Preparation and characterization of a rechargeable battery based on poly-(3,4-ethylenedioxythiophene) and aluminum in ionic liquids


This paper presents a feasibility study of a non-aqueous rechargeable battery based on aluminum and poly-(3,4-ethylenedioxythiophene) conductive polymer in a chloroaluminate ionic liquid. The polymer was electrodeposited on a vitreous carbon working electrode in a chloride aqueous solution and the structure was analyzed by scanning electron microscopy. The doping/de-doping mechanism of chloride ions into the polymer structure was studied using a quartz crystal microbalance and cyclic voltammetry. The deposition/dissolution of the aluminum negative electrode were investigated by electrochemical and microscopic methods. Performance data were obtained with a laboratory-scale aluminum-conductive polymer battery at constant current showing an average cell discharge voltage of 1 V and specific energies of at least 84 Wh kg−1 referred to the mass of the polymer and aluminum. The system is novel and the paper outlines further research to improve the cell performance.

Graphical Abstract


The long-term transformation of our energy landscape will involve high-performance energy storage technologies for sustainable energy sources such as intermittent photovoltaics and wind power. Batteries have currently a minor contribution to the challenges of the energy conversion; however, the continuous growth of sustainable energy sources will require a range of energy storage systems. Therefore, there is an urgent need for R&D in the state of the art batteries, to develop novel energy storage systems, like rechargeable batteries [1,2,3,4].

The main problems of the state of the art batteries, like lithium-based systems, are safety, availability of materials, and costs [5, 6]. The occurrence of lithium in the earth crust is approximately 20 ppm. The increasing demand of lithium-based batteries will require additional lithium production and recycling [7]. Great effort has been dedicated to improve the specific energy and power of lithium-ion batteries, while less attention has been directed to aluminum batteries in non-aqueous systems [8]. These systems merit study since aluminum is more abundant (~80,000 ppm), cost-effective, and safer than lithium [9,10,11,12,13]. In addition, the theoretical-specific capacity of aluminum (3.0 Ah g−1) is comparable to that of lithium (3.9 Ah g−1) [14, 15]; unlike lithium, aluminum batteries are not flammable and are not endangered by thermal runaway, which is still a very serious problem of lithium-ion batteries [16, 17].

Rechargeable batteries based on the reversible deposition and dissolution of aluminum in a Lewis acidic chloroaluminate ionic liquid have been reported [14, 18, 19]. Charge storage materials like three-dimensional graphitic foams [18], vanadium pentoxide nano-wires [19], and electro-polymerized polypyrrole and polythiophene [14] in ionic liquid have been used as positive electrodes. The storage mechanism of these materials consists on the reversible intercalation of chloroaluminate ion species in the porous three-dimensional structures of the graphitic foam [18] and nano-wires [19], whereas conductive polymers [14] store anions to compensate the positive charges in the oxidized polymer backbone. These battery systems showed high reversibility as well as stable electrochemical behavior of the charge storage materials (graphitic foams, nano-wires, and conductive polymers) as positive electrodes with high coulombic efficiencies approaching 100%. Cell voltages between 0.55 V [19] and 2 V [18] were reached with a wide electrochemical stability window [20], allowing the reversible redox reaction of aluminum (0 V vs Al/Al(III) [21]). The delivered specific discharge capacities are 70 Ah kg−1 (graphitic foam) [18], 273–305 Ah kg−1 (vanadium pentoxide nano-wires) [19], and 30–100 Ah kg−1 (conductive polymers) [14]. The reported specific capacities compete with those observed during the performance of positive active materials for lithium-ion batteries (50–300 Ah kg−1 [6]).

Proposed battery system

The battery proposed in this paper is based on the reversible deposition and dissolution of aluminum at the negative electrode while the conductive polymer PEDOT is doped and de-doped with chloride ions at the positive electrode in a Lewis acidic chloroaluminate ionic liquid.

In contrast to the use of bulky chloroaluminate anions as dopant described in the previous section [14, 18, 19], this work uses chloride ions as the dopant species for the conductive polymer that has been previously electro-polymerized in an aqueous solution. Chloride anions as dopant are preferred because they are smaller and more mobile than bulky chloroaluminate ions [20]. Furthermore, the smaller size of chloride ions could provide higher charge/discharge rates and high storage capacity.

The conductive polymer poly-(3,4-ethylenedioxythiophene) (PEDOT), used in this work, offers the advantageous characteristics of conventional polymers and high metal-like conductivity [22, 23]. This heterocyclic conducting polymer has a low oxidation potential in aqueous solutions (~1 V vs SHE [24]) and it is stable in the oxidized state as a p-type semiconductor. In addition, conductive polymers are called hybrid capacitors because they have the ability to store large amount of charge while acting as capacitor and battery at the same time [25]. PEDOT is able to store additional amount of charges by increasing the oxidation potential (doping potential). The amount of additional stored charges depends on the thickness and porosity of the film. Hybrid capacitors are potentially positive electrode materials for high-performance batteries, which require high capacities and cell potentials.

The charging reaction of PEDOT (Eq. 1), which is represented by one EDOT monomer, is an oxidation process from the neutral to the positively charged state and the simultaneous insertion of anions (doping). The oxidation causes positive-charged centers (sulfur or carbon) in the polymer backbone, which are compensated by the doping anions (Cl, AlCl4 , Al2Cl7 ) of the ionic liquid. Chloride anions are preferred as doping/de-doping species because of their small size and high mobility. The discharge reaction (Eq. 1) comprises the release of anions into the electrolyte and the transfer of the conductive polymer to the neutral state. The oxidation and reduction of PEDOT is characterized by a one electron transfer reaction.

$$ {\left[\mathrm{EDOT}\right]}_{1/ a}+{\mathrm{X}}^{-}\underset{\underset{disch \arg e}{\leftharpoondown }}{\overset{ch \arg e}{\rightharpoonup }}{\left[\mathrm{EDOT}\right]}_{1/ a}\mathrm{X}+{\mathrm{e}}^{-}\kern0.5em {\mathrm{X}}^{-}={\mathrm{Cl}}^{-},{{\kern0.2em \mathrm{Al}\mathrm{Cl}}_4}^{-},{\kern0.2em \mathrm{Al}}_2{\mathrm{Cl}}_7^{-}\kern10.1em $$

The degree of doping (α) is the ratio between the number of inserted chloride ions (n Cl ) and the number of monomer units (n EDOT+) (Eq. 2). The degree of doping varies from 0 to 1.

$$ \alpha =\frac{n\ \left({\mathrm{Cl}}^{-}\right)}{n\left({\mathrm{EDOT}}^{+}\right)} $$

The reversible deposition and dissolution of aluminum (Eq. 3) at the negative electrode is possible in a Lewis acidic chloroaluminate ionic liquid, containing heptachlorodialuminate ions (Al2Cl7 ) [20, 26,27,28,29,30,31,32,33,34,35,36].

$$ {4\mathrm{Al}}_2{\mathrm{Cl}}_7^{-}+{3\mathrm{e}}^{-}\underset{\underset{disch \arg e}{\leftharpoondown }}{\overset{ch \arg e}{\rightharpoonup }}\mathrm{Al}+{7\mathrm{AlCl}}_4^{-} $$

A Lewis basic chloroaluminate ionic liquid is composed of tetrachloroaluminate ions (AlCl4 ) and the organic cation compound 1-ethyl-3-methylimidazolium (EMIm+). The AlCl4 ions are reduced at potentials more negative than the organic cation EMIm+. Therefore, EMIm+ would be decomposed before the deposition of aluminum [20]. In order to avoid this decomposition, Lewis acidic mixtures of 1-ethyl-3-methylimidazolium chloride ([EMIm]Cl) and aluminum chloride (AlCl3) are prepared to favor the formation of Al2Cl7 (Eq. 4) [36]:

$$ {2\mathrm{AlCl}}_4^{-}{\rightleftharpoons \mathrm{Al}}_2{\mathrm{Cl}}_7^{-}+{\mathrm{Cl}}^{-} $$

The heptachlorodialuminate Al2Cl7 anion forms when the molar ratio of AlCl3 to the ionic liquid [EMIm]Cl is higher than unity (Lewis acidic ionic liquid). The deposition of aluminum from Al2Cl7 occurs before the decomposition of the ionic liquid.

The overall reaction of the battery (Eq. 5) arises from the half-cell reactions (Eqs. 1 and 3):

$$ {\ 3\mathrm{EDOT}}_{1/\alpha}+{4\mathrm{Al}}_2{\mathrm{Cl}}_7^{-}\rightleftharpoons {\ 3\mathrm{EDOT}}_{1/\alpha}^{+}+\mathrm{Al}+{7\mathrm{AlCl}}_4^{-} $$

A theoretical maximum specific capacity of 36 Ah kg−1 is calculated by using the overall reaction (Eq. 5) and a degree of doping α of 0.33, which is a typical value for PEDOT [23].

In this feasibility study, we propose a secondary non-aqueous aluminum-based battery operating at room temperature. The PEDOT-aluminum battery connects the two independent reactions, the reversible intercalation (doping/de-doping) of PEDOT with chloride anions and deposition and dissolution of aluminum in a Lewis acidic chloroaluminate ionic liquid in an advanced novel approach.


Preparation of PEDOT electrodes

The monomer 3,4-ethylenedioxythiophene (EDOT) (purity >98.0%) and potassium chloride (>99.5%) were supplied by Wako Chemicals. The PEDOT electrodes were prepared in a three-electrode cell at 28 °C and ambient atmosphere in an aqueous solution containing 0.01 mol dm−3 EDOT and KCl from 0.01 to 1.0 mol dm−3. EDOT was potentiostatically electro-polymerized at 1.2 V vs Ag/AgCl for 30 min on a planar vitreous carbon working electrode (WE) (4.5 cm2). A solid platinum plate electrode (0.5 cm2) was used as counter electrode (CE) and silver/silver chloride as reference electrode (RE) (Ag/AgCl 3 mol dm−3, 0.197 V vs SHE). The inter-electrode distance between the WE and CE was 1 cm. The RE was connected by a salt bridge filled with agar-agar powder (Wako, jelly strength 400~600 g cm−2) over a Haber-Luggin capillary tube with the cell. The distance between the tip of the capillary and WE was 0.3 cm. The cell potential was controlled with a potentiostat (BioLogic SP-240), using the commercial software package EC-LAB (version 10.32). After the deposition, the PEDOT films were dried in vacuum for at least 3 days. The mass of the vitreous carbon electrodes was measured in dried condition before and after electro-polymerization with an electrical balance (Sartorius, ±0.1 mg) to determine the deposited mass of PEDOT doped with chloride ions. The doped amount of chloride ions was calculated by the difference of the initial amount of chloride ions in the electro-polymerization solution and the remaining amount of chloride ions in the electro-polymerization solution after the polymerization. The remaining amount of chloride was determined by Mohr titration [37, 38]. The degree of doping (α) (Eq. 2) can be determined by the ratio between the amount of doped chloride ions (n Cl ) and the amount of EDOT monomers (n EDOT). The accuracy of the calculated degree of doping depends on the measured deposited mass of the polymerized and doped PEDOT film as well as on the measured amount of doped chloride ions by Mohr titration. In order to assess the accuracy of these values, the titration measurements were repeated at least five times.

Electrochemical characterization

The Lewis acidic ionic liquid (33.3 mol% [EMIm]Cl and 66.7 mol% AlCl3) was prepared by adding 87.64 g aluminum chloride (Kanto Chemicals, 98%) to 48.11 g 1-ethyl-3-methylimidazolium chloride (Merck, for synthesis) under continuous stirring and cooling, resulting in a translucent light yellow color liquid. The preparation of the ionic liquid and the half-cell tests and galvanostatic charging and discharging experiments in ionic liquid were performed in a glove box in an argon atmosphere (99.999%) with less than 50 ppm water content. The ionic liquid EMIm-AlCl3 is stable at a water content lower than 500 ppm [18].

The cyclic voltammetry (CV) experiments were performed in a cylindrical three-electrode glass cell (9.4 cm3) with an aluminum wire (1 mm diameter, 99.99%) as reference electrode. The inter-electrode distance between the rectangular counter electrode (vitreous carbon, 4.5 cm2) and rectangular working electrode (either PEDOT or aluminum with 99.99%, 4.5 cm2) was 0.4 cm. The electrodes were placed parallel to each other. The same cell was used for galvanostatic charge and discharge experiments of the PEDOT-aluminum battery. The battery was galvanostatically discharged at −0.02 mA cm−2 and charged at 0.2 mA cm−2. The cell was additionally equipped with a commercially available porous (pore size range of 0.03 to 0.8 mm) glass frit as support for the electrolyte solution, which was soaked with ionic liquid and placed between the electrodes. The thickness of the electrolyte support was 0.4 cm. The experiments were performed with and without the electrolyte support and the results compared.

The polymer can be doped with a mixture of anions (Cl, AlCl4 , Al2Cl7 ) in the ionic liquid electrolyte. For this reason, in situ quartz crystal microbalance (QCM) measurements in chloroaluminate electrolytes were performed to determine the molar mass of the doping species. A gold-coated quartz crystal (10 MHz; active crystal area (A) 0.2 cm2; density (ρ) 2.64 g cm−3; shear modulus (μ) 2.95 × 1011 g cm−1 s−2) was used as substrate for constant potential electro-polymerization of PEDOT films as working electrode at 1.2 V vs Ag/AgCl for 600 s in aqueous 0.01 mol dm−3 EDOT and 0.1 mol dm−3 KCl solution.

For the doping and de-doping experiments, a cylindrical cell with aluminum wires (1 mm diameter, 99.99%) as counter and reference electrodes was used. The resonant frequency (f), including the initial resonant frequency (f 0), of the quartz crystal was measured in argon atmosphere (water level <0.5 ppm, oxygen level 0.2 ppm) in ionic liquid electrolyte and before and after the measurement in absence of the electrolyte. Simultaneously, cyclic voltammetry measurements, from 0 to 2 V vs Al/Al(III), were performed to calculate the transferred anodic and cathodic charges. The cyclic voltammogram was first recorded in anodic and then in cathodic direction. The Sauerbrey equation (Eq. 6) [39] was used to determine the mass changes (∆m).

$$ \Delta f=-\frac{2{f}_0^2}{\sqrt{\mu \rho}}\cdotp \frac{\Delta m}{A} $$

Structural characterization

The structure of the aluminum electrodes and PEDOT electrodes, prepared at different molar ratios of KCl (0.01 to 1.0 mol dm−3) and EDOT (0.01 mol dm−3), was investigated by a JEOL JSM-6510LA scanning electron microscope (SEM). Their elemental composition was analyzed through an energy-dispersive X-ray (EDX) module (EX-230 BM). The images were taken with a secondary electron detector at different magnifications (max. 40,000), 5–20 kV, and WD 9 to 29 mm. All EDX spectra were measured at a magnification of 1500, 10 kV, WD 10 mm, and around 5000 cps. Poorly conductive samples were sputtered with gold at 30 mA for 30 s.

Results and discussion

Structure of electro-polymerized PEDOT

The SEM images (Fig. 1) of the PEDOT surfaces prepared by potentiostatic electro-polymerization in 0.01 mol dm−3 EDOT and 0.01 to 1.0 mol dm−3 KCl show that PEDOT forms a granular and porous structure on vitreous carbon. These porous grains have a high surface area and consequently a high number of accessible positive charged doping positions for chloride ions.

Fig. 1

SEM images of PEDOT deposited at 1.2 V vs Ag/AgCl for 30 min on vitreous carbon (4.5 cm2) in 0.01 mol dm−3 EDOT and a 0 mol dm−3 KCl, b 0.01 mol dm−3 KCl, c 0.1 mol dm−3 KCl, and d 0.5 mol dm−3 KCl

The structure of the PEDOT films, prepared in an increasing concentration of KCl in the electro-polymerization solution, strongly depends on the doping anion concentration. The density of the grains increases significantly with increasing chloride concentration up to 0.1 mol dm−3 KCl in the electro-polymerization solution (Fig. 1a–c). The structure and grain density remains similar for electrodes prepared in solutions with 0.1 to 1.0 mol dm−3 KCl (Fig. 1c, d).

The distribution of the grains, which were polymerized in aqueous solution containing 0.1 mol dm−3 KCl and 0.01 mol dm−3 EDOT, is very uniform at the surface of the vitreous carbon substrate (Fig. 1c). The randomly distributed agglomerates of PEDOT have an average size of 0.2 to 2 μm. The formation of three-dimensional grains on top of an initial uniform layer of the conductive polymer is typical for the material because of the higher adhesion of the agglomerates on a first thin layer of PEDOT than on the native vitreous carbon substrate [40,41,42]. The average ratio of the proportion of sulfur, which represents one monomer unit of EDOT per one chloride ion, was measured by EDX. The ratio corresponds to a degree of doping of 0.33 and is in accordance with literature value [23].

Undoped PEDOT (Fig. 1a), which was polymerized in 0.01 mol dm−3 EDOT and in the absence of KCl, is characterized by a smooth surface with very small and separated grains. A small amount of chloride ions (0.01 mol dm−3) (Fig. 1b) increases the growth of the grains, covering the whole surface (Fig. 1b–d). Agglomerated grains as well as flat structures were formed over the whole surface of the carbon electrode. The diffusion zones around the hemispherical nuclei have started to overlap, forming the agglomerated grain structure until a critical height of the layers is reached. The height might depend on the concentration of the doping anion. Therefore, the growth continues laterally and flat structures are formed. The formation of a dense structure of grains is attributable to the fact that the conductivity of the solution increases with the chloride concentration. The structures polymerized at a low chloride concentration (0.01 mol dm−3 KCl) show presumably the initial stage of the PEDOT layer formation. However, the polymerization continues if the oxidation potential remains sufficiently high to oxidize further EDOT to the radical cation. With an insufficient conductivity, the diffusion zones increase until the oxidation current cannot be maintained and the polymerization stops.

Cyclic voltammetry of PEDOT

The cyclic voltammograms (Fig. 2) of the PEDOT films, prepared in different concentrations of the doping component, show a clear influence of the amount of doping component on the capacity. Each cyclic voltammogram shows a constant capacity beyond cycle 10. Therefore, cycle 10 was used to compare peak positions and capacity.

Fig. 2

Cyclic voltammogram of the system PEDOT (4.5 cm2) (WE), vitreous carbon (4.5 cm2) (CE), and aluminum (RE) in Lewis acidic ionic liquid at 100 mV s−1, cycle 10, and 28 °C. PEDOT film deposited at 1.2 V vs Ag/AgCl for 30 min in 0.01 mol dm−3 EDOT and a 0.01 mol dm−3 KCl, b 0.1 mol dm−3 KCl, c 0.5 mol dm−3 KCl, and d 1.0 mol dm−3 KCl. e Bare vitreous carbon (WE, CE, 4.5 cm2) and aluminum (RE) in Lewis acidic ionic liquid

The cyclic voltammogram of the PEDOT film prepared in the lowest KCl concentration of 0.01 mol dm−3 (Fig. 2 (a)) shows neither anodic nor cathodic peaks. Thus, under these conditions, the PEDOT film seems to be electrochemically inactive. The PEDOT film polymerized in 0.1 mol dm−3 KCl (Fig. 2 (b)) is characterized by significant anodic and cathodic peaks as well as high capacity. A further increase of the doping component, to 0.5 mol dm−3 (Fig. 2 (c)) and 1.0 mol dm−3 KCl (Fig. 2 (d)) solution, shows lower currents compared to the film prepared in 0.1 mol dm−3 (Fig. 2 (b)) KCl. The shapes and the currents and consequently the capacities of the films deposited in 0.5 and 1.0 mol dm−3 KCl (Fig. 2 (c, d)) do not show significant differences. From these results, it can be suggested that the amount of chloride ions incorporated in the PEDOT film reaches a maximum. Regarding the decreasing current and capacity from the solutions containing 0.5 and 1.0 mol dm−3 chloride, it is assumed that an increasing saturation of the positive charges with doping anions in the polymer backbone transforms PEDOT into a less conductive state. The degree of doping, determined by Mohr titration [37, 38], increases with an increasing chloride concentration in the electro-polymerization electrolyte from 0.1 to 0.33. For the PEDOT film polymerized in 0.01 mol dm−3 EDOT and 0.1 mol dm−3 KCl, a degree of doping of 0.27 was determined, along with the highest capacity in the cyclic voltammogram (Fig. 2 (b)). The PEDOT films polymerized in 0.01 mol dm−3 EDOT and 0.5 mol dm−3 as well as 1.0 mol dm−3 (Fig. 2 (c, d)) have a degree of doping of 0.33, which agrees with the EDX results.

Performance of PEDOT in Lewis acidic ionic liquid

The cyclic voltammograms of PEDOT electrodes (prepared with 0.01 mol dm−3 EDOT and 0.1 mol dm−3 KCl) in a Lewis acidic ionic liquid from 0 to 2.7 V vs Al/Al(III) were recorded at 10, 25, and 50 cycles (Fig. 3). A vitreous carbon electrode was used as counter electrode and an aluminum wire as reference electrode. The oxidation and reduction reactions of the film in the Lewis acidic ionic liquid are characterized by four anodic and three cathodic waves, indicating different levels of doping and de-doping of the polymer. The anodic broad waves arise at 0.7 V (I), 1.45 V (II), 1.9 V (III), and 2.2 V (IV) vs Al/Al(III). The doping at 2.2 V (IV) occurs with the decomposition of the ionic liquid to chlorine gas. The cathodic wave around 1.85 V (V) correlates with the anodic wave at 1.9 V (III) vs Al/Al(III) and indicates a reversible doping and de-doping reaction. The second cathodic wave appears at 1.5 V (VI) and the third wave arises at 0.7 V (VII) vs Al/Al(III).

Fig. 3

Cyclic voltammogram of the system PEDOT (4.5 cm2) (WE), vitreous carbon (4.5 cm2) (CE), and aluminum (RE) in Lewis acidic ionic liquid at 100 mV s−1, different cycle numbers a cycle 10, b cycle 25, and c cycle 50, and 28 °C. d Bare vitreous carbon (WE, CE, 4.5 cm2) and aluminum (RE) in Lewis acidic ionic liquid

With an increasing cycle number, the anodic and cathodic currents decrease. A swelling of the PEDOT film was observed in the ionic liquid during doping and de-doping, which appears as blue cloud-like film around the electrode that causes the decrease in current, as there are less available active sites to accommodate chloride ions in the PEDOT backbone. The polymer film loses its adhesion on the vitreous carbon substrate and is partially detached. The stability of the polymer on the substrate can be improved by using rougher surfaces and three-dimensional carbon substrates to deposit PEDOT or by using pure porous PEDOT electrodes, as they are more stable due to the higher number of doping positions in contrast to flat thin films of PEDOT on the vitreous carbon surface. This approach will be a focus of future work.

Determination of the anion doping species

PEDOT films doped with chloride ions were formed on a gold-coated crystal quartz electrode of 0.2 cm2 area by polymerization of 0.01 mol dm−3 EDOT in 0.1 mol dm−3 KCl aqueous solution at a constant potential of 1.2 V vs Ag/AgCl for 600 s. The quartz with the PEDOT film were dried and transferred into a Lewis acidic ionic liquid and cycled from 0 to 2.0 V vs Al/Al(III) (Fig. 4 (a)). Simultaneously, the changes of the resonance frequency [39] (different resonance frequencies of the loaded and unloaded quartz crystal) (Δf) of the quartz crystal were measured (Fig. 4 (b)).

Fig. 4

a Current density, b change of resonance frequency (Δf, dotted line), and c change of damping (Δw, solid line) depending on potential of the system PEDOT (0.2 cm2) on a gold resonator (WE) and aluminum wire (CE and RE) in Lewis acidic ionic liquid at 100 mV s−1 and 28 °C

PEDOT could also been doped with AlCl4 and Al2Cl7 ions, which are present in the ionic liquid electrolyte, during cycling. The changes in mass (Δm), calculated by the changes in resonance frequency (Δf) with the Sauerbrey equation (Eq. 6), and the transferred anodic and cathodic charges (ΔQ) (Table 1) provide information about the doping species.

Table 1 Calculated values for molar mass (M doped anion) of the doped and de-doped anion species in PEDOT, electro-polymerized on the gold electrode of a quartz crystal, in the listed potential ranges (ΔE) of the cyclic voltammogram (Fig. 4). The specific charges (ΔQ spec) were determined by the transferred charges (ΔQ) measured by cyclic voltammetry and change of mass (Δm) of the polymer film calculated by the change of frequency of the resonator by Sauerbrey equation

The regions I and II (Table 1) indicate the doping potential window (ΔE) of PEDOT. The mass change (Δm) of the polymer, determined by quartz crustal microbalance measurement (Fig. 4 (b)), in these regions, refers to doped anion species. The transferred charge (ΔQ) was measured simultaneously with cyclic voltammetry (Fig. 4 (a)). The specific charge (Q spec) was calculated by the ratio of ΔQ and Δm. The cyclic voltammogram (Fig. 4 (a)) shows anodic waves from 0.4 to 0.8 V (I) and 1.0 to 1.9 V (II) vs Al/Al(III). The frequency (Δf) decreases approximately linearly at these anodic potentials (Fig. 4 (b)), which indicates the anion doping (p-doping) [39]. The subsequent cathodic waves from 1.4 to 1.8 V (III) and 0.35 to 0.65 V (IV) vs Al/Al(III) show the de-doping reaction, which also represents the increase of the frequency. PEDOT can be also doped with cations (n-doping) when the polymer carries negative charges. It is assumed that the cationic species EMIm+ is inserted in the PEDOT film from 0 to 0.4 V vs Al/Al(III). The oxidation shows an increase of the frequency in the same potential range, indicating a decrease of mass or removal of the cationic species.

The doping and de-doping reactions occur in the potential window 0.4 to 1.9 V vs Al|Al(III) (Table 1). As the damping changes (Δw) (Fig. 4 (c)) of the quartz crystal in this potential window are in the same order of magnitude as the frequency changes (Fig. 4 (b)), we can use the Sauerbrey equation (Eq. 6) to calculate the change of mass from the change of frequency. The calculated molar mass (M doped anion) for the doped anion species are 140 and 87 g mol−1 (Table 1), indicating that the doping proceeds via a mixture of Cl (M theo = 35.6 g mol−1) and AlCl4 (M theo = 169.4 g mol−1) (Table 1). It is assumed that bulky chloroaluminate ions are partially trapped and irreversibly inserted in the polymer film and causing a damage with subsequent detachment of the PEDOT film, which was observed as blue cloud-like film in the electrolyte (“Performance of PEDOT in Lewis acidic ionic liquid” section). The selective doping of PEDOT with smaller chloride ions might be realized in a Lewis basic ionic liquid, which contains an excess of free chloride ions.

Performance of aluminum dissolution and deposition in Lewis acidic ionic liquid

A Lewis acidic ionic liquid of [EMIm]Cl and AlCl3 contains an excess of AlCl3, which enables the electro-deposition of aluminum. The cyclic voltammogram (Fig. 5) shows the tenth cycle of the deposition and dissolution of aluminum on aluminum plate (4.5 cm2) between −0.5 V and 0.5 V vs Al/Al(III).

Fig. 5

Cyclic voltammogram of a Lewis acidic ionic liquid with aluminum (4.5 cm2) (WE), vitreous carbon (4.5 cm2) (CE), and aluminum (RE) at 100 mV s−1, cycle 10, and 28 °C

The reduction of the complex aluminum ion (Al2Cl7 ) starts at −0.175 V vs Al/Al(III). The deposition occurs with some over potential due to the nucleation process, which has been reported for many metals in ionic liquids [35]. The aluminum oxidation is characterized by a wide peak with a maximum around 0.25 V vs Al/Al(III). The stripping peak shows an anodic charge of 5.3 mC cm−2 whereas the charge of the cathodic electro-deposition is 7 mC cm−2 giving a stripping efficiency of 76%. The stripping efficiency remains approximately constant with the cycles of the cyclic voltammetry. It is assumed that the reduced stripping efficiency is caused by the formation of a porous deposit of ionic liquid compounds on the aluminum electrode surface (Fig. 6), inhibiting the oxidation of aluminum. However, the deposition and dissolution of aluminum in a Lewis acidic ionic liquid is acceptable and can be improved [26] and therefore suitable for the charging and discharging reactions of the PEDOT-aluminum system.

Fig. 6

SEM images of the aluminum electrode surface a with porous deposit and b circular deposits after cyclic voltammetry in Lewis acidic ionic liquid

The deposition of aluminum in the Lewis acidic ionic liquid shows a very porous surface (pore diameter ~0.4 to 1.4 μm) (Fig. 6a) on the aluminum electrode and circular deposits with a diameter of ~28 μm (Fig. 6b). It is proposed that the circular deposits are organic decomposition products of the ionic liquid, because the cyclic voltammetry was carried out until −0.5 V vs Al|Al(III). The aluminum deposition occurs at potentials lower than −0.2 V vs Al|Al(III) and the ionic liquid decomposition process starts at −0.5 V. Furthermore, the porous structure may be a thin film of organic depositions or decomposition products as well, which are permeable for aluminum ions.

Charge and discharge behavior of PEDOT-aluminum battery

The reference sample, prepared in 0.01 mol dm−3 EDOT and 0.1 mol dm−3 KCl supported on vitreous carbon plate (4.5 cm2), was introduced as the positive electrode and metallic aluminum plate (4.5 cm2) was used as negative electrode in the cell. The open circuit potential was measured before the galvanostatic cycling and before every charge and discharge cycle (Eqs. 1 and 3). The OCP before the first cycle is between 2.1 and 2.3 V and before cycle 2 to 10 between 1.3 and 1.6 V. The battery was galvanostatically discharged (Fig. 7 (a, c)) at −0.02 mA cm−2 and charged (Fig. 7 (b)) at 0.2 mA cm−2.

Fig. 7

Galvanostatic discharging at −0.02 mA cm−2 and charging at 0.22 mA cm−2 of the system PEDOT-aluminum in Lewis acidic ionic liquid at 28 °C. a First discharge cycle, b second charge cycle, and c second discharge cycle

The average cell voltage of the first discharge is 2 V for 124 mA s (Fig. 7 (a)). The first charge voltage is around 2.2 to 2.3 V for 1600 mA s (Fig. 7 (b)). The beginning of the charging curve after 1500 s shows a steep slope at 1.8 to 1.9 V. Assuming that the aluminum deposition is at 0 V vs Al/Al(III), the slope and the voltage plateau correlate with the peaks at 1.9 to 2.0 V and 2.2 V vs Al/Al(III) in the cyclic voltammogram (Fig. 3 potential regions III and IV), indicating the doping of chloride ions in the polymer. The charging cycle (Fig. 7 (b)) was terminated at 2.35 V because the electrolyte started to decompose. The subsequent discharge curve (Fig. 7 (c)) is characterized by a decreasing cell voltage from around 1.2 to 0.8 V for around 170 mA s and terminated at 0.5 V. The suggestion is that the first discharge is accompanied by the de-doping of chloride ions and the subsequent charge is characterized by the doping of AlCl4 in the polymer, influencing the OCP, discharge voltage, and capacity. In addition, the insertion of bulky ions like AlCl4 in the polymer could change the structure of the polymer film and cause a damage of the film and a loss of active mass.

The battery-related characteristics (Table 2), which are based on the deposited mass of PEDOT, the active mass of aluminum, applied discharge current, and discharge time, show a specific capacity of 84 Ah kg−1. This is 2.3 times higher than the maximum theoretical value. This discrepancy can be explained if it is assumed that the PEDOT electrode behaves like a capacitor and battery (also known as hybrid-capacitor). The sum of the non-faradaic cathodic-specific charges (52 Ah kg−1), obtained from the second cycle of the cyclic voltammogram (Fig. 3) of PEDOT in Lewis acidic ionic liquid, and the maximum theoretical capacity (36 Ah kg−1) equals approximately to the measured specific capacity (84 Ah kg−1). This additional capacity is probably provided by the capacitive double layer of anion species (Cl, AlCl4 , Al2Cl7 ) and cationic species (EMIm+) of the electrolyte.

Table 2 Comparison of battery characteristic values without and with electrolyte support. List of measured deposited mass (m active) of PEDOT and active mass of aluminum and OCP of the system PEDOT-aluminum as well as capacity (Q) calculated from the discharge time and the applied current, specific charge (Q spec) calculated by the capacity per mass, specific power (P spec) calculated by the average discharge voltage of 1 V, and the applied current per mass and specific energy (E spec) calculated by the average discharge voltage, applied current, and discharge time per active mass

Influence on the charge and discharge behavior with porous electrolyte support

In order to limit the loss of PEDOT mass due to swelling and detachment of the film from the electrode, a porous support for the electrolyte was used. The aim was to keep the PEDOT film as close as possible to the vitreous carbon electrode. The pore size was between 0.03 and 0.8 mm to allow the ions in the ionic liquid to move freely and maintain the ionic conductivity. In this new configuration, the PEDOT-aluminum system in Lewis acidic ionic liquid was galvanostically charged and discharged at 0.2 and −0.02 mA cm−2, respectively. The second discharge cycles without (Fig. 8 (a)) and with (Fig. 8 (b)) electrolyte support were compared.

Fig. 8

Galvanostatic discharging at −0.02 mA cm−2 a without separator and b with separator of the system PEDOT-aluminum in Lewis acidic ionic liquid at 28 °C

The discharge reaction for the cell with the porous electrolyte support is characterized by a significant longer discharge plateau over 600 mA s between 1.1 and 0.9 V (Fig. 8 (b)). The discharging was terminated at 0.9 V because of the low practical use of this cell potential. The cell with electrolyte support was charged between 2.2 and 2.3 V for 1600 mA s similar to the charging cycle of the cell without electrolyte support (Fig. 7 (b)). The coulombic efficiency is 38% for the cell with electrolyte support. The cell shows a discharge time, specific charge and capacity that are approximately three times larger (Table 2) than the cell without electrolyte support. The calculated energy densities, based on the active mass of aluminum and deposited mass of PEDOT, are 84 Wh kg−1 without electrolyte support and 228 Wh kg−1 with electrolyte support, which is in the order of nickel-metal-hydride batteries (60–100 Wh kg−1) and lithium-based battery systems (100–256 Wh kg−1), respectively [43]. The improved performance is due to the fact that the film was kept in place by the electrolyte support and the behavior of PEDOT as hybrid capacitor. A more porous conductive polymer electrode reaches a higher capacity due to proportional capacitance to sample volume. Future work will aim at a deeper understanding of whether the measured values were caused by the battery system or are an effect of the porous electrolyte support.


This work shows the feasibility of a rechargeable low-cost, novel, and safer PEDOT-aluminum battery system in a Lewis acidic ionic liquid, which was the premier aim of the study.

The system is based on the doping/de-doping of the conductive polymer PEDOT with ions from the ionic liquid and the deposition/dissolution of aluminum.

It has been shown that

  1. (a)

    The deposition and dissolution of aluminum as negative electrode is reversible with 76% coulombic efficiency.

  2. (b)

    The oxidation/reduction and simultaneous doping/de-doping of PEDOT as positive electrode are also reversible.

  3. (c)

    The doping of PEDOT involves chloride ions and bulky chloroaluminate ions (AlCl4 and Al2Cl7 ) from the Lewis acidic ionic liquid.

  4. (d)

    Loss of capacity and low coulombic efficiency occur due to the damage and detachment of the thin and planar PEDOT film during the doping with bulky ions. This can be avoided by using porous substrates for the conductive polymer and selective doping with smaller anions in a Lewis basic chloroaluminate ionic liquid at the positive electrode.

  5. (e)

    Specific energy and power of 84 Wh kg−1 and 179 W kg−1, respectively, in the absence of an electrolyte support and 228 Ah kg−1 and 143 W kg−1, respectively, with electrolyte support have been determined. These are comparable with nickel-metal-hydride batteries (without electrolyte support) and with lithium-based battery systems (with electrolyte support).


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This study was supported by the Faculty of Engineering of the Hokkaido University (Japan) during the academic visit by the first author T.S., in cooperation with the Technische Universität Ilmenau (Germany). T.S. is grateful to the Centre for Doctoral Training in Sustainable Infrastructure Systems from the University of Southampton [EP/L01582X/1] and the Lloyd’s Register Foundation for the financial support received from September 2016.

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Correspondence to T. Schoetz.

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Schoetz, T., Ueda, M., Bund, A. et al. Preparation and characterization of a rechargeable battery based on poly-(3,4-ethylenedioxythiophene) and aluminum in ionic liquids. J Solid State Electrochem 21, 3237–3246 (2017).

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  • Aluminum
  • Lewis acidic ionic liquid
  • PEDOT-aluminum battery
  • Poly-(3,4-ethylenedioxythiophene) (PEDOT)