This work is part of the inter-laboratory collaboration to study the stability of seven distinct sets of state-of-the-art organic photovoltaic (OPV) devices prepared by leading research laboratories. All devices have been shipped to and degraded at RIS?-DTU up to 1830 hours in accordance with established ISOS-3 protocols under defined illumination conditions. In this work, we apply the Incident Photon-to-Electron Conversion Efficiency (IPCE) and the in situ IPCE techniques to determine the relation between solar cell performance and solar cell stability. Different ageing conditions were considered: accelerated full sun simulation, low level indoor fluorescent lighting and dark storage. The devices were also monitored under conditions of ambient and inert (N(2)) atmospheres, which allows for the identification of the solar cell materials more susceptible to degradation by ambient air (oxygen and moisture). The different OPVs configurations permitted the study of the intrinsic stability of the devices depending on: two different ITO-replacement alternatives, two different hole extraction layers (PEDOT:PSS and MoO(3)), and two different P3HT-based polymers. The response of un-encapsulated devices to ambient atmosphere offered insight into the importance of moisture in solar cell performance. Our results demonstrate that the IPCE and the in situ IPCE techniques are valuable analytical methods to understand device degradation and solar cell lifetime. 相似文献
With conventional heating process, ultraviolet (UV) illumination, and microwave irradiation, we have successfully synthesized UV curable encapsulating adhesives with excellent gas barrier capabilities, good adhesive strength, moderate hardness, and high refractive indices. The experimental results manifest that the physical properties of lab-made encapsulating adhesives are highly dependent on their chemical structures and synthetic procedure. We also discover that the encapsulating adhesive prepared by microwave irradiation (i.e. encapsulating adhesive VI-MW) exhibits better adhesive strength and higher gas resistance than those prepared by conventional heating process and UV illumination. Furthermore, encapsulating adhesive VI-MW has also been applied for the package of organic light emitting diodes (OLEDs), flexible OLEDs, and organic solar cells. With encapsulating adhesive VI-MW, the entry of oxygen and moisture in the air into these organic optoelectronic devices has been blocked, therefore enhancing the lifetimes. 相似文献
ITO substrates were treated with organic solvent cleaning(OSC), SC1 treatment[V(NH4OH):V(H2O2): V(H2O)=1:1:5], O2 plasma and UV ozone, respectively. Combined investigations of atom force microscopy(AFM), water contact angle measurements, ultraviolet photoemission spectroscopy(UPS) and X-ray photoemission spectroscopy(XPS) demonstrated that UV ozone treatment could give rise to the smoothest surface, the most hydrophilic property and the highest work function(WF) of ITO due to the removal of hydrophobic C-O impurity from the ITO surface and the enrichments of more oxygen on the ITO surface. When PEDOT:PSS film[(poly(3,4-ethylenedioxy- thiophene):poly(styrene sulfonate)] was deposited on the ITO substrates treated with UV ozone, it showed a lower root-mean- square roughness in AFM images, a higher transmission in UV-Vis transmission spectra and a higher WF in UPS spectra than the PEDOT:PSS films deposited on the ITO substrates treated by other three methods. As a result, the power conversion efficiency of polymer solar cells(PSCs) based on PTB7:PC71BM as an active layer and ITO treated by UV ozone as an anode can reach 8.48% because of the simultaneously improved short circuit current, open circuit voltage and fill factor compared to the PSCs with ITO treated with other three methods. 相似文献
Novel conjugated polymers containing carbazole, phenothiazine or triphenylamine units in the main chain were designed and synthesized via Wittig, Knovenagel or Heck condensations respectively. A majority of them have good solubility in common organic solvents, high thermal stability and good hole-injection ability. Their diluted solutions in THF showed strong absorption with the absorption maximum in the range of 294∼470 nm and the optic band gaps located in the range of 1.90∼2.75 eV. When irradiated by ultraviolet or visible light, the diluted solutions in THF of the polymers emitted light from purple to yellow color with the emission maximum in the range of 347∼597 nm and the full width at half maximum located in the range of 59∼119 nm. Several polymeric light-emitting diodes (PLEDs) devices were fabricated using these polymers as light-emitting materials, and a double-layer device composed of ITO/PEDOT:PSS/PQTN/Mg:Ag showed a good performance, in which the maximum brightness was measured as 2434.0 cd/m2 under a 11.0 V forward bias voltage. Photovoltaic devices were also investigated using these polymers as an active layer, and a device composed of ITO/PNB/PTCDI-C13/Al showed a good performance, which was estimated to have external quantum efficiency at around 1% at 330 nm. From these preliminary experimental results, we may infer that these polymers are good light-emitting materials for PLEDs; while for photovoltaic applications, their absorption spectra need to be further improved to match the solar illumination. 相似文献
A simple and cost-effective successive ionic layer adsorption and reaction (SILAR) method was adopted to fabricate hydrophobic ZnO nanostructured surfaces on transparent indium-tin oxide (ITO), glass and polyethylene terephthalate (PET) substrates. ZnO films deposited on different substrates show hierarchical structures like spindle, flower and spherical shape with diameters ranging from 30 to 300 nm. The photo-induced switching behaviors of ZnO film surfaces between hydrophobic and hydrophilic states were examined by water contact angle and X-ray photoelectron spectroscopy (XPS) analysis. ZnO nanostructured films had contact angles of ~140° and 160°±2 on glass and PET substrates, respectively, exhibiting hydrophobic behavior without any surface modification or treatment. Upon exposure to ultraviolet (UV) illumination, the films showed hydrophilic behavior (contact angle: 15°±2), which upon low thermal stimuli revert back to its original hydrophobic nature. Such reversible and repeatable switching behaviors were observed upon cyclical exposure to ultraviolet radiation. These biomimetic ZnO surfaces exhibit good anti-reflective properties with lower reflectance of 9% for PET substrates. Thus, the present work is significant in terms of its potential application in switching devices, solar coatings and self-cleaning smart windows. 相似文献
The photodecomposition of dimethyl methylphosphonate (DMMP) and trimethyl phosphate (TMP) adsorbed on monoclinic WO3 powders when irradiated by ultraviolet light (UV) in air, oxygen, and under evacuation was investigated using infrared spectroscopy
(IR). The IR spectra show that DMMP decomposes into methyl phosphonate upon exposure to 254 nm UV for 2 h at room temperature
in air. The same decomposition of DMMP occurs only at temperatures above 300°C without UV illumination. TMP differs from DMMP
in that the photodecomposition product is not the same as the decomposition product obtained by heating above 300°C. Thermal
decomposition leads to formation of a phosphate on the surface, whereas photodecomposition leads to the same adsorbed methyl
phosphonate as found for the thermal or photodecomposition of DMMP. Since TMP does not contain a P-CH3 bond, the formation of a methyl phosphonate on the surface after UV illumination involves a mechanism where CH3 groups migrate from the methoxy group to the phosphorous central atom. No decomposition is observed at room temperature when
DMMP or TMP adsorbed on WO3 is irradiated under vacuum or in nitrogen atmosphere. Therefore, the photodecomposition of either DMMP or TMP adsorbed on
WO3 at room temperature does not involve a reaction with the lattice oxygen but rather a reaction with the oxygen radicals produced
by the decomposition of ozone. 相似文献
Summary: The electrochemical behaviour of four types of (phenylene ethynylene)‐alt‐(phenylene vinylene) hybrid polymers, 1 , 2 , 3 , and 4 have been investigated with respect to the influence of the grafted alkoxy side chains. In the case of the fully substituted polymers 2 , 3 , and 4 , the strong insulating nature of longer linear octadecyl or bulky branched 2‐ethylhexyl side chains lowers the HOMO levels of the polymers thereby increasing the discrepancy, ΔEg, between the electrochemical, Eequation/tex2gif-stack-1.gif, and the optical, Eequation/tex2gif-stack-2.gif, bandgap energies. Thus it is not possible to establish a direct correlation between the open circuit voltage, VOC, of bulk heterojunction solar cell devices of the configuration glass substrate/ITO/PEDOT:PSS/polymer 3 :PCBM(1:3, w/w)/LiF/Al and the HOMO energy levels of polymer 3 solely, as postulated in the literature. The photovoltaic (PV) parameters greatly depend on the grafted side chains.
Linear I–V curves of solar cell devices from polymers 3a – d , measured in the dark and under 100 mW · cm−2 solar simulator illumination. 相似文献
Electrodeposition approach was used to grow the ZnSe nanostructure on indium doped tin oxide (ITO) layered glass substrate. Due to low cost and high degree of absorption, binary semiconductors made from chalcogens such as CdSe, ZnO, ZnS and ZnSe provide significant features in photovoltaic and photoelectrochemical cells. The structural and morphological properties of deposited nanostructures were examined by XRD and SEM. X-ray diffraction analysis informed about cubic structure with a preferred orientation and the calculated crystal size was approximately 75 nm. The optical properties were examined by UV–visible absorbance spectra and optical band gap was measured using Tauc plot. The deposited ZnSe nanostructure has direct band gap ∼2.52 eV at room temperature which was less than 2.82 eV which is the band gap of bulk ZnSe. Investigations also focused on additional qualities like excellent optical transmission, low electrical resistance, and good photosensitivity. Because of the presence of defect states in the deposited nanostructure, the band gap energy is smaller than that of bulk material. The current-voltage characteristics were measured in dark mode and under illumination of normal tungsten filament light and LED. There was notable change in the current for both normal light and LED in comparison to dark mode. The findings of all the characterization methodologies suggested that for the production of solar cells low cost ZnSe may be used as an alternative environment friendly Cd-free window layer. 相似文献
The spatial distribution of reaction products in multilayer polymer solar cells induced by water and oxygen atmospheres was mapped and used to elucidate the degradation patterns and failure mechanisms in an inverted polymer solar cell. The active material comprised a bulk heterojunction formed by poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) sandwiched between a layer of zinc oxide and a layer of poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) that acted as, respectively, electron and hole transporting layers between the active material and the two electrodes indium-tin-oxide (ITO) and printed silver. X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (TOF-SIMS) in conjunction with isotopic labeling using H(2)(18)O and (18)O(2) enabled detailed information on where and to what extent uptake took place. A comparison was made between the use of a humid (oxygen-free) atmosphere and a dry oxygen atmosphere during testing of devices that were kept in the dark and devices that were subjected to illumination under simulated sunlight. It was found that the reactions taking place at the interface between the active layer and the PEDOT:PSS were the major cause of device failure in the case of these inverted devices, which are compatible with full roll-to-roll (R2R) coating and industrial manufacture. The PEDOT:PSS was found to phase separate, with the PEDOT-rich phase being responsible for most of the interface degradation in oxygen atmospheres. In water atmospheres, little chemically induced degradation was observed, whereas a large partially reversible dependence of the open circuit voltage on the relative humidity was observed. In addition, temporal aspects are discussed in regard to degradation mechanisms. Finally, analytical aspects in regard to storing devices are discussed. 相似文献
A novel polythienylenevinylene (PTV) and two new polythiophenes (PTs), featuring fused tetrathiafulvalene (TTF) units, have been prepared and characterized by ultraviolet-visible (UV-vis) and electron paramagnetic resonance (EPR) spectroelectrochemistry. All polymers undergo two sequential, reversible oxidation processes in solution. Structures in which the TTF species is directly linked to the polymer backbone (2 and 4) display redox behavior which is dictated by the fulvalene system. Once the TTF is spatially removed from the polymer chain by a nonconjugated link (polymer 3), the electroactivity of both TTF and polythiophene moieties can be detected. Computational studies confirm the delocalization of charge over both electroactive centers (TTF and PT) and the existence of a triplet dication intermediate. PTV 4 has a low band gap (1.44 eV), is soluble in common organic solvents, and is stable under ambient conditions. Organic solar cells of polymer 4:[6,6]-phenyl-C(61) butyric acid methyl ester (PCBM) have been fabricated. Under illumination, a photovoltaic effect is observed with a power conversion efficiency of 0.13% under AM1.5 solar simulated light. The onset of photocurrent at 850 nm is consistent with the onset of the pi-pi absorption band of the polymer. Remarkably, UV-vis spectroelectrochemistry of polymer 4 reveals that the conjugated polymer chain remains unchanged during the oxidation of the polymer. 相似文献
The design of narrow band gap (NBG) donors or acceptors and their application in organic solar cells (OSCs) are of great importance in the conversion of solar photons to electrons. Limited by the inevitable energy loss from the optical band gap of the photovoltaic material to the open‐circuit voltage of the OSC device, the improvement of the power conversion efficiency (PCE) of NBG‐based OSCs faces great challenges. A novel acceptor–donor–acceptor structured non‐fullerene acceptor is reported with an ultra‐narrow band gap of 1.24 eV, which was achieved by an enhanced intramolecular charge transfer (ICT) effect. In the OSC device, despite a low energy loss of 0.509 eV, an impressive short‐circuit current density of 25.3 mA cm−2 is still recorded, which is the highest value for all OSC devices. The high 10.9 % PCE of the NBG‐based OSC demonstrates that the design and application of ultra‐narrow materials have the potential to further improve the PCE of OSC devices. 相似文献
In this study, some crucial parameters were determined of flexible polymer–organic solar cells prepared from an active layer blend of poly(3-hexylthiophene) (P3HT) and the fullerene derivative [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) mixed in 1:1 mass ratio and deposited from chlorobenzene solution by spin-coating on poly(ethylene terephthalate) (PET)/ITO substrates. Additionally, the positive effect of an electron transport layer (ETL) prepared from zinc oxide nanoparticles (ZnO np) on flexible photovoltaic elements’ performance and stability was investigated. Test devices with above normal architecture and silver back electrodes deposed by magnetron sputtering were constructed under environmental conditions. They were characterized by current-voltage (I–V) measurements, quantum efficiency, impedance spectroscopy, surface morphology, and time–degradation experiments. The control over morphology of active layer thin film was achieved by post-deposition thermal treatment at temperatures of 110–120 °C, which led to optimization of device morphology and electrical parameters. The impedance spectroscopy results of flexible photovoltaic elements were fitted using two R||CPE circuits in series. Polymer–organic solar cells prepared on plastic substrates showed comparable current–voltage characteristics and structural properties but need further device stability improvement according to traditionally constructed cells on glass substrates. 相似文献
The design of narrow band gap (NBG) donors or acceptors and their application in organic solar cells (OSCs) are of great importance in the conversion of solar photons to electrons. Limited by the inevitable energy loss from the optical band gap of the photovoltaic material to the open‐circuit voltage of the OSC device, the improvement of the power conversion efficiency (PCE) of NBG‐based OSCs faces great challenges. A novel acceptor–donor–acceptor structured non‐fullerene acceptor is reported with an ultra‐narrow band gap of 1.24 eV, which was achieved by an enhanced intramolecular charge transfer (ICT) effect. In the OSC device, despite a low energy loss of 0.509 eV, an impressive short‐circuit current density of 25.3 mA cm−2 is still recorded, which is the highest value for all OSC devices. The high 10.9 % PCE of the NBG‐based OSC demonstrates that the design and application of ultra‐narrow materials have the potential to further improve the PCE of OSC devices. 相似文献