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Isobel McSweeney

Publications and source records attributed to Isobel McSweeney.

3 recordsLinked to original sources

Scalable Size- and Shape-Selective Purification of Colloidal Building Blocks via Excluded Volume Interactions

Excluded-volume interactions, arising solely from steric constraints, play a crucial role in determining the structure, dynamics, and phase behaviour of colloidal suspensions. This is particularly important for non-spherical particles, where orientation-dependent effects also become significant. In this study, we employ depletion-driven phase separation to develop a scalable, size-selective method for purifying spherical and non-spherical colloidal clusters that exhibit an interplay of concave and convex surface areas. Phase diagrams of charge-stabilised polystyrene spheres ranging in size from 267 to 1008 nm demonstrate that the mixing-demixing transition occurs across a range of surfactant concentrations rather than at a single threshold. Taking advantage of this transition width enables the purification of a single component from binary mixtures at size ratios as low as 1.6 in a single step. When the same approach is applied to tetrameric colloidal clusters, these are enriched fifteenfold relative to uncoordinated spheres. Importantly, the efficiency of sorting depends not only on the effective size but also on the geometry of the aggregate. For instance, anisotropic, weakly fused clusters separate more efficiently than spherical aggregates because their concave surface curvature is reduced compared to unfused clusters. These findings establish excluded-volume-driven sorting as a practical and scalable route for purifying colloidal building blocks for hierarchical assembly.

cond-mat.soft

Electron Correlation Enables Phase-Coherent One-Attosecond Pulse Trains

Attosecond synthesis is ultimately a phase problem: a broad spectrum produces an ultrashort waveform only if its harmonics remain phase-locked. We show theoretically that correlated two-electron high-harmonic generation in helium driven by a long, multicycle laser pulse supports a train of soft-x-ray bursts with durations approaching 1 as. Using a two-electron strong-field approximation, we calculate the complex harmonic spectrum and reconstruct the temporal emission while retaining its full intrinsic spectral phase, rather than imposing a flat-phase approximation. Despite the trajectory-dependent phase accumulated by two continuum electrons, the correlation-extended plateau contains a broad phase-coherent region reaching the keV range. Its superposition produces reproducible bursts separated by one half-cycle of the driving field. These results identify electron correlation not only as a mechanism for extending the high-harmonic cutoff, but also as a route toward phase-coherent x-ray waveforms on the zeptosecond timescale.

physics.atom-ph

Two-Electron Effects Extend High-Harmonic Generation into the keV Regime

Two-electron processes can generate high harmonics beyond the conventional single-active-electron cutoff. Motivated by recent experimental evidence of an extended secondary plateau in the helium high-harmonic spectrum [S. Wang et al, Optica, (2023); S. Wang et al, In Print in Nature Photon., (2026)], we present a two-electron generalisation of the strong-field approximation. We analyse the resulting expressions using the saddle-point method and determine the extended cutoff. We find good agreement with classical predictions of cutoff scalings of $4.7$ and $5.5$ times the ponderomotive energy, which significantly exceed the established single-electron scaling of 3.17. We calculate high-harmonic spectra generated via a two-electron process in helium atoms driven by an intense few-cycle infrared laser pulse. Our results demonstrate that the harmonic spectrum extends far beyond the water window, reaching photon energies up to $\approx 1.2\,\mathrm{keV}$ in the soft x-ray region. The large spectral bandwidth can support the generation of sub-attosecond soft x-ray pulses, which are of particular interest for probing ultrafast dynamics across matter, including applications in core-level spectroscopy and biological imaging.

physics.atom-ph