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Great Enhancement of Carbon Energy Storage through Narrow Pores and Hydrogen-Containing Functional Groups for Aqueous Zn-Ion Hybrid Supercapacitor

机译:锌离子混合超级电容器的窄孔和含氢官能团大大提高了碳储能

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摘要

The proton transfer mechanism on the carbon cathode surface has been considered as an effective way to boost the electrochemical performance of Zn-ion hybrid supercapacitors (SCs) with both ionic liquid and organic electrolytes. However, cheaper, potentially safer, and more environmental friendly supercapacitor can be achieved by using aqueous electrolyte. Herein, we introduce the proton transfer mechanism into a Zn-ion hybrid supercapacitor with the ZnSO4 aqueous electrolyte and functionalized activated carbon cathode materials (FACs). We reveal both experimentally and theoretically an enhanced performance by controlling the micropores structure and hydrogen-containing functional groups (–OH and –NH functions) of the activated carbon materials. The Zn-ion SCs with FACs exhibit a high capacitance of 435 F g−1 and good stability with 89% capacity retention over 10,000 cycles. Moreover, the proton transfer effect can be further enhanced by introducing extra hydrogen ions in the electrolyte with low pH value. The highest capacitance of 544 F g−1 is obtained at pH = 3. The proton transfer process tends to take place preferentially on the hydroxyl-groups based on the density functional theory (DFT) calculation. The results would help to develop carbon materials for cheaper and safer Zn-ion hybrid SCs with higher energy.
机译:碳阴极表面上的质子转移机制已被认为是提高具有离子液体和有机电解质的Zn离子混合超级电容器(SCs)电化学性能的有效方法。但是,可以通过使用水性电解质来获得更便宜,可能更安全和更环保的超级电容器。在这里,我们将质子传递机制引入具有ZnSO4水溶液电解质和功能化活性炭阴极材料(FAC)的Zn离子混合超级电容器中。通过控制活性炭材料的微孔结构和含氢官能团(–OH和–NH功能),我们在实验和理论上均显示出增强的性能。具有FAC的Zn-ion SC电容具有435 F g -1 的高电容,并具有良好的稳定性,在10,000次循环中的容量保持率为89%。此外,通过在pH值低的电解液中导入多余的氢离子,可以进一步提高质子传递效果。在pH = 3时可获得544 F g -1 的最大电容。基于密度泛函理论(DFT)的计算,质子转移过程倾向于优先发生在羟基上。该结果将有助于开发碳材料,用于具有更高能量的更便宜,更安全的Zn离子混合SC。

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