Vanadium Pentoxide-Based Composite Synthesized Using Microwave Water Plasma for Cathode Material in Rechargeable Magnesium Batteries.

Multivalent cation rechargeable batteries are expected to perform well as high-capacity storage devices. Rechargeable magnesium batteries have an advantage in terms of resource utilization and safety. Here, we report on sulfur-doped vanadium pentoxide (S-V₂O₅) as a potential material for the cathodes of such a battery; S-V₂O₅ showed a specific capacity of 300 mAh·g-1. S-V₂O₅ was prepared by a method using a low-temperature plasma generated by carbon felt and a 2.45 GHz microwave generator. This study investigates the ability of S-V₂O₅ to achieve high capacity when added to metal oxide. The highest recorded capacity (420 mAh·g-1) was reached with MnO₂ added to composite SMn-V₂O₅, which has a higher proportion of included sulfur than found in S-V₂O₅. Results from transmission electron microscopy, energy-dispersive X-ray spectroscopy, Micro-Raman spectroscopy, and X-ray photoelectron spectroscopy show that the bulk of the SMn-V₂O₅ was the orthorhombic V₂O₅ structure; the surface was a xerogel-like V₂O₅ and a solid solution of MnO₂ and sulfur.

1. Introduction

Recently, high-capacity rechargeable batteries have seen wide adoption as a power source for electric vehicles. Rechargeable magnesium batteries, which have been studied for a long time, have attracted attention for use in next-generation power storage applications. Aurbach et al. reported an electrolyte solution that allowed magnesium to dissolve and deposit reversibly [1,2].

However, there are a limited number of possible materials to use for the cathode of rechargeable magnesium batteries. In one case, Mg2+ is easily trapped in the cathode where it diffuses slowly. And, in another, repetitive insertion/desorption of Mg2+ at the cathode by use of high voltage can induce structural failure of the cathode or its dissolution into the electrolyte solution. Thus, one drawback of rechargeable magnesium batteries is the difficulty of maintaining their cycle characteristics because of their capacity fading [3,4].

For all of these reasons, there is high demand for cathode materials capable of stable insertion/desorption of Mg2+ in order to create a feasible rechargeable magnesium battery. The most commonly studied cathode materials are metal oxides [5,6] and metal sulfides [7,8]. As a rule, metal oxides possess stable crystal architecture but easily trap Mg2+. On the other hand, metal sulfides are less likely to trap Mg2+ because their structure is generally unsound. Since sulfides have generally rather lower bond-energy than oxides, those are thought to be unsuitable for the cathode material for lithium-ion batteries. Our research is advancing toward a solution to the above problem. A summary of our results is given below.

Sulfur-doped vanadium pentoxide (S-V2O5) prepared by the method described in Section 3.1 was tested as an adaptation for the cathode of a rechargeable magnesium battery [9]. Our method employs low-temperature plasma generated using carbon felt and a 2.45 GHz microwave generator (CF-MWP, Figure 1) [10]. Structural analysis and charge-discharge characteristic evaluation were performed for S-V2O5 prepared by CF-MWP.

Figure 1

Schematic diagram of carbon felt and a 2.45 GHz microwave generator (CF-MWP).

Charge-discharge capacity curves are shown in Figure 2. For the orthorhombic V2O5 (Figure 2a), the first-cycle discharge was 170 mAh g−1, and the second-cycle discharge was 70 mAh g−1. This result is similar to that reported by Yu et al. [11]. For the composite of V2O5 and sulfur (Figure 2b) formed by simple mixing, two plateau potentials (P1 and P2) appeared at 1.4 V and 1.0 V versus Mg/Mg2+ due to V2O5 and sulfur, respectively. P2 appeared in the first discharge cycle but did not appear after the second discharge cycle. One possible reason is that the sulfur may have been transferred to the electrolyte solution at the first Mg2+ desorption. However, the discharge capacity curve of S-V2O5 (Figure 2c) was 300 mAh·g−1 and decreased in a linear fashion from 1.6 V to 1.0 V versus Mg/Mg2+. This result implies that the surface of S-V2O5 became amorphous [12].

Figure 2

Charge-discharge curves: (a) V2O5; (b) Mixture of S and V2O5; and (c) S-V2O5.

The X-ray photoelectron spectroscopy (XPS) results for S-V2O5 (Figure 3) showed that the S2p spectrum shift occurred at low energy and the V2p3/2 spectrum shift occurred at a high energy. These results indicate a V-S bond-like state at the surface of S-V2O5 because of the solid solution formation of sulfur and V2O5. Results of FTIR, XRD, SEM, and EPMA testing indicate that the surface of S-V2O5 was amorphous, similar to a xerogel structure, and that the bulk was the orthorhombic V2O5.

Figure 3

X-ray photoelectron spectroscopy (XPS) narrow spectra of S-V2O5: (a) S2p; and (b) V2p3/2.

The electrolyte after a charge-discharge cycle of S-V2O5 electrode included sulfur, which it did not include originally. This suggests that sulfur leeched from the S-V2O5 electrode into the electrolyte through Mg2+ intercalation and desorption. Therefore, this study discusses the addition of a metal oxide material to inhibit sulfur elution.

2. Results and Discussion

2.1. Electrochemical Characteristics

Charge-discharge capacity curves are shown in Figure 4. The discharge capacities of the batteries containing metal oxides (MnO2, MoO3, Fe2O3, NiO, and ZrO2) as additives were 420 mAh g−1, 320 mAh g−1, 300 mAh g−1, 290 mAh g−1, and 230 mAh g−1, respectively. The highest capacity was reached in the case of MnO2 (SMn-V2O5). The discharge curve in the case of SMn-V2O5 decreased linearly from 1.5 V to 0.9 V versus Mg/Mg2+. This result demonstrates that the surface of the SMn-V2O5 was amorphous, similar to a xerogel structure; in this regard, it is similar to S-V2O5. Although the discharge curve obtained with added MoO3 decreased linearly from 1.5 V to 0.9 V versus Mg/Mg2+, its charge curve showed plateau potentials at around 1.8 V and 2.4 V. In the other curves, a plateau potential appeared at 1.5V, and each of the curves descended abruptly after the plateau potential. The cathode formed by the addition of NiO had the highest plateau potential at 1.65 V, different from other cases. This result shows that the addition of NiO might improve the high-voltage characteristics of the obtained material. The metal oxides other than MnO2 inhibited the formation of an S-V2O5 amorphous structure and showed a plateau potential.

Figure 4

Charge-discharge curves at second cycle: (a) MnO2; (b) MoO3; (c) Fe2O3; (d) NiO; and (e) ZrO2.

2.2. Structural Analysis

A transmission electron microscopy (TEM) image, electron beam diffraction image, and energy dispersive X-ray spectrometry (EDX) spectrum of SMn-V2O5 are shown in Figure 5 and Figure 6. The bulk of the SMn-V2O5 produced a clear image of electron diffraction. This result corresponds with the pattern of the orthorhombic V2O5. Therefore, the bulk of the SMn-V2O5 has maintained the V2O5 the orthorhombic structure without degradation. In the TEM image, the surface of SMn-V2O5 is seen as a thin layer with two types of morphology, shown in Figure 5 as Points 1 and 2. The diffraction image of Point 1 has a clear diffraction pattern and halo pattern. This diffraction pattern is slightly broader than the pattern for the orthorhombic V2O5, and the observation of the halo pattern indicates an amorphous structure. The EDX spectrum at Point 1 shows a strong V peak. These results indicate that Point 1 was a V2O5 xerogel or a similar structure. This is similar to the case of S-V2O5. The diffraction image of Point 2 shows only a halo pattern, and the EDX spectrum shows peaks for manganese and sulfur. Because these results indicate that Point 2 has an amorphous structure and consists of only manganese and sulfur, it is likely that Point 2 is a solid solution of MnO2 and sulfur.

Figure 5

Transmission electron microscopy (TEM) of S-Mn-V2O5 and electron beam diffraction at Points 1 and 2.

Figure 6

Energy dispersive X-ray spectrometry (EDX) at (a) Point 1; and (b) Point 2.

The micro-Raman spectrum of an SMn-V2O5 electrode is shown in Figure 7. The orthorhombic V2O5 peaks [13] and fluorescence can be seen, whereas there are no MnO2 and sulfur peaks. This result indicates fluorescence, possibly derived from MnO2 and sulfur. Thus, during Raman spectroscopy, although the area of fluorescence was low in intensity for V2O5, the orthorhombic V2O5 and the fluorescence area were separate. These results, together with the results from TEM and EDX tests, suggest that the fluorescence area was a solid solution of MnO2 and sulfur, indicating that SMn-V2O5 had a surface of the orthorhombic V2O5 covered with a solid solution. This is consistent with the TEM and EDX data.

Figure 7

Raman spectroscopy of SMn-V2O5 and Raman images of the surface of the SMn-V2O5 of (a) V2O5; and (b) the fluorescence area.

The XPS narrow spectrum of SMn-V2O5 is shown in Figure 8. The peaks for V2p3/2 and S2p at the same positions as S-V2O5 suggest a S-V bond-like state and indicate an amorphous structure. The FWHM of SMn-V2O5 increased 2-fold compared to S-V2O5. Therefore, there was considered that the oxidation state of V of SMn-V2O5 have slightly different compared to S-V2O5. Mn2p3/2 became a solid-solution formation with sulfur, according to another analysis. The ratio of manganese to sulfur was about 1:2. This ratio remained constant when the amount of sulfur was increased five-fold. These results demonstrate that MnO2 and sulfur were linked by mechanical force rather than by a chemical binding force. The ICP-MS analysis result shows that the molar ratio of V:Mn:S was 100:6.8:14.4. The sulfur content of SMn-V2O5 was twice that of S-V2O5 (V:S = 100:7.8). The ratio of manganese to sulfur was about 1:2 in SMn-V2O5; this result was arrived at by XPS analysis.

Figure 8

XPS narrow spectra of SMn-V2O5: (a) V2p3/2; (b) Mn2p3/2; and (c) S2p.

Balanced chemical reactions involving V2O5, MnO2, and S, along with their theoretical capacities, are shown below. V 2MnO S + Mg

From the results of ICP-MS analysis and the three equations above, average theoretical capacities of SMn-V2O5 and S-V2O5 through the surface to bulk are calculated to be 458 mAh·g−1 and 393 mAh·g−1, respectively. That is, the empirically obtained capacity of SMn-V2O5 was 91.7% of the theoretical capacity. Because the theoretical capacity of MnO2 is as high as that of V2O5, achieving a high capacity for SMn-V2O5 may be possible by increasing the amount of sulfur.

3. Experimental Section

3.1. Preparation of Cathode Material by CF-MWP

Vanadium pentoxide (V2O5), sulfur, and a metal oxide (MnO2, MoO3, Fe2O3, NiO, or ZrO2) were mixed at a molar ratio of 2:1:1 in a ball mill (P-6, Fritsch Co., Ltd.). Additionally, the composite added MnO2 was prepared the composite the ratio of 2:5:1 because of observing increase of sulfur contained amount. This composite was wetted down and left overnight, after which it was treated by our method involving low-temperature plasma generated using carbon felt and a 2.45 GHz microwave generator (CF-MWP). Specifically, 2.0 g of each raw material were placed between pieces of carbon felt (30 mm in diameter) and a 500 W, 2.45 GHz microwave was used to irradiate the material under reduced pressure (0.001 MPa) for 2 min (Figure 1) to synthesize the hybrid cathode materials. In this process, raw materials are treated by plasma formed from water in the raw materials as a result of electric discharge between the pieces of carbon felt. It is assumed that the water in the raw materials is distributed uniformly enough that the composite is treated uniformly. Furthermore, although the process was performed under reduced pressure and at the evaporating temperature of water, the process did not induce reduction of V2O5 and oxidation of sulfur.

3.2. Electrochemical Characteristics

The electrodes were prepared from a mixture of the cathode material, acetylene black, and a polyvinylidene fluoride binder with N-methyl-2-pyrrolidone with a weight ratio of 10:3:1. The resulting slurry was spread on carbon paper. The electrode was dried at 110 °C for 1.5 h. S-V2O5 was charged with magnesium ions and used as a counter electrode. This electrode showed the same potential changes as a magnesium alloy plate. A magnesium alloy plate was used as the reference electrode. For the electrolytic solution, 0.3 M Mg(ClO4)2 and 1.8 M H2O dissolved in propylene carbonate were used, and the electrode performance was evaluated using three-electrode cells. The electrolyte has been proven for metal oxides as cathode active materials to charge and discharge smoothly [4]. The stability of the Mg pseudo reference electrode used was preliminarily checked to be stable by observing the reproducibility of cyclic voltammograms of ferrocene using the electrolytic solution containing 0.2 M ferrocene, 0.3 M Mg(ClO4)2 and 1.8 M H2O in propylene carbonate solvent and an electrochemical system with a magnesium alloy plate as the reference electrode and platinum wires as working and counter electrodes. Charge-discharge tests were conducted between cut-off potentials from 2.4 V to 0.9 V versus Mg/Mg2+ at a constant current of 60 mA·g−1 (0.1 C). All trials were conducted at 25 °C.

3.3. Structural Analysis

The as-prepared samples were characterized by TEM (HF2000, Hitachi, Japan), EDX (Noran System SIX, Thermo Fisher Scientific, USA), micro-Raman spectroscopy (in Via Reflex/StreamLine, Renishaw, UK), and XPS (Quantum 2000, PHI, Inc.). The Raman spectroscopy measurements were taken after the electrodes were prepared.

4. Conclusions

As a cathode material for rechargeable magnesium batteries, we synthesized S-V2O5 with an added metal oxide prepared by CF-MWP and examined its crystal structure and electrode characteristics. The composite of V2O5, sulfur, and MnO2 (SMn-V2O5) synthesized by CF-MWP demonstrated the highest capacity of 420 mAh·g−1 of any of the prepared samples. The charge-discharge curves showed that the SMn-V2O5 capacity decreased linearly from 1.5 V to 0.9 V but that, for the other electrodes, a plateau potential appeared at 1.5 V. This result was interpreted to mean that only SMn-V2O5 had a surface structure resembling a xerogel. The composite of V2O5, sulfur, and MnO2 was treated by CF-MWP. The bulk of the resulting composite was orthorhombic V2O5, while the surface showed a xerogel-like structure of V2O5 and a solid solution of sulfur and MnO2.