posted on 2021-07-15, 19:06authored byJoshua Moncada, Tanguy Terlier, Ilia N. Ivanov, Mark D. Dadmun
Thin
films containing conjugated polymers have been used in a wide
array of optoelectronic devices, and much research has focused on
the conformation of the conjugated polymer as a key aspect to tuning
the performance of the resulting devices. White light exposure has
been studied as a post-processing method to alter the film’s
morphology and photoluminescence (PL) in systems composed of poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene]
(MEH-PPV) and polystyrene (PS). To date, there have been few studies
that correlate the changes in the depth profile with the PL performance
of MEH-PPV/PS films. This study is designed to address this gap in
knowledge. Thin films of MEH-PPV/dPS annealed above the glass transition
temperatures (Tg) in an illuminated environment
led to lower PL than that found in annealed samples that are not illuminated.
However, at higher MEH-PPV loading in the blend film, the extent of
variation of PL with illumination diminished. Time-of-flight secondary
ion mass spectrometry and small-angle neutron scattering document
the three-dimensional morphology of the films under illumination conditions,
which are correlated with the changes in PL. Illumination during annealing
compressed MEH-PPV-rich layers in the thin film blends at low loadings
of MEH-PPV (below 10 wt %) but resulted in significant in-plane phase
separation at higher loadings (above 15 wt %). Both changes increase
interchain interactions and lower the PL of the illuminated samples.
The changes in the depth profile significantly alter the PL of the
films, while the in-plane phase separation affected the optoelectronic
properties to a lesser degree. This work, therefore, provides insights
into how illumination and film composition can be utilized to predictably
alter the structure and optoelectronic performance of conjugated polymer
blend films.