电解质
化学
分子
溶解
接受者
阴极
锌
氢键
扩散
金属
离子
无机化学
物理化学
电极
有机化学
物理
热力学
凝聚态物理
作者
Ziyang Song,Ling Miao,Yaokang Lv,Lihua Gan,Mingxian Liu
出处
期刊:Angewandte Chemie
[Wiley]
日期:2023-07-29
卷期号:62 (38): e202309446-e202309446
被引量:91
标识
DOI:10.1002/anie.202309446
摘要
Abstract Organic small molecules as high‐capacity cathodes for Zn‐organic batteries have inspired numerous interests, but are trapped by their easy‐dissolution in electrolytes. Here we knit ultrastable lock‐and‐key hydrogen‐bonding networks between 2, 7‐dinitropyrene‐4, 5, 9, 10‐tetraone (DNPT) and NH 4 + charge carrier. DNPT with octuple‐active carbonyl/nitro centers (H‐bond acceptor) are redox‐exclusively accessible for flexible tetrahedral NH 4 + ions (H‐bond donator) but exclude larger and rigid Zn 2+ , due to a lower activation energy (0.14 vs . 0.31 eV). NH 4 + coordinated H‐bonding chemistry conquers the stability barrier of DNPT in electrolyte, and gives fast diffusion kinetics of non‐metallic charge carrier. A stable two‐step 4e − NH 4 + coordination with DNPT cathode harvests a high capacity (320 mAh g −1 ), a high‐rate capability (50 A g −1 ) and an ultralong life (60,000 cycles). This finding points to a new paradigm for H‐bond stabilized organic small molecules to design advanced zinc batteries.
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