Green production
of hydrogen is possible with photocatalytic water
splitting, where hydrogen is produced while water is reduced by using
energy derived from light. In this study, density functional theory
(DFT) is employed to gain insights into the photocatalytic performance
of La
5
Ti
2
AgS
5
O
7
and La
5
Ti
2
CuS
5
O
7
—two emerging
candidate materials for water splitting. The electronic structure
of both bulk materials was calculated by using hybrid DFT, which indicated
the band gaps and charge carrier effective masses are suitable for
photocatalytic water splitting. Notably, the unique one-dimensional
octahedral TiO
x
S
6–
x
and tetragonal MS
4
channels formed provide
a structural separation for photoexcited charge carriers which should
inhibit charge recombination. Band alignments of surfaces that appear
on the Wulff constructions of 12 nonpolar symmetric surface slabs
were calculated by using hybrid DFT for each of the materials. All
surfaces of La
5
Ti
2
AgS
5
O
7
have band edge positions suitable for hydrogen evolution; however,
the small overpotentials on the largest facets likely decrease the
photocatalytic activity. In La
5
Ti
2
CuS
5
O
7
, 72% of the surface area can support oxygen evolution
thermodynamically and kinetically. Based on their similar electronic
structures, La
5
Ti
2
AgS
5
O
7
and La
5
Ti
2
CuS
5
O
7
could
be effectively employed in Z-scheme photocatalytic water splitting.