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作为有机阴极材料的π共轭氧化还原活性二维聚合物

π-Conjugated redox-active two-dimensional polymers as organic cathode materials.

作者信息

Jin Zexin, Cheng Qian, Evans Austin M, Gray Jesse, Zhang Ruiwen, Bao Si Tong, Wei Fengkai, Venkataraman Latha, Yang Yuan, Nuckolls Colin

机构信息

Department of Chemistry, Columbia University New York New York 10027 USA

Department of Applied Physics and Applied Mathematics, Columbia University New York New York 10027 USA

出版信息

Chem Sci. 2022 Mar 8;13(12):3533-3538. doi: 10.1039/d1sc07157b. eCollection 2022 Mar 24.

Abstract

Redox-active two-dimensional polymers (RA-2DPs) are promising lithium battery organic cathode materials due to their regular porosities and high chemical stabilities. However, weak electrical conductivities inherent to the non-conjugated molecular motifs used thus far limit device performance and the practical relevance of these materials. We herein address this problem by developing a modular approach to construct π-conjugated RA-2DPs with a new polycyclic aromatic redox-active building block PDI-DA. Efficient imine-condensation between PDI-DA and two polyfunctional amine nodes followed by quantitative alkyl chain removal produced RA-2DPs TAPPy-PDI and TAPB-PDI as conjugated, porous, polycrystalline networks. In-plane conjugation and permanent porosity endow these materials with high electrical conductivity and high ion diffusion rates. As such, both RA-2DPs function as organic cathode materials with good rate performance and excellent cycling stability. Importantly, the improved design enables higher areal mass-loadings than were previously available, which drives a practical demonstration of TAPPy-PDI as the power source for a series of LED lights. Collectively, this investigation discloses viable synthetic methodologies and design principles for the realization of high-performance organic cathode materials.

摘要

氧化还原活性二维聚合物(RA-2DPs)由于其规整的孔隙率和高化学稳定性,是很有前景的锂电池有机阴极材料。然而,迄今为止所使用的非共轭分子基序固有的弱导电性限制了这些材料的器件性能和实际应用价值。我们在此通过开发一种模块化方法来构建具有新型多环芳族氧化还原活性结构单元PDI-DA的π共轭RA-2DPs,解决了这一问题。PDI-DA与两个多官能胺节点之间的高效亚胺缩合,随后定量去除烷基链,生成了作为共轭、多孔、多晶网络的RA-2DPs TAPPy-PDI和TAPB-PDI。面内共轭和永久孔隙率赋予这些材料高电导率和高离子扩散速率。因此,两种RA-2DPs均作为具有良好倍率性能和优异循环稳定性的有机阴极材料发挥作用。重要的是,改进后的设计能够实现比以前更高的面质量负载,这推动了TAPPy-PDI作为一系列LED灯电源的实际演示。总的来说,这项研究揭示了实现高性能有机阴极材料的可行合成方法和设计原则。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a594/8943886/60170e8745be/d1sc07157b-f1.jpg

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