氢
催化作用
分解水
贵金属
光化学
纳米技术
化学物理
作者
Yuanjun Chen,Shufang Ji,Wenming Sun,Yongpeng Lei,Qichen Wang,Ang Li,Wenxing Chen,Gang Zhou,Zedong Zhang,Yu Wang,Lirong Zheng,Qinghua Zhang,Lin Gu,Xiaodong Han,Dingsheng S. Wang,Yadong Li
标识
DOI:10.1002/ange.201912439
摘要
Abstract It is highly desirable but challenging to optimize the structure of photocatalysts at the atomic scale to facilitate the separation of electron–hole pairs for enhanced performance. Now, a highly efficient photocatalyst is formed by assembling single Pt atoms on a defective TiO 2 support (Pt 1 /def‐TiO 2 ). Apart from being proton reduction sites, single Pt atoms promote the neighboring TiO 2 units to generate surface oxygen vacancies and form a Pt‐O‐Ti 3+ atomic interface. Experimental results and density functional theory calculations demonstrate that the Pt‐O‐Ti 3+ atomic interface effectively facilitates photogenerated electrons to transfer from Ti 3+ defective sites to single Pt atoms, thereby enhancing the separation of electron–hole pairs. This unique structure makes Pt 1 /def‐TiO 2 exhibit a record‐level photocatalytic hydrogen production performance with an unexpectedly high turnover frequency of 51423 h −1 , exceeding the Pt nanoparticle supported TiO 2 catalyst by a factor of 591.
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