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Aging mechanisms of lithium cathode materials

机译:锂正极材料的时效机理

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Batteries for stationary and automotive applications are required to provide extended cycle life and calendar life. Lithium-manganese oxides (LiMn_2O_4) with spinel structure and lithium-nickel-cobalt mixed oxides (LiNiCoO_2) with layered structures have been extensively studied in the last few years for usage in high energy and high power batteries in order to replace lithium-cobalt oxide (LiCoO_2) as cathode material in terms of cost, abundance and performance. In this paper, we summarize some basic mechanisms responsible for capacity fading under cycling and different storage conditions for both types of cathode materials. Lithium-nickel-cobalt mixed oxides show excellent storage stability in the discharged state and low metal solubility in the electrolyte. The cycling stability is mainly influenced by structural changes in the delithiated state and thermal instability arises from oxygen release at elevated temperatures in the charged state. Small amounts of aluminum and magnesium dopants stabilize the layered structure and increase cycling stability of lithium-nickel-cobalt oxide. Different mechanisms of capacity fading especially at higher temperatures are discussed for lithium-manganese oxide spinels. Capacity fading is highly dependent on cycling and storage conditions and caused by structural changes as well as by side reactions with electrolyte catalyzed by decomposition products of LiPF(, conducting salt and H_2O impurities in the electrolyte.
机译:需要固定和汽车应用电池来延长循环寿命和日历寿命。近年来,具有尖晶石结构的锂锰氧化物(LiMn_2O_4)和具有层状结构的锂镍钴复合氧化物(LiNiCoO_2)已在高能量和高功率电池中得到广泛应用,以替代锂钴氧化物(LiCoO_2)作为阴极材料的成本,丰度和性能。在本文中,我们总结了两种类型的正极材料在循环和不同存储条件下导致容量衰减的一些基本机理。锂-镍-钴混合氧化物在放电状态下显示出极好的存储稳定性,并且在电解质中的金属溶解度低。循环稳定性主要受脱锂状态的结构变化影响,并且热不稳定性是由于在充电状态下在高温下释放氧气而引起的。少量的铝和镁掺杂剂可稳定层状结构并增加锂镍钴氧化物的循环稳定性。对于锂锰氧化物尖晶石,讨论了容量衰减的不同机理,尤其是在高温下。容量衰减在很大程度上取决于循环和存储条件,并且由结构变化以及与LiPF(电解质中的导电盐和H_2O杂质的分解产物)催化的电解质副反应引起。

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