Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries

The development of MnO2 as a cathode for aqueous zinc-ion batteries (AZIBs) is severely limited by the low intrinsic electrical conductivity and unstable crystal structure. Herein, a multifunctional modification strategy is proposed to construct N-doped KMn8 O16 with abundant oxygen vacancy and larg...

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Main Authors: Cui, Guodong, Zeng, Yinxiang, Wu, Jinfang, Guo, Yan, Gu, Xiaojun, Lou, David Xiong Wen
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2022
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Online Access:https://hdl.handle.net/10356/160810
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Institution: Nanyang Technological University
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spelling sg-ntu-dr.10356-1608102023-12-29T06:52:53Z Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries Cui, Guodong Zeng, Yinxiang Wu, Jinfang Guo, Yan Gu, Xiaojun Lou, David Xiong Wen School of Chemical and Biomedical Engineering Engineering::Chemical engineering Aqueous Zinc-Ion Batteries N-Doping The development of MnO2 as a cathode for aqueous zinc-ion batteries (AZIBs) is severely limited by the low intrinsic electrical conductivity and unstable crystal structure. Herein, a multifunctional modification strategy is proposed to construct N-doped KMn8 O16 with abundant oxygen vacancy and large specific surface area (named as N-KMO) through a facile one-step hydrothermal approach. The synergetic effects of N-doping, oxygen vacancy, and porous structure in N-KMO can effectively suppress the dissolution of manganese ions, and promote ion diffusion and electron conduction. As a result, the N-KMO cathode exhibits dramatically improved stability and reaction kinetics, superior to the pristine MnO2 and MnO2 with only oxygen vacancy. Remarkably, the N-KMO cathode delivers a high reversible capacity of 262 mAh g-1 after 2500 cycles at 1 A g-1 with a capacity retention of 91%. Simultaneously, the highest specific capacity can reach 298 mAh g-1 at 0.1 A g-1 . Theoretical calculations reveal that the oxygen vacancy and N-doping can improve the electrical conductivity of MnO2 and thus account for the outstanding rate performance. Moreover, ex situ characterizations indicate that the energy storage mechanism of the N-KMO cathode is mainly a H+ and Zn2+ co-insertion/extraction process. Published version The authors gratefully acknowledge the financial support from the National Natural Science Foundation of China (21701090, 21975015, and 21761025), the Science and Technology Projects of Inner Mongolia Autonomous Region (2021GG0195), and the Natural Science Foundation of Inner Mongolia Autonomous Region of China (2021MS02017). 2022-08-03T02:58:16Z 2022-08-03T02:58:16Z 2022 Journal Article Cui, G., Zeng, Y., Wu, J., Guo, Y., Gu, X. & Lou, D. X. W. (2022). Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries. Advanced Science, 9(10), 2106067-. https://dx.doi.org/10.1002/advs.202106067 2198-3844 https://hdl.handle.net/10356/160810 10.1002/advs.202106067 35142449 2-s2.0-85124624223 10 9 2106067 en Advanced Science © 2022 The Authors. Advanced Science published by Wiley-VCH GmbH.This is an open access article under the terms of the Creative CommonsAttribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic Engineering::Chemical engineering
Aqueous Zinc-Ion Batteries
N-Doping
spellingShingle Engineering::Chemical engineering
Aqueous Zinc-Ion Batteries
N-Doping
Cui, Guodong
Zeng, Yinxiang
Wu, Jinfang
Guo, Yan
Gu, Xiaojun
Lou, David Xiong Wen
Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries
description The development of MnO2 as a cathode for aqueous zinc-ion batteries (AZIBs) is severely limited by the low intrinsic electrical conductivity and unstable crystal structure. Herein, a multifunctional modification strategy is proposed to construct N-doped KMn8 O16 with abundant oxygen vacancy and large specific surface area (named as N-KMO) through a facile one-step hydrothermal approach. The synergetic effects of N-doping, oxygen vacancy, and porous structure in N-KMO can effectively suppress the dissolution of manganese ions, and promote ion diffusion and electron conduction. As a result, the N-KMO cathode exhibits dramatically improved stability and reaction kinetics, superior to the pristine MnO2 and MnO2 with only oxygen vacancy. Remarkably, the N-KMO cathode delivers a high reversible capacity of 262 mAh g-1 after 2500 cycles at 1 A g-1 with a capacity retention of 91%. Simultaneously, the highest specific capacity can reach 298 mAh g-1 at 0.1 A g-1 . Theoretical calculations reveal that the oxygen vacancy and N-doping can improve the electrical conductivity of MnO2 and thus account for the outstanding rate performance. Moreover, ex situ characterizations indicate that the energy storage mechanism of the N-KMO cathode is mainly a H+ and Zn2+ co-insertion/extraction process.
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Cui, Guodong
Zeng, Yinxiang
Wu, Jinfang
Guo, Yan
Gu, Xiaojun
Lou, David Xiong Wen
format Article
author Cui, Guodong
Zeng, Yinxiang
Wu, Jinfang
Guo, Yan
Gu, Xiaojun
Lou, David Xiong Wen
author_sort Cui, Guodong
title Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries
title_short Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries
title_full Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries
title_fullStr Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries
title_full_unstemmed Synthesis of nitrogen-doped KMn₈ O₁₆ with oxygen vacancy for stable zinc-ion batteries
title_sort synthesis of nitrogen-doped kmn₈ o₁₆ with oxygen vacancy for stable zinc-ion batteries
publishDate 2022
url https://hdl.handle.net/10356/160810
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