氢键供体对复合石墨烯电极/深共晶溶剂界面电化学性能的影响

A. T. Brandão, Renata Costa, A. F. Silva, C. Pereira
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引用次数: 2

摘要

性能更好的储能装置的开发依赖于创新材料和电解质的使用,旨在通过筛选低毒性电解质和无溶剂电极设计方案来减少碳足迹。利用高比表面积的纳米结构碳材料制备复合电极,被认为是提高储能装置功率和能量效率的一个有希望的起点。采用更环保、对环境影响更小的方法合成的非水电解质使深共晶溶剂(DES)成为电化学能量存储和转换应用的有前途的替代品。因此,本文提出了系统研究以二醇和酰胺为HBD(氢键供体:1,2-丙二醇和尿素)的DES的组成对石墨烯和石墨复合电极/DES电解质界面电化学性能的影响。选择玻碳(GC)作为裸电极材料衬底制备复合配方,因为它提供了电化学可复制的表面。测定了商用石墨烯和商用石墨/GC复合电极与氯化胆碱、1,2-丙二醇和尿素以1:2摩尔比络合为HBD接触时的重量电容。通过1、2和4 A g−1的充放电曲线来评估电化学稳定性。为了进行比较,我们用商用石墨进行了平行研究。当与1,2-丙二醇基DES接触时,用商业石墨烯(6.19 F g−1)取代商业石墨(1.70 F g−1)时,重量电容增加了4倍。当使用尿素基DES时,用商业石墨烯取代商业石墨时,重量电容没有显著变化。
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Hydrogen Bond Donors Influence on the Electrochemical Performance of Composite Graphene Electrodes/Deep Eutectic Solvents Interface
The development of energy storage devices with better performance relies on the use of innovative materials and electrolytes, aiming to reduce the carbon footprint through the screening of low toxicity electrolytes and solvent-free electrode design protocols. The application of nanostructured carbon materials with high specific surface area, to prepare composite electrodes, is being considered as a promising starting point towards improving the power and energy efficiency of energy storage devices. Non-aqueous electrolytes synthesized using greener approaches with lower environmental impact make deep eutectic solvents (DES) promising alternatives for electrochemical energy storage and conversion applications. Accordingly, this work proposes a systematic study on the effect of the composition of DES containing a diol and an amide as HBD (hydrogen bond donor: 1,2-propylene glycol and urea), on the electrochemical performance of graphene and graphite composite electrodes/DES electrolyte interface. Glassy carbon (GC) was selected as the bare electrode material substrate to prepare the composite formulations since it provides an electrochemically reproducible surface. Gravimetric capacitance was measured for commercial graphene and commercial graphite/GC composite electrodes in contact with choline chloride, complexed with 1,2-propylene glycol, and urea as the HBD in 1:2 molar ratio. The electrochemical stability was followed by assessing the charge/discharge curves at 1, 2, and 4 A g−1. For comparison purposes, a parallel study was performed using commercial graphite. A four-fold increase in gravimetric capacitance was obtained when replacing commercial graphite (1.70 F g−1) by commercial graphene (6.19 F g−1) in contact with 1,2-propylene glycol-based DES. When using urea based DES no significant change in gravimetric capacitance was observed when commercial graphite is replaced by commercial graphene.
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