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1.
Vincent M. Le Corre Azadeh Rahimi Chatri Nutifafa Y. Doumon L. Jan Anton Koster 《Liver Transplantation》2017,7(22)
Charge transport in organic photovoltaic (OPV) devices is often characterized by steady‐state mobilities. However, the suitability of steady‐state mobilities to describe charge transport has recently been called into question, and it has been argued that dispersion plays a significant role. In this paper, the importance of the dispersion of charge carrier motion on the performance of organic photovoltaic devices is investigated. An experiment to measure the charge extraction time under realistic operating conditions is set up. This experiment is applied to different blends and shows that extraction time is directly related to the geometrical average of the steady‐state mobilities. This demonstrates that under realistic operating conditions the steady‐state mobilities govern the charge extraction of OPV and gives a valuable insight in device performance. 相似文献
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Sebastian Engmann Chetan R. Singh Vida Turkovic Harald Hoppe Gerhard Gobsch 《Liver Transplantation》2013,3(11):1463-1472
This study correlates the device performance of organic solar cells and the electronic charge transport within polymer/fullerene films, directly to the optical order of the polymer. The optical order was measured by spectroscopic ellipsometry and evaluated by our previously derived model. We were able to determine the in‐depth distribution of higher and lower ordered poly(3‐hexylthiophene) (P3HT) domains within an [6,6]‐phenyl‐C61‐butyric acid methyl ester (PCBM) matrix. The over the film thickness integrated volume fraction of highly ordered P3HT domains could be directly correlated to the corresponding solar cell device performance. We are able to describe various thermally annealing conditions between room‐temperature and 200 °C. 相似文献
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Armantas Melianas Vytenis Pranculis Donato Spoltore Johannes Benduhn Olle Inganäs Vidmantas Gulbinas Koen Vandewal Martijn Kemerink 《Liver Transplantation》2017,7(20)
In organic solar cells continuous donor and acceptor networks are considered necessary for charge extraction, whereas discontinuous neat phases and molecularly mixed donor–acceptor phases are generally regarded as detrimental. However, the impact of different levels of domain continuity, purity, and donor–acceptor mixing on charge transport remains only semiquantitatively described. Here, cosublimed donor–acceptor mixtures, where the distance between the donor sites is varied in a controlled manner from homogeneously diluted donor sites to a continuous donor network are studied. Using transient measurements, spanning from sub‐picoseconds to microseconds photogenerated charge motion is measured in complete photovoltaic devices, to show that even highly diluted donor sites (5.7%–10% molar) in a buckminsterfullerene matrix enable hole transport. Hopping between isolated donor sites can occur by long‐range hole tunneling through several buckminsterfullerene molecules, over distances of up to ≈4 nm. Hence, these results question the relevance of “pristine” phases and whether a continuous interpenetrating donor–acceptor network is the ideal morphology for charge transport. 相似文献
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A correlation between the hole transport and corresponding structural properties of the bulk regioregular poly(3‐hexylthiophene) (rr‐P3HT) is studied as a function of temperature by the time‐of‐flight (TOF) and wide angle X‐ray diffraction (WAXD) techniques. The thermally‐reversible structural evolution along the (100) and (020) directions in a semi‐crystalline rr‐P3HT can be divided into two distinct temperature regions. At T > 120 °C, a large thermal expansion along the π–π stacking direction in the nanocrystals and a deteriorated ordering in the material result in negative slopes of temperature and electric field dependences of hole mobility. The WAXD data suggest that the hole transport is limited by a decrease in the crystallinity and by an increase in the hopping distance along the π‐π stacking direction, while the Gaussian Disorder Model (GDM) with temperature‐independent parameters cannot be applied. At T < 120 °C, the transport‐related structural changes are negligible and the temperature and electric field dependences of hole mobility can be described by the GDM with constant energetic (σ ～ 120 meV) and positional disorder parameters (Σ ～ 3.33). These values suggest that the hole transport is limited by the amorphous phase, as commonly seen in disordered polymers. Moreover, a regiorandom P3HT (rra‐P3HT), which shows a temperature‐independent intermolecular distance of ～15.3Å, provides a route for separate examination of the amorphous phase in rr‐P3HT. 相似文献
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Halide perovskites have remarkable properties for relatively crudely processed semiconductors, including large optical absorption coefficients and long charge carrier lifetimes. Thanks to such properties, these materials are now competing with established technologies for use in cost‐effective and efficient light‐harvesting and light‐emitting devices. Nevertheless, the fundamental understanding of the behavior of charge carriers in these materials—particularly on the nano‐ to microscale—has, on the whole, lagged behind empirical device performance. Such understanding is essential to control charge carriers, exploit new device structures, and push devices to their performance limits. Among other tools, optical microscopy and spectroscopic techniques have revealed rich information about charge carrier recombination and transport on important length scales. In this progress report, the contribution of time‐resolved optical microscopy techniques to the collective understanding of the photophysics of these materials is detailed. The ongoing technical developments in the field that are overcoming traditional experimental limitations in order to visualize transport properties over multiple time and length scales are discussed. Finally, strategies are proposed to combine optical microscopy with complementary techniques in order to obtain a holistic picture of local carrier photophysics in state‐of‐the‐art perovskite devices. 相似文献
7.
Ardalan Armin Gytis Juska Mujeeb Ullah Marappan Velusamy Paul L. Burn Paul Meredith Almantas Pivrikas 《Liver Transplantation》2014,4(4)
A novel technique based upon injection‐charge extraction by linearly increasing voltage (i‐CELIV) in a metal‐insulator‐semiconductor (MIS) diode structure is described for studying charge transport in organic semiconductors. The technique (MIS‐CELIV) allows selective measurement of both electron and hole mobilities of organic solar cells with active layers thicknesses representative of operational devices. The method is used to study the model high efficiency bulk heterojunction combination poly[N‐9′′‐heptadecanyl‐2,7‐carbazole‐alt‐5,5‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothiadiazole)] (PCDTBT) and [6,6]‐phenyl C70‐butyric acid methyl ester (PC70BM) at various blend ratios. The absence of bipolar transport in PCDTBT‐and‐PC70BM‐only diodes is shown and strongly imbalanced carrier mobility is found in the most efficient “optimized” blend ratios. The mobility measurements are correlated with overall device performance and it is found that balanced and high charge carrier mobility are not necessarily required for high efficiencies in thin film organic solar cells. 相似文献
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The electrical conductivity behavior of a fluorinated self‐assembled monolayer (FSAM) of a molybdenum oxide (MoOx)‐doped α‐naphthyl diamine derivative (α‐NPD) in organic light‐emitting diodes (OLEDs) was investigated. The current density of the MoOx‐doped α‐NPD/FSAM device was proportional to its voltage owing to smooth carrier injection through the FSAM and the high carrier density of its bulk. The temperature‐dependent characteristics of this device were investigated. The current density–voltage characteristics at different temperatures were almost the same owing to its very low activation energy. The activation energy of the device was estimated to be 1.056 × 10?2 [eV] and was very low due to the inelastic electron tunneling of FSAM molecules. Copyright © 2014 John Wiley & Sons, Ltd. 相似文献
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Thomas Heumueller Timothy M. Burke William R. Mateker Isaac T. Sachs‐Quintana Koen Vandewal Christoph J. Brabec Michael D. McGehee 《Liver Transplantation》2015,5(14)
The photoinduced open‐circuit voltage (Voc) loss commonly observed in bulk heterojunction organic solar cells made from amorphous polymers is investigated. It is observed that the total charge carrier density and, importantly, the recombination dynamics are unchanged by photoinduced burn‐in. Charge extraction is used to monitor changes in the density of states (DOS) during degradation of the solar cells, and a broadening over time is observed. It is proposed that the Voc losses observed during burn‐in are caused by a redistribution of charge carriers in a broader DOS. The temperature and light intensity dependence of the Voc losses can be described with an analytical model that contains the amount of disorder broadening in a Gaussian DOS as the only fit parameter. Finally, the Voc loss in solar cells made from amorphous and crystalline polymers is compared and an increased stability observed in crystalline polymer solar cells is investigated. It is found that solar cells made from crystalline materials have a considerably higher charge carrier density than those with amorphous materials. The effects of a DOS broadening upon aging are suppressed in solar cells with crystalline materials due to their higher carrier density, making crystalline materials more stable against Voc losses during burn‐in. 相似文献
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Eric T. Hoke Koen Vandewal Jonathan A. Bartelt William R. Mateker Jessica D. Douglas Rodrigo Noriega Kenneth R. Graham Jean M. J. Fréchet Alberto Salleo Michael D. McGehee 《Liver Transplantation》2013,3(2):220-230
Polymer:fullerene solar cells are demonstrated with power conversion efficiencies over 7% with blends of PBDTTPD and PC61BM. These devices achieve open‐circuit voltages (Voc) of 0.945 V and internal quantum efficiencies of 88%, making them an ideal candidate for the large bandgap junction in tandem solar cells. Voc’s above 1.0 V are obtained when the polymer is blended with multiadduct fullerenes; however, the photocurrent and fill factor are greatly reduced. In PBDTTPD blends with multiadduct fullerene ICBA, fullerene emission is observed in the photoluminescence and electroluminescence spectra, indicating that excitons are recombining on ICBA. Voltage‐dependent, steady state and time‐resolved photoluminescence measurements indicate that energy transfer occurs from PBDTTPD to ICBA and that back hole transfer from ICBA to PBDTTPD is inefficient. By analyzing the absorption and emission spectra from fullerene and charge transfer excitons, we estimate a driving free energy of –0.14 ± 0.06 eV is required for efficient hole transfer. These results suggest that the driving force for hole transfer may be too small for efficient current generation in polymer:fullerene solar cells with Voc values above 1.0 V and that non‐fullerene acceptor materials with large optical gaps (>1.7 eV) may be required to achieve both near unity internal quantum efficiencies and values of Voc exceeding 1.0 V. 相似文献
13.
Ardalan Armin Mike Hambsch Pascal Wolfer Hui Jin Jun Li Zugui Shi Paul L. Burn Paul Meredith 《Liver Transplantation》2015,5(3)
The high power conversion efficiencies (PCEs) of laboratory‐scale polymer‐based organic solar cells are yet to translate to large area modules because of a number of factors including the relatively large sheet resistance of available transparent conducting electrodes (TCEs), and the high defect densities associated with thin organic semiconductor junctions. The TCE problem limits device architectures to narrow connected strips (<1 cm) causing serious fabrication difficulties and extra costs. Thin junctions are required because of poor charge transport (imbalanced mobilities) in the constituent organic semiconductors. These issues are addressed using a combination of approaches to create thick junctions conformally coated on low sheet resistance metal grid TCEs. An essential feature of these thick junctions is balanced carrier mobilities, which affords high fill factors and efficient carrier extraction. Conformal coating is achieved by promoting enhanced intermolecular interactions in the coating solution using a high molecular weight polymeric semiconductor and appropriate solvent system. This combination of balanced mobilities, conformal coating and metallic grid TCEs is a simple and generic approach to the fabrication of defect‐free large area organic solar cells (OSCs). The approach is demonstrated with 25 cm2 monolithic devices possessing aperture‐corrected power conversion efficiencies of 5% and fill factors exceeding 0.5. 相似文献
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Charge‐transfer (CT) state electroluminescence is investigated in several polymer:fullerene bulk heterojunction solar cells. The ideality factor of the electroluminescence reveals that the CT emission in polymer:fullerene solar cells originates from free‐carrier bimolecular recombination at the donor‐acceptor interface, rather than a charge‐trap‐mediated process. The fingerprint of the presence of nonradiative trap‐assisted recombination, a voltage‐dependent CT electroluminescence quantum efficiency, is only observed for the P3HT:PCBM system, which is explained by a reduction of the competing bimolecular recombination rate. These results are in agreement with measurements of the illumination‐intensity dependence of the open‐circuit voltage. 相似文献
15.
Martin Stolterfoht Safa Shoaee Ardalan Armin Hui Jin Ivan Kassal Wei Jiang Paul Burn Paul Meredith 《Liver Transplantation》2017,7(4)
The origin of photocurrent losses in the power‐generating regime of organic solar cells (OSCs) remains a controversial topic, although recent literature suggests that the competition between bimolecular recombination and charge extraction determines the bias dependence of the photocurrent. Here the steady‐state recombination dynamics is studied in bulk‐heterojunction OSCs with different hole mobilities from short‐circuit to maximum power point. It is shown that in this regime, in contrast to previous transient extracted charge and absorption spectroscopy studies, first‐order recombination outweighs bimolecular recombination of photogenerated charge carriers. This study demonstrates that the first‐order losses increase with decreasing slower carrier mobility, and attributes them to either mobilization of charges trapped at the donor:acceptor interface through the Poole–Frenkel effect, and/or recombination of photogenerated and injected charges. The dependence of both first‐order and higher‐order losses on the slower carrier mobility explains why the field dependence of OSC efficiencies has historically been attributed to charge‐extraction losses. 相似文献
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Organic Electronics: The Roles of Structural Order and Intermolecular Interactions in Determining Ionization Energies and Charge‐Transfer State Energies in Organic Semiconductors (Adv. Energy Mater. 22/2016) 
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下载免费PDF全文 Kenneth R. Graham Guy O. Ngongang Ndjawa Sarah M. Conron Rahim Munir Koen Vandewal John J. Chen Sean Sweetnam Mark E. Thompson Alberto Salleo Michael D. McGehee Aram Amassian 《Liver Transplantation》2016,6(22)
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Kenneth R. Graham Guy O. Ngongang Ndjawa Sarah M. Conron Rahim Munir Koen Vandewal John J. Chen Sean Sweetnam Mark E. Thompson Alberto Salleo Michael D. McGehee Aram Amassian 《Liver Transplantation》2016,6(22)
The energy landscape in organic semiconducting materials greatly influences charge and exciton behavior, which are both critical to the operation of organic electronic devices. These energy landscapes can change dramatically depending on the phases of material present, including pure phases of one molecule or polymer and mixed phases exhibiting different degrees of order and composition. In this work, ultraviolet photoelectron spectroscopy measurements of ionization energies (IEs) and external quantum efficiency measurements of charge‐transfer (CT) state energies (ECT) are applied to molecular photovoltaic material systems to characterize energy landscapes. The results show that IEs and ECT values are highly dependent on structural order and phase composition. In the sexithiophene:C60 system both the IEs of sexithiophene and C60 shift by over 0.4 eV while ECT shifts by 0.5 eV depending on molecular composition. By contrast, in the rubrene:C60 system the IE of rubrene and C60 vary by ≤ 0.11 eV and ECT varies by ≤ 0.04 eV as the material composition varies. These results suggest that energy landscapes can exist whereby the binding energies of the CT states are overcome by energy offsets between charges in CT states in mixed regions and free charges in pure phases. 相似文献
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Photoinduced charge selective carrier extraction by linearly increasing voltage technique allows straightforward assessment of charge transport properties within planar and mesostructured perovskite solar cells with respect to light intensity and signal delay time. Charge sensitive device architecture is realized through implementation of insulating layer between the anode or cathode to prevent extraction of unwanted type of carriers. Resulting behavior of comparatively efficient mesoporous and planar solar cells exhibits well balanced charge transport with slight dependence of charge mobility on applied laser pulse fluence, for given pulse delay times. Very similar charge carrier mobilities are present within mesoporous devices, whereas holes trail approximately half an order of magnitude behind electrons in planar structured specimens. Moreover, dispersive transport is identified in the electron selective devices with titanium oxide electron transporter, suggesting considerable presence of trapping states at the perovskite interface, whereas no such behavior characterizes planar samples. Variation in delay time between laser pulse and extraction ramp only affects initial charge concentration present within the device, while transient outlay remains unchanged, indicating absence of film charging effect. 相似文献
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With power conversion efficiencies now exceeding 25%, hybrid perovskite solar cells require deeper understanding of defects and processing to further approach the Shockley‐Queisser limit. One approach for processing enhancement and defect reduction involves additive engineering—, e.g., addition of MASCN (MA = methylammonium) and excess PbI2 have been shown to modify film grain structure and improve performance. However, the underlying impact of these additives on transport and recombination properties remains to be fully elucidated. In this study, a newly developed carrier‐resolved photo‐Hall (CRPH) characterization technique is used that gives access to both majority and minority carrier properties within the same sample and over a wide range of illumination conditions. CRPH measurements on n‐type MAPbI3 films reveal an order of magnitude increase in carrier recombination lifetime and electron density for 5% excess PbI2 added to the precursor solution, with little change noted in electron and hole mobility values. Grain size variation (120–2100 nm) and MASCN addition induce no significant change in carrier‐related parameters considered, highlighting the benign nature of the grain boundaries and that excess PbI2 must predominantly passivate bulk defects rather than defects situated at grain boundaries. This study offers a unique picture of additive impact on MAPbI3 optoelectronic properties as elucidated by the new CRPH approach. 相似文献
20.
Dongmei Wang Ze Wang Lei Zhang Zhiyuan Li XiaoFei Tian Jun Fang Qingyou Lu Xin Zhang 《Bioelectromagnetics》2018,39(5):352-360