The astrophysical phenomenon of mimetic helical magnetic field (h B)-assisted self-assembly is herein introduced to build helical superstructures that display chiroptical properties. As a building block, magnetoplasmonic (MagPlas) Ag@Fe3O4 core–shell nanoparticles are used to guide plasmonic Ag nanoparticles onto a helical magnetic flux. The chirality of the assembled helical structures and tailored circular dichroism are successfully tuned in real time, and the handedness of the assembled structures is dynamically switched by the h B at the millisecond level, which is at least 6000-fold faster than other template-assisted methods. The peak position of circular dichroism can be reconfigured by altering the plasmonic resonance or coupling by controlling the size of the Ag core and magnetic flux density. The h B-induced chirality modulation represents a method to control the polarization state of light at the nexus of plasmonics, magnetic self-assembly, colloidal science, liquid crystals, and chirality. It presents active and dynamic chiral assemblies of magnetoplasmonic nanomaterials, enabling further practical applications in optical devices.

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The Lorentz or Kelvin force generated by an externally applied magnetic field may introduce additional convection of the electrolyte near the working electrode and consequently produces magnetocurrent (MC), which can be attributed to the magnetohydrodynamic (MHD) flow and an extra electrochemical reaction. A magnetoplasmonic (MagPlas) composite of metallic and superparamagnetic nanoparticles (NPs) with a permanent dipole or magnetic moment have additional degree or order, which corresponds to directional correlation to electric and magnetic dipoles. In particular, an ordered self-assembly may boost up the MHD flow on a collectively reactive surface, leading to remarkable electrochemical performance. In this article, a proof-of-concept work explores the effect of the magnetic field on the electrocatalytic activity of the oxygen reduction reaction (ORR) as well as [Fe­(CN)6]3–/4– redox probes using a precisely controlled three-dimensional (3D) nanostructure of a silver core and a porous magnetic shell (Ag@Fe3O4) assembly. Then, the reduction current was carefully monitored in the presence of a magnetic field (B, up to 380 mT), resulting in an extraordinary increment of reduction current (I R) of [Fe­(CN)6]3– by 23% and a 1.13-fold high ORR efficiency owing to the additional magnetic field (B in) from the 3D magnetoplasmonic nanoassembly. The computational simulation explained the plausible mechanism of current enhancement from the MagPlas nanoassembly. From our experimental and computational studies, it is probable that the 3D MagPlas nanoassembly is a unique and efficient catalyst under a low external magnetic field, which would be useful for further biomedical and energy-related applications.

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