Effect of β-Cyclodextrin on Physicochemical Properties of an Ionic Liquid Electrolyte Composed of N-Methyl-N-Propylpyrrolidinium bis(trifluoromethylsulfonyl)amide

Ionic liquids (ILs) are promising electrolyte materials for developing next-generation rechargeable batteries. In order to improve their properties, several kinds of additives have been investigated. In this study, β-cyclodextrin (β-CD) was chosen as a new additive in IL electrolytes because it can form an inclusion complex with bis(trifluoromethylsulfonyl)amide (TFSA) anions. We prepared the composites by mixing N-methyl-N-propylpyrrolidinium bis(trifluoromethylsulfonyl)amide/LiTFSA and a given amount of triacetyl-β-cyclodextrin (Acβ-CD). The thermal behaviors and electrochemical properties of the composites were analyzed by several techniques. In addition, pulse field gradient NMR measurements were conducted to determine the self-diffusion coefficients of the component ions. The addition of Acβ-CD to the IL electrolytes results in the decrease in the conductivity value and the increase in the viscosity value. In contrast, the addition of Acβ-CD to the IL electrolytes induced an improvement in the anodic stability because of the formation of an inclusion complex between the Acβ-CD and TFSA anions. CDs are potential candidates as additives in IL electrolytes for electrochemical applications.

Introduction

Ionic liquids (ILs) have been attractive as electrolyte materials because of their unique properties such as high ionic conductivity at room temperature and wide potential window (Armand et al., 2009). In addition, as ILs have a low vapor pressure and low flammability, they will be suitable for developing safer electrolytes instead of organic solvents (Ohno, 2011). Among onium cations, pyrrolidinium-based ILs are primarily being used as electrolytes in rechargeable batteries (Ishikawa et al., 2006; Matsumoto et al., 2006; Seki et al., 2008; Yoon et al., 2015). Pyrrolidinium-based ILs are superior in thermal and electrochemical stability as compared to those of other onium-based ILs. However, it is difficult to realize target ion transport with ions such as lithium ions or sodium ions in ILs, because the component ions of ILs as solvents also migrate along the potential gradient. New designs of ILs that address such drawback has been proposed by many researchers. For example, one candidate is poly(IL)s, which fix cation or anion species on the polymer chain (Yuan et al., 2013; Nishimura and Ohno, 2014; Qian et al., 2017). Another candidate is zwitterions, which have the cation and anion in the same molecule (Yoshizawa et al., 2004; Narita et al., 2006; Yoshizawa-Fujita et al., 2011). Nevertheless, it is still difficult to achieve a high ionic conductivity over 10⁻² S cm⁻¹ at room temperature and a high lithium transference number (t_Li+) over 0.5.

Rechargeable batteries, especially lithium-ion batteries (LIBs), employing ILs as the electrolyte materials have been developed (Ishikawa et al., 2006; Matsumoto et al., 2006; Seki et al., 2008; Ohno, 2011). For practical applications, a high energy density of LIBs is required. In order to improve the energy density of LIBs, the cells are needed to be operated at higher cut-off voltages. However, high cut-off voltages induce a significant decrease in the charge/discharge cycle stability of LIBs due to the decomposition of electrolytes. As a result, a passivation layer on the electrode is formed, even when ILs are used as electrolytes (Seki et al., 2008). The decomposition reaction of electrolytes should be suppressed at high cut-off voltages to allow the use of high-voltage cathode materials [e.g., LiCo_1/3Ni_1/3Mn_1/3O₂ (Yabuuchi and Ohzuku, 2003), LiNi_0.5Mn_1.5O₄ (Zhu et al., 2014)]. Various additives have been used to improve the anodic stability of electrolyte materials (Franco, 2015).

Cyclodextrin (CD) is a circular oligosaccharide composed of α-D(+)-glucopyranose units. The CD, which possesses seven glucose units, is called β-CD. They have a three-dimensional funnel-shaped architecture with a narrower rim molded by a hydrogen-bonding network built by primary OH groups (one group per glucose unit), and with a broader rim composed of secondary OH groups (two groups per glucose unit) (Crini, 2014). The two rims of the molecules are hydrophilic, while the interior of their cavity is hydrophobic. It is known that β-CD tends to form inclusion complexes with guest molecules with suitable characteristics of polarity and dimension in aqueous solutions (Silva et al., 2008; Baâzaoui et al., 2016). CD is among the most frequently used host molecule in supramolecular chemistry; this ability has been widely used in food and pharmaceutical studies (Szejtli, 1998; Crini, 2014). It has also been widely used in lithium battery research as a surfactant to effectively disperse solid substances in liquids and as an agent to promote complexation reactions, which is beneficial to material dispersion and molding (Chen et al., 2016).

Recently, Amajjahe et al. (2008) found that the anion of 1-butyl-3-vinylimidazolium bis(trifluoromethylsulfonyl)amide exclusively formed a host–guest complex with β-CD (Amajjahe and Ritter, 2008; Amajjahe et al., 2008). He et al. (2009) investigated the interaction of hydrophobic ILs and β-CD in detail (He et al., 2009). They found that the imidazolium cation did not interact with β-CD while its long alkyl side chain did. In addition, hydrophobic anions with fluorine atoms could interact with β-CD, and the interaction between the bis(trifluoromethylsulfonyl)amide (TFSA) anion and β-CD was stronger than those of BF₄ and PF₆ anions. These results prompted us to investigate the effect of β-CD on the physicochemical properties of ILs, and we expected that the anion trap ability of β-CD would contribute to the enhancement of the Li-ion conductivity and the improvement of the electrochemical stability. In this study, a pyrrolidinium-based IL with a TFSA anion, N-methyl-N-propylpyrrolidinium bis(trifluoromethylsulfonyl)amide ([C₃mpyr][TFSA]) (see Figure 1), was used as the electrolyte solution. Its LiTFSA composites were prepared and mixed with different amounts of β-CD, and their physicochemical and electrochemical properties were evaluated.

FIGURE 1

Figure 1. Chemical structures of [C₃mpyr][TFSA], and Acβ-CD.

Experimental

Materials

N-Methylpyrrolidine (Tokyo Chemical Industry Co., Ltd., > 98.0%), 1-chloropropane (Tokyo Chemical Industry Co., Ltd., > 99.0%), and lithium bis(trifluoromethylsulfonyl)amide (LiTFSA) (Kishida Chemical Co., Ltd., 99.0%) were purchased. N-Methylpyrrolidine and 1-chloropropane were purified by distillation in vacuo prior to use. Triacetyl-β-cyclodextrin (Acβ-CD) (Tokyo Chemical Industry Co., Ltd., > 97.0%) (see Figure 1) was used after drying.

[C₃mpyr][TFSA] was prepared as follows. N-Methyl-N-propylpyrrolidinium chloride ([C₃mpyr][Cl]) was synthesized according to a previously published procedure (Laus et al., 2008). [C₃mpyr][Cl] and LiTFSA were separately dissolved in deionized water. LiTFSA aq. was added dropwise to [C₃mpyr][Cl] aq. The resulting liquid was purified by washing repeatedly with deionized water until no residual chloride was detected with the use of AgNO₃ aq. [C₃mpyr][TFSA] was obtained as a colorless liquid at room temperature and characterized by ¹H NMR, fast atom bombardment mass spectrometry (FAB-MS), and elemental analysis. ¹H NMR (CD₂Cl₂, 300 MHz): δ (ppm) = 3.50 (2H, ddd, J = 10.22, 5.58, 3.01 Hz), 3.26 (1H, dt, J = 8.59, 4.04 Hz), 3.04 (1.5H, s), 2.27 (2H, s), 1.83 (1H, tt, J = 12.20, 5.61 Hz), 1.06 (1.5H, t, J = 7.39 Hz). MS (FAB⁺): m/z 128.2 [M], 536.4 [2M+X]⁺, MS (FAB⁻): m/z 280.0 [X], 688.0 [M+2X]⁻. Anal. Calcd. for C₁₀H₁₈F₆N₂O₄S₂ (%): C, 29.4; H, 4.44; N, 6.86; S, 15.7; Found (%): C, 29.2; H, 4.42; N, 6.78; S, 16.1.

A given amount of LiTFSA was dissolved in [C₃mpyr][TFSA] [IL:LiTFSA = 18 : 1 (molar ratio)], and then a given amount of Acβ-CD was added into IL/LiTFSA composites at molar ratios LiTFSA:Acβ-CD = 1.0 : 0.5, 1.0 : 1.0, and 1.0 : 1.5. Four kinds of samples were prepared to investigate the effect of Acβ-CD on the properties of the IL electrolyte. Their composites are abbreviated as the molar ratio of Acβ-CD. For example, the abbreviation of [C₃mpyr][TFSA] : LiTFSA : Acβ-CD = 18 : 1 : 1.5 is Acβ-CD1.5. These mixtures were stirred at 60°C for 24 h.

Measurements

Fourier-transform infrared (FT-IR) measurements were performed on a Nicolet 6700 (Thermo Fisher Scientific) by using KRS-5.

¹H and ¹⁹F NMR measurements were carried out with a Bruker Avance III HD 400 MHz at 25°C. Thermogravimetric analysis was conducted using a TG-DTA instrument (TG/DTA7200, Hitachi High-Technologies Corp.) under a nitrogen atmosphere at temperatures ranging from 25 to 500°C at a heating rate of 10°C min⁻¹. The thermal behavior was examined using differential scanning calorimetry (DSC) (DSC7020, Hitachi High-Technologies Corp.) at temperatures between −150 and 100°C at a heating/cooling rate of 10°C min⁻¹.

Impedance measurements were carried out using a VSP-300 (Bio-Logic Science Instruments) at frequencies ranging from 100 mHz to 1 MHz and temperatures ranging from 80 to −40°C. The temperature was controlled by a constant-temperature oven (SU-642, Espec Corp.). The composites were enclosed in a homemade glass cell having two platinum electrodes. The measurements were carried out by maintaining the cells at each temperature for 30 min. Viscosity measurements were carried out using a stabinger viscometer (SVM3000, Anton Paar) and temperature ranging from 80 to 20°C.

Pulse field gradient nuclear magnetic resonance (PFG-NMR) measurements were carried out with a Bruker Avance III HD 400 MHz at 80°C for ¹H, ⁷Li, and ¹⁹F nucleus. The ILs were filled into 5-mm NMR tubes, which were sealed. The measurements were carried out in 16 gradient steps per diffusion experiment. The gradient strength was 1,700 G cm⁻¹. The diffusion coefficients were calculated from the peak integration attenuation according to Equation 1 (Tanner and Stejskal, 1968):

$\begin{array}{ll}A=A_0-\text{exp}[{(\gamma \delta \text{G})}^2\text{D}(\Delta -\frac{\delta }{3})]& (1)\end{array}$

where A is the signal at a certain gradient (G), A₀ is the signal at a gradient of 0, δ is the width of the gradient pulse, Δ is the diffusion time, D is the diffusion coefficient, and γ is the gyromagnetic ratio of the nuclei.

Linear sweep voltammetry (LSV) measurements were carried out by using a VSP-300 (Bio-Logic Science Instruments) in the potential range of −0.2 and 6 V at 60°C at a scan rate of 1.0 mV s⁻¹. Li foils were used as the reference and counter electrodes, while Ni and Pt plates were used as working electrodes in the potential ranges of −0.2–3.0, and 3.0–6.0 V, respectively. The electrodes were separated by a glass filter to prevent short-circuiting. The cyclic voltammetric measurements of [C₃mpyr][TFSA]:LiTFSA:Acβ-CD = 18:1:1.0 composites were carried out using a VSP-300 (Bio-Logic Science Instruments) in the potential range of −0.25–1.0 V at 25, at a scan rate of 1.0 mV s⁻¹, with Li foils as the reference and counter electrodes, and the Ni plate was used as the working electrode. The electrodes were separated by a glass filter to prevent short-circuiting.

Results and Discussion

Interaction Between Acβ-CD and TFSA Anion

A given amount of β-CD was initially added into [C₃mpyr][TFSA] and its LiTFSA mixture. Unfortunately, the IL electrolytes could not dissolve β-CD at any concentration. β-CD possesses hydroxyl groups, which form hydrogen bonds. The Lewis basicity of the TFSA anion is weak, and the TFSA anion cannot break the hydrogen bond. In fact, ILs with anions such as chloride and acetate, which exhibit a stronger Lewis basicity, can dissolve cellulose (Ohno and Fukaya, 2009) as such anions interact with the hydroxyl groups of cellulose because of the strong electron-donating ability. The TFSA anion could not dissolve even oligosaccharides. Therefore, Acβ-CD was used in this study instead of β-CD. A given amount of Acβ-CD was added into the IL electrolytes. [C₃mpyr][TFSA] with a weak Lewis-base anion could dissolve Acβ-CD, which has an acetyl group instead of a hydroxyl group.

FT-IR measurements were conducted, and each peak was assigned according to the literatures (Liu et al., 2009; Roy et al., 2016; Li et al., 2017; Wu et al., 2017). Figure 2 presents FT-IR spectra of [C₃mpyr][TFSA]/LiTFSA and [C₃mpyr][TFSA]/LiTFSA/Acβ-CD composites. The FT-IR spectrum of [C₃mpyr][TFSA]/LiTFSA exhibits characteristic peaks for C-H stretching, CH₂ bending, and S = O stretching bands etc. The peaks in the range from 2,978 to 2,882 cm⁻¹ can be assigned to the C-H stretching and CH₂ bending modes. In the case of TFSA anion, the peaks of S = O stretching band and C-SO₂-N bond are observed at 1,349 and 1,136 cm⁻¹, respectively. In addition, CF₃ symmetric stretching modes are located in 1,195 cm⁻¹ and 1,056 cm⁻¹. For the spectrum of [C₃mpyr][TFSA]/LiTFSA/Acβ-CD, a new peak is observed at 1,746 cm⁻¹, which is assigned to C = O stretching mode for acetyl group, and the absorbance increases with increasing the Acβ-CD amount, indicating that the composites are formed by mixing [C₃mpyr][TFSA]/LiTFSA and Acβ-CD.

FIGURE 2

Figure 2. FT-IR spectra of [C₃mpyr][TFSA]/LiTFSA composites and their Acβ-CD composites.

¹⁹F NMR measurements were carried out to investigate the interaction between Acβ-CD and the TFSA anion. Figure 3 presents ¹⁹F NMR spectra of the CF₃ group in the TFSA anion for the [C₃mpyr][TFSA]/LiTFSA and [C₃mpyr][TFSA]/LiTFSA/Acβ-CD composites. The chemical shifts of the CF₃ group of the TFSA anion are −79.73, −79.80, −79.88, and −79.99 ppm for the Acβ-CD 1.5, 1.0, 0.5, and 0 composites, respectively. Zhang et al. (2014) performed ¹⁹F NMR measurements of 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)amide to detect the host–guest interaction between the β-CD and TFSA anion (Zhang et al., 2014). As the molar ratio of CD increases, downfield shifts for the fluorine atom of the CF₃ group in the TFSA anion are observed because of the formation of the complex for CD and the TFSA anion. In all the [C₃mpyr][TFSA]/LiTFSA/Acβ-CD composites, the CF₃ group chemically shifts to a lower magnetic field as compared to that of Acβ-CD 0, suggesting that Acβ-CD forms a complex with the TFSA anion.

FIGURE 3

Figure 3. ¹⁹F NMR spectra of [C₃mpyr][TFSA]/LiTFSA composites and their Acβ-CD composites.

Thermal Properties

To evaluate the thermal stability, onset thermal decomposition temperatures (T_d) were measured. Figure 4 shows TGA traces for the [C₃mpyr][TFSA]/LiTFSA and [C₃mpyr][TFSA]/LiTFSA/Acβ-CD composites. Acβ-CD 0 shows a T_d value at 386°C. Pyrrolidinium-based ILs with the TFSA anion are known to exhibit a higher thermal stability, and the T_d value of Acβ-CD 0 is consistent with the literature value (Yang et al., 2014). All the composites with Acβ-CD show similar T_d values, and their T_d values are about 300°C. This is due to the decomposition of Acβ-CD. The amount of weight loss is consistent with the amount of added Acβ-CD in the IL electrolytes.

FIGURE 4

Figure 4. TGA curves of [C₃mpyr][TFSA]/LiTFSA composites and their Acβ-CD composites.

DSC traces of the composites are presented in Figure 5. Acβ-CD 0 exhibits a melting point (T_m) of 8.0°C, which is consistent with the literature value (Wu et al., 2011). When the addition amount of Acβ-CD is 0.5 in the molar ratio, the glass transition temperature (T_g), two crystallization temperatures, and T_m are observed at −91, −33, −19, and 7.1°C, respectively. Acβ-CD 0.5 exhibits no crystallization temperature upon the cooling scan. In addition, the T_m value of Acβ-CD 0.5 slightly decreases as compared to that of Acβ-CD 0. The crystallization temperature and T_m cannot be observed in the composites in which the added amount of Acβ-CD is larger than the amount of Li salt in the molar ratio. Acβ-CD 1.0 and 1.5 exhibits T_g only and maintains low values below −79°C. These results suggest that the interaction between the Acβ-CD and TFSA anion prevents the crystallization of the IL.

FIGURE 5

Figure 5. DSC charts of [C₃mpyr][TFSA]/LiTFSA composites and their Acβ-CD composites.

Conductivity and Viscosity

Arrhenius plots of the ionic conductivities for the composite electrolytes are presented in Figure 6. Figure 7 exhibits a typical Nyquist plot for Acβ-CD 1.5 at 0°C. The ionic conductivity values were calculated from the touchdown point on the Z′-axis which exhibits the resistance of the compound. For Acβ-CD 0 and 0.5, the conductivity values were not obtained by means of our impedance apparatus, because of the crystallization of the electrolytes below 0°C, which is consistent with the DSC results. According to the DSC results, as Acβ-CD 1.0 and 1.5 are liquid in a wide temperature range, they exhibit a higher ionic conductivity even below 0°C, as shown in Figure 5. The ionic conductivities of the Acβ-CD 1.5, 1.0, 0.5, and 0 composites are 3.2 × 10⁻⁴, 5.1 × 10⁻⁴, 1.6 × 10⁻³, and 2.1 × 10⁻³ S cm⁻¹ at 25°C, respectively. The addition of Acβ-CD results in the decrease in the conductivity value, ascribable to the formation of an inclusion complex between Acβ-CD and the TFSA anion. This complex decreases the diffusivity of the component ions, thus decreasing the ionic conductivities. Roy and Roy (2017) used trihexyltetradecylphosphonium chloride as an IL, where a similar decrease in conductivity was observed as the amount of CD increased. The decrease in conductivity will be due to the encapsulation of guest molecules in the hydrophobic cavity of CD (Roy and Roy, 2017).

FIGURE 6

Figure 6. Arrhenius plots of ionic conductivities for [C₃mpyr][TFSA]/LiTFSA composites and their Acβ-CD composites.

FIGURE 7

Figure 7. A typical Nyquist plot for Acβ-CD 1.5 at 0°C.

Figure 8 shows the ionic conductivity at 25°C and viscosity at 30°C as a function of the molar ratio of Acβ-CD. The ionic conductivity monotonously decreases with the Acβ-CD content as mentioned above. The viscosity values of the Acβ-CD 1.5, 1.0, 0.5, and 0 composites are 19,000, 1,700, 250, and 60 mPa s at 30°C, respectively. The viscosity values increase steeply as Acβ-CD is added to the composites. In addition, the conductivities and viscosities are inversely proportional (Salminen et al., 2007). The viscosity increases with CD concentration probably because of the IL and CD interactions and solvation (Roy et al., 2016). Thus, it is considered that the ionic conductivities decrease because of the increase in the viscosities of the composites.

FIGURE 8

Figure 8. Correlation between ionic conductivity and viscosity for [C₃mpyr][TFSA]/LiTFSA composites and their Acβ-CD composites.

Diffusion Coefficients

The self-diffusion coefficients of C₃mpyr⁺ (D_H), Li⁺ (D_Li), and TFSA⁻ (D_TFSA) for the [C₃mpyr][TFSA]/LiTFSA and [C₃mpyr][TFSA]/LiTFSA/Acβ-CD composites were determined by means of PFG-NMR at 80°C, as shown in Figure 9. The D_H and D_TFSA values of these composites are almost the same at 80°C, while the D_Li value is lower than those of the D_H and D_TFSA values. The increase in the Acβ-CD content induces a large difference between the D_Li value and other values. The apparent lithium transfer number (t_Li+) was calculated from the diffusion coefficient values using Equation (2):

$\begin{array}{cc}{t}_{{\text{Li}}^{+}}=\frac{D_{\text{Li}}}{D_{\text{Li }}+D_{\text{TFSA }}+D_{\text{H }}}& (2)\end{array}$

FIGURE 9

Figure 9. Diffusion coefficients of [C₃mpyr][TFSA]/LiTFSA composites and their Acβ-CD composites as a function of mole ratio of Acβ-CD.

Unlike electrochemical techniques, the diffusion coefficients obtained using the PFG-NMR mwcies but also from non-ionic species (Horiuchi et al., 2017). The $t_{\text{Li}}^{+}$ values of the Acβ-CD 1.5, 1.0, 0.5, and 0 composites were 0.06, 0.08, 0.12, and 0.22, respectively. The decrease in the $t_{\text{Li}}^{+}$ values with the increase in Acβ-CD content suggests that an inclusion complex will be formed between LiTFSA and Acβ-CD. In addition, Acβ-CD would form an inclusion complex with not only LiTFSA but also the aggregation including a Li cation, similar to the combination of two TFSA anions and one Li cation because the large surface charge density of a Li cation induces the formation of cluster ions (Appetecchi et al., 2016).

Electrochemical Properties

The electrochemical stabilities of the [C₃mpyr][TFSA]/LiTFSA and [C₃mpyr][TFSA]/LiTFSA/Acβ-CD composites were investigated by LSV on a Ni electrode (from 3 to −0.2 V) and Pt electrode (from 3 to 6 V) at 60°C. The LSV results are presented in Figure 10. The electrochemical window (EW = E_anodic-E_cathodic) of all the IL electrolytes was determined from the values for the cathodic (E_cathodic) limit at −0.1 mA cm⁻² and anodic (E_anodic) limit at 0.1 mA cm⁻². The EW value of Acβ-CD 0 is 4.6 V vs. Li/Li⁺ and that of Acβ-CD 0.5 is 4.6 V vs. Li/Li⁺, which is almost the same as that of Acβ-CD 0. The EW values are about 5.5 V vs. Li/Li⁺ for both Acβ-CD 1.0 and 1.5 composites. As the addition amount of Acβ-CD increases, the oxidation stability improves. This improvement should be based on the formation of an inclusion complex between Acβ-CD and the TFSA anion because the anodic stability significantly improves, and the cathodic stability is almost the same regardless of the addition of Acβ-CD.

FIGURE 10

Figure 10. Linear sweep voltammograms of [C₃mpyr][TFSA]/LiTFSA composites and their Acβ-CD composites.

The reversible oxidation and reduction reactions of lithium were examined at room temperature for Acβ-CD 1.0. Figure 11 shows the cyclic voltammogram for Acβ-CD 1.0 on a Ni electrode. Acβ-CD 1.0 exhibits reduction and oxidation peaks for Li at about −0.1 and 0.1 V vs. Li/Li⁺, respectively. The current density decreases with the cycling number from 1st to 10th. After that, the current density maintains a constant value, and stable reversible redox reactions are observed during 20 cycles. At the initial anodic sweep, an anodic current is observed. This behavior is also observed for pyrrolidinium-based ILs (Towada et al., 2015; Horiuchi et al., 2016). In addition, the maximum current density of the anodic peak slightly shifts to a higher potential value with the increase in cycle number. These results suggest that a solid electrolyte interphase film is formed on the Ni electrode surface (Grande et al., 2015), even in the presence of Acβ-CD.

FIGURE 11

Figure 11. Cyclic voltammograms of Acβ-CD 1.0 at 25°C.

Conclusions

The effect of Acβ-CD on the properties of [C₃mpyr][TFSA]/LiTFSA was investigated by means of several techniques. The chemical shift of the CF₃ group of the TFSA anion shifted to a lower magnetic field with the increase in the Acβ-CD content. With the addition of Acβ-CD to the IL electrolyte, the T_m of the IL disappeared and the viscosity increased. These results suggest that an inclusion complex is formed between Acβ-CD and the TFSA anion. In contrast, the t_Li+ and D_Li values decreased with the increase in the Acβ-CD content in the composites. The anodic stability of [C₃mpyr][TFSA]/LiTFSA was significantly improved after adding a certain amount of Acβ-CD. Li plating and stripping in the [C₃mpyr][TFSA]/LiTFSA/Acβ-CD composite were repeatedly observed. According to these results, Acβ-CD will be an interesting additive for improving the electrochemical stability of ILs. It is known that there are three kinds of CD, α-CD, β-CD, and γ-CD, which have different cavity sizes. The physicochemical properties of various ILs with different anions could be controlled by choosing suitable CD derivatives.

Author Contributions

MS and MY-F designed the research. MS prepared the samples and measured the properties. MS and NK carried out the NMR measurements and the data collection. YT, MR, and MY-F participated in the data analysis. MS and MY-F wrote the manuscript.

Funding

This work was supported by a Sophia University Special Grant for Academic Research.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We thank Sophia University for instrumental analyses (FAB-MS and elemental analysis).

References

Amajjahe, S., Choi, S., Munteanu, M., and Ritter, H. (2008). Pseudopolyanions based on poly(NIPAAM-co-beta-cyclodextrin methacrylate) and ionic liquids. Angew. Chem. Int. Ed. Engl. 47, 3435–3437. doi: 10.1002/anie.200704995

PubMed Abstract | CrossRef Full Text | Google Scholar

Amajjahe, S., and Ritter, H. (2008). Anion complexation of vinylimidazolium salts and its influence on polymerization. Macromolecules 41, 716–718. doi: 10.1021/ma702271p

CrossRef Full Text | Google Scholar

Appetecchi, G. B., D'Annibale, A., Santilli, C., Genova, E., Lombardo, L., Navarra, M. A., et al. (2016). Novel functionalized ionic liquid with a sulfur atom in the aliphatic side chain of the pyrrolidinium cation. Electrochem. Commun. 63, 26–29. doi: 10.1016/j.elecom.2015.12.009

CrossRef Full Text | Google Scholar

Armand, M., Endres, F., MacFarlane, D. R., Ohno, H., and Scrosati, B. (2009). Ionic-liquid materials for the electrochemical challenges of the future. Nat. Mater. 8, 621–629. doi: 10.1038/nmat2448

PubMed Abstract | CrossRef Full Text | Google Scholar

Baâzaoui, M., Béjaoui, I., Kalfat, R., Amdouni, N., Hbaieb, S., and Chevalier, Y. (2016). Interfacial properties and thermodynamic behavior of cationic amphiphilic β-cyclodextrins substituted with one or seven alkyl chains. RSC Adv. 6, 72044–72054. doi: 10.1039/C6RA10597A

CrossRef Full Text | Google Scholar

Chen, R., Lai, J., Li, Y., Cao, M., Chen, S., and Wu, F. (2016). β-Cyclodextrin coated lithium vanadium phosphate as novel cathode material for lithium ion batteries. RSC. Adv. 6, 103364–103371. doi: 10.1039/C6RA22400H

CrossRef Full Text | Google Scholar

Crini, G. (2014). Review: a history of cyclodextrins. Chem. Rev. 114, 10940–10975. doi: 10.1021/cr500081p

PubMed Abstract | CrossRef Full Text | Google Scholar

Franco, A. A. (2015). Rechargeable Lithium Batteries. Cambridge: Woodhead/Elsevier Science.

Google Scholar

Grande, L., von Zamory, J., Koch, S. L., Kalhoff, J., Paillard, E., and Passerini, S. (2015). Homogeneous lithium electrodeposition with pyrrolidinium-based ionic liquid electrolytes. ACS Appl. Mater. Interfaces 7, 5950–5958. doi: 10.1021/acsami.5b00209

PubMed Abstract | CrossRef Full Text | Google Scholar

He, Y., Chen, Q., Xu, C., Zhang, J., and Shen, X. (2009). Interaction between ionic liquids and β-cyclodextrin: a discussion of association pattern. J. Phys. Chem. B 113, 231–238. doi: 10.1021/jp808540m

PubMed Abstract | CrossRef Full Text | Google Scholar

Horiuchi, S., Yoshizawa-Fujita, M., Takeoka, Y., and Rikukawa, M. (2016). Physicochemical and electrochemical properties of N-methyl-N-methoxymethylpyrrolidinium bis(fluorosulfonyl)amide and its lithium salt composites. J. Power Sources 325, 637–640. doi: 10.1016/j.jpowsour.2016.06.087

CrossRef Full Text | Google Scholar

Horiuchi, S., Zhu, H., Forsyth, M., Takeoka, Y., Rikukawa, M., and Yoshizawa-Fujita, M. (2017). Synthesis and evaluation of a novel pyrrolidinium-based zwitterionic additive with an ether side chain for ionic liquid electrolytes in high-voltage lithium-ion batteries. Electrochim. Acta 241, 272–280. doi: 10.1016/j.electacta.2017.04.165

CrossRef Full Text | Google Scholar

Ishikawa, M., Sugimoto, T., Kikuta, M., Ishiko, E., and Kono, M. (2006). Pure ionic liquid electrolytes compatible with a graphitized carbon negative electrode in rechargeable lithium-ion batteries. J. Power Sources 162, 658–662. doi: 10.1016/j.jpowsour.2006.02.077

CrossRef Full Text | Google Scholar

Laus, G., Bentivoglio, G., Kahlenberg, V., Griesser, U. J., Schottenberger, H., and Nauer, G. (2008). Syntheses, crystal structures, and polymorphism of quaternary pyrrolidinium chlorides. CrystEngComm. 10, 748–752. doi: 10.1039/b718917f

CrossRef Full Text | Google Scholar

Li, X., Zhang, Z., Li, S., Yang, K., and Yang, L. (2017). Polymeric ionic liquid-ionic plastic crystal all-solid-state electrolytes for wide operating temperature range lithium metal batteries. J. Mater. Chem. A. 5, 21362–21369. doi: 10.1039/C7TA04204C

CrossRef Full Text | Google Scholar

Liu, Z.-T., Shen, L.-H., Liu, Z.-W., and Lu, J. (2009). Acetylation of β-cyclodextrin in ionic liquid green solvent. J. Mater Sci. 44, 1813–1820. doi: 10.1007/s10853-008-3238-1

CrossRef Full Text | Google Scholar

Matsumoto, H., Sakaebe, H., Tatsumi, K., Kikuta, M., Ishiko, E., and Kono, M. (2006). Safety assessment of ionic liquid-based lithium-ion battery prototypes. J. Power Sources 160, 1308–1313. doi: 10.1016/j.jpowsour.2006.02.018

CrossRef Full Text

Narita, A., Shibayama, W., Sakamoto, K., Mizumo, T., Matsumi, N., and Ohno, H. (2006). Lithium ion conduction in an organoborate zwitterion–LiTFSI mixture. Chem. Commun. 1926–1928. doi: 10.1039/B517019B

PubMed Abstract | CrossRef Full Text | Google Scholar

Nishimura, N., and Ohno, H. (2014). 15th anniversary of polymerised ionic liquids. Polymer 55, 3289–3297. doi: 10.1016/j.polymer.2014.02.042

CrossRef Full Text | Google Scholar

Ohno, H. (2011). Electrochemical Aspects of Ionic Liquids, Second Ed. Hoboken, NJ: John Wiley & Sons, Inc.

Ohno, H., and Fukaya, Y. (2009). Task specific ionic liquids for cellulose technology. Chem. Lett. 38, 2–7. doi: 10.1246/cl.2009.2

CrossRef Full Text | Google Scholar

Qian, W., Texter, J., and Yan, F. (2017). Frontiers in poly(ionic liquid)s: syntheses and applications. Chem. Soc. Rev. 46, 1124–1159. doi: 10.1039/C6CS00620E

PubMed Abstract | CrossRef Full Text | Google Scholar

Roy, A., and Roy, M. N. (2017). Cage to cage study of ionic liquid and cyclic oligosaccharides to form inclusion complexes. RSC Adv. 7, 40803–40812. doi: 10.1039/C7RA08397A

CrossRef Full Text | Google Scholar

Roy, A., Saha, S., Datta, B., and Roy, M. N. (2016). Insertion behavior of imidazolium and pyrrolidinium based ionic liquids into α and β-cyclodextrins: mechanism and factors leading to host–guest inclusion complexes. RSC Adv. 6, 100016–100027. doi: 10.1039/C6RA19684E

CrossRef Full Text | Google Scholar

Salminen, J., Papaiconomou, N., Kumar, R. A., Lee, J.-M., Kerr, J., Newman, J., et al. (2007). Physicochemical properties and toxicities of hydrophobic piperidinium and pyrrolidinium ionic liquids. Fluid Phase Equilibria 261, 421–426. doi: 10.1016/j.fluid.2007.06.031

CrossRef Full Text | Google Scholar

Seki, S., Kobayashi, Y., Miyashiro, H., Ohno, Y., Mita, Y., Terada, N., et al. (2008). Compatibility of N-methyl-N-propylpyrrolidinium cation room-temperature ionic liquid electrolytes and graphite electrodes. J. Phys. Chem. C 112, 16708–16713. doi: 10.1021/jp805403e

CrossRef Full Text | Google Scholar

Seki, S., Ohno, Y., Miyashiro, H., Kobayashi, Y., Usami, A., Mita, Y., et al. (2008). Quaternary ammonium room-temperature ionic liquid/lithium salt binary electrolytes: electrochemical study. J. Electrochem. Soc. 155, A421–A427. doi: 10.1149/1.2899014

CrossRef Full Text | Google Scholar

Silva, O. F., Fernández, M. A., Pennie, S. L., Gil, R. R., and de Rossi, R. H. (2008). Synthesis and characterization of an amphiphilic cyclodextrin, a micelle with two recognition sites. Langmuir 24, 3718–3726. doi: 10.1021/la702962f

PubMed Abstract | CrossRef Full Text | Google Scholar

Szejtli, J. (1998). Introduction and general overview of cyclodextrin chemistry. Chem. Rev. 98, 1743–1754. doi: 10.1021/cr970022c

PubMed Abstract | CrossRef Full Text | Google Scholar

Tanner, J. E., and Stejskal, E. O. (1968). Restricted self-diffusion of protons in colloidal systems by the pulsed-gradient, spin-echo method. J. Chem. Phys. 49, 1768. doi: 10.1063/1.1670306

CrossRef Full Text | Google Scholar

Towada, J., Karouji, T., Sato, H., Kadoma, Y., Shimada, K., and Ui, K. (2015). Charge–discharge characteristics of natural graphite electrode in N, N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoromethylsulfonyl)amide containing lithium ion for lithium-ion secondary batteries. J. Power Sources 275, 50–54. doi: 10.1016/j.jpowsour.2014.10.101

CrossRef Full Text | Google Scholar

Wu, A., Lu, F., Sun, P., Qiao, X., Gao, X., and Zheng, L. I. (2017). Low-molecular-weight supramolecular ionogel based on host–guest interaction. Langmuir 33, 13982–13989. doi: 10.1021/acs.langmuir.7b03504

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, T.-Y., Su, S.-G., Wang, H.-P., Lin, Y.-C., Gung, S.-T., Lin, M.-W., et al. (2011). Electrochemical studies and self diffusion coefficients in cyclic ammonium based ionic liquids with allyl substituents. Electrochim. Acta 56, 3209–3218. doi: 10.1016/j.electacta.2011.01.040

CrossRef Full Text | Google Scholar

Yabuuchi, N., and Ohzuku, T. (2003). Novel lithium insertion material of LiCo_1/3Ni_1/3Mn_1/3O₂ for advanced lithium-ion batteries. J. Power Sources 119–121, 171–174. doi: 10.1016/S0378-7753(03)00173-3

CrossRef Full Text | Google Scholar

Yang, B., Li, C., Zhou, J., Liu, J., and Zhang, Q. (2014). Pyrrolidinium-based ionic liquid electrolyte with organic additive and LiTFSI for high-safety lithium-ion batteries. Electrochim. Acta 148, 39–45. doi: 10.1016/j.electacta.2014.10.001

CrossRef Full Text | Google Scholar

Yoon, H., Best, A. S., Forsyth, M., MacFarlane, D. R., and Howlett, P. C. (2015). Physical properties of high Li-ion content N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide based ionic liquid electrolytes. Phys. Chem. Chem. Phys. 17, 4656–4663. doi: 10.1039/C4CP05333H

PubMed Abstract | CrossRef Full Text | Google Scholar

Yoshizawa, M., Narita, A., and Ohno, H. (2004). Design of ionic liquids for electrochemical applications. Aust. J. Chem. 57, 139–144. doi: 10.1071/CH03240

CrossRef Full Text | Google Scholar

Yoshizawa-Fujita, M., Tamura, T., Takeoka, Y., and Rikukawa, M. (2011). Low-melting zwitterion: effect of oxyethylene units on thermal properties and conductivity. Chem. Commun. 47, 2345–2347. doi: 10.1039/C0CC03754K

PubMed Abstract | CrossRef Full Text | Google Scholar

Yuan, J., Mecerreyes, D., and Antonietti, M. (2013). Poly(ionic liquid)s: an update. Prog. Polym. Sci. 38, 1009–1036. doi: 10.1016/j.progpolymsci.2013.04.002

CrossRef Full Text | Google Scholar

Zhang, W., Yuan, C., Guo, J., Qiu, L., and Yan, F. (2014). Supramolecular ionic liquid gels for quasi-solid-state dye-sensitized solar cells. ACS Appl. Mater. Interfaces 6, 8723–8728. doi: 10.1021/am501523x

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, Z., Qilu, Z. D., and Yu, H. (2014). Preparation of spherical hierarchical LiNi_0.5Mn_1.5O₄ with high electrochemical performances by a novel composite co-precipitation method for 5 V lithium ion secondary batteries. Electrochim. Acta 115, 290–296. doi: 10.1016/j.electacta.2013.10.167

CrossRef Full Text | Google Scholar