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通过溶液处理实现碳电极的大容量增强以用于高密度储能

Large Capacity Enhancement of Carbon Electrodes by Solution Processing for High Density Energy Storage.

作者信息

Farquhar Anna K, Smith Scott R, Dyck Colin Van, McCreery Richard L

机构信息

Department of Chemistry, University of Alberta, 11227 Saskatchewan Drive, Edmonton, Alberta T6G 2G2, Canada.

Department of Physics, University of Mons, 20, place du Parc, 7000 Mons, Belgium.

出版信息

ACS Appl Mater Interfaces. 2020 Mar 4;12(9):10211-10223. doi: 10.1021/acsami.9b17420. Epub 2020 Feb 20.

Abstract

An inexpensive, solution phase modification of flat carbon electrodes by electrochemical reactions of a 1,8-diaminonaphthalene derivative results in a 120- to 700-fold increase in capacity by formation of a 15-22 nm thick organic film. Modification of high surface area carbon electrodes with the same protocol resulted in a 12- to 82-fold increase in capacity. The modification layer contains 9-15% nitrogen present as -NH- redox centers that result in a large Faradaic component involving one H ion for each electron. The electrodes showed no capacity loss after prolonged cycling in 0.1 M HSO and exhibited significantly higher charge density than similar reported electrodes based on graphene and polyaniline. Investigation of the deposition conditions revealed that N-doped oligomeric ribbons are formed both by diazonium ion reduction and diaminonaphthalene oxidation, and the 1,8 isomer is essential for the large capacity increases. The capacity increase has at least three contributions: increased microscopic surface area from ribbon formation, Faradaic reactions of nitrogen-containing redox centers, and changes in ribbon conductivity resulting from polaron formation. An aqueous fabrication process was developed which both increased capacity and improved stability and was amenable to industrial production. The high charge density, low-cost fabrication, and <25 nm thickness of the diaminonaphthalene-derived films should prove attractive toward practical application on both flat surfaces and in high surface area carbon electrodes.

摘要

通过1,8 - 二氨基萘衍生物的电化学反应对扁平碳电极进行廉价的溶液相修饰,通过形成15 - 22纳米厚的有机膜,使容量增加了120至700倍。用相同方法对高比表面积碳电极进行修饰,容量增加了12至82倍。修饰层含有9 - 15%的氮,以 -NH- 氧化还原中心的形式存在,这导致了一个大的法拉第分量,每个电子涉及一个氢离子。在0.1 M HSO中长时间循环后,电极没有容量损失,并且比基于石墨烯和聚苯胺的类似报道电极表现出显著更高的电荷密度。对沉积条件的研究表明,N掺杂的低聚带是通过重氮离子还原和二氨基萘氧化形成的,并且1,8异构体对于大容量增加至关重要。容量增加至少有三个贡献:带形成增加了微观表面积、含氮氧化还原中心的法拉第反应以及极化子形成导致的带导电性变化。开发了一种水性制造工艺,该工艺既增加了容量又提高了稳定性,并且适合工业生产。二氨基萘衍生膜的高电荷密度、低成本制造以及<25纳米的厚度应该对在平面表面和高比表面积碳电极上的实际应用具有吸引力。

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