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Structural evolution of electrodes in the NCR and CGR cathode-containing commercial lithium-ion batteries cycled between 3.0 and 4.5 V: an operando neutron powder-diffraction study

Journal Article


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Abstract


  • The dissimilar lattice-evolution of the isostructural layered Li(Ni,Co,Al)O2 (NCR) and Li(Ni,Co,Mn)O2 (CGR) cathodes in commercial lithium-ion batteries during overcharging/discharging was examined using operando neutron powder-diffraction. The stacking axis (c parameter) of both cathodes expands on initial lithiation and contracts on further lithiation. Although both the initial increase and later decrease are smaller for the CGR cathode, the overall change between battery charged and discharged states of the c parameter is larger for the CGR (1.29%) than for the NCR cathode (0.33%). We find these differences are correlated to the transition metal to oxygen bond (as measured through the oxygen positional-parameter) which is specific to the different cathode chemistries. Finally, we note the formation of and suggest a model for a LiC x intermediate between graphite and LiC12 in the anode of both batteries.

UOW Authors


  •   Pang, Wei Kong
  •   Alam, Moshiul (external author)
  •   Peterson, Vanessa K. (external author)
  •   Sharma, Neeraj (external author)

Publication Date


  • 2015

Citation


  • Pang, W., Alam, M., Peterson, V. K. & Sharma, N. (2015). Structural evolution of electrodes in the NCR and CGR cathode-containing commercial lithium-ion batteries cycled between 3.0 and 4.5 V: an operando neutron powder-diffraction study. Journal of Materials Research, 30 (3), 373-380.

Scopus Eid


  • 2-s2.0-84910679034

Ro Full-text Url


  • http://ro.uow.edu.au/cgi/viewcontent.cgi?article=4624&context=eispapers

Ro Metadata Url


  • http://ro.uow.edu.au/eispapers/3605

Number Of Pages


  • 7

Start Page


  • 373

End Page


  • 380

Volume


  • 30

Issue


  • 3

Abstract


  • The dissimilar lattice-evolution of the isostructural layered Li(Ni,Co,Al)O2 (NCR) and Li(Ni,Co,Mn)O2 (CGR) cathodes in commercial lithium-ion batteries during overcharging/discharging was examined using operando neutron powder-diffraction. The stacking axis (c parameter) of both cathodes expands on initial lithiation and contracts on further lithiation. Although both the initial increase and later decrease are smaller for the CGR cathode, the overall change between battery charged and discharged states of the c parameter is larger for the CGR (1.29%) than for the NCR cathode (0.33%). We find these differences are correlated to the transition metal to oxygen bond (as measured through the oxygen positional-parameter) which is specific to the different cathode chemistries. Finally, we note the formation of and suggest a model for a LiC x intermediate between graphite and LiC12 in the anode of both batteries.

UOW Authors


  •   Pang, Wei Kong
  •   Alam, Moshiul (external author)
  •   Peterson, Vanessa K. (external author)
  •   Sharma, Neeraj (external author)

Publication Date


  • 2015

Citation


  • Pang, W., Alam, M., Peterson, V. K. & Sharma, N. (2015). Structural evolution of electrodes in the NCR and CGR cathode-containing commercial lithium-ion batteries cycled between 3.0 and 4.5 V: an operando neutron powder-diffraction study. Journal of Materials Research, 30 (3), 373-380.

Scopus Eid


  • 2-s2.0-84910679034

Ro Full-text Url


  • http://ro.uow.edu.au/cgi/viewcontent.cgi?article=4624&context=eispapers

Ro Metadata Url


  • http://ro.uow.edu.au/eispapers/3605

Number Of Pages


  • 7

Start Page


  • 373

End Page


  • 380

Volume


  • 30

Issue


  • 3