We discovered for the first time that light can twist metal to control the chirality of metal nanostructures (hereafter, chiral metal nanoneedles). The helicity of optical vortices is transferred to the constituent elements of the irradiated material (mostly melted material), resulting in the formation of chiral metal nanoneedles. The chirality of these nanoneedles could be controlled by just changing the sign of the helicity of the optical vortex. The tip curvature of these chiral nanoneedles was measured to be <40 nm, which is less than 1/25th of the laser wavelength (1064 nm). Such chiral metal nanoneedles will enable us to selectively distinguish the chirality and optical activity of molecules and chemical composites on a nanoscale and they will provide chiral selectivity for nanoscale imaging systems (e.g., atomic force microscopes), chemical reactions on plasmonic nanostructures, and planar metamaterials.

We discovered that chiral nanoneedles fabricated by vortex laser ablation can be used to visualize the helicity of an optical vortex. The orbital angular momentum of light determines the chirality of the nanoneedles, since it is transferred from the optical vortex to the metal. Only the spin angular momentum of the optical vortex can reinforce the helical structure of the created chiral nanoneedles. We also found that optical vortices with the same total angular momentum (defined as the sum of the orbital and spin angular momenta) are degenerate, and they generate nanoneedles with the same chirality and spiral frequency.

Microneedle fabrication on a metal surface based on laser ablation using twisted light with spin was demonstrated, for the first time. The resulting needle showed a height of at least 10 μm above the target surface and a tip diameter of less than 0.3 μm. We also demonstrated the fabrication of a two-dimensional 5 × 6 microneedle array. The needles were uniformly well shaped with an average length and tip diameter of about 10 and 0.5 μm, respectively.

The formation of a monocrystalline silicon needle by picosecond optical vortex pulse illumination was demonstrated for the first time in this study. The dynamics of this silicon needle formation was further revealed by employing an ultrahigh-speed camera. The melted silicon was collected through picosecond pulse deposition to the dark core of the optical vortex, forming the silicon needle on a submicrosecond time scale. The needle was composed of monocrystalline silicon with the same lattice index (100) as that of the silicon substrate and had a height of approximately 14 μm and a thickness of approximately 3 μm. Overlaid vortex pulses allowed the needle to be shaped with a height of approximately 40 μm without any changes to the crystalline properties. Such a monocrystalline silicon needle can be applied to devices in many fields, such as core–shell structures for silicon photonics and photovoltaic devices as well as nano- or microelectromechanical systems.

We have discovered that a novel chiral structured surface relief (termed ‘conch’-shaped surface relief) with a height of over 1 μm can be formed in an azo-polymer film merely by employing circularly polarized optical vortex irradiation with a total angular momentum of j = ±2. The temporal evolution of the conch-shaped surface relief in the azo-polymer film was also observed. The results provide physical insight into how the angular momentum of light is transferred to a material through mass transport by cis-trans photo-isomerization. Such conch-shaped surface reliefs with chirality, in which functional chemical composites can be doped, enable new applications, such as planar chiral metamaterials, plasmonic holograms, and identification of chiral chemical composites.