Department of Applied Physics, Shri Shankaracharya Institute of Professional Management & Technology, Raipur - 492015, C.G., India

Abstract

Synthesis of new Ag⁺ ion conducting glass-polymer electrolytes (GPEs): (1-x) PEO: x [0.75(0.75AgI:0.25AgCl):0.25(Ag2O:P₂O₅)], where 0 < x < 50 wt. (%), are reported. GPEs have been casted using hot-press techniques. The highest conducting composition 70 PEO: 30 [0.75(0.75AgI:0.25AgCl):0.25(Ag2O:P₂O₅)], with conductivity (σ) ~ 6.0 × 10^-6 S cm^-1, was identified from the compositional dependent conductivity studies and this has been referred to as the Optimum Conducting Composition (OCC). Approximately three orders of conductivity enhancement have been achieved in GPE OCC from that of the pure polymer PEO. The glass-polymer complexation has been confirmed by SEM and DSC analysis. Ion transport parameters viz. ionic conductivity (σ), ionic mobility (μ), mobile ion concentration (n) and ionic transference number (tion) have been characterized using different experimental techniques. Solid-state polymeric batteries were fabricated using GPE OCC as electrolyte and the cell-potential discharge characteristics were studied under different load conditions at room temperature.

Keywords: glass polymer electrolytes, hot-press method, SEM, DSC, polymer battery.

Introduction

The development of new solid-state dry electrolytes with both high conductivity and limited reactivity with electrodes are of great attention recently [1, 2]. After the demonstration of the first solid polymer battery in 1979 [3], a large number of solid polymer electrolytes (SPEs), involving different mobile ions viz. Li⁺, Na⁺, K⁺, Ag⁺, etc., have been investigated. Among the known electrolytes, solid polymer electrolytes (SPEs) based on high molecular weight dielectric polymer hosts, generally polyethylene oxide (PEO), seem the most suitable electrolytes for solid state device applications. Their ether groups solvate lithium-ions in the same manner as crown ethers, and confer low reactivity, increasing safety. However, the room temperature conductivities of PEO-based polymer electrolytes are in the range of 10^-7 to 10^-8 S cm^-1 because of low effective carrier mobility in the largely crystalline material below the transition temperature [4, 5]. The PEO-based flexible solid polymer electrolytes (SPEs)/ glass-polymer electrolytes (GPEs) show tremendous technological potential to develop ion conducting devices viz. polymer batteries, sensors, smart windows and other electrochemical devices. In a recent work, a number of glass polymer electrolytes (GPEs) have been developed for solid state device applications, which show high ionic conductivity by stabilizing the highly conductive amorphous phase, improve the electrode-electrolyte interfacial stability by trapping residual impurities, extend shelf-life by decreasing PEO recrystallization rate and increase in ion-transference number [5-8]. SPE/ NCPE/ GPE films are prepared, in general, by a traditional solution-cast method. However, recently a novel hot- press technique has been developed for casting SPE/ NCPE films [9-13]. In the present paper, we report the synthesis of a new Ag⁺ ion conducting PEO- based glass polymer electrolyte (GPEs): (1-x) PEO: x [0.75(0.75AgI:0.25AgCl): 0.25(Ag2O:P₂O₅)], where 0 < x < 50 wt. (%), using the hot-press method. The glass-polymer complexation and materials characterization are also reported with the help of SEM and DSC analysis.

Experimental

The AR grade precursor chemicals: poly (ethylene oxide) PEO (105 Mw, Aldrich, USA), AgI (purity >98%, Reidel India), AgC1 (>99%, Reidel India), Ag2O (>98%, Reidel India) and P₂O₅ (>99%, Reidel India) have been used for synthesis of new Glass Polymer Electrolytes (GPEs): (1-x) PEO: x [0.75(0.75AgI:0.25AgCl): 0.25(Ag2O:P₂O₅)], where 0+ ion conducting phosphate glass 0.8(0.75AgI:0.25AgCl):0.2(Ag2O:P₂O₅) has been prepared using the melt-quenching technique [14]. This phosphate glass was used as a host salt for synthesis of GPEs. The dry powders of pure polymer PEO and salt in appropriate wt. (%) ratios were homogeneously mixed for ~ 30 min at room temperature, then heated separately at ~ 70 °C (close to the melting point of PEO) for ~ 30 min with mixing continued. It resulted into a soft lump/ slurry which was then pressed (~ 1.25 ton/ cm²) between two SS-cold blocks, giving rise to a uniform film of thickness ~ 0.013 cm. The details related to hot- press casting of other SPEs/ NCPEs have been given elsewhere in the literature [10-13]. Material characterizations were done with the help of SEM (model: JEOL, JXA-8100, Japan) and DSC (model: Perkin Elmer) techniques. The conductivity (σ)-measurements were carried out on different samples at a fixed frequency (i.e., 5 kHz) using an LCR-bridge (model: HIOKI 3520-01, Japan). The ionic transference number (t_ion) measurements were also carried out by using dc polarization technique at room temperature [15].

A new Ag⁺ ion conducting solid-state polymeric battery was also fabricated in the following cell configuration:

The cell performances were studied under different load conditions at room temperature.

Results and discussion

The conductivity of the glass system increased initially and attained a peak value of x = 0.75, then decreased. The highest conducting composition: 0.75 [0.75AgI: 0.25AgCl]: 0.25 [Ag2O: P₂O₅], with room temperature conductivity s ~ 5.5 × 10^-3 S cm^-1, has been used as a host salt for synthesis of glass polymer electrolytes (GPEs): (1-x) PEO: x [0.75(0.75AgI:0.25AgCl): 0.25(Ag2O: P₂O₅)], where 0 < x < 50 in wt. (%).

However, a moderate sized σ-maxima appears at x = 30 wt.(%) and then decreases on further addition of salts. The GPE films beyond 50 wt. (%) salt concentration were conductivity (σ ~ 6 × 10^-6 S cm^-1), exhibited optimum conductivity and this has brittle and appeared physically less stable. The GPE film: 70PEO: 30[0.75(0.75AgI:0.25AgCl): 0.25(Ag₂O:P₂O₅)], with room temperature been referred to as Optimum Conducting Composition (OCC). The three orders of conductivity enhancement in GPE OCC are due to the increase in the degree of amorphousity/ decrease in degree of crystallinity from that of the pure PEO.

The broad endothermic peak was observed in SPE OCC at ~ 65-67 °C and it corresponds to the melting point temperature of pure PEO. The slightly shifting in the melting point temperature towards lower side is due to the complexation of Ag⁺ ion to the ether oxygen of pure PEO and it is also indicative of the formation of GPEs.

where I_e is the electronic current and I_T is the total current of the cell: [SS / GPE OCC / SS]. tion ~ 0.98 has been obtained by using the above equation and it indicated that the majority of the charge carriers (~ 98 %) are cation Ag⁺, with only a very small contribution (~ 2 %) of the others. tion is close to unity and hence the present GPE systems are very much suitable for the preparation of solid-state electrochemical cells and other ion conducting devices.

The Open Circuit Voltage (OCV) ~ 0.68 V has been obtained for both the cells. It can be clearly noticed that except for the initial potential drop, OCV value remained practically stable for ~ 35 and ~ 15 hrs. when discharged through 100 & 50 kW, respectively (i.e., during a low current drain state). However, the cell potential decreased relatively faster when discharged through 50 kW load (i.e., during higher current drain states). Hence, a GPE based newly polymer battery, performed fairly satisfactorily especially under low current drains.

Conclusions

References

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