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用于阳光驱动香草醇向香草醛高选择性催化氧化并耦合析氢反应的NiS/Cd Zn S肖特基结双功能光催化剂

NiS/Cd Zn S Schottky Junction Bifunctional Photocatalyst for Sunlight-Driven Highly Selective Catalytic Oxidation of Vanillyl Alcohol Towards Vanillin Coupled with Hydrogen Evolution Reaction.

作者信息

Du Rui, Wang Chuantao, Guo Li, Soomro Razium Ali, Xu Bin, Yang Chunming, Fu Feng, Wang Danjun

机构信息

Shaanxi Key Laboratory of Chemical Reaction Engineering, College of Chemistry & Chemical Engineering, Yan'an University, Yan'an, 716000, P. R. China.

State Key Laboratory of Organic-Inorganic Composites Beijing Key Laboratory of Electrochemical Process and Technology for Materials, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

出版信息

Small. 2023 Sep;19(39):e2302330. doi: 10.1002/smll.202302330. Epub 2023 May 31.

DOI:10.1002/smll.202302330
PMID:37259262
Abstract

Selective oxidation of biomass-based molecules to high-value chemicals in conjunction with hydrogen evolution reaction (HER) is an innovative photocatalysis strategy. The key challenge is to design bifunctional photocatalysts with suitable band structures, which can achieve highly efficient generation of high-value chemicals and hydrogen. Herein, NiS/Cd Zn S Schottky junction bifunctional catalysts are constructed for sunlight-driven catalytic vanillyl alcohol (VAL) selective oxidation towards vanillin (VN) coupling HER. At optimal conditions, the 8% NiS/Cd Zn S photocatalyst achieves high activity of VN production (3.75 mmol g h ) and HER (3.84 mmol g h ). It also exhibits remarkable VAL conversion (66.9%), VN yield (52.1%), and selectivity (77.8%). The photocatalytic oxidation of VAL proceeds a carbon-centered radical mechanism via the cleavage of α bond. Experimental results and theoretical calculations show that NiS with metallic properties enhances the electron transfer capability. Importantly, a Ni-S-Cd "electron bridge" formed at the interface of NiS/Cd Zn S further improves the separation/transfer of electrone/h pairs and also furnishes HER active sites due to its smaller the |ΔG | value, thereby resulting in a remarkably HER activity. This work sheds new light on the selective catalytic oxidation VAL to VN coupling HER, with a new pathway towards achieving its efficient HER efficiency.

摘要

将基于生物质的分子选择性氧化为高价值化学品并同时进行析氢反应(HER)是一种创新的光催化策略。关键挑战在于设计具有合适能带结构的双功能光催化剂,以实现高价值化学品和氢气的高效生成。在此,构建了NiS/CdZnS肖特基结双功能催化剂,用于阳光驱动催化香草醇(VAL)选择性氧化为香草醛(VN)并耦合HER。在最佳条件下,8%的NiS/CdZnS光催化剂实现了高产率的VN生成(3.75 mmol g h)和HER(3.84 mmol g h)。它还表现出显著的VAL转化率(66.9%)、VN产率(52.1%)和选择性(77.8%)。VAL的光催化氧化通过α键的断裂以碳中心自由基机制进行。实验结果和理论计算表明,具有金属性质的NiS增强了电子转移能力。重要的是,在NiS/CdZnS界面形成的Ni-S-Cd“电子桥”进一步改善了电子/空穴对的分离/转移,并且由于其较小的|ΔG|值还提供了HER活性位点,从而产生了显著的HER活性。这项工作为VAL选择性催化氧化为VN并耦合HER提供了新的思路,为实现其高效HER效率开辟了一条新途径。

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