32 research outputs found
Optimisation of Quantum Trajectories Driven by Strong-field Waveforms
Quasi-free field-driven electron trajectories are a key element of
strong-field dynamics. Upon recollision with the parent ion, the energy
transferred from the field to the electron may be released as attosecond
duration XUV emission in the process of high harmonic generation (HHG). The
conventional sinusoidal driver fields set limitations on the maximum value of
this energy transfer, and it has been predicted that this limit can be
significantly exceeded by an appropriately ramped-up cycleshape. Here, we
present an experimental realization of such cycle-shaped waveforms and
demonstrate control of the HHG process on the single-atom quantum level via
attosecond steering of the electron trajectories. With our optimized optical
cycles, we boost the field-ionization launching the electron trajectories,
increase the subsequent field-to-electron energy transfer, and reduce the
trajectory duration. We demonstrate, in realistic experimental conditions, two
orders of magnitude enhancement of the generated XUV flux together with an
increased spectral cutoff. This application, which is only one example of what
can be achieved with cycle-shaped high-field light-waves, has farreaching
implications for attosecond spectroscopy and molecular self-probing
CEP-stable Tunable THz-Emission Originating from Laser-Waveform-Controlled Sub-Cycle Plasma-Electron Bursts
We study THz-emission from a plasma driven by an incommensurate-frequency
two-colour laser field. A semi-classical transient electron current model is
derived from a fully quantum-mechanical description of the emission process in
terms of sub-cycle field-ionization followed by continuum-continuum electron
transitions. For the experiment, a CEP-locked laser and a near-degenerate
optical parametric amplifier are used to produce two-colour pulses that consist
of the fundamental and its near-half frequency. By choosing two incommensurate
frequencies, the frequency of the CEP-stable THz-emission can be continuously
tuned into the mid-IR range. This measured frequency dependence of the
THz-emission is found to be consistent with the semi-classical transient
electron current model, similar to the Brunel mechanism of harmonic generation
Competition–colonization trade-offs in a ciliate model community
There is considerable theoretical evidence that a trade-off between competitive and colonization ability enables species coexistence. However, empirical studies testing for the presence of a competition–colonization (CC) trade-off and its importance for species coexistence have found mixed results. In a microcosm experiment, we looked for a CC trade-off in a community of six benthic ciliate species. For each species, we measured the time needed to actively disperse to and colonize an empty microcosm. By measuring dispersal rates and growth rates of the species, we were able to differentiate between these two important components of colonization ability. Competitive ability was investigated by comparing species’ growth with or without a competitor in all pairwise species combinations. Species significantly differed in their colonization abilities, with good colonizers having either high growth rates or high dispersal rates or both. Although species showed a clear competitive hierarchy, competitive and colonization ability were uncorrelated. The weakest competitors were also the weakest colonizers, and the strongest competitor was an intermediate colonizer. However, some of the inferior competitors had higher colonization abilities than the strongest competitor, indicating that a CC trade-off may enable coexistence for a subset of the species. Absence of a community-wide CC trade-off may be based on the lack of strong relationships between the traits underlying competitive and colonization ability. We show that temporal effects and differential resource use are alternative mechanisms of coexistence for the species that were both slow colonizers and poor competitors
Reorientational dynamics of organic cations in perovskite-like coordination polymers
Here we report the dynamics of organic cations as guest molecules in a perovskite host-framework. The molecular motion of CH3NH3+ (MAFe), (CH3)2NH2+ (DMAFe) and (CH3)3NH+ (TrMAFe) in the cage formed by KFe(CN)63− units was studied using a combination of experimental methods: (i) thermal analysis, (ii) dielectric and electric studies, (iii) optical observations, (iv) EPR and 1H NMR spectroscopy and (v) quasielastic neutron scattering (QENS). In the case of MAFe and TrMAFe, the thermal analysis reveals one solid-to-solid phase transition (PT) and two PTs for the DMAFe crystal. A markedly temperature-dependent dielectric constant indicates the tunable and switchable properties of the complexes. Also, their semiconducting properties are confirmed by a dc conductivity measurement. The broadband dielectric relaxation is analyzed for the TrMAFe sample in the frequency range of 100 Hz–1 GHz. QENS shows that we deal rather with the localized motion of the cation than a diffusive one. Three models, which concern the simultaneous rotation of the CH3 and/or NH3 group, π-flips and free rotations of the organic cation, are used to fit the elastic incoherent structure factor. The 1H NMR spin–lattice relaxation time for all compounds under study, as well as the second moments, has been measured in a wide temperature range. In all studied samples, the temperature dependence of the second moment of the proton NMR line indicated the gradual evolution of the molecular movements from the rigid state up to a highly disordered on
Soliton self-compression based HHG driver for water-window transient absorption experiments
Bendrojo ugdymo mokyklos veiklos kokybės įsivertinimo rekomendacijos
Projekto „Kokybės vadybos stiprinimas bendrojo ugdymo mokyklose (modelių sukūrimas)“ leidinysVytauto Didžiojo universitetasŠvietimo akademij
Bendrojo ugdymo mokyklos veiklos kokybės įsivertinimo modelis ir rodiklių sistema
Projekto „Kokybės vadybos stiprinimas bendrojo ugdymo mokyklose (modelių sukūrimas)“ leidinysVytauto Didžiojo universitetasŠvietimo akademij
3D printing hybrid organometallic polymer‐based biomaterials via laser two‐photon polymerization
Materials with microscale structures are gaining increasing interest due to their range of technical and medical applications. Additive manufacturing approaches to such objects via laser two‐photon polymerization, also known as multiphoton fabrication, enable the creation of new materials with diverse and tunable properties. Here, we investigate the properties of 3D structures composed of organometallic polymers incorporating aluminium, titanium, vanadium and zirconium. The organometallic polymer‐based materials were analysed using a variety of techniques including SEM, energy‐dispersive X‐ray spectroscopy, X‐ray photoelectron spectroscopy analysis and contact angle measurements and their biocompatibility was tested in vitro. Cell viability and mode of death were determined by 3‐(4,5‐dimethyl‐2‐thiazolyl)‐2,5‐diphenyl‐2H‐tetrazolium bromide (MTT) assay and acridine orange/ethidium bromide staining. Polymers incorporating Al, Ti and Zr supported cell adhesion and proliferation, and showed low toxicity in vitro, whereas the organometallic polymer incorporating V was shown to be cytotoxic. Inductively coupled plasma optical emission spectrometry suggested that leaching of the V from the organometallic polymer is the likely cause of this. The preparation of the organometallic polymers is straightforward and both simple 2D and complex 3D structures can be fabricated with ease. Resolution tests of the newly developed organometallic polymer incorporating Al show that suspended lines with widths down to 200 nm can be fabricated. We believe that the materials described in this work show promising properties for the development of objects with sub‐micron features for biomedical applications (e.g. biosensors, drug delivery devices, tissue scaffolds etc.)