Microscopic analysis of the octupole phase transition in Th isotopes

A shape phase transition between stable octupole deformation and octupole vibrations in Th nuclei is analyzed in a microscopic framework based on nuclear density functional theory. The relativistic functional DD-PC1 is used to calculate axially-symmetric quadrupole-octupole constrained energy surfaces. Observables related to order parameters are computed using an interacting-boson Hamiltonian, with parameters determined by mapping the microscopic energy surfaces to the expectation value of the Hamiltonian in the boson condensate. The systematics of constrained energy surfaces and low-energy excitation spectra point to the occurrence of a phase transition between octupole-deformed shapes and shapes characterized by octupole-soft potentials.Comment: 6 pages, 5 figures, accepted for publication in Physical Review C, Rapid Communicatio

Microfluidically fabricated pH-responsive anionic amphiphilic microgels for drug release

© 2016 The Royal Society of Chemistry. Amphiphilic microgels of different composition based on the hydrophilic, pH-responsive acrylic acid (AA) and the hydrophobic, non-ionic n-butyl acrylate (BuA) were synthesised using a lab-on-a-chip device. Hydrophobic droplets were generated via a microfluidic platform that contained a protected form of AA, BuA, the hydrophobic crosslinker, ethylene glycol dimethacrylate (EGDMA), and a free radical initiator in an organic solvent. These hydrophobic droplets were photopolymerised within the microfluidic channels and subsequently hydrolysed, enabling an integrated platform for the rapid, automated, and in situ production of anionic amphiphilic microgels. The amphiphilic microgels did not feature the conventional core-shell structure but were instead based on random amphiphilic copolymers of AA and BuA and hydrophobic crosslinks. Due to their amphiphilic nature they were able to encapsulate and deliver both hydrophobic and hydrophilic moieties. The model drug delivery and the swelling ability of the microgels were influenced by the pH of the surrounding aqueous solution and the hydrophobic content of the microgels

Tailoring pH-responsive acrylic acid microgels with hydrophobic crosslinks for drug release

Amphiphilic microgels based on the hydrophilic acrylic acid (AA) and hydrophobic crosslinks of different compositions were synthesised using a lab-on-a-chip device. The microgels were formed by polymerising hydrophobic droplets. The droplets were generated via a microfluidic platform and contained a protected form of AA, a hydrophobic crosslinker (ethylene glycol dimethacrylate, EGDMA) and a free radical initiator in an organic solvent. Following photopolymerisation and subsequent hydrolysis, AA based microgels of amphiphilic nature were produced and it was demonstrated that they can successfully deliver both hydrophilic as well as hydrophobic moieties. The model drug delivery and the swelling ability of the microgels were influenced by the pH of the aqueous solution as well as the crosslinking density and hydrophobic content of the microgels

Nonperturbative signatures in pair production for general elliptic polarization fields

The momentum signatures in nonperturbative multiphoton pair production for general elliptic polarization electric fields are investigated by employing the real-time Dirac-Heisenberg-Wigner formalism. For a linearly polarized electric field we find that the positions of the nodes in momenta spectra of created pairs depend only on the electric field frequency. The polarization of external fields could not only change the node structures or even make the nodes disappear but also change the thresholds of pair production. The momentum signatures associated to the node positions in which the even-number-photon pair creation process is forbid could be used to distinguish the orbital angular momentum of created pairs on the momenta spectra. These distinguishable momentum signatures could be relevant for providing the output information of created particles and also the input information of ultrashort laser pulses.Comment: 8 pages, 4 figures, submitted to Europhysics Letter

Determination of activation volumes of reversal in perpendicular media

We discuss a method for the determination of activation volumes of reversal in perpendicular media. This method does not require correction for the self-demagnetizing field normally associated with these media. This is achieved by performing time dependence measurements at a constant level of magnetization. From the difference in time taken for the magnetization to decay to a fixed value at two fields-separated by a small increment DeltaH, the activation volume can be determined. We report data for both CoCrPt alloy films and a multilayer film, typical of those materials under consideration for use as perpendicular media. We find activation volumes that are consistent with the hysteresis curves of the materials. The activation volume scales qualitatively with the exchange coupling. The alloy films have significantly lower activation volumes, implying that they would be capable of supporting a higher data density

Accurate determination of the Gaussian transition in spin-1 chains with single-ion anisotropy

The Gaussian transition in the spin-one Heisenberg chain with single-ion anisotropy is extremely difficult to treat, both analytically and numerically. We introduce an improved DMRG procedure with strict error control, which we use to access very large systems. By considering the bulk entropy, we determine the Gaussian transition point to 4-digit accuracy, $D_{c}/J = 0.96845(8)$, resolving a long-standing debate in quantum magnetism. With this value, we obtain high-precision data for the critical behavior of quantities including the ground-state energy, gap, and transverse string-order parameter, and for the critical exponent, $\nu = 1.472(2)$. Applying our improved technique at $J_{z} = 0.5$ highlights essential differences in critical behavior along the Gaussian transition line.Comment: 4 pages and 4 figure

Effect of Interactions on Molecular Fluxes and Fluctuations in the Transport Across Membrane Channels

Transport of molecules across membrane channels is investigated theoretically using exactly solvable one-dimensional discrete-state stochastic models. An interaction between molecules and membrane pores is modeled via a set of binding sites with different energies. It is shown that the interaction potential strongly influences the particle currents as well as fluctuations in the number of translocated molecules. For small concentration gradients the attractive sites lead to largest currents and fluctuations, while the repulsive interactions yield the largest fluxes and dispersions for large concentration gradients. Interaction energies that lead to maximal currents and maximal fluctuations are the same only for locally symmetric potentials, while they differ for the locally asymmetric potentials. The conditions for the most optimal translocation transport with maximal current and minimal dispersion are discussed. It is argued that in this case the interaction strength is independent of local symmetry of the potential of mean forces. In addition, the effect of the global asymmetry of the interaction potential is investigated, and it is shown that it also strongly affects the particle translocation dynamics. These phenomena can be explained by analyzing the details of the particle entering and leaving the binding sites in the channel.Comment: submitted to J. Chem. Phy