Ahmed H. Zewail

Time-resolved electron diffraction with atomic-scale spatial and temporal resolution was used to unravel the transformation pathway in the photoinduced structural phase transition of vanadium dioxide. Results from bulk crystals and single-crystalline thin-films reveal a common, stepwise mechanism: First, there is a femtosecond V−V bond dilation within 300 fs, second, an intracell adjustment in picoseconds and, third, a nanoscale shear motion within tens of picoseconds. Experiments at different ambient temperatures and pump laser fluences reveal a temperature-dependent excitation threshold required to trigger the transitional reaction path of the atomic motions.

Significance: One of the most significant advances made is the ability to visualize nanoscale objects and to determine their shapes (through imaging) and their atomic-scale structure (through diffraction). Furthermore, for optical excitation of the nanostructure the photon-induced near-field EM (PINEM) imaging results in the mapping of nanostructure plasmonics with high spatial–temporal resolution. Here, we show that PINEM can be exploited in the infrared region with greater sensitivity, and that diffraction can be implemented for structural dynamics. Just as importantly, the time resolution of ultrafast EM (UEM), which already far exceeds, by 10 orders of magnitude, that of conventional EM, may be further enhanced by IR PINEM and photon gating with the unprecedented energy resolution (0.63 eV) reported here for UEM.

Understanding the dynamical nature of the catalytic active site embedded in complex systems at the atomic level is critical to developing efficient photocatalytic materials. Here, we report, using 4D ultrafast electron microscopy, the spatiotemporal behaviors of titanium and oxygen in a titanosilicate catalytic material. The observed changes in Bragg diffraction intensity with time at the specific lattice planes, and with a tilted geometry, provide the relaxation pathway: the Ti⁴⁺=O²⁻ double bond transformation to a Ti³⁺−O¹⁻ single bond via the individual atomic displacements of the titanium and the apical oxygen. The dilation of the double bond is up to 0.8 Å and occurs on the femtosecond time scale. These findings suggest the direct catalytic involvement of the Ti³⁺−O¹⁻ local structure, the significance of nonthermal processes at the reactive site, and the efficient photo-induced electron transfer that plays a pivotal role in many photocatalytic reactions.

The phase transition of crystalline ordering is a general phenomenon, but its evolution in space and time requires microscopic probes for visualization. Here we report direct imaging of the transformation of amorphous titanium dioxide nanofilm, from the liquid state, passing through the nucleation step and finally to the ordered crystal phase. Single-pulse transient diffraction profiles at different times provide the structural transformation and the specific degree of crystallinity (η) in the evolution process. It is found that the temporal behaviour of η exhibits unique ‘two-step’ dynamics, with a robust ‘plateau’ that extends over a microsecond; the rate constants vary by two orders of magnitude. Such behaviour reflects the presence of intermediate structure(s) that are the precursor of the ordered crystal state. Theoretically, we extend the well-known Johnson–Mehl–Avrami–Kolmogorov equation, which describes the isothermal process with a stretched-exponential function, but here over the range of times covering the melt-to-crystal transformation.

Significance: In this contribution, we demonstrate a unique concept in the use of photon-induced near-field electron microscopy—combining one electron pulse and two optical pulses—as a probe for ultrafast dynamics of matter in electron microscopy. Photon–electron coupling permits the use of a short optical pulse to gate the electron pulse, which is serving as a probe of the ultrafast dynamics triggered by another optical pulse. This technique provides the high spatial and temporal resolution of the electron pulse and optical laser pulses, respectively, both in ultrafast electron microscopy (UEM) measurements. This development paves the way for numerous studies in imaging of matter not only with few femtosecond resolution but also with the potential for attosecond imaging in UEM.

Light–matter interactions at the nanoscale are fundamental to the rapidly developing fields of plasmonics and nanophotonics. These fields hold the promise of advancing both the speed of computers along with communications and may also provide methods to create a new generation of ultrasensitive molecular biosensors. While there are a variety of techniques that can provide static images of these devices with suboptical wavelength precision there are only a few that are capable of capturing the ultrafast dynamics of electromagnetic fields interacting with or produced by nanomaterials. In this Perspective, we aim to introduce the reader to the newly developed field of 4D ultrafast electron microscopy (4D UEM), which provides a unique window into ultrafast dynamics at the nanoscale. We will describe the basic technique and how internal structural, bulk electronic, and surface near-field dynamics can all be obtained with nanometer and femtosecond resolutions. In addition, we will discuss how a variety of different ultrafast electron microscopes have been used to map the evolution of photonics-related phenomena. Throughout, we discuss the direction of research that will help advance the understanding of light–matter interactions near the atomic scale in both space and time.

Phase-change materials (PCMs) represent the leading candidates for universal data storage devices, which exploit the large difference in the physical properties of their transitional lattice structures. On a nanoscale, it is fundamental to determine their performance, which is ultimately controlled by the speed limit of transformation among the different structures involved. Here, we report observation with atomic-scale resolution of transient structures of nanofilms of crystalline germanium telluride, a prototypical PCM, using ultrafast electron crystallography. A nonthermal transformation from the initial rhombohedral phase to the cubic structure was found to occur in 12 ps. On a much longer time scale, hundreds of picoseconds, equilibrium heating of the nanofilm is reached, driving the system toward amorphization, provided that high excitation energy is invoked. These results elucidate the elementary steps defining the structural pathway in the transformation of crystalline-to-amorphous phase transitions and describe the essential atomic motions involved when driven by an ultrafast excitation. The establishment of the time scales of the different transient structures, as reported here, permits determination of the possible limit of performance, which is crucial for high-speed recording applications of PCMs.

Significance: The biomechanics of amyloid underlies its function in living organisms. We use four-dimensional electron microscopy to systematically dissect the nanoscale origins of amyloid elasticity by measuring the bond stiffnesses of the intermolecular forces stabilizing each of its three characteristic packing interfaces. We find amyloid to have a pronounced mechanical anisotropy with longitudinal, hydrogen bonding 20 times stiffer than transverse, amphiphilic, and electrostatic interactions. Such strongly anisotropic elastic properties are likely to give rise to length-dependent mechanical behavior with short fibrils possessing significantly different material properties than longer fibrils. This is of great importance in understanding fibril–membrane interactions and fragmentation mechanisms, both of which are thought to play a crucial role in the spread of amyloid diseases.

We demonstrate ultrafast core-electron energy-loss spectroscopy in four-dimensional electron microscopy as an element-specific probe of nanoscale dynamics. We apply it to the study of photoexcited graphite with femtosecond and nanosecond resolutions. The transient core-loss spectra, in combination with ab initio molecular dynamics simulations, reveal the elongation of the carbon-carbon bonds, even though the overall behavior is a contraction of the crystal lattice. A prompt energy-gap shrinkage is observed on the picosecond time scale, which is caused by local bond length elongation and the direct renormalization of band energies due to temperature-dependent electron–phonon interactions.