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Electrolytic-anion-redox adsorption pseudocapacitance in nanosized lithium-free transition metal oxides as cathode materials for Li-ion batteries

机译:纳米锂无锂过渡金属氧化物中的电解 - 阴离子氧化还原吸附假偶像作为锂离子电池的阴极材料

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摘要

Conventional batteries (except redox flow batteries) react by involving only their electrode redox centers, with electrolyte ions shuttled between the cathode and the anode. However, this chemistry causes large electronic and structural changes in the bulk of the electrode materials, leading to performance degradation. Herein, we report that electrolytic-anion-redox adsorption pseudocapacitance, relayed by lithium intercalation in lithium-free transition metal oxide electrodes, can be exploited to boost the total energy density of a battery. Focused on the study of Mn3O4, we show that this pseudocapacitance is processed by the reversible adsorption/desorption of PF6- on the surface of transition metal oxides, with charge transfer between Mn3O4 and PF6- through Mn-F bond while fluoride ions acting as redox centers. This new electrolytic-anion-redox chemistry provides greater design freedom for high-capacity energy storage devices since it only involves a specific electrode surface and the electrolyte anion, rather than specially crystallized compounds for bulk reactions.
机译:传统的电池(除氧化还原电池除外)通过仅涉及它们的电极氧化还原中心而反应,电解质离子在阴极和阳极之间穿梭。然而,这种化学导致大量电极材料的电子和结构变化,导致性能下降。这里,我们报告说,通过锂无锂过渡金属氧化物电极锂嵌入的电解阴离子氧化还原吸附假偶联能够利用来提高电池的总能量密度。专注于MN3O4的研究,我们表明,该假偶像划分是通过在过渡金属氧化物表面上的可逆吸附/解吸处理,在Mn3O4和PF6-通过Mn-F之间的电荷转移,而氟化物离子作用作为氧化还原中心。这种新的电解阴离子氧化还原化学为高容量能量存储装置提供了更大的设计自由,因为它只涉及特定的电极表面和电解质阴离子,而不是特殊结晶的本体反应的化合物。

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