Nanostructures
of some metals can sustain light-driven electron
oscillations called localized surface plasmon resonances, or LSPRs,
that give rise to absorption, scattering, and local electric field
enhancement. Their resonant frequency is dictated by the nanoparticle
(NP) shape and size, fueling much research geared toward discovery
and control of new structures. LSPR properties also depend on composition;
traditional, rare, and expensive noble metals (Ag, Au) are increasingly
eclipsed by earth-abundant alternatives, with Mg being an exciting
candidate capable of sustaining resonances across the ultraviolet,
visible, and near-infrared spectral ranges. Here, we report numerical
predictions and experimental verifications of a set of shapes based
on Mg NPs displaying various twinning patterns including (101̅1),
(101̅2), (101̅3), and (112̅1), that create tent-,
chair-, taco-, and kite-shaped NPs, respectively. These are strikingly
different from what is obtained for typical plasmonic metals because
Mg crystallizes in a hexagonal close packed structure, as opposed
to the cubic Al, Cu, Ag, and Au. A numerical survey of the optical
response of the various structures, as well as the effect of size
and aspect ratio, reveals their rich array of resonances, which are
supported by single-particle optical scattering experiments. Further,
corresponding numerical and experimental studies of the near-field
plasmon distribution via scanning transmission electron
microscopy electron-energy loss spectroscopy unravels a mode nature
and distribution that are unlike those of either hexagonal plates
or cylindrical rods. These NPs, made from earth-abundant Mg, provide
interesting ways to control light at the nanoscale across the ultraviolet,
visible, and near-infrared spectral ranges.