Probing microphase separation and proton transport cooperativity in polymer‐tethered 1 H ‐tetrazoles

To elucidate the driving forces for phase separation and proton conductivity in polystyrenic alkoxy 1 H ‐tetrazole (PS‐Tet), an analogous polystyrenic alkoxy carboxylic acid (PS‐HA) was synthesized and the conductivity and chain dynamics of both materials measured. Proton and polymer motions illustr...

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Veröffentlicht in:Journal of polymer science. Part B, Polymer physics Polymer physics, 2014-11, Vol.52 (21), p.1375-1387
Hauptverfasser: Chaloux, Brian L., Ricks‐Laskoski, Holly L., Miller, Joel B., Saunders, Kaitlin M., Hickner, Michael A.
Format: Artikel
Sprache:eng
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Zusammenfassung:To elucidate the driving forces for phase separation and proton conductivity in polystyrenic alkoxy 1 H ‐tetrazole (PS‐Tet), an analogous polystyrenic alkoxy carboxylic acid (PS‐HA) was synthesized and the conductivity and chain dynamics of both materials measured. Proton and polymer motions illustrate dramatic differences in the nonaqueous behavior of carboxylic acids and 1 H ‐tetrazoles, belying similarities in their aqueous properties. Exceptional interactions between 1 H ‐tetrazoles drive phase separation not observed in PS‐HA or reported for other azole‐containing homopolymers. PS‐HA and PS‐Tet exhibit both dry (0% relative humidity) and hydrated proton dissociations proportional to their aqueous p K a s, with residual water acting as the proton acceptor in both polymers. While water is the sole contributor to mobility in PS‐HA, PS‐Tet exhibits dynamic interactions with water allowing 1 H ‐tetrazole moieties to contribute to proton conduction even in the hydrated state. © 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2014 , 52 , 1375–1387
ISSN:0887-6266
1099-0488
DOI:10.1002/polb.23573