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Sökning: WFRF:(Eriksson Therese 1992 ) > (2020) > Restricted Ion Tran...

Restricted Ion Transport by Plasticizing Side Chains in Polycarbonate-Based Solid Electrolytes

Ebadi, Mahsa (författare)
Uppsala universitet,Strukturkemi
Eriksson, Therese, 1992- (författare)
Uppsala universitet,Strukturkemi
Mandal, Prithwiraj (författare)
Uppsala universitet,Strukturkemi
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Costa, Luciano T. (författare)
Universidade Federal Fluminense, BRA,Univ Fed Fluminense, Inst Quim, Dept Fis Quim, BR-24020150 Niteroi, RJ, Brazil
Araujo, Carlos Moyses (författare)
Uppsala universitet,Materialteori
Mindemark, Jonas (författare)
Uppsala universitet,Strukturkemi
Brandell, Daniel, 1975- (författare)
Uppsala universitet,Strukturkemi
visa färre...
 (creator_code:org_t)
2020-01-31
2020
Engelska.
Ingår i: Macromolecules. - : American Chemical Society (ACS). - 0024-9297 .- 1520-5835. ; 53:3, s. 764-774
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Increasing the ionic conductivity has for decades been an overriding goal in the development of solid polymer electrolytes. According to fundamental theories on ion transport mechanisms in polymers, the ionic conductivity is strongly correlated to free volume and segmental mobility of the polymer for the conventional transport processes. Therefore, incorporating plasticizing side chains onto the main chain of the polymer host often appears as a clear-cut strategy to improve the ionic conductivity of the system through lowering of the glass transition temperature (T-g) This intended correlation between Tg and ionic conductivity is, however, not consistently observed in practice. The aim of this study is therefore to elucidate this interplay between segmental mobility and polymer structure in polymer electrolyte systems comprising plasticizing side chains. To this end, we utilize the synthetic versatility of the ion-conductive poly(trimethylene carbonate) (PTMC) platform. Two types of host polymers with side chains added to a PTMC backbone are employed, and the resulting electrolytes are investigated together with the side chain-free analogue both by experiment and with molecular dynamics (MD) simulations. The results show that while added side chains do indeed lead to a lower Tg, the total ionic conductivity is highest in the host matrix without side chains. It was seen in the MD simulations that while side chains promote ionic mobility associated with the polymer chain, the more efficient interchain hopping transport mechanism occurs with a higher probability in the system without side chains. This is connected to a significantly higher solvation site diversity for the Li+ ions in the side-chain-free system, providing better conduction paths. These results strongly indicate that the side chains in fact restrict the mobility of the Li+ ions in the polymer hosts.

Ämnesord

NATURVETENSKAP  -- Kemi -- Polymerkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Polymer Chemistry (hsv//eng)

Nyckelord

Physics
Fysik

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