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No small matter : science on the nanoscale
A small revolution is remaking the world. The only problem is, we can't see it. Images and descriptions reveal the virtually invisible realities and possibilities of nanoscience. An introduction to the science and technology of small things. An overview of recent scientific advances that have given us our ever-shrinking microtechnology - for instance, an information processor connected by wires only 1,000 atoms wide. New methods are described that are used to study nanostructures, suggest ways of understanding their often bizarre behavior, and outline their uses in technology. The various means of making nanostructures are explained and speculated about their importance for critical developments in information processing, computation, biomedicine, and other areas. No Small Matter considers both the benefits and the risks of nano/microtechnology - from the potential of quantum computers and single-molecule genomic sequencers to the concerns about self-replicating nanosystems.
Book
Atomic Clusters
This book delves into the fundamental principles of nanoscience, focusing on the physics of nano-objects and their impact on the properties of materials at the nanoscale, offering practical applications in fields ranging from insulator-metal transition to catalysis.
eBook
Bidirectional phonon emission in two-dimensional heterostructures triggered by ultrafast charge transfer
Photoinduced charge transfer in van der Waals heterostructures occurs on the 100 fs timescale despite weak interlayer coupling and momentum mismatch. However, little is understood about the microscopic mechanism behind this ultrafast process and the role of the lattice in mediating it. Here, using femtosecond electron diffraction, we directly visualize lattice dynamics in photoexcited heterostructures of WSe
2
/WS
2
monolayers. Following the selective excitation of WSe
2
, we measure the concurrent heating of both WSe
2
and WS
2
on a picosecond timescale—an observation that is not explained by phonon transport across the interface. Using first-principles calculations, we identify a fast channel involving an electronic state hybridized across the heterostructure, enabling phonon-assisted interlayer transfer of photoexcited electrons. Phonons are emitted in both layers on the femtosecond timescale via this channel, consistent with the simultaneous lattice heating observed experimentally. Taken together, our work indicates strong electron–phonon coupling via layer-hybridized electronic states—a novel route to control energy transport across atomic junctions.
Femtosecond electron diffraction and ab initio theory unravel ultrafast lattice dynamics in photoexcited two-dimensional heterostructures during charge transfer.
Journal Article
Towards single-species selectivity of membranes with subnanometre pores
Synthetic membranes with pores at the subnanometre scale are at the core of processes for separating solutes from water, such as water purification and desalination. While these membrane processes have achieved substantial industrial success, the capability of state-of-the-art membranes to selectively separate a single solute from a mixture of solutes is limited. Such high-precision separation would enable fit-for-purpose treatment, improving the sustainability of current water-treatment processes and opening doors for new applications of membrane technologies. Herein, we introduce the challenges of state-of-the-art membranes with subnanometre pores to achieve high selectivity between solutes. We then analyse experimental and theoretical literature to discuss the molecular-level mechanisms that contribute to energy barriers for solute transport through subnanometre pores. We conclude by providing principles and guidelines for designing next-generation single-species selective membranes that are inspired by ion-selective biological channels.Membranes with subnanometre pores have the potential to provide solute-to-solute selectivity. This Perspective explores challenges and provides guidelines for designing next-generation single-species selective membranes
Journal Article
Ultrafast dynamics in van der Waals heterostructures
Van der Waals heterostructures are synthetic quantum materials composed of stacks of atomically thin two-dimensional (2D) layers. Because the electrons in the atomically thin 2D layers are exposed to layer-to-layer coupling, the properties of van der Waals heterostructures are defined not only by the constituent monolayers, but also by the interactions between the layers. Many fascinating electrical, optical and magnetic properties have recently been reported in different types of van der Waals heterostructures. In this Review, we focus on unique excited-state dynamics in transition metal dichalcogenide (TMDC) heterostructures. TMDC monolayers are the most widely studied 2D semiconductors, featuring prominent exciton states and accessibility to the valley degree of freedom. Many TMDC heterostructures are characterized by a staggered band alignment. This band alignment has profound effects on the evolution of the excited states in heterostructures, including ultrafast charge transfer between the layers, the formation of interlayer excitons, and the existence of long-lived spin and valley polarization in resident carriers. Here we review recent experimental and theoretical efforts to elucidate electron dynamics in TMDC heterostructures, extending from timescales of femtoseconds to microseconds, and comment on the relevance of these effects for potential applications in optoelectronic, valleytronic and spintronic devices.
Journal Article