Postdoctoral Researcher, Institute for Bioengineering of Catalonia (IBEC)
My research in Beppe Battaglia's groups at IBEC and UCL focuses on characterising diffusioosmotic, diffusiophoretic and convective flows due to concentration gradients, and on developing the self-diffusiophoresis of lipid and polymer vesicles. The chemotactic response of a microscopic objects depends sensitively on the properties of its interface, and so I am investigating the connection between interfacial rheology, membrane penetration and fluid flow in the non-equilibrium conditions established by a concentration gradient.
Colloids in Adaptive Confinement
Interfacial colloids: Crystals, Clusters & Gels
I measured the response of lung surfactant monolayers to shear deformations and interpreted the observed phenomena in terms of the structure and morphology of condensed domains as observed via fluorescence imaging.
Chemotaxis is the mechanism by which microscopic biological objects navigate their environment by sensing gradients in particular chemicals and moving to regions containing (e.g.) plentiful nutrition. Developing chemotaxis in artificial nanodevices would allow selective targeting of particular regions in our bodies, therefore allowing us to deliver drugs to precisely the location they are required.
When molecules such as surfactants or proteins adsorb at an aqueous-air interface, the properties of that interface are often modified. For instance, pulmonary surfactants greatly reduce surface tension, an effect which is exploited by nature to allow easy breathing.
Using the magnetic microbutton microrheology technique developed in the Squires lab,
Colloidal spheres readily attach to oil-water interfaces where their interactions can be controlled, allowing the assembly of a variety of structures including crystals and gels. The response of these systems to shear can be probed using an interfacial microrheology technique developed in the Squires lab.
I am particularly interested in the way in which local structure determines rheological response and how rheology develops as an initially crystalline system undergoes gelation. Additionally I am taking a close look at how a crystalline system reorders itself near multi-particle clusters and the resulting defect structure.
The presence of aspherical impurities in a quasi-two-dimensional colloidal polycrystal influences both the local structure near the impurity and the overall polycrystalline texture of the entire material. Locally, impurities create defects in their neighbourhoods, disrupting the hexagonal lattice. An increased concentration of impurities is associated with smaller crystalline grains and a related decorrelation in orientational order over shorter lengthscales.
This research is published in the Journal of Physics: Condensed Matter and is the result of two undergraduate research projects performed at the University of Bristol by Andrew Gray and Lizzie Mould.
During my PhD I studied two-dimensional colloidal suspensions confined by light, resulting in the development of the colloidal corral, in which particles are confined by a circular boundary created using optical tweezers. The optical traps are soft, resulting in a flexible wall. This flexibility is the source of a number of interesting phenomena not seen in similar systems confined by a hard boundary. At high density, structural transitions are observed between concentrically layered configurations and highly hexagonal organisation reminiscent of the crystal observed in bulk. These structures exhibit markedly different dynamics due to the distribution of empty space in the system giving rise to multiple relaxation regimes. By controlling the stiffness of the boundary the interior structure and dynamics can be tuned. Furthermore, by measuring displacements of boundary particles from their optical traps mechanical measurements of pressure can be made, revealing further interesting features of adaptively confined materials.
Additionally, I investigated how the rheological response of insoluble surfactant monolayers is modified by the presence of soluble serum proteins in the aqueous subphase. The mechanical properties of a mixed phospholipid-serum protein monolayer depend strongly on the protocol by which they are mixed. When serum protein penetrates a lung surfactant monolayer, it adopts a structure determined by the initial monolayer morphology. Under the correct initial conditions, this results in a beautiful domain-templated interfacial protein network. This research is published in the Journal of the Royal Society Interface and Soft Matter.
I previously studied a microscopic rotational device driven by light, dubbed the colloidal washing machine. By driving colloidal spheres on a circular path torque is transmitted to additional confined spheres. Due to the soft nature of the colloidal ensemble, multiple transmission modes are observed dependent on internal density and the speed with which the device is driven. At microscopic lengthscales, thermal fluctuations are significant and so the colloidal washing machine operates very differently from a macroscopic machine. This research is published in and featured on the cover of Nature Physics.
Interfacial microrheology of lung surfactant & serum proteins