Construction of an S-scheme heterojunction with staggered
energy
band structures can facilitate the charge separation and reserve their
high redox potential. Herein, an S-scheme Ni3Se4/TiO2 heterojunction is successfully constructed via an
in situ hydrothermal method. The introduction of the Ni3Se4 nanoparticle can enhance the light absorption ability,
favor the charge transfer, and induce more abundant electrochemically
active sites of the composite. Based on the photocatalytic H2 evolution experiments, the H2 evolution rate of 10%-Ni3Se4/TiO2 reaches 8409.3 μmol·g–1
·h–1 under simulated sunlight irradiation using TEOA as the sacrificial
agent, which is 32.3 and 127.2 times than those of TiO2 and Ni3Se4, respectively. This composite also
exhibits excellent stability during four cycling tests. In addition,
the charge transfer between Ni3Se4 and TiO2 following the S-scheme route is confirmed by the core-level
alignment analysis and hydroxyl radical capture tests; this special
charge transfer can retain the active charges by consuming the inactive
electrons and holes. This work demonstrates that the Ni3Se4 nanoparticle as a reduction photocatalyst can be employed
to construct an S-scheme heterojunction with desired photocatalytic
performance.