Mode suppression in the non-Markovian limit by time-gated stimulated photon echo

It is demonstrated that enhanced mode suppression in stimulated photon echo experiments can be obtained by diagonal time gating of the echo. This technique is especially important when the optical dynamics of the system is non-Markovian. A two-mode Brownian oscillator model is used to analyze the effect of time gating on the stimulated photon echo. The method is demonstrated on a dye solution of DTTCI in ethylene glycol at room temperature. Experimentally, time gating of the echo is accomplished by means of femtosecond phase-locked heterodyne detected stimulated photon echo. The vibrational dynamics in this system are explored by conventional stimulated photon echo experiments, Especially stimulated photon echo-maximum shift measurements are found to be particularly useful. (C) 1996 American Institute of Physics

Hydrated Electron Dynamics at a Five Femtosecond Time Scale

Hydrated electrons are studied by frequency resolved pump probe with 5 fs time resolution in the spectral range from 600 nm to 1000 nm. A recurrence detected in the pumpprobe signal at —40 fs is tentatively assigned to coupling to librational motions in the electron's solvent cage

Magnetization of ferrofluids with dipolar interactions - a Born--Mayer expansion

For ferrofluids that are described by a system of hard spheres interacting via dipolar forces we evaluate the magnetization as a function of the internal magnetic field with a Born--Mayer technique and an expansion in the dipolar coupling strength. Two different approximations are presented for the magnetization considering different contributions to a series expansion in terms of the volume fraction of the particles and the dipolar coupling strength.Comment: 19 pages, 11 figures submitted to PR

Water Infiltration in Methylammonium Lead Iodide Perovskite: Fast and Inconspicuous

While the susceptibility of CH3NH3PbI3 to water is well documented, water influence on device performance is not well understood. Herein we use infrared spectroscopy to show that water infiltration into CH3NH3PbI3 occurs much faster and at much lower humidity than previously thought. We propose a molecular model where water molecules have a strong effect on the hydrogen bonding between the methylammonium cations and the Pb-I cage. Furthermore, the exposure of CH3NH3PbI3 to ambient environment increases the photocurrent of films in lateral devices by more than one order of magnitude. The observed slow component in the photocurrent buildup indicates that the effect is associated with enhanced proton conduction when light is combined with water and oxygen exposure.C.M. and M.S. acknowledge support by the Heidelberg Graduate School of Fundamental Physics. A.A.B. is a Royal Society University Research Fellow.This is the author accepted manuscript. The final version is available from the American Chemical Society via http://dx.doi.org/10.1021/acs.chemmater.5b0388

Magnetic properties of colloidal suspensions of interacting magnetic particles

We review equilibrium thermodynamic properties of systems of magnetic particles like ferrofluids in which dipolar interactions play an important role. The review is focussed on two subjects: ({\em i}) the magnetization with the initial magnetic susceptibility as a special case and ({\em ii}) the phase transition behavior. Here the condensation ("gas/liquid") transition in the subsystem of the suspended particles is treated as well as the isotropic/ferromagnetic transition to a state with spontaneously generated long--range magnetic order.Comment: Review. 62 pages, 4 figure

Excited state dynamics and exciton diffusion in triphenylamine/dicyanovinyl push-pull small molecule for organic optoelectronics

Triphenylamine-based small push-pull molecules have recently attracted substantial research attention due to their unique optoelectronic properties. Here, we investigate the excited state de-excitation dynamics and exciton diffusion in TPA-T-DCV-Ph-F small molecule, having simple chemical structure with asymmetrical architecture and end-capped with electron-withdrawing p-fluorodicyanovinyl group. The excited state lifetime in diluted solutions (0.04 ns in toluene and 0.4 ns in chloroform) are found to be surprisingly shorter compared to the solid state (3 ns in PMMA matrix). Time-dependent density functional theory indicates that this behavior originates from non-radiative relaxation of the excited state through a conical intersection between the ground and singlet excited state potential energy surfaces. Exciton diffusion length of similar to 16 nm in solution processed films was retrieved by employing time-resolved photoluminescence volume quenching measurements with Monte Carlo simulations. As means of investigating the device performance of TPA-T-DCV-Ph-F, we manufactured solution and vacuum processed bulk heterojunction solar cells that yielded efficiencies of similar to 1.5% and similar to 3.7%, respectively. Our findings demonstrate that the short lifetime in solutions does not hinder per se long exciton diffusion length in films thereby granting applications of TPA-T-DCV-Ph-F and similar push-pull molecules in vacuum and solution processable devices

Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals

Thiophene-phenylene co-oligomers (TPCOs) are among the most promising materials for organic light emitting devices. Here we report on record high among TPCO single crystals photoluminescence quantum yield reaching 60%. The solution-grown crystals are stronger luminescent than the vapor-grown ones, in contrast to a common believe that the vapor-processed organic electronic materials show the highest performance. We also demonstrate that the solution grown TPCO single crystals perform in organic field effect transistors as good as the vapor-grown ones. Altogether, the solution-grown TPCO crystals are demonstrated to hold great potential for organic electronics.</p

Theoretical study of the magnetization dynamics of non-dilute ferrofluids

The paper is devoted to the theoretical investigation of the magnetodipolar interparticle interaction effect on remagnetization dynamics in moderately concentrated ferrofluids. We consider a homogeneous (without particle aggregates) ferrofluid consisting of identical spherical particles and employ a rigid dipole model, where magnetic moment of a particle is fixed with respect to the particle itself. In particular, for the magnetization relaxation after the external field is instantly switched off, we show that the magnetodipolar interaction leads to the increase of the initial magnetization relaxation time. For the complex ac-susceptibility we find that the this interaction leads to an overall increase of the imaginary susceptibility part and shifts the peak on its frequency dependence towards lower frequencies. Comparing results obtained with our analytical approach (second order virial expansion) to numerical simulation data (Langevin dynamics method), we demonstrate that the employed virial expansion approximation gives a good qualitative description of the ferrofluid magnetization dynamics and provides a satisfactory quantitative agreement with numerical simulations for the dc magnetization relaxation - up to the particle volume fraction c ~ 10% and for the ac-susceptibility - up to c ~ 5 %.Comment: 12 pages, 6 figures, submitted to PR