Conducting polymer aerogels from supercritical CO2 drying PEDOT-PSS hydrogels
The organic conducting PEDOT-PSS aerogels can be prepared by supercritical CO 2 drying of metal ion crosslinked PEDOT-PSS supermolecular hydrogels. The PEDOT-PSS hydrogel precursors were synthesized by polymerizing 3,4-ethylenedioxythiophene with excess ferric nitrate as oxidizing agent as well as c...
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Veröffentlicht in: | Journal of materials chemistry 2010-01, Vol.2 (24), p.58-585 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The organic conducting PEDOT-PSS aerogels can be prepared by supercritical CO
2
drying of metal ion crosslinked PEDOT-PSS supermolecular hydrogels. The PEDOT-PSS hydrogel precursors were synthesized by polymerizing 3,4-ethylenedioxythiophene with excess ferric nitrate as oxidizing agent as well as crosslinking agent in the presence of poly(sodium 4-styrenesulfonate). The supermolecular crosslinking mechanism of the hydrogel precursors and the chemical composition of the resulting aerogels were revealed by X-ray photoelectron spectroscopy (XPS). The molecular structure of the resulting PEDOT-PSS aerogels was further confirmed by Raman and infra-red spectroscopy. The morphology and textural properties of the resultant aerogels were investigated by scanning electron microscopy (SEM), nitrogen adsorption/desorption, and X-ray powder diffraction (XRD) tests, respectively. The resulting aerogels show light weight (0.138-0.232 g cm
−3
), large BET surface area (170-370 m
2
g
−1
) and hierarchically porous structure with wide pore size distribution. The large surface area and wide pore size distribution, together with their electro-optical properties, would allow these organic conducting aerogels to be applied in many fields with unexpected performance.
The organic conducting PEDOT-PSS aerogels with light weight, large BET surface area and hierarchically porous structure,
etc.
have been prepared by supercritical CO
2
drying of metal ion crosslinked PEDOT-PSS supermolecular hydrogels. |
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ISSN: | 0959-9428 1364-5501 |
DOI: | 10.1039/c0jm00050g |