Evidences of photocurrent generation by hole–exciton interaction at organic semiconductor interfaces

The charge–exciton interaction at the donor/acceptor interface plays a significant role in the exciton dissociation processes, and thus influences the performance of organic solar cells. In this work, the evidences of photocurrent generation via hole–exciton interaction (HEI) at the organic semiconductor interface in organic solar cells, which is the counterpart of photocurrent generated by electron–exciton interaction, is demonstrated. A heterojunction, composed of copper phthalocyanine (CuPc) and fullerene (C₆₀), is used to provide free holes that interact with the excitons supplied by perfluorinated hexadecafluorophthalo-cyaninatozinc (F16ZnPc). The fact that photocurrent generation via HEI is well evidenced by: (1) a short circuit current of 0.38 mA cm⁻²; (2) the jump of an external quantum efficiency (EQE) around 800 nm after adding a bias light; (3) the EQE variations under bias light of different wavelengths and light intensities; and (4) the superlinear dependence of the photocurrent on the light intensity.     

Energy levels in dilute-donor organic solar cell photocurrent generation: A thienothiophene donor molecule study

To investigate photocurrent generation mechanisms in these organic solar cells (OSCs), we design and synthesize four thienothiophene (TT)-based small-molecule donors with the highest occupied molecular orbital (HOMO) levels varying from −6.4 eV to −5.1 eV, which span across the HOMO value of the [6,6]-phenyl-C70-butyric acid methyl ester (PC₇₁BM) acceptor. We measure TT-based donor:PC₇₁BM films’ electronic and optical properties, OSC current density-voltage characteristic, and external quantum efficiency, and perform density functional theory (DFT) calculations. Our results show that photocurrent generation depends strongly on the substitutions of the center TT groups, cyano (-CN) versus hexyloxy (-OHex). With 1 wt% donor, TTOHex:PC₇₁BM devices produce seven times, increasing to twelve times for 5 wt % donor, higher photocurrent than neat PC₇₁BM devices. In contrast, TTCN:PC₇₁BM devices do not generate additional photocurrent even with 10 wt% donor. The photocurrent generation in TT-based donor:PC₇₁BM devices depends critically on the HOMO value of the donor molecule with respect to that of PC₇₁BM, indicating the importance of type II energy level alignment to facilitate exciton dissociation at the donor-acceptor interface. The photovoltage of all TT:PC₇₁BM devices are comparable to neat PC₇₁BM devices, 0.85–0.90 V, with a low voltage loss due to non-radiative recombination. The fill factor of TTOHex:PC₇₁BM devices are low due to the low hole mobility, ~10⁻⁸ cm²/V. Following exciton dissociation, hole transport is analyzed according to three possible mechanisms: tunneling, percolation pathways, and hole back transfer. We find that the hole back transfer mechanism can explain all experimental results and therefore is the primary hole transport mechanism for photocurrent generation in TT-based donor:PC₇₁BM dilute-donor OSCs.     

Enhancement of power conversion efficiency of PTB7:PCBM-based solar cells by gate bias

We designed and fabricated poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl] [3-fluoro-2-[(2-ethylhexyl)carbonyl] thieno[3,4-b]thiophenediyl]] (PTB7): [6,6]-phenyl-C70-butyric-acid-methyl-ester (PC₇₀BM)–based solar cells with gate electrodes, which can introduce an additional electric field within the devices just as in organic thin film transistors (OTFTs). Our proposed realize the simple and convenient modulation of electric field within the device, and power conversion efficiency (PCE) of 8.1% is reached at 2.0 V gate bias, significantly higher than the PCE of 6.8% at the case of no gate structure. By calculating the carrier mobility and the rate of exciton dissociation efficiency in detail, the role of electric field to the exciton dissociation and carrier transport was investigated, respectively. Meanwhile, the feasibility of the proposed device structure in practical application was discussed. The results suggest that such a gate structure has a great of prospects in achieving high efficiency polymer solar cells.     

Enhanced power conversion efficiency of organic solar cells by embedding Ag nanoparticles in exciton blocking layer

We demonstrate the power conversion efficiency of bulk heterojunction organic solar cells can be enhanced by introducing Ag nanoparticles into organic exciton blocking layer. The Ag nanoparticles were incorporated into the exciton blocking layer by thermal evaporation. Compared with the conventional cathode contact materials such as Al, LiF/Al, devices with Ag nanoparticles incorporated in the exciton blocking layer showed lower series resistances and higher fill factors, leading to a 3.2% power conversion efficiency with a 60 nm active layer; whereas, the conventional devices have only 2.0–2.3% power conversion efficiency. Localized surface plasmon resonances by the Ag nanoparticles and their contribution to photocurrent were also discussed by simulating optical absorptions using a FDTD (finite-difference-time-domain) method.     

States confined in the barriers of type-III HgTe/CdTe superlattices

We present a theoretical study of states quasi-localized in CdTe barriers of HgTe/CdTe superlattices. We show that the quasi-localization of both electrons and holes will lead to strong Coulomb interaction, and thus to the formation of excitons. It is further demonstrated that such quasi-localized states, including excitons, exhibit confinement effect similar to those of loclaized states in quantum wells.     

Efficient small molecule-based bulk heterojunction photovoltaic cells with reduced exciton quenching in fullerene

Most highly efficient small molecule-based bulk heterojunction (BHJ) photovoltaic cells contain a large concentration of fullerene in their blend active layers. However, the excitons generated in fullerene can seriously quench at the surface of the commonly used MoO₃ buffer layer, becoming a key limitation to the photovoltaic performance of these cells. In this study, we’ve investigated various anode buffer layers in the thermally evaporated tetraphenyldibenzoperiflanthene (DBP) and C₇₀-based BHJ cells with high C₇₀ concentration. It’s been found that obviously enhanced power conversion efficiency (PCE) of up to 6.26% can be obtained in DBP and C₇₀-based BHJ cells via simply replacing the MoO₃ buffer by poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT: PSS), which is also a commonly used anode buffer material in polymer-based BHJ cells. Photoluminescence spectra results have confirmed the suppression of exciton quenching at the anode interface by inserting this PEDOT: PSS buffer. Moreover, after adding a C₇₀ interlayer for better electron extraction and the further suppression of exciton quenching, the DBP and C₇₀-based M-i-n photovoltaic cells show a remarkable PCE of 7.04% under illumination with 100 mW/cm², AM 1.5G simulated solar light.     

Effect of quantum dot shape on dynamical dephasing suppression in exciton qubits under applied electric field

We investigate the efficiency of periodic dynamical decoupling of an exciton qubit confined in a self-assembled quantum dot in the presence of an applied electric field. The shape of the quantum dot is found to have a large effect on the excitonic dephasing. It is shown that dynamical suppression of dephasing, through a simple series of equally spaced bit flips, is most efficient for quantum dots that are close to spherical. In addition, compared to the no field case, the presence of an electric field increases the efficiency of the decoupling technique as the quantum dot becomes more oblate. Our calculations show that dephasing can be significantly suppressed in GaAs/AlAs quantum dots suitable for quantum information processing.     

Exciton management by co-doping of blue triplet emitter as a lifetime improving method of blue thermally activated delayed fluorescent devices

Co-doping of a blue phosphorescent emitter in a thermally activated delayed fluorescent (TADF) emitter based emitting layer was developed as an approach to extend the lifetime of blue TADF devices by managing excitons and polarons in the emitting layer. The blue phosphorescent emitter was doped at a very low doping concentration below 1 wt% to suppress triplet-triplet and triplet-polaron quenching effect in the TADF emitting layer. The doping of the blue phosphorescent emitter led to great extension of the lifetime of the TADF devices by hole trapping effect of the blue triplet emitter which widened exciton formation zone in the TADF emitting layer. More than twice extension of the operational lifetime of the device was demonstrated by the co-doping approach irrespective of the doping concentration of the TADF emitter in the emitting layer.     

Efficient ternary polymer solar cells by optimizing photogenerated exciton dissociation and photon harvesting with a short wavelength absorption polymer acceptor as the third component

Ternary blend films, obtained by introducing a third component (a second acceptor as the third component) to a binary polymer solar cell (PSC), are a promising ternary strategy because the light absorption range, surface morphology, and charge carrier transport of the photoactive layer may be optimized, as can the energy level alignment between the donor and the acceptor. In this work, acceptors such as the short-wavelength-absorption polymer N2200 and the long-wavelength-absorption small molecule FOIC were combined with the donor PBDB-T-2F to construct ternary blends. The optimized ternary PSC could achieve a power conversion efficiency (PCE) of 13.98%, which is higher than the efficiencies of binary PSCs based on PBDB-T-2F:FOIC (12.65%) and PBDB-T-2F:N2200 (9.36%). The enhanced PCE of the ternary PSC is based on the high electron mobility, balanced charge transport, optimized surface morphology and charge carrier kinetics and the extended light absorption of the ternary photoactive layer, realized by adjusting the ratio of FOIC:N2200. Our results indicate that mixing a polymer acceptor into a binary photoactive layer to form a ternary blend photoactive layer is a valuable strategy for improving photovoltaic performance.