Luminescent solar concentrators (LSCs)
are solar-harvesting devices
fabricated from a transparent waveguide that is doped or coated with
lumophores. Despite their potential for architectural integration,
the optical efficiency of LSCs is often limited by incomplete harvesting
of solar radiation and aggregation-caused quenching (ACQ) of lumophores
in the solid state. Here, we demonstrate a multilumophore LSC design
that circumvents these challenges through a combination of nonradiative
Förster resonance energy transfer (FRET) and aggregation-induced
emission (AIE). The LSC incorporates a green-emitting poly(tetraphenylethylene),
p-O-TPE, as an energy donor and a red-emitting perylene bisimide molecular
dye (PDI-Sil) as the energy acceptor, within an organic–inorganic
hybrid diureasil waveguide. Steady-state photoluminescence studies
demonstrate the diureasil host induced AIE from the p-O-PTE donor
polymer, leading to a high photoluminescence quantum yield (PLQY)
of ∼45% and a large Stokes shift of ∼150 nm. Covalent
grafting of the PDI-Sil acceptor to the siliceous domains of the diureasil
waveguide also inhibits nonradiative losses by preventing molecular
aggregation. Due to the excellent spectral overlap, FRET was shown
to occur from p-O-TPE to PDI-Sil, which increased with acceptor concentration.
As a result, the final LSC (4.5 cm × 4.5 cm × 0.3 cm) with
an optimized donor–acceptor ratio (1:1 by wt %) exhibited an
internal photon efficiency of 20%, demonstrating a viable design for
LSCs utilizing an AIE-based FRET approach to improve the solar-harvesting
performance.