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Jones, E. Tracy Turner 2014-12-15T23:18:30Z 2014-12-15T23:18:30Z 10000-01-01 1985 1985 I. In general, only one member of a redox couple will be luminescent if redox activity and luminescence originate in the same molecular feature. Moreover, diffusion controlled quenching by the nonluminescent form, through energy or electron transfer, is a likely decay route for a long-lived excited state. Thin layer spectroelectrochemical theory for such a system was derived from the Nernst and Stern-Volmer equations. The tris(2,2'-bipyridine) complex of osmium(III/II) in 1.0 M H(,2)SO(,4) was chosen as a test case. The luminescence Os(bpy)(,3)('2+) *, emitted from an optically transparent thin layer electrode, was monitored as a function of potential. As in the absorbance mode experiment, analysis of the data via Nernst plots proved to be an excellent means of determining n and E('o)', despite the intrusion of photochemical processes in the test system. In addition, the luminescence mode experiment was found to be a useful probe of quenching behavior. II. Poly(styrenesulfonate, sodium salt) was spincoated on glassy carbon rotating disk electrodes (RDE's) for use as a matrix for the mediated oxidation of ferrocene-1,1'-disulfonate by electrostatically bound tris(2,2'-bipyridine)osmium(III). This particular mediator-substrate system is designated as case C in the terminology of the Andrieux-Saveant kinetic model for polymer modified electrodes. Case C systems are not catalytic; direct oxidation (reduction) of the substrate precedes oxidation (reduction) of the pre-mediator redox form. However, the existence of two plateau currents facilitates diagnosis of the factors that limit the mediated current. The Andrieux-Saveant theory was applied to voltammetric data obtained at rotating and stationary RDE's and to chronocoulometric data. Analysis of the data revealed that electron self-exchange among the densely packed mediator centers was an efficient process, whereas substrate diffusion through the film was hindered. Mediated oxidation of substrate occurred primarily at the film-solution boundary. Made available in DSpace on 2014-12-15T23:18:30Z (GMT). No. of bitstreams: 1 8521794.pdf: 3088551 bytes, checksum: c668a91343029ff3cf85f1b1c570d369 (MD5) Previous issue date: 1985 Embargo set by: Seth Robbins for item 70467 Lift date: Forever Reason: Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs Restricted to the U of I community idenfinitely during batch ingest of legacy ETDs U of I Only 121 p. Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 1985. http://hdl.handle.net/2142/70301 (UMI)AAI8521794 Chemistry, Analytical I. Luminescence Spectroelectrochemistry in Thin Layer Cells. Ii. Kinetics of Mediated Oxidation at a Polymer Modified Electrode text Chemistry Chemistry University of Illinois at Urbana-Champaign Dissertation Ph.D.