ABSTRACT
Graphene oxide (GO), a functional derivative of graphene, is a promising nanomaterial for a variety of optoelectronic applications as it exhibits fluorescence and maintains many of graphene's beneficial physical properties. although other graphene derivatives are chemically plausible and may serve to the benefit of the aforementioned applications, GO remains the one heavily used. the nature of optical behavior of other graphene derivatives has yet to be fully understood and studied. in this work we develop a variety of graphene derivatives and characterize their optical properties concomitantly suggesting a unified model for optical emission in graphene derivatives. in this process we examine the influence of different functional groups on the surface of graphene on its optoelectronic properties. mildly oxidized graphene (oxo-g1), nitrated graphene, arylated graphene, brominated graphene, and fluorinated graphene are obtained and characterized via TEM and EDX, FTIR and fluorescence spectroscopies with the latter indicating a potential band gap-derived fluorescence from each of the materials. this suggests that optical properties of graphene derivatives have minimal functional group dependence and are manifested by the localized environments within the flakes. this is confirmed by the hyperchem theoretical modeling of all aforementioned graphene derivatives indicating a similar electronic configuration for all, assessed by the pm3 semi-empirical approach. this work can further serve to describe and predict optical properties of similar graphene-based structures and promote graphene derivatives other than GO for utilization in research and industry.
ABSTRACT
With the advent of graphene, there has been an interest in utilizing this material and its derivative, graphene oxide (GO) for novel applications in nanodevices such as bio and gas sensors, solid-state supercapacitors and solar cells. Although GO exhibits lower conductivity and structural stability, it possesses an energy band gap that enables fluorescence emission in the visible/near infrared leading to a plethora of optoelectronic applications. In order to allow fine-tuning of its optical properties in the device geometry, new physical techniques are required that, unlike existing chemical approaches, yield substantial alteration of GO structure. Such a desired new technique is one that is electronically controlled and leads to reversible changes in GO optoelectronic properties. In this work, we for the first time investigate the methods to controllably alter the optical response of GO with the electric field and provide theoretical modeling of the electric field-induced changes. Field-dependent GO emission is studied in bulk GO/polyvinylpyrrolidone films with up to 6% reversible decrease under 1.6 V µm-1 electric fields. On an individual flake level, a more substantial over 50% quenching is achieved for select GO flakes in a polymeric matrix between interdigitated microelectrodes subject to two orders of magnitude higher fields. This effect is modeled on a single exciton level by utilizing Wentzel, Kremer, and Brillouin approximation for electron escape from the exciton potential well. In an aqueous suspension at low fields, GO flakes exhibit electrophoretic migration, indicating a degree of charge separation and a possibility of manipulating GO materials on a single-flake level to assemble electric field-controlled microelectronics. As a result of this work, we suggest the potential of varying the optical and electronic properties of GO via the electric field for the advancement and control over its optoelectronic device applications.