选择性
材料科学
苯甲醇
光催化
苯甲醛
催化作用
激进的
吸附
光化学
组合化学
纳米技术
有机化学
化学
作者
Ran Wang,Li Shi,Elena Yu. Konysheva,Xiaoxiang Xu
标识
DOI:10.1002/adfm.202418074
摘要
Abstract Photocatalytic conversion of benzyl alcohol (BA) is a promising means to coproduce H 2 with value‐added chemicals. However, there is a lack of an efficient strategy to regulate the selectivity of the BA conversion products. Here, by a simple cocatalyst engineering technique, the selective conversion of BA over Zn 2 In 2 S 5 nanosheets (ZIS) is maneuvered. Two types of cocatalysts, i.e., Pt and Cd, are photo‐deposited onto ZIS that can shift the selectivity to diverse products, namely, Pt to benzaldehyde (BAD) and Cd to the carbon‐carbon (C─C) coupling compounds. Mechanistic studies indicate that Cd has a high reducing capacity to convert BAD back to the ketyl radical (C 𝛼 radical), favoring the construction of the C─C bonds. Pt, however, facilitates the generation of C 𝛼 radicals but is energetically unfavorable for their coupling reactions, resulting in the generation of BAD as the main product. Theoretical calculation reveals that the distinct catalytic behaviors of Pt and Cd stem from their different electronic structures that govern the adsorption strength to the reaction intermediates and the reaction energy barriers of the C─C coupling step. This work not only addresses the challenge of selectivity regulation for BA conversion but also brings fresh mechanistic insights into the role of the cocatalysts.
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