Critical parameters influencing the material distribution produced by pulsed laser deposition

The parameters that control the thickness distribution of thin films produced by pulsed laser deposition are investigated. It is found that highly asymmetric material distribution profiles can be obtained in vacuum when high energy densities are used and the target surface is positioned at the lens focus. The asymmetries are due to asymmetries in the spatial distribution of the beam. Under Ar gas pressure, the profile becomes symmetric and the distribution narrows as a consequence of collisions between the ejected species and the gas. In vacuum, decreasing the energy density, by decreasing the laser energy output or by moving the lens to defocus the beam, leads to symmetric distribution profiles. Nevertheless, in the first case a quite broad distribution and a low deposition rate are obtained, whereas in the second case the distribution is narrow and the deposition rate increases.     

Families of discrete advection-reaction operators investigated via divided differences

An infinite matrix formulation of the families of discrete advection-reaction operators is given in order to investigate their relevance to interpolation theory. A basic characteristic under study is the connection of each iteration of the operators to a series of interpolation problems for the canonical polynomial base for selected initial conditions. In order to generalize our results, we extend the definition of advection-reaction operators to sequences of polynomials.     

Ultrashort-laser-pulse-driven rewritable phase-change optical recording in Sb-based films

This paper reviews the work we have carried out over the last years on the development of ultrashort-laser-pulse-driven, rewritable, phase-change optical memories. The materials we have tailored for this application are non-stoichiometric, Sb-rich amorphous thin films, which can be crystallized upon irradiation with ultrashort laser pulses, showing a large optical contrast upon transformation. This result makes them very promising for the development of rewritable phase-change optical memories under ultrashort pulses, since the reversibility of the process has also been demonstrated. Adequate control of the heat-flow conditions has allowed us to achieve a full transformation time faster than 400 ps for crystallization/amorphization using 30-ps pulses. The crystallization threshold fluence has been found to decrease upon irradiation with pulses shorter than 800 fs, thus suggesting the relevance of high-electronic-excitation-induced processes in the amorphous-to-crystalline phase transition. This has been confirmed by the observation of an ultrafast, non-thermal phase transition occurring 200–300 fs after the arrival of the laser pulse at the surface, for fluences above the crystallization threshold. The presence of this transient phase conditions the final state induced therefore enabling the applicability of this material as a rewritable recording medium using femtosecond pulses. Received: 11 October 2001 / Accepted: 9 July 2002 / Published online: 25 October 2002 RID="*" ID="*"Corresponding author. Fax: +34-91/564-5557, E-mail: J.Solis@io.cfmac.csic.es     

Optimization of ultra-fast interactions using laser pulse temporal shaping controlled by a deterministic algorithm

Femtosecond laser pulse temporal shaping techniques have led to important advances in different research fields like photochemistry, laser physics, non-linear optics, biology, or materials processing. This success is partly related to the use of optimal control algorithms. Due to the high dimensionality of the solution and control spaces, evolutionary algorithms are extensively applied and, among them, genetic ones have reached the status of a standard adaptive strategy. Still, their use is normally accompanied by a reduction of the problem complexity by different modalities of parameterization of the spectral phase. Exploiting Rabitz and co-authors’ ideas about the topology of quantum landscapes, in this work we analyze the optimization of two different problems under a deterministic approach, using a multiple one-dimensional search (MODS) algorithm. In the first case we explore the determination of the optimal phase mask required for generating arbitrary temporal pulse shapes and compare the performance of the MODS algorithm to the standard iterative Gerchberg–Saxton algorithm. Based on the good performance achieved, the same method has been applied for optimizing two-photon absorption starting from temporally broadened laser pulses, or from laser pulses temporally and spectrally distorted by non-linear absorption in air, obtaining similarly good results which confirm the validity of the deterministic search approach.     

A Layered Hybrid Perovskite Solar‐Cell Absorber with Enhanced Moisture Stability

Two‐dimensional hybrid perovskites are used as absorbers in solar cells. Our first‐generation devices containing (PEA)₂(MA)₂[Pb₃I₁₀] ( 1 ; PEA=C₆H₅(CH₂)₂NH₃⁺, MA=CH₃NH₃⁺) show an open‐circuit voltage of 1.18 V and a power conversion efficiency of 4.73 %. The layered structure allows for high‐quality films to be deposited through spin coating and high‐temperature annealing is not required for device fabrication. The 3D perovskite (MA)[PbI₃] ( 2 ) has recently been identified as a promising absorber for solar cells. However, its instability to moisture requires anhydrous processing and operating conditions. Films of 1 are more moisture resistant than films of 2 and devices containing 1 can be fabricated under ambient humidity levels. The larger bandgap of the 2D structure is also suitable as the higher bandgap absorber in a dual‐absorber tandem device. Compared to 2 , the layered perovskite structure may offer greater tunability at the molecular level for material optimization.     

Indirect determination of pepsin activity in human seric protein samples by polyphenol oxidase electrodes

We present a new chronoamperometric methodology for the indirect determination of pepsin activity in proteic solutions. The high-sensitive polyphenol oxidase (PPO) carbon paste bioelectrodes, prepared with 150–200 U of PPO adsorbed on the carbon paste surface and trapped behind a dialysis membrane were able to detect free -tyrosine ( -Tyr) as well as -Tyr-containing peptides, the product of pepsin hydrolysis on haemoglobin samples. The electroactive enzymatic products were determined by their reduction current at −0.050 V, a working potential low enough for preventing electrochemical interferences. The external diffusional barrier posed by the dialysis membrane and the high PPO-superficial concentrations allowed us to prevent electrode surface fouling and to reach stationary diffusional currents after 3 min. The electrochemical -Tyr concentrations measured with proper internal standards, were correlated to those determined by the spectrophotometric reference method (Folin–Ciocalteu), reaching a linear relationship with a slope of 1.05±0.04 and a linear regression coefficient of 0.9951. These results as well as a recovery assay of 98% and the detection limit lower than that of the spectrophotometric method indicate that the proposed methodology is very satisfactory and potentially useful for indirect determination of pepsin in biological samples. The technique was also applied for the determination of pepsin activity in hydrolysed immuno globulin solutions of different composition.     

Charge induced pattern formation on surfaces: segregation in cylindrical micelles of cationic-anionic peptide-amphiphiles

Micelles, vesicles, and films composed of two species of incompatible heterogeneous molecules exhibit full internal segregation of the component species. This macroscopic segregation can be inhibited by oppositely charging the two different molecular species. The degree of compatibility achieved by the charges leads to either fully homogenous mixtures or to local segregation and the possible formation of regular patterns. We investigate the induction of periodic surface patterns by the presence of opposite charges in flat films and cylindrical micelles. In the strong segregation limit the incompatibility between species can be described by a line tension parameter gamma. The size of the patterns formed is of the order of a characteristic size L approximately (gamma/sigma(2))(1/2), where sigma is the surface charge density. The pattern symmetry on flat surfaces is function only of the fraction of area covered by the components, f: lamellar for 0.34相似文献   

Null Screen Isoparametric Hypersurfaces in Lorentzian Space Forms

In this paper, we develop the notion of screen isoparametric hypersurface for null hypersurfaces of Robertson–Walker spacetimes. Using this formalism we derive Cartan identities for the screen principal curvatures of null screen isoparametric hypersurfaces in Lorentzian space forms and provide a local characterization of such hypersurfaces.