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Water can be vitrified if it is cooled at high rates, which makes it possible to outrun crystallization in so-called no man's land, a range of deeply supercooled temperatures where water crystallizes rapidly. Here, we study the reverse process in pure water samples by flash melting amorphous ice with microsecond laser pulses. Time-resolved electron diffraction reveals that the sample transiently crystallizes despite a heating rate of more than 5 × 106 K/s, even though under the same conditions, vitrification can be achieved with a similar cooling rate of 107 K/s. Moreover, we observe different crystallization kinetics for amorphous solid water and hyperquenched glassy water. These experiments open up new avenues for elucidating the crystallization mechanism of water and studying its dynamics in no man's land. They also add important insights into the laser melting and revitrification processes that are integral to the emerging field of microsecond time-resolved cryo-electron microscopy. [ABSTRACT FROM AUTHOR]

In ultrafast transmission electron microscopy, time zero can be accurately determined by making use of the photon-induced near-field electron microscopy (PINEM) effect, which causes electrons interacting with the near fields of a nanoparticle to coherently gain or lose energy in multiples of the photon energy when the laser pump and electron probe pulse overlap in time. If the instrument is not equipped with an energy filter, which is required to observe the PINEM effect, the response of a sample is frequently monitored instead. However, the gradual or delayed onset of this response can render an accurate measurement as challenging. Here, we demonstrate a simple and accurate method for determining time zero without an energy filter that is based on the observation that the outline of a nanoparticle blurs when the electron and laser pulse overlap in time. We show that this phenomenon arises from the PINEM effect, which causes some electrons to gain a large energy spread, thus blurring the image due to the chromatic aberration of the imaging system. This effect can also be used to characterize the instrument response and determine the laser polarization in situ. Furthermore, it may find applications for mapping out the near fields of a nanoparticle without the help of an energy filter. [ABSTRACT FROM AUTHOR]

Thanks to their high brightness, field emitters are the electron sources of choice in most high-end electron microscopes. Under typical operating conditions, the available emission current from these emitters is largely limited by practical considerations, and extracting significantly larger currents is usually not possible without reducing the lifetime of the emitter or even damaging it. Such limitations may, however, not apply if the emitter is only briefly subjected to extreme operating conditions so that damage can be outrun. Here, we demonstrate that it is possible to temporarily operate a Schottky emitter far outside its stable operating regime and significantly increase its emission current. We do so by locally heating the tip of the emitter with a microsecond laser pulse, which boosts the emission current by a factor of 3.7 to nearly 450 μA. We believe that the generation of intense microsecond electron pulses from a field emitter will particularly benefit the atomic-resolution imaging of fast processes that occur on the microsecond timescale. [ABSTRACT FROM AUTHOR]

The manipulation of liquids at nanoscale dimensions is a central goal of the emergent nanofluidics field. Such endeavors extend to nanodroplets, which are ubiquitous objects involved in many technological applications. Here, we employ time-resolved electron microscopy to elucidate the formation of so-called jumping nanodroplets on a graphene surface. We flash-melt a thin gold nanostructure with a laser pulse and directly observe how the resulting nanodroplet contracts into a sphere and jumps off its substrate, a process that occurs in just a few nanoseconds. Our study provides the first experimental characterization of these morphological dynamics through real-time observation and reveals new aspects of the phenomenon. We observe that friction alters the trajectories of individual droplets. Surprisingly, this leads some droplets to adopt dumbbell-shaped geometries after they jump, suggesting that they spin with considerable angular momentum. Our experiments open up new avenues for studying and controlling the fast morphological dynamics of nanodroplets through their interaction with structured surfaces. [ABSTRACT FROM AUTHOR]

[Display omitted] • A novel method for microsecond time-resolved electron microscopy is presented. • Cryo electron microscopy samples are rapidly melted in situ with a laser beam. • Microsecond protein dynamics are induced in a native liquid environment. • Revitrification traps particles in transient configurations so they can be imaged. Proteins typically undergo dynamics on the microsecond to millisecond timescale, which is much faster than the time resolution of cryo-electron microscopy. Here, we propose a novel approach for microsecond time-resolved cryo-electron microscopy that involves melting a cryo specimen in situ with a laser beam. The sample remains liquid for the duration of the laser pulse, offering a tunable time window in which the dynamics of embedded particles can be induced in a liquid environment. After the laser pulse, the sample vitrifies, trapping particles in their transient configurations. As a proof of principle, we study the disassembly of particles after they incur structural damage. [ABSTRACT FROM AUTHOR]