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Particle trapping and binding in optical potential wells provide a versatile platform for various biomedical applications. However, implementation systems to study multi-particle contact interactions in an optical lattice remain rare. By configuring an optofluidic lattice, we demonstrate the precise control of particle interactions and functions such as controlling aggregation and multi-hopping. The mean residence time of a single particle is found considerably reduced from 7 s, as predicted by Kramer's theory, to 0.6 s, owing to the mechanical interactions among aggregated particles. The optofluidic lattice also enables single-bacteria-level screening of biological binding agents such as antibodies through particle-enabled bacteria hopping. The binding efficiency of antibodies could be determined directly, selectively, quantitatively and efficiently. This work enriches the fundamental mechanisms of particle kinetics and offers new possibilities for probing and utilising unprecedented biomolecule interactions at single-bacteria level.

An interfacial monolayer of CuO in Cu-coated γ-Fe2O3 nanoparticles enables significantly decreased intrinsic surface spin disorder compared to bare γ-Fe2O3 nanoparticles. Element specific x-ray absorption spectroscopy at the L-edges for Cu and Fe indicates that the magnetic moment of the CuO in the shell interacts with the γ-Fe2O3 nanoparticle's surface magnetic moments. This exchange interaction cants the moments of the CuO resulting in a non-zero Cu moment, altering the γ-Fe2O3 nanomagnetism. [ABSTRACT FROM AUTHOR]

Iron disilicide in a bulk form is practically nonmagnetic. In contrast, nanoparticles of FeSi2 exhibit superparamagnetism with blocking temperatures ranging from 8 K (15 nm) to 34 K (55 nm). Their relatively low saturation magnetization suggests that the magnetic behavior is associated with only a small fraction of Fe ions, which have a sufficient number of other Fe as nearest neighbors. The chemical disorder is presumably induced in the formation of nanoparticles. A spin glass-type anomaly below 10 K observed in specific heat data gives a further evidence for the compositional heterogeneity. [ABSTRACT FROM AUTHOR]

Evidence of elemental copper magnetism in Cu-coated γ-Fe2O3 nanoparticles was revealed by element specific x-ray absorption spectroscopy and magnetic circular dichroism (XMCD). An interfacial layer of magnetic CuO was discovered that interacted with the Fe3+ surface magnetic moments. This unexpected exchange interaction canted the moments of the CuO, so that a non-zero net magnetic moment was measured. XMCD measurements as a function of field on the copper coated γ-Fe2O3 nanoparticles indicated that the CuO magnetic moment was aligned with the octahedral Fe3+ and its magnetization was modified by the changing applied field. With increasing copper thickness, a stronger field dependence of the Fe3+ and Cu2+ magnetization was observed. [ABSTRACT FROM AUTHOR]