Journal of Inorganic Materials ›› 2025, Vol. 40 ›› Issue (5): 481-488.DOI: 10.15541/jim20240495

• RESEARCH ARTICLE • Previous Articles     Next Articles

Organic Pollutant Fenton Degradation Driven by Self-activated Afterglow from Oxygen-vacancy-rich LiYScGeO4: Bi3+ Long Afterglow Phosphor

FAN Xiaoxuan(), ZHENG Yonggui, XU Lirong, YAO Zimin, CAO Shuo, WANG Kexin(), WANG Jiwei()   

  1. College of Physics, Liaoning University, Shenyang 110036, China
  • Received:2024-11-27 Revised:2025-01-24 Published:2025-05-20 Online:2025-02-13
  • Contact: WANG Kexin, lecturer. E-mail: wyf93jl@163.com;
    WANG Jiwei, professor. E-mail: wangjiwei@lnu.edu.cn
  • About author:FAN Xiaoxuan (1997-), female, PhD candidate. E-mail: fanxiaoxuan0314@163.com
  • Supported by:
    National Natural Science Foundation of China(12374181);Fundamental Research Funds for Public Universities in Liaoning(LJ212410140035);Natural Science Foundation of Shenyang(22-315-6-06);Youth Research Fund in Liaoning University(LDYBJC2401)

Abstract:

Self-activated long afterglow photocatalysts show great potential for all-weather wastewater treatment, with sustained photocatalytic activity even under dark conditions. However, the radiative combination of afterglow luminescence and photocatalytic degradation reaction has competitive utilization for photogenerated carriers, reducing afterglow duration and generating excessive hole accumulation, which significantly limits the efficiency of long afterglow driven photocatalytic degradation. Here, a long afterglow photocatalyst LiYGeO4: Bi3 based on oxygen vacancy (VO) was prepared, which released ultraviolet afterglow after activation by ultraviolet light irradiation and degraded organic pollutants via photocatalytic degradation driven by its own afterglow in dark condition. The trap concentration was improved by engineering oxygen vacancies and crystal fields, significantly enhancing the afterglow duration and intensity of VO-LiYScGeO4: Bi3+. A Fenton reaction system was constructed to further increase the concentration of active species, which maximized the photocatalytic degradation efficiency of VO-LiYScGeO4: Bi3+ during the afterglow duration. After 10 min UV irradiation to activate VO-LiYScGeO4: Bi3+ continuously released ultraviolet afterglow for photocatalytic degradation of Rhodamine B (RhB), reaching a degradation efficiency of 63% within 1 h in Fenton environment, which increased by 3.5 folds when compared to that of LiYScGeO4: Bi3+ in the initial environment. This work provides a new approach for the design of afterglow photocatalysts and their application in wastewater treatment.

Key words: photocatalysis, photo-Fenton, oxygen vacancy, long afterglow, phosphor

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