Bacterial
and organic pollutants are major problems with potential
adverse impacts on human health and the environment. A promising strategy
to alleviate these impacts consists in designing innovative photocatalysts
with a wider spectrum of application. In this paper, we report the
improved photocatalytic and antibacterial activities of chemically
precipitated Ag
3
PO
4
microcrystals by the incorporation
of W at doping levels 0.5, 1, and 2 mol %. The presence of W directly
influences the crystallization of Ag
3
PO
4
, affecting
the morphology, particle size, and surface area of the microcrystals.
Also, the characterization via experimental and theoretical approaches
evidenced a high density of disordered [AgO
4
], [PO
4
], and [WO
4
] structural clusters due to the substitution
of P
5+
by W
6+
into the Ag
3
PO
4
lattice. This leads to new defect-related energy states,
which decreases the band gap energy of the materials (from 2.27 to
2.04 eV) and delays the recombination of e′–h
•
pairs, leading to an enhanced degradation process. As a result of
such behaviors, W-doped Ag
3
PO
4
(Ag
3
PO
4
:W) is a better visible-light photocatalyst than Ag
3
PO
4
, demonstrated here by the photodegradation
of potential environmental pollutants. The degradation of rhodamine
B dye was 100% in 4 min for Ag
3
PO
4
:W 1%, and
for Ag
3
PO
4
, the obtained result was 90% of degradation
in 15 min of reaction. Ag
3
PO
4
:W 1% allowed the
total degradation of cephalexin antibiotic in only 4 min, whereas
pure Ag
3
PO
4
took 20 min to achieve the same
result. For the degradation of imidacloprid insecticide, Ag
3
PO
4
:W 1% allowed 90% of degradation, whereas Ag
3
PO
4
allowed 40%, both in 20 min of reaction. Moreover,
the presence of W-dopant results in a 16-fold improvement of bactericidal
performance against methicillin-resistant
Staphylococcus
aureus
. The outstanding results using the Ag
3
PO
4
:W material demonstrated its potential multifunctionality
for the control of organic pollutants and bacteria in environmental
applications.