| Literature DB >> 27801566 |
Wenpei Kang1, Denis Y W Yu, Pui-Kit Lee, Zhenyu Zhang, Haidong Bian, Wenyue Li, Tsz-Wai Ng, Wenjun Zhang, Chun-Sing Lee.
Abstract
Cu-Ni-Mn-based ternary P2-type NaxCu0.15Ni0.20Mn0.65O2 (x = 0.50, 0.67, and 0.75) cathodes for sodium-ion batteries (SIBs) are synthesized by a co-precipitation method. We find that Na content plays a key role on the structure, morphology, and the charge-discharge performances of these materials. For x = 0.67 and 0.75, superstructure from Na+-vacancy ordering is observed, while it is absent in the x = 0.50 sample. Despite the same synthesis conditions, materials with x = 0.67 and 0.75 show smaller particle sizes compared to that of the x = 0.50 sample. In addition, redox potentials of the materials differ significantly even though they have the same transition metal ratios. These differences are attributed to the changes in local structures of the as-prepared materials arising from the different amount of Na and possibly oxygen in the lattice. Materials with x = 0.67 and 0.75 show excellent rate performance and cycle stability when tested as cathode material of SIBs. Average discharge potential is as high as 3.41 V versus Na-Na+ with capacity of 87 mAh g-1 at 20 mA g-1. Excellent capacity and cycle stability are maintained even when they are tested with higher current rates. For instance, a capacity of 62.3 mAh g-1 is obtained from the x = 0.67 sample at 1000 mA g-1 after 1000 cycles between 3.0 and 4.2 V without any decrease in capacity.Entities:
Keywords: P2-type; cathode; high power; long life; sodium-ion battery
Year: 2016 PMID: 27801566 DOI: 10.1021/acsami.6b10841
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229