posted on 2016-09-22, 00:00authored byChao Zhang, Hangqi Zhao, Linan Zhou, Andrea E. Schlather, Liangliang Dong, Michael J. McClain, Dayne
F. Swearer, Peter Nordlander, Naomi J. Halas
Photocatalysis
uses light energy to drive chemical reactions. Conventional industrial
catalysts are made of transition metal nanoparticles that interact
only weakly with light, while metals such as Au, Ag, and Al that support
surface plasmons interact strongly with light but are poor catalysts.
By combining plasmonic and catalytic metal nanoparticles, the plasmonic
“antenna” can couple light into the catalytic “reactor”.
This interaction induces an optical polarization in the reactor nanoparticle,
forcing a plasmonic response. When this “forced plasmon”
decays it can generate hot carriers, converting the catalyst into
a photocatalyst. Here we show that precisely oriented, strongly coupled
Al–Pd nanodisk heterodimers fabricated using nanoscale lithography
can function as directional antenna–reactor photocatalyst complexes.
The light-induced hydrogen dissociation rate on these structures is
strongly dependent upon the polarization angle of the incident light
with respect to the orientation of the antenna–reactor pair.
Their high degree of structural precision allows us to microscopically
quantify the photocatalytic activity per heterostructure, providing
precise photocatalytic quantum efficiencies. This is the first example
of precisely designed heterometallic nanostructure complexes for plasmon-enabled
photocatalysis and paves the way for high-efficiency plasmonic photocatalysts
by modular design.