Aqueous Rechargeable Manganese/Iodine Battery

Author:

Soundharrajan Vaiyapuri1,Pham Duong Tung2,Piao Junji1,Nithiananth Subramanian3,Kim Jung Ho4,Kim Jaekook15ORCID

Affiliation:

1. Department of Materials Science and Engineering Chonnam National University 77 Yongbong-ro, Bukgu Gwangju 61186 Republic of Korea

2. School of Engineering Physics Hanoi University of Science and Technology No 1 Dai Co Viet Street 100000 Hanoi Viet Nam

3. Graduate School of Science and Technology Shizuoka University 3-5-1 Johoku, Naka-ku Hamamatsu Shizuoka 432–8011 Japan

4. Institute for Superconducting and Electronic Materials (ISEM) Australian Institute of Innovative Materials (AIIM) University of Wollongong North Wollongong New South Wales 2500 Australia

5. Research Center for Artificial Intelligence Assisted Ionics Based Materials Development Platform Chonnam National University Gwangju 61186 Republic of Korea

Abstract

AbstractCarbon neutralization has promoted the identification of new types of energy storage devices. Aqueous iodine batteries (AIBs) with reversible iodine redox activity are considered a viable candidate for stationary energy storage units and thus have recently drawn extensive research interest. Herein, we introduce an aqueous manganese iodine battery (AMIB), utilizing sodium iodide (NaI) as a redox‐active additive in the Mn(ClO4)2 (NMC) electrolyte, activated carbon (AC) as a redox host and Mn ions as the charge carrier. Taking advantage of enhanced kinetics facilitated by I2/2I redox activity, our suggested AMIBs can be electrochemically charged/discharged with only a 6 % loss in capacity after 2,000 cycles at a low current density of 0.3 A g−1 in an AC||AC coin cell configuration. Moreover, the AC||Zn−Mn hybrid full‐cell configuration is also established with AC and a Zn−Mn anode involving the NMC electrolyte, which retains a high energy of 185 Wh kg−1 at a specific power of 2,600 W kg−1. Overall, the AMIBs in this study preferred I2/I conversion chemistry, yielding stable cycle stability, rate performance, and low capacity loss per cycle when compared to Manganese Ion Batteries (MIBs) which are based on Mn2+ intercalation chemistry.

Funder

National Research Foundation of Korea

Trường Đại học Bách Khoa Hà Nội

Publisher

Wiley

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