posted on 2021-02-23, 21:13authored bySarah
A. Lindley, Qi An, William A. Goddard, Jason K. Cooper
We
offer a detailed investigation of the photophysical properties
of plasmonic solid and hollow gold nanospheres suspended in water
by combining ultrafast transient absorption (TA) spectroscopy with
molecular dynamics (MD) simulations. TA reveals that hollow gold nanospheres
(HGNs) exhibit faster excited state relaxation and larger amplitude
acoustic phonon modes than solid gold nanoparticles of the same outer
diameter. MD simulation carried out on full scale nanoparticle–water
models (over 10 million atoms) to simulate the temporal evolution
(0–100 ps) of the thermally excited particles (1000 or 1250
K) provides atomic-scale resolution of the spatiotemporal temperature
and pressure maps, as well as visualization of the lattice vibrational
modes. For the 1000 K HGN, temperatures upward of 500 K in the vicinity
of the shell surface were observed, along with pressures up to several
hundred MPa in the inner cavity, revealing potential use as a photoinduced
nanoreactor. Our approach of combining TA and MD provides a path to
better understanding how thermal–structural properties (such
as expansion and contraction) and thermal–optical properties
(such as modulated dielectrics) manifest themselves as TA signatures.
The detailed picture of heat transfer at interfaces should help guide
nanoparticle design for a wide range of applications that rely on
photothermal conversion, including photothermal coupling agents for
nanoparticle-mediated photothermal therapy and photocatalysts for
light-driven chemical reactions.