Electron emission represents the key mechanism enabling the development of devices that have revolutionized modern science and technology. Today, science still relies on advanced electron-emission devices for imaging, electronics, sensing, and high-energy physics. New generations of emission devices are continuously being improved based on innovative materials and the introduction of novel physical concepts. Recent advances are highlighted by emerging low-work-function and low-dimensional materials with unusual electronic and thermal properties. Nanotubes, nanowires, graphene, and electron-emission models are discussed in this issue, as well as original mechanisms, such as the thermoelectronic effect, thermionic emission, and heat trap processes. Advances in electron-emission materials and physics are driving a renaissance in the field, both opening up new applications, such as energy conversion and ultrafast electronics, as well as improving traditional applications in electron imaging and high-energy science.

Light-induced generation of free electrons is of interest for a wide variety of vacuum electronic devices and systems. The properties of nanomaterials, stemming from their geometry and the strong manifestation of quantum phenomena in them, have opened up new avenues for developing new cathodes and exploring and exploiting electron emission. This article presents the heat trap effect—efficient localized heating of carbon nanotube arrays using light, leading to electron emission through the thermionic mechanism. This process requires unexpectedly modest amounts of optical power—available from sources such as handheld lasers—and dramatically simplifies the electron emitter. Potential applications, including thermionic and thermoelectric conversion for solar-energy harvesting and simple electron-beam systems, are also highlighted.

Nucleation is the seminal process in the formation of ordered structures ranging from simple inorganic crystals to macromolecular matrices. Observations over the past 15 years have revealed a rich set of hierarchical nucleation pathways involving higher-order species ranging from multi-ion clusters to dense liquid droplets, as well as transient crystalline or amorphous phases. Despite this complexity, the pathways that lead to nucleation can be described by a holistic framework that is rooted in classical concepts, but which takes into account the coupled effects of perturbations in free-energy landscapes and the impact of dynamical factors. This article describes that framework using a series of in situ transmission electron microscopy and atomic force microscopy studies on inorganic, organic, and macromolecular systems to illustrate the evolution in nucleation processes as these perturbations and dynamical factors come into play. The results provide a common basis for understanding development of order in systems as diverse as simple salt crystals, branched semiconductor nanowires, and microbial membranes.

The resolution of the electron microscope is now largely limited by the performance of its electron source when various aberrations in the electron imaging system, especially spherical aberrations, are corrected. A nanowire tip could be an ideal point electron source, where electrons are emitted from a small physical area. In this article, we review recent advances in electric-field-induced electron emission using a single nanowire, specifically, single-crystalline lanthanum hexaboride (LaB6) nanowire, compared to the state-of-the-art contemporary tungsten cold-field electron emitter W(310) as well as single atom tip and single-carbon nanotube emitters. Owing to its low work function, improved emission stability, and high emission brightness, the LaB6 nanowire as a cold-field-emission electron source offers a new and exciting opportunity for developing the next generation of electron microscopes.

The theories of thermionic emission and field emission (also known as the Richardson–Dushman [RD] and Fowler–Nordheim [FN] Laws, respectively) were formulated more than 80 years ago for bulk materials. In single-layer graphene, electrons mimic massless Dirac fermions and follow relativistic carrier dynamics. Thus, their behavior deviates significantly from the nonrelativistic electrons that reside in traditional bulk materials with a parabolic energy-momentum dispersion relation. In this article, we assert that due to linear energy dispersion, the traditional thermionic emission and field emission models are no longer valid for graphene and two-dimensional Dirac-like materials. We have proposed models that show better agreement with experimental data and also show a smooth transition to the traditional RD and FN Laws.

Nanoscale electron sources with high electron-emitting performance are of great interest in vacuum nanoelectronics. Resembling traditional thermionic emission sources based on a hot tungsten filament, a hot carbon nanotube or graphene can function as a nanoscale electron source because of its excellent thermal stability and electrical conductivity. In this article, studies of thermionic emission from single hot carbon nanostructures are overviewed, emphasizing their differences in physics from macroscopic thermionic emission as well as potential applications in vacuum nanoelectronics. Due to their low dimensionality, nanoscale size, and nonequilibrium electron distribution, Richardson’s Law, which governs thermionic emission from macroscopic metals, breaks down in the case of thermionic emission from single carbon nanostructures, and an internal electric field in a carbon nanostructure can contribute directly to its thermionic emission. Graphene-based nanoscale thermionic emission sources, source arrays, and vacuum transistors have been fabricated and demonstrated to exhibit the advantages compared to those based on field emission. The advances imply the promise of realizing high-performance nanoscale electron sources and vacuum electronic devices based on thermionic emission.