Metal-organic supramolecular nanoarchitectures by Ru(Ⅱ)bis-(terpyridine)-bridged pillar[5]arene dimers with triphenylamine

A metal-organic photoinduced electron transfer(PET) supramolecular nanoarchitecture comprised of Ru(Ⅱ) bis(terpyridine)-modified pillar[5]arene(electron acceptor) and triazole triphenylamine amyl cyanide(electron donor) has been designed and constructed.Through the comparison of diverse solvents and acceptors,the two conditions,i.e.,modification of pillar[5]arene to donor and weak polar solvent are benefit for the occurrence of "efficient PET" because of shorter D-A distance in the presence of pillar[5]arene.Crucially,the fluorescence and PET process of the supramolecular assembly could be further modulated by solvent conversion and another competitive guest.The study provides a supramolecular method to design and construct tunable PET systems and PET-based smart materials.     

Use of sol–gels as solid matrixes for laser-induced breakdown spectroscopy

Silicon, zirconium and aluminum sol–gels were investigated as suitable starting materials for tunable matrix calibration standards for laser-induced breakdown spectroscopy. A fast and simple preparation method was developed, using aluminum i-propoxide as the precursor in the sol–gel synthesis, which allows one to quickly prepare solid calibration standards offering very homogenous analyte distribution in the matrix, low optical spectral background, as well as reproducible behavior towards laser ablation and vaporization. The surface of the calibration targets and the morphology of the ablation craters were examined by optical and scanning electron microscopy, and the material ejection process was observed by shadowgraph imaging. Low μg/g detection limits and 4–15% relative standard deviation were measured by laser induced breakdown spectroscopy for Pb, Cr and Be used as internal standards.     

中红外波长可调谐激光器及其在葡萄糖检测中的应用

提出一种激光器发射波长和功率控制与稳定的方法,研制出波长范围在9.19~9.77 μm,可应用于葡萄糖检测的中红外波长可调谐CO₂激光器,发射光谱半波宽度为4 cm-1,光谱分辨率达到2.7×104,最高功率为800 mW,功率波动性＜0.8%。根据葡萄糖在中红外指纹谱波段的吸收特性,选择激光器发射光谱9R和9P带的1 081,1 076,1 051,1 041和1 037 cm-1作为测量波长,利用ATR传感器测量了PBS溶液中葡萄糖浓度。结果表明五个测量波长下的吸收度与葡萄糖浓度呈现良好的线性关系(R2＞0.99,SD＜0.000 4,P＜0.000 1),且该波长可调谐激光光谱测量系统的灵敏度是传统FTIR光谱仪的4倍左右。     

A novel tunable cascaded IIR microwave photonic filter

A new tunable cascaded infinite impulse response (IIR) microwave photonic filter is presented, based on a novel configuration in which a semiconductor optical amplifier (SOA) is inserted between two active recirculating delay line (RDL) loops. Due to wavelength conversion with cross-gain modulation (XGM) in SOA, interferences between light beams traveling different paths are canceled, ensuring a stable transmission. By employing this configuration, a cascaded IIR microwave photonic filter is firstly achieved. The free spectral range (FSR) and the Q factor are both increased significantly by adopting “vernier effect” technique in the IIR filter. The structure is also tunable by adjusting the length of one RDL loop.     

Heterogeneous Electrospinning Nanofiber Membranes with pH-regulated Ion Gating for Tunable Osmotic Power Harvesting

Biological ion channels existing in organisms are critical for many biological processes. Inspired by biological ion channels, the heterogeneous electrospinning nanofiber membranes (HENM) with functional ion channels are constructed by electrospinning technology. The HENM successfully realizes ion-gating effects, which can be used for tunable energy conversions. Introduction of pyridine and carboxylic acid groups into the HENM plays an important role in generating unique and stable ion transport behaviors, in which gates become alternative states of open and close, responding to symmetric/asymmetric pH stimulations. Then we used the HENM to convert osmotic energy into electric energy which reach a maximum value up to 12.34 W m⁻² and the output power density of HENM-based system could be regulated by ion-gating effects. The properties of the HENM provide widespread potentials in application of smart nanofluidic devices, energy conversion, and water treatment.     

Tunable emission of AgIn5S8 and ZnAgIn5S8 nanocrystals: electrosynthesis,characterization and optical application

Ternary AgIn₅S₈ (AIS) and quaternary ZnAgIn₅S₈-alloy (ZAIS) nanocrystals, stabilized by L-glutathione, were produced by a clean and eco-friendly electrochemical method, eliminating the need of reducing agents. AIS-GSH colloidal solution was obtained by constant current electrolysis (i = 30 mA) in cavity cell. S^2? ions (0.051 mmol) were generated into a graphite powder macroelectrode, reacting in the intermediate compartment of the cell containing Ag⁺/In³⁺ aqueous solution at different ratios (0.5, 0.28, 0.18, and 0.14), and 0.025 mmol/L^?1 glutathione (GSH). ZAIS-GSH NCs were synthesized in the same cavity cell containing the previously prepared AIS-GSH solution. A paired electrolysis (i = 30 mA) was used for simultaneous production of Zn²⁺ and S^2? (Zn⁰ sacrificial anode and graphite powder macroelectrode/S⁰ cathode). The electrochemical method promoted a high reproducibility and efficient luminescence in the preparations of NCs. The sizes of the AIS-GSH and ZAIS-GSH nanoparticles were determined by HRTM (3.4 and 4.0 nm, respectively), and quantum yields reaching 16% (AIS-GSH, Ag⁺/In³⁺ = 0.18). The spectrophotometric characterization showed that Ag⁺/In³⁺ ratio can be used for the tuning of the AIS-GSH nanoparticle emission wavelength, which is associated to electronic defects introduced in the NCs lattice. XRD/EDS analysis of ZAIS-GSH nanoparticles point out to Zn²⁺ ion-exchange into the AIS-GSH lattice. XPS analysis was carried out at different etching levels of the ZAIS nanocrystals surface, making possible to identify the 2p Zn doublet signal, indicating two different Zn²⁺ sites in the alloy structure. Time-resolved spectroscopy measurements/decay curves were carried out to evaluate the effect of silver amount on radioactive and non-radioactive terms. Additionally, the AIS-GSH and ZAIS-GSH photoluminescence and stability were used to produce the active parts of commercial white LEDs, and modulate the colour perception from the respective emission bands.     

高强度黏附力可调控的水下超疏油铜网膜的制备

通过调控在铜网表面电镀铜的时间制备了一系列具有不同黏附性的水下超疏油铜网表面,并进一步在铜网表面包覆一层磷酸二氢铝(ADP)纳米涂层.在保持铜网表面原有微结构形貌不变的前提下,ADP纳米涂层有效增强了铜网表面微纳结构的机械强度及表面浸润特征的稳定性.研究结果表明,铜网表面不同微结构赋予了表面与油滴之间不同的接触状态,从而产生了不同的黏附性; ADP包覆后铜网表面微结构机械强度的增加,得益于包覆后表面微观结构在外力作用下最大应力和最大横向位移的明显降低.     

对当量为1的预混乙烯/氧气/氩气火焰的实验研究

A comprehensive experimental study of the premixed ethylene/oxygen/argon flame at 2.667 kPa with a stoichiometric equivalence ratio (φ=1) was performed with the tunable synchrotron photoionization and molecular-beam sampling mass spectrometry techniques. The isomers of most observed species in the flame were unambiguously identified by measurements of the photoionization efficiency spectra, e.g. C3H4, C2H4O and C4H4. The mole fraction profiles of species up to C7H8 were measured by scanning the burner position at the selected photon energies near ionization thresholds, and the flame temperature profile was obtained by using Pt/Pt-13%Rh thermocouple. Compared with the previous studies, a lot of new flame species:C3H2, C3H3, C3H5, C2H6O, C4H2, C4H4, C4H6, C3H4O, C3H6O, C3H8O, C5H6, C4H8O and C7H8, were observed. A series of free radicals in the flame are detected to be CH3, C2H3, C2H5, HCO, C3H3 and C3H5.Based on the experimental work, a reduced reaction mechanism was developed including 40 species and 223 reactions. Modeling and measurements agree well for the major species and most intermediates. A detailed kinetic model is desired for this flame.     

ZnxCd1-xS纳米线的可控合成及其可调的光学性质

采用简单的气相沉积法,合成了不同组成的Zn_xCd_1-xS (0< x <1)纳米线. 利用扫描电子显微镜、透射电子显微镜和电子能谱研究了所制得的纳米线的表面形貌和组成. 该方法以Au为催化剂,简单控制起始物质的相对用量和沉积温度,可以获得可控的Zn/Cd 比例. X射线衍射结果表明所制得的Zn_xCd_1-xS纳米线具有纤维锌矿的单晶结构. 根据制得纳米线的表面形貌讨论了纳米线可能的生长机理为“底部生长”机理. 利用拉曼光谱和光致发光光谱研究了Zn_xCd_1-xS纳米线的光学性质,其纵向光学(LO)声子的拉曼位移频率随着组成的变化在ZnS和CdS的拉曼位移频率之间连续变化. 光致发光光谱中同时存在带边发光和缺陷发光. Zn_xCd_1-xS纳米线的带间跃迁的频率可随着组成的调节而调节,纳米线的禁带宽度介于ZnS (3.63 eV)和CdS (2.41 eV)的禁带宽度之间.