Immobilization of
inorganic metal quantum dots (especially, noble
transition metals) onto organic polymers to synthesize nanometal–polymer
composites (NMPCs) has attracted considerable attention because of
their advanced optical, electrical, catalytic/photocatalytic, and
biological properties. Herein, novel, highly efficient, stable, and
visible light-active NMPC photocatalysts consisting of silver quantum
dots (Ag QDs) immobilized onto polymeric chitosan–polyethylene
oxide (CTS–PEO) blend sheets have been successfully prepared
by an in situ self-assembly facile casting method as a facile and
green approach. The CTS–PEO blend polymer acts as a reducing
and a stabilizing agent for Ag QDs which does not generate any environmental
chemical pollutant. The prepared x wt % Ag QDs/CTS–PEO
composites were fully characterized through X-ray diffraction, Fourier
transform infrared spectroscopy, transmission electron microscopy
(TEM), thermogravimetric analysis, and UV/visible spectroscopy. The
characterization results indicated the successful synthesis of the
Ag QDs/CTS–PEO composites by the interactions and complexation
between x wt % Ag QDs and CTS–PEO blend sheets.
TEM images revealed small granules randomly distributed onto the CTS–PEO
blend sheets, indicating the immobilization of Ag QDs onto CTS–PEO
composites. The presence of a surface plasmon resonance (SPR) band
and the shifting of the absorption edge toward higher wavelengths
in the UV/vis spectra indicated the formation of x wt % Ag QDs/CTS–PEO composites. The Ag QDs in the polymeric
blend matrix led to remarkable enhancement in the optical, thermal,
electrical, and photocatalytic properties of x wt
% Ag QDs/CTS–PEO composites. The photocatalytic efficiency
of the prepared composites was evaluated by the photodegradation of p-nitrophenol (PNP) under simulated sunlight. The maximum
photocatalytic degradation reached 91.1% efficiency within 3 h for
the 12.0 wt % Ag QDs/CTS–PEO photocatalyst. Generally, the
Ag QDs immobilized onto CTS–PEO blend composites significantly
enhance the SPR effect and the synergistic effect and reduce the band
gap, leading to a high photocatalytic activity.