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Integrating molecular design and crystal engineering approaches in non-humidified intermediate-temperature proton conductors based on a Dawson-type polyoxometalate and poly(ethylene glycol) derivatives
Ist Teil von
Nanoscale, 2021-05, Vol.13 (17), p.849-857
Ort / Verlag
England: Royal Society of Chemistry
Erscheinungsjahr
2021
Quelle
Alma/SFX Local Collection
Beschreibungen/Notizen
Anionic metal-oxygen clusters known as polyoxometalates (POMs) have been widely researched as components of proton conductors. While proton conduction under non-humidified intermediate-temperature (100-250 °C) conditions is advantageous from the viewpoint of kinetics, few solid-state materials, not to mention POM-based crystals, show truly effective proton conduction without the aid of water vapor. In this context, non-volatile proton-conductive polymers have been confined into POM-based frameworks, while fast proton conduction was infeasible. Herein, we demonstrate a new strategy to synthesize POM-polymer composites exhibiting fast proton conduction under non-humidified intermediate-temperature conditions. Specifically, a molecular design approach utilizing poly(ethylene glycol)s (PEGs) of different terminal groups or chain lengths controls the proton carrier density, and a crystal engineering approach using a large Dawson-type POM ([α-P
2
W
18
O
62
]
6−
) with an anisotropic molecular shape and alkali metal ions as counter cations fine-tunes the mobility of the confined PEGs as proton carriers. By integrating these approaches, proton conductivity over 10
−4
S cm
−1
at 150 °C, comparable to the well-known highly proton-conductive solid-state materials, is achieved. The proton conduction mechanism is discussed with alternative current impedance spectroscopy jointly with specific heat capacity measurements and solid-state NMR spectroscopy.
Crystalline composites of Dawson-type polyoxometalates, alkali-metal ions as counter cations, and poly(ethylene glycol)s offer efficient proton conduction under non-humidified conditions.