Ba0.6Sr0.4TiO3/聚偏氟乙烯-聚甲基丙烯酸甲酯复合材料的制备及其介电性能

采用流延热压工艺制备Ba_0.6Sr_0.4TiO₃(BST)/聚偏氟乙烯(PVDF)?聚甲基丙烯酸甲酯(PMMA)复合薄膜,研究了PMMA含量对复合材料微观组织结构和介电性能的影响规律。结果表明,BST相能够均匀分散在聚合物基体中,归因于PMMA与PVDF良好的相容性,2种聚合物之间的界面不分明;随着PMMA含量的增加,复合材料的介电常数先降低后升高,耐击穿强度和介电可调性先增加后减少。PMMA含量(体积分数)为15%的BST/PVDF?PMMA₁₅复合材料的综合性能最佳:介电常数为23.2,介电损耗为0.07,耐击穿强度为1412 kV·cm^-1,在550 kV·cm^-1偏压场下,介电可调性为26.2%。     

InAs Quantum Dots On (001) GaAs Substrate with two Groups of Different Sizes Under Arsenic Shutter Closed Condition

The effect of temperature on the self-assembled InAs quantum dots (QDs) grown on GaAs substrate under arsenic shutter closed condition has been studied. From atomic force microscopy (AFM), it was found that the size of InAs dots exhibited a transition from single-sized uniformly distributed quantum dot (QD) at a growth temperature of 490°C to two groups of different sizes QDs at 510°C. Since the desorption rate of In atoms from the substrate surface is very high at 510°C, a growth model is proposed that attributes the larger sized QDs to the enhanced capture of desorbed In atoms by a local random protrusion which initiates a regenerative capture and growth process and leads to explosive growth.     

Boron nitride nanosheet-assisted matrix solid-phase dispersion microextraction of alkaloids from lotus plumule by high-performance liquid chromatography coupled with ultraviolet detection and ion mobility quadrupole time-of-flight mass spectrometry

A boron nitride nanosheet (BNNS)-assisted matrix solid-phase dispersion method was established to microextract alkaloids from medicinal plants. The target compounds were identified by high-performance liquid chromatography coupled with ultraviolet detection and ion mobility quadrupole time-of-flight mass spectrometry. During the experimental process, several important parameters, including the type of dispersant, the amount of dispersant, the grinding time, and the type of elution solvent, were optimized. Finally, the BNNSs were chosen as the best dispersant, and their microcosmic morphologies were identified by scanning electron microscopy and transmission electron microscopy. Because of the special property of BNNSs, the cost of this experiment was greatly reduced, especially in elution volume, sample amount (50 mg), and extraction time (2 min). Under the best conditions, 50 mg of sample powder was dispersed with 50 mg of BNNSs, the grinding time was 120 s, the mixed powder was eluted with 200 μL of methanol, and good linearity (r² > 0.9993) and satisfactory recoveries (80–100%) were obtained. The inter- and intraday precisions were acceptable, with RSDs lower than 2.01 and 4.84%, respectively. The limits of detection ranged from 2.54 to 15.00 ng/mL, and the limits of quantitation were 8.47 to 50.00 ng/mL. The proposed method was successfully applied for the determination of liensinine, isoliensinine, and neferine in lotus plumule.     

The Influence of B<Subscript>2</Subscript>H<Subscript>6</Subscript> on the Growth of Silicon Nanowire

The un-doped and boron-doped silicon nanowires (SiNWs) were grown via vapor–liquid–solid (VLS) mechanism by low pressure chemical deposition (LPCVD). The diameters of un-doped and boron-doped SiNWs varied from 18.5 to 75.3 nm and 26.6 to 66.1 nm, respectively. The critical growth temperature of boron-doped SiNWs is 10°C lower than that of un-doped ones and the diameters of the boron-doped SiNWs is always larger than that of the un-doped ones under different growth temperatures. This is because that the introduction of diborane enhanced the dissociation of SiH₄ which determines the growth process of SiNW. A growth process of silicon nanowire is proposed to describe the influence of B₂H₆.     

The two-phase amphiphilic preconcentration based on surfactants to enrich phenolic compounds from diluted plant extracts and rat urine by micellar electrokinetic chromatography

A novel technology by two-phase amphiphilic preconcentration based on surfactants was established for enriching phenolic compounds by micellar electrokinetic chromatography (MEKC). The cationic surfactant cetyltrimethylammonium chloride (CTAC) was combined with the anionic analytes that existed in the sample solution before injection. The boundary was formed between CTAC and sodium dodecyl sulfate (SDS) in the background solution when the sample solution was injected into the capillary, where the analytes bound inside micelles were released due to the stronger electrostatic force between SDS and CTAC. This procedure accelerated the separation of analytes from CTAC and greatly improved the enrichment efficiency. The optimal conditions were obtained after a series of optimizations, and the sensitivity enrichment factors of the four analytes were in the range of 39–93 compared to typical injections in capillary zone electrophoresis. Good linearity for matrix-matched calibrations was established for all analytes with R² values of 0.9993–0.9997. The limits of detection (S/N = 3) for kaempferol, quercetin, salvianolic acid C, and salvianolic acid B were 0.0166, 0.0292, 0.0215, and 0.0195 µg/ml, respectively. The intracapillary RSDs of the analytes ranged from 0.8% to 1.3% for migration time and from 0.4% to 1.8% for peak areas. The developed method was successfully applied to the determination of phenolic compounds, the main compounds of Salvia miltiorrhiza Bge., and had been validated for the determination of spiked recoveries in rat urine.     

Cu对K-LaZrO2异丁醇合成催化剂的影响

采用X射线衍射(XRD)、程序升温脱附(TPD)、X射线光电子能谱(XPS)、傅里叶变换红外(FTIR)光谱技术及富集法考察了K-LaZrO₂和K-CuLaZrO₂催化剂结构、CO和H₂在锆基催化剂上的吸附行为及异丁醇合成活性的影响. 结果表明, 催化剂添加Cu后, 与Zr形成较好的固溶体, 促进了CuO的分散, 且抑制了ZrO₂结晶, 增强Cu-Zr相互作用, 提高了催化活性. CO-TPD结果显示, 引入Cu后, 催化剂表面CO吸附量明显增加, 有利于碳链增长; H₂-TPD结果显示, 与活性相关的低温脱附氢量也明显增加. 另外, FTIR及富集法结果发现, Cu的引入促进了表面C₁物种的形成, 增加了表面C₁物种含量, 促进了碳链增长, 明显改善了异丁醇的选择性. 在p=10.0 MPa, 空速(GHSV)=3000 h^-1, T=360℃, V(H₂)/V(CO)=1:1条件下,异丁醇选择性达到48.5%.     

Nonlocal hyperconcentration on entangled photons using photonic module system

Entanglement distribution will inevitably be affected by the channel and environment noise. Thus distillation of maximal entanglement nonlocally becomes a crucial goal in quantum information. Here we illustrate that maximal hyperentanglement on nonlocal photons could be distilled using the photonic module and cavity quantum electrodynamics, where the photons are simultaneously entangled in polarization and spatial-mode degrees of freedom. The construction of the photonic module in a photonic band-gap structure is presented, and the operation of the module is utilized to implement the photonic nondestructive parity checks on the two degrees of freedom. We first propose a hyperconcentration protocol using two identical partially hyperentangled initial states with unknown coefficients to distill a maximally hyperentangled state probabilistically, and further propose a protocol by the assistance of an ancillary single photon prepared according to the known coefficients of the initial state. In the two protocols, the total success probability can be improved greatly by introducing the iteration mechanism, and only one of the remote parties is required to perform the parity checks in each round of iteration. Estimates on the system requirements and recent experimental results indicate that our proposal is realizable with existing or near-further technologies.     

Hydrogenated amorphous silicon with substrate-dependent structure

Hydrogenated amorphous silicon (a-Si:H) thin films grown at 250°C on (1 0 0) crystalline substrate using plasma-enhanced chemical vapor deposition (PECVD) with SiH₄/H₂ gas flow ratio equal to 5/1 (sccm) are investigated by transmission electron microscopy. It is found that the thin film is totally amorphous when grown on a glass substrate. But when the substrate is changed to crystalline silicon, some crystalline grains are found embedded in the amorphous structure in certain regions even if the thickness of the film reaches 600 nm. It is suggested that the amorphous silicon film grown on a crystalline silicon substrate at a temperature of 250°C without heavy H₂ dilution is a mixed network of a small amount of crystalline silicon and the major portion of amorphous silicon.     

An InSb integrated photo-MOSFET fabricated by photo-enhanced chemical vapour deposition

A new output-controllable InSb infrared (i.r.) detector is proposed. The detector is fabricated by monolithically integrating an InSb p-n junction with an InSb p-channel enhancement mode metal oxide semiconductor field effect transistor (MOSFET). During operation, a photocurrent generated near the source junction is controllably switched to the drain terminal by a gate of the integrated MOSFET. The observed internal quantum efficiency in the on state is as high as 85%. Photocurrent on-off ratios are between 260 and 730, improving with increasing channel length. For longchannel devices, the photocurrent in the off state is limited by undesired leakage paths. The new structure can be used as an output-controllable i.r. detector.     

Silicon nanowires synthesized by vapor–liquid–solid growth on excimer laser annealed thin gold film

The fabrication of Si nanowires has been demonstrated using excimer laser annealed thin gold film as the catalyst and vapor–liquid–solid (VLS) growth. Au nanoparticles with mean diameters of 12, 13 and 15 nm were formed by excimer laser annealing (ELA) of Au film with thickness of 2.5, 5 and 10 nm, respectively. The results show that the silicon nanowires (SiNWs) with desired diameter can be obtained by controlling the Au film thickness and laser power density.