Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/168704
Title: A liquid crystal ionomer-type electrolyte toward ordering-induced regulation for highly reversible zinc ion battery
Authors: Yuan, Du
Li, Xin
Yao, Hong
Li, Yuhang
Zhu, Xiaobo
Zhao, Jin
Zhang, Haitao
Zhang, Yizhou
Jie, Ernest Tang Jun
Cai, Yi
Srinivasan, Madhavi
Keywords: Engineering::Materials
Issue Date: 2023
Source: Yuan, D., Li, X., Yao, H., Li, Y., Zhu, X., Zhao, J., Zhang, H., Zhang, Y., Jie, E. T. J., Cai, Y. & Srinivasan, M. (2023). A liquid crystal ionomer-type electrolyte toward ordering-induced regulation for highly reversible zinc ion battery. Advanced Science, 10(8), 2206469-. https://dx.doi.org/10.1002/advs.202206469
Project: A20H3g2140 
NRF-NRFI2017-08 
Journal: Advanced Science 
Abstract: Novel electrolyte is being pursued toward exploring Zn chemistry in zinc ion batteries. Here, a fluorine-free liquid crystal (LC) ionomer-type zinc electrolyte is presented, achieving simultaneous regulated water activity and long-range ordering of conduction channels and SEI. Distinct from water network or local ordering in current advances, long-range ordering of layered water channels is realized. Via manipulating water activity, conductivities range from ≈0.34 to 15 mS cm-1 , and electrochemical window can be tuned from ≈2.3-4.3 V. The Zn|Zn symmetric cell with LC gel exhibits highly reversible Zn stripping/plating at 5 mA cm-2 and 5 mAh cm-2 for 800 h, with retained ordering of water channels. The capability of gel for inducing in situ formation of long-range ordered layer SEI associated with alkylbenzene sulfonate anion is uncovered. V2 O5 /Zn cell with the gel shows much improved cycling stability comparing to conventional zinc electrolytes, where the preserved structure of V2 O5 is associated with the efficiently stabilized Zn anode by the gel. Via long-range ordering-induced regulation on ion transport, electrochemical stability, and interfacial reaction, the development of LC electrolyte provides a pathway toward advancing aqueous rechargeable batteries.
URI: https://hdl.handle.net/10356/168704
ISSN: 2198-3844
DOI: 10.1002/advs.202206469
Schools: School of Materials Science and Engineering 
Rights: © 2023 The Authors. Advanced Science published by Wiley-VCH GmbH.This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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