Tunable graphene bandgaps from superstrate mediated interactions

A theory is presented for the strong enhancement of graphene-on-substrate bandgaps by attractive interactions mediated through phonons in a polarizable superstrate. It is demonstrated that gaps of up to 1eV can be formed for experimentally achievable values of electron-phonon coupling and phonon frequency. Gap enhancements range between 1 and 4, indicating possible benefits to graphene electronics through greater bandgap control for digital applications, lasers, LEDs and photovoltaics through the relatively simple application of polarizable materials such as SiO2 and Si3N4.Comment: 4 pages, 4 figures, to appear in Phys. Rev.

Influence of Anomalous Dispersion on Optical Characteristics of Quantum Wells

Frequency dependencies of optical characteristics (reflection, transmission and absorption of light) of a quantum well are investigated in a vicinity of interband resonant transitions in a case of two closely located excited energy levels. A wide quantum well in a quantizing magnetic field directed normally to the quantum-well plane, and monochromatic stimulating light are considered. Distinctions between refraction coefficients of barriers and quantum well, and a spatial dispersion of the light wave are taken into account. It is shown that at large radiative lifetimes of excited states in comparison with nonradiative lifetimes, the frequency dependence of the light reflection coefficient in the vicinity of resonant interband transitions is defined basically by a curve, similar to the curve of the anomalous dispersion of the refraction coefficient. The contribution of this curve weakens at alignment of radiative and nonradiative times, it is practically imperceptible at opposite ratio of lifetimes . It is shown also that the frequency dependencies similar to the anomalous dispersion do not arise in transmission and absorption coefficients.Comment: 10 pages, 6 figure

Transmission of a Symmetric Light Pulse through a Wide QW

The reflection, transmission and absorption of a symmetric electromagnetic pulse, which carrying frequency is close to the frequency of an interband transition in a QW (QW), are obtained. The energy levels of a QW are assumed discrete, one exited level is taken into account. The case of a wide QW is considered when a length of the pulse wave, appropriate to the carrying frequency, is comparable to the QW's width. In figures the time dependencies of the dimensionless reflection, absorption are transmission are represented. It is shown, that the spatial dispersion and a distinction in refraction indexes influence stronger reflection.Comment: 8 pages,8 figures with caption

Principals of the theory of light reflection and absorption by low-dimensional semiconductor objects in quantizing magnetic fields at monochromatic and pulse excitations

The bases of the theory of light reflection and absorption by low-dimensional semiconductor objects (quantum wells, wires and dots) at both monochromatic and pulse irradiations and at any form of light pulses are developed. The semiconductor object may be placed in a stationary quantizing magnetic field. As an example the case of normal light incidence on a quantum well surface is considered. The width of the quantum well may be comparable to the light wave length and number of energy levels of electronic excitations is arbitrary. For Fourier-components of electric fields the integral equation (similar to the Dyson-equation) and solutions of this equation for some individual cases are obtained.Comment: 14 page

Phonon-affected steady-state transport through molecular quantum dots

We consider transport through a vibrating molecular quantum dot contacted to macroscopic leads acting as charge reservoirs. In the equilibrium and nonequilibrium regime, we study the formation of a polaron-like transient state at the quantum dot for all ratios of the dot-lead coupling to the energy of the local phonon mode. We show that the polaronic renormalization of the dot-lead coupling is a possible mechanism for negative differential conductance. Moreover, the effective dot level follows one of the lead chemical potentials to enhance resonant transport, causing novel features in the inelastic tunneling signal. In the linear response regime, we investigate the impact of the electron-phonon interaction on the thermoelectrical properties of the quantum dot device.Comment: 11 pages, 7 figures, FQMT11 Proceeding

Efficient DMFT-simulation of the Holstein-Hubbard Model

We present a method for solving impurity models with electron-phonon coupling, which treats the phonons efficiently and without approximations. The algorithm is applied to the Holstein-Hubbard model in the dynamical mean field approximation, where it allows access to strong interactions, very low temperatures and arbitrary fillings. We show that a renormalized Migdal-Eliashberg theory provides a reasonlable description of the phonon contribution to the electronic self energy in strongly doped systems, but fails if the quasiparticle energy becomes of order of the phonon frequency.Comment: Published versio

The nature of Ho magnetism in multiferroic HoMnO3

Using x-ray resonant magnetic scattering and x-ray magnetic circular dichroism, techniques that are element specific, we have elucidated the role of Ho3+ in multiferroic HoMnO3. In zero field, Ho3+ orders antiferromagnetically with moments aligned along the hexagonal c direction below 40 K, and undergoes a transition to another magnetic structure below 4.5 K. In applied electric fields of up to 1x10^7 V/m, the magnetic structure of Ho3+ remains unchanged.Comment: 4 pages, 3 figures Manuscript accepted for publication in Phys. Rev. Lett. 200

Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: A case report

Background: Sixty mutations of claudin 16 coding gene have been reported in familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) patients. Recent investigations revealed that a highly conserved glycine-leucine-tryptophan (115G-L-W117) motif in the first extracellular segment (ESC1) of claudin 16 might be essential for stabilization of the appropriately folded ECS1 structure and conservation of normal claudin 16 function. However, neither missense nor nonsense mutation has ever been described in this motif. Our study aimed at identifying mutations in a Chinese patient with FHHNC and exploring the association between genotype and phenotype. Case presentation: A 33-year-old female presented with 4 years history of recurrent acute pyelonephritis without other notable past medical history. Her healthy parents, who aged 56 and 53 respectively, were second cousins, and her only sibling died from renal failure without definite cause at age 25. Renal ultrasound imaging demonstrated atrophic kidneys and bilateral nephrocalcinosis. The laboratory workup revealed impaired renal function (Stage CKD IV), hypocalcemia and mild hypomagnesemia, accompanied with marked renal loss of magnesium and hypercalciuria. During the follow-up, treatment with calcitriol and calcium but not with magnesium was difficult to achieve normal serum calcium levels, whereas her serum magnesium concentration fluctuated within normal ranges. In the end, the patient unavoidably reached ESRD at 36 years old. The clinical features and family history suggested the diagnosis of FHHNC. To make a definite diagnosis, we use whole-exome sequencing to identify the disease-causing mutations and Sanger sequencing to confirm the mutation co-segregation in the family. As a result, a novel homozygous mutation (c.346C > G, p.Leu116Val) in115G-L-W117motif of claudin 16 was identified. Her parents, grandmother and one of her cousins carried heterozygous p.Leu116Val, whereas 200 unrelated controls did not carry this mutation. Conclusions: We described a delayed diagnosis patient with FHHNC in the Chinese population and identified a novel missense mutation in the highly conserved115G-L-W117motif of claudin 16 for the first time. According to the reported data and the information deduced from 3D modeling, we speculate that this mutation probably reserve partial residual function which might be related to the slight phenotype of the patient