米子银花的分类学鉴定与质量分析

目的鉴定米子银花的品种及评价其质量。方法通过性状鉴定、产地追踪、标本查阅和原植物鉴定确定米子银花的品种,通过主要有效成分的含量测定和体外抑菌试验研究,结合药材性状进行品质评价。结果米子银花品种为淡红忍冬,其主要有效成分含量在种内的差异很大,并对其优良居群进行了抑菌作用研究。结论有助于米子银花的利用和深入研究。

米子银花挥发油成分分析

目的分析米子银花挥发油化学成分。方法采用气相色谱-质谱联用(GC-MS)法,WILLEY138.L谱库自动检索。结果通过计算机自动检索,共鉴定出28个组分,并用面积归一化法计算出各组分的相对百分含量。结论为米子银花的品质评价提供参考。

路径积分与费米子行列式

本文利用路径积分的方法计算1+1维弯曲时空中 QCD_2模型与手征杂化袋模型中的费米子行列式,给出了有效拉氏量,在 QCD_2中矢量玻色子获得质量,同时存在着规范场与背景引力的相互作用,在手征杂化袋中,W-Z-W 项很自然地就是手征转动的 Jacobian。

Green synthesis of MIL⁃101/Au composite particles and their sensitivity to Raman detection of thiram

Metal⁃organic framework(MOF)MIL⁃101 and surface plasmon polariton(SPP)supported gold nanoparti⁃cles(Au NPs)hybrid systems were developed as a highly sensitive and reproducible surface⁃enhanced Raman scat⁃tering(SERS)detection platform,in which a green electrostatic self⁃assembly technology was adopted to construct the substrate.In an aqueous solution,the electronegativity of the particles can be used to prepare the composite sub⁃strate without any surface modifier.Due to the enrichment capacity of MIL⁃101 and the electromagnetic enhance⁃ment from Au NPs,the well⁃designed MIL⁃101/Au composites possessed ultrahigh sensitivity with the detection limit of Rhodamine 6G(R6G)as low as 10^(-10) mol·L^(-1).Meanwhile,the substrate exhibits high stability,excellent reproduc⁃ibility,and recyclability.Additionally,the novel substrate can be explored for direct capture,and sensitively detect pesticide residues such as thiram.

Witnessing quantum phase transition in a non-Hermitian trapped ion system via quantum Fisher information

Quantum Fisher information is used to witness the quantum phase transition in a non-Hermitian trapped ion system with balanced gain and loss,from the viewpoint of quantum parameter estimation.We formulate a general non-unitary dynamic of any two-level non-Hermitian system in the form of state vector.The sudden change in the dynamics of quantum Fisher information occurs at an exceptional point characterizing quantum criticality.The dynamical behaviors of quantum Fisher information are classified into two different ways which depends on whether the system is located in symmetry unbroken or broken phase regimes.In the phase regime where parity and time reversal symmetry are unbroken,the oscillatory evolution of quantum Fisher information is presented,achieving better quantum measurement precision.In the broken phase regime,quantum Fisher information undergoes the monotonically decreasing behavior.The maximum value of quantum estimation precision is obtained at the exceptional point.It is found that the two distinct kinds of behaviors can be verified by quantum entropy and coherence.Utilizing quantum Fisher information to witness phase transition in the non-Hermitian system is emphasized.The results may have potential applications to non-Hermitian quantum information technology.

Highly Sensitive Photodetectors Based on WS_(2) Quantum Dots/GaAs Heterostructures

The performance of the photodetector is significantly impacted by the inherent surface faults in GaAs nanowires(NWs).We combined three-dimensional(3D)gallium arsenide nanowires with zero-dimensional(0D)WS_(2) quantum dot(QDs)materials in a simple and convenient way to form a heterogeneous structure.Various performance enhancements have been realized through the formation of typeⅡenergy bands in heterostructures,opening up new research directions for the future development of photodetector devices.This work successfully fabricated a high-sensitivity photodetector based on WS_(2)QDs/GaAs NWs heterostructure.Under 660 nm laser excitation,the photodetector exhibits a responsivity of 368.07 A/W,a detectivity of 2.7×10^(12)Jones,an external quantum efficiency of 6.47×10^(2)%,a low-noise equivalent power of 2.27×10^(-17)W·Hz^(-1/2),a response time of 0.3 s,and a recovery time of 2.12 s.This study provides a new solution for the preparation of high-performance GaAs detectors and promotes the development of optoelectronic devices for GaAs NWs.

Enhancing zinc storage performance of Mn_(3)O_(4)cathode through Ag-doping and-crosslinking dual-modification strategy

Octahedral Mn_(3)O_(4)nanoparticles with an Ag-doping and nanoporous Ag(NPS)framework was simply fabricated through an alloying-etching engineering.The dual-modified Mn_(3)O_(4)(denoted as Ag−Mn_(3)O_(4)/NPS)consists of Ag-doped Mn_(3)O_(4)nanoparticles crosslinked with three dimensional nanoporous Ag framework.The incorporated Ag dopant is effective in improving the intrinsic ionic and electronic conductivities of Mn_(3)O_(4),while the NPS framework is introduced to improve the electron/mass transfer across the entire electrode.Profiting from the dual-modification strategy,the Ag−Mn_(3)O_(4)/NPS exhibits admirable rate capability and cycling stability.A high reversible capacity of 88.7 mA·h/g can still be retained for over 1000 cycles at a current density of 1 A/g.Moreover,a series of ex-situ experimental techniques indicate that for Ag−Mn_(3)O_(4)/NPS electrode during the zinc ion storage,Mn_(3)O_(4)is electrochemically oxidized into various MnOx(e.g.,Mn_(2)O_(3),MnO2)species in the initial charging,and the subsequent battery reaction is actually the intercalation/deintercalation of H+and Zn2+into MnOx.

Nitrogen⁃doped 3D graphene⁃carbon nanotube network for efficient lithium storage

A 3D nitrogen⁃doped graphene/multi⁃walled carbon nanotube(CS⁃GO⁃NCNT)crosslinked network mate⁃rial was successfully synthesized utilizing chitosan and melamine as carbon and nitrogen sources,concomitant with the incorporation of multi⁃wall carbon nanotubes and employing freeze drying technology.The material amalgamates the merits of 1D/2D hybrid carbon materials,wherein 1D carbon nanotubes confer robustness and expedited elec⁃tron transport pathways,while 2D graphene sheets facilitate rapid ion migration.Furthermore,the introduction of nitrogen heteroatoms serves to furnish additional active sites for lithium storage.When served as an anode material for lithium⁃ion batteries,the CS⁃GO⁃NCNT electrode delivered a reversible capacity surpassing 500 mAh·g^(-1),mark⁃edly outperforming commercial graphite anodes.Even after 300 cycles at a high current density of 1 A·g^(-1),it remained a reversible capacity of up to 268 mAh·g^(-1).

Formation mechanism of nanopores in dense films of anodic alumina

Constant-current anodization of pure aluminum was carried out in non-corrosive capacitor working electrolytes to study the formation mechanism of nanopores in the anodic oxide films.Through comparative experiments,nanopores are found in the anodic films formed in the electrolytes after high-temperature storage(HTS)at 130°C for 240 h.A comparison of the voltage-time curves suggests that the formation of nanopores results from the decrease in formation efficiency of anodic oxide films rather than the corrosion of the electrolytes.FT-IR and UV spectra analysis shows that carboxylate and ethylene glycol in electrolytes can easily react by esterification at high temperatures.Combining the electronic current theory and oxygen bubble mold effect,the change in electrolyte composition could increase the electronic current in the anodizing process.The electronic current decreases the formation efficiency of anodic oxide films,and oxygen bubbles accompanying electronic current lead to the formation of nanopores in the dense films.The continuous electronic current and oxygen bubbles are the prerequisites for the formation of porous anodic oxides rather than the traditional field-assisted dissolution model.

Electrodeposition and corrosion resistance of Ni-P-TiN composite coating on AZ91D magnesium alloy

In order to improve the corrosion resistance and microhardness of AZ91D magnesium alloy, TiN nanoparticles were addedto fabricate Ni-P-TiN composite coating by electrodeposition. The surface, cross-section morphology and composition wereexamined using SEM, EDS and XRD, and the corrosion resistance was checked by electrochemical technology. The results indicatethat TiN nanoparticles were doped successfully in the Ni-P matrix after a series of complex pretreatments including activation, zincimmersion and pre-electroplating, which enhances the stability of magnesium alloy in electrolyte and the adhesion betweenmagnesium alloy and composite coating. The microhardness of the Ni-P coating increases dramatically by adding TiN nanoparticlesand subsequent heat treatment. The corrosion experimental results indicate that the corrosion resistance of Ni-P-TiN compositecoating is much higher than that of uncoated AZ91D magnesium alloy and similar with Ni-P coating in short immersion time.However, TiN nanoparticles play a significant role in long-term corrosion resistance of composite coatings.

Preparation and Fluorescence Properties of Co-doped Nanocomposite Film Based on Supra Molecular Structure

A novel materials design procedure based on the co-doping of metal nanoparticle and azo dye compound （MNPADC） is developed to improve the properties of functional molecules. The synthesized materials were characterized by transmission electron micrograph （TEM）, ultraviolet-visible absorption spectra （UV-Vis） and fluorescence spectra （FS）. It was found that the fluorescence intensity of methyl orange （MO） was enhanced by 5 times in the aqueous composite system doped with silver nanoparticles whereas it was reduced by 15% and 20% in composite films with co-mixing and coating structures, respectively. The results indicate that the properties of functional molecules can be greatly improved in composite film with supra molecular structure and that the procedure presented here is effective.

Adsorption behavior and adsorption mechanism of Cu(Ⅱ) ions on amino-functionalized magnetic nanoparticles

Amino-functionalized magnetic nanoparticle （NH2-MNP） were prepared by a sol-gel approach. The adsorption behavior of Cu（II） ions on NH2-MNP was discussed systematically by batch experiments. The effects of initial Cu（II） ions concentration, time, pH and temperature were investigated. In kinetic studies, the pseudo-second-order model was successfully employed, and the pseudo-first-order model substantiated that Cu（II） adsorption on NH2-MNP was a diffusion-based process. Langmuir model and Dubinin-Radushkevich model （R2〉0.99） were more corresponded with the adsorption isotherm data of Cu（II） ions than Freundlich model. The adsorption capacity was increased with the increment of temperature and pH. NH2-MNP remains excellent Cu（II） recoveries after reusing five adsorption and desorption cycles, making NH2-MNP a promising candidate for repetitively removing heavy metal ions from environmental water samples. According to the results obtained from adsorption activation energy and thermodynamic studies, it can be inferred that the main adsorption mechanism between absorbent and Cu（II） ions is ion exchange-surface complexation.

Catalytic performance of cobalt oxide-supported gold-palladium nanocatalysts for the removal of toluene and o-xylene

Using the molten salt and polyvinyl alcohol-protected reduction method,we fabricated Co3O4 octahedron-supported Au-Pd（x（AuPdy）/Co3O4;x =（0.18,0.47,and 0.96） wt%;y（Pd/Au molar ratio） =1.85-1.97） nanocatalysts.The molten salt-derived Co3O4 sample possessed well-defined octahedral morphology,with an edge length of 300 nm.The Au-Pd nanoparticles,with sizes of 2.7-3.2 nm,were uniformly dispersed on the surface of Co3O4.The 0.96（AuPd1.92）/Co3O4 sample showed the highest catalytic activity for toluene and o-xylene oxidation,and the temperature required for achieving 90%conversion of toluene and o-xylene was 180 and 187 ℃,respectively,at a space velocity of 40000 mL/（g·h）.The high catalytic performance of Co3O4 octahedron-supported Au-Pd nanocatalysts was associated with the interaction between Au-Pd nanoparticles and Co3O4 and high concentration of adsorbed oxygen species.

Tribological effects of oxide based nanoparticles in lubricating oils

In order to enhance the tribological properties of lubricating oil, suitable surfactants such as Tween-20, Tween-60, Span-20 and Sodium sodecylbenzenesulfonate were selected and lubricating oils containing CeO2 and TiO2 nanoparticles were prepared. The morphology and size of CeO2 and TiO2 nanoparticles were examined with a transmission electron microscope （TEM）. The tribological properties of the oils were tested using an MRS-1J four-ball tribotester. The research results show that when the proportion by weight of CeO2 nanoparticles to TiO2 nanoparticles is 1：3, and the total weight fraction is 0.6%, the lubricating oil has optimal anti-wear and friction reducing properties. The addition of CeO2 nanoparticles reduces the required amount of TiO2 nanoparticles.

Preparation, Structures Nano TiO_2 Particles, and the properties of TiH_2 Coated with Nano TiO_2

The surface of Titanium Hydride (TiH 2) is coated by Nano Titanium Dioxide (TiO 2) particles prepared in both of methods of hydrolysis reaction of Ti(OC 4H 9) 4 and base precipitation reaction of Ti(SO 4) 2. TiH 2 coated with nano TiO 2 particles, in which there is an oxidation film on its surface, shown in the experiments, will obviously achieve good effects on releasing hydrogen slowly in high temperature. There are different structures and properties of TiH 2 coated by nano TiO 2 particles prepared in different ways in high temperature, which can influence on releasing hydrogen.

Synthesis,characterization and photocatalytic performance of rod-shaped Pt/PbWO_4 composite microcrystals

Rod-shaped PbW O4 microcrystals of length 1 μm were fabricated by a hydrothermal route and subsequent calcination. Pt nanoparticles（NPs） of different contents（0.5 wt%,1 wt% and 2 wt%） were subsequently deposited on the PbW O4 microcrystals,producing robust Pt/PbW O4 composite microcrystals. The PbW O4 microcrystals and Pt/PbW O4 photocatalysts were characterized by X-ray diffraction,N2 sorption measurements,scanning electron microscopy,transmission electron microscopy,and X-ray photoelectron,photoluminescence,Fourier-transform infrared,and ultraviolet-visible diffuse reflectance spectroscopies. The photocatalytic performances of the catalysts were evaluated by the consecutive photocatalytic degradation of acid orange II dye. The Pt/PbW O4 composite microcrystals exhibited high photocatalytic activity and stability. The deposition of Pt NPs produced surface plasmon resonance（SPR）,which induced a large visible light absorption. A Pt NP content of 1-2 wt% resulted in an ~2 times increase in photocatalytic activity,compared with the activity of Pt/PbW O4. The crystal structure and high crystallinity of PbW O4 resulted in its favorable photocatalytic property,and the SPR effect of the Pt NPs promoted visible light harvesting. The Pt NPs also enhanced the separation of photo-generated electrons and holes,which further promoted the photocatalytic reaction.

Effect of electron beam irradiation on multi-walled carbon nanotubes

Multi-walled carbon nanotubes （MWCNTs） were irradiated with focused electron beams in a transmission electron microscope at room temperature. The results showed that carbon nanotubes had no obvious structural damages but only shell bending under 100 keV electron beam irradiation. However, when the electron energy increased to 200 keV, the nanotubes were damaged and amorphization, pits and gaps were detected. Furthermore, generating of carbon onions and welding between two MWCNTs occurred under 200 keV electron irradiation. It was easy to destroy the MWCNTs as the electron beams exceeded the displacement threshold energy that was calculated to be 83-110 keV. Conversely, the energy of electron beams below the threshold energy was not able to damage the tubes. The damage mechanism is sputtering and atom displacement.

Ni@Pd core-shell nanoparticles supported on a metal-organic framework as highly efficient catalysts for nitroarenes reduction

Ni@Pd core-shell nanoparticles with a mean particle size of 8–9 nm were prepared by solvothermal reduction of bivalent nickel and palladium in oleylamine and trioctylphosphine.Subsequently,the first-ever deposition of Ni@Pd core-shell nanoparticles having different compositions on a metal-organic framework（MIL-101）was accomplished by wet impregnation in n-hexane.The Ni@Pd/MIL-101 materials were characterized by powder X-ray diffraction,Fourier transform infrared spectroscopy,transmission electron microscopy,and energy-dispersive X-ray spectroscopy and also investigated as catalysts for the hydrogenation of nitrobenzene under mild reaction conditions.At 30 °C and 0.1 MPa of H2 pressure,the Ni@Pd/MIL-101 gives a TOF as high as 375 h–1 for the hydrogenation of nitrobenzene and is applicable to a wide range of substituted nitroarenes.The exceptional performance of this catalyst is believed to result from the significant Ni-Pd interaction in the core-shell structure,together with promotion of the conversions of aromatics by uncoordinated Lewis acidic Cr sites on the MIL-101 support.

Isolation and Structural Analysis of DRE-Binding Transcription Factor from Maize (Zea mays L.)

Dehydration-responsive element-binding (DREB) proteins specifically binding with dehydration-responsive element (DRE) have been identified as a kind of important transcription activator of plants under drought, high salt and cold stress. The conserved amino, acid residues of Val (14th residue) and Glu (19th residue) in AP2/EREBP domain of DREB1A have been identified to be two key points in determining the binding ability of DREB gene with DRE element. Using the yeast one-hybrid system, we isolated one maize DREB gene named maDREB1 by screening cDNA library. Trans-activation experiment in yeast reporter strain demonstrated that maDREB1 protein could function as a DREB transcription factor activating target gene expression by specifically binding to the DRE cis-element. To assess the functional significance of these two residues in maDREB1, the V14 and E19 were substituted individually or doubly by Ala and Asp. Point mutation analysis showed that V14 substitution made significant loss of binding ability with DRE element, while point mutation of E19 had less effect. If the substitution happened simultaneously to these two residues, it would lead to great loss of the ability of binding with DRE element. It suggested that V14 and E19 were both important in protein-DNA interacting in maDREB1, though 14V was more essential. The copy number and expression pattern of maDREB1 was discussed.