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Highly Efficient Photocatalytic H<sub>2</sub> Evolution from Water using Visible Light and Structure‐Controlled Graphitic Carbon Nitride

David James MartinSolar Energy Group, Department of Chemical Engineering, UCL, Torrington Place, London, WC1E 7JE (UK)Kaipei QiuDepartment of Chemistry, UCL, 20 Gordon Street, London, WC1H 0AJ (UK)Stephen A. ShevlinDepartment of Chemistry, UCL, 20 Gordon Street, London, WC1H 0AJ (UK)Albertus D. HandokoSolar Energy Group, Department of Chemical Engineering, UCL, Torrington Place, London, WC1E 7JE (UK)Xiaowei ChenDepartamento de Ciencia de los Materiales, Ingeniería Metalúrgica y Química Inorgánica, Facultad de Ciencias, Universidad de Cádiz, Puerto Real (Cádiz) (Spain)Zhengxiao GuoDepartment of Chemistry, UCL, 20 Gordon Street, London, WC1H 0AJ (UK)Junwang TangSolar Energy Group, Department of Chemical Engineering, UCL, Torrington Place, London, WC1E 7JE (UK)
2014en
ABI

Аннотация

The major challenge of photocatalytic water splitting, the prototypical reaction for the direct production of hydrogen by using solar energy, is to develop low-cost yet highly efficient and stable semiconductor photocatalysts. Herein, an effective strategy for synthesizing extremely active graphitic carbon nitride (g-C3N4) from a low-cost precursor, urea, is reported. The g-C3N4 exhibits an extraordinary hydrogen-evolution rate (ca. 20,000 μmol h(-1) g(-1) under full arc), which leads to a high turnover number (TON) of over 641 after 6 h. The reaction proceeds for more than 30 h without activity loss and results in an internal quantum yield of 26.5% under visible light, which is nearly an order of magnitude higher than that observed for any other existing g-C3N4 photocatalysts. Furthermore, it was found by experimental analysis and DFT calculations that as the degree of polymerization increases and the proton concentration decreases, the hydrogen-evolution rate is significantly enhanced.

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