肉桂醛
催化作用
选择性
碳化
碳纤维
材料科学
转移加氢
X射线光电子能谱
电子转移
金属
无机化学
化学
化学工程
光化学
有机化学
扫描电子显微镜
复合数
钌
复合材料
工程类
作者
Yongwang Ren,Huizhong Xu,Beibei Han,Jing Xu
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2023-05-17
卷期号:28 (10): 4136-4136
被引量:9
标识
DOI:10.3390/molecules28104136
摘要
At present, the selective hydrogenation of α, β-unsaturated aldehydes remains a challenge due to competition between unsaturated functional groups (C=C and C=O). In this study, N-doped carbon deposited on silica-supported nickel Mott–Schottky type catalysts (Ni/SiO2@NxC) was prepared for the selective hydrogenation of cinnamaldehyde (CAL) by using the respective hydrothermal method and high-temperature carbonization method. The prepared optimal Ni/SiO2@N7C catalyst achieved 98.9% conversion and 83.1% selectivity for 3-phenylpropionaldehyde (HCAL) in the selective hydrogenation reaction of CAL. By constructing the Mott–Schottky effect, the electron transfer from metallic Ni to N-doped carbon at their contact interface was promoted, and the electron transfer was demonstrated by XPS and UPS. Experimental results indicated that by modulating the electron density of metallic Ni, the catalytic hydrogenation of C=C bonds was preferentially performed to obtain higher HCAL selectivity. Meanwhile, this work also provides an effective way to design electronically adjustable type catalysts for more selective hydrogenation reactions.
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