Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering
Aqueous rechargeable zinc-ion batteries are emerging as attractive alternatives for post-lithium-ion batteries. However, their electrochemical performances are restricted by the narrow working window of materials in aqueous electrolytes. Herein, a Ni-mediated VO2–B nanobelt [(Ni)VO2] has been design...
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sg-ntu-dr.10356-1475512023-07-14T16:01:06Z Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering Cai, Yi Chua, Rodney Kou, Zongkui Ren, Hao Yuan, Du Huang, Shaozhuan Kumar, Sonal Verma, Vivek Amonpattaratkit, Penphitcha Srinivasan, Madhavi School of Materials Science and Engineering Energy Research Institute @ NTU (ERI@N) Engineering::Materials Zn-ion Battery Aqueous Aqueous rechargeable zinc-ion batteries are emerging as attractive alternatives for post-lithium-ion batteries. However, their electrochemical performances are restricted by the narrow working window of materials in aqueous electrolytes. Herein, a Ni-mediated VO2–B nanobelt [(Ni)VO2] has been designed to optimize the intrinsic electronic structure of VO2–B and thus achieve much more enhanced zinc-ion storage. Specifically, the Zn/(Ni)VO2 battery yields a good rate capability (182.0 mA h g–1 at 5 A g–1) with a superior cycling stability (130.6 mA h g–1 at 10 A g–1 after 2000 cycles). Experimental and theoretical methods reveal that the introduction of Ni2+ in the VO2 tunnel structure can effectively provide high surface reactivity and improve the intrinsic electronic configurations, thus resulting in good kinetics. Furthermore, H+ and Zn2+ cointercalation processes are determined via in situ X-ray diffraction and supported by ex situ characterizations. Additionally, quasi-solid-state Zn/(Ni)VO2 soft-packaged batteries are assembled and provide flexibility in battery design for practical applications. The results provide insights into the interrelationships between the intrinsic electronic structure of the cathode and the overall electrochemical performance. National Research Foundation (NRF) Accepted version R.C. and Y.C. contributed equally to this work. This work was financially supported by the National Research Foundation of Singapore (NRF) Investigatorship award number NRFI2017-08/NRF2016NRF-NRFI001-22. The authors thank Synchro-tron Light Research Institute (Public Organization), Muang, Nakhon Ratchasima, 30000, Thailand, for XANES measure-ments in Beamline 8. 2021-04-16T06:15:26Z 2021-04-16T06:15:26Z 2020 Journal Article Cai, Y., Chua, R., Kou, Z., Ren, H., Yuan, D., Huang, S., Kumar, S., Verma, V., Amonpattaratkit, P. & Srinivasan, M. (2020). Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering. ACS Applied Materials & Interfaces, 12(32), 36110-36118. https://dx.doi.org/10.1021/acsami.0c09061 1944-8244 https://hdl.handle.net/10356/147551 10.1021/acsami.0c09061 32 12 36110 36118 en NRFI2017-08/NRF2016NRF-NRFI001-22 ACS Applied Materials & Interfaces This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Materials & Interfaces, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsami.0c09061 application/pdf |
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Engineering::Materials Zn-ion Battery Aqueous Cai, Yi Chua, Rodney Kou, Zongkui Ren, Hao Yuan, Du Huang, Shaozhuan Kumar, Sonal Verma, Vivek Amonpattaratkit, Penphitcha Srinivasan, Madhavi Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering |
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Aqueous rechargeable zinc-ion batteries are emerging as attractive alternatives for post-lithium-ion batteries. However, their electrochemical performances are restricted by the narrow working window of materials in aqueous electrolytes. Herein, a Ni-mediated VO2–B nanobelt [(Ni)VO2] has been designed to optimize the intrinsic electronic structure of VO2–B and thus achieve much more enhanced zinc-ion storage. Specifically, the Zn/(Ni)VO2 battery yields a good rate capability (182.0 mA h g–1 at 5 A g–1) with a superior cycling stability (130.6 mA h g–1 at 10 A g–1 after 2000 cycles). Experimental and theoretical methods reveal that the introduction of Ni2+ in the VO2 tunnel structure can effectively provide high surface reactivity and improve the intrinsic electronic configurations, thus resulting in good kinetics. Furthermore, H+ and Zn2+ cointercalation processes are determined via in situ X-ray diffraction and supported by ex situ characterizations. Additionally, quasi-solid-state Zn/(Ni)VO2 soft-packaged batteries are assembled and provide flexibility in battery design for practical applications. The results provide insights into the interrelationships between the intrinsic electronic structure of the cathode and the overall electrochemical performance. |
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School of Materials Science and Engineering |
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School of Materials Science and Engineering Cai, Yi Chua, Rodney Kou, Zongkui Ren, Hao Yuan, Du Huang, Shaozhuan Kumar, Sonal Verma, Vivek Amonpattaratkit, Penphitcha Srinivasan, Madhavi |
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Cai, Yi Chua, Rodney Kou, Zongkui Ren, Hao Yuan, Du Huang, Shaozhuan Kumar, Sonal Verma, Vivek Amonpattaratkit, Penphitcha Srinivasan, Madhavi |
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Cai, Yi |
title |
Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering |
title_short |
Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering |
title_full |
Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering |
title_fullStr |
Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering |
title_full_unstemmed |
Boosting Zn-ion storage performance of bronze-type VO2 via Ni-mediated electronic structure engineering |
title_sort |
boosting zn-ion storage performance of bronze-type vo2 via ni-mediated electronic structure engineering |
publishDate |
2021 |
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https://hdl.handle.net/10356/147551 |
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1773551199065210880 |