Abstract
The electrodes of a hybrid electrochemical capacitor which utilize the quinone (Q)-hydroquinone (QH2) couple, a prototypical organic redox system known to provide fast and reversible proton-coupled electron-transfer reactions, are deterministically mesostructured via a colloidal templating strategy to provide good ion and electron transport pathways, enabling a high rate performance. Specifically, a conducting polymer, polypyrrole (PPy), is functionalized with a pseudocapacitive material, a Q/QH2-containing catechol derivative, by noncovalent interactions. The mesostructure of this hybrid material is formed into an ordered 3D porous structure by a polystyrene colloidal crystal template-assisted electrosynthesis. The catechol derivative is sufficiently bound to the PPy through noncovalent interactions to provide a volumetric capacitance as high as ≈130 F cm-3 and a capacitance retention of ≈75% over 10 000 charging/discharging cycles. When compared with a randomly structured electrode, the deterministically structured electrode exhibits an improved rate performance due to the mesostructure facilitated electron and ion transport.
Original language | English (US) |
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Pages (from-to) | 903-910 |
Number of pages | 8 |
Journal | Advanced Functional Materials |
Volume | 26 |
Issue number | 6 |
DOIs | |
State | Published - Feb 9 2016 |
Keywords
- catechol
- energy storage
- polypyrrole
- pseudocapacitor
- quinone
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- General Chemistry
- Condensed Matter Physics
- General Materials Science
- Electrochemistry
- Biomaterials