- Original paper
- Open Access
Polystyrene-Al2O3 composite solid polymer electrolyte for lithium secondary battery
© Lim et al; licensee Springer. 2012
- Received: 23 September 2011
- Accepted: 5 January 2012
- Published: 5 January 2012
In a common salt-in-polymer electrolyte, a polymer which has polar groups in the molecular chain is necessary because the polar groups dissolve lithium salt and coordinate cations. Based on the above point of view, polystyrene [PS] that has nonpolar groups is not suitable for the polymer matrix. However, in this PS-based composite polymer-in-salt system, the transport of cations is not by segmental motion but by ion-hopping through a lithium percolation path made of high content lithium salt. Moreover, Al2O3 can dissolve salt, instead of polar groups of polymer matrix, by the Lewis acid-base interactions between the surface group of Al2O3 and salt. Notably, the maximum enhancement of ionic conductivity is found in acidic Al2O3 compared with neutral and basic Al2O3 arising from the increase of free ion fraction by dissociation of salt. It was revealed that PS-Al2O3 composite solid polymer electrolyte containing 70 wt.% salt and 10 wt.% acidic Al2O3 showed the highest ionic conductivity of 9.78 × 10-5 Scm-1 at room temperature.
- solid polymer electrolyte
- polymer-in-salt system
- lithium secondary battery
A lithium secondary battery using solid polymer electrolyte [SPE] is an attractive energy source for portable devices since the use of SPE makes the fabrication of safe batteries possible and permits the development of thin batteries with design flexibility. Most of the efforts to date have focused on poly(ethylene oxide) [PEO] as the host material for SPE [1–3]. However, it has a major drawback of having a low ionic conductivity (10-8 to 10-5 Scm-1) at room temperature . Thus, many researchers [5–7] have focused on the SPE consisting of the polymer with low glass transition temperature [Tg] and moderate concentrations of salt in order to overcome the low ionic conductivity of SPE, but high ambient conductivity has not yet been reached. Low ionic conductivity can be achieved from the fact that the ionic mobility strongly depends on the polymer segmental motion and that the cation transport number is low in the SPE at a high salt concentration. Therefore, new materials with unconventional conduction mechanisms are clearly needed .
In common SPEs, a polymer which has polar groups in the chain is necessary for electrolyte formation. The polar groups dissolve lithium salt and coordinate cations. The cations can move between coordinating sites in one chain or in neighboring chains, promoted by the segmental motion . From this point of view, a polymer which has nonpolar groups is not suitable for the polymer matrix in common SPEs. However, in this new composite SPE consisting of polystyrene [PS] and having nonpolar groups, LiCF3SO3 and Al2O3 with polymer-in-salt system, the transport of cations is done by ion-hopping through an ion percolation path made of high content lithium salt instead of segmental motion. Moreover, Al2O3 can cause conductivity enhancement depending on the nature of the filler surface group . In this work, the ionic conductivity of PS-Al2O3 composite SPE according to the salt content was checked, and the effect of Al2O3 type and content on ion conduction properties in PS-based composite SPE was investigated.
Polystyrene (Sigma-Aldrich Corporation, St. Louis, MO, USA) with a number average molecular weight (M n ) of 170,000 was used as received without undergoing further purification process. As salt, LiCF3SO3 (Sigma-Aldrich Corporation) was dried and stored in a desiccator under nitrogen. Three types of aluminum oxides [Al2O3] (Sigma-Aldrich Corporation) with acidic, neutral, and basic surface groups as fillers were also used. As an organic solvent, N-butyl acetate (Junsei Chemical Co., Ltd., Chuo-ku, Tokyo, Japan) was used in order to dissolve the materials.
Preparation of PS-based composite SPE films
An appropriate amount of PS was introduced into N-butyl acetate and stirred for 24 h; after that, a definitive amount of LiCF3SO3 was added to the solution and stirred again for 24 h. At the same time of the PS/LiCF3SO3 solution preparation, 5, 10, 15, and 20 wt.% Al2O3 were added to N-butyl acetate. Then, the solution was sonicated for 10 min and stirred for 24 h for dispersion. PS-based SPE was prepared by mixing the PS/LiCF3SO3 and Al2O3 solutions for 4 days. The solutions were directly cast on 3 × 3 cm2 stainless steel plates after mixing and then allowed to dry in a vacuum oven for 5 days at 40°C.
Ionic conductivity of the sample was measured by Gamry Instruments' (Warminster, PA, USA) Reference 600 impedance analyzer. Deconvolution of the composite bands of the Fourier transform infrared [FT-IR] spectra was accomplished by the best fits of constituent Gaussian peaks, and the fractions of salt forms were calculated by the peak fitting program of Origin 7.0 software (OriginLab Corporation, Northampton, MA, USA) to analyze the change of salt forms in SPEs. Scanning electron microscopy [SEM] was also used to observe the morphology of the specimen.
Ionic conductivities of PS-based composite SPEs with salt content
Moreover, Al2O3 can dissolve the lithium salt instead of the polar groups in the polymer matrix using Lewis acid-base interactions between the surface group of Al2O3 and salt . The sample consisting 70 wt.% salt and 10 wt.% Al2O3 shows the highest ionic conductivity of 5.83 × 10-5 Scm-1.
Ionic conductivity of PS-based composite SPE according to Al2O3 type and content
FT-IR evidence of dissociated ions
In the polymer-in-salt system, ion clouds made of ion aggregates and ion pairs play an important role in ion conduction , so it is necessary to investigate the change of salt form of the SPE films as salt concentrations increase. FT-IR spectra have confirmed the presence of ion pairs and aggregates in SPEs based upon poly(propylene oxide) [12–16] and PEO [17–24]. A clear distinction between free (dissociated) ions, contact ion pairs, and more aggregates may be observed in the vibrational spectra of the internal mode of anions, such as the triflate anion [Tf-]. Ion association occurs at the SO3 end of the anion; thus, the symmetric SO3 stretching mode is highly sensitive to change in the coordination state of the anion. Band fitting of these regions has provided information pertaining to the types of aggregation and strengths of ionic interactions occurring in the SPEs.
Some band assignments for triflate species
Wave number (cm-1)
Free Tf- ions, solvent-separated pairs
Ion pairs (LiTf), LiTf2-, LiTf32-
Composite SPEs based on PS, LiCF3SO3, and Al2O3 were prepared, and the effect of the Al2O3 type and content on ion conduction properties of SPEs was investigated. As the salt content increased, the ionic conductivities increased continuously. In contrary of the common SPE, PS-based composite SPE has no decrease in ionic conductivity because PS does not contribute to the dissociation of salts and transport of cations. As the Al2O3 content increased, the ionic conductivity increased until the content of Al2O3 reached 10 wt.%. Then, the sample consisting 70 wt.% salt and 10 wt.% Al2O3 shows the highest ionic conductivity of 5.83 × 10-5 Scm-1. The maximum ionic conductivity was found in SPE with acidic Al2O3. The ionic conductivity decreased in the order of SPEs with acidic, neutral, and basic Al2O3. This tendency may be related to the number of free ions by dissociation of salt. The SEM images show that the fillers are well dispersed, and there is no aggregate of fillers until 10 wt.% Al2O3 is reached. On the other hand, as more Al2O3 contents were added, the aggregates of fillers appeared. It seems that the aggregates of fillers disturb the ion transport, so the ionic conductivity increased up to 10 wt.% Al2O3, and then the ionic conductivity decreased. The highest ionic conductivity of 9.78 × 10-5 Scm-1 could be obtained at 10 wt.% acidic Al2O3.
This work was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (no. 2011-0026644).
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