共查询到20条相似文献,搜索用时 265 毫秒
1.
Andreas Distler Tobias Sauermann Hans‐Joachim Egelhaaf Sheila Rodman Dave Waller Kap‐Soo Cheon Mike Lee Dirk M. Guldi 《Liver Transplantation》2014,4(1)
Increasing the lifetime of polymer based organic solar cells is still a major challenge. Here, the photostability of bulk heterojunction solar cells based on the polymer poly[4,4′‐bis(2‐ethylhexyl)dithieno[3,2‐b:2′,3′‐d]silole)‐2,6‐diyl‐alt‐[2,5‐bis(3‐tetradecylthiophen‐2‐yl)thiazole[5,4‐d]thiazole)‐1,8‐diyl] (PDTSTzTz) and the fullerene [6,6]‐phenyl‐C61‐butyric acid methyl ester (PC60BM) under inert atmosphere is investigated. Correlation of electrical measurements on complete devices and UV‐vis absorption measurements as well as high‐performance liquid chromatography (HPLC) analysis on the active materials reveals that photodimerization of PC60BM is responsible for the observed degradation. Simulation of the electrical device parameters shows that this dimerization results in a significant reduction of the charge carrier mobility. Both the dimerization and the associated device performance loss turn out to be reversible upon annealing. BisPC60BM, the bis‐substituted analog of PC60BM, is shown to be resistant towards light exposure, which in turn enables the manufacture of photostable PDTSTzTz:bisPC60BM solar cells. 相似文献
2.
Toxicity of Thiophenes from Echinops transiliensis (Asteraceae) against Aedes aegypti (Diptera: Culicidae) Larvae 下载免费PDF全文
Hiroshi Nakano Abbas Ali Junaid Ur Rehman Leonid K. Mamonov Charles L. Cantrell Ikhlas A. Khan 《化学与生物多样性》2014,11(7):1001-1009
Structure? activity relationships of nine thiophenes, 2,2′: 5′,2″‐terthiophene ( 1 ), 2‐chloro‐4‐[5‐(penta‐1,3‐diyn‐1‐yl)thiophen‐2‐yl]but‐3‐yn‐1‐yl acetate ( 2 ), 4‐(2,2′‐bithiophen‐5‐yl)but‐3‐yne‐1,2‐diyl diacetate ( 3 ), 4‐[5‐(penta‐1,3‐diyn‐1‐yl)thiophen‐2‐yl]but‐3‐yne‐1,2‐diyl diacetate ( 4 ), 4‐(2,2′‐bithiophen‐5‐yl)‐2‐hydroxybut‐3‐yn‐1‐yl acetate ( 5 ), 2‐hydroxy‐4‐[5‐(penta‐1,3‐diyn‐1‐yl)thiophen‐2‐yl]but‐3‐yn‐1‐yl acetate ( 6 ), 1‐hydroxy‐4‐[5‐(penta‐1,3‐diyn‐1‐yl)thiophen‐2‐yl]but‐3‐yn‐2‐yl acetate ( 7 ), 4‐(2,2′‐bithiophen‐5‐yl)but‐3‐yne‐1,2‐diol ( 8 ), and 4‐[5‐(penta‐1,3‐diyn‐1‐yl)thiophen‐2‐yl]but‐3‐yne‐1,2‐diol ( 9 ), isolated from the roots of Echinops transiliensis, were studied as larvicides against Aedes aegypti. Structural differences among compounds 3, 5 , and 8 consisted in differing AcO and OH groups attached to C(3″) and C(4″), and resulted in variations in efficacy. Terthiophene 1 showed the highest activity (LC50, 0.16 μg/ml) among compounds 1 – 9 , followed by bithiophene compounds 3 (LC50, 4.22 μg/ml), 5 (LC50, 7.45 μg/ml), and 8 (LC50, 9.89 μg/ml), and monothiophene compounds 9 (LC50, 12.45 μg/ml), 2 (LC50, 14.71 μg/ml), 4 (LC50, 17.95 μg/ml), 6 (LC50, 18.55 μg/ml), and 7 (LC50, 19.97 μg/ml). These data indicated that A. aegypti larvicidal activities of thiophenes increase with increasing number of thiophene rings, and the most important active site in the structure of thiophenes could be the tetrahydro‐thiophene moiety. In bithiophenes, 3, 5 , and 8 , A. aegypti larvicidal activity increased with increasing number of AcO groups attached to C(3″) or C(4″), indicating that AcO groups may play an important role in the larvicidal activity. 相似文献
3.
Shuyan Shao Jian Liu Jonas Bergqvist Shengwei Shi Clemens Veit Uli Würfel Zhiyuan Xie Fengling Zhang 《Liver Transplantation》2013,3(3):349-355
A solution‐processed neutral hole transport layer is developed by in situ formation of MoO3 in aqueous PEDOT:PSS dispersion (MoO3‐PEDOT:PSS). This MoO3‐PEDOT:PSS composite film takes advantage of both the highly conductive PEDOT:PSS and the ambient conditions stability of MoO3; consequently it possesses a smooth surface and considerably reduced hygroscopicity. The resulting bulk heterojunction polymer solar cells (BHJ PSC) based on poly[2,3‐bis‐(3‐octyloxyphenyl)quinoxaline‐5,8‐diyl‐alt‐thiophene‐2,5‐diyl] (TQ1):[6,6]‐phenyl‐C71‐butyric acid methyl ester (PC70BM) blends using MoO3‐PEDOT:PSS composite film as hole transport layer (HTL) show considerable improvement in power conversion efficiency (PCE), from 5.5% to 6.4%, compared with the reference pristine PEDOT:PSS‐based device. More importantly, the device with MoO3‐PEDOT:PSS HTL shows considerably improved stability, with the PCE remaining at 80% of its original value when stored in ambient air in the dark for 10 days. In comparison, the reference solar cell with PEDOT:PSS layer shows complete failure within 10 days. This MoO3‐PEDOT:PSS implies the potential for low‐cost roll‐to‐roll fabrication of high‐efficiency polymer solar cells with long‐term stability at ambient conditions. 相似文献
4.
Interplay of Optical,Morphological, and Electronic Effects of ZnO Optical Spacers in Highly Efficient Polymer Solar Cells 下载免费PDF全文
Sadok Ben Dkhil David Duché Meriem Gaceur Anil K. Thakur Fatima Bencheikh Aboura Ludovic Escoubas Jean‐Jacques Simon Antonio Guerrero Juan Bisquert Germà Garcia‐Belmonte Qinye Bao Mats Fahlman Christine Videlot‐Ackermann Olivier Margeat Jörg Ackermann 《Liver Transplantation》2014,4(18)
Optical spacers based on metal oxide layers have been intensively studied in poly(3‐hexylthiophene) (P3HT) based polymer solar cells for optimizing light distribution inside the device, but to date, the potential of such a metal oxide spacer to improve the electronic performance of the polymer solar cells simultaneously has not yet be investigated. Here, a detailed study of performance improvement in high efficient polymer solar cells by insertion of solution‐processed ZnO optical spacer using ethanolamine surface modification is reported. Insertion of the modified ZnO optical spacer strongly improves the performance of polymer solar cells even in the absence of an increase in light absorption. The electric improvements of the device are related to improved electron extraction, reduced contact barrier, and reduced recombination at the cathode. Importantly, it is shown for the first time that the morphology of optical spacer layer is a crucial parameter to obtain highly efficient solar cells in normal device structures. By optimizing optical spacer effects, contact resistance, and morphology of ZnO optical spacers, poly[[4,8‐bis[(2‐ethylhexyl)oxy]benzo[1,2‐b:4,5‐b′]dithiophene‐2,6diyl] [3‐fluoro‐2‐[(2‐ethylhexyl)carbonyl] thieno[3,4‐b]thiophenediyl]] (PTB7):[6,6]‐phenyl‐C71‐butyric acid (PC70BM) bulk heterojunction solar cells with conversion efficiency of 7.6% are obtained in normal device structures with all‐solution‐processed interlayers. 相似文献
5.
Brian J. Worfolk Tate C. Hauger Kenneth D. Harris David A. Rider Jordan A. M. Fordyce Serge Beaupré Mario Leclerc Jillian M. Buriak 《Liver Transplantation》2012,2(3):361-368
A water‐soluble cationic polythiophene derivative, poly[3‐(6‐{4‐tert‐butylpyridiniumyl}‐hexyl)thiophene‐2,5‐diyl] [P3(TBP)HT], is combined with anionic poly(3,4‐ethylenedioxythiophene):poly(p‐styrenesulfonate) (PEDOT:PSS) on indium tin oxide (ITO) substrates via electrostatic layer‐by‐layer (eLbL) assembly. By varying the number of eLbL layers, the electrode's work function is precisely controlled from 4.6 to 3.8 eV. These polymeric coatings are used as cathodic interfacial modifiers for inverted‐mode organic photovoltaics that incorporate a photoactive layer composed of either poly[(3‐hexylthiophene)‐2,5‐diyl] (P3HT) and the fullerene acceptor [6,6‐phenyl‐C61‐butyric acid methyl ester (PC61BM) or the low bandgap polymer [poly({4,8‐di(2‐ethylhexyloxyl)benzo[1,2‐b:4,5‐b′]dithiophene}‐2,6‐diyl)‐alt‐({5‐octylthieno[3,4‐c]pyrrole‐4,6‐dione}‐1,3‐diyl) (PBDTTPD)] and the electron acceptor [6,6‐phenyl‐C71‐butyric acid methyl ester (PC71BM)]. The power conversion efficiency (PCE) of the resulting photovoltaic device is dependent on the composition of the eLbL‐assembled interface and permits the fabrication of devices with efficiencies of 3.8% and 5.6% for P3HT and PBDTTPD donor polymers, respectively. Notably, these devices demonstrate significant stability with a P3HT:PC61BM system maintaining 83% of its original PCE after 1 year of storage and a PBDTTPD:PC71BM system maintaining 97% of its original PCE after over 1000 h of storage in air, according to the ISOS‐D‐1 shelf protocol. 相似文献
6.
Sebastian Engmann Felicia A. Bokel Hyun Wook Ro Dean M. DeLongchamp Lee J. Richter 《Liver Transplantation》2016,6(10)
A method to study the structural evolution of organic bulk heterojunctions via real‐time, in‐situ, steady‐state photoluminescence (PL) is presented. In‐situ PL, in combination with real‐time transmission and reflection measurements, allows us to quantitatively describe the progression of intimate mixing during blade coating of two OPV systems: the common model system poly(3‐hexylthiophene‐2,5‐diyl)/phenyl‐C61‐butyric‐acid‐methyl ester (P3HT/PCBM), and the higher power conversion efficiency system 7,7′‐(4,4bis(2‐ethylhexyl)‐4H‐silolo[3,2‐b:4,5‐b′]dithiophene‐2,6‐diyl)bis(6‐fluoro‐5‐(5′‐hexyl‐[2,2′‐bithiophen]‐5‐yl)benzo[c][1,2,5]thiadiazaole), p‐DTS(FBTTh2)2/[70]PCBM. Evaluating the time dependence of the PL intensity during drying using a 3D‐random‐walk diffusion model allows for the quantitative determination of the ratio of characteristic domain size to exciton diffusion length during solidification in the presence of the processing additives 1‐chloronaphtalene (CN), 1,8‐octanedithiol (ODT), and 1,8‐diiodooctane (DIO). In both cases, the obtained results are in good agreement with the typically observed fibril widths and grain sizes, for P3HT and p‐DTS(FBTTh2)2, respectively. 相似文献
7.
Paul E. Schwenn Ke Gui Alexandre M. Nardes Karsten B. Krueger Kwan H. Lee Karyn Mutkins Halina Rubinstein‐Dunlop Paul E. Shaw Nikos Kopidakis Paul L. Burn Paul Meredith 《Liver Transplantation》2011,1(1):73-81
Organic bulk heterojunction photovoltaic devices predominantly use the fullerene derivatives [C60]PCBM and [C70]PCBM as the electron accepting component. This report presents a new organic electron accepting small molecule 2‐[{7‐(9,9‐di‐n‐propyl‐9H‐fluoren‐2‐yl)benzo[c][1,2,5]thiadiazol‐4‐yl}methylene]malononitrile (K12) for organic solar cell applications. It can be processed by evaporation under vacuum or by solution processing to give amorphous thin films and can be annealed at a modest temperature to give films with much greater order and enhanced charge transport properties. The molecule can efficiently quench the photoluminescence of the donor polymer poly(3‐n‐hexylthiophene‐2,5‐diyl) (P3HT) and time resolved microwave conductivity measurements show that mobile charges are generated indicating that a truly charge separated state is formed. The power conversion efficiencies of the photovoltaic devices are found to depend strongly on the acceptor packing. Optimized K12:P3HT bulk heterojunction devices have efficiencies of 0.73±0.01% under AM1.5G simulated sunlight. The efficiencies of the devices are limited by the level of crystallinity and nanoscale morphology that was achievable in the blend with P3HT. 相似文献
8.
Significance of Average Domain Purity and Mixed Domains on the Photovoltaic Performance of High‐Efficiency Solution‐Processed Small‐Molecule BHJ Solar Cells 下载免费PDF全文
Subhrangsu Mukherjee Christopher M. Proctor Guillermo C. Bazan Thuc‐Quyen Nguyen Harald Ade 《Liver Transplantation》2015,5(21)
Whereas the role of molecularly mixed domains in organic photovoltaic devices for charge generation is extensively discussed in the literature, the impact on charge recombination and thus fill factor is largely unexplored. Here, a combination of soft X‐ray techniques enables the quantification of phases at multiple length scales to reveal their role regarding charge recombination in a highly efficient solution processed small molecule system 7,7′‐(4,4‐bis(2‐ethylhexyl)‐4H‐silolo[3,2‐b:4,5‐b′]dithiophene‐2,6‐diyl)bis(6‐fluoro‐4‐(5′‐hexyl‐[2,2′‐bithiophen]‐5‐yl)benzo[c][1,2,5]thiadiazole) (p‐DTS(FBTTh2)2) . A quantitative (linear) relationship between the average composition variations and the device fill‐factor is observed. The results establish the complex interrelationship between average phase purity, domain size, and structural order and highlight the requirement of achieving sufficient phase purities to diminish bimolecular and geminate recombination in solution processed small molecule solar cells. 相似文献
9.
Paul E. Schwenn Ke Gui Alexandre M. Nardes Karsten B. Krueger Kwan H. Lee Karyn Mutkins Halina Rubinstein‐Dunlop Paul E. Shaw Nikos Kopidakis Paul L. Burn Paul Meredith 《Liver Transplantation》2011,1(1):72-72
Organic bulk heterojunction photovoltaic devices predominantly use the fullerene derivatives [C60]PCBM and [C70]PCBM as the electron accepting component. This report presents a new organic electron accepting small molecule 2‐[{7‐(9,9‐di‐n‐propyl‐9H‐fluoren‐2‐yl)benzo[c][1,2,5]thiadiazol‐4‐yl}methylene]malononitrile (K12) for organic solar cell applications. It can be processed by evaporation under vacuum or by solution processing to give amorphous thin films and can be annealed at a modest temperature to give films with much greater order and enhanced charge transport properties. The molecule can efficiently quench the photoluminescence of the donor polymer poly(3‐n‐hexylthiophene‐2,5‐diyl) (P3HT) and time resolved microwave conductivity measurements show that mobile charges are generated indicating that a truly charge separated state is formed. The power conversion efficiencies of the photovoltaic devices are found to depend strongly on the acceptor packing. Optimized K12:P3HT bulk heterojunction devices have efficiencies of 0.73±0.01% under AM1.5G simulated sunlight. The efficiencies of the devices are limited by the level of crystallinity and nanoscale morphology that was achievable in the blend with P3HT. 相似文献
10.
Ternary Organic Solar Cells with >11% Efficiency Incorporating Thick Photoactive Layer and Nonfullerene Small Molecule Acceptor 下载免费PDF全文
Currently, constructing ternary organic solar cells (OSCs) and developing nonfullerene small molecule acceptors (n‐SMAs) are two pivotal avenues to enhance the device performance. However, introducing n‐SMAs into the ternary OSCs to construct thick layer device is still a challenge due to their inferior charge transport property and unclear aggregation mechanism. In this work, a novel wide band gap copolymer 4,8‐bis(4,5‐dioctylthiophen‐2‐yl) benzo[1,2‐b:4,5‐b′]dithiophene‐2,6‐diyl‐alt‐N‐(2‐hexyldecyl)‐5,5′‐bis(thiophen‐2‐yl)‐2,2′‐bithiophene‐3,3′‐dicarboximide (PDOT) is designed and blend of PDOT:PC71BM achieves a power conversion efficiency (PCE) of 9.5% with active layer thickness over 200 nm. The rationally selected n‐SMA based on a bulky seven‐ring fused core (indacenodithieno[3,2‐b]thiophene) end‐capped with 2‐(3‐oxo‐2,3‐dihydroinden‐1‐ylidene) malononitrile groups (ITIC) is introduced into the host binary PDOT:PC71BM system to extend the absorption range and reduce the photo energy loss. After fully investigating the morphology evolution of the ternary blends, the different aggregation behavior of n‐SMAs with respect to their fullerene counterpart is revealed and the adverse effect of introducing n‐SMAs on charge transport is successfully avoided. The ternary OSC delivers a PCE of 11.2% with a 230 nm thick active layer, which is among the highest efficiencies of thick layer OSCs. The results demonstrate the feasibility of using n‐SMAs to construct a thick layer ternary device for the first time, which will greatly promote the efficiency of thick layer ternary devices. 相似文献
11.
Miao Zeng Xiaojing Wang Ruijie Ma Weiya Zhu Yuan Li Zhongxin Chen Jiawen Zhou Wenqiang Li Tao Liu Zhicai He He Yan Fei Huang Yong Cao 《Liver Transplantation》2020,10(25)
Poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) has been is applied as hole transport material in organic electronic devices for more than 20 years. However, the redundant sulfonic acid group of PEDOT:PSS has often been overlooked. Herein, PEDOT:PSS‐DA is prepared via a facile doping of PEDOT:PSS with dopamine hydrochloride (DA·HCl) which reacts with the redundant sulfonic acid of PSS. The PEDOT:PSS‐DA film exhibits enhanced work function and conductivity compared to those of PEDOT:PSS. PEDOT:PSS‐DA‐based devices show a power conversion efficiency of 16.55% which is the highest in organic solar cells (OSCs) with (poly[(2,6‐(4,8‐bis(5‐(2‐ethylhexyl)‐4‐fluorothiophen‐2‐yl)benzo[1,2‐b:4,5‐b′]dithio‐phene))‐co‐(1,3‐di(5‐thiophene‐2‐yl)‐5,7‐bis(2‐ethylhexyl)‐benzo[1,2‐c:4,5‐c′]dithiophene‐4,8‐dione))] (PM6):(2,2′‐((2Z,2′Z)‐((12,13‐bis(2‐ethylhexyl)‐3,9‐diundecyl‐12,13‐dihydro‐[1,2,5]thiadiazolo[3,4‐e]thieno[2′′,3′:4′,5′]thieno[2′,3′:4,5]pyrrolo[3,2‐g]thieno[2′,3′:4,5]thieno[3,2‐b]indole‐2,10‐diyl)bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile) (Y6) as the active layer. Furthermore, PEDOT:PSS‐DA also exhibits enhanced performance in three other donor/acceptor systems, exhibiting high compatibility in OSCs. This work demonstrates that doping PEDOT:PSS with various amino derivatives is a potentially efficient strategy to enhance the performance of PEDOT:PSS in organic electronic devices. 相似文献
12.
Germanium‐ and Silicon‐Substituted Donor–Acceptor Type Copolymers: Effect of the Bridging Heteroatom on Molecular Packing and Photovoltaic Device Performance 下载免费PDF全文
Jong Soo Kim Zhuping Fei Sebastian Wood David T. James Myungsun Sim Kilwon Cho Martin J. Heeney Ji‐Seon Kim 《Liver Transplantation》2014,4(18)
The effects of heteroatom substitution from a silicon atom to a germanium atom in donor‐acceptor type low band gap copolymers, poly[(4,4′‐bis(2‐ethylhexyl)dithieno[3,2‐b:2′,3′‐d]silole)‐2,6‐diyl‐alt‐(2,1,3‐benzothiadiazole)‐4,7‐diyl] (PSiBTBT) and poly[(4,4′‐bis(2‐ethylhexyl)dithieno[3,2‐b:2′,3′‐d]germole)‐2,6‐diyl‐alt‐(2,1,3‐benzothiadiazole)‐4,7‐diyl] (PGeBTBT), are studied. The optoelectronic and charge transport properties of these polymers are investigated with a particular focus on their use for organic photovoltaic (OPV) devices in blends with phenyl‐C70‐butyric acid methyl ester (PC70BM). It is found that the longer C‐Ge bond length, in comparison to C‐Si, modifies the molecular conformation and leads to a more planar chain conformation in PGeBTBT than PSiBTBT. This increase in molecular planarity leads to enhanced crystallinity and an increased preference for a face‐on backbone orientation, thus leading to higher charge carrier mobility in the diode configuration. These results provide important insight into the impact of the heavy atom substitution on the molecular packing and device performance of polymers based on the poly[2,6‐(4,4‐bis‐(2‐ethylhexyl)‐4H‐cyclopenta[2,1‐b;3,4‐b]‐dithiophene)‐alt‐4,7‐(2,1,3‐benzothiadiazole) (PCPDTBT) backbone. 相似文献
13.
A New Interconnecting Layer of Metal Oxide/Dipole Layer/Metal Oxide for Efficient Tandem Organic Solar Cells 下载免费PDF全文
Shunmian Lu Xing Guan Xinchen Li Wei E. I. Sha Fengxian Xie Hongchao Liu Jiannong Wang Fei Huang Wallace C. H. Choy 《Liver Transplantation》2015,5(17)
A new metal‐oxide‐based interconnecting layer (ICL) structure of all‐solution processed metal oxide/dipole layer/metal oxide for efficient tandem organic solar cell (OSC) is demonstrated. The dipole layer modifies the work function (WF) of molybdenum oxide (MoO x ) to eliminate preexisted counter diode between MoO x and TiO2. Three different amino functionalized water/alcohol soluble conjugated polymers (WSCPs) are studied to show that the WF tuning of MoO x is controllable. Importantly, the results show that S‐shape current density versus voltage (J–V) characteristics form when operation temperature decreases. This implies that thermionic emission within the dipole layer plays critical role for helping recombination of electrons and holes. Meanwhile, the insignificant homotandem open‐circuit voltage (V oc) loss dependence on dipole layer thickness shows that the quantum tunneling effect is weak for efficient electron and hole recombination. Based on this ICL, poly(3‐hexylthiophene) (P3HT)‐based homotandem OSC with 1.20 V V oc and 3.29% power conversion efficiency (PCE) is achieved. Furthermore, high efficiency poly(4,8‐bis(5‐(2‐ethylhexyl)‐thiophene‐2‐yl)‐benzo[1,2‐b54,5‐b9]dithiophene‐alt alkylcarbonylthieno[3,4‐b]thiophene) (PBDTTT‐C‐T)‐based homotandem OSC with 1.54 V V oc and 8.11% PCE is achieved, with almost 15.53% enhancement compared to its single cell. This metal oxide/dipole layer/metal oxide ICL provides a new strategy to develop other qualified ICL with different hole transporting layer and electron transporting layer in tandem OSCs. 相似文献
14.
K. Xerxes Steirer Paul F. Ndione N. Edwin Widjonarko Matthew T. Lloyd Jens Meyer Erin L. Ratcliff Antoine Kahn Neal R. Armstrong Calvin J. Curtis David S. Ginley Joseph J. Berry Dana C. Olson 《Liver Transplantation》2011,1(5):813-820
We show enhanced efficiency and stability of a high performance organic solar cell (OPV) when the work‐function of the hole collecting indium‐tin oxide (ITO) contact, modified with a solution‐processed nickel oxide (NiOx) hole‐transport layer (HTL), is matched to the ionization potential of the donor material in a bulk‐heterojunction solar cell. Addition of the NiOx HTL to the hole collecting contact results in a power conversion efficiency (PCE) of 6.7%, which is a 17.3% net increase in performance over the 5.7% PCE achieved with a poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) HTL on ITO. The impact of these NiOx films is evaluated through optical and electronic measurements as well as device modeling. The valence and conduction band energies for the NiOx HTL are characterized in detail through photoelectron spectroscopy studies while spectroscopic ellipsometry is used to characterize the optical properties. Oxygen plasma treatment of the NiOx HTL is shown to provide superior contact properties by increasing the ITO/NiOx contact work‐function by 500 meV. Enhancement of device performance is attributed to reduction of the band edge energy offset at the ITO/NiOx interface with the poly(N‐9′‐heptadecanyl‐2,7‐carbazole‐alt‐5,5‐(4′,7′‐di‐2‐thienyl‐2′,1′,3′‐benzothidiazole) (PCDTBT):[6,6]‐phenyl‐C61 butyric acid methyl ester PCBM and [6,6]‐phenyl‐C71 butyric acid methyl ester (PC70BM) active layer. A high work‐function hole collecting contact is therefore the appropriate choice for high ionization potential donor materials in order to maximize OPV performance. 相似文献
15.
Harmonious Compatibility Dominates Influence of Side‐Chain Engineering on Morphology and Performance of Ternary Solar Cells 下载免费PDF全文
Tanya Kumari Sang Myeon Lee Kyu Cheol Lee Yongjoon Cho Changduk Yang 《Liver Transplantation》2018,8(22)
A growing number of recent studies have demonstrated the substantial impact of the alkyl side chains on the device performance of organic semiconductors. However, detailed investigation of the effect of side‐chain engineering on the blend morphology and performance of ternary organic solar cells (OSCs) has not yet been undertaken. In this study, the performance of ternary OSCs is investigated in a given poly(4,8‐bis(5‐(2‐ethylhexyl)thiophen‐2‐yl)benzo[1,2‐b;4,5‐b′]dithiophene‐2,6‐diyl‐alt‐(4‐(2‐ethylhexyl)‐3‐fluorothieno[3,4‐b]thiophene‐)‐2‐carboxylate‐2‐6‐diyl)):[6,6]‐phenyl‐C71‐butyric acid methyl ester (PTB7‐Th:PC71BM) host set by introducing various small molecule donors (SMDs) with different terminal side‐chain lengths. As expected, the performance of binary OSCs with SMDs depends greatly on the side‐chain length. In contrast, it is observed that all SMD‐based ternary OSCs exhibit almost identical and high power‐conversion efficiencies of 12.0–12.2%. This minor performance variation is attributed to good molecular compatibility between the two donor components, as evidenced by in‐depth electrical and morphological investigations. These results highlight that the alloy‐like structure formed due to the high compatibility of the donor molecules has a more significant effect on the overall performance than the side‐chain length, offering a new guideline for pairing donor components for achieving high‐performance ternary OSCs. 相似文献
16.
Alexander Colsmann Andreas Puetz Andreas Bauer Jonas Hanisch Erik Ahlswede Uli Lemmer 《Liver Transplantation》2011,1(4):599-603
Window integrated photovoltaics for automotive and building applications are a promising market segment for organic solar modules. Besides semi‐transparency, window integrated applications require a reasonable transparency perception and good color rendering properties in order to be suitable for realistic scene illumination. Here, the transmitted light through semi‐transparent organic solar cells comprising the polymer/fullerene blend poly[(4,4'‐bis(2‐ethylhexyl)dithieno[3,2‐b:2',3'‐d]silole)‐2,6‐diyl‐alt‐(2,1,3‐benzothiadiazole)‐4,7‐diyl]: [6,6]‐phenyl C71‐butric acid methyl ester (PSBTBT:PC70BM) as active layer and a sputtered aluminum doped zinc oxide cathode were found to exhibit a color neutral perception for the human eye and very good color rendering properties. Moreover, the electrical cell properties allow for efficient energy harvesting with an overall power conversion efficiency η ≈ 3%. 相似文献
17.
Overcoming Fill Factor Reduction in Ternary Polymer Solar Cells by Matching the Highest Occupied Molecular Orbital Energy Levels of Donor Polymers 下载免费PDF全文
Jihoon Lee Vellaiappillai Tamilavan Kyung Hwan Rho Sangha Keum Ki Hong Park Daehee Han Yun Kyung Jung Changduk Yang Youngeup Jin Jae‐Won Jang Jung Hyun Jeong Sung Heum Park 《Liver Transplantation》2018,8(9)
Despite the potential of ternary polymer solar cells (PSCs) to improve photocurrents, ternary architecture is not widely utilized for PSCs because its application has been shown to reduce fill factor (FF). In this paper, a novel technique is reported for achieving highly efficient ternary PSCs without this characteristic sharp decrease in FF by matching the highest occupied molecular orbital (HOMO) energy levels of two donor polymers. Our ternary device—made from a blend of wide‐bandgap poly[4,8‐bis(2‐ethylhexyloxy)benzo[1,2‐b:4,5‐b′]dithiophene‐alt‐2,5‐dioctyl‐4,6‐di(thiophen‐2‐yl)pyrrolo[3,4‐c]pyrrole‐1,3(2H,5H)‐dione) (PBDT‐DPPD) polymer, narrow‐bandgap poly[4,8‐bis[5‐(2‐ethylhexyl)‐2‐thienyl]benzo[1,2‐b:4,5‐b′]dithiophene‐alt‐(4‐(2‐ethylhexyl)‐3‐fluorothieno[3,4‐b]thiophene‐)‐2‐carboxylate‐2‐ 6‐diyl)] (PTB7‐Th) polymer, and [6,6]‐phenyl C70‐butyric acid methyl ester (PC70BM)—exhibits a maximum power conversion efficiency of 10.42% with an open‐circuit voltage of 0.80 V, a short‐circuit current of 17.61 mA cm?2, and an FF of 0.74. In addition, this concept is extended to quaternary PSCs made by using three different donor polymers with similar HOMO levels. Interestingly, the quaternary PSCs also yield a good FF (≈0.70)—similar to those of corresponding binary PSCs. This study confirms that the HOMO levels of the polymers used on the photoactive layer of PSCs are a crucial determinant of a high FF. 相似文献
18.
Electron Collection as a Limit to Polymer:PCBM Solar Cell Efficiency: Effect of Blend Microstructure on Carrier Mobility and Device Performance in PTB7:PCBM 下载免费PDF全文
Samuel Foster Florent Deledalle Akiko Mitani Toshio Kimura Ki‐Beom Kim Takayuki Okachi Thomas Kirchartz Jun Oguma Kunihito Miyake James R. Durrant Shuji Doi Jenny Nelson 《Liver Transplantation》2014,4(14)
The poor photovoltaic performance of state‐of‐the‐art blends of 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) and [6,6]‐phenyl‐C61‐butyric acid (PCBM) at large active layer thicknesses is studied using space‐charge‐limited current mobility and photovoltaic device measurements. The poor performance is found to result from relatively low electron mobility. This is attributed to the low tendency of PTB7 to aggregate, which reduces the ability of the fullerene to form a connected network. Increasing the PCBM content 60–80 wt% increases electron mobility and accordingly improves performance for thicker devices, resulting in a fill factor (FF) close to 0.6 at 300 nm. The result confirms that by improving only the connectivity of the fullerene phase, efficient electron and hole collection is possible for 300 nm‐thick PTB7:PCBM devices. Furthermore, it is shown that solvent additive 1,8‐diiodooctane (DIO), used in the highest efficiency PTB7:PCBM devices, does not improve the thickness dependence and, accordingly, does not lead to an increase in either hole or electron mobility or in the carrier lifetime. A key challenge for researchers is therefore to develop new methods to ensure connectivity in the fullerene phase in blends without relying on either a large excess of fullerene or strong aggregation of the polymer. 相似文献
19.
Domain Compositions and Fullerene Aggregation Govern Charge Photogeneration in Polymer/Fullerene Solar Cells 下载免费PDF全文
Sameer Vajjala Kesava Zhuping Fei Adam D. Rimshaw Cheng Wang Alexander Hexemer John B. Asbury Martin Heeney Enrique D. Gomez 《Liver Transplantation》2014,4(11)
The complex microstructure of organic semiconductor mixtures continues to obscure the connection between the active layer morphology and photovoltaic device performance. For example, the ubiquitous presence of mixed phases in the active layer of polymer/fullerene solar cells creates multiple morphologically distinct interfaces which are capable of exciton dissociation or charge recombination. Here, it is shown that domain compositions and fullerene aggregation can strongly modulate charge photogeneration at ultrafast timescales through studies of a model system, mixtures of a low band‐gap polymer, poly[(4,4′‐bis(2‐ethylhexyl)dithieno[3,2‐b:2′,3′‐d]germole)‐2,6‐diyl‐alt‐(2,1,3‐benzothia‐diazole)‐4,7‐diyl], and [6,6]‐phenyl‐C71‐butyric acid methyl ester. Structural characterization using energy‐filtered transmission electron microscopy (EFTEM) and resonant soft X‐ray scattering shows similar microstructures even with changes in the overall film composition. Composition maps generated from EFTEM, however, demonstrate that compositions of mixed domains vary significantly with overall film composition. Furthermore, the amount of polymer in the mixed domains is inversely correlated with device performance. Photoinduced absorption studies using ultrafast infrared spectroscopy demonstrate that polaron concentrations are highest when mixed domains contain the least polymer. Grazing‐incidence X‐ray scattering results show that larger fullerene coherence lengths are correlated to higher polaron yields. Thus, the purity of the mixed domains is critical for efficient charge photogeneration because purity modulates fullerene aggregation and electron delocalization. 相似文献
20.
8.0% Efficient All‐Polymer Solar Cells with High Photovoltage of 1.1 V and Internal Quantum Efficiency near Unity 下载免费PDF全文
Xiaofeng Xu Zhaojun Li Wei Zhang Xiangyi Meng Xianshao Zou Dario Di Carlo Rasi Wei Ma Arkady Yartsev Mats R. Andersson René A. J. Janssen Ergang Wang 《Liver Transplantation》2018,8(1)
In very recent years, growing efforts have been devoted to the development of all‐polymer solar cells (all‐PSCs). One of the advantages of all‐PSCs over the fullerene‐based PSCs is the versatile design of both donor and acceptor polymers which allows the optimization of energy levels to maximize the open‐circuit voltage (Voc). However, there is no successful example of all‐PSCs with both high Voc over 1 V and high power conversion efficiency (PCE) up to 8% reported so far. In this work, a combination of a donor polymer poly[4,8‐bis(5‐(2‐octylthio)thiophen‐2‐yl)benzo[1,2‐b:4,5‐b′]dithiophene‐2,6‐diyl‐alt‐(5‐(2‐ethylhexyl)‐4H‐thieno[3,4‐c]pyrrole‐4,6(5H)‐dione)‐1,3‐diyl] (PBDTS‐TPD) with a low‐lying highest occupied molecular orbital level and an acceptor polymer poly[[N,N′‐bis(2‐octyldodecyl)‐naphthalene‐1,4,5,8‐bis(dicarboximide)‐2,6‐diyl]‐alt‐thiophene‐2,5‐diyl] (PNDI‐T) with a high‐lying lowest unoccupied molecular orbital level is used, realizing high‐performance all‐PSCs with simultaneously high Voc of 1.1 V and high PCE of 8.0%, and surpassing the performance of the corresponding PC71BM‐based PSCs. The PBDTS‐TPD:PNDI‐T all‐PSCs achieve a maximum internal quantum efficiency of 95% at 450 nm, which reveals that almost all the absorbed photons can be converted into free charges and collected by electrodes. This work demonstrates the advantages of all‐PSCs by incorporating proper donor and acceptor polymers to boost both Voc and PCEs. 相似文献