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Isolation of Solid Solution Phases in Size‐Controlled LixFePO4 at Room Temperature
Authors:Genki Kobayashi  Shin‐ichi Nishimura  Min‐Sik Park  Ryoji Kanno  Masatomo Yashima  Takashi Ida  Atsuo Yamada
Affiliation:1. Department of Electronic Chemistry Interdisciplinary Graduate School of Science and Engineering Tokyo Institute of Technology 4259 Nagatsuta, Midori, Yokohama 226‐8502 (Japan);2. Department of Materials Science and Engineering Interdisciplinary Graduate School of Science and Engineering Tokyo Institute of Technology 4259 Nagatsuta, Midori, Yokohama 226‐8502 (Japan);3. Ceramics Research Laboratory Nagoya Institute of Technology Asahigaoka, Tajimi 507‐0071 (Japan)
Abstract:State‐of‐the‐art LiFePO4 technology has now opened the door for lithium ion batteries to take their place in large‐scale applications such as plug‐in hybrid vehicles. A high level of safety, significant cost reduction, and huge power generation are on the verge of being guaranteed for the most advanced energy storage system. The room‐temperature phase diagram is essential to understand the facile electrode reaction of LixFePO4 (0 < x < 1), but it has not been fully understood. Here, intermediate solid solution phases close to x = 0 and x = 1 have been isolated at room temperature. Size‐dependent modification of the phase diagram, as well as the systematic variation of lattice parameters inside the solid‐solution compositional domain closely related to the electrochemical redox potential, are demonstrated. These experimental results reveal that the excess capacity that has been observed above and below the two‐phase equilibrium potential is largely due to the bulk solid solution, and thus support the size‐dependent miscibility gap model.
Keywords:lithium‐ion batteries  phase diagrams  solid solution phases
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