The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate

Copper hexacyanoferrate (CuHCFe) is proved to be a potential cathode for potassium ion and sodium ion storage in aqueous system recently. However, its ability for lithium ion storage has not been well studied. Here, we synthesized CuHCFe by a low-cost and scalable co-precipitation method, and its el...

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Main Authors: Gao, Caitian, Liu, Yezhou, Zheng, Lu, Feng, Erxi, Sim, Soojin, Kim, Yeongae, Yun, Jeonghun, Kim, Moobum, Lee, Seok Woo
Other Authors: School of Electrical and Electronic Engineering
Format: Article
Language:English
Published: 2020
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Online Access:https://hdl.handle.net/10356/141908
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-1419082020-06-11T08:43:49Z The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate Gao, Caitian Liu, Yezhou Zheng, Lu Feng, Erxi Sim, Soojin Kim, Yeongae Yun, Jeonghun Kim, Moobum Lee, Seok Woo School of Electrical and Electronic Engineering School of Materials Science and Engineering Engineering::Electrical and electronic engineering Microphones Flow Rate Measurement Copper hexacyanoferrate (CuHCFe) is proved to be a potential cathode for potassium ion and sodium ion storage in aqueous system recently. However, its ability for lithium ion storage has not been well studied. Here, we synthesized CuHCFe by a low-cost and scalable co-precipitation method, and its electrochemical behavior as the cathode for lithium ion storage was investigated both in aqueous and organic systems. The CuHCFe electrode shows larger capacity and better rate capability in organic system compared with the performance in aqueous system. In addition, the capacity has 88% retention after 500 cycles. We further analyzed the strain generated during lithium ion intercalation by ex-situ X-ray diffraction (XRD) method in both types of electrolyte. The lattice of CuHCFe shows shrinkage with ion intercalation in both systems. The measured strains are 0.70% and 0.83% in aqueous and organic system, respectively. The results indicate that the large open framework and small strain are the essential factors for the promising electrochemical performance. ASTAR (Agency for Sci., Tech. and Research, S’pore) Published version 2020-06-11T08:43:49Z 2020-06-11T08:43:49Z 2019 Journal Article Gao, C., Liu, Y., Zheng, L., Feng, E., Sim, S., Kim, Y., . . . Lee, S. W. (2019). The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate. Journal of The Electrochemical Society, 166(10), A1732-A1737. doi:10.1149/2.0331910jes 0013-4651 https://hdl.handle.net/10356/141908 10.1149/2.0331910jes 2-s2.0-85073204825 10 166 A1732 A1737 en Journal of the Electrochemical Society © The Electrochemical Society, Inc. 2019. All rights reserved. Except as provided under U.S. copyright law, this work may not be reproduced, resold, distributed, or modified without the express permission of The Electrochemical Society (ECS). The archival version of this work was published in Journal of The Electrochemical Society, 166, 10, A1732-A1737. application/pdf
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
topic Engineering::Electrical and electronic engineering
Microphones
Flow Rate Measurement
spellingShingle Engineering::Electrical and electronic engineering
Microphones
Flow Rate Measurement
Gao, Caitian
Liu, Yezhou
Zheng, Lu
Feng, Erxi
Sim, Soojin
Kim, Yeongae
Yun, Jeonghun
Kim, Moobum
Lee, Seok Woo
The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate
description Copper hexacyanoferrate (CuHCFe) is proved to be a potential cathode for potassium ion and sodium ion storage in aqueous system recently. However, its ability for lithium ion storage has not been well studied. Here, we synthesized CuHCFe by a low-cost and scalable co-precipitation method, and its electrochemical behavior as the cathode for lithium ion storage was investigated both in aqueous and organic systems. The CuHCFe electrode shows larger capacity and better rate capability in organic system compared with the performance in aqueous system. In addition, the capacity has 88% retention after 500 cycles. We further analyzed the strain generated during lithium ion intercalation by ex-situ X-ray diffraction (XRD) method in both types of electrolyte. The lattice of CuHCFe shows shrinkage with ion intercalation in both systems. The measured strains are 0.70% and 0.83% in aqueous and organic system, respectively. The results indicate that the large open framework and small strain are the essential factors for the promising electrochemical performance.
author2 School of Electrical and Electronic Engineering
author_facet School of Electrical and Electronic Engineering
Gao, Caitian
Liu, Yezhou
Zheng, Lu
Feng, Erxi
Sim, Soojin
Kim, Yeongae
Yun, Jeonghun
Kim, Moobum
Lee, Seok Woo
format Article
author Gao, Caitian
Liu, Yezhou
Zheng, Lu
Feng, Erxi
Sim, Soojin
Kim, Yeongae
Yun, Jeonghun
Kim, Moobum
Lee, Seok Woo
author_sort Gao, Caitian
title The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate
title_short The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate
title_full The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate
title_fullStr The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate
title_full_unstemmed The effect of electrolyte type on the Li ion intercalation in copper hexacyanoferrate
title_sort effect of electrolyte type on the li ion intercalation in copper hexacyanoferrate
publishDate 2020
url https://hdl.handle.net/10356/141908
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