posted on 2017-05-02, 00:00authored byD. M. Tobaldi, M. J. Hortigüela Gallo, G. Otero-Irurueta, M. K. Singh, R. C. Pullar, M. P. Seabra, J. A. Labrincha
We
report titania nanoheterostructures decorated with silver, exhibiting
tuneable photochromic properties for the first time when stimulated
only by visible white light (domestic indoor lamp), with no UV wavelengths.
Photochromic materials show reversible color changes under light exposure.
However, all inorganic photochromic nanoparticles (NPs) require UV
light to operate. Conventionally, multicolor photochromism in Ag–TiO2 films involves a change in color to
brownish-gray during UV-light irradiation (i.e., reduction of Ag+ to Ag0) and a (re)bleaching (i.e., (re)oxidation
of Ag0 to colorless Ag+) upon visible-light
exposure. In this work, on the contrary, we demonstrate visible-light-induced
photochromism (ranging from yellow to violet) of 1–10 mol %
Ag-modified titania NPs using both spectroscopic and colorimetric
CIEL*a*b* analyses.
This is not a bleaching of the UV-induced color but a change in color
itself under exposure to visible light, and it is shown to be a completely
different mechanismdriven by the interfacial charge transfer
of an electron from the valence band of TiO2 to that of
the AgxO clusters that surround the titaniato
the usual UV-triggered photochromism reported in titania-based materials.
The quantity of Ag or irradiation time dictated the magnitude and
degree of tuneability of the color change, from pale yellow to dark
blue, with a rapid change visible only after a few seconds, and the
intensity and red shift of surface plasmon resonance induced under
visible light also increased. This effect was reversible after annealing
in the dark at 100 °C/15 min. Photocatalytic activity under visible
light was also assessed against the abatement of nitrogen oxide pollutants,
for interior use, therefore showing the coexistence of photochromism
and photocatalysisboth triggered by the same wavelengthin
the same material, making it a multifunctional material. Moreover,
we also demonstrate and explain why X-ray photoelectron spectroscopy
is an unreliable technique with such materials.