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InP quantum dots on g-C3N4 nanosheets to promote molecular oxygen activation under visible light
Affiliation:1. State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation, Southwest Petroleum University, Chengdu 610500, China;2. The Center of New Energy Materials and Technology, School of New Energy and Materials, Southwest Petroleum University, Chengdu 610500, China;1. School of Materials Science and Engineering, Southwest Petroleum University, Chengdu 610500, China;2. Chengdu Institute of Organic Chemistry, Chinese Academy of Science, Chengdu 610041, China;1. The Center of New Energy Materials and Technology, School of Materials Science and Engineering, Southwest Petroleum University, Chengdu, 610500, China;2. State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation, Southwest Petroleum University, Chengdu 610500, China;1. Research Center for Environmental Science & Technology, Institute of Fundamental and Frontier Sciences, University of Electronic Science and Technology of China, Chengdu 611731, China;2. School of Resources and Environment, University of Electronic Science and Technology of China, Chengdu 611731, China;3. Department of Environmental Science and Engineering, Fuzhou University, Fuzhou 350108, China;4. The Center of New Energy Materials and Technology, School of New Energy and Materials, Southwest Petroleum University, Chengdu 610500, China;5. College of Materials Science and Engineering, Chongqing University, Chongqing 400044, China
Abstract:Largely limited by the high dissociation energy of the Osingle bondO bond, the photocatalytic molecular oxygen activation is highly challenged, which restrains the application of photocatalytic oxidation technology for atmospheric pollutants removal. Herein, we design and fabricate the InP QDs/g-C3N4 compounds. The introduction of InP QDs promotes the charge transfer within the interface resulting in the effective separation of photo-generated carriers. Furthermore, InP QDs greatly facilitates the activation of molecular oxygen and promote the formation of O2radical dot? under visible-light illumination. These conclusions are identified by experimental and calculation results. Hence, NO can be combined with the O2radical dot? to form Osingle bondOsingle bondNsingle bondO intermediate to direct conversion into NO3?. As a result, the NO removal ratio of g-C3N4 has a onefold increase after InP QDs loaded and the generation of NO2 is effectively inhibited. This work may provide a strategy to design highly efficient materials for molecular oxygen activation.
Keywords:InP quantum dots  Molecular oxygen activation  Photocatalytic NO removal
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