4.8 Article

Synthesis and Electrochemical Properties of LiNi0.5Mn1.5O4 for Li-Ion Batteries by the Metal-Organic Framework Method

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 10, Issue 16, Pages 13625-13634

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.8b02553

Keywords

cathode material; LiNi05Mn15O4; crystal surface orientation; metal-organic framework; lithium-ion batteries

Funding

  1. National Science Foundation of China [51371198]
  2. Technology Project of Changsha [K1202039-11]

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A LiNi0.5Mn1.5O4 cathode material with high surface orientation was prepared via a complexing reaction coupled with the elevated-temperature solid-state method. First, a bimetal organic framework containing Ni2+ and Mn2+ ions was synthesized via a self assembly route using pyromellitic acid (PMA) as a dispersant and complexing agent. This step was followed by calcination with lithium acetate using PMA as a structure-directing agent. The resulting LiNi(0.5)Mni(1.5)O(4) (M-LNMO) cathode material was investigated using Xray diffraction, transmission and scanning electron microscopies, X-ray photoelectron spectroscopy, energy-dispersive X-ray spectroscopy, cyclic voltammetry, electrochemical impedance spectroscopy, and charge/discharge tests. For comparison, LiNia(5)Mn(1.5)O(4) samples were prepared by coprecipitation and the solid-phase method under the same conditions. M-LNMO was highly crystalline with low impurity, uniform grain size, and a preferred orientation in the (111) and (110) planes. Owing to these advantages, the M-LNMO cathode material exhibited overwhelmingly high cyclic stability and rate capability and M-LNMO delivered a capacity of 145 mAh g(-1) at a discharge rate of 0.1C and a discharge capacity retention of 86.6% at SC after 1000 cycles. Even at an extremely high discharge rate (10C), the specific capacity was 112.7 mAh g(-1), and 78.7% of its initial capacity was retained over 500 cycles. The superior electrochemical performance, particularly during a low-rate operation, was conferred by improved crystallinity and the crystal orientation of the particles.

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