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改性石墨毡在五种用于氧化还原液流电池的蒽醌衍生物溶液中的电催化活性

Electrocatalytic Activity of Modified Graphite Felt in Five Anthraquinone Derivative Solutions for Redox Flow Batteries.

作者信息

Gao Fanfan, Li Xinyu, Zhang Yue, Huang Chengde, Zhang Wen

机构信息

Department of Applied Chemistry, School of Chemical Engineering and Technology, and State Key Laboratory of Chemical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China.

出版信息

ACS Omega. 2019 Aug 19;4(9):13721-13732. doi: 10.1021/acsomega.9b01103. eCollection 2019 Aug 27.

Abstract

Redox flow batteries have received wide attention because of their unique advantages such as high efficiency, long cycle life, low operating cost, and independent adjustment of energy power. In this study, five types of anthraquinone derivative organic redox couple were selected, and the surfaces of graphite felt were modified. When the number of functional groups is increased or the substitution position is closer to the carbonyl (C=O) groups, a more pronounced hindrance for the C=O reaction on the benzene ring is observed; thus, the electrochemical performance and reversibility decreases. Sodium 9,10-anthraquinone-2-sulfonate solution is the best organic redox couple in terms of both reversibility and electrochemical performance. It was also found that all the surface treatment methods of graphite felt are beneficial for improving their electrochemical performances. All these superior results demonstrate that the graphite felt treated under air exposure at 550 °C for 3 h exhibited the best electrochemical performance, which might be attributed to the increase in the content of C-OH functional groups.

摘要

氧化还原液流电池因其具有高效率、长循环寿命、低运行成本以及能量功率可独立调节等独特优势而受到广泛关注。在本研究中,选取了五种蒽醌衍生物有机氧化还原对,并对石墨毡表面进行了改性。当官能团数量增加或取代位置更靠近羰基(C=O)基团时,观察到苯环上C=O反应的阻碍更为明显;因此,电化学性能和可逆性降低。就可逆性和电化学性能而言,9,10-蒽醌-2-磺酸钠溶液是最佳的有机氧化还原对。还发现石墨毡的所有表面处理方法都有利于提高其电化学性能。所有这些优异结果表明,在550℃空气暴露下处理3小时的石墨毡表现出最佳的电化学性能,这可能归因于C-OH官能团含量的增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8104/6714531/e04f6b62968a/ao9b01103_0001.jpg

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