4.6 Article

F- Serve as Surface Trapping Sites to Promote the Charge Separation and Transfer of TiO2

Journal

ACS OMEGA
Volume 6, Issue 51, Pages 35799-35809

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.1c05891

Keywords

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Funding

  1. National Natural Science Foundation of China [21902140]
  2. Foundation of State Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering [2021-K47]
  3. Nanhu Scholars Program for Young Scholars of XYNU

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In this study, surface fluorination modification of TiO2 was found to enhance charge transfer and separation processes, resulting in improved photocatalytic activity. Surface F- may act as trapping sites to boost the efficiency of charge transfer and separation.
Finding an effective strategy to promote the charge transfer and separation of TiO2 is urgently needed. Herein, a surface fluorination (F-)- modified TiO2 (denoted as TO-xF, where x represents the volume of HF added in the solution) catalyst has been prepared by a mild and facile post-treatment method. The changes induced by surface F- on the morphological, structural, and surface electronic features and the charge separation and transfer efficiency of TiO2 were specifically examined. Compared with pristine TO, TO-0.4F exhibits enhanced photocatalytic degradation of methyl orange and phenol, production of hydroxyl radicals, and photocurrent response. The enhanced photocatalytic activities of TO-0.4F can be attributed to the role of surface F- as surface trapping sites in effectively boosting the charge transfer and separation processes, which is verified by the steady-state and time-resolved fluorescence spectroscopy, electrochemical impedance spectroscopy, Bode plot, transient photocurrent response, and open-circuit voltage measurements. This study emphasizes the role of surface F- in promoting the charge transfer and separation and improving the photocatalytic activity of TiO2.

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