Journal of Inorganic Materials

• Original article •     Next Articles

Ligand-hydroxylated UiO-66 for Enhanced Photothermally Catalytic VOCs Oxidation

CHEN Xiaochen1,2(), WANG Yang2, YANG Bin1, WANG Min2, A Bohan2, WANG Man2, ZHANG Lingxia1,2()   

  1. 1 School of Chemistry and Materials Science, Hangzhou Institute for Advanced Study, University of Chinese Academy of Sciences, Hangzhou 310024, China
    2 Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China
  • Received:2025-04-13 Revised:2025-06-26
  • Contact: ZHANG Lingxia, professor. E-mail: zhlingxia@mail.sic.ac.cn
  • About author:CHEN Xiaochen (1999-), male, Master candidate. E-mail: chenxiaochen22@mails.ucas.ac.cn
  • Supported by:
    National Natural Science Foundation of China (22405287); Science and Technology Commission of Shanghai (24DZ2201600, 24ZR1475800); China Postdoctoral Science Foundation (2024M760699)

Abstract:

The efficient removal of low-concentration volatile organic compounds (VOCs) in indoor and industrial environments remains a significant challenge. Metal-organic frameworks (MOFs) are potential oxidation catalysts due to their superior adsorption enrichment capability for low-concentration VOCs. In this work, hydroxyl-containing ligands were introduced into UiO-66, and the as-synthesized UiO-66-OH catalyst exhibited exceptional photothermal catalytic performance on oxidation of flowing low-concentration VOCs (an initial concentration of 0.075 mg/L for toluene and 0.064 mg/L for benzene, a weight hourly space velocity (WHSV) of 30000 mL/(g∙h)), achieving 97% and 90% conversion of toluene and benzene, respectively, surpassing the reported photothermal catalysts such as metal oxides and noble-metal-loaded catalysts. Such impressive activity is attributed to the synergy of thermal catalysis and photocatalysis. Ligand hydroxylation optimizes the electron structure and the ligand-to-metal charge transfer (LMCT) effect, enhancing light absorption, improving electron-hole separation efficiency and photothermal properties of UiO-66. Hydroxyl introduction promotes the formation of oxygen vacancies, facilitating oxygen adsorption/activation to sustain lattice oxygen (Olatt) and generate superoxide radical (∙O2-), which are the dominant reactive species in VOCs oxidation. This work not only presents the potential of MOFs as efficient photothermal catalysts for the oxidation of low-concentration VOCs but also shows prospective on facile modulation of electron structure by ligand engineering to enhance the photothermal properties of MOFs.

Key words: volatile organic compound, low concentration, metal-organic framework, photothermal catalysis, ligand-to-metal charge transfer effect

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