Self-assembled ZnO-carbon dots anode materials for high performance nickel-zinc alkaline batteries

After incorporation of a few Carbon Dots (CDs), ZnO anodes process thin carbon shells, refined microstructures and special univalent zinc sites, which result in better reactivity, higher corrosion resistance, more effective electron paths to enhance electrochemical performance in high capacity, exce...

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Published inChemical engineering journal (Lausanne, Switzerland : 1996) Vol. 425; p. 130660
Main Authors Wei, Ji-Shi, Zhu, Ze-Yang, Zhao, Xiao, Song, Tian-Bing, Huang, Jian-Hang, Zhang, Yi-Xiao, Liu, Xi, Chen, Liwei, Niu, Xiao-Qing, Wang, Yong-Gang, Xiong, Huan-Ming
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.12.2021
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Abstract After incorporation of a few Carbon Dots (CDs), ZnO anodes process thin carbon shells, refined microstructures and special univalent zinc sites, which result in better reactivity, higher corrosion resistance, more effective electron paths to enhance electrochemical performance in high capacity, excellent rate capability and long cycling stability in the Ni-Zn alkaline battery. [Display omitted] •1. CDs efficiently control morphology of ZnO for sufficient electrochemical reactions.•2. With the assistance of CDs, ZnO will process conformal carbon shells with few layers.•3. Univalent zinc sites constructed by CDs play a key role during charging process. The development of high-performance nickel-zinc (Ni-Zn) alkaline batteries is mainly plagued by short life span and poor rate performance of ZnO anode materials. To improve the cycling stability and rate capability of Ni-Zn batteries, carbon dots (CDs) are employed to construct clustered ZnO-CDs nanocomposites, coating ZnO with protective shells of carbon layers and providing electron paths to enhance conductivity of the nanocomposites. Univalent zinc species are found at the interfaces between CDs derivatives and ZnO, which are embedded in the nanoclusters and protected well by carbon coating. Theoretical calculations show univalent zinc species change the electronic structures of ZnO surface, so as to accelerate the charging process of ZnO anode materials. Such ZnO-CDs derived nanocomposites exhibit excellent rate capability (95.3%, 84.7% and 75.0% of capacity retention rate at 2, 5 and 10 A g−1, respectively) and outstanding cycling stability with 92.0% of capacity retention rate after 5000 cycles, which is far better than ZnO based anodes without the protection of CDs (39.1% retention rate from 1 to 10 A g−1 and 71.6% of capacity retention rate after 500 cycles).
AbstractList After incorporation of a few Carbon Dots (CDs), ZnO anodes process thin carbon shells, refined microstructures and special univalent zinc sites, which result in better reactivity, higher corrosion resistance, more effective electron paths to enhance electrochemical performance in high capacity, excellent rate capability and long cycling stability in the Ni-Zn alkaline battery. [Display omitted] •1. CDs efficiently control morphology of ZnO for sufficient electrochemical reactions.•2. With the assistance of CDs, ZnO will process conformal carbon shells with few layers.•3. Univalent zinc sites constructed by CDs play a key role during charging process. The development of high-performance nickel-zinc (Ni-Zn) alkaline batteries is mainly plagued by short life span and poor rate performance of ZnO anode materials. To improve the cycling stability and rate capability of Ni-Zn batteries, carbon dots (CDs) are employed to construct clustered ZnO-CDs nanocomposites, coating ZnO with protective shells of carbon layers and providing electron paths to enhance conductivity of the nanocomposites. Univalent zinc species are found at the interfaces between CDs derivatives and ZnO, which are embedded in the nanoclusters and protected well by carbon coating. Theoretical calculations show univalent zinc species change the electronic structures of ZnO surface, so as to accelerate the charging process of ZnO anode materials. Such ZnO-CDs derived nanocomposites exhibit excellent rate capability (95.3%, 84.7% and 75.0% of capacity retention rate at 2, 5 and 10 A g−1, respectively) and outstanding cycling stability with 92.0% of capacity retention rate after 5000 cycles, which is far better than ZnO based anodes without the protection of CDs (39.1% retention rate from 1 to 10 A g−1 and 71.6% of capacity retention rate after 500 cycles).
ArticleNumber 130660
Author Chen, Liwei
Zhang, Yi-Xiao
Xiong, Huan-Ming
Wei, Ji-Shi
Liu, Xi
Niu, Xiao-Qing
Zhao, Xiao
Huang, Jian-Hang
Zhu, Ze-Yang
Wang, Yong-Gang
Song, Tian-Bing
Author_xml – sequence: 1
  givenname: Ji-Shi
  surname: Wei
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  organization: Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials, Fudan University, Shanghai 200438, PR China
– sequence: 2
  givenname: Ze-Yang
  surname: Zhu
  fullname: Zhu, Ze-Yang
  organization: Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials, Fudan University, Shanghai 200438, PR China
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  givenname: Xiao
  surname: Zhao
  fullname: Zhao, Xiao
  organization: Institute for Computation in Molecular and Materials Science, School of Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, PR China
– sequence: 4
  givenname: Tian-Bing
  surname: Song
  fullname: Song, Tian-Bing
  organization: Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials, Fudan University, Shanghai 200438, PR China
– sequence: 5
  givenname: Jian-Hang
  surname: Huang
  fullname: Huang, Jian-Hang
  organization: Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials, Fudan University, Shanghai 200438, PR China
– sequence: 6
  givenname: Yi-Xiao
  surname: Zhang
  fullname: Zhang, Yi-Xiao
  organization: School of Chemistry and Chemical Engineering, In-situ Center for Physical Science, and Frontiers Science Center for Transformative Molecules, Shanghai Jiao Tong University, Shanghai 200240, PR China
– sequence: 7
  givenname: Xi
  surname: Liu
  fullname: Liu, Xi
  organization: School of Chemistry and Chemical Engineering, In-situ Center for Physical Science, and Frontiers Science Center for Transformative Molecules, Shanghai Jiao Tong University, Shanghai 200240, PR China
– sequence: 8
  givenname: Liwei
  surname: Chen
  fullname: Chen, Liwei
  organization: School of Chemistry and Chemical Engineering, In-situ Center for Physical Science, and Frontiers Science Center for Transformative Molecules, Shanghai Jiao Tong University, Shanghai 200240, PR China
– sequence: 9
  givenname: Xiao-Qing
  surname: Niu
  fullname: Niu, Xiao-Qing
  organization: Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials, Fudan University, Shanghai 200438, PR China
– sequence: 10
  givenname: Yong-Gang
  surname: Wang
  fullname: Wang, Yong-Gang
  organization: Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials, Fudan University, Shanghai 200438, PR China
– sequence: 11
  givenname: Huan-Ming
  surname: Xiong
  fullname: Xiong, Huan-Ming
  email: hmxiong@fudan.edu.cn
  organization: Department of Chemistry, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Laboratory of Advanced Materials, Fudan University, Shanghai 200438, PR China
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Keywords Carbon dots
Univalent Zinc
ZnO anode
Surface coating
Nickel-zinc alkaline battery
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Snippet After incorporation of a few Carbon Dots (CDs), ZnO anodes process thin carbon shells, refined microstructures and special univalent zinc sites, which result...
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elsevier
SourceType Enrichment Source
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Publisher
StartPage 130660
SubjectTerms Carbon dots
Nickel-zinc alkaline battery
Surface coating
Univalent Zinc
ZnO anode
Title Self-assembled ZnO-carbon dots anode materials for high performance nickel-zinc alkaline batteries
URI https://dx.doi.org/10.1016/j.cej.2021.130660
Volume 425
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