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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

机译:炭黑负载Ru基核壳纳米粒子的原位合成及其在胺硼烷脱氢中的高催化活性

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摘要

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_(H_2)min~(-1))mol_(Ru)~(-1) and activation energy (E_a) 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 SiO_2 and γ-Al_2O_3.
机译:炭黑上负载的分散良好的核-壳Ru @ M(M = Co,Ni,Fe)纳米颗粒(NPs)已通过一种简便的原位一步法在环境条件下合成。首次合成并表征了核壳Ru @ Co NP。合成后的Ru @ Co和Ru @ Ni NP在氨硼烷的水解中显示出比其单金属和合金对应物更好的催化活性。 Ru @ Co / C NPs的反应性最高,其周转频率(TOF)值为320(mol_(H_2)min〜(-1))mol_(Ru)〜(-1),活化能(E_a)为21.16 kJ mol〜(-1)。居第二位的是Ru @ Ni / C NP,而居第二位的是Ru @ Fe / C NP。另外,负载在炭黑上的合成后的NPs表现出比其他常规载体(如SiO_2和γ-Al_2O_3)上更高的催化活性。

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