| Literature DB >> 30222306 |
Qiong Yang1, Peng-Fei Wang2,3, Jin-Zhi Guo1, Zi-Ming Chen1, Wei-Lin Pang1, Ke-Cheng Huang1, Yu-Guo Guo2,3, Xing-Long Wu1,4,5, Jing-Ping Zhang1.
Abstract
As a promising cathode material of sodium-ion battery, P2-type Na2/3Ni1/3Mn2/3O2 (NNMO) possesses a theoretically high capacity and working voltage to realize high energy storage density. However, it still suffers from poor cycling stability mainly incurred by the undesirable P2-O2 phase transition. Herein, the electrochemically active Fe3+ ions are introduced into the lattice of NNMO, forming Na2/3Ni1/3Mn2/3- xFe xO2 ( x = 0, 1/24, 1/12, 1/8, 1/6) to effectively stabilize the P2-type crystalline structure. In such Fe-substituted materials, both Ni2+/Ni4+ and Fe3+/Fe4+ couples take part in the redox reactions, and the P2-O2 phase transition is well restrained during cycling, as verified by ex situ X-ray diffraction. As a result, the optimized Na2/3Ni1/3Mn7/12Fe1/12O2 (1/12-NNMF) has a long-term cycling stability with the fading rate of 0.05% per cycle over 300 cycles at 5 C. Furthermore, the 1/12-NNMF delivers excellent rate capabilities (65 mA h g-1 at 25 C) and superior low-temperature performance (the capacity retention of 94% at -25 °C after 80 cycles) owing to the enhanced Na diffusion upon Fe doping, which is deduced by the studies of electrode kinetics. More significantly, the 1/12-NNMF also displays remarkable sodium-ion full-cell properties when merged with an LS-Sb@G anode, thus implying the possibility of their practical application.Entities:
Keywords: full cell; high-performance cathode; iron substitution; low-temperature performance; sodium-ion battery
Year: 2018 PMID: 30222306 DOI: 10.1021/acsami.8b12204
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229