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High-capacity electrode materials for rechargeable lithium batteries: Li 3 NbO 4 -based system with cation-disordered rocksalt structure

锂(药物) 材料科学 自然键轨道 氧化物 氧化还原 氧化锂 氧烷 离子 电极 吸收(声学) 化学 化学物理 电化学 光谱学 密度泛函理论 磷酸钒锂电池 物理化学 计算化学 冶金 物理 有机化学 内分泌学 复合材料 医学 量子力学
作者
Naoaki Yabuuchi,Mitsue Takeuchi,Masanobu Nakayama,Hiromasa Shiiba,Masahiro Ogawa,Keisuke Nakayama,Toshiaki Ohta,Daisuke Endo,Tetsuya Ozaki,Tokuo Inamasu,Kei Sato,Shinichi Komaba
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:112 (25): 7650-7655 被引量:480
标识
DOI:10.1073/pnas.1504901112
摘要

Rechargeable lithium batteries have rapidly risen to prominence as fundamental devices for green and sustainable energy development. Lithium batteries are now used as power sources for electric vehicles. However, materials innovations are still needed to satisfy the growing demand for increasing energy density of lithium batteries. In the past decade, lithium-excess compounds, Li2MeO3 (Me = Mn(4+), Ru(4+), etc.), have been extensively studied as high-capacity positive electrode materials. Although the origin as the high reversible capacity has been a debatable subject for a long time, recently it has been confirmed that charge compensation is partly achieved by solid-state redox of nonmetal anions (i.e., oxide ions), coupled with solid-state redox of transition metals, which is the basic theory used for classic lithium insertion materials, such as LiMeO2 (Me = Co(3+), Ni(3+), etc.). Herein, as a compound with further excess lithium contents, a cation-ordered rocksalt phase with lithium and pentavalent niobium ions, Li3NbO4, is first examined as the host structure of a new series of high-capacity positive electrode materials for rechargeable lithium batteries. Approximately 300 mAh ⋅ g(-1) of high-reversible capacity at 50 °C is experimentally observed, which partly originates from charge compensation by solid-state redox of oxide ions. It is proposed that such a charge compensation process by oxide ions is effectively stabilized by the presence of electrochemically inactive niobium ions. These results will contribute to the development of a new class of high-capacity electrode materials, potentially with further lithium enrichment (and fewer transition metals) in the close-packed framework structure with oxide ions.
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