Christopher C. S. Chan
University of Oxford
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Featured researches published by Christopher C. S. Chan.
Applied Physics Letters | 2013
Christopher C. S. Chan; Benjamin P. L. Reid; Robert A. Taylor; YiDing Zhuang; Philip A. Shields; D. W. E. Allsopp; Wei Jia
Time-resolved and time-integrated microphotoluminescence studies at 4.2 K were performed on a single InGaN/GaN nanorod light emitting diode, fabricated in an array, on a wafer scale by nanoimprint lithography. Emission properties and carrier dynamics of the single nanorods are presented. Sharp peaks of 2 meV line-width were observed. The single nanorods possess longer decay rates than an unprocessed wafer at delay-times above 50 ns after excitation. The time evolution of the photoluminescence spectra implies that the slower decay times are due to surface related localisation near the perimeter of the nanorods, resulting in a spatial separation of the recombining carriers at low excitation densities.
Applied Physics Letters | 2014
Benjamin P. L. Reid; Claudius Kocher; Tongtong Zhu; Fabrice Oehler; Robert M. Emery; Christopher C. S. Chan; Rachel A. Oliver; Robert A. Taylor
Experimental observation of Rabi rotations between an exciton excited state and the crystal ground state in a single non-polar InGaN quantum dot is presented. The exciton excited state energy is determined by photoluminescence excitation spectroscopy using two-photon excitation from a pulsed laser. The population of the exciton excited state is seen to undergo power dependent damped Rabi oscillations.
Nano Letters | 2015
Youngsin Park; Geunsik Lee; Mark J. Holmes; Christopher C. S. Chan; Benjamin P. L. Reid; Jack A. Alexander-Webber; R. J. Nicholas; Robert A. Taylor; Kwang S. Kim; Sang W. Han; Woochul Yang; Y. J. Jo; J.H. Kim; Hyunsik Im
We investigate nontrivial surface effects on the optical properties of self-assembled crystalline GaN nanotubes grown on Si substrates. The excitonic emission is observed to redshift by ∼100 meV with respect to that of bulk GaN. We find that the conduction band edge is mainly dominated by surface atoms, and that a larger number of surface atoms for the tube is likely to increase the bandwidth, thus reducing the optical bandgap. The experimental findings can have important impacts in the understanding of the role of surfaces in nanostructured semiconductors with an enhanced surface/volume ratio.
Japanese Journal of Applied Physics | 2013
Benjamin P. L. Reid; Tongtong Zhu; Tim J. Puchtler; Luke J. Fletcher; Christopher C. S. Chan; Rachel A. Oliver; Robert A. Taylor
We report on optical characterization of self-assembled InGaN quantum dots (QDs) grown on three GaN pseudo-substrates with differing threading dislocation densities. QD density is estimated via microphotoluminscence on a masked sample patterned with circular apertures, and appears to increase with dislocation density. A non-linear excitation technique is used to observe the sharp spectral lines characteristic of QD emission. Temporal variations of the wavelength of emission from single QDs are observed and attributed to spectral diffusion. The magnitude of these temporal variations is seen to increase with dislocation density, suggesting locally fluctuating electric fields due to charges captured by dislocations are responsible for the spectral diffusion in this system.
Optics Express | 2013
Frederic S. F. Brossard; Benjamin P. L. Reid; Christopher C. S. Chan; Xiulai Xu; Jonathan Griffiths; D. A. Williams; R. Murray; Robert A. Taylor
We study the coupling of cavities defined by the local modulation of the waveguide width using confocal photoluminescence microscopy. We are able to spatially map the profile of the antisymmetric (antibonding) and symmetric (bonding) modes of a pair of strongly coupled cavities (photonic molecule) and follow the coupled cavity system from the strong coupling to the weak coupling regime in the presence of structural disorder. The effect of disorder on this photonic molecule is also investigated numerically with a finite-difference time-domain method and a semi-analytical approach, which enables us to quantify the light localization observed in either cavity as a function of detuning.
Journal of Applied Physics | 2011
Mark J. Holmes; Young Soo Park; Xu Wang; Christopher C. S. Chan; Anas F. Jarjour; Robert A. Taylor; Jamie H. Warner; Jun Luo; Haitham A. R. El-Ella; Rachel A. Oliver
Time-integrated and time-resolved microphotoluminescence studies have been performed on Inx Ga1−xN quantum disks at the tips of GaN nanocolumns. The results are analyzed in the context of current theories regarding an inhomogeneous strain distribution in the disk which is theorized to generate lateral charge separation in the disks by strain induced band bending, an inhomogeneous polarization field distribution, and Fermi surface pinning. It is concluded that no lateral separation of carriers occurs in the quantum disks under investigation. Internal field screening by an increased carrier density in the QDisks at higher excitation densities is observed via a blue-shift of the emission and a dynamically changing decay time. Other possible explanations for these effects are discussed and discounted. Cathodoluminescence studies have also been carried out on the nanocolumns to provide insight into the physical origin of the luminescence.
Applied Physics Letters | 2015
Benjamin P. L. Reid; Claudius Kocher; Tongtong Zhu; Fabrice Oehler; Christopher C. S. Chan; Rachel A. Oliver; Robert A. Taylor
Polarization sensitive photoluminescence is performed on single non-polar InGaN quantum dots. The studied InGaN quantum dots are found to have linearly polarized emission with a common polarization direction defined by the [0001] crystal axis. Around half of ∼40 studied dots have a polarization degree of 1. For those lines with a polarization degree less than 1, we can resolve fine structure splittings between −800 μeV and +800 μeV, with no clear correlation between fine structure splitting and emission energy.
Applied Physics Letters | 2011
Mark J. Holmes; Young Soo Park; Xu Wang; Christopher C. S. Chan; Benjamin P. L. Reid; Heedae Kim; Robert A. Taylor; Jamie H. Warner; Jun Luo
Microphotoluminescence studies were carried out on a single GaN nanocolumn containing a single InGaN quantum disk (QDisk) that had been removed from its growth substrate and dispersed onto a patterned grid. An analysis of the dynamics of the carriers in the nanocolumn is presented. Suppression of the GaN luminescence from the area of the column in the vicinity of the InGaN QDisk in addition to a delayed emission from the QDisk relative to the GaN is observed. Time resolved spatial maps of the luminescence intensity from the column are also presented, illustrating the evolution of the carrier density in the system.
Optical Materials Express | 2015
Young S. Park; Christopher C. S. Chan; Benjamin P. L. Reid; Mark J. Holmes; David M. Coles; Jack A. Alexander-Webber; R. J. Nicholas; Robert A. Taylor; Seung-Woong Lee; Woochul Yang; Hyunsik Im
The optical transitions of the three-dimensionally confined GaN/AlGaN asymmetric multi quantum disks were characterized by micro photoluminescence and time-resolved photoluminescence. Several fine emission lines, originating from the wide and narrow quantum disks, were observed around 3.7 eV from a single nanocolumn dispersed on a patterned SiO2 substrate. The photoluminescence from the wide quantum disk shifts a little with increasing excitation power, while that from the narrow quantum disk does not shift. This effect can be explained by carrier tunneling for the 3-dimensionally confined quantum disks. Kelvin probe force microscopy results confirm that the GaN/AlGaN multiquantum disks are surrounded by a GaN shell, which has a higher potential than core GaN.
ACS Nano | 2017
Youngsin Park; Yooseok Kim; Chang Woo Myung; Robert A. Taylor; Christopher C. S. Chan; Benjamin P. L. Reid; Tim J. Puchtler; R. J. Nicholas; Laishram Tomba Singh; Geunsik Lee; Chan-Cuk Hwang; Chong-Yun Park; Kwang S. Kim
Despite having outstanding electrical properties, graphene is unsuitable for optical devices because of its zero band gap. Here, we report two-dimensional excitonic photoluminescence (PL) from graphene grown on a Cu(111) surface, which shows an unexpected and remarkably sharp strong emission near 3.16 eV (full width at half-maximum ≤3 meV) and multiple emissions around 3.18 eV. As temperature increases, these emissions blue shift, displaying the characteristic negative thermal coefficient of graphene. The observed PL originates from the significantly suppressed dispersion of excited electrons in graphene caused by hybridization of graphene π and Cu d orbitals of the first and second Cu layers at a shifted saddle point 0.525(M+K) of the Brillouin zone. This finding provides a pathway to engineering optoelectronic graphene devices, while maintaining the outstanding electrical properties of graphene.