Single-Crystalline, Semiconductive Layered Organic Cathode Powers High-Energy All-Solid-State Batteries

IF 11.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Central Science Pub Date : 2026-05-27 Epub Date: 2026-05-06 DOI:10.1021/acscentsci.6c00267
Junyong Mo, , , Jiande Wang, , and , Mircea Dincă*, 
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引用次数: 0

Abstract

All-solid-state batteries (ASSBs) offer a pathway to improved safety and increased energy density but remain limited by sluggish ion transport and low active material loading in composite cathodes. Organic cathode materials provide a sustainable alternative to metal-based systems, yet their implementation in solid-state architectures is constrained by poor electronic conductivity and inefficient electrode microstructures. Here, we integrate a high-capacity, semiconductive, single-crystalline layered organic cathode into ASSBs and demonstrate an electrochemical performance comparable to that of conventional systems. Systematic optimization of cathode composition identifies a configuration that delivers a specific capacity of 310 mAh g–1 at 25 mA g–1 with stable cycling over 100 cycles at room temperature under moderate pressure. At this rate, the architecture achieves an active-material-level energy density of 638 Wh kg–1. Performance limitations are mitigated through compositing with single-walled carbon nanotubes and operation at an elevated temperature. Electrochemical impedance spectroscopy indicates simplified interfacial behavior and suppressed side reactions relative to conventional solid-state cathodes, while in situ measurements reveal volcano-shaped lithium-ion diffusion behavior arising from the interplay between structural evolution and site occupancy. These results define design constraints for organic solid-state cathodes and establish their viability as functional components in next-generation solid-state energy storage.

单晶半导电层状有机阴极为高能全固态电池提供动力
全固态电池(assb)提供了改善安全性和提高能量密度的途径,但仍然受到离子传输缓慢和复合阴极中活性材料负载低的限制。有机阴极材料为金属基系统提供了可持续的替代方案,但其在固态结构中的实施受到电子导电性差和电极微结构效率低下的限制。在这里,我们将高容量,半导体,单晶层状有机阴极集成到assb中,并展示了与传统系统相当的电化学性能。系统优化阴极成分确定了一种配置,该配置在25 mA g-1时提供310 mAh g-1的比容量,在室温和中等压力下稳定循环超过100次。在这个速率下,该架构实现了638 Wh kg-1的活性材料级能量密度。通过单壁碳纳米管复合和在高温下操作,可以减轻性能限制。电化学阻抗谱表明,相对于传统的固态阴极,其界面行为简化,副反应抑制,而原位测量显示,结构演化和位置占用之间的相互作用产生了火山状锂离子扩散行为。这些结果定义了有机固态阴极的设计约束,并确立了其作为下一代固态储能功能组件的可行性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Central Science
ACS Central Science Chemical Engineering-General Chemical Engineering
CiteScore
25.50
自引率
0.50%
发文量
194
审稿时长
10 weeks
期刊介绍: ACS Central Science publishes significant primary reports on research in chemistry and allied fields where chemical approaches are pivotal. As the first fully open-access journal by the American Chemical Society, it covers compelling and important contributions to the broad chemistry and scientific community. "Central science," a term popularized nearly 40 years ago, emphasizes chemistry's central role in connecting physical and life sciences, and fundamental sciences with applied disciplines like medicine and engineering. The journal focuses on exceptional quality articles, addressing advances in fundamental chemistry and interdisciplinary research.
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