Colloidal Cu/ZnO catalysts for the hydrogenation of carbon dioxide to methanol: investigating catalyst preparation and ligand effects

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Title: Colloidal Cu/ZnO catalysts for the hydrogenation of carbon dioxide to methanol: investigating catalyst preparation and ligand effects
Author(s): Pike, SD
Garcia-Trenco, A
White, ER
Leung, AHM
Weiner, J
Shaffer, MSP
Williams, CK
Item Type: Journal Article
Abstract: The production of methanol from CO2 hydrogenation is a promising potential route to a renewable liquid fuel and renewable energy vector. Herein, three distinct routes to make colloidal catalysts based on mixtures of Cu(0) and ZnO nanoparticles (NPs) and using low-temperature organometallic procedures are reported. The colloids are surface coordinated by a phosphinate ligand: dioctylphosphinate ([DOPA]−), which delivers a high solubility in organic solvents. Further, the synthetic routes allow fine control of the ZnO:Cu and ligand loadings. The catalysts are prepared by mixing small NPs (2 nm) of either Cu(0) or air-stable Cu2O NPs with ZnO NPs (3 nm), or by the synthesis of Cu(0) in presence of ZnO NPs (ZnO: 2 nm, Cu: 6 nm). The resulting colloidal catalysts are applied in the liquid phase hydrogenation of CO2 to methanol (210 °C, 50 bar, 3 : 1 molar ratio of CO2 : H2). The catalysts typically exhibit 3 times higher rates when compared to a heterogeneous Cu–ZnO–Al2O3 commercial catalyst (21 vs. 7 mmolMeOH gCuZnO−1 h−1). The characterisation of the post-catalysis colloids show clear Cu/ZnO interfaces (HR-TEM), which are formed under reducing conditions, as well as differences in the Cu(0) NP size (from 3 to 7 nm) and nanoscale restructuring of the catalysts. The combination of characterisation and catalytic results indicate that the activity is mostly dictated by the Cu(0) particle size and ligand loading. Smaller Cu(0) NPs exhibited lower turnover frequency (TOF) values, whereas higher ligand loadings ([DOPA]−:(Cu + Zn) of 0.2–1.1) lead to smaller Cu(0) NPs and reduce the formation of Cu/ZnO interfaces. UV-vis spectroscopy reveals that the Cu(0) NPs are more stable to oxidation under air after catalysis than beforehand, potentially due to migration of ZnO onto the Cu surface whilst under catalytic conditions.
Publication Date: 11-Aug-2017
Date of Acceptance: 26-Jul-2017
URI: http://hdl.handle.net/10044/1/52988
DOI: https://dx.doi.org/10.1039/c7cy01191a
ISSN: 2044-4753
Publisher: Royal Society of Chemistry
Start Page: 3842
End Page: 3850
Journal / Book Title: Catalysis Science and Technology
Volume: 7
Issue: 17
Copyright Statement: This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Sponsor/Funder: Engineering & Physical Science Research Council (EPSRC)
Funder's Grant Number: EP/K035274/1
Keywords: Science & Technology
Physical Sciences
Chemistry, Physical
Chemistry
METAL-SUPPORT INTERACTIONS
LIQUID-PHASE METHANOL
CO2 HYDROGENATION
PALLADIUM NANOPARTICLES
NANOCRYSTAL SURFACES
PARTICLE-SIZE
ACTIVE-SITES
CU
ZNO
GAS
Science & Technology
Physical Sciences
Chemistry, Physical
Chemistry
METAL-SUPPORT INTERACTIONS
LIQUID-PHASE METHANOL
CO2 HYDROGENATION
PALLADIUM NANOPARTICLES
NANOCRYSTAL SURFACES
PARTICLE-SIZE
ACTIVE-SITES
CU
ZNO
GAS
Publication Status: Published
Appears in Collections:Chemistry
Faculty of Natural Sciences



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