Tailoring a Dynamic Metal-Polymer Interaction to Improve Catalyst Selectivity and Longevity in Hydrogenation

被引:21
作者
Hyun, Kyunglim [1 ]
Park, Younghwan [1 ]
Lee, Songhyun [1 ]
Lee, Jueun [1 ]
Choi, Yeonwoo [1 ]
Shin, Seung-Jae [2 ]
Kim, Hyungjun [2 ]
Choi, Minkee [1 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Chem & Biomol Engn, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol KAIST, Dept Chem, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
DMPI; metal– support interactions; palladium; partial hydrogenation; polymers;
D O I
10.1002/anie.202100814
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Controlling metal-support interactions is important for tuning the catalytic properties of supported metal catalysts. Here, premade Pd particles are supported on stable polymers containing different ligating functionalities to control the metal-polymer interactions and their catalytic properties in industrially relevant acetylene partial hydrogenation. The polymers containing strongly ligating groups (e.g., Ar-SH and Ar-S-Ar) can form a polymer overlayer on the Pd surface, which enables selective acetylene adsorption and partial hydrogenation to ethylene without deactivation. In contrast, polymers with weakly ligating groups (e.g., Ar-O-Ar) do not form an overlayer, resulting in non-selective hydrogenation and fast deactivation, similar to Pd catalysts on conventional inorganic supports. The results imply that tuning the metal-polymer interactions via rational polymer design can provide an efficient way of synthesizing selective and stable catalysts for hydrogenation.
引用
收藏
页码:12482 / 12489
页数:8
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