Abstract
Well-dispersed core-shell Ru@M (M=Co, Ni, Fe) nanoparticles (NPs) supported on carbon black have been synthesized via a facile in situ one-step procedure under ambient condition. Core-shell Ru@Co NPs were synthesized and characterized for the first time. The as-synthesized Ru@Co and Ru@Ni NPs exhibit superior catalytic activity in the hydrolysis of ammonia borane compared with their monometallic and alloy counterparts. The Ru@Co/C NPs are the most reactive, with a turnover frequency (TOF) value of 320 (mol H2 min-1) molRu-1 and activation energy (Ea) of 21.16 kJ mol-1. Ru@Ni/C NPs are the next most active, whereas Ru@Fe/C NPs are almost inactive. Additionally, the as-synthesized NPs supported on carbon black exhibit higher catalytic activity than catalysts on other conventional supports, such as SiO2 and γ-Al2O3. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Cao, N., Su, J., Hong, X., Luo, W., & Cheng, G. (2014). In situ facile synthesis of Ru-based core-shell nanoparticles supported on carbon black and their high catalytic activity in the dehydrogenation of amine-boranes. Chemistry - An Asian Journal, 9(2), 562–571. https://doi.org/10.1002/asia.201301171
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