| 1. |
- Diaz de Zerio Mendaza, Amaia, et al.
(författare)
-
A fullerene alloy based photovoltaic blend with a glass transition temperature above 200 degrees C
- 2017
-
Ingår i: Journal of Materials Chemistry A. - : ROYAL SOC CHEMISTRY. - 2050-7488 .- 2050-7496. ; 5:8, s. 4156-4162
-
Tidskriftsartikel (refereegranskat)abstract
- Organic solar cells with a high degree of thermal stability require bulk-heterojunction blends that feature a high glass transition, which must occur considerably above the temperatures encountered during device fabrication and operation. Here, we demonstrate for the first time a polymer : fullerene blend with a glass transition temperature above 200 degrees C, which we determine by plasmonic nanospectroscopy. We achieve this strong tendency for glass formation through the use of an alloy of neat, unsubstituted C-60 and C-70, which we combine with the fluorothieno-benzodithiophene copolymer PTB7. A stable photovoltaic performance of PTB7 : C60 : C70 ternary blends is preserved despite annealing the active layer at up to 180 degrees C, which coincides with the onset of the glass transition. Rapid deterioration of the power conversion efficiency from initially above 5% only occurs upon exceeding the glass transition temperature of 224 degrees C of the ternary blend.
|
|
| 2. |
- Diaz de Zerio Mendaza, Amaia, 1986, et al.
(författare)
-
A Fullerene Alloy Based Photovoltaic Blend with a Glass Transition Temperature above 200 °C
- 2017
-
Ingår i: Journal of Materials Chemistry A. - 2050-7488 .- 2050-7496. ; 5:8, s. 4156-4162
-
Tidskriftsartikel (refereegranskat)abstract
- Organic solar cells with a high degree of thermal stability require bulk-heterojunction blends that feature a high glass transition, which must occur considerably above the temperatures encountered during device fabrication and operation. Here, we demonstrate for the first time a polymer : fullerene blend with a glass transition temperature above 200 °C, which we determine by plasmonic nanospectroscopy. We achieve this strong tendency for glass formation through the use of an alloy of neat, unsubstituted C60 and C70, which we combine with the fluorothieno-benzodithiophene copolymer PTB7. A stable photovoltaic performance of PTB7 : C60 : C70 ternary blends is preserved despite annealing the active layer at up to 180 °C, which coincides with the onset of the glass transition. Rapid deterioration of the power conversion efficiency from initially above 5% only occurs upon exceeding the glass transition temperature of 224 °C of the ternary blend.
|
|
| 3. |
- Felekidis, Nikolaos, et al.
(författare)
-
The Role of Delocalization and Excess Energy in the Quantum Efficiency of Organic Solar Cells and the Validity of Optical Reciprocity Relations
- 2020
-
Ingår i: The Journal of Physical Chemistry Letters. - : AMER CHEMICAL SOC. - 1948-7185. ; 11:9, s. 3563-3570
-
Tidskriftsartikel (refereegranskat)abstract
- The photon energy dependence of long-range charge separation is studied for two prototypical polymer:fullerene systems. The internal quantum efficiency (IQE) of PCDTBT:PC61BM is experimentally shown to be independent of the excitation energy. In contrast, for TQ1:PC71BM the IQE is strongly energy-dependent for excitation energies close to charge transfer (CT) electroluminescence peak maximum while it becomes energy-independent at higher excitation energies. Kinetic Monte Carlo simulations reproduce the experimental IQE and reveal that the photon energy-dependence of the IQE is governed by charge delocalization. Efficient long-range separation at excitation energies corresponding to the CT electroluminescence peak maximum or lower requires an initial separation of the hole- electron pair by similar to 4-5 nm, whereas delocalization is less important for charge separation at higher photon energies. Our modeling results suggest that a phenomenological reciprocity between CT electroluminescence and external quantum efficiency does not necessarily prove that commonly employed reciprocity relations between these spectra are valid from a fundamental perspective.
|
|
| 4. |
- Kroon, Renee, 1982, et al.
(författare)
-
Comparison of selenophene and thienothiophene incorporation into pentacyclic lactam-based conjugated polymers for organic solar cells
- 2015
-
Ingår i: Polymer Chemistry. - : Royal Society of Chemistry (RSC). - 1759-9954 .- 1759-9962. ; 6:42, s. 7402-7409
-
Tidskriftsartikel (refereegranskat)abstract
- In this work, we compare the effect of incorporating selenophene versus thienothiophene spacers into pentacyclic lactam-based conjugated polymers for organic solar cells. The two cyclic lactam-based copolymers were obtained via a new synthetic method for the lactam moiety. Selenophene incorporation results in a broader and red-shifted optical absorption while retaining a deep highest occupied molecular orbital level, whereas thienothienophene incorporation results in a blue-shifted optical absorption. Additionally, grazing-incidence wide angle X-ray scattering data indicates edge- and face-on solid state order for the selenophene-based polymer as compared to the thienothiophene-based polymer, which orders predominantly edge-on with respect to the substrate. In polymer : PC71BM bulk heterojunction solar cells both materials show a similar open-circuit voltage of similar to 0.80-0.84 V, however the selenophene-based polymer displays a higher fill factor of similar to 0.70 vs. similar to 0.65. This is due to the partial face-on backbone orientation of the selenophene-based polymer, leading to a higher hole mobility, as confirmed by single-carrier diode measurements, and a concomitantly higher fill factor. Combined with improved spectral coverage of the selenophene-based polymer, as confirmed by quantum efficiency experiments, it offers a larger short-circuit current density of similar to 12 mA cm(-2). Despite the relatively low molecular weight of both materials, a very robust power conversion efficiency similar to 7% is achieved for the selenophene-based polymer, while the thienothiophene-based polymer demonstrates only a moderate maximum PCE of similar to 5.5%. Hence, the favorable effects of selenophene incorporation on the photovoltaic performance of pentacyclic lactam-based conjugated polymers are clearly demonstrated.
|
|
| 5. |
- Murthy, D H K, et al.
(författare)
-
Origin of Reduced Bimolecular Recombination in Blends of Conjugated Polymers and Fullerenes
- 2013
-
Ingår i: Advanced Functional Materials. - : Wiley-VCH Verlag. - 1616-301X .- 1616-3028. ; 23:34, s. 4262-4268
-
Tidskriftsartikel (refereegranskat)abstract
- Bimolecular charge carrier recombination in blends of a conjugated copolymer based on a thiophene and quinoxaline (TQ1) with a fullerene derivative ((6,6)-phenyl-C-71-butyric acidmethyl ester, PC71BM) is studied by two complementary techniques. TRMC (time-resolved microwave conductance) monitors the conductance of photogenerated mobile charge carriers locally on a timescale of nanoseconds, while using photo-CELIV (charge extraction by linearly increasing voltage) charge carrier dynamics are monitored on a macroscopic scale and over tens of microseconds. Despite these significant differences in the length and time scales, both techniques show a reduced Langevin recombination with a prefactor close to 0.05. For TQ1:PC71BM blends, the value is independent of temperature. On comparing TRMC data with electroluminescence measurements it is concluded that the encounter complex and the charge transfer state have very similar energetic properties. The value for annealed poly(3-hexylthiophene) (P3HT):(6,6)-phenyl-C-61-butyric acid methyl ester (PC61BM) is approximately 10(-4), while for blend systems containing an amorphous polymer values are close to 1. These large differences can be related to the extent of charge delocalization of opposite charges in an encounter complex. Insight is provided into factors governing the bimolecular recombination process, which forms a major loss mechanism limiting the efficiency of polymer solar cells.
|
|
| 6. |
- Roland, Steffen, et al.
(författare)
-
Equilibrated Charge Carrier Populations Govern Steady-State Nongeminate Recombination in Disordered Organic Solar Cells
- 2019
-
Ingår i: The Journal of Physical Chemistry Letters. - : AMER CHEMICAL SOC. - 1948-7185. ; 10:6, s. 1374-1381
-
Tidskriftsartikel (refereegranskat)abstract
- We employed bias-assisted charge extraction techniques to investigate the transient and steady-state recombination of photogenerated charge carriers in complete devices of a disordered polymer-fullerene blend. Charge recombination is shown to be dispersive, with a significant slowdown of the recombination rate over time, consistent with the results from kinetic Monte Carlo simulations. Surprisingly, our experiments reveal little to no contributions from early time recombination of nonequilibrated charge carriers to the steady-state recombination properties. We conclude that energetic relaxation of photogenerated carriers outpaces any significant nongeminate recombination under application-relevant illumination conditions. With equilibrated charges dominating the steady-state recombination, quasi-equilibrium concepts appear suited for describing the open-circuit voltage of organic solar cells despite pronounced energetic disorder.
|
|
| 7. |
- Wilken, Sebastian, et al.
(författare)
-
Experimentally Calibrated Kinetic Monte Carlo Model Reproduces Organic Solar Cell Current–Voltage Curve
- 2020
-
Ingår i: Solar RRL. - : Wiley. - 2367-198X. ; 4:6
-
Tidskriftsartikel (refereegranskat)abstract
- Kinetic Monte Carlo (KMC) simulations are a powerful tool to study the dynamics of charge carriers in organic photovoltaics. However, the key characteristic of any photovoltaic device, its current–voltage (J–V) curve under solar illumination, has proven challenging to simulate using KMC. The main challenges arise from the presence of injecting contacts and the importance of charge recombination when the internal electric field is low, i.e., close to open-circuit conditions. Herein, an experimentally calibrated KMC model is presented that can fully predict the J–V curve of a disordered organic solar cell. It is shown that it is crucial to make experimentally justified assumptions on the injection barriers, the blend morphology, and the kinetics of the charge transfer state involved in geminate and nongeminate recombination. All of these properties are independently calibrated using charge extraction, electron microscopy, and transient absorption measurements, respectively. Clear evidence is provided that the conclusions drawn from microscopic and transient KMC modeling are indeed relevant for real operating organic solar cell devices.
|
|
