Optoelectronic and stability properties of quasi-2D alkylammonium based perovskites.

Electronic and stability properties of quasi-2D alkylammonium perovskites are investigated using density functional theory (DFT) calculations and validated experimentally on selected classes of compounds. Our analysis is focused on perovskite structures of formula (A)2(A')n-1PbnX3n+1, with large cations A = butyl-, pentyl-, hexylammonium (BA, PA, HXA), small cations A' = methylammonium, formamidinium, ethylammonium, guanidinium (MA, FA, EA, GA) and halogens X = I, Br, Cl. The role of the halogen ions is outlined for the band structure, stability and defect formation energies. Two opposing trends are found for the absorption efficiency versus stability, the latter being assessed with respect to possible degradation mechanisms. Experimental validation is performed on quasi-2D perovskites based on pentylammonium cations, namely: (PA)2PbX4 and (PA)2(MA)Pb2X7, synthesized by antisolvent-assisted vapor crystallization. Structural and optical analysis are inline with the DFT based calculations. In addition, the thermogravimetric analysis shows an enhanced stability of bromide and chloride based compounds, in agreement with the theoretical predictions.

Core-shell copper-gold nanoparticles modified at the boron-doped diamond electrode for oxygen sensors.

Bimetallic copper-gold (Cu@Au) nanoparticles were synthesized and utilised to modify boron-doped diamond (BDD) electrodes. Nanorod particles with a diameter size of around 10 nm and a length of around 20 nm were successfully synthesized. These nanoparticles were then attached to the BDD surface by using allylamine as the bridge. Comparison among the BDD modified with Cu@Au and individual gold nanoparticles showed that Cu@Au nanoparticles created around 3 times higher gold coverage on the BDD surface than normal gold nanoparticles. It was also found that the use of allylamine as the bridge can attach more gold than copper nanoparticles. Moreover, around two times higher current responses of oxygen reduction reaction were observed at Cu@Au-modified BDD. Good linearity in a concentration range from 2 to 9 ppm could be achieved with a sensitivity of 0.0138 mA ppm-1 and limit detection of 1.98 ppm. An application of the modified BDD for a biochemical oxygen demand (BOD) sensor using Rhodotorula mucilaginosa UICC Y-181 as the biosensing agent was also demonstrated with glucose solutions as the solution model. Sensitivity equivalent to 17.4 µA mM-1 BOD could be achieved. The system showed good stability with an RSD of 3.45% in 10 measurements.

Equivalence between fractional exclusion statistics and self-consistent mean-field theory in interacting-particle systems in any number of dimensions.

We describe a mean field interacting particle system in any number of dimensions and in a generic external potential as an ideal gas with fractional exclusion statistics (FES). We define the FES quasiparticle energies, we calculate the FES parameters of the system and we deduce the equations for the equilibrium particle populations. The FES gas is "ideal," in the sense that the quasiparticle energies do not depend on the other quasiparticle levels' populations and the sum of the quasiparticle energies is equal to the total energy of the system. We prove that the FES formalism is equivalent to the semiclassical or Thomas Fermi limit of the self-consistent mean-field theory and the FES quasiparticle populations may be calculated from the Landau quasiparticle populations by making the correspondence between the FES and the Landau quasiparticle energies. The FES provides a natural semiclassical ideal gas description of the interacting particle gas.

Lateral mobility of polyelectrolyte chains in multilayers.

In this work, the lateral mobility of polyelectrolyte multilayers was investigated by means of the fluorescence recovery after photobleaching (FRAP) technique, with special attention to the effect of relevant parameters during and after preparation. Different polyelectrolytes with respect to charge density, stiffness, and hydrophilicity were compared. From the experimental results emerged that the density of charged sites along the polymer is the most important parameter controlling the formation of polymer complexes. At higher charge density, more complexes are formed, and the diffusion coefficient decreases. It was observed that the intrinsic backbone stiffness reduces the interpenetration of polyelectrolyte layers and the formation of complexes promoting the lateral mobility. In addition, the lateral mobility increases with increasing ionic strength and with decreasing hydration shell of the added anion in the polyelectrolyte solution. The effect of heating or annealing in electrolyte solution after preparation was also investigated along with the embedding of the probing layer at controlled distances to the multilayer surface.

Determination of the relative impact of chromatographic conditions and solute structures on the retention behaviour of non-ionic surfactants in RP-HPLC.

The retention behaviour of non-ionic surfactants containing different hydrophobic moiety and various lengths of polar ethylene oxide chain was studied on RP-8 and RP-18 columns using methanol and acetonitrile as organic modifiers. The relative impact of the chromatographic conditions on the retention strength was determined using stepwise regression analysis. Non-ionic surfactants can be separated according to the character of the hydrophobic moiety, but not according to the length of the polar ethylene oxide chain. Calculations proved that the organic modifier exerted the highest impact on the retention; the effect of the number of carbon atoms in the hydrophobic moiety, column temperature and the length of the hydrophobic ligand on the surface of silica support are of secondary importance.

Effects of cetyltrimethylammonium bromide (CTAB) surfactant upon the dielectric properties of yeast cells.

The dielectric properties of yeast cells in the absence and presence of cetyltrimethylammonium bromide (CTAB) were investigated. The surfactant concentration range was between 0.0 and 1.0 mM. The experimental permittivity and conductivity spectra of frequency were analyzed by means of the two-shell electrical cell model (Irimajiri et al., Bull. Inst. Chem. Res., Kyoto Univ. 69 (1991) 421-438), and the electrical phase parameters of cells were subsequently evaluated. The cytoplasm conductivity and the conductivity of the vacuole interior decreased drastically by treating the cells with surfactant. The apparent capacitance of the plasma membrane increased systematically from 0.65 microF/cm2, for untreated cells, up to about 0.75 microF/cm2, at 0.3 mM CTAB. This growth was ascribed to the increase in the folding of the membrane surface associated with the surfactant-induced cell shrinkage. A further addition of the surfactant entailed a gradual decrease of the capacitance that was assigned to the membrane solubilization by the surfactant molecules. Within the accuracy of the data, the specific capacitance of the vacuole membrane was nearly constant (0.544+/-0.021 microF/cm2) over the whole surfactant concentration range. Also, the cytoplasm permittivity remained constant at 64.3+/-4.5.