TY - GEN
T1 - Water-gas shift reaction on Cu and Au nanoparticles supported on CeO2 and ZnO
T2 - 233rd ACS National Meeting
AU - Rodriguez, Jose A.
AU - Wang, Xianqin
AU - Liu, Ping
AU - Hanson, Jonathan C.
AU - Hrbek, Jan
PY - 2007
Y1 - 2007
N2 - Synchrotron-based techniques (high-resolution photoemission, in-situ X-ray absorption spectroscopy, and time-resolved X-ray diffraction) have been used to study the water-gas shift (WGS, CO + H2O → H2 + CO2) reaction on a series catalysts. Au and Cu nanoparticles supported on CeO2(111) display an extraordinary catalytic activity for the WGS reaction that is not seen on a ZnO(000i) support or for the bulk metal. The behaviour of Au/ceria in the WGS illustrates the essential role that an oxide can have for the activity of supported Au nanocatalysts. In-situ time-resolved x-ray diffraction and x-ray absorption spectroscopy were used to monitor the behavior of nanostructured {Au+AuOx}-CeO2 catalysts under the WGS reaction. At temperatures above 250 C, a complete AuOx→Au transformation was observed with high catalytic activity. The active sites in {Au + AuOx}/ceria catalysts involve pure gold nanoparticles in contact with O vacancies of the oxide support.
AB - Synchrotron-based techniques (high-resolution photoemission, in-situ X-ray absorption spectroscopy, and time-resolved X-ray diffraction) have been used to study the water-gas shift (WGS, CO + H2O → H2 + CO2) reaction on a series catalysts. Au and Cu nanoparticles supported on CeO2(111) display an extraordinary catalytic activity for the WGS reaction that is not seen on a ZnO(000i) support or for the bulk metal. The behaviour of Au/ceria in the WGS illustrates the essential role that an oxide can have for the activity of supported Au nanocatalysts. In-situ time-resolved x-ray diffraction and x-ray absorption spectroscopy were used to monitor the behavior of nanostructured {Au+AuOx}-CeO2 catalysts under the WGS reaction. At temperatures above 250 C, a complete AuOx→Au transformation was observed with high catalytic activity. The active sites in {Au + AuOx}/ceria catalysts involve pure gold nanoparticles in contact with O vacancies of the oxide support.
UR - http://www.scopus.com/inward/record.url?scp=37349072256&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=37349072256&partnerID=8YFLogxK
M3 - Conference contribution
AN - SCOPUS:37349072256
SN - 084127438X
SN - 9780841274389
T3 - ACS National Meeting Book of Abstracts
BT - 233rd ACS National Meeting, Abstracts of Scientific Papers
Y2 - 25 March 2007 through 29 March 2007
ER -