Bi2Te3拓扑绝缘体表面颗粒化铅膜诱导的超导邻近效应

拓扑绝缘体的出现为寻找拓扑超导体和Majorana费米子提供了一种可能的途径. 在拓扑绝缘体Bi₂Te₃表面沉积极薄的不连续铅膜, 试图通过邻近效应感应出大片的超导区, 为下一步研究拓扑超导电性创造条件.借助四引线电输运测量实验, 在0.25 K的低温下看到了超流现象, 表明沉积在Bi₂Te₃表面的厚度小于20 nm的颗粒化铅膜能够诱导邻近效应, 并且使大片Bi₂Te₃超导. 关键词： 超导邻近效应 S-N-S结 拓扑绝缘体     

Comparative Study of Tribological Properties of Polyphenylene Sulfide (PPS), Polyethersulfone (PES), and Polysulfone (PSU)

The tribological properties of polyphenylene sulfide (PPS), polyethersulfone (PES) and polysulfone (PSU), which have similar molecular structures, were investigated using an end-face contact tribometer and a reciprocating tribometer. The thermomechanical behavior of the polymers was analyzed using dynamic mechanical analysis (DMA). PPS exhibited a maximum friction coefficient with increasing load and sliding speed, while the friction coefficients of PES and PSU decreased only slightly. The wear rate of PPS was much lower than that of PES and PSU under high loads and speeds. It is suggested that the main factors influencing the friction and wear properties of the neat polymers are their condensed state and heat resistance. Amorphous PES and PSU showed liquid-like behavior and very low friction when the frictional surface was in the molten-flow state. The macromolecular crystals of crystallizable PPS give it some solid-like behavior and load-carrying capacity; hence PPS exhibited lower wear than PES and PSU.     

Effect of Surface Structure of Nano-CaCO3 Particles on Mechanical and Rheological Properties of PVC Composites

To study the effect of different surface structures on resultant mechanical and rheological properties, nano-CaCO₃ particles were treated with isopropyl tri-stearyl titanate (H928), isopropyl tri-(dodecylbenz-enesulfonyl) titanate (JN198), and isopropyl tri-(dioctylpyrophosphato) titanate (JN114). Scanning electron microscopy (SEM) and dynamic mechanic analysis (DMA), carried out to characterize the effective interfacial interaction between the nano-CaCO₃ particles and a poly(vinyl chloride) (PVC) matrix, indicated that JN114 treated nano-CaCO₃ particles had the strongest interfacial interaction with a PVC matrix, while H928 treated nano-CaCO₃ had the weakest. The rheological and mechanical properties of PVC/nano-CaCO₃ composites were investigated as a function of surface structure and filler volume fraction. The tensile yield stress and elongation at break decreased with the increasing of calcium carbonate content while tensile modulus increased. PVC filled with JN114 treated nano-CaCO₃ had the highest tensile modulus and tensile yield stress, while those filled with H928 treated nano-CaCO₃ had the highest elongation at break at the same filler content. The impact strength of PVC/nano-CaCO₃ composites increased with the increasing of CaCO₃ content, and PVC composites filled with JN198 treated nano-CaCO₃ particle had a higher impact strength than those with JN114 or H928 treated, with the value reaching 23.9 ± 0.7 kJ/m² at 11 vol% CaCO₃, four times as high as that of pure PVC. Rheological properties indicated that a suitable interfacial interaction and a good dispersion of inorganic filler in a PVC matrix could reduce the viscosity of PVC/nano-CaCO₃ composites. The interfacial interaction was quantitatively characterized by semiempirical parameters calculated from the tensile strength of PVC/nano-CaCO₃ composites to confirm the results from the SEM and DMA experiments.     

Preparation and Characterization of Isotactic Polypropylene Reinforced with Hydroxyapatite Nanorods

Isotactic polypropylene (PP) composites filled with hydroxyapatite nanorods (nHAs) were fabricated using a melt compounding process. The effects of nHA additions on the structure, thermal, and mechanical properties as well as bioactivity of PP were investigated. Wide-angle X-ray diffraction and differential scanning calorimetry results showed that PP crystallized exclusively in the α-form when adding nHAs. Dynamic mechanical analysis showed that nHAs enhanced the storage modulus of PP. Mechanical measurements showed that nHAs stiffened and reinforced PP but reduced its tensile ductility and impact strength considerably. Furthermore, the PP/nHA nanocomposites were found to exhibit excellent bioactivity upon immersion in a simulated body fluid solution. This was attributed to the formation of apatite mineral crystals on the nanocomposite surfaces as revealed by scanning electron microscopy and energy dispersive X-ray analysis.     

Preparation,Characterization, and Humidity-Control Performance of Organobentonite/Sodium Polyacrylate Mortar

Organobentonite (OBT)/sodium polyacrylate (PAAS) composite material was prepared. The OBT/PAAS humidity-control cement-based mortars were prepared by mixing OBT/PAAS in mortar. Its morphology and structure were characterized by environmental scanning electron microscope (ESEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and the Brunauer-Emmett-Teller (BET) method. The results showed that the morphology and humidity-control capacity of OBT/PAAS mortar are superior to those of the original mortar. The OBT/PAAS mortar had larger pore specific surface area and larger pore volume, corresponding to the most probable pore diameter, than that of mortar. There was no chemical reaction between mortar and OBT/PAAS and there was no new crystal structure generated. The prepared, solidified OBT-PAAS mortar can maintain humidity in a desiccator at 38～62 RH%.     

Improving the precision of fluorescence lifetime measurement using a streak camera

Streak camera has high temporal resolution and high sensitivity, and is a powerful tool in biomedical study to measure fluorescence lifetime and perform fluorescence lifetime imaging. However, nonuniformity of the gain in the streak tube and nonlinearity of the sweeping speed limit the precision of fluorescence lifetime measurement, particularly when fluorescence lifetimes are short. We have constructed a two-photon excitation fluorescence lifetime measurement system that is based on a synchroscan streak camera and have developed accordingly a method to correct the effect of gain nonuniformity and nonlinearity of sweeping speed on the measurement precision. A continuous-wave laser of high stability is used to calibrate the gain of the streak camera, and a Fabry-Perot etalon is used to calibrate the nonlinearity of the sweeping speed. Fitting algorithms are used to correct the gain of the streak camera and nonlinearity of the sweeping speed respectively, which significantly improves the measurement precision of the system, as characterized through the fluorescence lifetime of the short-lived fluorescence dye, Rose Bengal. Experimental results show that the measurement fluctuation of the lifetime has been improved from more than 10% to 2% after correcting the effects of gain nonuniformity and sweeping speed nonlinearity.     

Zirconium-doped hybrid films patterned by soft lithography for distributed-feedback lasers

Zirconium (Zr)-doped hybrid films containing Rhodamine 6G (Rh6G) were prepared by spin-coating on glass substrates with different Zr–Si molar ratio. Second-order distributed-feedback (DFB) resonators with large surface-relief modulation depth over 160 nm could be fabricated by soft lithographic technique using a polydimethylsiloxane (PDMS) replica. Optically pumped by a pulsed frequency-doubled Q-switched Nd:YAG laser, the emission wavelength of the DFB-lasers can be tuned over 16 nm by changing the grating period. With the optimization of the Zr–Si molar ratio, low laser threshold of 3 μJ/mm² was obtained.     

Optical pumping of nuclear spin magnetization in GaAs/AlAs quantum wells of variable electron density

We report the use of time-resolved Faraday rotation to induce and probe the polarization of nuclear spins within a set of quantum wells with varying background electron density. The electron density was controlled over a broad range by making use of structures of mixed type-I/type-II GaAs/AlAs quantum wells that spatially separate photoexcited electron–hole pairs. We find that the optically detected nuclear magnetic field decreases quasi-monotonically with increasing electron density. The likely factors responsible for this behavior are increased electron spin-lattice relaxation, increased electron spin delocalization, and dilution of the electron spin polarization.     

The transition form factors for semi-leptonic weak decays of J/ψ in QCD sum rules

Within the standard model, we investigate the semi-leptonic weak decays of J/ψ. The various form factors of J/ψ making the transition to a single charmed meson (D^(*) _(d,s)) are studied in the framework of QCD sum rules. These form factors fully determine the rates of the weak semi-leptonic decays of J/ψ and provide valuable information on non-perturbative QCD effects. Our results indicate that the decay rate of the semi-leptonic weak decay mode J/ψ→D^(*)- _s+e⁺+ν_e is at the order of 10^-10. PACS 13.20.Gd; 13.25.Gv; 11.55.Hx     

<Emphasis Type="Italic">In situ</Emphasis> X-ray diffraction study of structural evaluation in Fe<Subscript>73</Subscript>Cu<Subscript>1.5</Subscript>Nd<Subscript>3</Subscript>Si<Subscript>13.5</Subscript>B<Subscript>9</Subscript> amorphous alloy at high temperature

The thermodynamics structural relaxation of Fe₇₃Cu_1.5Nd₃Si_13.5B₉ amorphous alloy from room temperature to 400°C has been investigated by measuring the structure factor with in situ X-ray diffraction. The structural information of the atomic configuration such as radial distribution function (RDF) and neighbor atomic distance was gained by Fourier transformation. The research result shows that the amorphous structure remains stable in the temperature range of 30 to 400°C but exhibits distinct changes in local atomic configuration with the increase of temperature. The quantitative determination of the neighbor atomic distance suggests that the degree of short-range order changes by the temperature altering the second nearest neighbor local atomic configuration of the amorphous when structural relaxation occurs. Supported by the Natural Science Foundation of Hebei Province of China (Grant No. A2007000296), the National Natural Science Foundation of China (Grant No. 50731005), SKPBRC (Grant Nos. 2007CB616915 and 2006CB605201), and PCSIRT (Grant No. IRT0650)