4.5 Article

Fabrication of flexible sheets of Cu/CuO/Cu2O heterojunction nanodisks: A dominant performance of multiple photocatalytic sheets under natural sunlight

出版社

ELSEVIER
DOI: 10.1016/j.mseb.2020.114652

关键词

Flexible sheet; CuO nanodisk; Cu/CuO/Cu2O heterojunction; Sunlight photocatalyst; Optical materials and properties; Nanocrystalline materials

资金

  1. Brain Pool program - Ministry of Science and ICT through the National Research Foundation of Korea [NRF-2019H1D3A2A01102099]
  2. National Research Foundation of Korea [2019H1D3A2A01102099] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Development of immobilized photocatalyst on a flexible sheet is an urgent need for wastewater treatment in industry. A facile method is established to fabricate flexible Cu/CuO/Cu2O heterojunction nanodisks. The existence of both phases of CuO and Cu2O are identified by XRD, oS and Raman spectroscopy. The combined CuO and Cu2O phases having different bandgaps are responsible for an improved photodegradation due to increased charge separation efficiency and an extended range of photoexcitation while decreasing recombination of photogenerated electrons and holes. For the first time, a single to several sheets of Cu/CuO/Cu2O heterojunction nanodisk are introduced to investigate the performance of photodegradation and continued to maximum of eight sheets. The superior photocatalytic performance of Cu/CuO/Cu2O heterojunction on rhodamine dye solution is observed and compared with recent reports related to the similar architecture. It is identified that the part of photoexcited electrons are consumed to oxidizes O-2 to generate superoxide radicals due to the closer oxidation potential between O-2/center dot O-2(-) and Cu2O, besides the transfer to the conduction band of CuO. Hence, the proposed flexible photocatalytic sheet benefits for the stable and continuous usage in a large-scale process to degrade toxic pollutants without sacrificing their photocatalytic activity.

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