光催化
可见光谱
水溶液
石墨氮化碳
材料科学
分解
色散(光学)
离子键合
氮化物
氮化碳
分解水
人工光合作用
光化学
催化作用
碳纤维
纳米技术
化学
离子
光电子学
有机化学
复合材料
物理
光学
复合数
图层(电子)
作者
Kazuhiko Maeda,Xinchen Wang,Yasushi Nishihara,Daling Lu,Markus Antonietti,Kazunari Domen
摘要
Graphitic carbon nitride (g-C3N4) with a band gap of 2.7 eV is studied as a nonmetallic photocatalyst for H2 or O2 evolution from water under ultraviolet (UV) and visible light. The g-C3N4 catalyst exhibits activities for water reduction into H2 or water oxidation into O2 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 H2 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 O2 from an aqueous silver nitrate solution upon UV irradiation (λ > 300 nm), although N2 release due to self-decomposition of g-C3N4 by photogenerated holes takes place. Modification of g-C3N4 with RuO2 improves not only O2 evolution activity but also stability against the self-decomposition, resulting in stable visible-light-driven O2 evolution (λ > 420 nm).
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