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Understanding the Capacity Fading Mechanisms of O3‐Type Na[Ni 0.5 Mn 0.5 ]O 2 Cathode for Sodium‐Ion Batteries
Author(s) -
Yu TaeYeon,
Ryu HoonHee,
Han Geumjae,
Sun YangKook
Publication year - 2020
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.202001609
Subject(s) - materials science , cathode , capacity loss , electrochemistry , intercalation (chemistry) , electrolyte , ion , coprecipitation , structural stability , chemical engineering , inorganic chemistry , electrode , chemistry , organic chemistry , structural engineering , engineering
A spherical O3‐type Na[Ni 0.5 Mn 0.5 ]O 2 cathode, composed of compactly‐packed nanosized primary particles, is synthesized by the coprecipitation method to examine its capacity fading mechanism. The electrochemical performance cycled at different upper cut‐off voltages demonstrate that the P3′ to O3′ phase transition above 3.6 V is primarily responsible for the loss of the structural stability of the O3‐type Na[Ni 0.5 Mn 0.5 ]O 2 cathode. The capacity retention is greatly improved by avoiding the P3′ to O3′ phase transition, and 94.2% and 90.7% of the initial capacities (108.9 mAh g −1 at 3.35 V and 125.4 mAh g −1 at 3.58 V) are retained after 100 cycles. During cycling at 4.0 V, rapid capacity fading (75.5% of 147.5 mAh g −1 after 100 cycles) is observed. The poor Na + ion intercalation stability is directly attributed to the extent of microcracks caused by the abrupt change in the lattice structure. Microcracks traversing the entire secondary particle compromise the mechanical integrity of the cathode and accelerate electrolyte infiltration into the particle interior, causing the subsequent degradation of the exposed internal surfaces. Thus, suppressing microcracks in secondary particles is one of the key challenges for improving the cycling stability of hierarchical structured O3‐type Na[Ni 0.5 Mn 0.5 ]O 2 cathodes.