Details
| Original language | English |
|---|---|
| Pages (from-to) | 153-159 |
| Number of pages | 7 |
| Journal | SOLID STATE IONICS |
| Volume | 112 |
| Issue number | 1-2 |
| Publication status | Published - 2 Sept 1998 |
Abstract
Temperature-dependent 7Li nuclear magnetic resonance (NMR) spin-lattice relaxation time (T1) data of a lithium monoconducting polymer electrolyte based on maleic anhydride-styrene copolymers are examined in an effort to understand the mechanism of how plasticizers affect significant changes in the observed ionic conductivity (σ). The use of strong polar organic plasticizers, such as propylene carbonate, is believed to induce changes in the charge-carrier separation, which is expected to facilitate the transport of ions in these materials. Cationic monoconducting gel electrolytes consisting of polyelectrolytes with immobilized carboxylic anions, charge compensating mobile Li+ ions, and various combinations of poly(ethylene glycol) dimethyl ether, dimethylsulfoxide, propylene carbonate, and BF3 exhibit ambient σ values from 10-3 to 10-6 S cm-1. For systems not containing BF3 the T1 data as a function of inverse temperature and the value of the T1 at its minimum are found to be independent of the electrolyte composition in spite of the fact that the δ values are observed to increase by 1 to 3 orders of magnitude in these samples. For these samples it is suggested that the Li+ ions find comparable sites possibly in the form of contact ion pairs with the carboxylic anions and that they are dynamically coupled to the motion of the polymer host. The observed increase in conductivity upon addition of the plasticizers is assumed to arise from a weakening of the ion-polymer interactions and not from a fundamental change in the ionic conductivity mechanism. Upon addition of BF3, however, a shift in the T1 minimum to lower temperatures and a decrease in the depth of the T1 minimum are observed. These observations suggest that the Li+ ions interact preferentially with -O-B⊖F3 moieties and are consistent with the existence of an alternate conduction path such that the ion motions are decoupled from the local motions of the polymer host.
Keywords
- Li NMR relaxation times, Ionic conductivity, Plasticizers, Polymer electrolytes
ASJC Scopus subject areas
- Chemistry(all)
- General Chemistry
- Materials Science(all)
- General Materials Science
- Physics and Astronomy(all)
- Condensed Matter Physics
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In: SOLID STATE IONICS, Vol. 112, No. 1-2, 02.09.1998, p. 153-159.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Enhancement of ionic conductivity by the addition of plasticizers in cationic monoconducting polymer electrolytes
AU - Chung, S. H.
AU - Heitjans, P.
AU - Winter, R.
AU - Bzäucha, W.
AU - Florjańczyk, Z.
AU - Onoda, Y.
N1 - Funding Information: Financial supports for this project from the Deutsche Forschungsgemeinschaft (SFB 173), Fonds der Chemischen Industrie, and the Science and Technology Agency (STA) of Japan are gratefully acknowledged. We thank W. Wieczorek and A. Zalewska for providing T g and ionic conductivity data of the samples. ZF and WB gratefully acknowledge financial support from the Polish State Committee for Scientfic Research (3/TO9B/04809). SHC would like to express his appreciation to Professor Heitjans and Dr. Onoda for their kind hospitality during his stay in their respective laboratories.
PY - 1998/9/2
Y1 - 1998/9/2
N2 - Temperature-dependent 7Li nuclear magnetic resonance (NMR) spin-lattice relaxation time (T1) data of a lithium monoconducting polymer electrolyte based on maleic anhydride-styrene copolymers are examined in an effort to understand the mechanism of how plasticizers affect significant changes in the observed ionic conductivity (σ). The use of strong polar organic plasticizers, such as propylene carbonate, is believed to induce changes in the charge-carrier separation, which is expected to facilitate the transport of ions in these materials. Cationic monoconducting gel electrolytes consisting of polyelectrolytes with immobilized carboxylic anions, charge compensating mobile Li+ ions, and various combinations of poly(ethylene glycol) dimethyl ether, dimethylsulfoxide, propylene carbonate, and BF3 exhibit ambient σ values from 10-3 to 10-6 S cm-1. For systems not containing BF3 the T1 data as a function of inverse temperature and the value of the T1 at its minimum are found to be independent of the electrolyte composition in spite of the fact that the δ values are observed to increase by 1 to 3 orders of magnitude in these samples. For these samples it is suggested that the Li+ ions find comparable sites possibly in the form of contact ion pairs with the carboxylic anions and that they are dynamically coupled to the motion of the polymer host. The observed increase in conductivity upon addition of the plasticizers is assumed to arise from a weakening of the ion-polymer interactions and not from a fundamental change in the ionic conductivity mechanism. Upon addition of BF3, however, a shift in the T1 minimum to lower temperatures and a decrease in the depth of the T1 minimum are observed. These observations suggest that the Li+ ions interact preferentially with -O-B⊖F3 moieties and are consistent with the existence of an alternate conduction path such that the ion motions are decoupled from the local motions of the polymer host.
AB - Temperature-dependent 7Li nuclear magnetic resonance (NMR) spin-lattice relaxation time (T1) data of a lithium monoconducting polymer electrolyte based on maleic anhydride-styrene copolymers are examined in an effort to understand the mechanism of how plasticizers affect significant changes in the observed ionic conductivity (σ). The use of strong polar organic plasticizers, such as propylene carbonate, is believed to induce changes in the charge-carrier separation, which is expected to facilitate the transport of ions in these materials. Cationic monoconducting gel electrolytes consisting of polyelectrolytes with immobilized carboxylic anions, charge compensating mobile Li+ ions, and various combinations of poly(ethylene glycol) dimethyl ether, dimethylsulfoxide, propylene carbonate, and BF3 exhibit ambient σ values from 10-3 to 10-6 S cm-1. For systems not containing BF3 the T1 data as a function of inverse temperature and the value of the T1 at its minimum are found to be independent of the electrolyte composition in spite of the fact that the δ values are observed to increase by 1 to 3 orders of magnitude in these samples. For these samples it is suggested that the Li+ ions find comparable sites possibly in the form of contact ion pairs with the carboxylic anions and that they are dynamically coupled to the motion of the polymer host. The observed increase in conductivity upon addition of the plasticizers is assumed to arise from a weakening of the ion-polymer interactions and not from a fundamental change in the ionic conductivity mechanism. Upon addition of BF3, however, a shift in the T1 minimum to lower temperatures and a decrease in the depth of the T1 minimum are observed. These observations suggest that the Li+ ions interact preferentially with -O-B⊖F3 moieties and are consistent with the existence of an alternate conduction path such that the ion motions are decoupled from the local motions of the polymer host.
KW - Li NMR relaxation times
KW - Ionic conductivity
KW - Plasticizers
KW - Polymer electrolytes
UR - http://www.scopus.com/inward/record.url?scp=0032475079&partnerID=8YFLogxK
U2 - 10.1016/s0167-2738(98)00229-x
DO - 10.1016/s0167-2738(98)00229-x
M3 - Article
AN - SCOPUS:0032475079
VL - 112
SP - 153
EP - 159
JO - SOLID STATE IONICS
JF - SOLID STATE IONICS
SN - 0167-2738
IS - 1-2
ER -