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Transfer Printed Flexible and Stretchable Thin Film Solar Cells Using a Water‐Soluble Sacrificial Layer
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Jiyoon Nam Youngjoo Lee Wonjung Choi Chang Su Kim Hogyoung Kim Jongbok Kim Dong‐Ho Kim Sungjin Jo 《Liver Transplantation》2016,6(21)
Recently, the rapid and significant progress in the development of various stretchable electronics has triggered intense research interest. Although the remarkable features of transfer printing processes have enabled the use of inorganic crystalline semiconductors in various types of stretchable devices, including solar cells, light‐emitting diodes, circuits, and photodetectors, there are few examples of stretchable electronics using thin film semiconductors. Transfer printing of inorganic amorphous thin film semiconductors remains a challenge because no suitable sacrificial layer is available. To meet this challenge, a water‐soluble germanium oxide sacrificial layer is developed. Stretchable inorganic amorphous thin film solar cells are produced using a transfer printing process with a water‐soluble sacrificial layer. This first attempt to fabricate stretchable solar cells with inorganic amorphous thin film semiconductors significantly broadens the scope of solar cell applications. Moreover, the germanium oxide sacrificial layer can be used in other thin film electronics applications. 相似文献
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Huanping Zhou Tze‐Bin Song Choong‐Heui Chung Bao Lei Brion Bob Rui Zhu Hsin‐Sheng Duan Chia‐Jung Hsu Yang Yang 《Liver Transplantation》2012,2(11):1368-1374
As a wide‐bandgap semiconductor, titanium dioxide (TiO2) with a porous structure has proven useful in dye‐sensitized solar cells, but its application in low‐cost, high‐efficiency inorganic photovoltaic devices based on materials such as Cu(InGa)Se2 or Cu2ZnSnS4 is limited. Here, a thin film made from solution‐processed TiO2 nanocrystals is demonstrated as an alternative to intrinsic zinc oxide (i‐ZnO) as the window layer of CuInSxSe1?x solar cells. The as‐synthesized, well‐dispersed, 6 nm TiO2 nanocrystals are assembled into thin films with controllable thicknesses of 40, 80, and 160 nm. The TiO2 nanocrystal films with thicknesses of 40 and 80 nm exhibit conversion efficiencies (6.2% and 6.33%, respectively) that are comparable to that of a layer of the typical sputtered i‐ZnO (6.42%). The conversion efficiency of the devices with a TiO2 thickness of 160 nm decreases to 2.2%, owing to the large series resistance. A 9‐hour reaction time leads to aggregated nanoparticles with a much‐lower efficiency (2%) than that of the well‐dispersed TiO2 nanoparticles prepared using a 15‐hour reaction time. Under optimized conditions, the champion TiO2 nanocrystal‐film‐based device shows even higher efficiency (9.2%) than a control device employing a typical i‐ZnO film (8.6%). 相似文献
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Thomas H. Reilly III Alexander W. Hains Hsiang‐Yu Chen Brian A. Gregg 《Liver Transplantation》2012,2(4):455-460
Solid films of a water‐soluble dicationic perylene diimide salt, perylene bis(2‐ethyltrimethylammonium hydroxide imide), Petma+OH?, are strongly doped n‐type by dehydration and reversibly de‐doped by hydration. The hydrated films consist almost entirely of the neutral perylene diimide, PDI, while the dehydrated films contain ~50% PDI anions. The conductivity increases by five orders of magnitude upon dehydration, probably limited by film roughness, while the work function decreases by 0.74 V, consistent with an n‐type doping density increase of ~12 orders of magnitude. Remarkably, the PDI anions are stable in dry air up to 120 °C. The work function of the doped film, ? (3.96 V vs. vacuum), is unusually negative for an O2‐stable contact. Petma+OH? is also characterized as an interfacial layer, IFL, in two different types of organic photovoltaic cells. Results are comparable to state of the art cesium carbonate IFLs, but may improve if film morphology can be better controlled. The films are stable and reversible over many months in air and light. The mechanism of this unusual self‐doping process may involve the change in relative potentials of the ions in the film caused by their deshielding and compaction as water is removed, leading to charge transfer when dry. 相似文献
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Dan Li Zuo Xiao Shizhe Wang Xinjian Geng Shangfeng Yang Junfeng Fang Huai Yang Liming Ding 《Liver Transplantation》2018,8(20)
An aromatic lactam acceptor unit, thieno[3,2‐c]isoquinolin‐5(4H)‐one (TIQ), is developed. Compared with its analogues, dithieno[3,2‐b:2′,3′‐d]pyridin‐5(4H)‐one (DTP) and phenanthridin‐6(5H)‐one (PN), TIQ shows its advantage in constructing donor–acceptor (D–A) copolymers for efficient solar cells. TIQ‐based D–A copolymer PTIQ4TFBT delivers a power conversion efficiency (PCE) of 10.16% in polymer:fullerene solar cells, while those based on DTP and PN copolymers, PDTP4TFBT and PPN4TFBT, afford PCEs around 8.5%. The higher performance of PTIQ4TFBT:PC71BM solar cells originates from enhanced short‐circuit current density (Jsc) and fill factor (FF), because of favorable morphology, less bimolecular recombination, and balanced charge transport in the active layer. Moreover, the performance for PTIQ4TFBT:PC71BM solar cells is less sensitive to active layer thickness than PDTP4TFBT:PC71BM and PPN4TFBT:PC71BM solar cells. Over 8% PCEs can be obtained from PTIQ4TFBT:PC71BM solar cells when the active layer thickness is over 500 nm. 相似文献
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Hong Jia Shu Hong Zheng Cheng Xu Wei Bo Chen Jue Chen Wang Xiao Feng Liu Jian Rong Qiu 《Liver Transplantation》2015,5(2)
Utilization of photons of sub‐bandgap energy, mostly near‐infrared (NIR) photons, is highly desirable for photovoltaic devices. We show that (NaYF4:Yb‐Tm)/(Cu2O) composite films formed by electrodeposition exhibit robust photoactive current generation under NIR light excitation. The composite films consist of homogeneous crystalline particles of the fluoride and Cu2O in sub‐micrometer size. From spectroscopic characterization, it is found that the NaYF4:Yb‐Tm layer in the composite film converts NIR radiation by up‐conversion into visible emission, which is efficiently absorbed by the covering semiconducting Cu2O film, producing photoelectrons. Accordingly, the composite films exhibit highly photoactive current generation by means of a photoelectrochemical process driven by NIR irradiation. The methodology demonstrated here may have certain implications for the utilization of NIR radiation in solar cells, photocatalysts, and infrared photodetectors. 相似文献
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Possible antagonism of (Z)‐2‐hexenyl (E)‐3‐hexenoate against the attractiveness of (E)‐2‐hexenyl (Z)‐3‐hexenoate to Ooencyrtus nezarae (Hymenoptera: Encyrtidae)
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C. G. Park 《Journal of Applied Entomology》2018,142(3):327-332
Ooencyrtus nezarae (Hymenoptera: Encyrtidae) is an egg parasitoid of bean bug Riptortus pedestris (Hemiptera: Alydidae) which is a major pest of beans. Females of O. nezarae are attracted to (E)‐2‐hexenyl (Z)‐3‐hexenoate (EZ), one of the components of aggregation pheromone of R. pedestris. Effects of three isomers (ZE, EE and ZZ) of EZ on the attractiveness of O. nezarae were tested using electroantennography (EAG) and field bioassays. EAG analyses revealed that the response of O. nezarae to ZE was significantly higher than those to air, hexane and two other isomers, even though the response was lower than that to EZ. ZE affected the attractiveness of EZ dose‐dependently in the field. Addition of ZE (100 mg) to EZ (10 mg) caused a significant reduction in the catches of O. nezarae females. Single or binary addition of two other isomers (EE and ZZ) to EZ could not decrease or increase significantly the number of O. nezarae catches of EZ. Even though addition of ZZ (10, 50 or 100 mg) to EZ (10 mg) caused dose‐dependent reduction in the number of O. nezarae female catches, the reductions were not significantly different from that of EZ. EZ and its three isomers were not attractive to O. nezarae males at all. 相似文献
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The stereocontrolled synthesis of fully protected (2S,4S,6S)‐2‐amino‐6‐hydroxy‐4‐methyl‐8‐oxodecanoic acid was accomplished using a glutamate derivative as starting material. The key steps of this stereochemical synthetic pathway involved an Evans asymmetric alkylation, a Sharpless asymmetric epoxidation, and a Grignard reaction. Copyright © 2012 European Peptide Society and John Wiley & Sons, Ltd. 相似文献
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We studied the effects of hand weeding of second‐year plants of the biennial garlic mustard (Alliaria petiolata) on first‐year plants (seedlings) and native ground layer vegetation. Garlic mustard is a Eurasian species that has invaded deciduous forest ground layers in eastern North America. Treatments consisted of a control and an early or late weeding of second‐year garlic mustard. The early treatment (early March) was applied before garlic mustard seeds had germinated and when most native species were dormant. The late treatment (mid‐May) occurred after plants had bolted, flowering was occurring, and most native species and new garlic mustard seedlings were actively growing. Pre‐treatment data were obtained in 2004 and treated and control plots were sampled in 2005, 2006, and 2007. No significant treatment effects were observed in 2004 or 2005. In 2006, mean cover of first‐year plants was higher in the early weeding treatment than in the late weeding treatment and control. In 2007, mean cover of first‐year garlic mustard was higher in the control than in either of the two weeding treatments. There were no significant treatment effects in any year on native vegetation cover, bare ground, or the five most abundant native species. Our data indicate that (1) late weeding of garlic mustard provided more effective control than early weeding because late weeding allows second‐year plants to compete with garlic mustard seedlings for a longer period of time and (2) competition between first‐ and second‐year plants is responsible for alternating dominance of first‐year and second‐year garlic mustard plants. 相似文献
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Synthesis by Ring‐Closing Alkyne Metathesis with Selective Hydrogenation,and Olfactory Comparison of (7E)‐ and (7Z)‐Cyclohexadec‐7‐enone (Aurelione®)
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Both C?C‐bond isomers of cyclohexadec‐7‐enone ( 6 , Aurelione®) were selectively synthesized via cyclohexadec‐7‐ynol ( 16 ) by ring‐closing alkyne metathesis of icosa‐2,18‐diyn‐9‐ol ( 15 ), employing an in situ‐formed catalyst from Mo(CO)6 and 4‐(trifluoromethyl)phenol. Pyridinium chlorochromate (PCC) oxidation and subsequent Lindlar hydrogenation afforded the (7Z)‐configured isomer (7Z)‐ 6 , while hydrosilylation of the intermediate cyclohexadec‐7‐ynone ( 17 ), followed by desilylation, provided the (7E)‐configured cyclohexadec‐7‐enone ((7E)‐ 6 ). The substrate for the alkyne metathesis was prepared from cycloheptanone ( 7 ) by cycloaddition of chloromethylcarbene to its trimethylsilyl enol ether 8 , and subsequent ring enlargement of the adduct 9 under rearrangement to 2‐methylcyclooct‐2‐enone ( 10 ), which was subjected to Weitz? Scheffer epoxidation and Eschenmoser? Ohloff fragmentation to non‐7‐ynal ( 12 ). Its reaction with the Grignard reagent of 11‐bromoundec‐2‐yne ( 14 ), prepared from the corresponding alcohol 13 by Appel? Lee bromination, furnished the icosa‐2,18‐diyn‐9‐ol ( 15 ). While both isomers of cyclohexadec‐7‐enone ( 6 ) possess warm and powdery musk odors with tobacco‐type ambery accents, (7Z)‐ 6 is more animalic and waxy, whereas (7E)‐ 6 was found to be more floral, sweet, and hay‐like in tonality. Interestingly, however, with odor detection thresholds of 2.0 ng/l air and 2.3 ng/l air, respectively, both (7Z)‐ 6 and (7E)‐ 6 were found to be almost identical in their odor strength, with the (7Z)‐ 6 being only very slightly more powerful. 相似文献
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Epidemiological studies corroborate a correlation between pesticide use and Parkinson's disease (PD). Thiocarbamate and dithiocarbamate pesticides are widely used and produce neurotoxicity in the peripheral nervous system. Recent evidence from rodent studies suggests that these compounds also cause dopaminergic (DAergic) dysfunction and altered protein processing, two hallmarks of PD. However, DAergic neurotoxicity has yet to be documented. We assessed DAergic dysfunction in Caenorhabditis elegans (C. elegans) to investigate the ability of thiocarbamate pesticides to induce DAergic neurodegeneration. Acute treatment with either S‐ethyl N,N‐dipropylthiocarbamate (EPTC), molinate, or a common reactive intermediate of dithiocarbamate and thiocarbamate metabolism, S‐methyl‐N,N‐diethylthiocarbamate (MeDETC), to gradual loss of DAergic cell morphology and structure over the course of 6 days in worms expressing green fluorescent protein (GFP) under a DAergic cell specific promoter. HPLC analysis revealed decreased DA content in the worms immediately following exposure to MeDETC, EPTC, and molinate. In addition, worms treated with the three test compounds showed a drastic loss of DAergic‐dependent behavior over a time course similar to changes in DAergic cell morphology. Alterations in the DAergic system were specific, as loss of cell structure and neurotransmitter content was not observed in cholinergic, glutamatergic, or GABAergic systems. Overall, our data suggest that thiocarbamate pesticides promote neurodegeneration and DAergic cell dysfunction in C. elegans, and may be an environmental risk factor for PD. 相似文献
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Torsten Bronger Paul H. Wöbkenberg Jan Wördenweber Stefan Muthmann Ulrich W. Paetzold Vladimir Smirnov Stephan Traut Ümit Dagkaldiran Stephan Wieber Michael Cölle Anna Prodi‐Schwab Odo Wunnicke Matthias Patz Martin Trocha Uwe Rau Reinhard Carius 《Liver Transplantation》2014,4(11)
Solution‐based semiconductors give rise to the next generation of thin‐film electronics. Solution‐based silicon as a starting material is of particular interest because of its favorable properties, which are already vastly used in conventional electronics. Here, the application of a silicon precursor based on neopentasilane for the preparation of thin‐film solar cells is reported for the first time, and, for the first time, a performance similar to conventional fabrication methods is demonstrated. Because three different functional layers, n‐type contact layer, intrinsic absorber, and p‐type contact layer, have to be stacked on top of each other, such a device is a very demanding benchmark test of performance of solution‐based semiconductors. Complete amorphous silicon n‐i‐p solar cells with an efficiency of 3.5% are demonstrated, which significantly exceeds previously reported values. 相似文献
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《Chirality》2017,29(6):273-281
Enantiomeric 1H and 13C NMR signal separation behaviors of various α‐amino acids and DL‐tartarate were investigated by using the samarium(III) and neodymium(III) complexes with (S ,S )‐ethylenediamine‐N ,N' ‐disuccinate as chiral shift reagents. A relatively smaller concentration ratio of the lanthanide(III) complex to substrates was suitable for the neodymium(III) complex compared with the samarium(III) one, striking a balance between relatively greater signal separation and broadening. To clarify the difference in the signal separation behavior, the chemical shifts of β‐protons for fully bound D‐ and L‐alanine (δb(D) and δb(L)) and their adduct formation constants (K s) were obtained for both metal complexes. Preference for D‐alanine was similarly observed for both complexes, while it was revealed that the difference between the δb(D) and δb(L) values is the significant factor to determine the enantiomeric signal separation. The neodymium(III) and samarium(III) complexes can be used complementarily for higher and smaller concentration ranges of substrates, respectively, because the neodymium(III) complex gives the larger difference between the δb(D) and δb(L) values with greater signal broadening compared to the samarium(III) complex. 相似文献
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Layer‐by‐Layer Na3V2(PO4)3 Embedded in Reduced Graphene Oxide as Superior Rate and Ultralong‐Life Sodium‐Ion Battery Cathode
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Yanan Xu Qiulong Wei Chang Xu Qidong Li Qinyou An Pengfei Zhang Jinzhi Sheng Liang Zhou Liqiang Mai 《Liver Transplantation》2016,6(14)
Na3V2(PO4)3 (NVP) is regarded as a promising cathode for advanced sodium‐ion batteries (SIBs) due to its high theoretical capacity and stable sodium (Na) super ion conductor (NASICON) structure. However, strongly impeded by its low electronic conductivity, the general NVP delivers undesirable rate capacity and fails to meet the demands for quick charge. Herein, a novel and facile synthesis of layer‐by‐layer NVP@reduced graphene oxide (rGO) nanocomposite is presented through modifying the surface charge of NVP gel precursor. The well‐designed layered NVP@rGO with confined NVP nanocrystal in between rGO layers offers high electronic and ionic conductivity as well as stable structure. The NVP@rGO nanocomposite with merely ≈3.0 wt% rGO and 0.5 wt% amorphous carbon, yet exhibits extraordinary electrochemical performance: a high capacity (118 mA h g?1 at 0.5 C attaining the theoretical value), a superior rate capability (73 mA h g?1 at 100 C and even up to 41 mA h g?1 at 200 C), ultralong cyclability (70.0% capacity retention after 15 000 cycles at 50 C), and stable cycling performance and excellent rate capability at both low and high operating temperatures. The proposed method and designed layer‐by‐layer active nanocrystal@rGO strategy provide a new avenue to create nanostructures for advanced energy storage applications. 相似文献
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Thin‐Film Solar Cells: Atomic‐Scale Observation of Oxygen Substitution and Its Correlation with Hole‐Transport Barriers in Cu2ZnSnSe4 Thin‐Film Solar Cells (Adv. Energy Mater. 6/2016)
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Jin Hyun Kim Si‐Young Choi Minseok Choi Talia Gershon Yun Seog Lee Wei Wang Byungha Shin Sung‐Yoon Chung 《Liver Transplantation》2016,6(6)