4.7 Article

In-situ derived hierarchical ZnO/Zn-C nanofiber with high photocatalytic activity and recyclability under solar light

Journal

APPLIED SURFACE SCIENCE
Volume 491, Issue -, Pages 350-359

Publisher

ELSEVIER
DOI: 10.1016/j.apsusc.2019.06.159

Keywords

C-doped ZnO; 1-D nanofibers; Electrospinning; Photocurrent; Dye degradation

Funding

  1. Basic Science Research Program through the National Research Foundation of Korea (NRF) - Ministry of Education [2018R1D1A1B07048146]
  2. Korea Institute of Energy Technology Evaluation and Planning (KETEP) Grants - Ministry of Trade, Industry and Energy (MOTIE) [20174010201160]
  3. National Research Foundation of Korea [2018R1D1A1B07048146] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Carbon-doping in the crystal structure of ZnO has been proven to promote visible light induced photocatalytic activity. However, experimental procedures reported in literature to date for the fabrication of C-doped ZnO generally follow cumbersome steps and environmentally unfriendly techniques. In this study, we present a simple, relatively green and adaptable two-step synthesis using electrospinning and calcination techniques for the fabrication of C-doped ZnO nanofiber photocatalyst. Extensive characterization of the as-prepared nanofiber photocatalysts was made by XRD, XPS, FE-SEM, FE-TEM, EDS, N-2 adsorption, TGA, FT-IR, LSV and EIS analysis techniques. Depending on the calcination temperature, the crystallinity of the ZnO nanoparticles and amount of the polymer matrix on the nanofibers differ, which in turn tune the photocatalytic performance. Crystal structure and chemical state analysis confirm the C-doping and introduction of new energy level (Zn-C) in the ZnO crystal. Photoelectrochemical analysis proved the enhanced photocurrent response and reduced charge carrier recombination in the C-doped ZnO. The as-prepared photocatalyst exhibited high degradation efficiency (96% in 30 min) for the solar light mediated photodegradation of Methylene blue dye. The fibrous nature of the photocatalyst, with Carbon matrix wrapping around it, alleviates the recovery of the as-prepared photocatalyst from the reaction mixture and ensures its recyclability and protection against photo-corrosion. Considering the scalability and easiness of the experimental procedure, together with the enhanced photocatalytic activity and recyclability of the photocatalyst prepared, we believe this study open doors for the fabrication of high-performance photocatalytic materials at large scale.

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