Rengshausen Simon, Van Stappen Casey, Levin Natalia, Tricard Simon, Luska Kylie L, DeBeer Serena, Chaudret Bruno, Bordet Alexis, Leitner Walter
Max Planck Institute for Chemical Energy Conversion, Stiftstrasse 34-36, Mülheim an der Ruhr, 45470, Germany.
Institut für Technische und Makromolekulare Chemie, RWTH Aachen University, Worringerweg 2, Aachen, 52074, Germany.
Small. 2021 Feb;17(5):e2006683. doi: 10.1002/smll.202006683. Epub 2020 Dec 21.
The synthesis, characterization, and catalytic properties of bimetallic cobalt-rhodium nanoparticles of defined Co:Rh ratios immobilized in an imidazolium-based supported ionic liquid phase (Co Rh @SILP) are described. Following an organometallic approach, precise control of the Co:Rh ratios is accomplished. Electron microscopy and X-ray absorption spectroscopy confirm the formation of small, well-dispersed, and homogeneously alloyed zero-valent bimetallic nanoparticles in all investigated materials. Benzylideneacetone and various bicyclic heteroaromatics are used as chemical probes to investigate the hydrogenation performances of the Co Rh @SILP materials. The Co:Rh ratio of the nanoparticles is found to have a critical influence on observed activity and selectivity, with clear synergistic effects arising from the combination of the noble metal and its 3d congener. In particular, the ability of Co Rh @SILP catalysts to hydrogenate 6-membered aromatic rings is found to experience a remarkable sharp switch in a narrow composition range between Co Rh (full ring hydrogenation) and Co Rh (no ring hydrogenation).
本文描述了固定在咪唑基负载离子液体相(Co Rh@SILP)中的具有特定Co:Rh比例的双金属钴 - 铑纳米颗粒的合成、表征及催化性能。采用有机金属方法实现了对Co:Rh比例的精确控制。电子显微镜和X射线吸收光谱证实了在所有研究材料中均形成了小尺寸、高度分散且均匀合金化的零价双金属纳米颗粒。使用亚苄基丙酮和各种双环杂芳烃作为化学探针来研究Co Rh@SILP材料的氢化性能。发现纳米颗粒的Co:Rh比例对观察到的活性和选择性具有关键影响,贵金属与其3d同族元素的组合产生了明显的协同效应。特别是,发现Co Rh@SILP催化剂在Co Rh(完全环氢化)和Co Rh(无环氢化)之间的狭窄组成范围内,对六元芳环进行氢化的能力经历了显著的急剧转变。