Liu Yixuan, Xue Wenhua, Ye Jian, Zhang Ruilong, Rangappa Akkammagari Putta, Zhao Jun
Sino-Forest Applied Research Centre for Pearl River Delta Environment Department of Biology, Hong Kong Baptist University, Kowloon Tong, Hong Kong SAR, 999077, China.
Institute of Advanced Materials, Hong Kong Baptist University, Kowloon Tong, Hong Kong SAR, 999077, China.
Small. 2025 Apr;21(17):e2409005. doi: 10.1002/smll.202409005. Epub 2025 Mar 19.
The photocatalytic conversion of biomass feedstock represents a promising and environmentally friendly strategy for achieving selective transformation and value addition. The slow charge dynamics and sluggish hole transfer in the oxidation reactions severely limit the photocatalytic activity. Here, the heterojunction is fabricated by synthesizing ultra thin ZnInS nanoflower with spinel CuCoO. The internal and interfacial electric fields are successfully constructed, which shows superior 5-hydroxymethylfurfural (HMF) valorization. HMF undergoes severe mineralization when ZnInS is used as the catalyst, resulting in 0.9% 2,5-diformylfuran (DFF) yield in water, while the ZnInS/CuCoO heterojunction catalyst exhibits 77% DFF selectivity with 88.6% HMF conversion, The cascaded bulk and internal electric fields greatly reduce the oxidation potential of holes and enhance the charge separation efficiency, thus give a remarkable 70-fold increase in DFF yield. This work overcomes the limitations of ZnInS application for HMF and similar alcohol oxidation reactions that typically require organic solvents, achieving a high DFF evolution rate of 724.9 µmol·g·h in water within the first hour of the reaction, surpassing most reports of photocatalytic HMF selective oxidation.
生物质原料的光催化转化是实现选择性转化和增值的一种有前景且环境友好的策略。氧化反应中缓慢的电荷动力学和迟缓的空穴转移严重限制了光催化活性。在此,通过合成超薄的ZnInS纳米花与尖晶石CuCoO制备异质结。成功构建了内部和界面电场,其显示出优异的5-羟甲基糠醛(HMF)增值性能。当使用ZnInS作为催化剂时,HMF会发生严重矿化,在水中2,5-二甲基呋喃(DFF)产率为0.9%,而ZnInS/CuCoO异质结催化剂表现出77%的DFF选择性和88.6%的HMF转化率。级联的体相和内部电场极大地降低了空穴的氧化电位并提高了电荷分离效率,从而使DFF产率显著提高了70倍。这项工作克服了ZnInS在HMF及类似醇氧化反应应用中的局限性,这些反应通常需要有机溶剂,在反应的第一个小时内,在水中实现了724.9 µmol·g·h的高DFF生成速率,超过了大多数光催化HMF选择性氧化的报道。