The influence of large cations on the electrochemical properties of tunnel-structured metal oxides

Metal oxides with a tunnelled structure are attractive as charge storage materials for rechargeable batteries and supercapacitors, since the tunnels enable fast reversible insertion/extraction of charge carriers (for example, lithium ions). Common synthesis methods can introduce large cations such a...

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Published in:Nature communications Vol. 7; no. 1; p. 13374
Main Authors: Yuan, Yifei, Zhan, Chun, He, Kun, Chen, Hungru, Yao, Wentao, Sharifi-Asl, Soroosh, Song, Boao, Yang, Zhenzhen, Nie, Anmin, Luo, Xiangyi, Wang, Hao, Wood, Stephen M., Amine, Khalil, Islam, M. Saiful, Lu, Jun, Shahbazian-Yassar, Reza
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 21-11-2016
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Summary:Metal oxides with a tunnelled structure are attractive as charge storage materials for rechargeable batteries and supercapacitors, since the tunnels enable fast reversible insertion/extraction of charge carriers (for example, lithium ions). Common synthesis methods can introduce large cations such as potassium, barium and ammonium ions into the tunnels, but how these cations affect charge storage performance is not fully understood. Here, we report the role of tunnel cations in governing the electrochemical properties of electrode materials by focusing on potassium ions in α-MnO 2 . We show that the presence of cations inside 2 × 2 tunnels of manganese dioxide increases the electronic conductivity, and improves lithium ion diffusivity. In addition, transmission electron microscopy analysis indicates that the tunnels remain intact whether cations are present in the tunnels or not. Our systematic study shows that cation addition to α-MnO 2 has a strong beneficial effect on the electrochemical performance of this material. Metal oxides with a tunnelled structure are attractive as charge storage materials for rechargeable batteries and supercapacitors. Here, the authors investigate the role of tunnel cations in governing and enhancing the electrochemical properties of electrode materials.
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USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
AC02-06CH11357
These authors contributed equally to this work
ISSN:2041-1723
2041-1723
DOI:10.1038/ncomms13374