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Neil R. Champness

Publications and source records attributed to Neil R. Champness.

3 recordsLinked to original sources

From London to Morse via Binnig, Quate, and Gerber

In their landmark paper introducing the atomic force microscope [Phys. Rev. Lett. \textbf{56}, 930 (1986)], Binnig, Quate, and Gerber presciently anticipated that the technique would ultimately be capable of probing interactions running the gamut from weak van der Waals interactions to strong covalent bonding. They also highlighted that the tip-sample forces central to AFM are present, and often highly influential, in scanning tunnelling microscopy; indeed, this realisation directly inspired the invention of the force microscope. In this perspective for the \textit{Forty Years of AFM} special issue, we review selected aspects of two decades of work from our group at the University of Nottingham that span the force range highlighted by BQG and are united by a common, central theme: the probe as active participant rather than passive observer. Our selection of results also covers length- and correlation-scales from the microscopic right down to the single chemical bond limit, tracking a spectrum of interactions from van der Waals/Hamaker forces, through hydrogen bonding, to covalent bonds and, finally, atom-by-atom assembly of metal clusters via vertical tip-sample transfer. Echoing BQG's own observations on the prevalence of probe-sample forces in STM, we also discuss recent evidence that tip-induced heterogeneity underpins first-passage dynamics in molecular diffusion and highlight the challenges in acquiring non-invasive measurements of diffusion barriers for adsorbed molecules that are readily perturbed by the probe. We close with a perspective on machine learning's growing role in automating tip-driven atomic and molecular manipulation.

cond-mat.mes-hall

Common physical framework explains phase behavior and dynamics of atomic, molecular and polymeric network-formers

We show that the self-assembly of a diverse collection of building blocks can be understood within a common physical framework. These building blocks, which form periodic honeycomb networks and nonperiodic variants thereof, range in size from atoms to micron-scale polymers, and interact through mechanisms as different as hydrogen bonds and covalent forces. A combination of statistical mechanics and quantum mechanics shows that one can capture the physics that governs assembly of these networks by resolving only the geometry and strength of building block interactions. The resulting framework reproduces a broad range of phenomena seen experimentally, including periodic and nonperiodic networks in thermal equilibrium, and nonperiodic supercooled and glassy networks away from equilibrium. Our results show how simple `design criteria' control assembly of a wide variety of networks, and suggest that kinetic trapping can be a useful way of making functional assemblies.

cond-mat.stat-mech

Broken symmetry and the variation of critical properties in the phase behaviour of supramolecular rhombus tilings

The degree of randomness, or partial order, present in two-dimensional supramolecular arrays of isophthalate tetracarboxylic acids is shown to vary due to subtle chemical changes such as the choice of solvent or small differences in molecular dimensions. This variation may be quantified using an order parameter and reveals a novel phase behaviour including random tiling with varying critical properties as well as ordered phases dominated by either parallel or non-parallel alignment of neighbouring molecules, consistent with long-standing theoretical studies. The balance between order and randomness is driven by small differences in the intermolecular interaction energies, which we show, using numerical simulations, can be related to the measured order parameter. Significant variations occur even when the energy difference is much less than the thermal energy highlighting the delicate balance between entropic and energetic effects in complex self-assembly processes.

cond-mat.stat-mech