We investigate theoretically Rabi-like splitting and Fano resonance in absorption spectra of quantum dots(QDs)based on a hybrid QD-semiconducting nanowire/superconductor(SNW/SC)device mediated by Majorana fermions(MFs).Under the condition of pump on-resonance and off-resonance,the absorption spectrum experiences the conversion from Fano resonance to Rabi-like splitting in different parametric regimes.In addition,the Fano resonances are accompanied by the rapid normal phase dispersion,which will indicate the coherent optical propagation.The results indicate that the group velocity index is tunable with controlling the interaction between the QD and MFs,which can reach the conversion between the fast-and slow-light.Fano resonance will be another method to detect MFs and our research may indicate prospective applications in quantum information processing based on the hybrid QD-SNW/SC devices. 相似文献
Let A and B be two factor von Neumann algebras. For A, B ∈ A, define by [A, B]_*= AB-BA~*the skew Lie product of A and B. In this article, it is proved that a bijective map Φ : A → B satisfies Φ([[A, B]_*, C]_*) = [[Φ(A), Φ(B)]_*, Φ(C)]_*for all A, B, C ∈ A if and only if Φ is a linear *-isomorphism, or a conjugate linear *-isomorphism, or the negative of a linear *-isomorphism, or the negative of a conjugate linear *-isomorphism. 相似文献
Studies on N2 activation and transformation by transition metal hydride complexes are of particular interest and importance. The synthesis and diverse transformations of a dinitrogen dititanium hydride complex bearing the rigid acridane-based acriPNP-pincer ligands {[(acriPNP)Ti]2(μ2-η1:η2-N2)(μ2-H)2} are presented. This complex enabled N2 cleavage and hydrogenation even without additional H2 or other reducing agents. Furthermore, diverse transformations of the N2 unit with a variety of organometallic compounds such as ZnMe2, MgMe2, AlMe3, B(C6F5)3, PinBH, and PhSiH3 have been well established at the rigid acriPNP-ligated dititanium framework, such as reversible bonding-mode change between the end-on and side-on/end-on fashions, diborylative N=N bond cleavage, the formal insertion of two dimethylaluminum species into the N=N bond, and the formal insertion of two silylene units into the N=N bond. This work has revealed many unprecedented aspects of dinitrogen reaction chemistry. 相似文献
Ocotillol, pseudo-ginsenoside RT5 (RT5), and pseudo-ginsenoside F11 (PF11) are ocotillol-type saponins that have the same aglycone structure but with different numbers of glucose at the C-6 position. In this study, the metabolites of ocotillol, RT5, and PF11 in rat plasma, stomach, intestine, urine, and feces after oral administration were investigated by ultra-performance liquid chromatography coupled with time-of-flight mass spectrometry. The results showed that RT5 was easily biotransformed into metabolites in vivo, whereas PF11 and RT5 were difficult to be biotransformed. Hydrogenation, dehydrogenation, dehydration, deglycosylation, deoxygenation, hydration, phosphorylation, deoxidation, glucuronidation, and reactions combining amino acid were speculated to be involved in the biotransformation of ocotillol, RT5, and PF11. Based on the structural analysis of metabolites, it was deduced that hydrogenation, dehydration, deoxidation, and reactions combining amino acid occurred on the aglycone structure, whereas deglycosylation, hydration, and phosphorylation occurred on the glycosyl chain. Further, metabolites in plasma, urine, feces, and tissues were different: First, glucuronidation products were found in urine, stomach, intestine, and feces, but not in plasma. Second, the ocotillol prototype was not identified in urine samples. Third, the RT5 prototype was found in stomach, intestine, feces, and urine, but not in plasma. 相似文献
Indeno[1,2‐b]fluorene‐based [2,2]cyclophanes with 4n/4n and 4n/[4n+2] π‐electron systems were prepared, and their structures were identified by X‐ray crystallography. With short π–π distances around 3.0 Å, [2.2](5,11)indeno[1,2‐b]fluorenophane and its precursor [2.2](5,11)indeno[1,2‐b]fluorene‐6,12‐dionophane exhibit remarkable transannular interactions, leading to their unusual electrochemical and photophysical properties. With the aid of femtosecond transient absorption spectroscopy, the transition from the monomeric excited state to the redshifted H‐type dimeric state was first observed, correlating to the calculated excitonic energy splitting and the steady‐state absorption spectra induced by charge‐transfer‐mediated superexchange interaction. 相似文献
In this study, three different volume expansion ratios of expanded graphite (EG) are prepared and investigated to enhance the heat transfer efficiency of the sodium acetate trihydrate (SAT) composites. A series of SAT composite phase change materials (CPCMs) with EG were prepared. The influence of volume expansion ratio and mass fraction of EG on thermodynamic characteristics of SAT CPCMs was examined, including thermal conductivity, phase change temperature, enthalpy, latent heat storage and release time, and the degree of supercooling. Results showed that SAT CPCMs can be absorbed adequately by EG, and EG could enhance the heat transfer efficiency effectively. But it also brought some problems with the addition of all the three volume expansion ratios of EG, such as the poor enthalpy and serious supercooling. Particularly, the situation gets worse with the increase in mass and expansion ratio of EG. Therefore, it is better to choose the EG with proper expansion ratio or reduce the proportion of the EG which possesses higher expansion ratio. Besides, thermal cycling test and thermogravimetric analysis revealed that the SAT CPCMs with 3 mass% EG showed a good thermal stability.
Acta Mathematicae Applicatae Sinica, English Series - This paper summarizes the parameter estimation of systems with set-valued signals, which can be classified to three catalogs: one-time... 相似文献
Fullerene (C60), the third carbon allotrope, has shown great potential in photoelectric materials and drug delivery. However, the low solubility of C60 in polar solvents, especially in water, is the major limiting factor for further applications. The use of ultrasound and amphiphilic block copolymers, poly(ethylene glycol)-block-poly(4-vinylpyridine) (PEG-b-P4VP), helped to disperse C60 in acidic aqueous solutions. As characterized by dynamic light scattering, transmission electron microscopy, and UV-visible spectroscopy, the C60 colloids had a core-shell structure with C60 aggregated in the micellar cores. The photosensitized generation of singlet oxygen using C60-bound polymer micelle was confirmed by the iodide method. More importantly, C60 and metalloporphyrin complexes could be synthesized by the self-assembly between PEG-b-P4VP/C60 micelle and metalloporphyrin. The stability of metalloporphyrin increased in the presence of the PEG-b-P4VP/C60 micelle. This study provides a method for the solubilization of C60 with many potential applications in biomedicals and photovoltaics. 相似文献