arXiv subjects

Simon D. Connell

Publications and source records attributed to Simon D. Connell.

4 recordsLinked to original sources

arXiv2025

Temperature gradient-driven motion of magnetic domains in a magnetic metal multilayer by entropic forces

We studied the displacement of magnetic domains under temperature gradients in perpendicularly magnetized Ta/[Pt/Co$_{68}$B$_{32}$/Ir]$_{\times 10}$/Pt multilayer tracks with microfabricated Pt heaters/thermometers by magnetic force microscopy (MFM). Subtracting out the effects of the Oersted field from the heating current reveals the pure temperature gradient-driven motion, which is always towards the heater. The higher the thermal gradient along the track (owing to proximity to the heater or larger heater currents), the greater the observed displacements of the domains, up to a velocity of around 1~nm/s in a temperature gradient of 20~K/$\mu$m. Quantitative estimates of the strength of different driving mechanisms show that entropic forces dominate over those arising from the spin Seebeck and spin-dependent Seebeck effects.

cond-mat.mes-hall↗

arXiv2019

Nanoscale Substrate Roughness Hinders Domain Formation in Supported Lipid Bilayers

Supported Lipid Bilayers (SLBs) are model membranes formed at solid substrate surfaces. This architecture renders the membrane experimentally accessible to surface sensitive techniques used to study their properties, including Atomic Force Microscopy (AFM), optical fluorescence microscopy, Quartz Crystal Microbalance (QCM) and X-Ray/Neutron Reflectometry, and allows integration with technology for potential biotechnological applications such as drug screening devices. The experimental technique often dictates substrate choice or treatment, and it is anecdotally recognised that certain substrates are suitable for the particular experiment, but the exact influence of the substrate has not been comprehensively investigated. Here, we study the behavior of a simple model bilayer, phase separating on a variety of commonly used substrates, including glass, mica, silicon and quartz, with drastically different results. The distinct micron scale domains observed on mica, identical to those seen in free-floating Giant Unilamellar Vesicles (GUVs), are reduced to nanometer scale domains on glass and quartz. The mechanism for the arrest of domain formation is investigated, and the most likely candidate is nanoscale surface roughness, acting as a drag on the hydrodynamic motion of small domains during phase separation. Evidence was found that the physico-chemical properties of the surface have a mediating effect, most likely due to changes in the lubricating interstitial water layer between surface and bilayer.

physics.bio-ph↗

arXiv2018

Coincident Molecular Auxeticity and Negative Order Parameter in a Liquid Crystal Elastomer

"Auxetic" materials have the counter-intuitive property of expanding rather than contracting perpendicular to an applied stretch, formally they have negative Poisson's Ratios (PRs).[1,2] This results in properties such as enhanced energy absorption and indentation resistance, which means that auxetics have potential for applications in areas from aerospace to biomedical industries.[3,4] Existing synthetic auxetics are all created by carefully structuring porous geometries from positive PR materials. Crucially, their geometry causes the auxeticity.[3,4] The necessary porosity weakens the material compared to the bulk and the structure must be engineered, for example, by using resource-intensive additive manufacturing processes.[1,5] A longstanding goal for researchers has been the development of a synthetic material that has intrinsic auxetic behaviour. Such "molecular auxetics" would avoid porosity-weakening and their very existence implies chemical tuneability.[1,4-9] However molecular auxeticity has never previously been proven for a synthetic material.[6,7] Here we present a synthetic molecular auxetic based on a monodomain liquid crystal elastomer (LCE). When stressed perpendicular to the alignment direction, the LCE becomes auxetic at strains greater than approximately 0.8 with a minimum PR of -0.8. The critical strain for auxeticity coincides with the occurrence of a negative liquid crystal order parameter (LCOP). We show the auxeticity agrees with theoretical predictions derived from the Warner and Terentjev theory of LCEs.[10] This demonstration of a synthetic molecular auxetic represents the origin of a new approach to producing molecular auxetics with a range of physical properties and functional behaviours. Further, it demonstrates a novel feature of LCEs and a route for realisation of the molecular auxetic technologies that have been proposed over the years.

cond-mat.soft↗

arXiv2010

Nano-scale mechanical probing of supported lipid bilayers with atomic force microscopy

We present theory and experiments for the force-distance curve $F(z_0)$ of an atomic force microscope (AFM) tip (radius $R$) indenting a supported fluid bilayer (thickness $2d$). For realistic conditions the force is dominated by the area compressibility modulus $κ_A$ of the bilayer, and, to an excellent approximation, given by $F= πκ_A R z_0^2/(2d-z_0)^2$. The experimental AFM force curves from coexisting liquid ordered and liquid disordered domains in 3-component lipid bilayers are well-described by our model, and provides $κ_A$ in agreement with literature values. The liquid ordered phase has a yield like response that we model by hydrogen bond breaking.

physics.bio-ph↗