Electrocatalysis on Pt/YSZ electrodes

dc.contributor.authorLuerssen, Bjoern
dc.contributor.authorJanek, Jürgen
dc.contributor.authorImbihl, R.
dc.date.accessioned2023-06-12T07:53:54Z
dc.date.available2005-09-14T09:00:00Z
dc.date.available2023-06-12T07:53:54Z
dc.date.issued2001
dc.description.abstractElectrochemical polarization of porous metal electrodes on solid electrolytes often leads to an increase of their catalytic activity in heterogeneous reactions. Thin microstructured Pt films on single crystalline YSZ (yttria stabilized zirconia) are investigated as structurally and geometrically well-defined model systems in order to understand the origin of this effect. Photoelectron emission microscopy (PEEM) and scanning photoelectron microscopy (SPEM) have been applied as spatially resolving methods in situ to study the processes in the vicinity of the three-phase boundary (tpb). Measurements with SPEM show that atomic oxygen is created under anodic polarization and covers the Pt film homogeneously. A specific spillover species is not found, rather the formation of atomic oxygen is detected, which has the same O1s binding energy as chemisorbed oxygen from the gas phase.en
dc.identifier.urihttp://nbn-resolving.de/urn:nbn:de:hebis:26-opus-23815
dc.identifier.urihttps://jlupub.ub.uni-giessen.de//handle/jlupub/16725
dc.identifier.urihttp://dx.doi.org/10.22029/jlupub-16103
dc.language.isoende_DE
dc.rightsIn Copyright*
dc.rights.urihttp://rightsstatements.org/page/InC/1.0/*
dc.subjectCatalysisen
dc.subjectElectrochemistryen
dc.subjectInterfacesen
dc.subjectPhotoelectron emission microscopyen
dc.subjectScanning photoelectron microscopyen
dc.subject.ddcddc:540de_DE
dc.titleElectrocatalysis on Pt/YSZ electrodesen
dc.typearticlede_DE
local.affiliationFB 08 - Biologie und Chemiede_DE
local.opus.fachgebietChemiede_DE
local.opus.id2381
local.opus.institutePhysikalisch-Chemisches Institutde_DE
local.source.freetextZuerst erschienen in: Solid State Ionics 141/142 (2001) 701-707: http://dx.doi.org/10.1016/S0167-2738(01)00783-4de_DE

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