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      Recent progress in high-voltage lithium ion batteries

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      Journal of Power Sources
      Elsevier BV

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          Nonaqueous liquid electrolytes for lithium-based rechargeable batteries.

          Kang Xu (2004)
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            Ionic liquids as electrolytes

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              High-energy cathode material for long-life and safe lithium batteries.

              Layered lithium nickel-rich oxides, Li[Ni(1-x)M(x)]O(2) (M=metal), have attracted significant interest as the cathode material for rechargeable lithium batteries owing to their high capacity, excellent rate capability and low cost. However, their low thermal-abuse tolerance and poor cycle life, especially at elevated temperature, prohibit their use in practical batteries. Here, we report on a concentration-gradient cathode material for rechargeable lithium batteries based on a layered lithium nickel cobalt manganese oxide. In this material, each particle has a central bulk that is rich in Ni and a Mn-rich outer layer with decreasing Ni concentration and increasing Mn and Co concentrations as the surface is approached. The former provides high capacity, whereas the latter improves the thermal stability. A half cell using our concentration-gradient cathode material achieved a high capacity of 209 mA h g(-1) and retained 96% of this capacity after 50 charge-discharge cycles under an aggressive test profile (55 degrees C between 3.0 and 4.4 V). Our concentration-gradient material also showed superior performance in thermal-abuse tests compared with the bulk composition Li[Ni(0.8)Co(0.1)Mn(0.1)]O(2) used as reference. These results suggest that our cathode material could enable production of batteries that meet the demanding performance and safety requirements of plug-in hybrid electric vehicles.
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                Author and article information

                Journal
                Journal of Power Sources
                Journal of Power Sources
                Elsevier BV
                03787753
                September 2013
                September 2013
                : 237
                :
                : 229-242
                Article
                10.1016/j.jpowsour.2013.03.024
                9803e380-4d41-4773-b382-98a3d6b342e0
                © 2013

                http://www.elsevier.com/tdm/userlicense/1.0/

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