Solid
state triplet–triplet annihilation (TTA) upconversion
(UC) systems may find application as elements in a wide range of practical
photon energy conversion technologies. One strategy to produce highly
efficient UC emission in the solid state is to create systems that
can efficiently transport generated triplets to distances significantly
longer than afforded by the Dexter mechanism under restriction of
molecular movement. In this work, we present a new solid state UC
system through integration of conjugated poly(p-phenylene
vinylene) (PPV) derivatives, with tethered and/or blended chromophores
of (9,10-bisphenylethynylanthracene (BPEA) as an emitter and palladium(II)
meso-tetraphenyltetrabenzoporphyrine (TBP)) as a sensitizer. Photoluminescence
spectroscopy reveals that the introduction of a small ratio (ca. 3%)
of covalently bound BPEA onto the PPV backbone enhances UC emission
around an order of magnitude compared to the homo-PPV when mixed with
2 wt % TBP. On the other hand, time-resolved measurements find more
rapid consumption of the generated sensitizer triplets with BPEA increased
concentrations (up to 50 mol %), suggesting that these BPEA units
provide accelerated triplet energy transfer (TET) compared to in homo-PPV,
however there exists a significant loss channel via energy back transfer
in PPV-BPEA with higher contents of the BPEA unit. Moreover, microsecond
time scale decay behavior, where a small population of triplets exist,
show that triplets were mainly transmitted through the conjugated
polymer phase.