Department of Colloid Chemistry, Max Planck Institute of Colloids and Interfaces, Am Mühlenberg 1, 14476, Potsdam, Germany.
ChemSusChem. 2020 Apr 7;13(7):1856-1863. doi: 10.1002/cssc.201903156. Epub 2020 Mar 5.
Although several recent publications describe cathodes for electrochemical energy storage materials made from regrown biomass in aqueous electrolytes, their transfer to lithium-organic batteries is challenging. To gain a deeper understanding, we investigate the influences on charge storage in model systems based on biomass-derived, redox-active compounds and comparable structures. Hybrid materials from these model polymers and porous carbon are compared to determine precisely the causes of exceptional capacity in lithium-organic systems. Besides redox activity, particularly, wettability influences capacity of the composites greatly. Furthermore, in addition to biomass-derived molecules with catechol functionalities, which are described commonly as redox-active species in lithium-bio-organic systems, we further describe guaiacol groups as a promising alternative for the first time and compare the performance of the respective compounds.
尽管最近有几篇出版物描述了在水溶液电解质中由再生物质制成的用于电化学储能材料的阴极,但将其转移到锂有机电池中具有挑战性。为了更深入地了解这一点,我们研究了基于生物质衍生的、具有氧化还原活性的化合物和类似结构的模型系统中对电荷存储的影响。比较了这些模型聚合物和多孔碳的混合材料,以准确确定在锂有机系统中异常容量的原因。除了氧化还原活性外,特别地,润湿性极大地影响复合材料的容量。此外,除了通常被描述为锂生物有机系统中具有氧化还原活性物质的具有儿茶酚官能团的生物质衍生分子之外,我们还首次进一步将愈创木酚基团描述为一种有前途的替代物,并比较了各自化合物的性能。