Xiong Renzhi, Liu Fangde, Xiao Xiao, Wu Yuhao, Xiao Yanhe, Cheng Baochang, Lei Shuijin
School of Physics and Materials Science, Nanchang University, Nanchang 330031, PR China.
School of Physics and Materials Science, Nanchang University, Nanchang 330031, PR China.
J Colloid Interface Sci. 2025 Aug 15;692:137555. doi: 10.1016/j.jcis.2025.137555. Epub 2025 Apr 9.
While photocatalytic oxidation of 5-hydroxymethylfurfural (HMF) into valuable chemicals represents a crucial strategy for advancing carbon neutrality, low conversion rates and poor product selectivity hinder commercialization. In this study, a dual-sulfur-vacancy (S)-mediated CuZnSnS/ZnInS all-multinary-sulfide p-n heterojunction was designed for high-efficiency photocatalysis. Specifically, S introduction significantly enhanced light absorption, photothermal properties, and interfacial electric fields (IEF). Consequently, the CuZnSnS/ZnInS heterostructure achieved outstanding photothermal-assisted photocatalytic oxidation of HMF to 2,5-diformylfuran (DFF), with an oxidation rate of 94.1%, which was 9.1 and 4.0 times higher than that of CuZnSnS and ZnInS, respectively. The selectivity of DFF reached 92.8%. Additionally, mechanistic analysis identified primary active species and possible reaction pathways. This study provides a potential strategy for the design of photocatalytic systems for efficient HMF oxidation.
虽然将5-羟甲基糠醛(HMF)光催化氧化为有价值的化学品是推进碳中和的关键策略,但低转化率和差的产物选择性阻碍了其商业化。在本研究中,设计了一种双硫空位(S)介导的CuZnSnS/ZnInS全多元硫化物p-n异质结用于高效光催化。具体而言,引入S显著增强了光吸收、光热性能和界面电场(IEF)。因此,CuZnSnS/ZnInS异质结构实现了将HMF光热辅助光催化氧化为2,5-二糠醛(DFF),氧化率为94.1%,分别比CuZnSnS和ZnInS高9.1倍和4.0倍。DFF的选择性达到92.8%。此外,机理分析确定了主要活性物种和可能的反应途径。本研究为设计高效HMF氧化光催化系统提供了一种潜在策略。