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Preparation and Friction Force Microscopy Measurements of Immiscible, Opposing Polymer Brushes
Published on: December 24, 2014
Charge Storage Mechanisms in Redox-Active Polymer Brushes
Oleg Rud1, Sergii Chertopalov2, Oleg Borisov3
1Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University, Prague 128 00, Czech Republic.
Abstract:
Electroconductive polymer brushes grafted to conductive electrodes are investigated as model electrodes for aqueous supercapacitors using the Scheutjens-Fleer self-consistent field (SF-SCF) framework. The model self-consistently resolves polymer conformations, ion partitioning, and redox-mediated electron hopping under applied potentials (0-0.7 V). We show that solvent quality and grafting density govern brush swelling and counterion uptake, thus shaping the charge-potential response. In a good solvent, brushes provide volumetric charge storage throughout a swollen layer, while in a poor solvent, charging drives a collapsed-to-swollen transition that produces sharp capacitance peaks. During this transition, the differential capacitance reaches 15-30 F/m2, an order of magnitude higher than the bare-electrode baseline. These results demonstrate how redox-active electroconductive brushes integrate electric double-layer and pseudocapacitive mechanisms, providing design principles for polymer-brush-modified electrodes in both supercapacitors and ion-selective membranes.
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