Introduction

Lithium-ion secondary batteries are expected to be applied as high energy–density devices for large-scale uses such as electric vehicles1,2. However, commercially available lithium-ion secondary batteries are at risk for liquid leakage and ignition because of the use of organic liquid electrolytes. Therefore, it is necessary to improve their safety. To fulfill this requirement, all-solid-state lithium-ion secondary batteries with non-flammable solid electrolytes are attracting attention. As shown in Figure 1, the use of solid electrolytes enables the stacking of multiple electric cells in series within a single package3,4,5; this allows us to reduce the weight of the package and attain a higher energy density as compared to a single-layered cell. However, the availability of materials is limited to solid electrolytes that have high lithium-ion conductivity and are stable towards lithium metals6,7,8. Further, there have been reports that suggested that it is difficult to form a good interface between cathode active materials and electrolytes when using solid electrolytes9. Therefore, the development of novel solid electrolyte materials that can resolve these problems is required.

Figure 1
figure 1

Schematic of (a) conventional stacked Li-ion battery using a liquid electrolyte and (b) bipolar stacked all-solid-state Li battery.

Ionic liquids are expected to be high-performance electrolyte materials because of their high conductivity, wide potential window, low vapor pressure and flame resistance, etc10,11,12. In recent years, Watanabe's research group has proposed novel complex-type ionic liquids and reported the proper operation of devices containing tetraethylene glycol dimethyl ether (Tetraglyme, G4) and Li-TFSA, i.e., ether-type solvents with an equimolar complex13,14,15,16,17,18. Ionic liquids can be handled as quasi-solid-states or gels because of their interactions with oxides19,20,21,22,23,24,25,26 and are being studied for energy-device applications such as dye-sensitized solar cells20 and lithium-ion secondary batteries22,23,24,25,26. Our research group has developed solid electrolytes that could be handled as quasi-solid-states because of the strong interactions between the ionic liquids and oxide nanoparticles; these materials showed similar transport properties as bulk ionic liquids. We also investigated the quasi-solidification of the Li-Glyme complex as an ionic liquid complex; an all-solid-state lithium battery with this electrolyte was proven to operate properly25,26 and are for the preliminarily tested bipolar multilayered device in our previous reports27. Therefore, in this study, we prepared high-voltage bipolar stacked batteries using a quasi-solid-state electrolyte containing a Li-Glyme complex and the performance of this device was evaluated.

Results

Evaluation of bipolar stacked all-solid-state Li battery

Single-layer all-solid-state battery was prepared by stacking LiFePO4 cathode composite, quasi-soild-state electrolyte sheet and a Li metal anode. As shown in Figure 2, bipolar stacked all-solid-state batteries were fabricated by layering two or three single-layer batteries and trapping them with current collectors in the same CR2032 module of a coin cell. Figure 3 (a) shows the 10th charge–discharge profiles of the single-layered (one cell unit), double-layered (two cell units) and triple-layered (three cell units) all-solid-state lithium batteries at 35°C and 0.1 C. For the single-layered battery, the 10th discharge capacity was 161 mAh/g and the cathode utilization ratio was as high as 94%. For the double-layered and triple-layered batteries, the 10th discharge capacities were 155 and 156 mAh/g, respectively and the cathode utilization ratios were 91% and 91%, respectively. The cathode utilization ratios of the double-layered and triple-layered batteries were as high as that of the single-layered battery. The double-layered and triple-layered batteries showed plateau potentials of 6.7–6.8 and 10.0–10.2 V, respectively. These values for double-layered and triple-layered batteries were two and three times than that (3.4 V) of the single-layered battery, respectively, confirming that the electric cells within a single package did not have internal short-circuits and the stacked batteries operated successfully.

Figure 2
figure 2

(a) Structure of the device of a triple-layered bipolar stacked all-solid-state Li battery and (b) photograph of the components of a bipolar stacked cell.

Figure 3
figure 3

(a) 10th charge–discharge profiles of bipolar stacked all-solid-state Li batteries containing one, two and three cell units at the C-rate of 0.1 C. (b) 1st and 100th charge-discharge profiles and (c) cycling properties of double-layered all-solid-state Li batteries at 35°C at 0.1 C (red), 0.2 C (green) and 0.5 C (blue) rates.

Figure 3 (b) shows the charge–discharge profiles of the first and 100th cycles for the double-layered all-solid-state lithium battery at rates of 0.1 C, 0.2 C and 0.5 C. The initial capacities at 0.2 C and 0.5 C were 140 and 118 mAh/g, respectively and plateau potentials were observed at 6.6–6.7 and 6.4–6.5 V, respectively. These results indicated that, at 0.2 C and 0.5 C, the double-layered battery showed a high cathode utilization ratio, i.e., similar to that of the single-layered battery and showed that the device could be operated successfully without any internal short-circuiting. Figure 3 (c) shows the cycling properties and coulombic efficiencies of the double-layered all-solid-state device at 0.1 C, 0.2 C and 0.5 C. The coulombic efficiencies at 0.1 C, 0.2 C and 0.5 C were as high as 99, 98 and 99%, respectively. After the 200th cycle, the device retained 91, 89 and 99% of the capacity after the 10th cycle at each C-rate, respectively, indicating good cycling properties. Figure 4 shows the 10th and 100th charge–discharge profiles of the triple-layered all-solid-state lithium battery at rate of 0.2 C. The 10th and 100th discharge capacities were 98 and 96 mAh/g, respectively, indicating good cycle performance. Only a few studies on stacked all-solid-state devices have been reported to date and, although stacked devices using polymer electrolytes3,5 or Li3PO44 have been investigated, they showed low cathode utilization ratios because of their high internal electrolyte resistance. Furthermore, there have been a few studies on evaluation of cycle property to date. Thus, to the best of our knowledge, this is the first report on stacked all-solid-state lithium batteries which indicates good cycle properties and we successfully developed the high-voltage all-solid-state lithium devices in 6 and 10 V classes.

Figure 4
figure 4

The 10th and 100th charge-discharge curves of triple-layered bipolar stacked cell at 35°C and 0.2 C.

Cross-sectional SEM image of all-solid-state Li cell

Figure 5(a) shows a cross-sectional SEM image of the all-solid-state lithium battery and Figure 5(b) shows the EDX mapping results. The red region represents P derived from LiFePO4 and the blue region represents Si derived from fumed SiO2. This SEM image indicated the formation of a continuous and proper interface between the cathode and electrolyte. Furthermore, the SEM images of the cathode composite in Figures 5(c) and (d) confirmed the formation of a good lithium-ion transport interface between LiFePO4 and the quasi-solid-state electrolyte in the cathode composite, which led to the high efficiency of the cathode for the stacked all-solid-state batteries prepared in this study.

Figure 5
figure 5

(a) Cross-sectional SEM image and (b) Si (blue) and P (red) distributions of the all-solid-state Li battery. (c) SEM image and (d) Si (blue) and P (red) distributions of the cathode composite containing LiFePO4 and quasi-solid electrolyte using fumed SiO2.

Discussion

High-voltage stacked lithium batteries using quasi-solid-state electrolytes containing a Li-Glyme complex were prepared and the performances of the devices were evaluated via charge–discharge testing. It was confirmed that no internal short-circuits occurred within the single packages containing double- and triple-layered devices and these devices operated successfully. We successfully developed stacked lithium batteries with high cathode utilization ratio and good cycling properties.

Methods

Preparation of quasi-solid-state electrolyte

Equimolar amounts of lithium bis(trifluoromethanesulfonyl)amide powder (Li-TFSA,>99%, Kishida Chemical Co.) and tetraethylene glycol dimethyl ether (Tetraglyme, G4, 99%, Sigma-Aldrich Co.) were mixed to obtain a [Li(G4)][TFSA] solution. This [Li(G4)][TFSA] solution and fumed silica nanoparticles (Sigma-Aldrich Co., specific surface area: 390 m2 g−1, particle size: 7 nm) were then mixed and stirred in methanol for 3 h to achieve a volume fraction of 80%. The resulting mixture was dried on a hot plate at 60°C for 12 h to obtain a quasi-solid-state electrolyte powder. The resulting quasi-solid-state electrolyte powder and polytetrafluoroethylene (PTFE, Teflon-J, DuPont-Mitsui Fluorochemicals Co., Ltd.) were mixed to obtain a 5 wt% mixture, which was used to prepare a free-standing films with 200 μm thickness and 12 mm diameter.

Performance evaluation of bipolar stacked all-solid-state lithium batteries

LiFePO4 (Tatung Fine Chemicals Co., theoretical capacity: 170 mAh/g), acetylene black (AB), the quasi-solid-state electrolyte powder and PTFE were mixed (weight fraction of 34:11:45:10) and a cathode composite with cathode weight of 2 mg, 100 μm thickness and 4 mm diameter was prepared. A single-layered all-solid-state lithium secondary battery was prepared by directly stacking cathode composite, φ 12 mm quasi-solid-state electrolyte sheet with 200 μm thickness and φ 10 mm lithium metal anode with 100 μm thickness. As shown in Figure 2, two or three single-layered all-solid-state batteries were sandwiched between current collectors (SUS304L) and stacked in the same CR2032 module of a coin cell to prepare high-voltage stacked all-solid-state batteries. The cut-off voltage was set at 2.0–4.0 V for the single-layered battery, while those of the double-layered and triple-layered batteries were set at 5.0–8.0 V and 7.0–12.0 V, respectively. Charge–discharge measurements were performed on a HOKUTO Denko Corp. 8CH charge/discharge unit for the single-layered and double-layered batteries and a HOKUTO Denko Corp. HZ-7000 electrochemical measurement system for the triple-layered battery at 35 °C and 0.1 C and 0.2 C. The charge-discharge characteristics of double-layered cells were evaluated at 0.1 C, 0.2 C and 0.5 C.

Cross-sectional SEM image of all-solid-state cell

A scanning electron microscope (SEM, SU-6600, HITACHI) and an energy dispersive X-ray spectrometer (EDX, Incas-act, Oxford Instruments) were used to characterize the cathode composite. Cross-section polisher (IB-09020CP, JEOL) was used to prepare cross-sectional all-solid-state device for observation.