Effects of shell composition,dosage and alkali type on the morphology of polymer hollow microspheres

Polymer hollow microspheres were prepared by performing alkali treatment on the multilayer core/shell polymer latex particles containing carboxyl groups. Effects of the shell composition and dosage as well as alkali type on the morphology of the microspheres were investigated. Results showed that in comparison with acrylonitrile(AN) and methacrylic acid(MAA), using butyl acrylate(BA) as the shell co-monomer decreased the glass transition temperature(T_g) of shell effectively and was beneficial to the formation of uniform and big hollow structure. Along with the increase of the shell dosage, the alkali-treated microspheres sequentially presented porous and hollow morphology, and the size of microspheres increased, while the hollow diameter increased first and then decreased, and the maximum hollow ratio reached 39.5%. Furthermore, the multilayer core/shell microspheres had better tolerance to NH_3·H_2O than to NaOH. When the molar ratio of alkali to methacrylic acid(MR_(alkali/acid)) for Na OH ranged from 1.15 to 1.30 or MRalkali/acid for NH_3·H_2O ranged from 1.30 to 2.00, the regular polymer hollow microspheres could be obtained.     

Polyaniline encapsulated silicon nanocomposite as high-performance anode materials for lithium ion batteries

Polyaniline encapsulated silicon (Si/PANI) nanocomposite as anode materials for high-capacity lithium ion batteries has been prepared by an in situ chemical polymerization of aniline monomer in the suspension of Si nanoparticles. The obtained Si/PANI nanocomposite demonstrates a reversible specific capacity of 840 mAh g^?1 after 100 cycles at a rate of 100 mA g^?1 and excellent cycling stability. The enhanced electrochemical performance can be due to that the polyaniline (PANI) matrix offers a continuous electrically conductive network as well as enhances the compatibility of electrode materials and electrolyte as a result of suppressing volume stress of Si during cycles and preventing the agglomeration of Si nanoparticles.     

Natural graphite enhanced the electrochemical performance of Li<Subscript>3</Subscript>V<Subscript>2</Subscript>(PO<Subscript>4</Subscript>)<Subscript>3</Subscript> cathode material for lithium ion batteries

Natural graphite treated by mechanical activation can be directly applied to the preparation of Li₃V₂(PO₄)₃. The carbon-coated Li₃V₂(PO₄)₃ with monoclinic structure was successfully synthesized by using natural graphite as carbon source and reducing agent. The amount of activated graphite is optimized by X-ray diffraction, scanning electron microscope, transmission electron microscope, Raman spectrum, galvanostatic charge/discharge measurements, cyclic voltammetry, and electrochemical impedance spectroscopy tests. Our results show that Li₃V₂(PO₄)₃ (LVP)-10G exhibits the highest initial discharge capacity of 189 mAh g^?1 at 0.1 C and 162.9 mAh g^?1 at 1 C in the voltage range of 3.0–4.8 V. Therefore, natural graphite is a promising carbon source for LVP cathode material in lithium ion batteries.     

Double-walled core-shell structured Si@SiO2@C nanocomposite as anode for lithium-ion batteries

Double-walled core-shell structured Si@SiO₂@C nanocomposite has been prepared by calcination of silicon nanoparticles in air and subsequent carbon coating. The obtained Si@SiO₂@C nanocomposite demonstrates a reversible specific capacity of about 786 mAh g^?1 after 100 cycles at a current density of 100 mA g^?1 with a capacity fading of 0.13 % per cycle. The enhanced electrochemical performance can be due to that the double walls of carbon and SiO₂ improve the electronic conductivity and enhance the compatibility of electrode materials and electrolyte as a result of accommodating the significant volumetric change during cycles. The interlayer SiO₂ may release the mechanical strain and enhance the interfacial adhesion between carbon shell and silicon core.     

One-pot facile synthesis of CuS/graphene composite as anode materials for lithium ion batteries

CuS/graphene composite has been synthesized by the one-pot hydrothermal method using thiourea as the sulfur source and reducing agent. The formation of CuS nanoparticles and the reduction of graphene oxide occur simultaneously during the hydrothermal process, which enables a uniform dispersion of CuS nanoparticles on the graphene nanosheets. The electrochemical performance of CuS/graphene composite was studied as anode materials for lithium ion batteries. The obtained CuS/graphene composite exhibits a relative high reversible capacity and good cycling stability. The good electrochemical performance of CuS/graphene composite can be attributed to graphene, which improves the electronic conductivity of composite and enhances the interfacial stability of electrode and electrolyte.     

Cyclometallated iridium phosphors with amino acid ancillary ligand for intracellular imaging

Two new iridium complexes, (dfppy)₂Ir(L-alanine) (dfppy=2-(2,4-difluorophenyl)pyridine) and (piq)₂Ir(L-alanine) (piq=L-phenylisoquinoline) were prepared with L-alanine as ancillary ligand. The two complexes show bright greenish-blue and red emission respectively. Theoretic study demonstrated that the emission nature of these complexes is mainly determined by the main ligand. And their improved aqueous solubility and the retained quantum yield favor their application in cell imaging. Intracellular imaging suggested that these two complexes have fine cell membrane permeability and is mainly distributed in cytoplasm. This study displayed a new strategy to design aqueous soluble phosphorescent cyclometallated Ir(Ⅲ) complex via introducing amino acid as ancillary ligand.     

Kraus Operator-Sum Solution to the Master Equation Describing the Single-Mode Cavity Driven by an Oscillating External Field in the Heat Reservoir

Exploiting the thermo entangled state approach, we successfully solve the master equation for describing the single-mode cavity driven by an oscillating external field in the heat reservoir and then get the analytical time-evolution rule for the density operator in the infinitive Kraus operator-sum representation. It is worth noting that the Kraus operator M _{l, m} is proved to be a trace-preserving quantum operation. As an application, the time-evolution for an initial coherent state ρ _|β〉 = |β〉〈β| in such an environment is investigated, which shows that the initial coherent state decays to a new mixed state as a result of thermal noise, however the coherence can still be reserved for amplitude damping.     

高效产生任意矢量光场的一种方法

提出一种高效产生任意矢量光场的方法.利用两个光束偏移器分别对两个正交线偏振分量进行分束与合束,将传统激光模式转化为任意矢量光场.所产生矢量光场的偏振态和相位分布通过相位型空间光调制器(SLM)加载相应的相位实时调控.由于光路系统中不涉及任何衍射光学元件和振幅分光元件,光场转换效率高,仅取决于SLM的反射率,并且光路系统结构紧凑、稳定,同轴性易于调节.实验结果显示,采用反射率为79%的相位型SLM产生矢量光场的转换效率可达到58%.     

Synergistic Cu/Pd-Catalyzed Asymmetric Allenylic Alkylation of Azomethine Ylides for the Construction of α-Allene-Substituted Nonproteinogenic α-Amino Acids

An unprecedented asymmetric allenylic alkylation of readily available imine esters, which was enabled by a synergistic Cu/Pd catalysis, has been developed. This dual catalytic system possesses good substrate compatibility, delivering a diverse array of nonproteinogenic α-allenylic α-mono- or α,α-disubstituted α-amino acids (α-AAs) with high yields and generally excellent enantioselectivities. Furthermore, the scalability and practicability of the current synthetic protocol were proven by performing gram-scale reactions and by the first catalytic asymmetric synthesis of naturally occurring (S)-γ-allenic α-amino acid, respectively.