Enhanced catalytic activity of high index faceted palladium nanoparticles in Suzuki-Miyaura coupling due to efficient leaching mechanism

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TY  - JOUR
  - Collins, G.; Schmidt, M.; O’Dwyer, C.; McGlacken, G.; Holmes, J. D.
  - 2014
  - August
  - ACS Catalysis
  - Enhanced catalytic activity of high index faceted palladium nanoparticles in Suzuki-Miyaura coupling due to efficient leaching mechanism
  - Published
  - Altmetric: 1 ()
  - 4
  - 9
  - 3105
  - 3111
  - The structure−property relationship of palladium (Pd) catalysts in Suzuki−Miyaura cross-coupling reactions was investigated using Pd nanocrystals of uniform size and shape. Superior catalytic reactivity was observed for Pd nanoparticles with high-index {730} surface facets compared to low-index {100} facets. Although the nanocrystal morphologies were maintained during the reaction, the presence of Pd clusters, identified by high-resolution transmission electron microscopy (TEM), indicates a leaching mechanism. The nature of the surface facets on the nanoparticles was observed to influence the rate of Pd leaching during the Suzuki coupling reaction. The enhanced reactivity observed for the high-index facet catalysts stems from the greater number of leachable atoms of low abstraction energy available on high-index planes.
  - Washington, DC, USA
  - http://pubs.acs.org/journal/accacs
  - 10.1021/cs5008014
DA  - 2014/08
ER  - 
@article{V268042230,
   = {Collins, G. and  Schmidt, M. and  O’Dwyer, C. and  McGlacken, G. and  Holmes, J. D.},
   = {2014},
   = {August},
   = {ACS Catalysis},
   = {Enhanced catalytic activity of high index faceted palladium nanoparticles in Suzuki-Miyaura coupling due to efficient leaching mechanism},
   = {Published},
   = {Altmetric: 1 ()},
   = {4},
   = {9},
  pages = {3105--3111},
   = {{The structure−property relationship of palladium (Pd) catalysts in Suzuki−Miyaura cross-coupling reactions was investigated using Pd nanocrystals of uniform size and shape. Superior catalytic reactivity was observed for Pd nanoparticles with high-index {730} surface facets compared to low-index {100} facets. Although the nanocrystal morphologies were maintained during the reaction, the presence of Pd clusters, identified by high-resolution transmission electron microscopy (TEM), indicates a leaching mechanism. The nature of the surface facets on the nanoparticles was observed to influence the rate of Pd leaching during the Suzuki coupling reaction. The enhanced reactivity observed for the high-index facet catalysts stems from the greater number of leachable atoms of low abstraction energy available on high-index planes.}},
   = {Washington, DC, USA},
   = {http://pubs.acs.org/journal/accacs},
   = {10.1021/cs5008014},
  source = {IRIS}
}
AUTHORSCollins, G.; Schmidt, M.; O’Dwyer, C.; McGlacken, G.; Holmes, J. D.
YEAR2014
MONTHAugust
JOURNAL_CODEACS Catalysis
TITLEEnhanced catalytic activity of high index faceted palladium nanoparticles in Suzuki-Miyaura coupling due to efficient leaching mechanism
STATUSPublished
TIMES_CITEDAltmetric: 1 ()
SEARCH_KEYWORD
VOLUME4
ISSUE9
START_PAGE3105
END_PAGE3111
ABSTRACTThe structure−property relationship of palladium (Pd) catalysts in Suzuki−Miyaura cross-coupling reactions was investigated using Pd nanocrystals of uniform size and shape. Superior catalytic reactivity was observed for Pd nanoparticles with high-index {730} surface facets compared to low-index {100} facets. Although the nanocrystal morphologies were maintained during the reaction, the presence of Pd clusters, identified by high-resolution transmission electron microscopy (TEM), indicates a leaching mechanism. The nature of the surface facets on the nanoparticles was observed to influence the rate of Pd leaching during the Suzuki coupling reaction. The enhanced reactivity observed for the high-index facet catalysts stems from the greater number of leachable atoms of low abstraction energy available on high-index planes.
PUBLISHER_LOCATIONWashington, DC, USA
ISBN_ISSN
EDITION
URLhttp://pubs.acs.org/journal/accacs
DOI_LINK10.1021/cs5008014
FUNDING_BODY
GRANT_DETAILS