To obtain the maximum luminous efficiency from an organic material, it is n
ecessary to harness both the spin-symmetric and anti-symmetric molecular ex
citations (bound electron-hole pairs, or excitons) that result from electri
cal pumping. This is possible if the material is phosphorescent, and high e
fficiencies have been observed in phosphorescent(1,2) organic light-emittin
g devices(3), However, phosphorescence in organic molecules is rare at room
temperature. The alternative radiative process of fluorescence is more com
mon, but it is approximately 75% less efficient, due to the requirement of
spin-symmetry conservation(4) Here, we demonstrate that this deficiency can
be overcome by using a phosphorescent sensitizer to excite a fluorescent d
ye. The mechanism for energetic coupling between phosphorescent and fluores
cent molecular species is a long-range, non-radiative energy transfer: the
internal efficiency of fluorescence can be as high as 100%. As an example,
we use this approach to nearly quadruple the efficiency of a fluorescent re
d organic light-emitting device.