4.5 Article

Bromine doped g-C3N4 with enhanced photocatalytic reduction in U(VI)

Journal

RESEARCH ON CHEMICAL INTERMEDIATES
Volume 48, Issue 1, Pages 49-65

Publisher

SPRINGER
DOI: 10.1007/s11164-021-04568-7

Keywords

Bromine doping; Graphitic carbon nitride; Uranium; Visible-light photocatalysis; Semiconductor

Funding

  1. National Natural Science Foundation of China [21966003, 11765002]
  2. National Natural Science Foundation of Jiangxi [20181BAB203019]
  3. Open Fund of Jiangxi Province Key Laboratory of Synthetic Chemistry [JXSC202006]
  4. Research Foundation for Advanced Talents [DHBK2019131]

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This study utilized NH4Br as a source of bromide to conduct bromine doping in g-C3N4, aiming to enhance its light absorption and efficiency in photocatalytic reduction of uranium. The resulting materials demonstrated a smaller band gap, indicating an extended light absorption range. Compared to bulk carbon nitride, the efficiency of photocatalytic reduction of uranium was increased by 2.2 times, with good stability over five cycles.
In the process of uranium mining and smelting, large quantities of low-concentration uranium-containing wastewater have been produced. It is an ideal solution to remove and recover dissociative uranium from contaminated sites and water systems particularly with the method of photocatalysis. Due to the unique electronic structure and optical properties, graphitic carbon nitrides (g-C3N4) cover ranges of photocatalytic applications in the environment and energy fields. However, g-C3N4 still face some inherent defects, such as high recombination rate of charge carriers, low electrical conductivity and lack of visible-light absorption. In order to improve its light absorption and the efficiency of photocatalytic reduction in uranium, NH4Br was used as the bromide source to conduct bromine doping in g-C3N4. The resulting materials show a smaller band gap, proving an extended light absorption range. Compared with bulk carbon nitride, the efficiency of photocatalytic reduction in uranium is increased by 2.2 times with good stability in five cycles. This study provides an effective strategy to construct a stable and efficient visible-light-responsive photocatalyst in the reduction in radioactive uranium.

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