Compensation effect in carbon nanotube quantum dots coupled to polarized electrodes in the presence of spin-orbit coupling

We study theoretically the Kondo effect in carbon nanotube quantum dot attached to polarized electrodes. Since both spin and orbit degrees of freedom are involved in such a system, the electrode polarization contains the spin- and orbit-polarizations as well as the Kramers polarization in the presence of the spin-orbit coupling. In this paper we focus on the compensation effect of the effective fields induced by different polarizations by applying magnetic field. The main results are i) while the effective fields induced by the spin- and orbit-polarizations remove the degeneracy in the Kondo effect, the effective field induced by the Kramers polarization enhances the degeneracy through suppressing the spin-orbit coupling; ii) while the effective field induced by the spin-polarization can not be compensated by applying magnetic field, the effective field induced by the orbit-polarization can be compensated; and iii) the presence of the spin-orbit coupling does not change the compensation behavior observed in the case without the spin-orbit coupling. These results are observable in an ultraclean carbon-nanotube quantum dot attached to ferromagnetic contacts under a parallel applied magnetic field along the tube axis and it would deepen our understanding on the Kondo physics of the carbon nanotube quantum dot.Comment: 8 pages, 6 figure

Kondo effect of an adatom in graphene and its scanning tunneling spectroscopy

We study the Kondo effect of a single magnetic adatom on the surface of graphene. It was shown that the unique linear dispersion relation near the Dirac points in graphene makes it more easy to form the local magnetic moment, which simply means that the Kondo resonance can be observed in a more wider parameter region than in the metallic host. The result indicates that the Kondo resonance indeed can form ranged from the Kondo regime, to the mixed valence, even to the empty orbital regime. While the Kondo resonance displays as a sharp peak in the first regime, it has a peak-dip structure and/or an anti-resonance in the remaining two regimes, which result from the Fano resonance due to the significant background leaded by dramatically broadening of the impurity level in graphene. We also study the scanning tunneling microscopy (STM) spectra of the adatom and they show obvious particle-hole asymmetry when the chemical potential is tuned by the gate voltages applied to the graphene. Finally, we explore the influence of the direct tunneling channel between the STM tip and the graphene on the Kondo resonance and find that the lineshape of the Kondo resonance is unaffected, which can be attributed to unusual large asymmetry factor in graphene. Our study indicates that the graphene is an ideal platform to study systematically the Kondo physics and these results are useful to further stimulate the relevant experimental studies on the system.Comment: 8 pages, 5 figure

Global modeling of nitrate and ammonium: Interaction of aerosols and tropospheric chemistry

Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/95603/1/jgrd12466.pd

A simulation study on the measurement of D0-D0bar mixing parameter y at BES-III

We established a method on measuring the \dzdzb mixing parameter $y$ for BESIII experiment at the BEPCII $e^+e^-$ collider. In this method, the doubly tagged $\psi(3770) \to D^0 \overline{D^0}$ events, with one $D$ decays to CP-eigenstates and the other $D$ decays semileptonically, are used to reconstruct the signals. Since this analysis requires good $e/\pi$ separation, a likelihood approach, which combines the $dE/dx$, time of flight and the electromagnetic shower detectors information, is used for particle identification. We estimate the sensitivity of the measurement of $y$ to be 0.007 based on a $20fb^{-1}$ fully simulated MC sample.Comment: 6 pages, 7 figure

Genome-Wide Association Study Identifies ALDH7A1 as a Novel Susceptibility Gene for Osteoporosis

Osteoporosis is a major public health problem. It is mainly characterized by low bone mineral density (BMD) and/or low-trauma osteoporotic fractures (OF), both of which have strong genetic determination. The specific genes influencing these phenotypic traits, however, are largely unknown. Using the Affymetrix 500K array set, we performed a case-control genome-wide association study (GWAS) in 700 elderly Chinese Han subjects (350 with hip OF and 350 healthy matched controls). A follow-up replication study was conducted to validate our major GWAS findings in an independent Chinese sample containing 390 cases with hip OF and 516 controls. We found that a SNP, rs13182402 within the ALDH7A1 gene on chromosome 5q31, was strongly associated with OF with evidence combined GWAS and replication studies (P = 2.08×10−9, odds ratio = 2.25). In order to explore the target risk factors and potential mechanism underlying hip OF risk, we further examined this candidate SNP's relevance to hip BMD both in Chinese and Caucasian populations involving 9,962 additional subjects. This SNP was confirmed as consistently associated with hip BMD even across ethnic boundaries, in both Chinese and Caucasians (combined P = 6.39×10−6), further attesting to its potential effect on osteoporosis. ALDH7A1 degrades and detoxifies acetaldehyde, which inhibits osteoblast proliferation and results in decreased bone formation. Our findings may provide new insights into the pathogenesis of osteoporosis

Genetic Association Study of Common Mitochondrial Variants on Body Fat Mass

Mitochondria play a central role in ATP production and energy metabolism. Previous studies suggest that common variants in mtDNA are associated with several common complex diseases, including obesity. To test the hypothesis that common mtDNA variants influence obesity-related phenotypes, including BMI and body fat mass, we genotyped a total of 445 mtSNPs across the whole mitochondrial genome in a large sample of 2,286 unrelated Caucasian subjects. 72 of these 445 mtSNPs passed quality control criteria, and were used for subsequent analyses. We also classified all subjects into nine common European haplogroups. Association analyses were conducted for both BMI and body fat mass with single mtSNPs and mtDNA haplogroups. Two mtSNPs, mt4823 and mt8873 were detected to be significantly associated with body fat mass, with adjusted P values of 4.94×10-3 and 4.58×10-2, respectively. The minor alleles mt4823 C and mt8873 A were associated with reduced fat mass values and the effect size (β) was estimated to be 3.52 and 3.18, respectively. These two mtSNPs also achieved nominally significant levels for association with BMI. For haplogroup analyses, we found that haplogroup X was strongly associated with both BMI (adjusted P = 8.31×10-3) and body fat mass (adjusted P = 5.67×10-4) Subjects classified as haplogroup X had lower BMI and fat mass values, with the β estimated to be 2.86 and 6.03, respectively. Our findings suggest that common variants in mitochondria might play a role in variations of body fat mass. Further molecular and functional studies will be needed to clarify the potential mechanism