67 research outputs found

    Excitonic properties of low-dimensional semiconductors:Magnetic field effects and impurity bound excitons

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    Magneto-excitons and Faraday rotation in single-walled carbon nanotubes and graphene nanoribbons

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    On the existence of impurity bound excitons in one-dimensional systems with zero range interactions

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    We consider a three-body one-dimensional Schr\"odinger operator with zero range potentials, which models a positive impurity with charge Îş>0\kappa > 0 interacting with an exciton. We study the existence of discrete eigenvalues as Îş\kappa is varied. On one hand, we show that for sufficiently small Îş\kappa there exists a unique bound state whose binding energy behaves like Îş4\kappa^4, and we explicitly compute its leading coefficient. On the other hand, if Îş\kappa is larger than some critical value then the system has no bound states

    Optical orientation with linearly polarized light in transition metal dichalcogenides

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    We study the optical properties of semiconducting transition metal dichalcogenide monolayers under the influence of strong out-of-plane magnetic fields, using the effective massive Dirac model. We pay attention to the role of spin-orbit-coupling effects, doping level, and electron-electron interactions, treated at the Hartree-Fock level. We find that optically induced valley and spin imbalance, commonly attained with circularly polarized light, can also be obtained with linearly polarized light in the doped regime. Additionally, we explore an exchange-driven mechanism to enhance the spin-orbit splitting of the conduction band, in n-doped systems, controlling both the carrier density and the intensity of the applied magnetic field.G.C. and J.F.-R. acknowledge financial support from Fundação para a Ciência e a Tecnologia (FCT) for the Grant No. P2020-PTDC/FIS-NAN/4662/2014. J.H. acknowledges financial support by the QUSCOPE Center, sponsored by the Villum foundation. J.F.-R. acknowledges financial support from FCT for the Grants No. P2020-PTDC/FISNAN/3668/2014 and No. UTAP-EXPL/NTec/0046/2017, as well as Generalitat Valenciana funding Prometeo2017/139 and MINECO-Spain (Grant No. MAT2016-78625-C2). N.M.R.P. acknowledges financial support from the European Commission through the project “Graphene-Driven Revolutions in ICT and Beyond” (Ref. No. 785219) and the Portuguese Foundation for Science and Technology (FCT) in the framework of the Strategic Financing Grant No. UID/FIS/04650/2013. Additionally, N.M.R.P. acknowledges COMPETE2020, PORTUGAL2020, FEDER and the Portuguese Foundation for Science and Technology (FCT) for the Grants No. PTDC/FIS-NAN/3668/2013 and No. POCI-01-0145-FEDER-028114

    Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest

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    Introduction: A previous genome-wide association study found three genetic loci, rs9388451, rs10428132, and rs11708996, to increase the risk of Brugada Syndrome (BrS). Since the effect of these loci in the general population is unknown, we aimed to investigate the effect on electrocardiogram (ECG) parameters and outcomes in the general population.Materials and Methods: A cohort of 6,161 individuals (median age 45 [interquartile range (IQR) 40–50] years, 49% males), with available digital ECGs, was genotyped and subsequently followed for a median period of 13 [IQR 12.6–13.4] years. Data on outcomes were collected from Danish administrative healthcare registries. Furthermore, ~400,000 persons from UK Biobank were investigated for associations between the three loci and cardiac arrest/ventricular fibrillation (VF).Results: Homozygote carriers of the C allele in rs6800541 intronic to SCN10A had a significantly larger J-point elevation (JPE) compared with wildtype carriers (11 vs. 6 μV, P < 0.001). There was an additive effect of carrying multiple BrS-associated risk alleles with an increased JPE in lead V1. None of the BrS-associated genetic loci predisposed to syncope, atrial fibrillation, or total mortality in the general Danish population. The rs9388451 genetic locus adjacent to the HEY2 gene was associated with cardiac arrest/VF in an analysis using the UK Biobank study (odds ratio = 1.13 (95% confidence interval: 1.08–1.18), P = 0.006).Conclusions: BrS-associated risk alleles increase the JPE in lead V1 in an additive manner, but was not associated with increased mortality or syncope in the general population of Denmark. However, the HEY2 risk allele increased the risk of cardiac arrest/VF in the larger population study of UK Biobank indicating an important role of this common genetic locus
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