A Dual-Functional Organic Electrolyte Additive with Regulating Suitable Overpotential for Building Highly Reversible Aqueous Zinc Ion Batteries

Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review

Autoren

  • Zixiang Liu
  • Rui Wang
  • Quanwei Ma
  • Jiandong Wan
  • Shilin Zhang
  • Longhai Zhang
  • Hongbao Li
  • Qiquan Luo
  • Jiang Wu
  • Tengfei Zhou
  • Jianfeng Mao
  • Lin Zhang
  • Chaofeng Zhang
  • Zaiping Guo

Organisationseinheiten

Externe Organisationen

  • Anhui University
  • University of Adelaide
  • Qinghai Nationalities University
Forschungs-netzwerk anzeigen

Details

OriginalspracheEnglisch
Aufsatznummer2214538
FachzeitschriftAdvanced functional materials
Jahrgang34
Ausgabenummer5
PublikationsstatusVeröffentlicht - 29 Jan. 2024

Abstract

Aqueous zinc ion batteries (AZIBs) with high safety, low cost, and eco-friendliness advantages show great potential in large-scale energy storage systems. However, their practical application is hindered by low Columbic efficiency and unstable zinc anode resulting from the side reactions and deterioration of zinc dendrites. Herein, tripropylene glycol (TG) is chosen as a dual-functional organic electrolyte additive to improve the reversibility of AZIBs significantly. Importantly, ab initio molecular dynamics theoretical simulations and experiments such as in situ electrochemical impedance spectroscopy, and synchrotron radiation-based in situ Fourier transform infrared spectroscopy confirm that TG participates in the solvation sheath of Zn2+, regulating overpotential and inhibiting side reactions; meanwhile, TG inhibits the deterioration of dendrites and modifies the direction of zinc deposition by constructing an adsorbed layer on the zinc anode. Consequently, a Zn-MnO2 full cell with TG electrolyte exhibited a specific capacity of 124.48 mAh g-1 after 1000 cycles at a current density of 4 A g-1. This quantitative regulation for suitable solvation sheath and adsorbed layer on zinc anode, and its easy scalability of the process can be of immediate benefit for the dendrite-free, high-performance, and low-cost energy storage systems.

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A Dual-Functional Organic Electrolyte Additive with Regulating Suitable Overpotential for Building Highly Reversible Aqueous Zinc Ion Batteries. / Liu, Zixiang; Wang, Rui; Ma, Quanwei et al.
in: Advanced functional materials, Jahrgang 34, Nr. 5, 2214538, 29.01.2024.

Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review

Liu, Z, Wang, R, Ma, Q, Wan, J, Zhang, S, Zhang, L, Li, H, Luo, Q, Wu, J, Zhou, T, Mao, J, Zhang, L, Zhang, C & Guo, Z 2024, 'A Dual-Functional Organic Electrolyte Additive with Regulating Suitable Overpotential for Building Highly Reversible Aqueous Zinc Ion Batteries', Advanced functional materials, Jg. 34, Nr. 5, 2214538. https://doi.org/10.1002/adfm.202214538
Liu, Z., Wang, R., Ma, Q., Wan, J., Zhang, S., Zhang, L., Li, H., Luo, Q., Wu, J., Zhou, T., Mao, J., Zhang, L., Zhang, C., & Guo, Z. (2024). A Dual-Functional Organic Electrolyte Additive with Regulating Suitable Overpotential for Building Highly Reversible Aqueous Zinc Ion Batteries. Advanced functional materials, 34(5), Artikel 2214538. https://doi.org/10.1002/adfm.202214538
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title = "A Dual-Functional Organic Electrolyte Additive with Regulating Suitable Overpotential for Building Highly Reversible Aqueous Zinc Ion Batteries",
abstract = "Aqueous zinc ion batteries (AZIBs) with high safety, low cost, and eco-friendliness advantages show great potential in large-scale energy storage systems. However, their practical application is hindered by low Columbic efficiency and unstable zinc anode resulting from the side reactions and deterioration of zinc dendrites. Herein, tripropylene glycol (TG) is chosen as a dual-functional organic electrolyte additive to improve the reversibility of AZIBs significantly. Importantly, ab initio molecular dynamics theoretical simulations and experiments such as in situ electrochemical impedance spectroscopy, and synchrotron radiation-based in situ Fourier transform infrared spectroscopy confirm that TG participates in the solvation sheath of Zn2+, regulating overpotential and inhibiting side reactions; meanwhile, TG inhibits the deterioration of dendrites and modifies the direction of zinc deposition by constructing an adsorbed layer on the zinc anode. Consequently, a Zn-MnO2 full cell with TG electrolyte exhibited a specific capacity of 124.48 mAh g-1 after 1000 cycles at a current density of 4 A g-1. This quantitative regulation for suitable solvation sheath and adsorbed layer on zinc anode, and its easy scalability of the process can be of immediate benefit for the dendrite-free, high-performance, and low-cost energy storage systems.",
keywords = "electrolyte additives, electrolyte modification, synchrotron, tripropylene glycol, zinc ion batteries",
author = "Zixiang Liu and Rui Wang and Quanwei Ma and Jiandong Wan and Shilin Zhang and Longhai Zhang and Hongbao Li and Qiquan Luo and Jiang Wu and Tengfei Zhou and Jianfeng Mao and Lin Zhang and Chaofeng Zhang and Zaiping Guo",
note = "Funding Information: Z.L., R.W., Q.M. contributed equally to this work. The authors thank the financial support from the National Natural Science Foundation of China (52172173, 51872071), the Natural Science Foundation of Anhui Province for Distinguished Young Scholars (2108085J25), the Excellent innovation team of Anhui Province (2022AH010001), the Natural Science Foundation of Anhui Province (2208085QE130), the Open Fund of Guangdong Provincial Key Laboratory of Advance Energy Storage Materials (AESM202106), and the Special Project of Qinghai Provincial Science and Technology Plan Project (2023‐NY‐016). The authors also acknowledge the High‐performance Computing Platform of Anhui University for providing computing resources. ",
year = "2024",
month = jan,
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language = "English",
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journal = "Advanced functional materials",
issn = "1616-301X",
publisher = "Wiley-VCH Verlag",
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Download

TY - JOUR

T1 - A Dual-Functional Organic Electrolyte Additive with Regulating Suitable Overpotential for Building Highly Reversible Aqueous Zinc Ion Batteries

AU - Liu, Zixiang

AU - Wang, Rui

AU - Ma, Quanwei

AU - Wan, Jiandong

AU - Zhang, Shilin

AU - Zhang, Longhai

AU - Li, Hongbao

AU - Luo, Qiquan

AU - Wu, Jiang

AU - Zhou, Tengfei

AU - Mao, Jianfeng

AU - Zhang, Lin

AU - Zhang, Chaofeng

AU - Guo, Zaiping

N1 - Funding Information: Z.L., R.W., Q.M. contributed equally to this work. The authors thank the financial support from the National Natural Science Foundation of China (52172173, 51872071), the Natural Science Foundation of Anhui Province for Distinguished Young Scholars (2108085J25), the Excellent innovation team of Anhui Province (2022AH010001), the Natural Science Foundation of Anhui Province (2208085QE130), the Open Fund of Guangdong Provincial Key Laboratory of Advance Energy Storage Materials (AESM202106), and the Special Project of Qinghai Provincial Science and Technology Plan Project (2023‐NY‐016). The authors also acknowledge the High‐performance Computing Platform of Anhui University for providing computing resources.

PY - 2024/1/29

Y1 - 2024/1/29

N2 - Aqueous zinc ion batteries (AZIBs) with high safety, low cost, and eco-friendliness advantages show great potential in large-scale energy storage systems. However, their practical application is hindered by low Columbic efficiency and unstable zinc anode resulting from the side reactions and deterioration of zinc dendrites. Herein, tripropylene glycol (TG) is chosen as a dual-functional organic electrolyte additive to improve the reversibility of AZIBs significantly. Importantly, ab initio molecular dynamics theoretical simulations and experiments such as in situ electrochemical impedance spectroscopy, and synchrotron radiation-based in situ Fourier transform infrared spectroscopy confirm that TG participates in the solvation sheath of Zn2+, regulating overpotential and inhibiting side reactions; meanwhile, TG inhibits the deterioration of dendrites and modifies the direction of zinc deposition by constructing an adsorbed layer on the zinc anode. Consequently, a Zn-MnO2 full cell with TG electrolyte exhibited a specific capacity of 124.48 mAh g-1 after 1000 cycles at a current density of 4 A g-1. This quantitative regulation for suitable solvation sheath and adsorbed layer on zinc anode, and its easy scalability of the process can be of immediate benefit for the dendrite-free, high-performance, and low-cost energy storage systems.

AB - Aqueous zinc ion batteries (AZIBs) with high safety, low cost, and eco-friendliness advantages show great potential in large-scale energy storage systems. However, their practical application is hindered by low Columbic efficiency and unstable zinc anode resulting from the side reactions and deterioration of zinc dendrites. Herein, tripropylene glycol (TG) is chosen as a dual-functional organic electrolyte additive to improve the reversibility of AZIBs significantly. Importantly, ab initio molecular dynamics theoretical simulations and experiments such as in situ electrochemical impedance spectroscopy, and synchrotron radiation-based in situ Fourier transform infrared spectroscopy confirm that TG participates in the solvation sheath of Zn2+, regulating overpotential and inhibiting side reactions; meanwhile, TG inhibits the deterioration of dendrites and modifies the direction of zinc deposition by constructing an adsorbed layer on the zinc anode. Consequently, a Zn-MnO2 full cell with TG electrolyte exhibited a specific capacity of 124.48 mAh g-1 after 1000 cycles at a current density of 4 A g-1. This quantitative regulation for suitable solvation sheath and adsorbed layer on zinc anode, and its easy scalability of the process can be of immediate benefit for the dendrite-free, high-performance, and low-cost energy storage systems.

KW - electrolyte additives

KW - electrolyte modification

KW - synchrotron

KW - tripropylene glycol

KW - zinc ion batteries

UR - http://www.scopus.com/inward/record.url?scp=85153375984&partnerID=8YFLogxK

U2 - 10.1002/adfm.202214538

DO - 10.1002/adfm.202214538

M3 - Article

AN - SCOPUS:85153375984

VL - 34

JO - Advanced functional materials

JF - Advanced functional materials

SN - 1616-301X

IS - 5

M1 - 2214538

ER -

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