SearcharxivSearch

arXiv subjects

Alex Saywell

Publications and source records attributed to Alex Saywell.

2 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

One-step synthesis of graphene containing topological defects

Chemical vapour deposition enables large-domain growth of ideal graphene, yet many applications of graphene require the controlled inclusion of specific defects. We present a one-step chemical vapour deposition procedure aimed at retaining the precursor topology when incorporated into the grown carbonaceous film. When azupyrene, the molecular analogue of the Stone-Wales defect in graphene, is used as a precursor, carbonaceous monolayers with a range of morphologies are produced as a function of the copper substrate growth temperature. The higher the substrate temperature during deposition, the closer the resulting monolayer is to ideal graphene. Analysis, with a set of complementary materials characterisation techniques, reveals morphological changes closely correlated with changes in the atomic adsorption heights, network topology, and concentration of 5-/7-membered carbon rings. The engineered defective carbon monolayers can be transferred to different substrates, potentially enabling applications in nanoelectronics, sensorics, and catalysis.

cond-mat.mtrl-sci