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首页> 外文期刊>ACS nano >Microwave Synthesis of Classically Immiscible Rhodium-Silver and Rhodium-Gold Alloy Nanoparticles: Highly Active Hydrogenation Catalysts
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Microwave Synthesis of Classically Immiscible Rhodium-Silver and Rhodium-Gold Alloy Nanoparticles: Highly Active Hydrogenation Catalysts

机译:微波合成经典的不混溶铑银和铑金合金纳米粒子:高活性加氢催化剂

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摘要

Noble metal alloys are important in large-scale catalytic processes. Alloying facilitates fine-tuning of catalytic properties via synergistic interactions between metals. It also allows for dilution of scarce and expensive metals using comparatively earth-abundant metals. RhAg and RhAu are classically considered to be immiscible metals. We show here that stable RhM (M = Ag, Au) nanoparticles with randomly alloyed structures and broadly tunable Rh:M ratios can be prepared using a microwave-assisted method. The alloyed nanostructures with optimized Rh:M compositions are significantly more active as hydrogenation catalysts than Rh itself: Rh is more dilute and more reactive when alloyed with Ag or Au, even though the latter are both catalytically inactive for hydrogenation. Theoretical modeling predicts that the observed catalytic enhancement is due to few-atom surface ensemble effects in which the overall reaction energy profile for alkene hydrogenation is optimized due to RhM d-band intermixing.
机译:贵金属合金在大规模催化过程中很重要。合金化通过金属之间的协同相互作用促进了催化性能的微调。它还可以使用相对丰富的地球金属来稀释稀有和昂贵的金属。 RhAg和RhAu通常被认为是不混溶的金属。我们在这里显示可以使用微波辅助方法制备具有随机合金结构和广泛可调的Rh:M比率的稳定RhM(M = Ag,Au)纳米粒子。具有优化的Rh:M组成的合金纳米结构作为氢化催化剂的活性明显高于Rh本身:与Ag或Au合金化时,Rh的稀释度和反应性更高,即使后者对氢化均无催化活性。理论模型预测,观察到的催化增强是由于很少的原子表面整体效应,其中由于RhM d波段混合,烯烃加氢的总反应能量分布得到了优化。

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