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J. C. Ekström

Publications and source records attributed to J. C. Ekström.

2 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↗

Anisotropy of Ultrafast Strain in $V_2O_3$ Thin Films: Out-of-Equilibrium Phase Transitions under Interfacial Clamping

Ultrafast photoinduced insulator-to-metal transitions in correlated materials are often mediated by lattice distortions, yet the role of interfacial lattice constraints in shaping nonequilibrium pathways remains largely unexplored. We use azimuth-resolved time-resolved X-ray diffraction to track orientation-dependent strain dynamics in granular V$_2$O$_3$ thin films on c-cut sapphire, where thermal-expansion mismatch imposes anisotropic interfacial strain. Across the thermal transition, the azimuthal profile of the (110)$_H$ strain inverts curvature, providing direct evidence of partial clamping of the hexagonal basal-plane lattice (a$_H$,b$_H$). After photoexcitation of the antiferromagnetic insulating phase, the structural response remains clamp-limited: weakly constrained grain families reach the full basal-plane contraction characteristic of the metallic-like state, whereas strongly constrained families exhibit a strongly reduced distortion. Fluence-dependent measurements further disentangle transformed fraction from clamping-limited lattice distortion. Our results show that interfacial clamping acts as a static selector for ultrafast phase switching and provide a general route to quantify anisotropic strain dynamics in heterostructures.

cond-mat.mtrl-sci↗