Ultrathin transparent semiconducting oxides have attracted
considerable
attention in multifunctional electronic and optoelectronic devices,
owing to their exciting physical properties and excellent stability.
However, due to their wide bandgap, absorption in the visible region
is very limited. Here, we show enhanced light–matter interactions
by integrating plasmonic gold nanoparticles onto ultrathin SnO2 nanosheets, leading to higher optical absorption in the visible
spectra. In this work, a vacuum-free liquid metal printing technique
is used to deposit large-area ∼1.9 nm thick SnO2 nanosheets, which were then decorated with gold nanoparticles by
utilizing an electrostatic self-assembly technique. The enhancement
of the electric field due to localized surface plasmon resonance and
plasmon-induced hot electron generation at the Au–SnO2 interface is verified utilizing COMSOL simulations. Moreover, experimental
observations of fabricated photodetectors based on the Au–SnO2 hybrid structure demonstrate a broadband spectral response
ranging from ultraviolet to visible wavelengths. In particular, we
observe an improved room temperature photoresponsivity of ∼950
mA W–1 and a 17-fold enhancement in photocurrent
at a 400 nm wavelength as compared to bare SnO2. This work
provides a viable route to tune the optical properties of wide bandgap
2D functional oxides, making them attractive for large-area nanoscale
broadband photodetectors and optoelectronic devices.