Institute of Energy and Climate Research (IEK-9), Forschungszentrum Jülich GmbH, 52425, Jülich, Germany.
Institute of Technical and Macromolecular Chemistry, RWTH Aachen University, 52056, Aachen, Germany.
Sci Rep. 2023 Jul 6;13(1):10934. doi: 10.1038/s41598-023-37308-5.
Organic radical batteries (ORBs) represent a viable pathway to a more sustainable energy storage technology compared to conventional Li-ion batteries. For further materials and cell development towards competitive energy and power densities, a deeper understanding of electron transport and conductivity in organic radical polymer cathodes is required. Such electron transport is characterised by electron hopping processes, which depend on the presence of closely spaced hopping sites. Using a combination of electrochemical, electron paramagnetic resonance (EPR) spectroscopic, and theoretical molecular dynamics as well as density functional theory modelling techniques, we explored how compositional characteristics of cross-linked poly(2,2,6,6-tetramethyl-1-piperidinyloxy-4-yl methacrylate) (PTMA) polymers govern electron hopping and rationalise their impact on ORB performance. Electrochemistry and EPR spectroscopy not only show a correlation between capacity and the total number of radicals in an ORB using a PTMA cathode, but also indicates that the state-of-health degrades about twice as fast if the amount of radical is reduced by 15%. The presence of up to 3% free monomer radicals did not improve fast charging capabilities. Pulsed EPR indicated that these radicals readily dissolve into the electrolyte but a direct effect on battery degradation could not be shown. However, a qualitative impact cannot be excluded either. The work further illustrates that nitroxide units have a high affinity to the carbon black conductive additive, indicating the possibility of its participation in electron hopping. At the same time, the polymers attempt to adopt a compact conformation to increase radical-radical contact. Hence, a kinetic competition exists, which might gradually be altered towards a thermodynamically more stable configuration by repeated cycling, yet further investigations are required for its characterisation.
有机自由基电池 (ORB) 代表了一种比传统锂离子电池更具可持续性的储能技术途径。为了进一步开发具有竞争力的能量和功率密度的材料和电池,需要更深入地了解有机自由基聚合物正极中的电子输运和电导率。这种电子输运的特点是电子跳跃过程,这取决于紧密间隔的跳跃位点的存在。我们使用电化学、电子顺磁共振 (EPR) 光谱、理论分子动力学以及密度泛函理论建模技术的组合,探索了交联聚(2,2,6,6-四甲基-1-哌啶氧基-4-基甲基丙烯酸酯)(PTMA)聚合物的组成特性如何控制电子跳跃并合理地解释其对 ORB 性能的影响。电化学和 EPR 光谱不仅表明使用 PTMA 阴极的 ORB 的容量与自由基总数之间存在相关性,而且还表明如果自由基的数量减少 15%,则健康状态的退化速度快两倍。存在高达 3%的游离单体自由基并没有提高快速充电能力。脉冲 EPR 表明这些自由基很容易溶解在电解质中,但不能显示其对电池退化的直接影响。然而,也不能排除定性影响。该工作进一步说明了硝酮单元与导电炭黑添加剂具有很高的亲和力,表明其可能参与电子跳跃。同时,聚合物试图采用紧凑构象来增加自由基-自由基接触。因此,存在动力学竞争,通过反复循环可能逐渐向热力学更稳定的构型转变,但需要进一步研究其特性。