糠醛
选择性
催化作用
呋喃
原子层沉积
化学
沉积(地质)
吸附
纳米颗粒
化学工程
生物量(生态学)
图层(电子)
多相催化
化学气相沉积
有机化学
古生物学
海洋学
沉积物
工程类
生物
地质学
作者
Hongbo Zhang,Xiang‐Kui Gu,Christian P. Canlas,A. Jeremy Kropf,Payoli Aich,Jeffrey Greeley,Jeffrey W. Elam,Randall J. Meyers,James A. Dumesic,Peter C. Stair,Christopher L. Marshall
标识
DOI:10.1002/anie.201407236
摘要
Abstract The terraces, edges, and facets of nanoparticles are all active sites for heterogeneous catalysis. These different active sites may cause the formation of various products during the catalytic reaction. Here we report that the step sites of Pd nanoparticles (NPs) can be covered precisely by the atomic layer deposition (ALD) method, whereas the terrace sites remain as active component for the hydrogenation of furfural. Increasing the thickness of the ALD‐generated overcoats restricts the adsorption of furfural onto the step sites of Pd NPs and increases the selectivity to furan. Furan selectivities and furfural conversions are linearly correlated for samples with or without an overcoating, though the slopes differ. The ALD technique can tune the selectivity of furfural hydrogenation over Pd NPs and has improved our understanding of the reaction mechanism. The above conclusions are further supported by density functional theory (DFT) calculations.
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