Singlet molecular oxygen (
1
O
2
)
has been reported
in wide arrays of applications ranging from optoelectronic to photooxygenation
reactions and therapy in biomedical proposals. It is also considered
a major determinant of photodynamic therapy (PDT) efficacy. Since
the direct excitation from the triplet ground state (
3
O
2
) of oxygen to the singlet excited state
1
O
2
is spin forbidden; therefore, a rational design and development
of heterogeneous sensitizers is remarkably important for the efficient
production of
1
O
2
. For this purpose, quantum
dots (QDs) have emerged as versatile candidates either by acting individually
as sensitizers for
1
O
2
generation or by working
in conjunction with other inorganic materials or organic sensitizers
by providing them a vast platform. Thus, conjoining the photophysical
properties of QDs with other materials, e.g., coupling/combining with
other inorganic materials, doping with the transition metal ions or
lanthanide ions, and conjugation with a molecular sensitizer provide
the opportunity to achieve high-efficiency quantum yields of
1
O
2
which is not possible with either component
separately. Hence, the current review has been focused on the recent
advances made in the semiconductor QDs, perovskite QDs, and transition
metal dichalcogenide QD-sensitized
1
O
2
generation
in the context of ongoing and previously published research work (over
the past eight years, from 2015 to 2023).