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J. -E. Pudell

Publications and source records attributed to J. -E. Pudell.

3 recordsLinked to original sources

Ultrafast Dissipative Localization of Electronic Energy in AuPt Superlattices

Controlling the spatial distribution of absorbed optical energy is central to nanoscale photothermal chemistry, plasmonics, and ultrafast materials control. Here, we show that a metallic AuPt superlattice concentrates electronic energy in Pt within a few hundred femtoseconds, regardless of the initial energy distribution between the two constituents. Ultrafast X-ray diffraction follows this energy redistribution through the amplitude of a coherent 570 GHz superlattice phonon driven by the stress imbalance at the AuPt interfaces. Despite the nearly homogeneous absorption at 400 nm, the observed lattice motion is identical to that produced by 800 nm excitation, which is absorbed predominantly in Pt. This dissipation driven localization of energy arises from the large electronic heat capacity of Pt and rapid electronic transport through the superlattice, providing a route to femtosecond control of nanoscale energy distributions.

cond-mat.mtrl-sci↗

Phonon-dominated energy transport in purely metallic heterostructures

We use ultrafast x-ray diffraction to quantify the transport of energy in laser-excited nanoscale Au/Ni bilayers. Electron transport and efficient electron-phonon coupling in Ni convert the laser-deposited energy in the conduction electrons within a few picoseconds into a strong non-equilibrium between hot Ni and cold Au phonons at the bilayer interface. Modeling of the subsequent equilibration dynamics within various two-temperature models confirms that for ultrathin Au films the thermal transport is dominated by phonons instead of conduction electrons because of the weak electron-phonon coupling in Au.

cond-mat.mes-hall↗

Full spatiotemporal control of laser-excited periodic surface deformations

We demonstrate full control of acoustic and thermal periodic deformations at solid surfaces down to sub-nanosecond time scales and few-micrometer length scales via independent variation of the temporal and spatial phase of two optical transient grating (TG) excitations. For this purpose, we introduce an experimental setup that exerts control of the spatial phase of subsequent time-delayed TG excitations depending on their polarization state. Specific exemplary coherent control cases are discussed theoretically and corresponding experimental data are presented in which time-resolved x-ray reflectivity measures the spatiotemporal surface distortion of nanolayered heterostructures. Finally, we discuss examples where the application of our method may enable the control of functional material properties via tailored spatiotemporal strain fields.

physics.app-ph↗