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

被引:365
作者
Wang, Yuxiang [1 ]
Chen, Daoming [1 ]
Zhang, Jingnan [2 ]
Balogun, M-Sadeeq [3 ]
Wang, Pingshan [1 ]
Tong, Yexiang [2 ]
Huang, Yongchao [1 ]
机构
[1] Guangzhou Univ, Inst Environm Res Greater Bay, Key Lab Water Qual & Conservat Pearl River Delta, Minist Educ, Guangzhou 510006, Peoples R China
[2] Sun Yat Sen Univ, Sch Chem, Guangzhou 510275, Peoples R China
[3] Hunan Univ, Coll Mat Sci & Engn, Changsha 410082, Peoples R China
关键词
bismuth vanadate; carbon doping; carbon quantum dots; dual carbon-actions; photoelectrochemical water oxidation; BISMUTH VANADATE; OXYGEN VACANCIES; QUANTUM DOTS; BAND-EDGE; PHOTOANODES; OXIDATION; FERRIHYDRITE; SEPARATION; EFFICIENCY;
D O I
10.1002/adfm.202112738
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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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页数:9
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