材料科学
聚酰亚胺
介孔材料
聚合物
烷基
阴极
共轭体系
傅里叶变换红外光谱
化学工程
纳米技术
多孔性
自组装
光谱学
红外光谱学
储能
高分子化学
化学稳定性
普鲁士蓝
介孔二氧化硅
热稳定性
分子工程
作者
Nihao Cai,Yu Zhou,Xiaohao Jia,Chengxiang Chen,Pan Yang,Bowen Zhao,Jinghao Huang,Han Yu,Haoming Luo,Peng Zhao,Fuwu Zhang,Chao Luo
出处
期刊:ACS Nano
[American Chemical Society]
日期:2026-08-03
标识
DOI:10.1021/acsnano.6c10110
摘要
Abstract The development of affordable and sustainable Na-ion batteries (NIBs) and K-ion batteries (KIBs) is critical for grid-scale energy storage owing to the low cost and natural abundance of sodium and potassium resources. However, state-of-the-art cathode materials exhibit limitations in terms of cycling stability, power density, and performance under extreme-temperature conditions. To address these challenges, we developed three-dimensional mesoporous polyimides with engineered flexible alkyl chains and rigid conjugated structures to manipulate cross-linked structures and porosity in the polyimides for high structural stability and fast reaction kinetics in NIBs and KIBs. The mesoporous polyimide cathode delivers a high specific capacity of 152.7 mAh g–1 at 500 mA g–1 at 80 °C, fast-charging capability at up to 5 A g–1, and a long cycle life of 10,000 cycles at 1 A g–1 in NIBs, representing one of the most durable organic cathodes to date. The superior performances are extended to KIBs and low-temperature NIBs at −40 °C, demonstrating great promise for practical applications. To gain insight into the mechanism behind the performance, Fourier transform infrared spectroscopy (FTIR), electron paramagnetic resonance (EPR), and solid-state nuclear magnetic resonance (NMR) spectroscopy were leveraged to confirm reversible redox reaction, free-radical intermediate formation, and high structural stability of mesoporous polyimide cathodes, providing guidance for rational structure design of redox-active polymers for fast-charging and wide-temperature-range batteries.
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