We report the redox mediation of glucose oxidase (GOx) in a
self-assembled structure of cationic poly(allylamine) modified by ferrocene (PAA-Fc) and anionic GOx deposited
electrostatically layer-by-layer on
negatively charged alkanethiol-modified Au surfaces. Successive
PAA-Fc and GOx layers were deposited
by alternate immersion of the thiol-modified Au in the respective
polyelectrolyte and enzyme solutions.
The uptake of thiol, redox polymer, and GOx on the surface was
monitored by quartz crystal microbalance.
Cyclic voltammetry shows nearly ideal surface waves of ferrocene
in the polymer with charge independent
of sweep rate; the redox surface concentration was obtained from
integration of the ferrocene/ferricinium
voltammetric peaks. The redox charge increases in step with the
number of PAA-Fc layers deposited.
Enzyme catalysis for the oxidation of β-d-glucose
was achieved with a multilayer PAA-Fc/GOx assembly,
with each GOx layer contributing equally to the catalytic response.
Only a small fraction of the active
assembled GOx molecules are “electrically wired” by the ferrocene
polymer although all of the enzyme
could be oxidized by soluble ferrocenesulfonate when added to
solution.
In situ infrared subtractive normalized Fourier transform infrared spectroscopy (SNIFTIRS) experiments performed simultaneously with the electroreduction of oxygen on gold and platinum cathodes in LiPF 6 dimethyl sulfoxide (DMSO) electrolyte have shown that the solvent is stable with respect to nucleophilic attack by the electrogenerated superoxide radical anion. However, long-term experiments with KO 2 solutions in DMSO have shown a slow formation of dimethyl sulfone. Evidence of dimethyl sulfone formation by anodic oxidation of DMSO above 4.2 V (Li/Li + ) in the presence of trace water has been obtained on gold. On platinum, this unwanted reaction in the charging cycle of a lithium−air battery takes place at lower potentials, i.e., 3.5 V.
Redox polyelectrolyte multilayers have been assembled with use of the layer-by-layer (LBL) deposition technique with cationic poly(allylamine) modified with Os(bpy)(2)ClPyCHO (PAH-Os) and anionic poly(styrene)sulfonate (PSS) or poly(vinyl)sulfonate (PVS). Different behavior has been observed in the formal redox potential of the Os(II)/Os(III) couple in the polymer film with cyclic voltammetry depending on the charge of the outermost layer and the electrolyte concentration and pH. The electrochemical quartz crystal microbalance (EQCM) has been used to monitor the exchange of ions and solvent with the external electrolyte during redox switching. At low ionic strength Donnan permselectivity of anions or cations is apparent and the nature of the ion exclusion from the film is determined by the charge of the topmost layer and solution pH. At high electrolyte concentration Donnan breakdown is observed and the osmium redox potential approaches the value for the redox couple in solution. Exchange of anions and water with the external electrolyte under permselective conditions and salt and water under Donnan breakdown have been observed upon oxidation of the film at low pH for the PAH-Os terminating layer. Moreover, at high pH values and with PVS as the terminating layer EQCM mass measurements have shown that cation release was masked by water exchange.
The uptake of glucose oxidase (GOx) onto a polycationic redox polymer (PAA-Os)-modified surface, by adsorption from dilute aqueous GOx solutions, was followed by the quartz crystal microbalance (QCM) and shows double exponential kinetics. The electrochemistry of the layer-by-layer-deposited redox-active polymer was followed by cyclic voltammetry in glucose-free solutions, and the enzyme catalysis mediated by the redox polymer was studied in beta-D-glucose-containing solutions. AFM studies of the different layers showed the existence of large two dimension enzyme aggregates on the osmium polymer for 1 microM GOx and less aggregation for 50 nM GOx solutions. When the short alkanethiol, 2,2'-diaminoethyldisulfide was preadsorbed onto gold, a monoexponential adsorption law was observed, and single GOx enzyme molecules could be seen on the surface where the enzyme was adsorbed from 50 nM GOx in water.
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