4.6 Article

Characteristic studies of Ta3N5/BSC@PANI nanocomposites for hydrogen production via water-splitting under visible light irradiation

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CHEMICAL ENGINEERING RESEARCH & DESIGN
卷 197, 期 -, 页码 572-580

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ELSEVIER
DOI: 10.1016/j.cherd.2023.07.050

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Biomass soot carbon (BSC); Polyaniline (PANI); Photocatalyst; H-2 production

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The production of hydrogen in water-splitting can be greatly enhanced by designing efficient and cost-effective photocatalysts. This study focuses on investigating the photocatalytic activity of soot carbon-based metal nitrides nanocomposites under solar light exposure. The results show that by modifying a Ta3N5/PANI composite photocatalyst with biomass soot carbon, the hydrogen production rate can be significantly increased compared to pure Ta3N5, thanks to the formation of a p-n heterojunction at the interface of PANI and Ta3N5.
Hydrogen (H-2) production in water-splitting could be significantly increased by designing cost-effective photocatalysts with remarkable performance. The main objective of this study is to recognize the behavior of soot carbon-based metal nitrides nanocomposites on its photocatalytic activity when exposed to solar lights. This study synthesized a p-n heterojunction Ta3N5/PANI composite photocatalyst modified by eco-friendly and low-cost biomass soot carbon (BSC) using hydrothermal and chemisorption methods. BSC materials are photoactive when exposed to UV light because of their band gap (E-g < 4 eV), indicating they behave as semiconductors. Compared to pure Ta3N5, the hydrogen production rate of a photocatalyst containing polyaniline (PANI) can reach up to 76.9 mu mol g(-1) h(-1), equivalent to 3.42 times superior to pristine Ta3N5. The formation of a p-n heterojunction at the interface of PANI and Ta3N5 was primarily responsible for improving the H-2 evolution activity. This successfully prevents the self-photocorrosion of Ta3N5 by providing a rapid route for the migration and separation of photogenerated charges. It also confirms the long-term stability of the materials by repeating the experiments up to 6 cycles with more than 95 %.

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