703287]
  2. Natural Science Foundation of Shandong Province [ZR2017MB006, ZR2017BB027]
  3. Major Program of Shandong Province Natural Science Foundation [ZR2017ZB0315]
  4. Fundamental Research Funds for the Central Universities [18CX02052A, 19CX05002A]
  5. Taishan Scholar Program of Shandong Province [ts201712019]
  6. Postgraduate Innovation Project of China University of Petroleum [YCX2018076]
  7. China Postdoctoral Science Foundation [2020M672162]
  8. Independent Innovation Project of China University of Petroleum (East China) [20CX0603A]

向作者/读者索取更多资源

Heterojunction strategy has proven to be an effective approach for overcoming the quick photoexcited charge carrier recombination of graphitic carbon nitride (g-C3N4) and facilitating its photocatalytic performances. Bearing the merits of transition metal dichalcogenides (TMDs) in mind, in this work, a novel flower-like ReS2 coupled with layered g-C3N4 was constructed via a facile hydrothermal route. The hybrid ReS2/g-C3N4 catalysts create excellent photocatalytic hydrogen evolution without any additional co-catalyst. Under visible-light irradiation, the optimized 3 wt % ReS2/g-C3N4 heterojunction exhibited a hydrogen evolution rate 8 times that of pristine g-C3N4, maintaining a stable heterojunction after multiple photocatalytic cycles. ReS2/g-C3N4 integrates the merits of both the configuration of a heterojunction and the formation of spatially conductive network, which effectively accelerate the transfer of photoinduced carrier. This work not only presents a marked ReS2/g-C3N4 heterojunction photocatalyst, but provides more possibility for expanding applications in electrocatalysis, photothermal catalysis and energy storage.

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