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      Utilization of native oxygen in Eu(RE)-doped GaN for enabling device compatibility in optoelectronic applications

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          Abstract

          The detrimental influence of oxygen on the performance and reliability of V/III nitride based devices is well known. However, the influence of oxygen on the nature of the incorporation of other co-dopants, such as rare earth ions, has been largely overlooked in GaN. Here, we report the first comprehensive study of the critical role that oxygen has on Eu in GaN, as well as atomic scale observation of diffusion and local concentration of both atoms in the crystal lattice. We find that oxygen plays an integral role in the location, stability, and local defect structure around the Eu ions that were doped into the GaN host. Although the availability of oxygen is essential for these properties, it renders the material incompatible with GaN-based devices. However, the utilization of the normally occurring oxygen in GaN is promoted through structural manipulation, reducing its concentration by 2 orders of magnitude, while maintaining both the material quality and the favorable optical properties of the Eu ions. These findings open the way for full integration of RE dopants for optoelectronic functionalities in the existing GaN platform.

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          Surface-plasmon-enhanced light emitters based on InGaN quantum wells.

          Since 1993, InGaN light-emitting diodes (LEDs) have been improved and commercialized, but these devices have not fulfilled their original promise as solid-state replacements for light bulbs as their light-emission efficiencies have been limited. Here we describe a method to enhance this efficiency through the energy transfer between quantum wells (QWs) and surface plasmons (SPs). SPs can increase the density of states and the spontaneous emission rate in the semiconductor, and lead to the enhancement of light emission by SP-QW coupling. Large enhancements of the internal quantum efficiencies (eta(int)) were measured when silver or aluminium layers were deposited 10 nm above an InGaN light-emitting layer, whereas no such enhancements were obtained from gold-coated samples. Our results indicate that the use of SPs would lead to a new class of very bright LEDs, and highly efficient solid-state light sources.
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            Narrow-band red-emitting Sr[LiAl3N4]:Eu2+ as a next-generation LED-phosphor material

            To facilitate the next generation of high-power white-light-emitting diodes (white LEDs), the discovery of more efficient red-emitting phosphor materials is essential. In this regard, the hardly explored compound class of nitridoaluminates affords a new material with superior luminescence properties. Doped with Eu(2+), Sr[LiAl3N4] emerged as a new high-performance narrow-band red-emitting phosphor material, which can efficiently be excited by GaN-based blue LEDs. Owing to the highly efficient red emission at λ(max) ~ 650 nm with a full-width at half-maximum of ~1,180 cm(-1) (~50 nm) that shows only very low thermal quenching (>95% relative to the quantum efficiency at 200 °C), a prototype phosphor-converted LED (pc-LED), employing Sr[LiAl3N4]:Eu(2+) as the red-emitting component, already shows an increase of 14% in luminous efficacy compared with a commercially available high colour rendering index (CRI) LED, together with an excellent colour rendition (R(a)8 = 91, R9 = 57). Therefore, we predict great potential for industrial applications in high-power white pc-LEDs.
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              A GaN bulk crystal with improved structural quality grown by the ammonothermal method.

              The realization of high-performance optoelectronic devices, based on GaN and other nitride semiconductors, requires the existence of a high-quality substrate. Non-polar or semipolar substrates have recently been proven to provide superior optical devices to those on conventional c-plane substrates. Bulk GaN growth enables GaN substrates sliced along various favourable crystal orientations. Ammonothermal growth is an attractive method for bulk GaN growth owing to its potential to grow GaN ingots at low cost. Here we report on improvement in the structural quality of GaN grown by the ammonothermal method. The threading dislocation densities estimated by plan-view transmission electron microscopy observations were less than 1 x 10(6) cm(-2) for the Ga face and 1 x 10(7) cm(-2) for the N face. No dislocation generation at the interface was observed on the Ga face, although a few defects were generated at the interface on the N face. The improvement in the structural quality, together with the previous report on growth rate and scalability, demonstrates the commercial feasibility of the ammonothermal GaN growth.
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                Author and article information

                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group
                2045-2322
                04 January 2016
                2016
                : 6
                : 18808
                Affiliations
                [1 ]Department of Physics and Astronomy, University of Mount. Union, 1972 Clark Ave, Alliance , OH, 44601, USA
                [2 ]Division of Materials and Manufacturing Science, Graduate School of Engineering, Osaka University , Suita, Osaka 565-0871, Japan
                [3 ]Center for Nanophase Materials Sciences, Oak Ridge National Laboratory , Oak Ridge, TN 37831, USA
                [4 ]Instituto Superior Técnico, Campus Tecnológico e Nuclear , Estrada Nacional 10, P-2695-066 Bobadela LRS, Portugal
                [5 ]Department of Physics and Astronomy, Lehigh University , 16 Memorial Dr. E, Bethlehem, PA, 18015, USA
                Author notes
                Article
                srep18808
                10.1038/srep18808
                4698738
                26725651
                8729eb1c-fb90-4681-98c4-e27efff79129
                Copyright © 2016, Macmillan Publishers Limited

                This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

                History
                : 17 July 2015
                : 23 November 2015
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