Photo-induced Magnetic Force Between Nanostructures

TL;DR

This paper theoretically investigates photo-induced magnetic forces between nanostructures at optical frequencies, demonstrating the potential for magnetic force detection using engineered nanoprobes in microscopy and spectroscopy.

Contribution

It introduces two nanostructure examples capable of generating strong optical magnetic dipolar fields and evaluates their magnetic forces, highlighting their detection feasibility.

Findings

Magnetic forces of piconewtons are achievable with nanoprobes.

Engineered nanostructures can generate measurable optical magnetic dipoles.

Magnetic force detection can advance optical magnetic transition studies.

Abstract

Photo-induced magnetic force between nanostructures, at optical frequencies, is investigated theoretically. Till now optical magnetic effects are not used in scanning probe microscopy because of the vanishing natural magnetism with increasing frequency. On the other hand, artificial magnetism in engineered nanostructures led to the development of measurable optical magnetism. Here, two examples of nanoprobes that are able to generate strong magnetic dipolar fields at optical frequency are investigated: first an ideal magnetically polarizable nanosphere and then a circular cluster of silver nanospheres that has a loop-like collective plasmonic resonance equivalent to a magnetic dipole. Magnetic forces are evaluated based on nanostructure polarizabilities, i.e. induced magnetic dipoles, and magnetic-near field evaluations. As an initial assessment on the possibility of a magnetic nanoprobe to detect magnetic forces, we consider two identical magnetically polarizable nanoprobes and observe magnetic forces in the order of piconewtons thereby bringing it within detection limits of conventional atomic force microscopes at ambient pressure and temperature. The detection of magnetic force is a promising method in studying optical magnetic transitions that can be the basis of innovative spectroscopy applications.