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Coupling Piezocatalysis and Photocatalysis in Bi 4 NbO 8 X (X = Cl, Br) Polar Single Crystals
Author(s) -
Hu Cheng,
Huang Hongwei,
Chen Fang,
Zhang Yihe,
Yu Hai,
Ma Tianyi
Publication year - 2020
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.201908168
Subject(s) - photocatalysis , materials science , natural bond orbital , catalysis , radical , hydrogen peroxide , photochemistry , oxygen , nanotechnology , chemistry , molecule , organic chemistry
Reactive oxygen species (ROS) as green oxidants are of great importance for environmental and biological applications. Photocatalysis is one of the major routes for ROS evolution, which is seriously restricted by rapid charge recombination. Herein, piezocatalysis and photocatalysis (i.e., piezo–photocatalysis) are coupled to efficiently produce superoxide radicals (•O 2 − ), hydrogen peroxide (H 2 O 2 ), and hydroxyl radicals (•OH) via oxygen reduction reaction (ORR), by using Bi 4 NbO 8 X (X = Cl, Br) single crystalline nanoplates. Significantly, the piezo‐photocatalytic process leads to the highest ORR performance of the Bi 4 NbO 8 Br nanoplates, exhibiting •O 2 − , H 2 O 2 , and •OH evolution rates of 98.7, 792, and 33.2 µmol g −1 h −1 , respectively. The formation of a polarized electric field and band bending allows directional separation of charge carriers, promoting the catalytic activity. Furthermore, the reductive active sites are found enriched on all the facets in the piezo–photocatalytic process, also contributing to the ORR. By piezo–photodeposition of Pt to artificially plant reductive reactive sites, the Bi 4 NbO 8 Br plates demonstrate largely enhanced photocatalytic H 2 production activity with a rate of 203.7 µmol g −1 h −1 . The present work advances piezo–photocatalysis as a new route for ROS generation, but also discloses the potential of piezo–photocatalytic active sites enriching for H 2 evolution.