锰
阴极
电化学
过渡金属
插层(化学)
碱金属
材料科学
无机化学
锂(药物)
钠离子电池
钠
空位缺陷
电池(电)
化学
离子
冶金
结晶学
电极
物理化学
物理
有机化学
热力学
功率(物理)
催化作用
内分泌学
法拉第效率
医学
生物化学
作者
Raphaële J. Clément,Peter G. Bruce,Clare P. Grey
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2015-01-01
卷期号:162 (14): A2589-A2604
被引量:427
摘要
Sodium transition metal oxides (NaMO2) with a P2 structure exhibit good Na+ ion conductivity and are promising sodium-ion battery cathode materials. Manganese-based compounds have a high working potential vs. Na+/Na, and high capacity. Yet, the layered nature of these materials means that they are prone to structural rearrangements at high voltage/low Na contents, the phase transformations and Na+ ion/vacancy ordering transitions resulting in capacity fade and poor reversibility. This review discusses the latest advances in the field and focuses mainly on recent work on NayMn1-xMxO2 (x, y ≤ 1, M = Ni, Mg, Li) compounds. We compare the different lithium and sodium transition metal layered oxides (P2, O3, etc.) and describe the structures and mechanisms observed on alkali (de)intercalation. The strategies used to enhance the electrochemical properties and stabilize the structural framework of sodium transition metal oxides are reviewed. We show how X-ray diffraction and 7Li/23Na solid-state Nuclear Magnetic Resonance can be combined to provide a detailed insight into the structural and electronic processes occurring upon electrochemical cycling of these materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI