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类球形正交LiMnO_2的制备、微结构和电化学性能 被引量:5

Preparation,Microstructure and Electrochemical Properties of Spherical-like Orthorhombic LiMnO_2
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摘要 以共沉淀法得到的类球形MnCO3为前驱物,制备了类球形正交LiMnO2(So-LiMnO2),采用XRD、SEM和N2吸附技术对样品进行表征;与非球形正交LiMnO2(No-LiMnO2)进行了对比研究。结果表明:o-LiMnO2的堆垛层错度、结晶状况、颗粒形貌和大小与前驱物的微结构密切相关;在80次电化学循环测试过程中,So-LiMnO2经15次循环可达最大的放电容量152mAh·g-1,其容量衰减平均每次循环0.58mAh·g-1;而No-LiMnO2要经过38次循环才能达到最大放电容量128mAh·g-1,容量衰减平均每次循环高达1.24mAh·g-1。TEM和EDS分析证明:由一次粒子团聚的类球形So-LiMnO2能有效地抑制电解液对材料的腐蚀、减少Mn的溶解,从而提高了电化学循环能力。 Spherical-like morphology orthorhombic LiMnO2 (So-LiMnO2) powders were prepared using spherical MnCO3 precursors obtained by a carbonate co-precipitation method. The materials were characterized using XRD, SEM and low temperature nitrogen adsorption desorption. Non-spherical orthorhombic LiMnO2 (No-LiMnO2) powders were also studied for comparison. The characteristics of o-LiMnO2 such as the stacking faults, crystallization, particles morphology and size were significantly dependent on the microstructure of precursors. The electrochemical performances of o-LiMnO2-based cathodes were tested during 80 cycles. The So-LiMnO2 cathode had a maximum capacity of 152 mAh·g^-1 on the 15th cycle, and exhibited an average capacity decay of approximately 0.58 mAh·g^-1 per cycle. By contrast, the No-LiMnO2 sample had a maximum capacity of 128 mAh·g^-1 on the 38th cycle, and experienced an average capacity decay of 1.24 mAh·g^-1 per cycle. TEM observation and EDS analysis confirmed that So-LiMnO2 particle, agglomerated by primary particles, could reduce the erosion of positive material by electrolytes and the dissolution of manganese, which results in the enhanced electrochemical cycleability.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2007年第6期963-968,共6页 Chinese Journal of Inorganic Chemistry
基金 国家自然科学基金项目(No.50372058)。
关键词 共沉淀法 正交LiMnO2 类球形颗粒 电化学循环能力 co-precipitation method orthorhombic LiMnO2 spherical-like particle electrochemical cycleability
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  • 1Whittingham M S.Chem.Rev.,2004,104:4271~4301
  • 2Guo Z P,Konstantinov K,Wang G X.J.Power Sources,2003,119~121:221~225
  • 3Sakurai T,Kimura T,Sugihara T.J.Power sources,2001,97~98:366~370
  • 4Robertson A D,Armstrong A R,Bruce P G.Chem.Mater,2001,13:2380~2386
  • 5Kim K S,Lee S W,Moon H S,et al.J.Power Sources,2004,129:319~323
  • 6Croguennec L,Deniard P,Brec R.J.Electrochem.Soc.,1997,144:3323~3330
  • 7Croguennec L,Deniard P,Brec R,et al.Solid State Ionics,1996,89:127~137
  • 8Cho J,Kim Y J,Kim T J,et al.J.Electrochem.Soc.2002,149(2):A 127~132
  • 9Cho J,Kim Y J,Kim T J,et al.Chem.Mater.,2001,13:18~20
  • 10Tu X Y,Lu G L,Zeng Y W.J.Mater.Sci.Technol.2006,22:1~3

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