posted on 2016-10-24, 00:00authored byDavid
T. Valley, Vivian E. Ferry, David J. Flannigan
We
report real-space, time-resolved imaging of coherently excited
acoustic phonon modes in plasmonic nanoparticles via femtosecond electron
imaging with an ultrafast electron microscope. The particles studied
were cetyl trimethylammonium bromide stabilized Au nanorods (40 ×
120 nm), and the particular specimen configurations for which photoinduced
vibrational modes were visualized consisted of a single, isolated
nanocrystal and a cluster of four irregularly arranged and randomly
oriented particles, all supported on an amorphous Si3N4 membrane. In both configurations, we are able to resolve
discrete intraparticle acoustic phonon modes via diffraction-contrast
modulation with bright-field femtosecond electron imaging. For the
single nanorod, we spatiotemporally mapped the intraparticle vibrational
energy distribution and decay times. With Fourier filtering, acoustic
phonons ranging from 4 to 30 GHz (250 to 33 ps periods, respectively)
were visualized, corresponding to bending, extensional, and higher-order
modes. Furthermore, heterogeneously distributed intraparticle decay
times, ranging from 3 to 10 ns, were spatially mapped, indicating
a strong dependence on coupling of the mode to the underlying substrate.
For a cluster of four randomly oriented nanorods, we are able to image
acoustic phonon modes that are strongly localized to particular particle–particle
contact regions within the aggregate. A vibrational mode occurring
at 27 GHz (37 ps period) was observed to occur at a 10 nm side-to-end
contact region, with other intraparticle points at distances of 20
and 50 nm from the region showing no such dynamics, although the initial
few-picosecond diffraction-contrast response was observed changing
sign in moving from the end to the center of the particle. Excellent
agreement is found between the spatiotemporally mapped vibrational-mode
symmetries and finite-element simulations of supported modes in a
polymer-coated Au nanorod supported on a Si3N4 membrane. This experiment resolves both the structure and dynamic
properties of the plasmonic assembly, providing insight into the characteristics
of complex plasmonic assemblies that ultimately determine their response
to ultrafast excitation.