Photocatalysis
is an effective technology to convert solar energy
into chemical energy, which has attracted great attention for the
degradation of water pollutants and the hydrogen production by water
splitting. The nonmetallic polymer g-C3N4 (GCN)
can meet the thermodynamic conditions of photocatalytic water splitting,
but its performances are not satisfying due to its narrow light absorption
range and high recombination rate of photogenerated charge carriers.
Among metal sulfide semiconductors, Ag–In sulfide quantum dots
(AIS QDs), such as AgInS2, show excellent visible light
absorption and promising photoactivity. In this work, AIS QDs-modified
GCN is synthesized by an in situ growth method in mild conditions.
The photocatalytic activity of the AIS-QDs/GCN nanocomposite is notably
higher than that of the pure phase g-C3N4. Especially,
the sample containing 10 wt % AIS QDs has the best activity in both
tetracycline degradation and hydrogen generation, reaching 48.5% degradation
efficiency in 1 h of visible light exposure (3.2 times that of GCN)
and a hydrogen evolution rate of 62.3 μmol·g–1·h–1 (that of bare GCN being negligible).
The optical and photoelectrochemical characterization highlights the
interplay between the two components, suggesting that the enhanced
photocatalytic activity of AIS-QDs/GCN is mainly due to the broadening
of the light absorption range, the acceleration of charge transfer,
and the reduction of the carrier pair recombination rate due to the
formation of a type-II heterojunction inside the composite catalyst.
This work is among the first attempts to modify g-C3N4 with polysulfide quantum dots to improve its catalytic performance,
and the results provide an important step for advances in the application
of these systems.