Continuous illumination picosecond imaging using a delay line detector in a transmission electron microscope.

Progress towards analysing transitions between steady states demands improvements in time-resolved imaging, both for fundamental research and for applications in information technology. Transmission electron microscopy is a powerful technique for investigating the atomic structure, chemical composition and electromagnetic properties of materials with high spatial resolution and precision. However, the extraction of information about dynamic processes in the ps time regime is often not possible without extensive modification to the instrument while requiring careful control of the operation conditions to not compromise the beam quality. Here, we avoid these drawbacks by combining a delay line detector with continuous illumination in a transmission electron microscope. We visualize the gyration of a magnetic vortex core in real space and show that magnetization dynamics up to frequencies of 2.3 GHz can be resolved with down to ∼122ps temporal resolution by studying the interaction of an electron beam with a microwave magnetic field. In the future, this approach promises to provide access to resonant dynamics by combining high spatial resolution with sub-ns temporal resolution.

Magnetic Skyrmions and Skyrmion Clusters in the Helical Phase of Cu_{2}OSeO_{3}.

Skyrmions are nanometric spin whirls that can be stabilized in magnets lacking inversion symmetry. The properties of isolated Skyrmions embedded in a ferromagnetic background have been intensively studied. We show that single Skyrmions and clusters of Skyrmions can also form in the helical phase and investigate theoretically their energetics and dynamics. The helical background provides natural one-dimensional channels along which a Skyrmion can move rapidly. In contrast to Skyrmions in ferromagnets, the Skyrmion-Skyrmion interaction has a strong attractive component and thus Skyrmions tend to form clusters with characteristic shapes. These clusters are directly observed in transmission electron microscopy measurements in thin films of Cu_{2}OSeO_{3}. Topological quantization, high mobility, and the confinement of Skyrmions in channels provided by the helical background may be useful for future spintronics devices.

Filming the formation and fluctuation of skyrmion domains by cryo-Lorentz transmission electron microscopy.

Magnetic skyrmions are promising candidates as information carriers in logic or storage devices thanks to their robustness, guaranteed by the topological protection, and their nanometric size. Currently, little is known about the influence of parameters such as disorder, defects, or external stimuli on the long-range spatial distribution and temporal evolution of the skyrmion lattice. Here, using a large (7.3 × 7.3 µm(2)) single-crystal nanoslice (150 nm thick) of Cu2OSeO3, we image up to 70,000 skyrmions by means of cryo-Lorentz transmission electron microscopy as a function of the applied magnetic field. The emergence of the skyrmion lattice from the helimagnetic phase is monitored, revealing the existence of a glassy skyrmion phase at the phase transition field, where patches of an octagonally distorted skyrmion lattice are also discovered. In the skyrmion phase, dislocations are shown to cause the emergence and switching between domains with different lattice orientations, and the temporal fluctuation of these domains is filmed. These results demonstrate the importance of direct-space and real-time imaging of skyrmion domains for addressing both their long-range topology and stability.

Electronically driven fragmentation of silver nanocrystals revealed by ultrafast electron crystallography.

We report an ultrafast electron diffraction study of silver nanocrystals under surface plasmon resonance excitation, leading to a concerted fragmentation. By examining simultaneously transient structural, thermal, and Coulombic signatures of the prefragmented state, an electronically driven nonthermal fragmentation scenario is proposed.

The development and applications of ultrafast electron nanocrystallography.

We review the development of ultrafast electron nanocrystallography as a method for investigating structural dynamics for nanoscale materials and interfaces. Its sensitivity and resolution are demonstrated in the studies of surface melting of gold nanocrystals, nonequilibrium transformation of graphite into reversible diamond-like intermediates, and molecular scale charge dynamics, showing a versatility for not only determining the structures, but also the charge and energy redistribution at interfaces. A quantitative scheme for 3D retrieval of atomic structures is demonstrated with few-particle (<1,000) sensitivity, establishing this nanocrystallographic method as a tool for directly visualizing dynamics within isolated nanomaterials with atomic scale spatio-temporal resolution.

Direct observation of optically induced transient structures in graphite using ultrafast electron crystallography.

We use ultrafast electron crystallography to study structural changes induced in graphite by a femtosecond laser pulse. At moderate fluences of < or =21 mJ/cm2, lattice vibrations are observed to thermalize on a time scale of approximately 8 ps. At higher fluences approaching the damage threshold, lattice vibration amplitudes saturate. Following a marked initial contraction, graphite is driven nonthermally into a transient state with sp3-like character, forming interlayer bonds. Using ab initio density functional calculations, we trace the governing mechanism back to electronic structure changes following the photoexcitation.

Dynamics of size-selected gold nanoparticles studied by ultrafast electron nanocrystallography.

We report the studies of ultrafast electron nanocrystallography on size-selected Au nanoparticles (2-20 nm) supported on a molecular interface. Reversible surface melting, melting, and recrystallization were investigated with dynamical full-profile radial distribution functions determined with subpicosecond and picometer accuracies. In an ultrafast photoinduced melting, the nanoparticles are driven to a nonequilibrium transformation, characterized by the initial lattice deformations, nonequilibrium electron-phonon coupling, and, upon melting, the collective bonding and debonding, transforming nanocrystals into shelled nanoliquids. The displasive structural excitation at premelting and the coherent transformation with crystal/liquid coexistence during photomelting differ from the reciprocal behavior of recrystallization, where a hot lattice forms from liquid and then thermally contracts. The degree of structural change and the thermodynamics of melting are found to depend on the size of nanoparticle.