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Performance study of g-C3N4/carbon black/BiOBr@Ti3C2/MoS2 photocatalytic fuel cell for the synergistic degradation of different types of pollutants

  • Carbon Letters
  • Abbr : Carbon Lett.
  • 2023, 33(3), pp.847-862
  • DOI : 10.1007/s42823-023-00465-8
  • Publisher : Korean Carbon Society
  • Research Area : Natural Science > Natural Science General > Other Natural Sciences General
  • Received : September 23, 2022
  • Accepted : December 21, 2022
  • Published : May 1, 2023

Guo Huilin 1,  Yu Tingting 1,  Zhao Lei 1,  Qian Jun 2,  Yu Jiahe 1,  Zhang Yu 3,  Teng Yongyue 4,  Zhu Chunshui 1,  Yang Tao 1,  Chen Wenbin 1,  Gong Picheng 1,  Jiang Cuishuang 1,  Gao Changfei 5,  Yang Bing 1,  Yang Chenyu 1

1School of Environmental and Chemical Engineering, Jiangsu Ocean University
2CECEP Zhaosheng Environmental Protection Co.
3Lianyungang Gaopin Renewable Resources Co.
4School of Ecological and Environmental Sciences, East China Normal University
5School of Environmental and Material Engineering, Yantai University

Accredited

ABSTRACT

In this study, a bipolar visible light responsive photocatalytic fuel cell (PFC) was constructed by loading a Z-scheme g-C3N4/carbon black/BiOBr and a Ti3C2/MoS2 Schottky heterojunction on the carbon brush to prepare the photoanode and photocathode, respectively. It greatly improved the electron transfer and achieved efficient degradation of organic pollutants such as antibiotics and dyes simultaneously in two chambers of the PFC system. The Z-scheme g-C3N4/carbon black/BiOBr formed by adding highly conductive carbon black to g-C3N4/BiOBr not only effectively separates the photogenerated carriers, but also simultaneously retains the high reduction of the conduction band of g-C3N4 and the high oxidation of the valence band of BiOBr, improving the photocatalytic performance. The exceptional performance of Ti3C2/MoS2 Schottky heterojunction originated from the superior electrical conductivity of Ti3C2 MXene, which facilitated the separation of photogenerated electron–hole pairs. Meanwhile, the synergistic effect of the two photoelectrodes further improved the photocatalytic performance of the PFC system, with degradation rates of 90.9% and 99.9% for 50 mg L−1 tetracycline hydrochloride (TCH) and 50 mg L−1 rhodamine-B (RhB), respectively, within 180 min. In addition, it was found that the PFC also exhibited excellent pollutant degradation rates under dark conditions (79.7%, TCH and 97.9%, RhB). This novel pollutant degradation system is expected to provide a new idea for efficient degradation of multiple pollutant simultaneously even in the dark.

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Scopus Citation Counts (13) This is the result of checking the information with the same ISSN, publication year, volume, and start page between articles in KCI and the SCOPUS journals. (as of 2024-07-01)

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