In
photocatalysis, imperative photoredox behavior and narrow band
gap are important properties to exploit solar light for water splitting
reaction. Nanostructured ceria (cerium dioxide/CeO2) with
Ce3+/Ce4+ (photoredox couple) shows significant
enhancement in photocatalytic activity, however, no significant activity
for water splitting reaction. The present study mainly focuses on
incorporation of Pt on nanostructured mesoporous ceria by wet-impregnation
method and its evaluation for donor assisted photocatalytic water
splitting reaction. The BET analysis shows much higher surface area
(119–131 m2 g–1) for unmodified
as well as Pt modified mesoceria samples as compared to commercial
ceria (24.4 m2 g–1), although structure
was not ordered. The incorporation of Pt on mesoceria shows remarkable
influence on photocatalytic hydrogen generation activity, and 1 wt
% Pt was found to be optimized content, with broader light absorption.
This photocatalyst was optimized with respect to photocatalyst dose,
use of different sacrificial donors and their concentrations as well
as other experimental parameters, with 34 h time course evaluation,
yielding cumulative 1.52 mmol of hydrogen, under visible-NIR light
irradiation and using ethanol as a sacrificial donor. The XPS, BET
and photoluminescence studies imply that the enhanced photocatalytic
hydrogen evolution in the case of mesoceria is due to the unison of
high surface area, reduced recombination of photogenerated charge
carrier and lower Ce3+ concentration in the case of mesoceria.
This article deals with the synthesis of broad band absorption material which extends absorption response up to the infrared region by using plasmonic metal nanoparticles and upconverting host. The synergistic effect of surface plasmon resonance of the Au nanoparticle and upconversion property of (Yb,Er)NYF significantly enhances broad band absorption and photogenerated charge generation and transfer. Au as a plasmonic nanoparticle on (Yb,Er)NYF-TiO 2 plays multiple role of harvesting solar energy and exhibiting excellent catalytic activity. The synthesized heterostructure (Yb,Er)NYF-TiO 2 /Au tested for donor-assisted photocatalytic hydrogen generation shows a steady and remarkably high hydrogen generation rate of 350 μmol h −1 under solar AM 1.5 which is approximately 3.1 times higher than Au/TiO 2 (Degussa P-25). Moreover, a simple synthesis procedure has been rationally designed (Yb,Er)NYF-TiO 2 /Au which shall provide a pathway for futuristic design of plasmon-enhanced broad band absorption material.
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