Highly efficient photocatalytic degradation of different hazardous contaminants by CaIn2S4-Ti3C2Tx Schottky heterojunction: An experimental and mechanism study

Zhihao Zhuge, Xinjuan Liu, Taiqiang Chen, Yinyan Gong, Can Li, Lengyuan Niu, Shiqing Xu, Xingtao Xu, Zeid A. Alothman, Chang Q. Sun, Joseph G. Shapter, Yusuke Yamauchi

Research output: Contribution to journalArticlepeer-review

154 Citations (Scopus)

Abstract

The low charge transfer efficiency of isolated semiconductors is an urgent challenge in the photocatalytic degradation of hazardous contaminants. In this work, CaIn2S4/MXene Ti3C2Tx Schottky heterojunctions are synthesized via a simple hydrothermal method and applied for tetracycline hydrochloride degradation and Cr(VI) reduction. Results show that Ti3C2Tx as a cocatalyst can limit the charge recombination and boost the absorption of visible light, thus promoting the photocatalytic efficiency of pure CaIn2S4. An optimized CaIn2S4-Ti3C2Tx hybrid has the highest catalytic rate in the degradation of tetracycline hydrochloride (96%) and reduction of Cr(VI) (98%). Studies probing the mechanism indicate that the photogenerated superoxide radicals and holes play a key role in the tetracycline hydrochloride degradation process, while electrons are core to the Cr(VI) reduction reaction. Besides the high photocatalytic efficiency, the CaIn2S4-Ti3C2Tx hybrids also exhibit outstanding photo-stability in the present conditions, suggesting the potential for practical use.

Original languageEnglish
Article number127838
JournalChemical Engineering Journal
Volume421
DOIs
Publication statusPublished - 1 Oct 2021

Bibliographical note

Publisher Copyright:
© 2020 Elsevier B.V.

Keywords

  • CaInS
  • Charge separation
  • Co-catalyst
  • MXene
  • Schottky heterojunction

Fingerprint

Dive into the research topics of 'Highly efficient photocatalytic degradation of different hazardous contaminants by CaIn2S4-Ti3C2Tx Schottky heterojunction: An experimental and mechanism study'. Together they form a unique fingerprint.

Cite this