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Probing the effect of Mg doping on triclinic Na2Mn3O7 transition metal oxide as cathode material for sodium-ion batteries

Siriwardena, D. P. (författare)
Fernando, J. F. S. (författare)
Wang, T. (författare)
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Firestein, K. L. (författare)
Zhang, C. (författare)
Brand, H. E. A. (författare)
Jones, M. W. M. (författare)
Kewish, C. M. (författare)
Berntsen, P. (författare)
Jenkins, T. (författare)
Lewis, C. -EM. (författare)
von Treifeldt, J. E. (författare)
Dubal, D. P. (författare)
Golberg, D. V. (författare)
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Elsevier Ltd, 2021
2021
Engelska.
Ingår i: Electrochimica Acta. - : Elsevier Ltd. - 0013-4686 .- 1873-3859. ; 394
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Triclinic Na2Mn3O7 has been identified as a promising material for high-capacity sodium-ion batteries. However, the knowledge on the effect of doping of metal ions and structural transformations of Na2Mn3O7 during dis(charge) is limited. Integration of alkali metal-ions, specially Mg2+ can enhance the electrochemical properties in transition metal oxides. Herein, a series of Mg2+ doped triclinic Na2Mn3O7 cathode materials was explored for the first time. Electrochemical analysis revealed that Mg2+ improves specific capacities, and rate capabilities. Ex situ X-ray diffraction (XRD) and Galvanostatic charge discharge cycling (GCD) showed that the triclinic phase reversibly converts into two monoclinic phases at high Na+ insertion levels. Na+ extraction at high potentials is supported by another biphasic region which converts to a major triclinic phase at the end of the charge. GCD, cyclic voltammetry (CV) and ex situ X-ray absorption spectroscopy (XAS) documented that the capacity mainly evolved through a Mn4+/3+ redox couple and a reversible O2-/n− redox reaction. CV and Galvanostatic intermittent titration techniques (GITT) showed that Mg2+ reduces the Na+-vacancy ordering and improves the Na+ diffusion. The 2 mol.% Mg-doped material exhibited a high specific capacity of 143 mAh/g after 30 cycles and a rate capability of 93 mAh/g (at 500 mA/g). GCD analysis demonstrated that O2-/n− redox is remarkably stable up to at least 90 cycles. Full cells made using the 0.5 mol.% Mg-doped material displayed a promising discharge specific capacity of 80 mAh/g. The effects of cation doping into the complex crystal structures, phase transformations during Na+ de(intercalation) and the importance of O2-/n− redox for achieving high capacities were uncovered. The findings of this work will guide the design of novel cathode materials for sodium-ion batteries. © 2021

Nyckelord

Anion redox
Cathode materials
Full cell
Na2Mn3O7
Sodium-ion batteries
Cathodes
Cyclic voltammetry
Doping (additives)
Electric discharges
Metal ions
Redox reactions
Sodium compounds
Transition metal oxides
Transition metals
X ray absorption spectroscopy
Cathodes material
Charge discharge cycling
Galvanostatic charge/discharge
Mg$-2$
Mg$-2$
Mg-doping
Sodium ion batteries
Transition-metal oxides
Manganese compounds

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