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Intercalation Host Using Defective FePO4-Carbon Composite for Magnesium Rechargeable Battery Cathode

Thursday, 4 October 2018: 08:20
Galactic 7 (Sunrise Center)
Y. Orikasa (Department of Applied Chemistry, Ritsumeikan University), K. Kisu, E. Iwama (Tokyo University of Agriculture & Technology), W. Naoi (K & W Inc), Y. Yamaguchi (Ritsumeikan University), T. Munesada, M. Hattori (Kyoto University), K. Yamamoto (Human and Environmental Studies, Kyoto University), P. Rozier (CIRIMAT-CNRS, University of Toulouse III Paul Sabatier), P. Simon (CIRIMAT, UMR CNRS 5085), and K. Naoi (Tokyo University of Agriculture & Technology)
Magnesium rechargeable batteries are expected as one of candidates for next generation rechargeable batteries. The advantages of magnesium metal anode are the high theoretical capacity, high reserve amount of magnesium metal, and no dendrite formation. However, divalent magnesium ions are hard to diffuse in solid electrodes, and intercalation hosts that can operate at room temperature are limited to Chevrel type structures at present[1].

In this study, we investigated the applicability of FePO4-carbon composite prepared by ultracentrifugation (UC) method as magnesium-ion host structure. For nano-hybrid capacitor electrode, the electrode materials prepared by the UC method reported so far are capable of ultrafast lithium-ion insertion and extraction reaction[2]. Therefore, magnesium-ions could diffuse in the structure with a moderate condition. Since the irreversible magnesium ion insertion-extraction reaction in crystalline olivine type FePO4 has been reported[3], in this study, non-crystalline FePO4 with carbon composite was used.

FePO4-carbon composite was prepared by UC process[2]. The composite was mixed with PTFE. with the weight ratio of 9:1. The electrodes were charged using 1M LiPF6 in a 3:7 volume ratio of ethylene carbonate and diethyl carbonate. The charged electrodes were washed with DME and then, three-electrode cell with an Ag+/Ag double junction reference electrode was assembled. The counter electrode was an active carbon, and the electrolyte was 0.5 M magnesium bis(trifluoromethanesulfonyl)imide in acetonitrile. Charge-discharge measurements were performed at 25oC. The valence state of Fe in the charged / discharged electrodes were examined by X-ray absorption spectroscopy, which was measured in a transmission mode.

Reversible charge / discharge capacity was observed after the first discharge. In operation at 25oC and a rate of 1/20 C, a capacity of apploximately 150 mAh/g and the potential of about 2 V versus magnesium metal are observed. From the TEM-EDX measurements, the structure of FePO4 particles embedded in carbon and the intensity of magnesium is observed only in regions where FePO4 particles exist. X-ray absorption edge at Fe K-edge shifts downward in energy for the discharge reaction, reflecting the reduction of iron ions to maintain electrical neutrality upon magnesium-ion insertion in the discharge reaction.

References:

[1] D. Aurbach, Z. Lu, A. Schechter, Y. Gofer, H. Gizbar, R. Turgeman, Y. Cohen, M. Moshkovich, E. Levi, Nature 407, 724-727 (2000).

[2] K. Naoi, K. Kisu, E. Iwama, S. Nakashima, Y. Sakai, Y. Orikasa, P. Leone, N. Dupre, T. Brousse, P. Rozier, W. Naoi, P. Simon, Energy Environ. Sci. 9, 2143-2151 (2016).

[3] R. Zhang, C. Ling, ACS Appl. Mater. Interfaces 8, 18018-18026 (2016).

See more of: Multivalent-ion Batteries
See more of: A05: Beyond Lithium-Ion Batteries
See more of: Batteries and Energy Storage
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