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1.
Kammasandra Nanjunda Shivananda Irit Cohen Elena Borzin Yulia Gerchikov Michal Firstenberg Olga Solomeshch Nir Tessler Yoav Eichen 《Advanced functional materials》2012,22(7):1489-1501
Sequence‐independent or “click” chemistry is applied for the preparation of a series of novel and structurally similar π‐conjugated oligomers. The new oligomers are prepared using Wittig–Horner chemistry from bifunctional building blocks that can be interconnected to one another at any desired sequence. The bifunctional building blocks consist of aromatic skeletons with acetal protected aldehyde groups on one side and a phosphonic acid diethyl ester group para to the aldehyde functionality. The first step in the arylenevinylene formation is a Wittig–Horner coupling of a functionalized aldehyde with the methyl phosphonate ester ylide of a bifunctional monomer. A stepwise protection–deprotection process is applied for the preparation of structurally similar π‐conjugated oligo‐phenylene vinylenes. New di‐, tri‐, penta‐, and hepta‐phenylenevinylenes are prepared and characterized. Selected penta‐arylenevinylenes are incorporated as the semiconductor channel in organic field‐effect transistors. 相似文献
2.
Difluorobenzothiadiazole‐Based Small‐Molecule Organic Solar Cells with 8.7% Efficiency by Tuning of π‐Conjugated Spacers and Solvent Vapor Annealing
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Jin‐Liang Wang Fei Xiao Jun Yan Zhuo Wu Kai‐Kai Liu Zheng‐Feng Chang Ru‐Bo Zhang Hui Chen Hong‐Bin Wu Yong Cao 《Advanced functional materials》2016,26(11):1803-1812
The synthesis of a series of tetrafluorine‐substituted, wide‐bandgap, small molecules consisting of various π‐conjugated spacers (furan, thiophene, selenophene) between indacenodithiophene as the electron‐donating core and the electron‐deficient difluorobenzothiadiazole unit is reported and the effect of the π‐conjugated spacers on the photovoltaic properties is investigated. The alteration of the π‐conjugated spacer enables fine‐tuning of the photophysical properties and energy levels of the small molecules, and allows the adjustment of the charge‐transport properties, the morphology of the photoactive films, as well as their photovoltaic properties. Moreover, most of these devices exhibit superior device performances after CH2Cl2 solvent annealing than without annealing, with a high fill factor (0.70–0.75 for all cases). Notably, the devices based on the new molecule BIT4FTh (with thiophene as the spacer) show an outstanding PCE of 8.7% (with an impressive FF of 0.75), considering its wide‐bandgap (1.81 eV), which is among the highest efficiencies reported so far for small‐molecules‐based solar cells. The morphologies of the photoactive layers with/without CH2Cl2 solvent annealing are characterized by atomic force microscopy, transmission electron microscopy and two‐dimensional grazing incidence X‐ray diffraction analysis. The results reported here clearly indicate that highly efficient small‐molecules‐based solar cells can be achieved through rational design of their molecular structure and optimization of the phase‐separated morphology via an adapted solvent–vapor annealing process. 相似文献
3.
Ran Kim Paul S. K. Amegadze Il Kang Hui‐Jun Yun Yong‐Young Noh Soon‐Ki Kwon Yun‐Hi Kim 《Advanced functional materials》2013,23(46):5719-5727
A high‐performance naphthalene diimide (NDI)‐based conjugated polymer for use as the active layer of n‐channel organic field‐effect transistors (OFETs) is reported. The solution‐processable n‐channel polymer is systematically designed and synthesized with an alternating structure of long alkyl substituted‐NDI and thienylene–vinylene–thienylene units (PNDI‐TVT). The material has a well‐controlled molecular structure with an extended π‐conjugated backbone, with no increase in the LUMO level, achieving a high mobility and highly ambient stable n‐type OFET. The top‐gate, bottom‐contact device shows remarkably high electron charge‐carrier mobility of up to 1.8 cm2 V?1 s?1 (Ion/Ioff = 106) with the commonly used polymer dielectric, poly(methyl methacrylate) (PMMA). Moreover, PNDI‐TVT OFETs exhibit excellent air and operation stability. Such high device performance is attributed to improved π–π intermolecular interactions owing to the extended π‐conjugation, apart from the improved crystallinity and highly interdigitated lamellar structure caused by the extended π–π backbone and long alkyl groups. 相似文献
4.
Layer‐by‐Layer Conjugated Extension of a Semiconducting Polymer for High‐Performance Organic Field‐Effect Transistor
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Mi Jang Se Hyun Kim Han‐Koo Lee Yun‐Hi Kim Hoichang Yang 《Advanced functional materials》2015,25(25):3833-3839
A donor–acceptor (D–A) semiconducting copolymer, PDPP‐TVT‐29, comprising a diketopyrrolopyrrole (DPP) derivative with long, linear, space‐separated alkyl side‐chains and thiophene vinylene thiophene (TVT) for organic field‐effect transistors (OFETs) can form highly π‐conjugated structures with an edge‐on molecular orientation in an as‐spun film. In particular, the layer‐like conjugated film morphologies can be developed via short‐term thermal annealing above 150 °C for 10 min. The strong intermolecular interaction, originating from the fused DPP and D–A interaction, leads to the spontaneous self‐assembly of polymer chains within close proximity (with π‐overlap distance of 3.55 Å) and forms unexpectedly long‐range π‐conjugation, which is favorable for both intra‐ and intermolecular charge transport. Unlike intergranular nanorods in the as‐spun film, well‐conjugated layers in the 200 °C‐annealed film can yield more efficient charge‐transport pathways. The granular morphology of the as‐spun PDPP‐TVT‐29 film produces a field‐effect mobility (μ FET) of 1.39 cm2 V?1 s?1 in an OFET based on a polymer‐treated SiO2 dielectric, while the 27‐Å‐step layered morphology in the 200 °C‐annealed films shows high μ FET values of up to 3.7 cm2 V?1 s?1. 相似文献
5.
π‐Conjugated Molecules Crosslinked Graphene‐Based Ultrathin Films and Their Tunable Performances in Organic Nanoelectronics
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Xiaowei Ou Penglei Chen Lang Jiang Yunfan Shen Wenping Hu Minghua Liu 《Advanced functional materials》2014,24(4):543-554
Graphene‐based ultrathin films with tunable performances, controlled thickness, and high stability are crucial for their uses. The currently existing protocols, however, could hardly simultaneously meet these requirements. Using amino‐substituted π‐conjugated compounds, including 1,4‐diaminobenzene (DABNH2), benzidine (BZDNH2), and 5,10,15,20‐tetrakis (4‐aminophenyl)‐21H,23H‐porphine (TPPNH2), as cross‐linkages, a new protocol through which graphene oxide (GO) nanosheets can be anchored on solid supports with a high stability and controlled thickness via a layer‐by‐layer method is presented. A thermal annealing leads to the reduction of the films, and the qualities of the samples can be inherited by the as‐produced reduced GO films (RGO). When RGO films are integrated as source/drain electrodes in OFETs, tunable performances can be realized. The devices based on the BZDNH2‐crosslinked RGO electrodes exhibit similar electrical behaviors as those based on the non‐π‐conjugated compound crosslinked electrodes, while improved performances can be gained when those crosslinked by DABNH2 are used. The performances can be further improved when RGO films crosslinked by TPPNH2 are employed. This work likely paves a new avenue for graphene‐based films of tunable performances, controlled thickness, and high stability. 相似文献
6.
Suzhi Cai Huifang Shi Dan Tian Huili Ma Zhichao Cheng Qi Wu Mingxing Gu Ling Huang Zhongfu An Qian Peng Wei Huang 《Advanced functional materials》2018,28(9)
Efficient ultralong organic phosphorescent materials have potential applications in some fields, such as bioimaging, anti‐counterfeiting, and sensors. Nevertheless, phosphorescence efficiencies of metal‐free organic materials are low due to weak spin–orbit coupling and vigorous nonradiative transitions under ambient conditions. Here a chemical strategy to improve phosphorescence efficiency with intermolecular π‐type halogen bonding construction via isomerism is presented. X‐ray single crystal analysis reveals that different halogen bonding is formed among p‐BrTCz, m‐BrTCz, and o‐BrTCz crystals. Phosphorescence efficiency of m‐BrTCz in solid can reach 13.0%, seven times of o‐BrTCz in solid owing to effective π‐type halogen bonding, which is further confirmed by theoretical calculations. However, ultralong phosphorescence lifetimes are little affected, 155, 120, and 156 ms for p‐BrTCz, m‐BrTCz, and o‐BrTCz in the solid state, respectively. Furthermore, a simple pattern for data encryption and decryption is first demonstrated under sunlight. This result will provide an approach for improving the phosphorescent efficiency of metal‐free organic phosphors with ultralong luminescence. 相似文献
7.
Yali Qiao Mohammed Sayful Islam Kuo Han Eric Leonhardt Jiuyang Zhang Qing Wang Harry J. Ploehn Chuanbing Tang 《Advanced functional materials》2013,23(45):5638-5646
The discovery of nanodipolar π‐conjugated oligomer‐containing polymers as high performance nanodielectric materials with high permittivity and low dielectric loss over a wide range of frequency (100 Hz–4 MHz) is reported. Terthiophene‐containing methacrylate polymers are synthesized by reversible addition fragmentation transfer (RAFT) polymerization. Both X‐ray and thermal studies indicate the formation of small crystalline domains of terthiophene side chains dispersed in amorphous matrix. The highly polarizable and fast‐responsive nanodipoles from the nanoscale crystalline domains (<2 nm) are believed to dictate the performance. These polymers uniquely satisfy nanodipole architectures conjectured two decades ago to guide the design of high performance nanodielectric materials. This unprecedented approach can be generalized to a variety of π‐conjugated oligomer‐containing polymers for the development of high energy density capacitor materials. 相似文献
8.
N. Drolet J.‐F. Morin N. Leclerc S. Wakim Y. Tao M. Leclerc 《Advanced functional materials》2005,15(10):1671-1682
We have fabricated organic field‐effect transistors based on thin films of 2,7‐carbazole oligomeric semiconductors 1,4‐bis(vinylene‐(N‐hexyl‐2‐carbazole))phenylene (CPC), 1,4‐bis(vinylene‐(N′‐methyl‐7′‐hexyl‐2′‐carbazole))benzene (RCPCR), N‐hexyl‐2,7‐bis(vinylene‐(N‐hexyl‐2‐carbazole))carbazole (CCC), and N‐methyl‐2,7‐bis(vinylene‐(7‐hexyl‐N‐methyl‐2‐carbazole))carbazole (RCCCR). The organic semiconductors are deposited by thermal evaporation on bare and chemically modified silicon dioxide surfaces (SiO2/Si) held at different temperatures varying from 25 to 200 °C during deposition. The resulting thin films have been characterized using UV‐vis and Fourier‐transform infrared spectroscopies, scanning electron microscopy, and X‐ray diffraction, and the observed top‐contact transistor performances have been correlated with thin‐film properties. We found that these new π‐conjugated oligomers can form highly ordered structures and reach high hole mobilities. Devices using CPC as the active semiconductor have exhibited mobilities as high as 0.3 cm2 V–1 s–1 with on/off current ratios of up to 107. These features make CPC and 2,7‐carbazolenevinylene‐based oligomers attractive candidates for device applications. 相似文献
9.
Yan Zhao Zhiguang Xu Haitao Niu Xungai Wang Tong Lin 《Advanced functional materials》2015,25(3):437-444
Liquid marbles exhibit great potential for use as miniature labs for small‐scale laboratory operations, such as experiment and measurement. While important progress has been made recently in exploring their applications as microreactions, “on‐line” measurement of the components inside the liquid still remains a challenge. Herein, it is demonstrated that “on‐line” detection can be realized on magnetic liquid marbles by taking advantage of their unique magnetic opening feature. By partially opening the particle shell, electrochemical measurement is carried out with a miniaturized three‐electrode probe and the application of this technique for quantitative measurement of dopamine is demonstrated. Fully opened magnetic liquid marble makes it feasible to detect the optical absorbance of the liquid in a transmission mode. With this optical method, a glucose assay is demonstrated. Moreover, when magnetic particle shell contains low melting point material, e.g., wax, the liquid marble shows a unique encapsulation ability to form a rigid shell after heating, which facilitates the storage of the non‐volatile ingredients. These unique features, together with the versatile use as microreactors, enable magnetic liquid marbles to function as a miniature lab (or called “lab in a droplet”), which may find applications in clinical diagnostics, biotechnology, chemical synthesis, and analytical chemistry. 相似文献
10.
Simultaneous Edge‐on to Face‐on Reorientation and 1D Alignment of Small π‐Conjugated Molecules Using Room‐Temperature Mechanical Rubbing
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Jean‐Charles Ribierre Toshihiko Tanaka Li Zhao Yuki Yokota Shinya Matsumoto Daisuke Hashizume Kazuto Takaishi Tsuyoshi Muto Benoît Heinrich Stéphane Méry Fabrice Mathevet Toshinori Matsushima Masanobu Uchiyama Chihaya Adachi Tetsuya Aoyama 《Advanced functional materials》2018,28(19)
In this study, room‐temperature mechanical rubbing is used to control the 3D orientation of small π‐conjugated molecular systems in solution‐processed polycrystalline thin films without using any alignment substrate. High absorption dichroic ratio and significant anisotropy in charge carrier mobilities (up to 130) measured in transistor configuration are obtained in rubbed organic films based on the ambipolar quinoidal quaterthiophene (QQT(CN)4). Moreover, a solvent vapor annealing treatment of the rubbed film is found to improve the optical and charge transport anisotropy due to an increased crystallinity. X‐ray diffraction and atomic force microscopy measurements demonstrate that rubbing does not only lead to an excellent 1D orientation of the QQT(CN)4 molecules over large areas but also modifies the orientation of the crystals, moving molecules from an edge‐on to a face‐on configuration. The reasons why a mechanical alignment technique can be used at room temperature for such a polycrystalline film are rationalized, by the plastic characteristics of the QQT(CN)4 layer and the role of the flexible alkyl side chains in the molecular packing. This nearly complete conversion from edge‐on to face‐on orientation by mechanical treatment in polycrystalline small‐molecule‐based thin films opens perspectives in terms of fundamental research and practical applications in organic optoelectronics. 相似文献
11.
G. Li Y. Yao H. Yang V. Shrotriya G. Yang Y. Yang 《Advanced functional materials》2007,17(10):1636-1644
The self‐organization of the polymer in solar cells based on regioregular poly(3‐hexylthiophene) (RR‐P3HT):[6,6]‐phenyl C61‐butyric acid methyl ester (PCBM) is studied systematically as a function of the spin‐coating time ts (varied from 20–80 s), which controls the solvent annealing time ta, the time taken by the solvent to dry after the spin‐coating process. These blend films are characterized by photoluminescence spectroscopy, UV‐vis absorption spectroscopy, atomic force microscopy, and grazing incidence X‐ray diffraction (GIXRD) measurements. The results indicate that the π‐conjugated structure of RR‐P3HT in the films is optimally developed when ta is greater than 1 min (ts ~ 50 s). For t s < 50 s, both the short‐circuit current (JSC) and the power conversion efficiency (PCE) of the corresponding polymer solar cells show a plateau region, whereas for 50 < ts < 55 s, the JSC and PCE values are significantly decreased, suggesting that there is a major change in the ordering of the polymer in this time window. The PCE decreases from 3.6 % for a film with a highly ordered π‐conjugated structure of RR‐P3HT to 1.2 % for a less‐ordered film. GIXRD results confirm the change in the ordering of the polymer. In particular, the incident photon‐to‐electron conversion efficiency spectrum of the less‐ordered solar cell shows a clear loss in both the overall magnitude and the long‐wavelength response. The solvent annealing effect is also studied for devices with different concentrations of PCBM (PCBM concentrations ranging from 25 to 67 wt %). Under “solvent annealing” conditions, the polymer is seen to be ordered even at 67 wt % PCBM loading. The open‐circuit voltage (VOC) is also affected by the ordering of the polymer and the PCBM loading in the active layer. 相似文献
12.
Ying Liu Ying Wang Weiping Wu Yunqi Liu Hongxia Xi Limin Wang Wenfeng Qiu Kun Lu Chunyan Du Gui Yu 《Advanced functional materials》2009,19(5):772-778
The synthesis, characterization, and field‐effect transistor (FET) properties of a new class of thieno[3,2‐b]thieno[2′,3′:4,5]thieno[2,3‐d]thiophene derivatives are described. The optical spectra of their films show the presence of stronger interactions between molecules in the solid state. Thermal analyses reveal that the three materials are thermally stable and have no phase transitions at low temperature. The crystal structures are determined, and show π‐stacked structures and intermolecular S···S contacts. These organic materials exhibit p‐type FET behavior with hole mobilities as high as 0.14 cm2 V?1 s?1 and an on/off current ratio of 106. These results indicate that thieno[3,2‐b]thieno [2′,3′:4,5]thieno[2,3‐d]thiophene, as a linear π‐conjugated system, is an effective building block for developing high‐performance organic semiconductors. 相似文献
13.
Enhancement in Organic Photovoltaic Efficiency through the Synergistic Interplay of Molecular Donor Hydrogen Bonding and π‐Stacking
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Nathan T. Shewmon Davita L. Watkins Johan F. Galindo Raghida Bou Zerdan Jihua Chen Jong Keum Adrian E. Roitberg Jiangeng Xue Ronald K. Castellano 《Advanced functional materials》2015,25(32):5166-5177
For organic photovoltaic (OPV) cells based on the bulk heterojunction (BHJ) structure, it remains challenging to rationally control the degree of phase separation and percolation within blends of donors and acceptors to secure optimal charge separation and transport. Reported is a bottom‐up, supramolecular approach to BHJ OPVs wherein tailored hydrogen bonding (H‐bonding) interactions between π‐conjugated electron donor molecules encourage formation of vertically aligned donor π‐stacks while simultaneously suppressing lateral aggregation; the programmed arrangement facilitates fine mixing with fullerene acceptors and efficient charge transport. The approach is illustrated using conventional linear or branched quaterthiophene donor chromophores outfitted with terminal functional groups that are either capable or incapable of self‐complementary H‐bonding. When applied to OPVs, the H‐bond capable donors yield a twofold enhancement in power conversion efficiency relative to the comparator systems, with a maximum external quantum efficiency of 64%. H‐bond promoted assembly results in redshifted absorption (in neat films and donor:C60 blends) and enhanced charge collection efficiency despite disparate donor chromophore structure. Both features positively impact photocurrent and fill factor in OPV devices. Film structural characterization by atomic force microscopy, transmission electron microscopy, and grazing incidence wide angle X‐ray scattering reveals a synergistic interplay of lateral H‐bonding interactions and vertical π‐stacking for directing the favorable morphology of the BHJ. 相似文献
14.
Monodisperse stearic acid coated titanium dioxide nanoparticles (< 3 nm) have been prepared and characterized. The nanoparticles are soluble in common apolar organic solvents and bind to carboxylic acid functionalized π‐conjugated oligomers to form heterosupramolecular assemblies. When [2,2′;5′,2″]terthiophene‐5‐carboxylic acid was coupled to the nanoparticles, the fluorescence of the terthiophene moiety of the heterosupramolecular system was completely quenched due to a photoinduced electron transfer from terthiophene to titanium dioxide. Time‐resolved fluorescence and Stern–Volmer analysis revealed that the quenching is predominantly static rather than dynamic and occurs in apolar solvents. 相似文献
15.
Moyuan Cao Kan Li Zhichao Dong Cunming Yu Shuai Yang Cheng Song Kesong Liu Lei Jiang 《Advanced functional materials》2015,25(26):4114-4119
Antigravity transportation of water, which is often observed in nature, is becoming a vital demand for advanced devices and new technology. Many studies have been devoted to the motion of a single droplet on a horizontal or inclined substrate under specific assistance. However, the self‐propelled water motion, especially continuous antigravity water delivery, still remains a considerable challenge. Here, a novel self‐ascending phenomenon driven only by the surface energy release of water droplets is found, and a superhydrophobic mesh to pump water up to a height of centimeter scale is designed. An integrated antigravity transportation system is also demonstrated to continuously and spontaneously pump water droplets without additional driving forces. The present novel finding and integrated devices should serve as a source of inspiration for the design of advanced materials and for the development of new technology with exciting applications in microfluidics, microdetectors, and intelligent systems. 相似文献
16.
“Chemical Weathering” Exfoliation of Atom‐Thick Transition Metal Dichalcogenides and Their Ultrafast Saturable Absorption Properties
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Gang Zhao Shuo Han Aizhu Wang Yongzhong Wu Mingwen Zhao Zhengping Wang Xiaopeng Hao 《Advanced functional materials》2015,25(33):5292-5299
2D transition metal dichalcogenides are attracting increased attention because of their excellent electronic and optical properties. Inspired by the natural weathering exfoliation of seaside rocks, a “chemical weathering” concept for fabricating atom‐thick 2D materials from their bulk counterparts is proposed. It is experimentally demonstrated that chemical weathering‐assisted exfoliation mechanism is a simple and efficient method of preparing atom‐thick MoS2 and WS2 monolayers. These monolayers are difficult to prepare using other approaches. Interestingly, the as‐prepared MoS2 and WS2 monolayers exhibit excellent saturable absorption and mode‐locking properties in all‐solid‐state lasers because of intermediate states resulting from S‐vacancy defects. The obtained passively Q‐switched laser operation with 60 ns pulse width and ultrafast mode locking with 8.6 ps pulse width are promising for all‐solid‐state laser application. 相似文献
17.
Jia Guan Wei Chen Yafei Li Guangtao Yu Zhiming Shi Xuri Huang Chiachung Sun Zhongfang Chen 《Advanced functional materials》2013,23(12):1507-1518
Under first‐principles computations, a simple strategy is identified to modulate the electronic and magnetic properties of zigzag graphene nanoribbons (zGNRs). This strategy takes advantage of the effect of the floating dipole field attached to zGNRs via π–π interactions. This dipole field is induced by the acceptor/donor functional groups, which decorate the ladder‐structure polydiacetylene derivatives with an excellent delocalized π‐conjugated backbone. By tuning the acceptor/donor groups, –C≡C– number, and zGNR width, greatly enriched electronic and magnetic properties, e.g., spin gapless semiconducting, half‐metallic, and metallic behaviors, with the antiferromagnetic?ferromagnetic conversion can be achieved in zGNRs with perfect, 57‐reconstructed, and partially hydrogenated edge patterns. 相似文献
18.
Kazi M. Alam Abhay P. Singh Ryan Starko‐Bowes Srikrishna C. Bodepudi Sandipan Pramanik 《Advanced functional materials》2012,22(15):3298-3306
π‐conjugated molecular organics such as rubrene, Alq3, fullerene, and PCBM have been used extensively over the last few decades in numerous organic electronic devices, including solar cells, thin‐film transistors, and large‐area, low‐cost flexible displays. Rubrene and Alq3, have emerged as promising platforms for spin‐based classical and quantum information processing, which has triggered significant research activity in the relatively new area of organic spintronics. Synthesis of these materials in a nanowire geometry, with feature sizes in the sub‐100 nm regime, is desirable as it often enhances device performance and is essential for development of high‐density molecular electronic devices. However, fabrication techniques that meet this stringent size constraint are still largely underdeveloped. Here, a novel, versatile, and reagentless method that enables growth of nanowire arrays of the above‐mentioned organics in the cylindrical nanopores of anodic aluminum oxide (AAO) templates is demonstrated. This method 1) allows synthesis of high‐density organic nanowire arrays on arbitrary substrates, 2) provides electrical access to the nanowire arrays, 3) offers tunability of the array geometry in a range overlapping with the relevant physical length scales of many organic devices, and 4) can potentially be extended to synthesize axially and radially heterostructured organic nanowires. Thus prepared nanowires are characterized extensively with an aim to identify their potential applications in diverse areas such as organic optoelectronics, photovoltaics, molecular nanoelectronics, and spintronics. 相似文献
19.
Molecular Consideration for Small Molecular Acceptors Based on Ladder‐Type Dipyran: Influences of O‐Functionalization and π‐Bridges
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Lisi Yang Miao Li Jinsheng Song Yuanyuan Zhou Zhishan Bo Hua Wang 《Advanced functional materials》2018,28(8)
Molecular engineering of nonfullerene acceptors (NFAs) plays a vital role in the development of organic photovoltaics. Oxygen as an electron donating atom is incorporated into the NFA system as alkoxyl forms at central, terminal, or central conjugated moieties due to the tunability at structural conformation, solubility, electron donating ability, absorption, energy levels, etc. In this work, a novel dipyran‐based ladder‐type building block ( Ph‐DTDP ), which possesses two oxygen atoms in the conjugated skeleton, is designed and facilely synthesized. It is applied as the donor core for the acceptor–donor–acceptor‐type NFA design and such functionalized‐O efficiently enhances the electron donating ability, lowers the band gap, redshifts and extends the absorption spectra. In addition, the π‐bridge effects are considered as well. Photovoltaic performances are systematically investigated and a high power conversion efficiency of 9.21% can be afforded with an energy loss of 0.57 eV. Meanwhile, the morphologies as well as the carrier mobilities of the blend films are studied to assist further understanding of the structure–property relationships. Overall, the study in this work provides a new promising ladder‐type dipyran building block and brings in a novel way to use oxygen in NFA molecular structure design. 相似文献
20.
Q.‐D. Liu J. Lu J. Ding M. Day Y. Tao P. Barrios J. Stupak K. Chan J. Li Y. Chi 《Advanced functional materials》2007,17(6):1028-1036
Four monodisperse starburst oligomers bearing a 4,4′,4″‐tris(carbazol‐9‐yl)‐triphenylamine (TCTA) core and six oligofluorene arms are synthesized and characterized. The lengths of oligofluorene arms vary from one to four fluorene units, giving the starburst oligomers molecular weights ranging from 3072 to 10 068 Da (1 Da = 1.66 × 10–27 kg). All of the starburst oligomers have good film‐forming capabilities, and display bright, deep‐blue fluorescence (λmax = 395–416 nm) both in solution and in the solid state, with the quantum efficiencies of the films (ΦPL) varying between 27 and 88 %. Electrochemical studies demonstrate that these materials have large energy gaps, and are stable for both p‐doping and n‐doping processes. Electroluminescent devices are successfully fabricated using these materials as hole‐transporting emitters, and emit deep‐blue light. Devices with luminance values up to 1025 cd m–2 at 11 V and luminous efficiencies of 0.47 cd A–1 at 100 cd m–2 have been produced, which translates to an external quantum efficiency of 1.4 %. In addition, these large‐energy‐gap starburst oligomers are good host materials for red electrophosphorescence. The luminance of the red electrophosphorescent devices is as high as 4452 cd m–2, with a luminous efficiency of 4.31 cd A–1 at 15 mA cm–2: This value is much higher than those obtained from the commonly used hole‐transporting materials, such as poly(vinyl carbazole) (PVK) (1.10 cd A–1 at 16 mA cm–2). 相似文献