Boosting Aqueous Zn2+ Storage in 1,4,5,8‐Naphthalenetetracarboxylic Dianhydride through Nitrogen Substitution

The research of organic materials thrives for lithium‐ion and sodium‐ion batteries but lacks for aqueous Zn2+ batteries. Herein, we prepared 1,4,5,8‐naphthalene diimide (NTCDI), which is derived from 1,4,5,8‐naphthalenetetracarboxylic dianhydride, through nitrogen substitution with the assistance of...

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Veröffentlicht in:ChemElectroChem 2019-07, Vol.6 (14), p.3644-3647
Hauptverfasser: Wang, Xiaoshuang, Chen, Ling, Lu, Feng, Liu, Jingyan, Chen, Xiangcheng, Shao, Guangjie
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container_start_page 3644
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creator Wang, Xiaoshuang
Chen, Ling
Lu, Feng
Liu, Jingyan
Chen, Xiangcheng
Shao, Guangjie
description The research of organic materials thrives for lithium‐ion and sodium‐ion batteries but lacks for aqueous Zn2+ batteries. Herein, we prepared 1,4,5,8‐naphthalene diimide (NTCDI), which is derived from 1,4,5,8‐naphthalenetetracarboxylic dianhydride, through nitrogen substitution with the assistance of ammonia solution. NTCDI is first applied in aqueous Zn2+ batteries, which can give a high reversible capacity of 240 mAh g−1 at 0.1 A g−1. The electrochemical kinetics analysis indicates that the diffusion‐control process dominates in the electrode reaction. NTCDI can keep 73.7 % of the initial capacity of 152 mAh g−1 after 2000 continuous charge/discharge cycles at 1 A g−1, showing great potential for zinc storage. If the shoe fits: Highly activated 1,4,5,8‐naphthalene diimide (NTCDI) is prepared by dissolving 1,4,5,8‐naphthalenetetracarboxylic dianhydride (NTCDA) in ammonia solution. Two C=O groups of adjacent NTCDI molecules can accommodate Zn2+ efficiently in aqueous zin‐ion batteries (ZIBs). The contact possibility of Zn2+ and C=O bonds increases among NTCDI molecules with smaller crystal size, which is conducive to advancing the electrochemical performance. The exploration of NTCDA in ZIBs creates a strategy for designing organic materials for zinc storage.
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Herein, we prepared 1,4,5,8‐naphthalene diimide (NTCDI), which is derived from 1,4,5,8‐naphthalenetetracarboxylic dianhydride, through nitrogen substitution with the assistance of ammonia solution. NTCDI is first applied in aqueous Zn2+ batteries, which can give a high reversible capacity of 240 mAh g−1 at 0.1 A g−1. The electrochemical kinetics analysis indicates that the diffusion‐control process dominates in the electrode reaction. NTCDI can keep 73.7 % of the initial capacity of 152 mAh g−1 after 2000 continuous charge/discharge cycles at 1 A g−1, showing great potential for zinc storage. If the shoe fits: Highly activated 1,4,5,8‐naphthalene diimide (NTCDI) is prepared by dissolving 1,4,5,8‐naphthalenetetracarboxylic dianhydride (NTCDA) in ammonia solution. Two C=O groups of adjacent NTCDI molecules can accommodate Zn2+ efficiently in aqueous zin‐ion batteries (ZIBs). The contact possibility of Zn2+ and C=O bonds increases among NTCDI molecules with smaller crystal size, which is conducive to advancing the electrochemical performance. The exploration of NTCDA in ZIBs creates a strategy for designing organic materials for zinc storage.</description><identifier>ISSN: 2196-0216</identifier><identifier>EISSN: 2196-0216</identifier><identifier>DOI: 10.1002/celc.201900750</identifier><language>eng</language><publisher>Weinheim: John Wiley &amp; Sons, Inc</publisher><subject>Ammonia ; aqueous Zn2+ batteries ; Dianhydrides ; Diimide ; energy conversion ; Lithium ; molecular electrochemistry ; Naphthalene ; nitrogen substitution ; Organic materials ; Reaction kinetics ; Rechargeable batteries ; Substitution reactions</subject><ispartof>ChemElectroChem, 2019-07, Vol.6 (14), p.3644-3647</ispartof><rights>2019 Wiley‐VCH Verlag GmbH &amp; Co. 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Herein, we prepared 1,4,5,8‐naphthalene diimide (NTCDI), which is derived from 1,4,5,8‐naphthalenetetracarboxylic dianhydride, through nitrogen substitution with the assistance of ammonia solution. NTCDI is first applied in aqueous Zn2+ batteries, which can give a high reversible capacity of 240 mAh g−1 at 0.1 A g−1. The electrochemical kinetics analysis indicates that the diffusion‐control process dominates in the electrode reaction. NTCDI can keep 73.7 % of the initial capacity of 152 mAh g−1 after 2000 continuous charge/discharge cycles at 1 A g−1, showing great potential for zinc storage. If the shoe fits: Highly activated 1,4,5,8‐naphthalene diimide (NTCDI) is prepared by dissolving 1,4,5,8‐naphthalenetetracarboxylic dianhydride (NTCDA) in ammonia solution. Two C=O groups of adjacent NTCDI molecules can accommodate Zn2+ efficiently in aqueous zin‐ion batteries (ZIBs). 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subjects Ammonia
aqueous Zn2+ batteries
Dianhydrides
Diimide
energy conversion
Lithium
molecular electrochemistry
Naphthalene
nitrogen substitution
Organic materials
Reaction kinetics
Rechargeable batteries
Substitution reactions
title Boosting Aqueous Zn2+ Storage in 1,4,5,8‐Naphthalenetetracarboxylic Dianhydride through Nitrogen Substitution
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