Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/98134
Title: Quantum confinement-induced tunable exciton states in graphene oxide
Authors: Lee, Jaichan
Cole, Jacqueline M.
Lee, Dongwook
Seo, Jiwon
Zhu, Xi
Lee, Jiyoul
Shin, Hyeon-Jin
Shin, Taeh
Lee, Hangil
Su, Haibin
Issue Date: 2013
Source: Lee, D., Seo, J., Zhu, X., Lee, J., Shin, H. J., Cole, J. M., Shin, T., Lee, J., Lee, H.,& Su, H. (2013). Quantum confinement-induced tunable exciton states in graphene oxide. Scientific Reports, 3.
Series/Report no.: Scientific reports
Abstract: Graphene oxide has recently been considered to be a potential replacement for cadmium-based quantum dots due to its expected high fluorescence. Although previously reported, the origin of the luminescence in graphene oxide is still controversial. Here, we report the presence of core/valence excitons in graphene-based materials, a basic ingredient for optical devices, induced by quantum confinement. Electron confinement in the unreacted graphitic regions of graphene oxide was probed by high resolution X-ray absorption near edge structure spectroscopy and first-principles calculations. Using experiments and simulations, we were able to tune the core/valence exciton energy by manipulating the size of graphitic regions through the degree of oxidation. The binding energy of an exciton in highly oxidized graphene oxide is similar to that in organic electroluminescent materials. These results open the possibility of graphene oxide-based optoelectronic device technology.
URI: https://hdl.handle.net/10356/98134
http://hdl.handle.net/10220/13316
ISSN: 2045-2322
DOI: 10.1038/srep02250
Schools: School of Materials Science & Engineering 
Rights: © 2013 Nature Publishing Group. This is Open Access Journals.This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported license. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:MSE Journal Articles

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