4.6 Article

Facile synthesis and the exploration of the zinc storage mechanism of β-MnO2 nanorods with exposed (101) planes as a novel cathode material for high performance eco-friendly zinc-ion batteries

Journal

JOURNAL OF MATERIALS CHEMISTRY A
Volume 5, Issue 44, Pages 23299-23309

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ta07170a

Keywords

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Funding

  1. Global Frontier Hybrid Interface Materials (GFHIM) of the National Research Foundation of Korea (NRF) - Ministry of Science, ICT & Future Planning [2013M3A6B1078875]
  2. National Research Foundation of Korea (NRF) - Korea government (MSIP) [2017R1A2A1A17069397]
  3. National Research Foundation of Korea [2017R1A2A1A17069397, 2013M3A6B1078875] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Aqueous Zn-ion batteries (ZIBs) have emerged as promising and eco-friendly next-generation energy storage systems to substitute lithium-ion batteries. Therefore, discovering new electrode materials for ZIBs with high performance and unraveling their electrochemical reactions during Zn-ion insertion/extraction are of great interest. Here, we present, for the first time, tunnel-type beta-MnO2 nanorods with exposed (101) planes, prepared via a facile microwave-assisted hydrothermal synthesis within only 10 min, for use as a high performance cathode for ZIBs. In contrast to its bulk counterpart, which showed no electrochemical reactivity, the present beta-MnO2 nanorod electrode exhibited a high discharge capacity of 270 mA h g(-1) at 100 mA g(-1), high rate capability (123 and 86 mA h g(-1) at 528 and 1056 mA g(-1), respectively), and long cycling stability (75% capacity retention with 100% coulombic efficiency at 200 mA g(-1)) over 200 cycles. The Zn-ion storage mechanism of the cathode was also unraveled using in situ synchrotron, ex situ X-ray diffraction, ex situ X-ray photoelectron spectroscopy, and ex situ X-ray absorption spectroscopy. Our present study indicates that Zn intercalation occurred via a combination of solid solution and conversion reactions. During initial cycles, the beta-MnO2 cathode was able to maintain its structure; however, after prolonged cycles, it transformed into a spinel structure. The present results challenge the common views on the beta-MnO2 electrode and pave the way for the further development of ZIBs as cost-effective and environmentally friendly next-generation energy storage systems.

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