Molecular cocrystals
have received much attention for tuning physicochemical
properties in pharmaceutics, luminescence, organic electronics, and
so on. However, the effective methods for the formation of orderly
cocrystal thin films are still rather limited, which have largely
restricted their photofunctional and optoelectronic applications.
In this work, a fast crystallization-deposition procedure is put forward
to obtain acridine (AD)-based cocrystals, which are self-assembled
with three typical isophthalic acid derivatives (IPA, IPB, and TMA).
The obtained donor–acceptor cocrystal complexes exhibit an
adjustable energy level, wide range of photoluminescence color, and
rotational angle-dependent polarized emission. The orderly and uniform
cocrystal thin films further present tunable one-/two-photon up-conversion
and different semiconductor properties. Particularly, AD-TMA cocrystal
thin film shows a rare example of a molecule level heterojunction
with the alternating arrangement of AD electronic acceptor layers
and TMA electronic donor layers, and thus, provides a way for efficient
mobility and separation of electron–hole pairs. A large on–off
photocurrent ratio of more than 10
4
can be achieved for
the AD-TMA thin film, which is higher than state-of-the-art molecular
semiconductor systems. Therefore, this work extends the application
scopes of orderly cocrystal thin film materials for future luminescent
and optoelectronic micro-/nanodevices.