Effect of Temperature and Discharge Rate on Electrochemical Performance of Fiber Nickel–Cadmium Cell

Russian Journal of Electrochemistry - The effect of temperature and discharge rate on the discharge capacity of nickel–cadmium (Ni?Cd) cell is investigated quantitatively. Ni–Cd...     

Electric field induced switching of poly(ethylene glycol) terminated self-assembled monolayers: a parallel molecular dynamics simulation

Effects of electric field on the structure of poly(ethylene glycol) (PEG) terminated alkanethiol self-assembled monolayer (SAM) on gold have been studied using parallel molecular dynamics method. An applied electric field triggers a conformational transition from all-trans to a mostly gauche conformation. The polarity of the electric field has a significant effect on the surface structure of PEG leading to a profound effect on the hydrophilicity of the surface. The electric field applied antiparallel to the surface normal causes a reversible transition to an ordered state in which the oxygen atoms are exposed. On the other hand, an electric field applied in a direction parallel to the surface normal introduces considerable disorder in the system and the oxygen atoms are buried inside. The parallel field affects the overall tilt structure of SAMs more adversely than the antiparallel field.     

Bioinspired synthesis of morphologically controlled SrCO3 superstructures by natural gum acacia

Crystallization of strontium carbonate is performed in aqueous solution using Gum Acacia (GA) as crystal growth modifier. A novel study of hierarchical assembly, specifically interacting inorganic and natural component without introduction of other additives was studied. SrCO₃structures exhibiting the morphologies of well defined nanocrystallites in the form of clusters of hexagonal rods, flower shaped, cross like, doughnut shaped and rice grain shaped are identified by optimizing the conditions and concentration of GA. In continuation, morphology was also examined for mixed metal carbonates (Sr‐LaCO₃, Sr‐TbCO₃). The results indicate that –OH, –COOH and ‐NH₂ functional group moieties of GA play a remarkable role in inhibiting growth morphology of metal carbonates and mixed metal carbonates. Structural characterization of the synthesized materials was investigated by Powder X‐ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive analysis (EDAX), Transmission electron microscopy (TEM), Thermogravimetric analysis (TGA) coupled Mass (MS) and Fourier transform infrared spectroscopy (FT‐IR). This synthesis method can be easily extended to a variety of inorganic nanoparticles, thereby enabling exact control over material properties. (© 2011 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Computational insights of two-dimensional infrared spectroscopy under electric fields in phosphorylcholine

Influence of static electric field in biological cells causes electroporation, which results in the increase of permeability of the cells and phospholipid bilayer. However, the precise mode of action of electric fields on phospholipid bilayer and their quantum mechanics are still unclear. Therefore, to understand the quantum-based biological effect, we aimed to study two-dimensional infrared (2D-IR) spectra-adopted quantum mechanics/molecular mechanics (QM/MM) simulations under the influence of static electric fields on Phosphorylcholine, an important component in phospholipid membrane. Initially, QM/MM studies were performed under the influence of electric field, ranging from −1.543 to 1.028 V/nm. A multilayer ONIOM model (in combination with DFT/B3LYP/6-31G [d, p] and DREIDING force fields) was used to obtain 2D-IR simulated spectra to calculate electrostatic interaction in the biological system. The results demonstrated that the phosphate group played an important role on α-rotation in LUMO and the chlorine atom had a major contribution in HOMO. In addition, decreased number of hydrogen bonds demonstrated that uncoupling reaction of the P-O stretching vibrations while the electric field was −1.542 V/nm. Moreover, we observed that the electric field is −1.028 V/nm, there is no rotational isomerization in phosphorylcholine. We concluded that the static electric fields significantly affect the anharmonic frequencies, vibration coupling and the structure of the phosphorylcholine.     

Phase transitions of a single polyelectrolyte in a poor solvent with explicit counterions

Conformational properties of a single flexible polyelectrolyte chain in a poor solvent are studied using constant temperature molecular dynamics simulation. The effects of counterions are explicitly taken in to account. Structural properties of various phases and the transition between these phases are studied by tracking the values of asphericity, radius of gyration, fraction of condensed counterions, number of non-bonded neighbours, and Coulomb interaction energies. From our simulations, we find strong evidence for a first-order phase transition from extended to collapsed phase consistent with earlier theoretical predictions. We also identify a continuous phase transition associated with the condensation of counterions and estimate the critical exponents associated with the transition. Finally, we argue that previous suggestions of existence of an independent intermediate phase between extended and collapsed phases is only a finite size effect.     

Ab initio calculations of intramolecular parameters for a class of arylamide polymers

Using DFT methods, we have determined intramolecular parameters for an important class of arylamide polymers displaying antimicrobial and anticoagulant inhibitory properties. A strong link has been established between these functions and the conformation that the polymers adopt in solution and at lipid bilayer interfaces. Thus, it is imperative for molecular dynamics simulations designed to probe the conformational behavior of these systems to accurately describe the torsional degrees of freedom. Standard force fields were shown to be deficient in this respect. Therefore, we have computed the relevant torsional energy profiles using a series of constrained geometry optimizations. We have also determined electrostatic parameters using our results in combination with standard RESP charge optimization. Force constants for bond and angle potentials were calculated by iteratively matching quantum and classical normal modes via a Monte Carlo scheme. The resulting new set of parameters accurately described the conformation and dynamical behavior of the arylamide polymers.