Bismuth vanadate/MXene (BiVO4/Ti3C2) heterojunction composite: enhanced interfacial control charge transfer for highly efficient visible light photocatalytic activity

We have synthesized BiVO 4 /Ti 3 C 2 nanocomposite via a low-cost hydrothermal method and investigate its photocatalytic degradation activity against monoazo (methyl orange) and diazo dye (Congo red) in an aqueous solution under visible light. The physiochemical characterization exhibited that the a...

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Published in:Environmental science and pollution research international Vol. 28; no. 27; pp. 35911 - 35923
Main Authors: Sajid, Muhammad Munir, Khan, Sadaf Bashir, Javed, Yasir, Amin, Nasir, Zhang, Zhengjun, Shad, Naveed Akhtar, Zhai, Haifa
Format: Journal Article
Language:English
Published: Berlin/Heidelberg Springer Berlin Heidelberg 01-07-2021
Springer Nature B.V
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Summary:We have synthesized BiVO 4 /Ti 3 C 2 nanocomposite via a low-cost hydrothermal method and investigate its photocatalytic degradation activity against monoazo (methyl orange) and diazo dye (Congo red) in an aqueous solution under visible light. The physiochemical characterization exhibited that the addition of MXene in pristine BiVO 4 nanocomposite led to an increase in specific surface area and reduction in optical band gap energy. MXene also helps in enhancing visible light response via a higher electron-hole pair generation rate and long lifetime. The synthesized BiVO 4 /Ti 3 C 2 heterojunction composite exhibited 99.5 % degradation efficiency within 60 min for Congo red and 99.1 % for methyl orange solution in 130 min owed to a large specific surface area (1.79 m 2 /g), reduced band gap (1.99 eV), and low recombination rate of charge carriers. The chemical mechanism for BiVO 4 /Ti 3 C 2 nanocomposite proposes that Ti 3 C 2 role-plays as electron capture because of the higher potential of MXenes, tuning band gap energy which paves the way to excellent photocatalytic action. This work opens a new basis for developing Ti 3 C 2 based promising and inexpensive co-catalyst for efficient solar utilization in photocatalytic-related applications in the future.
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ISSN:0944-1344
1614-7499
DOI:10.1007/s11356-021-13315-9