The
synthesis of hybrid 0D-2D dot–disk Au-CIS heterostructures
is enabled through nucleating wurtzite ternary I–III–VI
CuInS<sub>2</sub> (CIS) semiconductor nanostructures on cubic Au particles
via thiol-activated interface reactions. Chemistry of formation of
these unique hybrid metal–semiconductor nanostructures is established
by correlating successive X-ray diffraction patterns and microscopic
images. Furthermore, these nanostructures are explored as an efficient
photocathode material for photoelectrochemical (PEC) production of
hydrogen from water. Although CIS nanostructures are extensively used
as PEC active materials for solar-to-hydrogen conversion, the coupled
structures with Au for their exciton–plasmon coupling is observed
in producing a higher photocurrent with efficient evolution of hydrogen.
In the comparison of materials properties, it is observed that the
cathodic photocurrent, onset potential, and the half-cell solar-to-hydrogen
efficiency (HC-STH) are recorded to be superior to all CIS-based photocathodes
reported up to the current time. These results suggest that designing
proper heterostructured functional materials can enhance the hydrogen
production in the PEC cell and would be helpful for the ongoing technological
needs for a greener way of generating and storing hydrogen energy