Refine
Has Fulltext
- no (101) (remove)
Year of publication
- 2009 (101) (remove)
Document Type
- Article (84)
- Doctoral Thesis (11)
- Monograph/Edited Volume (6)
Is part of the Bibliography
- yes (101)
Institute
- Institut für Physik und Astronomie (101) (remove)
A new globally uniform Lagrangian transport scheme for large ensembles of passive tracer particles is presented and applied to wind data from a coupled atmosphere-ocean climate model that includes interactive dynamical feedback with stratospheric chemistry. This feedback from the chemistry is found to enhance large-scale meridional air mass exchange in the northern winter stratosphere as well as intrusion of stratospheric air into the troposphere, where both effects are due to a weakened polar vortex.
Carrier transport and recombination have been studied in single component layers and blends of the soluble PPV- derivative poly[2,5-dimethoxy-1,4-phenylenevinylene-2-methoxy-5-(2-ethyl-hexyloxy)- 1,4-phenylenevinylene] (M3EH-PPV) and the small molecule acceptor 4,7-bis(2-(1-hexyl-4,5-dicyanoimidazole-2-yl)vinyl) benzo[c][1,2,5]-thiadiazole (HV-BT). Measurements on single carrier devices show significantly smaller electron mobility in the blend compared to the pure HV- BT layer, which is suggestive of the formation of isolated clusters of the acceptor in a continuous polymer matrix. The significant change in fill factor (FF) with increasing illumination intensity is consistently explained by a model taking into account bimolecular recombination and space charge effects. The decay of the carrier density after photoexcitation has been studied by performing photo-CELIV measurements on pure and blend layers. It is found that the decay at long delay times follows a power-law dependence, which is, however, not consistent with a Langevin-type bimolecular recombination of free charges. A good description of the data is obtained by assuming trimolecular recombination to govern the charge carrier dynamics in these systems.
The authors present organic photovoltaic (OPV) devices comprising a small molecule electron acceptor based on 2- vinyl-4,5-dicyanoimidazole (Vinazene (TM)) and a soluble poly(p-phenylenevinylene) derivative as the electron donor. A strong dependence of the fill factor (FF) and the external quantum efficiency [incident photons converted to electrons (IPCE)] on the heterojunction topology is observed. As-prepared blends provided relatively low FF and IPCE values of 26% and 4.5%, respectively, which are attributed to significant recombination of geminate pairs and free carriers in a highly intermixed blend morphology. Going to an all-solution processed bilayer device, the FF and IPCE dramatically increased to 43% and 27%, respectively. The FF increases further to 57% in devices comprising thermally deposited Vinazene layers where there is virtually no interpenetration at the donor/acceptor interface. This very high FF is comparable to values reported for OPV using fullerenes as the electron acceptor. Furthermore, the rather low electron affinity of Vinazene compound near 3.5 eV enabled a technologically important open circuit voltage (V-oc) of 1.0 V.
Stripe-array diode lasers naturally operate in an anti-phase supermode. This produces a sharp double lobe far field at angles ña depending on the period of the array. In this paper a 40 emitter gain guided stripe-array laterally coupled by off-axis filtered feedback is investigated experimentally and numerically. We predict theoretically and confirm experimentally that at doubled feedback angle 2a a stable higher order supermode exists with twice the number of emitters per array period. The theoretical model is based on time domain traveling wave equations for optical fields coupled to the carrier density equation taking into account diffusion of carriers. Feedback from the external reflector is modeled using Fresnel integration.
Polymer composites are currently suggested for use as improved dielectric materials in many applications. Here, the effect of particle size and dispersion on the electrical properties of composites of rutile TiO2 and poly(styrene- ethylene-butadiene-styrene) (SEBS) are investigated. Both 15 and 300 nm particles are mixed with SEBS, with amounts of sorbitan monopalmitate surfactant from 0 to 3.3 vol%, and their dielectric and mechanical properties are measured. Composites with the 300 nm TiO2 particles result in increases of 170% in relative permittivity over the pure polymer, far above those predicted by standard theories, such as Bruggeman (140%) and Yamada (114%), and improving dispersion with surfactant has little effect. The composites with 15 nm particles showed surprisingly large relative permittivity increases (350%), but improving the dispersion by the addition of any surfactant causes the relative permittivity to decrease to 240% of the pure polymer value. We suggest that the increase is due to the formation of a highly conductive layer in the polymer around the TiO2 particles.
Nanocrystalline carbonitrides were performed by pulsed plasma electrolytic carbonitriding on hard chromium coating deposited on AISI 1035 substrate by electroplating. The electroplated samples were connected cathodically to a high-current pulsed power supply and biased to a negative voltage. The treatment times were 30, 60 and 60 min. A thick compound layer was formed on the surface of Cr coating with microhardness of about 1200 HV0.15. The nanostructure of the treated layers depends strongly on the applied voltage. The wear resistance of the treated layers depended on process parameters. Overall mechanical properties of treated samples show strong relation to morphology and distribution of complex carbonitride nanocrystallites.
We present conditions for the local and global synchronizations in coupled-map networks using the matrix measure approach. In contrast to many existing synchronization conditions, the proposed synchronization criteria do not depend on the solution of the synchronous state and give less limitation on the network connections. Numerical simulations of the coupled quadratic maps demonstrate the potentials of our main results.