CO2 hydrogenation with shape-controlled Pd nanoparticles embedded in mesoporous silica: Elucidating stability and selectivity issues

被引：55

作者：

Martins, J. ^{[1
]}

Batail, N. ^{[1
]}

Silva, S. ^{[1
]}

Rafik-Clement, S. ^{[1
]}

Karelovic, A. ^{[2
]}

Debecker, D. P. ^{[2
]}

Chaumonnot, A. ^{[1
]}

Uzio, D. ^{[1
]}

机构：

[1] IFP Energies Nouvelles, IFPEN Lyon, F-69360 Solaize, France

[2] Catholic Univ Louvain, Inst Condensed Matter & Nanosci MOl Solids & Reac, B-1348 Louvain, Belgium

来源：

CATALYSIS COMMUNICATIONS | 2015年 / 58卷

关键词：

CO2; methanation; Embedded palladium nanopartides; Nanoparticles morphology; Mesoporous silica; Core-shell catalysts; SEED-MEDIATED SYNTHESIS; SUPPORTED PALLADIUM; METHANATION; CATALYSTS; TEMPERATURE; ADSORPTION; SIZE; NANOSTRUCTURES; SPECTROSCOPY; MECHANISM;

D O I：

10.1016/j.catcom.2014.08.027

中图分类号：

O64 [物理化学（理论化学）、化学物理学];

学科分类号：

070304 ; 081704 ;

摘要：

Shape-controlled Pd nanocubes and nanopolyedra particles were embedded in mesoporous silica shells and their catalytic properties for the CO2 hydrogenation were compared to a reference Pd/SiO2 catalyst prepared by wetness impregnation. Whereas the Pd impregnated silica exhibits a strong deactivation, the activity of both embedded solids is remarkably stable. This difference is due to a significant Pd particles sintering in the reference catalyst while no increase of particle size is observed for the core@shell solids. CH4 selectivity is shown to be correlated to the mean coordination number of surface atoms which controls the adsorption strength of CO as intermediate species. (C) 2014 Elsevier B.V. All rights reserved.

引用

页码：11 / 15

页数：5

共 35 条

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