The work function and surface property of ZnO can be
simply tuned by the self-assembled monolayer (SAM) molecules derived
from benzoic acid such as 4-methoxybenzoic acid (MBA), 4-tert-butylbenzoic acid (BBA), and 4-fluorobenzoic acid (FBA), which have
different dipole orientation and magnitude. MBA, BBA, and FBA treated
ZnO layers were used as an electron injection/transporting layer for
inverted type polymer solar cells (PSCs) with a structure of ITO/SAM
treated ZnO/active layer (P3HT:PC61BM)/MoO3/Ag.
The power conversion efficiency (PCE) of PSCs based on MBA and BBA
treated ZnO reaches 3.34 and 2.94%, respectively, while the PCE of
the device based on untreated ZnO is 2.47%. In contrary, the PCE of
the device with FBA treated ZnO is 1.81%. The open circuit voltage
(V
oc) of the device with MBA, BBA, and
FBA treated ZnO is 0.63 and 0.62 V, respectively, while the V
oc of PSC with untreated ZnO is 0.60 V. Contrarily,
the V
oc of the device with FBA treated
ZnO is 0.53 V. The PCE and V
oc of PSCs
based on MBA and BBA treated ZnO are better than those of the other
devices. This seems to be related with the direction of dipole moment
of benzoic acid derivatives. Also, the morphology of the active layer
seems to be affected by the substituent on the 4-position of benzoic
acid. The active layer on MBA treated ZnO shows optimized morphology,
and its device shows the best performances. We demonstrate that the
work function and morphology of the active layer can be controlled
by SAM treatment of the ZnO surface with different dipole orientation
and a substituent on the 4-position of benzoic acid. These are very
simple and effective methods for improving the performances of PSCs.
The results provide an alternative strategy to improve the interface
property between inorganic and organic materials in organic electronic
devices.
A nonconjugated anionic polyelectrolyte, poly(sodium 4-styrenesulfonate) (PSS-Na), was applied to the optoelectronic devices as an interfacial layer (IFL) at the semiconducting layer/cathode interface. The ultraviolet photoelectron spectroscopy and the Kelvin probe microscopy studies support the formation of a favorable interface dipole at the organic/cathode interface. For polymer light-emitting diodes (PLEDs), the maximum luminance efficiency (LEmax) and the turn-on voltage (Von) of the device with a layer of PSS-Na spin-coated from the concentration of 0.5 mg/mL were 3.00 cd/A and 5.5 V, which are dramatically improved than those of the device without an IFL (LEmax = 0.316 cd/A, Von = 9.5 V). This suggests that the PSS-Na film at the emissive layer/cathode interface improves the electron injection ability. As for polymer solar cells (PSCs), the power conversion efficiency (PCE) of the device with a layer of PSS-Na spin-coated from the concentration of 0.5 mg/mL was 2.83%, which is a 16% increase compared to that of the PSC without PSS-Na. The PCE improvement is mainly due to the enhancement of the short-circuit current (12% increase). The results support that the electron collection and transporting increase by the introduction of the PSS-Na film at the photoactive layer/cathode interface. The improvement of the efficiency of the PLED and PSC is due to the reduction of the Schottky barrier by the formation of a favorable interface as well as the better Ohmic contact at the cathode interface.
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