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1.
    
Photogenerated charge carriers for blend films of poly[2‐methoxy‐5‐(3,7‐dimethyloctyloxy)‐1,4‐phenylenevinylene] (MDMO‐PPV) and [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM) have been investigated by transient absorption spectroscopy. The blend film with a low PCBM fraction (<10 wt %) exhibits a wide absorption that ranges from 900 to 1000 nm, which is characteristic of the MDMO‐PPV hole polaron and PCBM radical anion. On the other hand, the blend film with a higher PCBM fraction (> 30 wt %) exhibits a major absorption band at ∼900 nm, which is characteristic of the PCBM radical cation. For identification of charge carriers, the absorption spectrum and molar absorption coefficient of each charged species have been evaluated separately using various combinations of electron donor and acceptor materials. Consequently, the MDMO‐PPV hole polaron has been found to have a broad absorption at ∼950 nm and the PCBM radical anion and cation show a distinct absorption at 1020 and 890 nm, respectively. On the basis of these absorption spectra, the transient spectra observed for the blend films have been simulated. The spectrum for a low PCBM fraction is well reproduced by superposition of the absorption spectra of the MDMO‐PPV hole polaron and PCBM radical anion. On the other hand, the spectrum for a high PCBM fraction is well reproduced by superposition of the absorption spectra of the MDMO‐PPV hole polaron, PCBM radical anion, and PCBM radical cation, which indicates that the PCBM radical cation is formed in the blend films with PCBM at a high concentration. Possible mechanisms for the formation of the PCBM radical cation in the blend are also discussed.  相似文献   

2.
Cu(In,Ga)Se2 (CIGS) thin films were deposited by electron beam evaporation of ball-milled powders containing various amounts of gallium. The effects of the gallium concentration in the Cu(In,Ga)Se2 on the structure, surface morphology and optical properties of the films were investigated using X-ray diffraction, energy-dispersive X-ray analysis, atomic force microscopy and optical spectroscopy. All of the films, which were deposited at 450 °C, were polycrystalline and exhibited a chalcopyrite structure with a (112) preferred orientation. The optical constants of the films were calculated. The grain size, the roughness and the band gap increased with increasing amounts of gallium in the films. A glass/TCO/CdS/CIGS/Au solar cell with 12.87% efficiency was prepared directly from the powdered material.  相似文献   

3.
    
A new donor (D)–acceptor (A) conjugate, benzodithiophene‐rhodanine–[6,6]‐phenyl‐C61 butyric acid methyl ester (BDTRh–PCBM) comprising three covalently linked blocks, one of p‐type oligothiophene containing BDTRh moieties and two of n‐type PCBM, is designed and synthesized. A single component organic solar cell (SCOSC) fabricated from BDTRh–PCBM exhibits the power conversion efficiency (PCE) of 2.44% and maximum external quantum efficiency of 46%, which are the highest among the reported efficiencies so far. The SCOSC device shows efficient charge transfer (CT, ≈300 fs) and smaller CT energy loss, resulting in the higher open‐circuit voltage of 0.97 V, compared to the binary blend (BDTRh:PCBM). Because of the integration of the donor and acceptor in a single molecule, BDTRh‐PCBM has a specific D–A arrangement with less energetic disorder and reorganization energy than blend systems. In addition, the SCOSC device shows excellent device and morphological stabilities, showing no degradation of PCE at 80 °C for 100 h. The SCOSC approach may suggest a great way to suppress the large phase segregation of donor and acceptor domains with better morphological stability compared to the blend device.  相似文献   

4.
    
All-small-molecule organic solar cells (ASM-OSCs), which consist of small-molecule donors and acceptors, have recently been studied extensively to eliminate the batch-to-batch variation from polymer-based donor or acceptor. On the other hand, the control of their active layer morphology is more challenging due to the similar chemical structure and miscibility of small-molecule donor and small-molecule accepter. Hence, this study develops a dual-additive-driven morphology optimization method for ASM-OSCs based on BTR-Cl:Y6. One solid additive – 1,4-diiodobenzene (DIB) and one liquid additive – diiodomethane (DIM) are selected, making use of their distinct interaction mechanisms with Y6 and BTR-Cl. It is found that DIB can form a eutectic phase with Y6, which can increase the intermolecular interactions and modulate the acceptor phase separation, while the simultaneous volatilization of DIM suppresses the over-aggregation of BTR-Cl during the film casting process. As a result of the synergistic morphology tuning, the optimized device delivers a power conversion efficiency (PCE) as high as 15.2%, among the highest PCE reported to date for binary ASM-OSCs without solvent annealing treatment. This work demonstrates the potential of morphology tuning via the incorporation of dual additives into ASM-OSCs, enabling them to achieve comparable efficiencies to those of conventional polymer/small-molecule based OSCs.  相似文献   

5.
    
This paper firstly reports the effect of deoxyribonucleic acid (DNA) molecules extracted from chickpea and wheat plants on the injection/recombination of photogenerated electrons and sensitizing ability of dye‐sensitized solar cells (DSSCs). These high‐yield DNA molecules are applied as both linker bridging unit as well as thin tunneling barrier (TTB) at titanium dioxide (TiO2 )/dye interface, to build up high‐efficient DSSCs. With its favorable energy levels, effective linker bridging role, and double helix structure, bifunctional DNA modifier shows an efficient electron injection, suppressed charge recombination, longer electron lifetime, and higher light harvesting efficiency, which leads to higher photovoltaic performance. In particular, a photoconversion efficiency (PCE) of 9.23% is achieved by the binary chickpea and wheat DNA‐modified TiO2 (CW@TiO2) photoanode. Furthermore, time‐resolved fluorescence spectroscopy measurements confirm a better electron transfer kinetics for DNA‐modified TiO2 photoanodes, implying a higher electron transfer rate (kET). This work highlights a great contribution for the photoanodes that are linked with DNA molecule, which act as both bridging unit and TTB to control the charge recombination and injection dynamics, and hence, boost the photovoltaic performance in the DSSCs.  相似文献   

6.
Capacitance transient spectroscopy is used to study defects in chips of fully fabricated silicon solar cells. Characteristic differences are observed as a function of the crystal growth type (crucible grown or float zoned) and dopant (boron or aluminum) of the starting material, processing variables (diffused or implanted junctions, electron beam or furnace annealing) and radiation environment (1 MeV electron irradiation).  相似文献   

7.
    
Organic semiconducting polymers exhibit complex microstructure and disorder over a wide range of length scales, which impact the electronic transport properties relevant for the development of photovoltaic devices. Typical transport measurements blur together intermolecular and intramolecular conduction processes, making it difficult to develop an understanding of how disorder on different length scales impacts device performance. This work uses time‐resolved terahertz (THz) spectroscopy to selectively study intramolecular carrier transport in poly(3‐hexylthiophene) (P3HT). At 2 THz, P3HT polymers with different side chain regularity have fast THz carrier mobility ranging from 0.1 to 0.4 cm2 V−1 s−1, and the mobility dependence on the side chain regularity is much smaller than studied by other macroscopic mobility measurements. The fast local carrier mobility allows us to understand how the efficiency of charge‐transfer state splitting is high in these polymers and shows that local disorder does not strongly impact intramolecular transport processes. Moreover, the local mobility does not exhibit changes with temperature or time within the 1 ns duration probed, indicating that local carrier transport is always fast. To fully understand the differences in time and temperature dependence on carrier transport at different length scales, a transport model that separates local transport from intermolecular carrier hopping is required.  相似文献   

8.
    
Ultrafast charge transfer dynamics in hybrid blend films of a low band‐gap polymer poly(2,6‐(N‐(1‐octylnonyl)dithieno[3,2‐b:20,30‐d]pyrrole)‐alt‐4,7‐(2,1,3‐benzothiadiazole)) (PDBT) and PbS quantum dots (QDs) are studied by using ultrafast transient transmission spectroscopy. It is observed that the transient bleaching signal arising from excitons of the PDBT displays a much faster recovery, within the time delay of ≈5 ps, in hybrid films than in the neat PDBT film. In contrast, the bleaching signal resulting from the electron filling of the QDs in hybrid films shows an extra rising component during ≈1–5 ps, which is absent in the pristine QDs. These results indicate the ultrafast electron transfer from the lowest unoccupied molecular orbital energy level of the PDBT to the conduction band of the QDs in the time scale of several ps after laser excitation. A transient absorption signal within 1 ps in the hybrid films is also found, indicating the emergence of charge transfer states (CTs). The CTs formed at the interface of the hybrid blend may facilitate the charge separation and transfer. It is estimated that over 80% of the photoexcited electrons in the PDBT may be transferred into the QDs. The transfer efficiencies show a positive correlation with the power conversion efficiencies of the corresponding hybrid solar cells.  相似文献   

9.
    
Developing highly efficient photocatalysts for artificial photosynthesis is one of the grand challenges in solar energy conversion. Among advanced photoactive materials, conjugated porous polymers (CPPs) possess a powerful combination of high surface areas, intrinsic porosity, cross-linked nature, and fully π-conjugated electronic systems. Here, based on these fascinating properties, organic–inorganic hybrid heterostructures composed of CPPs and TiO2 for the photocatalytic CO2 reduction and H2 evolution from water are developed. The study is focused on CPPs based on the boron dipyrromethene (BODIPY) and boron pyrrol hydrazine (BOPHY) families of compounds. It is shown that hybrid photocatalysts are active for the conversion of CO2 mainly into CH4 and CO, with CH4 production 4 times over the benchmark TiO2. Hydrogen evolution from water surpassed by 37.9-times that of TiO2, reaching 200 mmol gcat−1 and photonic efficiency of 20.4% in the presence of Pt co-catalyst (1 wt% Pt). Advanced photophysical studies, based on time-resolved photoluminescence and transient absorption spectroscopy, reveal the creation of a type II heterojunction in the hybrids. The unique interfacial interaction between CPPs and TiO2 results in longer carriers’ lifetimes and a higher driving force for electron transfer, opening the door to a new generation of photocatalysts for artificial photosynthesis.  相似文献   

10.
    
The insertion of a DNA nanolayer into polymer based solar cells, between the electron transport layer (ETL) and the active material, is proposed to improve the charge separation efficiency. Complete bulk heterojunction donor–acceptor solar cells of the layered type glass/electrode (indium tin oxide)/ETL/P3HT:PC70BM/hole transport layer/electrode (Ag) are investigated using femtosecond transient absorption spectroscopy both in the NIR and the UV–vis regions of the spectrum. The transient spectral changes indicate that when the DNA is deposited on the ZnO nanoparticles (ZnO‐NPs) it can imprint a different long range order on the poly(3‐hexylthiophene) (P3HT) polymer with respect to the non‐ZnO‐NPs/DNA containing cells. This leads to a larger delocalization of the initially formed exciton and its faster quenching which is attributed to more efficient exciton dissociation. Finally, the temporal response of the NIR absorption shows that the DNA promotes more efficient production of charge transfer states and free polarons in the P3HT cation indicating that the increased exciton dissociation correlates with increased charge separation.  相似文献   

11.
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12.
    
Colloidal metal chalcogenide quantum dots (QDs) have excellent quantum efficiency in light–matter interactions and good device stability. However, QDs have been brought to the forefront as viable building blocks in bottom‐up assembling semiconductor devices, the development of QD solar cell (QDSC) is still confronting considerable challenges compared to other QD technologies due to their low performance under natural sunlight, as a consequence of untapped potential from their quantized density‐of‐state and inorganic natures. This report is designed to address this long‐standing challenge by accessing the feasibility of using QDSC for indoor and concentration PV (CPV) applications. This work finds that above bandgap photon energy irradiation of QD solids can generate high densities of excitons via multi‐photon absorption (MPA), and these excitons are not limited to diffuse by Auger recombination up to 1.5 × 1019 cm?3 densities. Based on these findings, a 19.5% (2000 lux indoor light) and an 11.6% efficiency (1.5 Suns) have been facilely realized from ordinary QDSCs (9.55% under 1 Sun). To further illustrate the potential of the MPA in QDSCs, 21.29% efficiency polymer lens CPVs (4.08 Suns) and viable sensor networks powered by indoor QDSCs matrix have been demonstrated.  相似文献   

13.
    
The electrical properties of Cu(In,Ga)Se2/Mo junctions were characterized with respect of MoSe2 orientation and Na doping level using an inverse transmission line method, in which the Cu(In,Ga)Se2 (CIGS)/Mo contact resistance could be measured separately from the CIGS film sheet resistance. The MoSe2 orientation was controlled by varying the Mo surface density, with the c‐axis parallel and normal orientations favored on Mo surfaces of lower and higher density, respectively. The effect of Na doping was compared by using samples with and without a SiOx film on sodalime glass. The conversion of the MoSe2 orientation from c‐axis normal to parallel produced a twofold reduction in CIGS/Mo contact resistance. Measurements of the contact resistances as a function of temperature showed that the difference in CIGS/Mo contact resistance between the samples with different MoSe2 orientations was due to different barrier heights at the back contact. Comparison between Na‐doped and Na‐reduced samples revealed that the contact resistance for the Na‐reduced system was four times of that of the doped sample, which showed more pronounced Schottky‐junction behavior at lower temperature, indicating that Na doping effectively reduced the barrier height at the back contact. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

14.
    
In this work, for the first time, the addition of aluminum oxide nanostructures (Al2O3 NSs) grown by glancing angle deposition (GLAD) is investigated on an ultrathin Cu(In,Ga)Se2 device (400 nm) fabricated using a sequential process, i.e., post‐selenization of the metallic precursor layer. The most striking observation to emerge from this study is the alleviation of phase separation after adding the Al2O3 NSs with improved Se diffusion into the non‐uniformed metallic precursor due to the surface roughness resulting from the Al2O3 NSs. In addition, the raised Na concentration at the rear surface can be attributed to the increased diffusion of Na ion facilitated by Al2O3 NSs. The coverage and thickness of the Al2O3 NSs significantly affects the cell performance because of an increase in shunt resistance associated with the formation of Na2SeX and phase separation. The passivation effect attributed to the Al2O3 NSs is well studied using the bias‐EQE measurement and J–V characteristics under dark and illuminated conditions. With the optimization of the Al2O3 NSs, the remarkable enhancement in the cell performance occurs, exhibiting a power conversion efficiency increase from 2.83% to 5.33%, demonstrating a promising method for improving ultrathin Cu(In,Ga)Se2 devices, and providing significant opportunities for further applications.  相似文献   

15.
    
There is currently a worldwide effort to develop materials for solar energy harvesting which are efficient and cost effective, and do not emit significant levels of CO2 during manufacture. When a researcher fabricates a novel device from a novel material system, it often takes many weeks of experimental effort and data analysis to understand why any given device/material combination produces an efficient or poorly optimized cell. It therefore takes the community tens of years to transform a promising material system to a fully optimized cell ready for production (perovskites are a contemporary example). Herein, developed is a new and rapid approach to understanding device/material performance, which uses a combination of machine learning, device modeling, and experiment. Providing a set of electrical device parameters (charge carrier mobilities, recombination rates, trap densities, etc.) in a matter of seconds thus offers a fast way to directly link fabrication conditions to device/material performance, pointing a way to further and more rapid optimization of light harvesting devices. The method is demonstrated by using it to understand annealing temperature and surfactant choice and in terms of charge carrier dynamics in organic solar cells made from the P3HT:PCBM, PBTZT‐stat‐BDTT‐8:PCBM, and PTB7:PCBM material systems.  相似文献   

16.
    
Organic bulk heterojunction solar cells are often regarded as near‐equilibrium devices, whose kinetics are set by well‐defined charge carrier mobilities, and relaxation in the density of states is commonly ignored or included purely phenomenologically. Here, the motion of photocreated charges is studied experimentally with picosecond time resolution by a combination of time‐resolved optical probing of electric field and photocurrent measurements, and the data are used to define parameters for kinetic Monte Carlo modelling. The results show that charge carrier motion in a prototypical polymer:fullerene solar cell under operational conditions is orders of magnitude faster than would be expected on the basis of corresponding near‐equilibrium mobilities, and is extremely dispersive. There is no unique mobility. The distribution of extraction times of photocreated charges in operating organic solar cells can be experimentally determined from the charge collection transients measured under pulsed excitation. Finally, a remarkable distribution of the photocurrent over energy is found, in which the most relaxed charge carriers in fact counteract the net photocurrent.  相似文献   

17.
    
In organic solar cells, high open circuit voltages may be obtained by choosing materials with a high offset between the donor highest occupied molecular orbital (HOMO) and acceptor lowest unoccupied molecular orbital (LUMO). However, increasing this energy offset can also lead to photophysical processes that compete with charge separation. In this paper the formation of triplet states is addressed in blends of polyfluorene polymers with a series of PCBM multi‐adducts. Specifically, it is demonstrated that the formation of such triplets occurs when the offset energy between donor ionization potential and acceptor electron affinity is ～1.6 eV or greater. Spectroscopic measurements support a mechanism of resonance energy transfer for triplet formation, influenced by the energy levels of the materials, but also demonstrate that the competition between processes at the donor–acceptor interface is strongly influenced by morphology.  相似文献   

18.
    
Charge separation at the donor–acceptor interface is a key step for high efficiency in organic solar cells. If interfacial hybrid states exist already in the dark it is plausible that they can have a major impact on the dissociation of optically generated excitations. In this work we probe such interfacial states via steady state absorption spectroscopy. A substantial bleaching of the absorption spectrum is found near the absorption edge when an electron‐accepting layer of either trinitrofluorenone (TNF), C60, or a perylene‐diimide derivative is deposited on top of a layer of electron‐donating conjugated polymers, such as MEH‐PPV or various poly‐phenylene. This is in part attributed to the formation of ground state complexes with low oscillator strength. The experiments bear out a correlation between the reduction of the absorbance with the energy gap between the donor‐HOMO and acceptor‐LUMO, the effective conjugation length of the donor, and the efficiency of exciton dissociation in the solar cell. The effect originates from mixing of the donor‐HOMO and the acceptor LUMO. Calculations using density functional theory support this reasoning. Implications for efficiency of organic solar cells will be discussed.  相似文献   

19.
    
Organic solar cells (OSCs) based on small molecular acceptors (SMAs) have made great development with a power conversion efficiency (PCE) over 16% due to the design of novel materials and advances in device preparation technology. This work fabricates two bulk-heterojunction photovoltaic devices containing the same wide-bandgap donor PM6, respectively, matched with popular Y6 and ITIC SMAs. The PM6:Y6-based device achieves a much higher PCE of 15.21% than the PM6:ITIC-based device of 9.02%. On the basis of comparisons of macroscopic performances in the quasistatic regime, transient absorption spectroscopy (TAS) is further performed to better understand the microscopic dynamics difference in charge separation processes between the two photovoltaic blends. According to the TAS results, the calculated hole transfer efficiency in PM6:Y6 is 71.4%, far greater than the efficiency of 13.1% in PM6:ITIC, demonstrating favorable charge separation at donor/acceptor interfaces via hole transfer channel in PM6:Y6. The favorable hole transfer in PM6:Y6 is accounted for by its better mutual miscibility between the donor and acceptor, and the formation of long-lived delocalized intramoiety excimer state in the acceptor. These results highlight the important role of proper molecular design strategy with strong intermolecular coupling and beneficial film morphology on facilitating charge generation in OSCs adopting SMAs.  相似文献   

20.
    
A combination of transient photovoltage (TPV), voltage dependent charge extraction (CE), and time delayed collection field (TDCF) measurements is applied to 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‐C71‐butyric acid (PC71BM) bulk heterojunction solar cells to analyze the limitations of photovoltaic performance. Devices are processed from pure chlorobenzene (CB) solution and a subset is optimized with 1,8‐diiodooctane (DIO) as co‐solvent. The dramatic changes in device performance are discussed with respect to the dominating loss processes. While in the devices processed from CB solution severe geminate and nongeminate recombination is observed, the use of DIO facilitates efficient polaron pair dissociation and minimizes geminate recombination. Thus, from the determined charge carrier decay rate under open circuit conditions and the voltage dependent charge carrier densities n(V), the nongeminate loss current Jloss of the samples with DIO alone enables the reconstruction of the current/voltage (j/V) characteristics across the whole operational voltage range. Geminate and nongeminate losses are considered to describe the j/V response of cells prepared without additive, but lead to a clearly overestimated device performance. The deviation between measured and reconstructed j/V characteristics is attributed to trapped charges in isolated domains of pure fullerene phases.  相似文献   

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