4.8 Article

Non-equilibrium Structural Evolution of the Lithium-Rich Li1+yMn2O4 Cathode within a Battery

Journal

CHEMISTRY OF MATERIALS
Volume 25, Issue 5, Pages 754-760

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/cm303851w

Keywords

in situ neutron diffraction; structure-property relationships; lithium occupancy; battery; lithium manganate; cathode; neutron scattering

Funding

  1. ANSTO within the Bragg Institute
  2. MOST [2010DFA61770]
  3. NSFC [21073046]

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Lithium-ion batteries are undergoing rapid development to meet the energy demands of the transportation and renewable energy-generation sectors. The capacity of a lithium-ion battery is dependent on the amount of lithium that can be reversibly incorporated into the cathode. This work directly quantifies the time- and current-dependent lithium transfer within a cathode functioning under conventional charge-discharge cycling. We examine Li1+yMn2O4 under real working conditions using in situ neutron powder diffraction and link the atomic-scale structure to the battery performance. The lithium location and content, oxygen positional parameter, and lattice parameter of the cathode are measured and linked to the battery's charge/discharge characteristics. Lithium insertion (discharge) differs from extraction (charge), a feature that may explain the relative ease of discharge (compared with charge) of this material. An atomic-scale understanding of cathode functionality, such as revealed here, will direct improvements in battery performance at both the practical and the fundamental level.

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