选择性
材料科学
氢氧化物
催化作用
纳米线
膜
化学工程
X射线光电子能谱
肉桂醛
无机化学
纳米技术
有机化学
化学
生物化学
工程类
作者
Pengtang Wang,Qi Shao,Xiaoneng Cui,Xing Zhu,Xiaoqing Huang
标识
DOI:10.1002/adfm.201705918
摘要
Abstract Rational design of effective catalysts with both high activity and selectivity is highly significant and desirable for hydrogenation reaction. In this paper, for the first time an efficient approach to controllably construct 1D metal nanowires (NWs) coated with hydroxide (Ni x M(OH) 2 (M = Mn, Fe, Co, Cu, and Al)) membranes as highly active and selective hydrogenation catalysts is reported. The optimized Ni 32 Cu(OH) 2 membrane coated Pt 3 Ni nanowires show much enhanced selectivity of 87.9% for the hydrogenation of cinnamaldehyde to hydrocinnamaldehyde instead of hydrocinnamyl alcohol, in contrast with the pristine Pt 3 Ni nanowires and Pt 3 Ni nanowires on Ni(OH) 2 membranes. The enhanced selectivity of Pt 3 Ni@Ni 32 Cu(OH) 2 ‐2 NWs is ascribed to confinement/poisoning effects of the coated Ni 32 Cu(OH) 2 membranes as well as the intimate interaction between the Pt 3 Ni NWs and Ni 32 Cu(OH) 2 membranes, as confirmed by X‐ray photoelectron spectroscopy. The coated structures also show good stability after five recycle runs. The present work highlights the importance of surface engineering for the design of multicomponent composites with desirable activity and selectivity toward hydrogenation reaction and beyond.
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