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紫精晶体作为锂电池阴极的电荷存储机制及结构演变

Charge Storage Mechanism and Structural Evolution of Viologen Crystals as the Cathode of Lithium Batteries.

作者信息

Ma Ting, Liu Luojia, Wang Jiaqi, Lu Yong, Chen Jun

机构信息

Key Laboratory of Advanced Energy Materials, Chemistry (Ministry of Education), Renewable Energy Conversion and Storage Center (RECAST), College of Chemistry, Nankai University, Tianjin, 300071, China.

出版信息

Angew Chem Int Ed Engl. 2020 Jul 6;59(28):11533-11539. doi: 10.1002/anie.202002773. Epub 2020 May 11.

Abstract

Although organic ionic crystals represent an attractive class of active materials for rechargeable batteries owing to their high capacity and low solubility in electrolytes, they generally suffer from limited electronic conductivity and moderate voltage. Furthermore, the charge storage mechanism and structural evolution during the redox processes are still not clearly understood. Here we describe ethyl viologen iodide (EVI ) and ethyl viologen diperchlorate (EV(ClO ) ) as cathode materials of lithium batteries which crystallize in a monoclinic system with alternating organic EV layers and inorganic I /ClO layers. The EVI electrode exhibits a high initial discharge plateau of 3.7 V (vs. Li /Li) because of its anion storage ability. When I is replaced by ClO , the obtained EV(ClO ) electrode displays excellent rate performance with a theoretical capacity of 78 % even at 5 C owing to the good electron conductivity of ClO layers. EVI and EV(ClO ) also show excellent cycling stability (capacity retention >96 % after 200 cycles).

摘要

尽管有机离子晶体由于其高容量和在电解质中的低溶解度,是一类用于可充电电池的有吸引力的活性材料,但它们通常存在电子电导率有限和电压适中的问题。此外,氧化还原过程中的电荷存储机制和结构演变仍不清楚。在这里,我们描述了碘化乙基紫精(EVI)和高氯酸二乙酯基紫精(EV(ClO₄)₂)作为锂电池的阴极材料,它们在单斜晶系中结晶,具有交替的有机EV层和无机I⁻/ClO₄⁻层。由于其阴离子存储能力,EVI电极表现出3.7 V(相对于Li⁺/Li)的高初始放电平台。当I⁻被ClO₄⁻取代时,由于ClO₄⁻层良好的电子导电性,所得到的EV(ClO₄)₂电极即使在5 C时也具有78 %的理论容量,表现出优异的倍率性能。EVI和EV(ClO₄)₂还表现出优异的循环稳定性(200次循环后容量保持率>96 %)。

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