posted on 2013-02-13, 00:00authored byJonathan A. Scholl, Aitzol García-Etxarri, Ai Leen Koh, Jennifer A. Dionne
The plasmon resonances of two closely spaced metallic
particles
have enabled applications including single-molecule sensing and spectroscopy,
novel nanoantennas, molecular rulers, and nonlinear optical devices.
In a classical electrodynamic context, the strength of such dimer
plasmon resonances increases monotonically as the particle gap size
decreases. In contrast, a quantum mechanical framework predicts that
electron tunneling will strongly diminish the dimer plasmon strength
for subnanometer-scale separations. Here, we directly observe the
plasmon resonances of coupled metallic nanoparticles as their gap
size is reduced to atomic dimensions. Using the electron beam of a
scanning transmission electron microscope (STEM), we manipulate pairs
of ∼10-nm-diameter spherical silver nanoparticles on a substrate,
controlling their convergence and eventual coalescence into a single
nanosphere. We simultaneously employ electron energy-loss spectroscopy
(EELS) to observe the dynamic plasmonic properties of these dimers
before and after particle contact. As separations are reduced from
7 nm, the dominant dipolar peak exhibits a redshift consistent with
classical calculations. However, gaps smaller than ∼0.5 nm
cause this mode to exhibit a reduced intensity consistent with quantum
theories that incorporate electron tunneling. As the particles overlap,
the bonding dipolar mode disappears and is replaced by a dipolar charge
transfer mode. Our dynamic imaging, manipulation, and spectroscopy
of nanostructures enables the first full spectral mapping of dimer
plasmon evolution and may provide new avenues for in situ nanoassembly
and analysis in the quantum regime.