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调整有机氮化合物的化学性质以促进全有机阴离子可充电电池的发展。

Tuning the Chemistry of Organonitrogen Compounds for Promoting All-Organic Anionic Rechargeable Batteries.

作者信息

Jouhara Alia, Quarez Eric, Dolhem Franck, Armand Michel, Dupré Nicolas, Poizot Philippe

机构信息

Institut des Matériaux Jean Rouxel (IMN), UMR CNRS 6502, Université de Nantes, 2 rue de la Houssinière, B.P. 32229, 44322, Nantes Cedex 3, France.

Laboratoire de Glycochimie, des Antimicrobiens et des Agroressources (LG2A), UMR CNRS 7378, Université de Picardie Jules Verne, 33 rue Saint-Leu, 80039, Amiens Cedex, France.

出版信息

Angew Chem Int Ed Engl. 2019 Oct 28;58(44):15680-15684. doi: 10.1002/anie.201908475. Epub 2019 Sep 18.

DOI:10.1002/anie.201908475
PMID:31429162
Abstract

The ever-increasing demand for rechargeable batteries induces significant pressure on the worldwide metal supply, depleting resources and increasing costs and environmental concerns. In this context, developing the chemistry of anion-inserting electrode organic materials could promote the fabrication of molecular (metal-free) rechargeable batteries. However, few examples have been reported because little effort has been made to develop such anionic-ion batteries. Here we show the design of two anionic host electrode materials based on the N-substituted salts of azaaromatics (zwitterions). A combination of NMR, EDS, FTIR spectroscopies coupled with thermal analyses and single-crystal XRD allowed a thorough structural and chemical characterization of the compounds. Thanks to a reversible electrochemical activity located at an average potential of 2.2 V vs. Li /Li, the coupling with dilithium 2,5-(dianilino)terephthalate (Li DAnT) as the positive electrode enabled the fabrication of the first all-organic anionic rechargeable batteries based on crystallized host electrode materials capable of delivering a specific capacity of ≈27 mAh/g with a stable cycling over dozens of cycles (≈24 Wh/kg ).

摘要

对可充电电池不断增长的需求给全球金属供应带来了巨大压力,导致资源枯竭、成本上升以及环境问题。在这种背景下,开发阴离子插入电极有机材料的化学性质可促进分子(无金属)可充电电池的制造。然而,由于在开发此类阴离子电池方面投入的精力较少,鲜有相关实例报道。在此,我们展示了基于氮杂芳烃(两性离子)的N-取代盐设计的两种阴离子主体电极材料。核磁共振(NMR)、能谱分析(EDS)、傅里叶变换红外光谱(FTIR)结合热分析和单晶X射线衍射(XRD)对这些化合物进行了全面的结构和化学表征。由于在相对于Li/Li平均电位为2.2 V处具有可逆的电化学活性,与作为正极的2,5-(二苯胺基)对苯二甲酸二锂(Li DAnT)耦合,使得基于结晶主体电极材料制造出了首个全有机阴离子可充电电池,该电池能够提供约27 mAh/g的比容量,并在几十次循环中实现稳定循环(≈24 Wh/kg)。

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