Integrated Approaches in Nanomaterials Design: From Metal- Free Photocatalysts to Metal Oxo Clusters for Enhanced Catalytic Performance.
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IISER Mohali
Abstract
Visible light-driven hydrogen (H 2 ) evolution from water (H 2 O) has triggered an extensive
demand for high-abundant, low-cost semiconducting photocatalysts towards sustainable
energy harvesting. Even though graphitic carbon nitride (g-C 3 N 4 ) heralds great promise
as a metal-free inexpensive photocatalyst, its efficiency has been limited due to low
visible light absorption, stacked layers-driven restricted mass transfer, and poor charge-
transfer dynamics. Although many attempts have been made to exfoliate the layers and
tune the photophysics but finally end up with either complex synthetic steps or very low
yield. Herein, we have decorated the surface of g-C 3 N 4 by carbon nanotube (CNT) by
two composite formation strategies. The composite made under hydrothermal conditions
and calcination technique showed around 6 and 3 times higher H 2 evolution rates
respectively under visible light irradiation compared to the bare g-C 3 N 4 . The enhanced
photocatalytic hydrogen production can be attributed to facile charge transfer through the
network of CNT spread on the photoactive surface of g-C 3 N 4 . This work highlights the
potential of metal-free composites to realize highly efficient heterogeneous
photocatalytic systems for solar hydrogen production.
II
Synthesis of various metal oxo clusters, including those of Zr and Hf using fatty acids as
stabilizing ligands commonly employed in oxide nanocrystal stabilization. Our focus was
on the M 6 O 4 (OH) 4 (OOCR) 12 type clusters, recognized as pivotal in materials science.
We successfully synthesized different types of Zr, Hf, and Ti clusters. Exploring the
catalytic potential of zirconium and hafnium derivatives in esterification, we discovered
the superiority of oxo clusters over traditional forms like MOFs and nanocrystals.
Specifically, comparing UiO-66 MOF and ZrO 2 nanocrystals with Zr12 clusters revealed
the remarkable catalytic efficiency of clusters, attributed to their enhanced surface-to-
volume ratio. Moreover, our analysis, including Pair Distribution Function studies,
affirmed the structural integrity of the clusters, reinforcing their efficacy as catalysts in
homogeneous, zirconium/hafnium-mediated esterification reactions. These findings
provide crucial insights into the active catalytic species and pave the way for advanced
applications in catalysis and materials science