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ACS Appl Mater Interfaces ; 12(9): 10211-10223, 2020 Mar 04.
Artigo em Inglês | MEDLINE | ID: mdl-32040296

RESUMO

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 H2SO4 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.

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