排序方式: 共有16条查询结果,搜索用时 390 毫秒
1.
Ion Migration and the Role of Preconditioning Cycles in the Stabilization of the J–V Characteristics of Inverted Hybrid Perovskite Solar Cells
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2.
Comparison of the Morphology Development of Polymer–Fullerene and Polymer–Polymer Solar Cells during Solution‐Shearing Blade Coating
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Xiaodan Gu Hongping Yan Tadanori Kurosawa Bob C. Schroeder Kevin L. Gu Yan Zhou John W. F. To Stefan D. Oosterhout Victoria Savikhin Francisco Molina‐Lopez Christopher J. Tassone Stefan C. B. Mannsfeld Cheng Wang Michael F. Toney Zhenan Bao 《Liver Transplantation》2016,6(22)
In this work, the detailed morphology studies of polymer poly(3‐hexylthiophene‐2,5‐diyl) (P3HT):fullerene(PCBM) and polymer(P3HT):polymer naphthalene diimide thiophene (PNDIT) solar cell are presented to understand the challenge for getting high performance all‐polymer solar cells. The in situ X‐ray scattering and optical interferometry and ex situ hard and soft X‐ray scattering and imaging techniques are used to characterize the bulk heterojunction (BHJ) ink during drying and in dried state. The crystallization of P3HT polymers in P3HT:PCBM bulk heterojunction shows very different behavior compared to that of P3HT:PNDIT BHJ due to different mobilities of P3HT in the donor:acceptor glass. Supplemented by the ex situ grazing incidence X‐ray diffraction and soft X‐ray scattering, PNDIT has a lower tendency to form a mixed phase with P3HT than PCBM, which may be the key to inhibit the donor polymer crystallization process, thus creating preferred small phase separation between the donor and acceptor polymer. 相似文献
3.
Christopher G. Shuttle Neil D. Treat Jessica D. Douglas Jean M. J. Fréchet Michael L. Chabinyc 《Liver Transplantation》2012,2(1):111-119
The nature of energetic disorder in organic semiconductors is poorly understood. In photovoltaics, energetic disorder leads to reductions in the open circuit voltage and contributes to other loss processes. In this work, three independent optoelectronic methods were used to determine the long‐lived carrier populations in a high efficiency N‐alkylthieno[3,4‐c]pyrrole‐4,6‐dione (TPD) based polymer: fullerene solar cell. In the TPD co‐polymer, all methods indicate the presence of a long‐lived carrier population of ~ 1015 cm?3 on timescales ≥ 100 μs. Additionally, the behavior of these photovoltaic devices under optical bias is consistent with deep energetic lying trap states. Comparative measurements were also performed on high efficiency poly‐3‐hexylthiophene (P3HT): fullerene solar cells; however a similar long‐lived carrier population was not observed. This observation is consistent with a higher acceptor concentration (doping) in P3HT than in the TPD‐based copolymer. 相似文献
4.
John G. Labram James Kirkpatrick Donal D. C. Bradley Thomas D. Anthopoulos 《Liver Transplantation》2011,1(6):1176-1183
The clustering and diffusion of C71‐butyric acid methyl ester (PC71BM) in poly(3‐hexylthiophene) (P3HT) has been studied using single layer blend and bilayer organic field‐effect transistors (OFETs) and by atomic force microscopy (AFM). P3HT:PC71BM blend based OFETs were found to undergo phase‐segregation upon annealing, which was detectable as a fall in electron mobility with increasing annealing temperature. By employing carefully designed bilayer P3HT:PC71BM OFETs, the diffusion‐properties of PC71BM in P3HT could additionally be inferred from electron mobility measurements. It was found that the prerequisite annealing temperatures for detectable PC71BM clustering and diffusion in P3HT was approximately 20 °C higher than for PC61BM. The diffusion coefficient of PC61BM in P3HT was found to be several times higher that that of PC71BM. The present work provides unique insights into the diffusion process of fullerenes in conjugated polymers and could prove highly valuable for future materials development and device optimization. 相似文献
5.
Andrew J. Parnell Adam Hobson Robert M. Dalgliesh Richard A. L. Jones Alan D. F. Dunbar 《Journal of visualized experiments : JoVE》2014,(83)
The spin echo resolved grazing incidence scattering (SERGIS) technique has been used to probe the length-scales associated with irregularly shaped crystallites. Neutrons are passed through two well defined regions of magnetic field; one before and one after the sample. The two magnetic field regions have opposite polarity and are tuned such that neutrons travelling through both regions, without being perturbed, will undergo the same number of precessions in opposing directions. In this case the neutron precession in the second arm is said to "echo" the first, and the original polarization of the beam is preserved. If the neutron interacts with a sample and scatters elastically the path through the second arm is not the same as the first and the original polarization is not recovered. Depolarization of the neutron beam is a highly sensitive probe at very small angles (<50 μrad) but still allows a high intensity, divergent beam to be used. The decrease in polarization of the beam reflected from the sample as compared to that from the reference sample can be directly related to structure within the sample.In comparison to scattering observed in neutron reflection measurements the SERGIS signals are often weak and are unlikely to be observed if the in-plane structures within the sample under investigation are dilute, disordered, small in size and polydisperse or the neutron scattering contrast is low. Therefore, good results will most likely be obtained using the SERGIS technique if the sample being measured consist of thin films on a flat substrate and contain scattering features that contains a high density of moderately sized features (30 nm to 5 µm) which scatter neutrons strongly or the features are arranged on a lattice. An advantage of the SERGIS technique is that it can probe structures in the plane of the sample. 相似文献
6.
Benjamin J. Leever Christopher A. Bailey Tobin J. Marks Mark C. Hersam Michael F. Durstock 《Liver Transplantation》2012,2(1):120-128
Time‐dependent charge transport in operating poly(3‐hexylthiophene):[6,6]‐phenyl‐C61‐butyric acid methyl ester (P3HT:PCBM) bulk heterojunction organic photovoltaic (OPV) devices has been characterized with impedance spectroscopy. Devices with varied composition and morphology were measured over a range of illumination intensities ranging from dark conditions to 1 sun and applied bias voltages ranging from 0.0 V to 0.75 V. Using an equivalent circuit model, materials properties such as dielectric constant and conductivity were determined and found to be in agreement with values measured by other methods. Average carrier lifetimes were also extracted from the model and found to correlate with measured power conversion efficiencies. At the short circuit condition and ~1 sun illumination, the average electron lifetime was found to vary from 7.8 to 22 μs for devices with power conversion efficiencies ranging from 2.0 to 2.5%. These results suggest that impedance spectroscopy is an effective tool for predicting how processing parameters can impact device performance in organic bulk heterojunction photovoltaic devices. 相似文献
7.
Circumventing UV Light Induced Nanomorphology Disorder to Achieve Long Lifetime PTB7‐Th:PCBM Based Solar Cells
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Quan Liu Johann Toudert Feng Liu Paola Mantilla‐Perez Miguel Montes Bajo Thomas P. Russell Jordi Martorell 《Liver Transplantation》2017,7(21)
Large area flexible electronics rely on organic or hybrid materials prone to degradation limiting the device lifetime. For many years, photo‐oxidation has been thought to be one of the major degradation pathways. However, intense illumination may lead to a burn‐in or a rapid decrease in performance for devices completely isolated from corrosive elements as oxygen or moisture. The experimental studies which are presented in here indicate that a plausible triggering for the burn‐in is a spin flip after a UV photon absorption leading to the accumulation of electrostatic potential energy that initiates a rapid destruction of the nanomorpholgy in the fullerene phase of a polymer cell. To circumvent this and achieve highly stable and efficient devices, a robust nanocrystalline ordering is induced in the PCBM phase prior to UV illumination. In that event, PTB7‐Th:PC71BM cells are shown to exhibit T80 lifetimes larger than 1.6 years under a continuous UV‐filtered 1‐sun illumination, equivalent to 7 years for sunlight harvesting at optimal orientation and 10 years for vertical applications. 相似文献
8.
Nicholas M. Bedford Matthew B. Dickerson Lawrence F. Drummy Hilmar Koerner Kristi M. Singh Milana C. Vasudev Michael F. Durstock Rajesh R. Naik Andrew J. Steckl 《Liver Transplantation》2012,2(9):1136-1144
Nanofibers consisting of the bulk heterojunction organic photovoltaic (BHJ–OPV) electron donor–electron acceptor pair poly(3‐hexylthiophene):phenyl‐C61‐butyric acid methyl ester (P3HT:PCBM) are produced through a coaxial electrospinning process. While P3HT:PCBM blends are not directly electrospinnable, P3HT:PCBM‐containing fibers are produced in a coaxial fashion by utilizing polycaprolactone (PCL) as an electrospinnable sheath material. Pure P3HT:PCBM fibers are easily obtained after electrospinning by selectively removing the PCL sheath with cyclopentanone (average diameter 120 ± 30 nm). These fibers are then incorporated into the active layer of a BHJ–OPV device, which results in improved short‐circuit current densities, fill factors, and power‐conversion efficiencies (PCE) as compared to thin‐film devices of identical chemical composition. The best‐performing fiber‐based devices exhibit a PCE of 4.0%, while the best thin‐film devices have a PCE of 3.2%. This increase in device performance is attributed to the increased in‐plane alignment of P3HT polymer chains on the nanoscale, caused by the electrospun fibers, which leads to increased optical absorption and subsequent exciton generation. This methodology for improving device performance of BHJ–OPVs could also be implemented for other electron donor–electron acceptor systems, as nanofiber formation is largely independent of the PV material. 相似文献
9.
Sara Trost Kirill Zilberberg Andreas Behrendt Andreas Polywka Patrick Görrn Philip Reckers Julia Maibach Thomas Mayer Thomas Riedl 《Liver Transplantation》2013,3(11):1437-1444
A common phenomenon of organic solar cells (OSCs) incorporating metal‐oxide electron extraction layers is the requirement to expose the devices to UV light in order to improve device characteristics – known as the so‐called “light‐soaking” issue. This behaviour appears to be of general validity for various metal‐oxide layers, various organic donor/acceptor systems, and regardless if single junction devices or multi stacked cells are considered. The requirement of UV exposure of OSCs may impose severe problems if substrates with limited UV transmission, UV blocking filters or UV to VIS down‐conversion concepts are applied. In this paper, we will demonstrate that this issue can be overcome by the use of Al doped ZnO (AZO) as electron extraction interlayer. In contrast to devices based on TiOx and ZnO, the AZO devices show well‐behaved solar cell characteristics with a high fill factor (FF) and power conversion efficiency (PCE) even without the UV spectral components of the AM1.5 solar spectrum. As opposed to previous claims, our results indicate that the origin of s‐shaped characteristics of the OSCs is the metal‐oxide/organic interface. The electronic structures of the TiOx/fullerene and AZO/fullerene interfaces are studied by photoelectron spectroscopy, revealing an electron extraction barrier for the TiOx/fullerene case and facilitated electron extraction for AZO/fullerene. These results are of general relevance for organic solar cells based on various donor acceptor active systems. 相似文献
10.
Effect of Electron‐Transport Material on Light‐Induced Degradation of Inverted Planar Junction Perovskite Solar Cells
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Azat F. Akbulatov Lyubov A. Frolova Monroe P. Griffin Ioana R. Gearba Andrei Dolocan David A. Vanden Bout Sergey Tsarev Eugene A. Katz Alexander F. Shestakov Keith J. Stevenson Pavel A. Troshin 《Liver Transplantation》2017,7(19)
This paper presents a systematic study of the influence of electron‐transport materials on the operation stability of the inverted perovskite solar cells under both laboratory indoor and the natural outdoor conditions in the Negev desert. It is shown that all devices incorporating a Phenyl C61 Butyric Acid Methyl ester ([60]PCBM) layer undergo rapid degradation under illumination without exposure to oxygen and moisture. Time‐of‐flight secondary ion mass spectrometry depth profiling reveals that volatile products from the decomposition of methylammonium lead iodide (MAPbI3) films diffuse through the [60]PCBM layer, go all the way toward the top metal electrode, and induce its severe corrosion with the formation of an interfacial AgI layer. On the contrary, alternative electron‐transport material based on the perylendiimide derivative provides good isolation for the MAPbI3 films preventing their decomposition and resulting in significantly improved device operation stability. The obtained results strongly suggest that the current approach to design inverted perovskite solar cells should evolve with respect to the replacement of the commonly used fullerene‐based electron‐transport layers with other types of materials (e.g., functionalized perylene diimides). It is believed that these findings pave a way toward substantial improvements in the stability of the perovskite solar cells, which are essential for successful commercialization of this photovoltaic technology. 相似文献