嵌入
激光器
化学
组合化学
光学
物理
计算机科学
人工智能
作者
Jiulong Wang,Jie Jian,Xixiang Jing,Yazhou Shuang,Shiyuan Wang,Fang Wang,Zelin Ma,Pengfei Guo,Dmitry G. Shchukin,В. А. Винокуров,А. А. Новиков,А. P. Glotov,Junmin Xue,Tengfei Cao,Xiaoli Fan,Hongqiang Wang
标识
DOI:10.1016/j.cej.2024.153334
摘要
Selective hydrogenation of vinyl groups (C = C) and carbonyl groups (C = O) is of significance to effectively convert low-value organic compounds into high-value target chemicals, while a challenge remains on the hydrogenation of C = C bond that is in π-bond conjugation with the C = O bond. Herein, we address this challenge based on a synergetic modulation strategy on electronic structure and adsorption configurations to achieve a highly selective hydrogenation of the C = C bond, achieved by laser-assisted embedding of PdxCu bimetals in the ZIF-8 bulk phase (x represents the Pd/Cu molar ratio in PdCu nanoparticles). It is revealed that laser assisted synthesis of PdxCu bimetals not only inhibits the hydrogenation of C = O and promotes the hydrogenation of C = C, but also results in an arched absorption configuration for substrate molecules that facilitates the selective hydrogenation of vinyl groups. Exemplified by cinnamaldehyde (CAL), the present work achieves 98.03 % conversion of CAL and 100 % selectivity of the hydrocinnamaldehyde (HCAL) (70 °C, 1 MPa H2, 1 h), indicating the potential of laser-matter interaction to tackle the trade-off between conversion efficiency and selectivity in thermal catalysis.
科研通智能强力驱动
Strongly Powered by AbleSci AI