Construction of a BiOI/g-C 3 N 4 heterojunction photocatalyst: visible light-mediated efficient and selective oxidation of 5-hydroxymethylfurfural
The escalating demand for sustainable energy has intensified the search for photocatalysts capable of harnessing solar energy for chemical conversions, with a particular focus on non-noble metal catalysts. This study presents the synthesis of a novel BiOI/g-C 3 N 4 heterojunction photocatalyst via a...
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Veröffentlicht in: | New journal of chemistry 2025-01, Vol.49 (5), p.1607-1618 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The escalating demand for sustainable energy has intensified the search for photocatalysts capable of harnessing solar energy for chemical conversions, with a particular focus on non-noble metal catalysts. This study presents the synthesis of a novel BiOI/g-C 3 N 4 heterojunction photocatalyst via an ultrasound-assisted co-precipitation method, demonstrating its efficiency in the visible light-mediated oxidation of 5-hydroxymethylfurfural (HMF) to 5-hydroxymethyl-2-furancarboxylic acid (HMFCA). The innovative synthesis approach ensures a well-crystallized and uniformly dispersed composite, critical for optimizing photocatalytic performance. By meticulously adjusting the composite ratio, this study fine-tunes the electronic structure and optoelectronic properties, enhancing light absorption and charge carrier dynamics. The BiOI/g-C 3 N 4 photocatalyst achieved a maximum HMFCA yield of 43.6% and selectivity of 68.1% under visible light irradiation, showcasing its potential for sunlight-driven biomass conversion. Moreover, the catalyst exhibited excellent stability and reusability, retaining performance after five recycling cycles with only a 6.6% decrease in HMFCA yield. This work not only advances the understanding of non-noble metal photocatalysts for sustainable biomass conversion but also aligns with the principles of green chemistry by employing a renewable resource-based approach and minimizing environmental impact. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/D4NJ04937C |