4 research outputs found
Synergistic Amplification of Short-Circuit Current for Organic Solar Cells via Modulation of P3HT:PCBM Spatial Distribution with Solvent Treatment
Efficient
charge transport across proper interfacial contacts is
crucial in organic solar cells. In this paper, the surface of the
P3HT:PCBM bulk heterojunction (BHJ) layer is treated with ethylene
glycol monomethyl ether (EGME) prior to cathode buffer layer and top
cathode deposition. Comparing to the nontreated P3HT:PCBM active layers,
enhancement of short-circuit current (<i>J</i><sub>sc</sub>) to about 11 mA/cm<sup>2</sup> is observed in the EGME-treated P3HT:PCBM
BHJ layers. On the other hand, two cathode buffer layers, ZnO nanoparticles
(ZnO NPs) and LiF, are utilized to block holes and diminish the electron–hole
recombination near the cathode, which consequently promote the open-circuit
voltage (<i>V</i><sub>oc</sub>) to about 0.6 V. To integrate
these two approaches, the EGME-treated P3HT:PCBM active layer and
the ZnO NPs or LiF cathode buffer layer are applied concurrently.
These two approaches work synergistically to enhance the <i>J</i><sub>sc</sub> to 16.3 mA/cm<sup>2</sup> or higher. With the distinct <i>J</i><sub>sc</sub> performance, the efficiencies of P3HT:PCBM
cells using EGME treatment in combination with the ZnO/Al and LiF/Al
cathodes are successfully amplified to 4.68% and 4.32%, respectively.
The mechanism behind the synergistic amplification on <i>J</i><sub>sc</sub> will be analyzed based on the superficial morphology
of the P3HT:PCBM active layer
Enhanced and Anisotropic Charge Transport in Polymer-Based Thin-Film Transistors by Guiding Polymer Growth
Ideal molecular features
and microstructural properties of organic
semiconducting thin films are being explored to achieve high-performance
organic thin-film transistors (OTFTs). We prepared and processed hexamethylbenzene
(HMB)/polyÂ(3-hexylthiophene) (P3HT) mixtures using a thermal gradient
system to fabricate P3HT-based OTFTs. In the thermal gradient system,
the HMB separated from the HMB/P3HT mixtures and crystallized along
the sample movement direction. The crystallized HMB affected and guided
the growth behavior of P3HT at the molecular level. Observations from
joint microscopic and spectroscopic analyses revealed that the HMB-processed
P3HT (H-P3HT) thin film possessed anisotropic and improved microstructures,
particularly in crystalline domains. The improved molecular features
and microstructural properties of the H-P3HT thin film enhanced the
intramolecular and intermolecular charge transport by extending the
Ï€-conjugation, decreasing the reorganization energy, and strengthening
the π–π overlaps. The electrical performance of
the H-P3HT OTFT was augmented significantly with respect to that of
the spin-coated P3HT OTFT. In addition, the H-P3HT OTFT exhibited
an anisotropic charge transport property, correlating with microstructure
directionality and resulting from the difference in the directions
of the π–π overlaps. This effective and simple
technique can be applied to other device types and has the potential
to achieve high-performance organic electronic/photonic devices
Lithium-Induced Defect Levels in ZnO Nanoparticles To Facilitate Electron Transport in Inverted Organic Photovoltaics
In this work, lithium-doped zinc
oxide nanoparticles (LZO NPs)
with different Li/Zn molar ratios (Li/Zn = 0, 0.05, 0.2) are successfully
prepared to form an electron transporting layer (cathode buffer layer)
in the inverted-type P3HT:ICBA organic photovoltaic (OPV) devices.
As compared with the undoped ZnO NPs buffer layer, a considerable
improvement OPVs from 2.344% to 2.946% is obtained by using 5%-LZO
NPs as a buffer layer, which owns <i>J</i><sub>sc</sub> of
7.22 mA/cm<sup>2</sup>, <i>V</i><sub>oc</sub> of 0.86 V,
and FF of 47.4%. X-ray absorption near-edge structure (XANES) spectra
show the increase of unoccupied O 2p-derived states in 5%-LZO NPs,
which leads to better carrier conductance. The energy levels of defects
in 5%-LZO NPs analyzed by photoluminescence are found to facilitate
electron extraction to the cathode. Impedance measurement results
indicate that the carrier lifetime is effectively increased to 2176
μs by applying the 5%-LZO NPs buffer layer, showing the improvement
of carrier extraction efficiency and resulting in its progressive
performance
Synergistic Effects of Binary-Solvent Annealing for Efficient Polymer–Fullerene Bulk Heterojunction Solar Cells
Conjugated polymer–fullerene-based
bulk-heterojunction (BHJ) organic solar cells (OSCs) have attracted
tremendous attention over the past two decades because of their potential
to develop low-cost and easy methods to produce energy from light.
The complicated microstructure and morphology with randomly organized
architecture of these polymer–fullerene-based active layers
(ALs) is a key factor that limits photovoltaic performance. In this
study, a binary-solvent annealing (BSA) approach was established to
improve the polyÂ(3-hexylthiophene):indene-C<sub>60</sub> bisadduct-based
AL for efficient BHJ-type OSCs by varying the second solvents with
different boiling points (BP). Thus, we were able to change the evaporation
behavior of cosolvents and consequently obtain the various microstructural
properties of the AL. An in-depth study was conducted on the solvent-evaporation
driven morphology of the active layer under various cosolvent conditions
and its effect on the photovoltaic parameters of OSCs. Under the BSA
processes, we found that the specimens with low-BP second solvents
allows us to observe a more ideal AL for increasing photon absorption
and efficient charge transport and collection at the respective electrodes,
resulting in enhanced PCE of the corresponding OSCs. By contrast,
the specimens with high-BP second solvents exhibit random microstructures,
which are detrimental to charge transport and collection and lead
to diminished PCE of the corresponding OSCs. By appropriately selecting
the composition of a binary solvent, BSA can be employed as an easy
method for the effective manipulation of the microstructures of ALs.
BSA is a promising technique for the performance enhancement of not
only OSCs but also other organic/polymeric-based electronic devices