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Thin Heterojunctions and Spatially Separated Cocatalysts To Simultaneously Reduce Bulk and Surface Recombination in Photocatalysts
Author(s) -
Li Ang,
Chang Xiaoxia,
Huang Zhiqi,
Li Chengcheng,
Wei Yijia,
Zhang Lei,
Wang Tuo,
Gong Jinlong
Publication year - 2016
Publication title -
angewandte chemie
Language(s) - English
Resource type - Journals
eISSN - 1521-3757
pISSN - 0044-8249
DOI - 10.1002/ange.201605666
Subject(s) - photocatalysis , heterojunction , mesoporous material , materials science , absorption (acoustics) , thin film , chemical engineering , charge carrier , nanoparticle , photochemistry , nanotechnology , optoelectronics , chemistry , catalysis , composite material , organic chemistry , engineering
Efficient charge separation and light absorption are crucial for solar energy conversion over solid photocatalysts. This paper describes the construction of Pt@TiO 2 @In 2 O 3 @MnO x mesoporous hollow spheres (PTIM‐MSs) for highly efficient photocatalytic oxidation. TiO 2 –In 2 O 3 double‐layered shells were selectively decorated with Pt nanoparticles and MnO x on the inner and outer surfaces, respectively. The spatially separated cocatalysts drive electrons and holes near the surface to flow in opposite directions, while the thin heterogeneous shell separates the charges generated in the bulk phase. The synergy between the thin heterojunctions and the spatially separated cocatalysts can simultaneously reduce bulk and surface/subsurface recombination. In 2 O 3 also serves as a sensitizer to enhance light absorption. The PTIM‐MSs exhibit high photocatalytic activity for both water and alcohol oxidation.