Chiral plasmonic nanostructures have emerged as promising objects for numerous applications in nanophotonics, optoelectronics, biosensing, chemistry, and pharmacy. Here, we propose a novel method to induce strong chirality in achiral ensembles of gold nanoparticles via irradiation with circularly-polarized light of a picosecond Nd:YAG laser. Embedding of gold nanoparticles into a nanoporous silicate matrix leads to the formation of a racemic mixture of metal nanoparticles of different chirality that is enhanced by highly asymmetric dielectric environment of the nanoporous matrix. Then, illumination with intense circularly-polarized light selectively modifies the particles with the chirality defined by the handedness of the laser light, while their “enantiomers” survive the laser action almost unaffected. This novel modification of the spectral hole burning technique leads to the formation of an ensemble of plasmonic metal nanoparticles that demonstrates circular dichroism up to 100 mdeg. An unforeseen peculiarity of the chiral nanostructures obtained in this way is that 2D and 3D nanostructures contribute almost equally to the observed circular dichroism signals. Thus, the circular dichroism is neither even nor odd under reversal of direction of light propagation. These findings will help guide the development of a passive optical modulator and nanoplatform for enhanced chiral sensing and catalysis.

The compositional asymmetry of Janus micro- and nanoparticles gives unprecedented opportunities to manipulate such particles with different stimuli to achieve enhanced optical, magnetic, and photothermal responses, which can be exploited for sensing, phototherapy, and nanoscale robotic applications. This perspective overviews recent advances in optical and magnetic manipulation of plasmonic Janus particles and their implications for biomedical applications. In particular, a brief summary of optical, plasmonic, and magnetic manipulation of Janus particles of various compositions are presented. Moreover, the potentials of plasmonic Janus particles for targeted drug delivery, photothermal therapy, hyperthermia, bio-imaging, bio-detection, and neuromodulation are briefly discussed. Finally, a perspective on the rational design and applications of this particular family of asymmetric particles is forwarded.

Solid‐state nanopores offer a powerful platform for nanoscale analysis of individual analytes, including biomolecules and functionalized nanoparticles, by confining them within a precisely defined sensing region. However, their inherently passive operation restricts practical applications, as they cannot precisely control particle position or dynamics inside the pore. Here, we introduce magnetic nanopore architectures that integrate a ferromagnetic layer into the nanopore system. Acting as a magnetic discontinuity within an otherwise uniformly magnetized film, the nanopore generates localized stray magnetic fields that enable magnetic tweezing of magnetic nanoparticles, which can be functionalized with fluorescent biomolecules. Importantly, the nanopore geometry is designed to reversibly switch between a nearly uniform magnetization state and a magnetic flux‐closure state through the application of momentary magnetic fields of predetermined amplitude. This capability allows the magnetic tweezing effect to be selectively activated or deactivated, enabling controlled capture and release of tagged biomolecules on demand. As a proof of concept, we demonstrate the selective magnetic trapping of fluorescent magnetic particles. Our work establishes a robust and controllable approach for reconfigurable, on‐chip magnetic nanopore platforms capable of selective trapping and high‐throughput single‐particle detection.