Triplet–triplet
annihilation photon upconversion (TTA-UC)
is a process in which triplet excitons combine to form emissive singlets
and holds great promise in biological applications and for improving
the spectral match in solar energy conversion. While high TTA-UC quantum
yields have been reported for, for example, red-to-green TTA-UC systems,
there are only a few examples of visible-to-ultraviolet (UV) transformations
in which the quantum yield reaches 10%. In this study, we investigate
the performance of six annihilators when paired with the sensitizer
2,3,5,6-tetra(9
H
-carbazol-9-yl)benzonitrile (4CzBN),
a purely organic compound that exhibits thermally activated delayed
fluorescence. We report a record-setting internal TTA-UC quantum yield
(Φ
UC,g
) of 16.8% (out of a 50% maximum) for 1,4-bis((triisopropylsilyl)ethynyl)naphthalene,
demonstrating the first example of a visible-to-UV TTA-UC system approaching
the classical spin-statistical limit of 20%. Three other annihilators,
of which 2,5-diphenylfuran has never been used for TTA-UC previously,
also showed impressive performances with Φ
UC,g
above
12%. In addition, a new method to determine the rate constant of TTA
is proposed, in which only time-resolved emission measurements are
needed, circumventing the need for more challenging transient absorption
measurements. The results reported herein represent an important step
toward highly efficient visible-to-UV TTA-UC systems that hold great
potential for driving high-energy photochemical reactions.