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Visible Light-Driven Pure Water Splitting by a Nature-Inspired Organic Semiconductor-Based System
Author(s) -
David James Martin,
Philip James Thomas Reardon,
Savio J. A. Moniz,
Junwang Tang
Publication year - 2014
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja506386e
Subject(s) - chemistry , water splitting , graphitic carbon nitride , photocatalysis , oxygen evolution , artificial photosynthesis , semiconductor , oxygen , visible spectrum , redox , photosynthesis , carbon nitride , hydrogen , photochemistry , chemical engineering , chemical physics , inorganic chemistry , optoelectronics , electrochemistry , organic chemistry , catalysis , electrode , biochemistry , engineering , physics
For the first time, it is demonstrated that the robust organic semiconductor g-C3N4 can be integrated into a nature-inspired water splitting system, analogous to PSII and PSI in natural photosynthesis. Two parallel systems have been developed for overall water splitting under visible light involving graphitic carbon nitride with two different metal oxides, BiVO4 and WO3. Consequently, both hydrogen and oxygen can be evolved in an ideal ratio of 2:1, and evolution rates in both systems have been found to be dependent on pH, redox mediator concentration, and mass ratio between the two photocatalysts, leading to a stable and reproducible H2 and O2 evolution rate at 36 and 18 μmol h(-1) g(-1) from water over 14 h. Our findings demonstrate g-C3N4 can serve as a multifunctional robust photocatalyst, which could also be used in other systems such as PEC cells or coupled solar cell systems.

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