4.8 Article

Charge Relays via Dual Carbon-Actions on Nanostructured BiVO4 for High Performance Photoelectrochemical Water Splitting

期刊

ADVANCED FUNCTIONAL MATERIALS
卷 32, 期 13, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202112738

关键词

bismuth vanadate; carbon doping; carbon quantum dots; dual carbon-actions; photoelectrochemical water oxidation

资金

  1. Natural Science Foundation of Guangdong Province [2020A1515010798]
  2. Natural Science Foundation of China [21706295]
  3. Science and Technology Research Project of Guangzhou [202002010007]
  4. Innovation training program for college students of Guangzhou University [202011078020]
  5. Qing Yuan Huayuan Institute of Science and Technology Collaborative Innovation Co., Ltd.

向作者/读者索取更多资源

Carbon doping and introduction of carbon quantum dots can improve the electronic conductivity and light absorption capability of BiVO4, thus enhancing the separation and transfer of photo-generated charges. Electroplating a polyaniline layer onto the catalyst can sustain a stable photocurrent density for a long time.
Photoelectrochemical water splitting based on nanostructured bismuth vanadate (BiVO4) can be a promising strategy to produce low-cost and green H-2 to replace fossil fuels and realize carbon neutrality. Herein, a simple chemical way to realize in situ carbon doping into BiVO4 crystalline structure is designed and obtained carbon-doped BiVO4, namely C-BiVO4, can improve the electronic conductivity of BiVO4. In addition, the introduction of the synthesized carbon quantum dots (CQDs) as a co-catalyst, immobilizes CQDs onto the C-BiVO4 nanosheet and acquires the optimized C-BiVO4/CQDs heterogeneous structure, which not only boosts light absorption, but also enhances the separation and transfer of the photo-generated charges. Stemming from the dual carbon actions, the as-prepared C-BiVO4/CQDs photoanode exhibits an excellent photocurrent density of 4.83 mA cm(-2) at 1.23 V versus the RHE without the use of any hole scavengers. To assure the practical application of the sensitive photocatalyst, a polyaniline layer is electroplated onto the C-BiVO4/CQDs catalyst as a conducting, electroactive, and protective layer to sustain a remarkable long-term photocurrent density of 2.75 mA cm(-2) for 9 hours. This work suggests that the proposed low-cost, environmentally friendly dual carbon actions can modify photocatalyst and achieve green production of H-2.

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