In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries
Hydrogels hold great promise as electrolytes for emerging aqueous batteries, for which establishing a robust electrode-hydrogel interface is crucial for mitigating side reactions. Conventional hydrogel electrolytes fabricated by ex situ polymerization through either thermal stimulation or photo expo...
Main Authors: | , , , , , , , , |
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Format: | Journal Article |
Language: | English |
Published: |
2024
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Online Access: | https://hdl.handle.net/10356/179013 |
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author | Chen, Liangyuan Xiao, Tuo Yang, Jin-Lin Liu, Yipu Xian, Jinglin Liu, Kang Zhao, Yan Fan, Hong Jin Yang, Peihua |
author2 | School of Physical and Mathematical Sciences |
author_facet | School of Physical and Mathematical Sciences Chen, Liangyuan Xiao, Tuo Yang, Jin-Lin Liu, Yipu Xian, Jinglin Liu, Kang Zhao, Yan Fan, Hong Jin Yang, Peihua |
author_sort | Chen, Liangyuan |
collection | NTU |
description | Hydrogels hold great promise as electrolytes for emerging aqueous batteries, for which establishing a robust electrode-hydrogel interface is crucial for mitigating side reactions. Conventional hydrogel electrolytes fabricated by ex situ polymerization through either thermal stimulation or photo exposure cannot ensure complete interfacial contact with electrodes. Herein, we introduce an in situ electropolymerization approach for constructing hydrogel electrolytes. The hydrogel is spontaneously generated during the initial cycling of the battery, eliminating the need of additional initiators for polymerization. The involvement of electrodes during the hydrogel synthesis yields well-bonded and deep infiltrated electrode-electrolyte interfaces. As a case study, we attest that, the in situ-formed polyanionic hydrogel in Zn-MnO2 battery substantially improves the stability and kinetics of both Zn anode and porous MnO2 cathode owing to the robust interfaces. This research provides insight to the function of hydrogel electrolyte interfaces and constitutes a critical advancement in designing highly durable aqueous batteries. |
first_indexed | 2024-10-01T03:54:16Z |
format | Journal Article |
id | ntu-10356/179013 |
institution | Nanyang Technological University |
language | English |
last_indexed | 2024-10-01T03:54:16Z |
publishDate | 2024 |
record_format | dspace |
spelling | ntu-10356/1790132024-07-22T15:34:30Z In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries Chen, Liangyuan Xiao, Tuo Yang, Jin-Lin Liu, Yipu Xian, Jinglin Liu, Kang Zhao, Yan Fan, Hong Jin Yang, Peihua School of Physical and Mathematical Sciences Physics Aqueous Zn battery Single-ion conduction Hydrogels hold great promise as electrolytes for emerging aqueous batteries, for which establishing a robust electrode-hydrogel interface is crucial for mitigating side reactions. Conventional hydrogel electrolytes fabricated by ex situ polymerization through either thermal stimulation or photo exposure cannot ensure complete interfacial contact with electrodes. Herein, we introduce an in situ electropolymerization approach for constructing hydrogel electrolytes. The hydrogel is spontaneously generated during the initial cycling of the battery, eliminating the need of additional initiators for polymerization. The involvement of electrodes during the hydrogel synthesis yields well-bonded and deep infiltrated electrode-electrolyte interfaces. As a case study, we attest that, the in situ-formed polyanionic hydrogel in Zn-MnO2 battery substantially improves the stability and kinetics of both Zn anode and porous MnO2 cathode owing to the robust interfaces. This research provides insight to the function of hydrogel electrolyte interfaces and constitutes a critical advancement in designing highly durable aqueous batteries. Ministry of Education (MOE) Submitted/Accepted version P.Y. acknowledges the National Natural Science Foundationof China (22209124), the Fundamental Research Funds for the Central Universities (2042023kf0115) and startup funding of Wuhan University. H.J.F. acknowledges financial support from the Singapore Ministry of Education by AcRFTier 2 (MOE-T2EP50121-0006). 2024-07-16T02:51:11Z 2024-07-16T02:51:11Z 2024 Journal Article Chen, L., Xiao, T., Yang, J., Liu, Y., Xian, J., Liu, K., Zhao, Y., Fan, H. J. & Yang, P. (2024). In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries. Angewandte Chemie International Edition, 63(21), e202400230-. https://dx.doi.org/10.1002/anie.202400230 1433-7851 https://hdl.handle.net/10356/179013 10.1002/anie.202400230 38520070 2-s2.0-85190643212 21 63 e202400230 en MOE-T2EP50121-0006 Angewandte Chemie International Edition © 2024 Wiley-VCH GmbH. All rights reserved. This article may be downloaded for personal use only. Any other use requires prior permission of the copyright holder. The Version of Record is available online at http://doi.org/10.1002/anie.202400230. application/pdf |
spellingShingle | Physics Aqueous Zn battery Single-ion conduction Chen, Liangyuan Xiao, Tuo Yang, Jin-Lin Liu, Yipu Xian, Jinglin Liu, Kang Zhao, Yan Fan, Hong Jin Yang, Peihua In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries |
title | In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries |
title_full | In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries |
title_fullStr | In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries |
title_full_unstemmed | In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries |
title_short | In-situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries |
title_sort | in situ spontaneous electropolymerization enables robust hydrogel electrolyte interfaces in aqueous batteries |
topic | Physics Aqueous Zn battery Single-ion conduction |
url | https://hdl.handle.net/10356/179013 |
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