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The effects of hydrogen incorporation into beta-Ga2O3 thin films have been investigated by chemical, electrical and optical characterization techniques. Hydrogen incorporation was achieved by remote plasma doping without any structural alterations of the film; however, X-ray photoemission reveals major changes in the oxygen chemical environment. Depth-resolved cathodoluminescence (CL) reveals that the near-surface region of the H-doped Ga2O3 film exhibits a distinct red luminescence (RL) band at 1.9 eV. The emergence of the H-related RL band is accompanied by an enhancement in the electrical conductivity of the film by an order of magnitude. Temperature-resolved CL points to the formation of abundant H-related donors with a binding energy of 28 +/- 4 meV. The RL emission is attributed to shallow donor-deep acceptor pair recombination, where the acceptor is a VGa-H complex and the shallow donor is interstitial H. The binding energy of the VGa-H complex, based on our experimental considerations, is consistent with the computational results by Varley et al [J. Phys.: Condens. Matter, 23, 334212, 2011]., Comment: 3 figures

Large reflection losses at interfaces in light emitting semiconductor devices cause a significant reduction in their light emission and energy efficiencies. Metal nanoparticle (NP) surface coatings have been demonstrated to increase the light extraction efficiency from planar high refractive index semiconductor surfaces. This emission enhancement in Au NP-coated ZnO is widely attributed to involvement of a green (~ 2.5 eV) deep level ZnO defect exciting localized surface plasmons in the NPs that non-radiatively decay into hot electrons, which return to ZnO and radiatively recombine. In this work, we achieve a 6 times enhancement of the ultra-violet excitonic emission in ZnO nanorods that are coated with 5 nm Au NPs without the aid of ZnO defects. Cathodoluminescence (CL), photoluminescence (PL) and a novel concurrent CL-PL technique as well as time resolved PL spectroscopy revealed that the increase in UV emission is due to the formation of an additional fast excitonic relaxation pathway that increases the exciton spontaneous emission rate. Concurrent CL-PL measurements ruled out the presence of charge transfer mechanism in the emission enhancement process. While time resolved PL results confirmed the existence of a new excitonic recombination channel that is attributed to exciton relaxation via the plasmon-assisted excitation of rapid non-radiative Au interband transitions. Our results establish that ZnO defect levels ~ 2.5 eV are not required to facilitate Au NP induced enhancement of the ZnO UV emission.

The UV enhancement of Al-coated ZnO single crystals with a wide range of carrier densities is systematically studied using depth-resolved cathodoluminescence (CL) and photoluminescence (PL) as well as valence band X-ray photoemission spectroscopy (VB-XPS). AN up to 17-fold enhanced PL UV emission for Al-coated ZnO with the highest carrier density (2 x 10^17 cm^-3) was measured, which falls to a 12-fold increase for the lowest carrier density (3 x 10^13 cm^-3). Depth-resolved CL measurements confirm that the enhancement is strongest near the metal coating-ZnO interface consistent with an increased UV emission due to an exciton-localized surface plasmon coupling mechanism. Correlative CL, PL and VB-XPS studies reveal that a number of additional effects to the presence of the Al surface coating also contribute to the UV enhancement factor. These include increased UV enhancement due to the formation of a surface depletion layer induced by the metal surface coating, which also passivates competitive non-radiative surface recombination channels found in uncoated ZnO. Significantly, it was established that the magnitude of the emission enhancement factor can be raised in a controlled way by reducing the thickness of the depletion layer by increasing the carrier density. The contribution of these effects collectively provides an explanation for the large span of enhancement factors reported in the literature., Comment: 22 pages, 10 figures

Metal nanoparticle (NP) surface coatings are known to significantly enhance the ultra-violet luminescence intensity of ZnO. Although there is general agreement that resonantly excited Localized Surface Plasmons (LSPs) in metal NPs can directly couple to excitons in the semiconductor increasing their spontaneous emission rate, the exact mechanisms involved in this phenomenon are currently not fully understood. In this work, LSP-exciton coupling in a ZnO single crystal and ZnO nanorods coated with a 2 nm Al layer has been investigated using correlative photoluminescence and depth-resolved cathodoluminescence and time-resolved photoluminescence spectroscopy. Temperature-resolved cathodoluminescence and photoluminescence measurements from 10 K to 250 K show enhancement factors up to 12 times of the free exciton (FX) emission at 80 K. The FX couple more efficiently to the LSPs in Al compared to the localized donor-bound excitons. Furthermore, a strong polarization dependence of the LSPs with respect to the FX was observed with higher enhanced FX transitions polarized in the same direction as the electric field of the incident excitation. These results indicate that selective enhancement of the ultra-violet excitonic PL in ZnO can be achieved by careful alignment of the crystallographic axes of the ZnO relative to the electric vector of the excitation source., Comment: 20 pages, 9 figures

Online social media, periodically serves as a platform for cascading polarizing topics of conversation. The inherent community structure present in online social networks (homophily) and the advent of fringe outlets like Gab have created online "echo chambers" that amplify the effects of polarization, which fuels detrimental behavior. Recently, in October 2018, Gab made headlines when it was revealed that Robert Bowers, the individual behind the Pittsburgh Synagogue massacre, was an active member of this social media site and used it to express his anti-Semitic views and discuss conspiracy theories. Thus to address the need of automated data-driven analyses of such fringe outlets, this research proposes novel methods to discover topics that are prevalent in Gab and how they cascade within the network. Specifically, using approximately 34 million posts, and 3.7 million cascading conversation threads with close to 300k users; we demonstrate that there are essentially five cascading patterns that manifest in Gab and the most "viral" ones begin with an echo-chamber pattern and grow out to the entire network. Also, we empirically show, through two models viz. Susceptible-Infected and Bass, how the cascades structurally evolve from one of the five patterns to the other based on the topic of the conversation with upto 84% accuracy.

Groups of humans are often able to find ways to cooperate with one another in complex, temporally extended social dilemmas. Models based on behavioral economics are only able to explain this phenomenon for unrealistic stateless matrix games. Recently, multi-agent reinforcement learning has been applied to generalize social dilemma problems to temporally and spatially extended Markov games. However, this has not yet generated an agent that learns to cooperate in social dilemmas as humans do. A key insight is that many, but not all, human individuals have inequity averse social preferences. This promotes a particular resolution of the matrix game social dilemma wherein inequity-averse individuals are personally pro-social and punish defectors. Here we extend this idea to Markov games and show that it promotes cooperation in several types of sequential social dilemma, via a profitable interaction with policy learnability. In particular, we find that inequity aversion improves temporal credit assignment for the important class of intertemporal social dilemmas. These results help explain how large-scale cooperation may emerge and persist., Comment: 15 pages, 8 figures

New insights into controlling nanowire merging phenomena are demonstrated in growth of thin ZnO nanowires using monodispersed Au colloidal nanoparticles as catalyst. Both nanowire diameter and density were found to be strongly dependent on the density of Au nanoparticles. Structural analysis and spectral cathodoluminescence imaging of the c-plane nanowire cross-sections reveal that thin isolated nanowires growing from the Au nanoparticles begin to merge and coalesce with neighbouring nanowires to form larger nanowires when their separation reaches a threshold distance. Green luminescence, which is originated from the remnants of constituent nanowires before merging, is detected at the core of fused nanowires. The distribution of nanowire diameters and green emission were found to be strongly dependent on the density of the Au nanoparticles. The merging phenomenon is attributed to electrostatic interactions between nanowire c-facets during growth and well-described by a cantilever bending model.

Single photon sources are required for a wide range of applications in quantum information science, quantum cryptography and quantum communications. However, so far majority of room temperature emitters are only excited optically, which limits their proper integration into scalable devices. In this work, we overcome this limitation and present room temperature electrically triggered light emission from localized defects in zinc oxide (ZnO) nanoparticles and thin films. The devices emit at the red spectral range and show excellent rectifying behavior. The emission is stable over an extensive period of time, providing an important prerequisite for practical devices. Our results open up possibilities to build new ZnO based quantum integrated devices that incorporate solid-state single photon sources for quantum information technologies.

Room temperature single photon emitters are very important resources for photonics and emerging quantum technologies. In this work we study single photon emission from defect centers in 20 nm zinc oxide (ZnO) nanoparticles. The emitters exhibit bright broadband fluorescence in the red spectral range centered at 640 nm with polarized excitation and emission. The studied emitters showed continuous blinking, however, bleaching can be suppressed using a polymethyl methacrylate (PMMA) coating. Furthermore, hydrogen termination increased the density of single photon emitters. Our results will contribute to the identification of quantum systems in ZnO.

The uniaxial stress dependence of the band structure and the exciton-polariton transitions in wurtzite ZnO is thoroughly studied using modern first-principles calculations based on the HSE+G0W0 approach, k p modeling using the deformation potential framework, and polarized photoluminescence measurements. The ordering of the valence bands [A(G7), B(G9), C(G7)] is found to be robust even for high uniaxial and biaxial strains. Theoretical results for the uniaxial pressure coefficients and splitting rates of the A, B, and C valence bands and their optical transitions are obtained including the effects of the spin-orbit interaction. The excitonic deformation potentials are derived and the stress rates for hydrostatic pressure are determined based on the results for uniaxial and biaxial stress. In addition, the theory for the stress dependence of the exchange interaction and longitudinal-transversal splitting of the exciton-polaritons is developed using the basic exciton functions of the quasi-cubic approximation and taking the interaction between all exciton states into account. It is shown that the consideration of these effects is crucial for an accurate description of the stress dependence of the optical spectra in ZnO. The theoretical results are compared to polarized photoluminescence measurements of different ZnO substrates as function of uniaxial pressure and experimental values reported in the literature demonstrating an excellent agreement with the computed pressure coefficients., Comment: 16 pages with 9 figures and 5 tables