TY - JOUR
T1 - Larger cations can move faster in solid polymer electrolytes
AU - Ohno, Hiroyuki
AU - Kobayashi, Norihisa
AU - Takeoka, Shinji
AU - Ishizaka, Hajime
AU - Tsuchida, Eishun
N1 - Funding Information:
This work was partly supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science and Culture, Japan.
PY - 1990/8
Y1 - 1990/8
N2 - Poly[(ω-carboxy)-oligo(oxyethylene)methacrylate] alkali metal salts (P(CMEnM)s) are synthesized as solid polymer electrolytes which can transfer only cations. The conductivity of a series of alkali metal ions such as Li+, Na+, K+, Rb+, and Cs+ is measured, and the results are summarized with the reduced temperature (T-Tg:Tg=glass transition temperature) to neutralize the effect of segmental motion on the relative conductivity. They show a linear relation between the logarithm of conductivity at T-Tg=60°C and the logarithm of radius of the carrier cations. The ion-dipole interaction is suggested to be the most effective factor to control the mobility in the solid polymer electrolytes. Cations having larger ionic radius such as Rb+ or Cs+ are suggested to have weaker interaction force with ether oxygens, reflecting the faster ion exchange between possible adjacent sites in the polymer matrix.
AB - Poly[(ω-carboxy)-oligo(oxyethylene)methacrylate] alkali metal salts (P(CMEnM)s) are synthesized as solid polymer electrolytes which can transfer only cations. The conductivity of a series of alkali metal ions such as Li+, Na+, K+, Rb+, and Cs+ is measured, and the results are summarized with the reduced temperature (T-Tg:Tg=glass transition temperature) to neutralize the effect of segmental motion on the relative conductivity. They show a linear relation between the logarithm of conductivity at T-Tg=60°C and the logarithm of radius of the carrier cations. The ion-dipole interaction is suggested to be the most effective factor to control the mobility in the solid polymer electrolytes. Cations having larger ionic radius such as Rb+ or Cs+ are suggested to have weaker interaction force with ether oxygens, reflecting the faster ion exchange between possible adjacent sites in the polymer matrix.
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U2 - 10.1016/0167-2738(90)90091-5
DO - 10.1016/0167-2738(90)90091-5
M3 - Article
AN - SCOPUS:0025468123
SN - 0167-2738
VL - 40-41
SP - 655
EP - 658
JO - Solid State Ionics
JF - Solid State Ionics
IS - PART 2
ER -