噻吩
电池(电)
电化学
材料科学
电解质
电极
电压
有机自由基电池
离子
对偶(语法数字)
光电子学
化学工程
电气工程
化学
有机化学
功率(物理)
热力学
物理化学
物理
艺术
文学类
工程类
作者
R. Russo,Jean‐Noël Chotard,Grégory Gachot,Christine Frayret,Gwenaëlle Toussaint,Philippe Stevens,Matthieu Bécuwe
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-10-11
卷期号:8 (11): 4597-4607
被引量:6
标识
DOI:10.1021/acsenergylett.3c01456
摘要
Dual-ion organic batteries are attracting much more attention because of the need to replace critical materials (Ni, Co, and V). Because of its particular mechanism, this battery technology has several advantages but is still limited in terms of output voltage and energy density. Here we present the evaluation of p-type positive molecular materials based on thianthrene and their use to build a high-performance, all-organic battery. Thanks to a substitution in the 2,7-position with a donating or withdrawing group, electrochemical properties and material stability were tuned to maximize storage performances. In addition, through a series of post-mortem analyses coupled with electrolyte engineering, the electrochemical properties of thianthrene-based electrodes in half-cells were optimized. The best electrodes were then coupled to a negative electrode material (dilithium naphthalene dicarboxylate, Li2-NDC), to build the first all-organic dual-ion battery with an output voltage of 3.4 V and an outstanding energy density of 78–105 Wh kg–1 based on the electrode mass (49–66.5 Wh kg–1 by also considering the anion counterpart) after 100 cycles, one of the highest values reported in the literature.
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