Mn-doped
lead halide perovskites exhibit long-lived dopant luminescence
and enhanced host excitonic quantum yield. The contention between
energy and charge transfer in sensitizing dopant luminescence in Mn-doped
perovskites is investigated by state-of-the-art DFT calculations on
APbX
3
perovskites (X = Cl, Br, and I). We quantitatively
simulate the electronic structure of Mn-doped perovskites in various
charge and spin states, providing a structural/mechanistic analysis
of Mn sensitization as a function of the perovskite composition. Our
analysis supports both energy- and charge-transfer mechanisms, with
the latter probably preferred in Mn:CsPbCl
3
due to small
energy barriers and avoidance of spin and orbital restrictions. An
essential factor determining the dopant luminescence quantum yield
in the case of charge transfer is the energetics of intermediate oxidized
species, while bandgap resonance can well explain energy transfer.
Both aspects are mediated by perovskite host band edge energetics,
which is tuned in turn by the nature of the halide X.