Gadolinium-doped LiGd x Mn 2−x O 4 was synthesized by a sol-gel method and applied as cathode material in Li ion batteries. Gd-doping significantly changed the unit cell parameter and atomic arrangement. With an increase of x, a cell dimension contracts from 8.2419(2) to 8.2375(8) (x = 0.02), 8.2295(3) (x = 0.04), and 8.2120(6) Å (x = 0.08), with concomitant changes in bond length. The LiO 4 tetrahedron expands to facilitate a fast electrochemical process and the MnO 6 octahedron shrinks to provide structural integrity. The former contributes to a better high-rate performance and the latter leads to a variation in the cell dimensions during charge-discharge cycles that is less than that found in LiMn 2 O 4 (structure-stabilization). The strong octahedral framework eventually results in minimized contraction of the unit cell after repeated cycles and in good capacity retention. A less capacity fading of LiGd 0.02 Mn 2.98 O 4 can be correlated to a smaller dimensional variation between charged and discharged states (LiMn 2 O 4 : 8.1366 and 8.0460 Å (two phases, charged) and 8.2419 Å (discharged) vs. LiGd 0.02 Mn 2.98 O 4 : 8.1472 Å (single phase, charged) to 8.2375 Å (discharged)) and, thus, the less unit cell contraction for LiGd 0.02 Mn 2.98 O 4 after repeated cycling (LiMn 2 O 4 : 8.2419 Å to 8.218 Å vs. LiGd 0.02 Mn 2.98 O 4 : 8.2375 Å to 8.229 Å).
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Han et al. (2012) studied this question.
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