Interfacial synergy of Pd sites and defective BiOBr for promoting the solar-driven selective oxidation of toluene
Author:
Affiliation:
1. Department of Chemistry
2. School of Science
3. Zhejiang Sci-Tech University
4. Hangzhou 310018
5. China
6. Institute of Optoelectronic Materials and Devices
7. College of Optical and Electronic Technology
8. China Jiliang University
Abstract
The enhanced charge separation and molecule activation at the Pd–BiOBr interface greatly promote the photocatalytic selective oxidation of toluene to benzaldehyde.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Zhejiang Province
Zhejiang Sci-Tech University
Publisher
Royal Society of Chemistry (RSC)
Subject
General Materials Science,Renewable Energy, Sustainability and the Environment,General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2020/TA/D0TA05733A
Reference75 articles.
1. C−H Bond Activation and Organometallic Intermediates on Isolated Metal Centers on Oxide Surfaces
2. Solvent-Free Oxidation of Primary Carbon-Hydrogen Bonds in Toluene Using Au-Pd Alloy Nanoparticles
3. Efficient and selective oxidation of toluene to benzaldehyde on manganese tungstate nanobars: a noble metal-free approach
4. Production of benzaldehyde: a case study in a possible industrial application of phase-transfer catalysis
5. A photochromic composite with enhanced carrier separation for the photocatalytic activation of benzylic C–H bonds in toluene
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