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Synergetic catalysis enhancement between H2O2 and TiO2 with single-electron-trapped oxygen vacancy
The TIO 2 -H 2 O 2 system possesses excellent oxidation activity even under dark conditions. However, the mechanism of this process is unclear and inconsistent. In this work, the binary component system containing TiO 2 nanoparticles (NPs) with single electron-trapped oxygen vacancy (SETOV, Vo) and...
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Published in: | Nano research 2020-02, Vol.13 (2), p.551-556 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The TIO
2
-H
2
O
2
system possesses excellent oxidation activity even under dark conditions. However, the mechanism of this process is unclear and inconsistent. In this work, the binary component system containing TiO
2
nanoparticles (NPs) with single electron-trapped oxygen vacancy (SETOV, Vo) and H
2
O
2
exhibit excellent oxidative performance for tetracycline, RhB, and MO even without light irradiation. We systematically investigated the mechanism for the high activity of the TIO
2
-H
2
O
2
under dark condition. Reactive oxygen species (ROS) induced from H
2
O
2
play a significant role in improving the catalytic degradation activities. X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR) results firstly confirm that H
2
O
2
is primarily activated by SETOVs derived from the TiO
2
NPs through direct contribution of electrons, producing both 02-/·AOOH and ·OH, which are responsible for the excellent reactivity of TiO
2
-H
2
O
2
system. This work not only provides a new perspective on the role of SETOVs playing in the H
2
O
2
activation process, but also expands the application of TiO
2
in environmental conservation. |
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ISSN: | 1998-0124 1998-0000 |
DOI: | 10.1007/s12274-020-2650-y |