Rational optimization of 2D Bi2MoO6 nanopiece@2D g‐C3N4 nanoflake composite for boosting photocatalytic performance of hydrogen evolution rate and organic dye removal

BACKGROUND Preparing catalysts with heterojunction structures is a strategy to achieve efficient charge separation and transfer of charges to enhance photocatalytic activity of photocatalysts. To optimize the graphitic carbon nitride (g‐C3N4)‐based photocatalysts, Bi2MoO6@ 2D g‐C3N4 catalyst was pre...

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Veröffentlicht in:Journal of chemical technology and biotechnology (1986) 2024-03, Vol.99 (3), p.674-684
Hauptverfasser: Wang, Zhentao, Wang, Jingjing, Iqbal, Waheed, Qiao, Yuxin, Liu, Shuxin, Qin, Chuanguang
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Sprache:eng
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Zusammenfassung:BACKGROUND Preparing catalysts with heterojunction structures is a strategy to achieve efficient charge separation and transfer of charges to enhance photocatalytic activity of photocatalysts. To optimize the graphitic carbon nitride (g‐C3N4)‐based photocatalysts, Bi2MoO6@ 2D g‐C3N4 catalyst was prepared. RESULTS 2D Bi2MoO6 nanopiece@2D g‐C3N4 nanoflake composites in different proportions were prepared by the hydrothermal method. The prepared materials were characterized by various modern instrumental analyses, and their photocatalytic ability to decompose water and degrade rhodamine B under visible light irradiation was tested. Compared with pure Bi2MoO6 nanopiece and g‐C3N4 nanoflake, the hydrogen evolution rate of Bi2MoO6 nanopiece@g‐C3N4 nanoflake (1:10) composite was highest, at 4847 μmol h−1 g−1. The composite (3:10) exhibited significantly enhanced photocatalytic rhodamine B degradation for organic dye removal due to the formation of an excellent heterojunction to improve the separation and migration efficiency of photogenerated carriers. CONCLUSION O2− and •OH were the two main active species in the photocatalytic degradation of rhodamine B. Bi2MoO6 formed a heterojunction with g‐C3N4, which accelerated separation and migration efficiency, thereby enhancing the photocatalytic activity. © 2023 Society of Chemical Industry (SCI).
ISSN:0268-2575
1097-4660
DOI:10.1002/jctb.7572