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Comparing thermal and chemical removal of nanoparticle stabilizing ligands - effect on catalytic activity and stability
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Accepted Version
Supporting Information
Date
2018-11-16
Authors
Collins, Gillian
Davitt, Fionán
O'Dwyer, Colm
Holmes, Justin D.
Journal Title
Journal ISSN
Volume Title
Publisher
American Chemical Society
Published Version
Abstract
The use of stabilizers is an essential part of colloidal catalyst preparation, however their impact on catalytic behavior is challenging to elucidate. This report evaluates three commonly used nanoparticle (NP) stabilizing ligands, oleylamine (OAm), dodecanethiol (DDT) and the polymer polyvinylpyrrolidone (PVP). Stabilizing ligands are removed using thermal and chemical pre-treatments and the surface chemistry of the NPs is assessed using X-ray photoelectron spectroscopy (XPS). The method of ligand removal significantly altered the catalytic behavior of colloidal NPs. Chemical treatment was less effective in completely removing the capping ligands, however catalytic activity could be improved by partial ligand removal. Thermal pre-treatment decreased the activity of all the catalysts, even when the catalyst diameter and Pd surface chemistry was reasonably preserved. XPS analysis further revealed changes in the interfacial chemistry of the treated catalysts such as the formation of oxidized sulfur species formed during annealing DDT-Pd NPs and conformational changes in PVP capping ligands as a result of thermal treatment.
Description
Keywords
Nanoparticles , Capping ligands , Palladium , Surface chemistry , XPS , Suzuki coupling
Citation
Collins, G., Davitt, F., O'Dwyer, C. and Holmes, J. D. (2018) 'Comparing thermal and chemical removal of nanoparticle stabilizing ligands - effect on catalytic activity and stability', ACS Applied Nano Materials. doi:10.1021/acsanm.8b02019
Copyright
© 2018, American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Nano Materials after technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/abs/10.1021/acsanm.8b02019