High loading LiFePO<Subscript>4</Subscript> on activated carbon fiber cloth as a high capacity cathode for Li-ion battery

The LiFePO₄/carbon fiber (LFP/CF) cathodes were prepared by using activated carbon fiber cloth as current collector in place of conventional Al foil. The electrochemical properties of LFP/CF electrodes were analyzed by the cyclic voltammetry and galvanostatic charge/discharge tests. The results indicate that the activated carbon fiber cloth with high specific surface area and high porosity makes the LFP/CF electrode that possesses higher mass loading of 18–21 mg cm^–2 and stronger redox reaction ability compared with Al foil-based electrode. The LFP/CF electrode shows excellent rate performance and cycle stability. At 0.1C, the discharge capacity is up to 190.1 mAh g^–1 that exceeds the theoretical capacity due to the combination effect of battery and capacitor. Furthermore, the LFP/CF electrode shows an initial capacity of 150.4 mAh g^–1 at 1C with a capacity retention of 74.7% after 425 cycles, which is higher than 62.4% for LFP/Al foil electrode, and an initial discharge capacity of 130 mAh g^–1 at 5C with a capacity retention of 61.5% after 370 cycles. But this composite electrode is not suitable for charging/discharging at higher rate as 10C due to too much mass loading.     

Ultrasensitive electrochemical biosensor for specific detection of DNA based on molecular beacon mediated circular strand displacement polymerization and hyperbranched rolling circle amplification

Using a cascade signal amplification strategy, an ultrasensitive electrochemical biosensor for specific detection of DNA based on molecular beacon (MB) mediated circular strand displacement polymerization (CSDP) and hyperbranched rolling circle amplification (HRCA) was proposed. The hybridization of MB probe to target DNA resulted in a conformational change of the MB and triggered the CSDP in the presence of bio-primer and Klenow fragment (KF exo⁻), leading to multiple biotin-tagged DNA duplex. Furthermore, the HRCA was implemented to product amounts of double-stranded DNA (ds-DNA) fragments using phi29 DNA polymerase via biotin-streptavidin interaction. After the product of HRCA binded numerous biotinylated detection probes, an ultrasensitive electrochemical readout by further employing the streptavidin-alkaline phosphatase. The proposed biosensor exhibited excellent detection sensitivity and specificity with a log-linear response to target DNA from 0.01 fM to 10 pM as low as 8.9 aM. The proposed method allowed DNA detection with simplicity, rapidness, low cost and high specificity, which might have the potential for application in clinical molecular diagnostics and environmental monitoring.     

ESR Studies on a Friedel‐Crafts Alkylation Reaction in [bmim]Cl‐AlCl3 Ionic Liquid

The paramagnetic complexes formed in Friedel‐Crafts alkylation reaction systems are invistigated by electron spin resonance (ESR) spectroscopy, in room temperature ionic liquids system 1‐butyl‐3‐methyl‐limidazolium chloride‐aluminium chloride ([bmim]Cl‐AlCl₃). The results indicate that ESR spectra observed are due to polycyclic aromatic radical cations formed from their parent hydrocarbons. ESR spectrum of spin adduct is obtained in an ionic liquid system composed of [bmim]Cl‐AlCl₃. In acidic solution the ¹⁴N hyperfine coupling constant of 4‐oxo‐TEMPO, 2.15 mT, is appreciably larger due to an adduct formed with AlCl₃.     

One‐Step Synthesis of Folic Acid Protected Gold Nanoparticles and Their Receptor‐Mediated Intracellular Uptake

We report here a facile method to obtain folic acid (FA)‐protected gold nanoparticles (Au NPs) by heating an aqueous solution of HAuCl₄/FA in which FA acts as both the reducing and stabilizing agent. The successful formation of FA‐protected Au NPs is demonstrated by UV/Vis spectroscopy, transmission electron microscopy (TEM), selected‐area electron diffraction (SAED), X‐ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FTIR). The intracellular uptake of these nanoparticles is facilitated by HeLa cells overexpressing the folate reporter, which itself is significantly inhibited by free FA in a competitive assay as quantified by inductively coupled plasma mass spectroscopy (ICP‐MS). This simple one‐step approach affords a new perspective for creating functional nanomaterials, and the resulting biocompatible, functional Au NPs may find some prospective applications in various biomedical fields.     

Energy transfer channels at the diffraction-anomaly in transparent gratings and applications in sensors

Diffraction anomaly corresponds to an energy re-distribution in the reflected and transmitted light beams and in different diffraction orders of a grating, which leads to sharp modulations on the transmission and reflection spectra. In gratings sitting on a transparent substrate, this portion of the energy is actually transferred to channels separated from the reflected and transmitted beams. These channels are based on multiple degenerated diffraction processes at the same wavelength as the diffraction anomaly. The spectroscopic response of these channels is sensitive to the change in the environmental refractive index and can be utilized in sensor devices.     

低温/高温复合超导磁体的研究进展

低温/高温复合超导体的研究是当前超导领域比较新的一个课题,文章介绍了低温/高温复合超导体的结构以及加工工艺,并结合相关数值模拟和实验结果对复合超导体电流分布、热传导性质、理论机理和稳定性研究等相关问题进行了讨论与探索。     

Crucial factors affecting the physicochemical properties of sol–gel produced Fe3O4@SiO2–NH2 core–shell nanomaterials

Multifunctional nanomaterials with task-specific physicochemical properties, especially core?Cshell nanostructures with Fe₃O₄ core and NH₂-functional shells (Fe₃O₄@SiO₂?CNH₂), have been extensively investigated as high-performance adsorbents, catalysts and catalyst supports; and in most cases the controllable sol?Cgel technique is the choice for fabrication of this kind of widely applied materials. Herein, we demonstrated that mono-dispersed and spherical Fe₃O₄@SiO₂?CNH₂ nanomaterials with magnetic response core, NH₂-functional shell structure can be facilely prepared by co-condensation of TEOS with APTMS using a versatile sol?Cgel process. It was shown that the proper usage of APTMS and appropriate pre-hydrolysis time of TEOS were crucial and key steps for formation of highly uniform and desirable amino loading Fe₃O₄@SiO₂?CNH₂ materials. The TEOS pre-hydrolysis and the critical time (around 90?min) before the addition of APTMS prove to be vital for uniform structure evolution, while the appropriate concentration of APTMS (~2.28?mmol?L^?1 in our system) leads to well-dispersed materials with relatively high loading of amino functionality. The as-prepared Fe₃O₄@SiO₂?CNH₂ magnetic nanoparticles prepared under optimum conditions possessing superparamagnetic behavior, uniform core?Cshell structure (~200?nm in diameter), relatively large BET surface area (~138?m²/g) and high incorporation of amino-functionality (~2.90?wt?%).     

A 2-dimensional gradual period photonic heterostructure possessing omnidirectional band gap in visible range made by holography

A 2-dimensional gradual period photonic heterostructure was made with holography by use of non-uniform swelling effect of dichromated gelatin during processing. In this structure, the symmetric point group of triangle lattice was debased to C_2V from C_6V. Theoretical analysis and experimental results show that omnidirectional band gap in visible range can be achieved with this kind of heterostructure made by low refractive index materials.     

Hydrolysis kinetics of silane coupling agents studied by near-infrared spectroscopy plus partial least squares model

Abstract

A method of Fourier transform near-infrared (FT-NIR) spectroscopy combined with partial least squares (PLS) model was successfully applied to investigate the hydrolysis kinetics of four kinds of silane coupling agents (phenyltriethoxysilane, vinyltriethoxysilane, 3-mercaptopropyltriethoxysilane, 3-chloropropyltriethoxysilane) in an acid-catalyzed EtOH system. The fast scanning speed and high sensitivity of the FT-NIR spectroscopy, and the powerful data processing ability of the PLS, enabled the method to quantitatively and accurately catch the fast changing H₂O concentration during the hydrolysis processes without delay, realizing the study of the fast-paced hydrolysis reactions of the silane coupling agents. The results showed that electrophilic substitution occurred in the hydrolysis reactions, which followed second-order reactions and greatly depend on the catalyst concentration and reaction temperature. The hydrolysis rate constants, activation energy, and Arrhenius Frequency factors were gained. In conclusion, the FT-NIR PLS model is a powerful tool for hydrolysis kinetics researching of the silane coupling agents.     

Study of Chiral Ionic Liquid as Stationary Phases for GC

Due to the synthetic flexibility and special enantioselectivity, chiral ionic liquids (CILs) have heightened interest and an increasing number of CILs has been designed and utilized. In this work, CIL named l-1-butyl-3-(2-propionic-1-ether) imidazolium bromide ([BAlaIM]Br) derived from natural amino acids was synthesized, with chiral center at cation moiety. Chiral stationary phases for gas chromatography were then prepared by mixing the CIL with polymeric ionic liquid ([PSOMIM][NTf₂], homemade) at different ratios (4:1, 2:1, and 1:1). The column efficiency was measured to be about 3,200 plates m^?1 (8 m × 0.25 mm i.d.) when the content of [BAlaIM]Br was 50 % (mass percent) in the mixed stationary phase. All columns were coated via the static coating method using 0.30 % (w/v) of stationary phases dissolved in methanol. The results showed that the CIL contributed to the selectivity of stationary phase toward positional isomers dichlorobenzenes, methylnaphthalenes and pinenes, etc. Meanwhile, [BAlaIM]Br showed better selectivity for enantiomers such as carvones, citronellals, limonenes and camphors. The interactions between chiral selector and enantiomers were also discussed.