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dc.contributor.authorTao, Franklin Feng
dc.contributor.authorMa, Zhen
dc.date.accessioned2015-10-29T14:40:49Z
dc.date.available2015-10-29T14:40:49Z
dc.date.issued2013-06-18
dc.identifier.citationTao, Franklin (Feng), and Zhen Ma. "Water–gas Shift on Gold Catalysts: Catalyst Systems and Fundamental Studies." Phys. Chem. Chem. Phys. Physical Chemistry Chemical Physics 15.37 (2013): 15260. http://dx.doi.org/10.1039/C3CP51326Ben_US
dc.identifier.urihttp://hdl.handle.net/1808/18747
dc.descriptionThis is the published version. ©Copyright 2013 Royal Society of Chemistryen_US
dc.description.abstractSince the pioneering finding by Haruta et al. that small gold nanoparticles on reducible supports can be highly active for low-temperature CO oxidation, the synthesis, characterization, and application of supported gold catalysts have attracted much attention. The water–gas shift reaction (WGSR: CO + H2O = CO2 + H2) is important for removing CO and upgrading the purity of H2 for fuel cell applications, ammonia synthesis, and selective hydrogenation processes. In recent years, much attention has been paid to exploration the possibility of using supported gold nanocatalysts for WGSR and understanding the fundamental aspects related to catalyst deactivation mechanisms, nature of active sites, and reaction mechanisms. Here we summarize recent advances in the development of supported gold catalysts for this reaction and fundamental insights that can be gained, and furnish our assessment on the status of research progress.en_US
dc.publisherRoyal Society of Chemistryen_US
dc.titleWater–gas shift on gold catalysts: catalyst systems and fundamental studiesen_US
dc.typeArticle
kusw.kuauthorTao, Franklin Feng
kusw.kudepartmentChemical & Petroleum Engren_US
dc.identifier.doi10.1039/C3CP51326B
kusw.oaversionScholarly/refereed, publisher version
kusw.oapolicyThis item meets KU Open Access policy criteria.
dc.rights.accessrightsopenAccess


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