4.6 Article

Hydrothermal synthesis of GO wrapped BiOCl nanosheet and its application in visible light assited catalytic degradation of Rhodamine B dye

Journal

MATERIALS CHEMISTRY AND PHYSICS
Volume 279, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.matchemphys.2022.125796

Keywords

BiOCl (Bismuth oxychloride); GO (Graphene oxide); BOC-GO (Nano-composite); Photocatalysis; Water remediation

Funding

  1. CSIR (Council of Scientific and Industrial Research) [09/096 (0872) /2016-EMR-I, 09/096 (0869) /2016-EMR-I, 09/096 (0896) /2017-EMR-I]
  2. DST (Department of Science and Technology) [IF170684]
  3. SERB [SERB/EEQ/2017/000092]
  4. UGC (University Grants Commission) [F-1-10/12]
  5. DST Nanomission
  6. DST (Department of Science and Technology)

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A nano-composite material, BOC-GO, based on BiOCl and GO was successfully synthesized using a two-step procedure involving chemical treatment and hydrothermal technique. BOC-GO exhibited efficient photocatalytic degradation of organic dye Rhodamine B (RhB), with a degradation rate of 99.6% within 60 min. The composite material showed good reusability and high catalytic performance due to the formation of heterojunction between GO and BiOCl, which improved charge carrier separation under visible light irradiation.
A two-step synthesis procedure involving chemical treatment followed by hydrothermal technique was applied for the development of a nano-composite (BOC-GO) material based on Bismuth oxychloride (BiOCl) and Graphene oxide (GO). BOC-GO was employed as an efficient photocatalyst to degrade organic textile dye Rhodamine B (RhB) up to 99.6% within 60 min. Moreover, the sample retained impressive degradation efficiency even after 3 catalytic cycles, which demonstrated the good reusability property of the catalyst. The appreciable catalytic performance has been associated with the improvement in the separation of charge carriers under visible light irradiation due to the formation of heterojunction between GO & BiOCl. The center dot O-2(-) (superoxide radical) & h(+) (photoinduced hole) highly contribute to the redox reactions. The crystal structures of both samples exhibited a significantly exposed (001) lattice plane along with highly crystalline nature, as evident from PXRD and HRTEM analyses. The composite material showed a higher BET surface area and average pore diameter which in turn facilitated the catalytic activity to a great extent.

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