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Synthesis of PbO–TiO 2 Nanocomposites for Advanced Photocatalytic and Antimicrobial Applications
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ABSTRACT
PbO‐TiO
2
nanocomposites were synthesized via hydrothermal route to overcome the limitations of pristine TiO
2
photocatalysts, including poor visible‐light activation, and rapid charge recombination. Composites with varying PbO:TiO
2
ratios (25:75 and 50:50) were prepared using titanium (IV) butoxide and lead nitrate precursors at 180 °C for 6 h, followed by calcination at 500 °C. XRD analysis confirmed successful formation of binary composites comprising anatase TiO
2
and α,β‐PbO, while FTIR revealed interfacial chemical bonding through Pb‐O‐Ti lattice vibrations. The 25:75 PbO‐TiO
2
composite demonstrated superior photocatalytic performance with 70.0% Congo red degradation in the first hour versus 56.8% for pure TiO
2
, representing a 1.23‐fold enhancement (2.80 versus 2.27 mg g
−
1
), primarily governed by heterojunction‐induced charge separation and bandgap narrowing that suppress electron–hole recombination and enhance reactive oxygen species generation. Antimicrobial evaluation against gram‐positive (
S. aureus
,
L. monocytogenes
) and gram‐negative (
E. coli
,
S. abony
) bacteria plus
C. albicans
revealed composition‐dependent enhancement, with 50:50 composite achieving inhibition zones of 10.9 ± 0.29 mm against
E. coli
and
S. aureus
. The enhanced antimicrobial efficacy operates through synergistic mechanisms combining photocatalytic reactive oxygen species generation with direct Pb
2
+
ion toxicity targeting membrane integrity, enzymatic functions, and DNA structure. These findings establish PbO‐TiO
2
composites as multifunctional platforms addressing conventional TiO
2
limitations while offering enhanced antimicrobial properties for environmental and biomedical applications.
Title: Synthesis of PbO–TiO
2
Nanocomposites for Advanced Photocatalytic and Antimicrobial Applications
Description:
ABSTRACT
PbO‐TiO
2
nanocomposites were synthesized via hydrothermal route to overcome the limitations of pristine TiO
2
photocatalysts, including poor visible‐light activation, and rapid charge recombination.
Composites with varying PbO:TiO
2
ratios (25:75 and 50:50) were prepared using titanium (IV) butoxide and lead nitrate precursors at 180 °C for 6 h, followed by calcination at 500 °C.
XRD analysis confirmed successful formation of binary composites comprising anatase TiO
2
and α,β‐PbO, while FTIR revealed interfacial chemical bonding through Pb‐O‐Ti lattice vibrations.
The 25:75 PbO‐TiO
2
composite demonstrated superior photocatalytic performance with 70.
0% Congo red degradation in the first hour versus 56.
8% for pure TiO
2
, representing a 1.
23‐fold enhancement (2.
80 versus 2.
27 mg g
−
1
), primarily governed by heterojunction‐induced charge separation and bandgap narrowing that suppress electron–hole recombination and enhance reactive oxygen species generation.
Antimicrobial evaluation against gram‐positive (
S.
aureus
,
L.
monocytogenes
) and gram‐negative (
E.
coli
,
S.
abony
) bacteria plus
C.
albicans
revealed composition‐dependent enhancement, with 50:50 composite achieving inhibition zones of 10.
9 ± 0.
29 mm against
E.
coli
and
S.
aureus
.
The enhanced antimicrobial efficacy operates through synergistic mechanisms combining photocatalytic reactive oxygen species generation with direct Pb
2
+
ion toxicity targeting membrane integrity, enzymatic functions, and DNA structure.
These findings establish PbO‐TiO
2
composites as multifunctional platforms addressing conventional TiO
2
limitations while offering enhanced antimicrobial properties for environmental and biomedical applications.
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