光电阴极
光电流
分解水
化学
法拉第效率
光电化学电池
非阻塞I/O
能量转换效率
半导体
光电化学
光化学
电化学
光电子学
析氧
异质结
制氢
催化作用
光催化
材料科学
电极
物理
物理化学
电解质
有机化学
电子
量子力学
作者
Christopher D. Windle,Hiromu Kumagai,Masanobu Higashi,Romain Brisse,Sébastian Bold,Bruno Jousselme,Murielle Chavarot‐Kerlidou,Kazuhiko Maeda,Ryu Abe,Osamu Ishitani,Vincent Artero
摘要
A push-pull organic dye and a cobaloxime catalyst were successfully cografted on NiO and CuGaO2 to form efficient molecular photocathodes for H2 production with >80% Faradaic efficiency. CuGaO2 is emerging as a more effective p-type semiconductor in photoelectrochemical cells and yields a photocathode with 4-fold higher photocurrent densities and 400 mV more positive onset photocurrent potential compared to the one based on NiO. Such an optimized CuGaO2 photocathode was combined with a TaON|CoO x photoanode in a photoelectrochemical cell. Operated in this Z-scheme configuration, the two photoelectrodes produced H2 and O2 from water with 87% and 88% Faradaic efficiency, respectively, at pH 7 under visible light and in the absence of an applied bias, equating to a solar to hydrogen conversion efficiency of 5.4 × 10-3%. This is, to the best of our knowledge, the highest efficiency reported so far for a molecular-based noble metal-free water splitting Z-scheme.
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