光催化
氢化物
光化学
纳米片
掺杂剂
材料科学
氢原子
密度泛函理论
催化作用
兴奋剂
氢
无机化学
化学
纳米技术
计算化学
有机化学
光电子学
烷基
作者
Shintaro Ida,Kenta Sato,Tetsuya Nagata,Hidehisa Hagiwara,Motonori Watanabe,Namhoon Kim,Yoshihito Shiota,Michio Koinuma,Sakae Takenaka,Takaaki Sakai,Elif Ertekin,Tatsumi Ishihara
标识
DOI:10.1002/anie.201803214
摘要
Abstract The hydrogen evolution reaction using semiconductor photocatalysts has been significantly improved by cocatalyst loading. However, there are still many speculations regarding the actual role of the cocatalyst. Now a photocatalytic hydrogen evolution reaction pathway is reported on a cocatalyst site using TiO 2 nanosheets doped with Rh at Ti sites as one‐atom cocatalysts. A hydride species adsorbed on the one‐atom Rh dopant cocatalyst site was confirmed experimentally as the intermediate state for hydrogen evolution, which was consistent with the results of density functional theory (DFT) calculations. In this system, the role of the cocatalyst in photocatalytic hydrogen evolution is related to the withdrawal of photo‐excited electrons and stabilization of the hydride intermediate species; the presence of oxygen vacancies induced by Rh facilitate the withdrawal of electrons and stabilization of the hydride.
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