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双氧化还原离子蒽醌偶联乙基紫精复合材料实现锂有机电池的可逆多电子氧化还原化学。

Biredox-Ionic Anthraquinone-Coupled Ethylviologen Composite Enables Reversible Multielectron Redox Chemistry for Li-Organic Batteries.

作者信息

Wang Zhongju, Fan Qianqian, Guo Wei, Yang Changchun, Fu Yongzhu

机构信息

College of Chemistry, Zhengzhou University, Zhengzhou, 450001, P. R. China.

出版信息

Adv Sci (Weinh). 2022 Jan;9(1):e2103632. doi: 10.1002/advs.202103632. Epub 2021 Oct 29.

Abstract

Organic compounds bearing redox-active ionic pairs as electrode materials for high-performance rechargeable batteries have gained growing attention owing to the properties of synthetic tunability, high theoretical capacity, and low solubility. Herein, an innovative biredox-ionic composite, i.e., ethylviologen dianthraquinone-2-sulfonate (EV-AQ ), affording multiple and reversible active sites as a cathode material in lithium-organic batteries is reported. EV-AQ exhibits a high initial capacity of 199.2 mAh g at 0.1 C rate, which corresponds to the transfer of two electrons from one redox couple EV /EV and four electrons from two redox-active AQ anions. It is notable that EV-AQ shows remarkably improved cyclability compared to the precursors. The capacity retention is 89% and the Coulombic efficiency approaches 100% over 120 cycles at 0.5 C rate. The results offer evidence that AQ into the EV scaffold with multiple redox sites are promising in developing high-energy-density organic rechargeable batteries.

摘要

由于具有合成可调性、高理论容量和低溶解度等特性,带有氧化还原活性离子对的有机化合物作为高性能可充电电池的电极材料受到了越来越多的关注。在此,报道了一种创新的双氧化还原离子复合材料,即乙基紫精二蒽醌 -2- 磺酸盐(EV-AQ),它作为锂有机电池的阴极材料提供多个可逆活性位点。EV-AQ在0.1 C倍率下表现出199.2 mAh g的高初始容量,这对应于一个氧化还原对EV²⁺/EV的两个电子转移以及两个氧化还原活性AQ阴离子的四个电子转移。值得注意的是,与前体相比,EV-AQ的循环稳定性有显著提高。在0.5 C倍率下经过120次循环后,容量保持率为89%,库仑效率接近100%。这些结果表明,将具有多个氧化还原位点的AQ引入EV支架在开发高能量密度有机可充电电池方面具有潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a16/8728824/fa3c0408f84e/ADVS-9-2103632-g006.jpg

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