A carbon–LiFePO<Subscript>4</Subscript> nanocomposite as high-performance cathode material for lithium-ion batteries

A cathode material of an electrically conducting carbon–LiFePO₄ nanocomposite is synthesized by wet ball milling and spray drying of precursor powders prior to a solid-state reaction. The structural characterization shows that the composite is composed of LiFePO₄ crystals and 4.8 wt.% amorphous carbon. Galvanostatic charge/discharge measurements indicate that the composite exhibits a superior high energy and high cycling stability. This composite delivers a discharge capacity of 159.1 mAh g⁻¹ at 0.1 C, 150.8 mAh g⁻¹ at 1 C, and 140.1 mAh g⁻¹ at 2 C rate. The capacity retention of 99% is achieved after 200 cycles at 2 C. The 18,650 cylindrical batteries are assembled using the composite as cathode materials and demonstrate the capacity of 1,400 mAh and the capacity retention of 97% after 100 cycles at 1 C. These results reveal that the as-prepared LiFePO₄–carbon composite is one of the promising cathode materials for high-performance, advanced lithium-ion batteries directed to the hybrid electric vehicle and pure electric vehicle markets.     

Magneto-electric response functions for simple atomic systems

We consider a simple atomic two-body bound state system that is overall charge neutral and placed in a static electric and magnetic field, and calculate the magneto-electric response function as a function of frequency. This is done from first principles using a two-particle Hamiltonian for both an harmonic oscillator and Coulomb binding potential. In the high frequency limit, the response function falls off as 1/ω ² whilst at low frequencies it tends to a constant value.     

An overview of quantification methods in energy-dispersive X-ray fluorescence analysis

This paper reviews the major factors influencing the accuracy of the energy-dispersive X-ray fluorescence (EDXRF) analysis including physical and chemical matrix effects (resulting from particle size, surface irregularity, mineralogy, moisture, absorption and enhancement) as well as the correction procedures with emphasis on the analysis of unprepared samples. Quantification methods for thin samples, samples with intermediate thickness and thick samples are presented including fundamental parameter methods, influence coefficient algorithms, empirical coefficient algorithms and quantification methods based on scattered primary radiation. Quality control procedures are also reviewed.     

Effects of surfactants on properties of polymer-coated magnetic nanoparticles for drug delivery application

The objective of this research was to compare the effects of two different surfactants on the physicochemical properties of thermo-responsive poly(N-isopropylacrylamide-acrylamide-allylamine) (PNIPAAm-AAm-AH)-coated magnetic nanoparticles (MNPs). Sodium dodecyl sulfate (SDS) as a commonly used surfactant in nanoparticle formulation process and Pluronic F127 as an FDA approved material were used as surfactants to synthesize PNIPAAm-AAm-AH-coated MNPs (PMNPs). The properties of PMNPs synthesized using SDS (PMNPs-SDS) and PF127 (PMNPs-PF127) were compared in terms of size, polydispersity, surface charge, drug loading efficiency, drug release profile, biocompatibility, cellular uptake, and ligand conjugation efficiency. These nanoparticles had a stable core–shell structure with about a 100-nm diameter and were superparamagnetic in behavior with no difference in the magnetic properties in both types of nanoparticles. In vitro cell studies showed that PMNPs-PF127 were more cytocompatible and taken up more by prostate cancer cells than that of PMNPs-SDS. Cells internalized with these nanoparticles generated a dark negative contrast in agarose phantoms for magnetic resonance imaging. Furthermore, a higher doxorubicin release at 40 °C was observed from PMNPs-PF127, and the released drugs were pharmacologically active in killing cancer cells. Finally, surfactant type did not affect the conjugation efficiency to the nanoparticles when folic acid was used as a targeting ligand model. These results indicate that PF127 might be a better surfactant to form polymer-coated magnetic nanoparticles for targeted and controlled drug delivery.     

A molecular dynamics study on melting point and specific heat of Ni<Subscript>3</Subscript>Al alloy

Using the Embedding Atom Method (EAM) for highly undercooled Ni₃Al alloy, the melting point and the specific heat were studied by a molecular dynamics simulation. The simulation of melting point was carried out by means of the sandwich method and the NVE ensemble method, and the results show a good agreement, whereas are larger than the experimental value of 1663 K. This difference is attributed to the influence of surface melting on experimental results, which causes the smaller measurements compared with the thermodynamic melting point. The simulated specific heat of Ni₃Al alloy weakly and linearly increases with the increase of undercooling in the temperature range from 800 K to 2000 K. Supported by the National Natural Science Foundation of China (Grant No. 50395101)     

Thermodynamics of Squeezed State for Mesoscopic RLC Circuits

We present a density matrix of a mesoscopic RLC circuits to make it possible to analyze the connection between the initial condition and the certain temperature. Our results show that the quantum state evolution will be closely related to the initial condition; the system evolves to generalized coherent state if it is in ground state initially, and evolves to squeezed state if it is in excited state initially. In addition, we also obtain squeezed minimum uncertainty state with satisfying certain condition in mesoscopic RLC circuit.     

Structural investigation on PEO-based polymer electrolytes dispersed with Al<Subscript>2</Subscript>O<Subscript>3</Subscript> nanoparticles

Thin solid polymer electrolytes based on polyethylene oxide (PEO) and silver triflate (AgCF₃SO₃) dispersed with various concentrations of aluminum oxide (Al₂O₃) nanoparticles have been prepared by solution casting technique. These thin polymer films are found to have thickness of the order of 30 to 100 μm. The X-ray diffraction (XRD) patterns have indicated the amorphous nature of the polymer electrolyte. The differential scanning calorimeter (DSC) traces showed slight change in the glass transition temperature (T _g) whereas the degree of crystallization (X _c) decreases markedly due to the addition of alumina nanoparticles. Fourier transform infrared (FTIR) spectral analysis of all these samples has revealed the presence of absorption bands around 1,000 cm⁻¹; thus indicating the complexation of silver ions with oxygen in PEO. Employing the Wagner’s polarization technique as the standard method, the total ionic transference number for the complexed polymer electrolyte was found to be approximately unity thereby revealing that the significant contribution to electrical conduction was due to ions only. Paper presented at the Third International Conference on Ionic Devices (ICID 2006), Chennai, Tamilnadu, India, December 7–9, 2006     

Isotopic Liftings of Clifford Algebras and Applications in Elementary Particle Mass Matrices

Isotopic liftings of algebraic structures are investigated in the context of Clifford algebras, where it is defined a new product involving an arbitrary, but fixed, element of the Clifford algebra. This element acts as the unit with respect to the introduced product, and is called isounit. We construct isotopies in both associative and non-associative arbitrary algebras, and examples of these constructions are exhibited using Clifford algebras, which although associative, can generate the octonionic, non-associative, algebra. The whole formalism is developed in a Clifford algebraic arena, giving also the necessary pre-requisites to introduce isotopies of the exterior algebra. The flavor hadronic symmetry of the six u,d,s,c,b,t quarks is shown to be exact, when the generators of the isotopic Lie algebra are constructed, and the unit of the isotopic Clifford algebra is shown to be a function of the six quark masses. The limits constraining the parameters, that are entries of the representation of the isounit in the isotopic group SU(6), are based on the most recent limits imposed on quark masses.     

One-neutron stripping reactions of <Superscript>11</Superscript>Be and <Superscript>19</Superscript>C on light target

We have calculated the one-neutron absorption cross-section and the longitudinal momentum distribution of the core fragment coming out from the breakup of ¹¹Be and ¹⁹C on ⁹Be target at 63 MeV/A and 88 MeV/A beam energies respectively. The reaction mechanism is treated within the framework of the eikonal approximation. The effective range of the nuclear interaction between the core and the valence neutron within the projectile has been determined by comparing the predicted stripping cross-section with the recently measured one. The effective range for ¹⁹C has been found to be smaller than that for ¹¹Be. It qualitatively indicates that ¹⁹C is slightly more halo than ¹¹Be. The smaller width, predicted as well as measured, of the LMD of ¹⁸C than ¹⁰Be also strengthens this fact. The experimental data concerning the LMD of core fragments have been well represented.      

Independence of Yang-Mills Equations with Respect to the Invariant Pairing in the Lie Algebra

It is proved that the Euler–Lagrange equations of a Yang-Mills type Lagragian is independent with respect to the chosen pairing in the Lie algebra. Moreover, the Hamilton-Cartan equations of these Lagrangians are obtained and proved to be also independent with respect to the pairing. PACS Numbers 2003: 02.20.Qs, 02.20.Sv, 02.20.Tw, 02.40.Ma, 02.40.Vh, 11.10.Ef, 11.15.Kc Mathematics Subject Classification 2000: Primary 70S15, Secondary 58A20, 58E15, 58E30, 70S05, 70S10, 81T13