Photocatalytic Activities of Graphitic Carbon Nitride Powder for Water Reduction and Oxidation under Visible Light

被引:758
作者
Maeda, Kazuhiko [2 ]
Wang, Xinchen [1 ,3 ]
Nishihara, Yasushi [4 ]
Lu, Daling [5 ]
Antonietti, Markus [1 ]
Domen, Kazunari [2 ]
机构
[1] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, D-14424 Potsdam, Germany
[2] Univ Tokyo, Dept Chem Syst Engn, Bunkyo Ku, Tokyo 1138656, Japan
[3] Fuzhou Univ, State Key Lab Breeding Base Photocatalysis, Res Inst Photocatalysis, Fuzhou 350002, Peoples R China
[4] Okayama Univ, Grad Sch Nat Sci & Technol, Div Chem & Biochem, Okayama 7668530, Japan
[5] Tokyo Inst Technol, Ctr Adv Mat Anal, Meguro Ku, Tokyo 1528550, Japan
关键词
HYDROGEN-PRODUCTION; DRIVEN PHOTOCATALYST; SOLID-SOLUTION; OXYSULFIDE SM2TI2S2O5; STABLE PHOTOCATALYST; OXYGEN EVOLUTION; CATALYSTS; IRRADIATION; TIO2; NM;
D O I
10.1021/jp809119m
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Graphitic carbon nitride (g-C3N4) with a band gap of 2.7 eV is studied as a nonmetallic photocatalyst for H-2 or O-2 evolution from water under ultraviolet (UV) and visible light. The g-C3N4 catalyst exhibits activities for water reduction into H-2 or water oxidation into O-2 in the presence of a proper sacrificial electron donor or acceptor, respectively, even without the need for precious metal cocatalysts. When bis(1,5-cyclooctadiene)platinum complex [Pt(cod)(2)] (a nonionic complex) is used as a precursor of Pt cocatalyst instead of H2PtCl6 (an ionic complex), enhanced H-2) evolution activity is acquired. This difference in activity is primarily due to the better dispersion of Pt nanoparticles on g-C3N4, which is considered to originate from the better access of Pt(cod)(2) to the g-C3N4 surface, as compared to that of H2PtCl6 in the preparation process. Unmodified g-C3N4 produces O-2 from an aqueous silver nitrate solution upon UV irradiation (lambda > 300 nm), although N-2, release due to self-decomposition of g-C3N4 by photogenerated holes takes place. Modification of g-C3N4 with RuO2, improves not only O-2 evolution activity but also stability against the self-decomposition, resulting in stable visible-light-driven O-2 evolution (lambda > 420 nm).
引用
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页码:4940 / 4947
页数:8
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