Background::
Bimetallic nanocomposites have currently gained significant importance for enhanced catalytic
applications relative to monometallic analogues. The synergistic interactions modified electronic and optical properties in
the bimetallic (M1@M2) structural morphology e.g., core-shell /alloy nanostructures resulted in a better co-catalytic
performance for TiO2 photocatalysis.
Objective::
Hence, this article discusses the preparation, characterization, and co-catalytic activity of different bimetallic
nanostructures namely, Cu@Zn, Pd@Au, Au@Ag, and Ag@Cu, etc.
Method::
These bimetallic co-catalysts deposited on TiO2 possess the ability to absorb visible light due to surface plasmonic
absorption and are also expected to display the new properties due to synergy between two distinct metals. As a result, they
reveal the highest level of activity than the monometal deposited TiO2.
Result::
Their optical absorption, emission, charge carrier dynamics, and surface structural morphology are explained for
the improved photocatalytic activity of M1@M2 loaded TiO2 for the hydrogenation of certain organic compounds e.g.,
quinoline, crotonaldehyde, and 1,3-dinitrobenzene, etc. under UV/ visible light irradiation.
Conclusion::
It revealed that the use of bimetallic core@shell co-catalyst for hydrogenation of important industrial organics
by M1@M2-TiO2 nanocomposite demonstrates beneficial reactivity in many instances relative to conventional transition
metal catalysts.
Uniform synthesis of palladium species confined in a small-pore zeolite via full ion-exchange investigated by cryogenic electron microscopy
