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      Graphene-contact electrically driven microdisk lasers

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          Abstract

          Active nanophotonic devices are attractive due to their low-power consumption, ultrafast modulation speed and high-density integration. Although electrical operation is required for practical implementation of these devices, it is not straightforward to introduce a proper current path into such a wavelength-scale nanostructure without affecting the optical properties. For example, to demonstrate electrically driven nanolasers, complicated fabrication techniques have been used thus far. Here we report an electrically driven microdisk laser using a transparent graphene electrode. Current is injected efficiently through the graphene sheet covering the top surface of the microdisk cavity, and, for the first time, lasing operation was achieved with a low-threshold current of ~300 μA at room temperature. In addition, we measured significant electroluminescence from a graphene-contact subwavelength-scale single nanopillar structure. This work represents a new paradigm for the practical applications of integrated photonic systems, by conformally mounting graphene on the complex surfaces of non-planar three-dimensional nanostructures.

          Abstract

          Microdisk lasers are useful for compact wavelength-scale photonic devices and circuits, but their operation by electrical injection can hamper their optical properties. Kim et al. show that a graphene-contact electrode provides efficient electrical injection while minimising optical losses.

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          Most cited references15

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          Single-nanowire electrically driven lasers.

          Electrically driven semiconductor lasers are used in technologies ranging from telecommunications and information storage to medical diagnostics and therapeutics. The success of this class of lasers is due in part to well-developed planar semiconductor growth and processing, which enables reproducible fabrication of integrated, electrically driven devices. Yet this approach to device fabrication is also costly and difficult to integrate directly with other technologies such as silicon microelectronics. To overcome these issues for future applications, there has been considerable interest in using organic molecules, polymers, and inorganic nanostructures for lasers, because these materials can be fashioned into devices by chemical processing. Indeed, amplified stimulated emission and lasing have been reported for optically pumped organic systems and, more recently, inorganic nanocrystals and nanowires. However, electrically driven lasing, which is required in most applications, has met with several difficulties in organic systems, and has not been addressed for assembled nanocrystals or nanowires. Here we investigate the feasibility of achieving electrically driven lasing from individual nanowires. Optical and electrical measurements made on single-crystal cadmium sulphide nanowires show that these structures can function as Fabry-Perot optical cavities with mode spacing inversely related to the nanowire length. Investigations of optical and electrical pumping further indicate a threshold for lasing as characterized by optical modes with instrument-limited linewidths. Electrically driven nanowire lasers, which might be assembled in arrays capable of emitting a wide range of colours, could improve existing applications and suggest new opportunities.
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            Graphene thickness determination using reflection and contrast spectroscopy.

            We have clearly discriminated the single-, bilayer-, and multiple-layer graphene (<10 layers) on Si substrate with a 285 nm SiO2 capping layer by using contrast spectra, which were generated from the reflection light of a white light source. Calculations based on Fresnel's law are in excellent agreement with the experimental results (deviation 2%). The contrast image shows the reliability and efficiency of this new technique. The contrast spectrum is a fast, nondestructive, easy to be carried out, and unambiguous way to identify the numbers of layers of graphene sheet. We provide two easy-to-use methods to determine the number of graphene layers based on contrast spectra: a graphic method and an analytical method. We also show that the refractive index of graphene is different from that of graphite. The results are compared with those obtained using Raman spectroscopy.
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              Organic light-emitting diodes on solution-processed graphene transparent electrodes.

              Theoretical estimates indicate that graphene thin films can be used as transparent electrodes for thin-film devices such as solar cells and organic light-emitting diodes, with an unmatched combination of sheet resistance and transparency. We demonstrate organic light-emitting diodes with solution-processed graphene thin film transparent conductive anodes. The graphene electrodes were deposited on quartz substrates by spin-coating of an aqueous dispersion of functionalized graphene, followed by a vacuum anneal step to reduce the sheet resistance. Small molecular weight organic materials and a metal cathode were directly deposited on the graphene anodes, resulting in devices with a performance comparable to control devices on indium-tin-oxide transparent anodes. The outcoupling efficiency of devices on graphene and indium-tin-oxide is nearly identical, in agreement with model predictions.
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                Author and article information

                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Pub. Group
                2041-1723
                09 October 2012
                : 3
                : 1123
                Affiliations
                [1 ]Department of Physics, Korea University , Seoul 136-701, Republic of Korea.
                [2 ]Department of Physics, Chung-Ang University , Seoul 156-756, Republic of Korea.
                [3 ]Division of Materials Science and Engineering, Hanyang University , Seoul 133-791, Republic of Korea.
                [4 ]These authors contributed equally to this work.
                Author notes
                Article
                ncomms2137
                10.1038/ncomms2137
                3493654
                23047681
                86ee6f89-c070-4e31-937b-43b2829674a0
                Copyright © 2012, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.

                This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/

                History
                : 20 August 2012
                : 17 September 2012
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