Heptacene: Synthesis and Its Hole-Transfer Property in Stable Thin Films.

Heptacene (1) has been produced via a monoketone precursor, 2, which was prepared from 1,2,4,5-tetrabromobenzene in nine steps in a total yield of 10 %. Compound 2 was converted to 1 quantitatively by heating at 202 °C. Heptacene exhibited high thermal stability in the solid state without any observable change over two months. To investigate the potential value of 1 as a material for p-type organic field-effect transistors (OFETs), top-contact OFET devices were fabricated by vacuum deposition of 1 onto a hexamethyldisilazane (HMDS)/SiO2 /Si substrate. The best hole mobility performance was 2.2 cm2  V-1 s-1 . This is the first report of stable heptacene being used in an effective device and examined for its charge carrier properties.

High-Performance Organic Dyes with Electron-Deficient Quinoxalinoid Heterocycles for Dye-Sensitized Solar Cells under One Sun and Indoor Light.

A series of Y-shaped sensitizers incorporating quinoxaline or quinoxalinoid moieties were prepared and applied in dye-sensitized solar cells (DSSCs). By the introduction of quinoxalinoid functionalities, the absorption extinction coefficients could be enhanced. The molecular structures were modified by introducing an extra acceptor group (A) between a donor (D) and a π-bridge (D-A-π-A) and also by incorporating electron-donating substituents at various positions of the quinoxalinoid moiety. Some of the dyes and mixtures thereof were found to exhibit good light-harvesting efficiencies under both sunlight and indoor light, with efficiencies up to 7.92 % under one sun (AM 1.5G). When operated under indoor light, the efficiency could be boosted to 27.76, 28.74, and 30.45 % under 600, 1000, 2500 lux illumination, respectively. The best performance could be ascribed partly to an improved dye coverage on the TiO2 surface.

Synthesis and physical properties of brominated hexacene and hole-transfer properties of thin-film transistors.

A halide-substituted higher acene, 2-bromohexacene, and its precursor with a carbonyl bridge moiety were synthesized. The precursor was synthesized through 7 steps in a total yield of 2.5%. The structure of precursor and thermally converted 2-bromohexacene were characterized by solid state NMR, IR, and absorption spectra, as well as by DFT computation analysis. It exhibited high stability in the solid state over 3 months, therefore can be utilized in the fabrication of opto-electronic devices. The organic thin-film transistors (OFETs) were fabricated by using 2-bromohexacene and parent hexacene through vaccum deposition method. The best film mobility of 2-bromohexacene was observed at 0.83 cm2 V-1 s-1 with an on/off ratio of 5.0 × 104 and a threshold of -52 V, while the best film mobility of hexacene was observed at 0.076 cm2 V-1 s-1 with an on/off ratio of 2.4 × 102 and a threshold of -21 V. AFM measurement of 2-bromohexacene showed smooth film formation. The averaged mobility of 2-bromohexacene is 8 fold higher than the non-substituted hexacene.

Nitrogen-Free Bifunctional Bianthryl Leads to Stable White-Light Emission in Bilayer and Multilayer OLED Devices.

White organic light-emitting diodes (WOLEDs) are at the center stage of OLED research today because of their advantages in replacing the high energy-consuming lighting technologies in vogue for a long time. New materials that emit white light in simple devices are much sought after. We have developed two novel electroluminescent materials, referred to as BABZF and BATOMe, based on a twisted bianthryl core, which are brilliantly fluorescent, thermally highly stable with high T d and T g, and exhibit reversible redox property. Although inherently blue emissive, BABZF leads to white-light emission (CIE ≈ 0.28, 0.33) with a moderate power efficiency of 2.24 lm/W and a very high luminance of 15 600 cd/m2 in the fabricated multilayer nondoped OLED device. This device exhibited excellent color stability over a range of applied potential. Remarkably, similar white-light emission was captured even from a double-layer device, attesting to the innate hole-transporting ability of BABZF despite it being non-nitrogenous, that is, lacking any traditional hole-transporting di-/triarylamino group(s). Similar studies with BATOMe led to inferior device performance results, thereby underscoring the importance of dibenzofuryl groups in BABZF. Experimental as well as theoretical studies suggest the possibility of emission from multiple species involving BABZF and its exciplex and electroplex in the devices. The serendipitously observed white-light emission from a double-layer device fabricated with an unconventional hole-transporting material (HTM) opens up new avenues to create new non-nitrogenous HTMs that may lead to more efficient white-light emission in simple double-layer devices.

Performance Characterization of Dye-Sensitized Photovoltaics under Indoor Lighting.

Indoor utilization of emerging photovoltaics is promising; however, efficiency characterization under room lighting is challenging. We report the first round-robin interlaboratory study of performance measurement for dye-sensitized photovoltaics (cells and mini-modules) and one silicon solar cell under a fluorescent dim light. Among 15 research groups, the relative deviation in power conversion efficiency (PCE) of the samples reaches an unprecedented 152%. On the basis of the comprehensive results, the gap between photometry and radiometry measurements and the response of devices to the dim illumination are identified as critical obstacles to the correct PCE. Therefore, we use an illuminometer as a prime standard with a spectroradiometer to quantify the intensity of indoor lighting and adopt the reverse-biased current-voltage (I-V) characteristics as an indicator to qualify the I-V sampling time for dye-sensitized photovoltaics. The recommendations can brighten the prospects of emerging photovoltaics for indoor applications.

Helicenes as All-in-One Organic Materials for Application in OLEDs: Synthesis and Diverse Applications of Carbo- and Aza[5]helical Diamines.

A set of eight helical diamines were designed and synthesized to demonstrate their relevance as all-in-one materials for multifarious applications in organic light-emitting diodes (OLEDs), that is, as hole-transporting materials (HTMs), EMs, bifunctional hole transporting + emissive materials, and host materials. Azahelical diamines function very well as HTMs. Indeed, with high Tg values (127-214 °C), they are superior alternatives to popular N,N'-di(1-naphthyl)-N,N'-diphenyl-(1,1'-biphenyl)-4,4'-diamine (NPB). All the helical diamines exhibit emissive properties when employed in nondoped as well as doped devices, the performance characteristics being superior in the latter. One of the carbohelical diamines (CHTPA) serves the dual function of hole transport as well as emission in simple double-layer devices; the efficiencies observed were better by quite some margin than those of other emissive helicenes reported. The twisting endows helical diamines with significantly high triplet energies such that they also function as host materials for red and green phosphors, that is, [Ir(btp)2 acac] (btp=2-(2'-benzothienyl)pyridine; acac=acetylacetonate) and [Ir(ppy)3 ] (ppy=2-phenylpyridine), respectively. The results of device fabrications demonstrate how helicity/ helical scaffold may be diligently exploited to create molecular systems for maneuvering diverse applications in OLEDs.

Hole-Transporting Materials Based on Twisted Bimesitylenes for Stable Perovskite Solar Cells with High Efficiency.

A new class of hole-transport materials (HTMs) based on the bimesitylene core designed for mesoporous perovskite solar cells is introduced. Devices fabricated using two of these derivatives yield higher open-circuit voltage values than the commonly used spiro-OMeTAD. Power conversion efficiency (PCE) values of up to 12.11% are obtained in perovskite-based devices using these new HTMs. The stability of the device made using the highest performing HTM (P1) is improved compared with spiro-OMeTAD as evidenced through long-term stability tests over 1000 h.

Benzophenones as Generic Host Materials for Phosphorescent Organic Light-Emitting Diodes.

Despite the fact that benzophenone has traditionally served as a prototype molecular system for establishing triplet state chemistry, materials based on molecular systems containing the benzophenone moiety as an integral part have not been exploited as generic host materials in phosphorescent organic light-emitting diodes (PhOLEDs). We have designed and synthesized three novel host materials, i.e., BP2-BP4, which contain benzophenone as the active triplet sensitizing molecular component. It is shown that their high band gap (3.91-3.93 eV) as well as triplet energies (2.95-2.97 eV) permit their applicability as universal host materials for blue, green, yellow, and red phosphors. While they serve reasonably well for all types of dopants, excellent performance characteristics observed for yellow and green devices are indeed the hallmark of benzophenone-based host materials. For example, maximum external quantum efficiencies of the order of 19.2% and 17.0% were obtained from the devices fabricated with yellow and green phosphors using BP2 as the host material. White light emission, albeit with rather poor efficiencies, has been demonstrated as a proof-of-concept by fabrication of co-doped and stacked devices with blue and yellow phosphors using BP2 as the host material.

Amorphous host materials based on Tröger's base scaffold for application in phosphorescent organic light-emitting diodes.

Tröger's bases (TBs) functionalized with carbazoles (TB-Czs) and phosphine oxides (TB-POs) were designed and synthesized as host materials for application in phosphorescent organic light-emitting diodes. The TB scaffold is shown to impart thermal stability with high Tg values (171-211 °C) as well as high triplet energies in the range of 2.9-3.0 eV. With a limited experimentation of the devices, it is shown that the TBs doped with a green phosphor, namely, Ir(ppy)3, permit impressive external efficiencies on the order of ca. 16% with a high brightness of ca. 3000-4000 cd/m2. Better device performance results are demonstrated by a small structural manipulation of the TB scaffold involving substitution of methyl groups in the core scaffold.

Acenes generated from precursors and their semiconducting properties.

Acenes are a class of aromatic hydrocarbons composed of linearly fused benzene rings. Noteworthy features of these molecules include their extended flat structure and the narrow gap between the HOMO and LUMO energy levels. However, the preparation of larger acenes, those that are larger than pentacene, has been challenging. These molecules are relatively unstable and have low solubility in typical solvents. Recently researchers have developed a new synthesis route for higher acenes using stable and soluble "precursors," which generate these structures on demand by either heating or irradiation of light. Using this method, nonsubstituted hexacene, heptacene, octacene, and nonacene were successfully prepared. In this Account, we summarize the preparation of nonsubstituted acenes from corresponding precursors, describe their physical properties, and discuss potential applications including potential usage in organic semiconductor devices. We first introduced the concept of using a precursor in the work with pentacene. Overall, we divide this methodology into two categories: masking pentacene itself with a dienophile to form a cycloadduct and the construction of higher acenes through conventional synthetic procedures. For the first category, a diverse array of dienophiles could be chosen, depending on the processing needs, especially for use in field-effect transistors (FETs). For the second category, researchers synthesized the pentacene precursor molecules using a multistep procedure. Upon proper activation, these molecules expel small fragments to generate pentacene readily. This strategy enabled the production of pentacene andunprepared higher acenes ranging from hexacene to nonacene. This new method provides a way to unravel the fascinating chemistry of higher acenes.

A soluble precursor of hexacene and its application in thin film transistors.

A soluble precursor of hexacene is prepared from a cycloaddition of hexacene and diethyl ketomalonate in high yield. It can be used to make hexacene thin-films through spin-coating for the fabrication of organic field effect transistors.

Reaction-based colorimetric and ratiometric fluorescence sensor for detection of cyanide in aqueous media.

A stilbene-based compound (1) has been prepared and was highly selective for the detection of cyanide anion in aqueous media even in the presence of other anions, such as F(-), Cl(-), Br(-), I(-), ClO(4)(-), H(2)PO(4)(-), HSO(4)(-), NO(3)(-), and CH(3)CO(2)(-). A noticeable change in the color of the solution, along with a prominent fluorescence enhancement, was observed upon the addition of cyanide. The color change was observed upon the nucleophilic addition of the cyanide anion to the electron-deficient cyanoacrylate group of 1. The spectral changes induced by the reaction were analyzed by comparison with two model compounds, such as compound 2 with dimethyl substituents and compound 3 without a cyanoacrylate group. An intramolecular charge-transfer (ICT) mechanism played a key role in the sensing properties, and the mechanism was supported by DFT/TDDFT calculations.

The synthesis, crystal structure and charge-transport properties of hexacene.

Acenes can be thought of as one-dimensional strips of graphene and they have the potential to be used in the next generation of electronic devices. However, because acenes larger than pentacene have been found to be unstable, it was generally accepted that they would not be particularly useful materials under normal conditions. Here, we show that, by using a physical vapour-transport method, platelet-shaped crystals of hexacene can be prepared from a monoketone precursor. These crystals are stable in the dark for a long period of time under ambient conditions. In the crystal, the molecules are arranged in herringbone arrays, quite similar to that observed for pentacene. A field-effect transistor made using a single crystal of hexacene displayed a hole mobility significantly higher than that of pentacene. This result suggests that it might be instructive to further explore the potential of other higher acenes.

Solution processed high performance pentacene thin-film transistors.

High performance thin-film transistors were fabricated using a new precursor of pentacene through a multiple spin-heat procedure. High quality pentacene thin films can be prepared by this method and hence a FET device can be made in a top-contact configuration. The device exhibited a remarkable field-effect mobility of 0.38 cm(2) V(-1) s(-1) with an on/off ratio of 10(6).

High-performance organic materials for dye-sensitized solar cells: triarylene-linked dyads with a 4-tert-butylphenylamine donor.

A series of organic dyes were prepared that displayed remarkable solar-to-energy conversion efficiencies in dye-sensitized solar cells (DSSCs). These dyes are composed of a 4-tert-butylphenylamine donor group (D), a cyanoacrylic-acid acceptor group (A), and a phenylene-thiophene-phenylene (PSP) spacer group, forming a D-π-A system. A dye containing a bulky tert-butylphenylene-substituted carbazole (CB) donor group showed the highest performance, with an overall conversion efficiency of 6.70%. The performance of the device was correlated to the structural features of the donor groups; that is, the presence of a tert-butyl group can not only enhance the electron-donating ability of the donor, but can also suppress intermolecular aggregation. A typical device made with the CB-PSP dye afforded a maximum photon-to-current conversion efficiency (IPCE) of 80% in the region 400-480 nm, a short-circuit photocurrent density J(sc) =14.63 mA cm(-2), an open-circuit photovoltage V(oc) =0.685 V, and a fill factor FF=0.67. When chenodeoxycholic acid (CDCA) was used as a co-absorbent, the open-circuit voltage of CB-PSP was elevated significantly, yet the overall performance decreased by 16-18%. This result indicated that the presence of 4-tert-butylphenyl substituents can effectively inhibit self-aggregation, even without CDCA.

[2.2]Paracyclophane as a bridging unit in the design of organic dyes for sensitized solar cells.

Organic dyes consisting of a [2.2]paracyclophane unit along the main chromophore are examined for their application in sensitized solar cells. These materials exhibit considerably high values of open-circuit voltage (V(oc)) ranging 0.69-0.72 V, and an overall efficiency up to 3.8%.

Nondoped pure-blue OLEDs based on amorphous phenylenevinylene-functionalized twisted bimesitylenes.

The twisted bimesitylene scaffold hinders crystallization and imparts amorphous nature to the oligophenylenevinylenes (OPVs) generated by 2- and/or 4-fold functionalization. The resultant phenylenevinylenes 1-5 with unique molecular topology exhibit excellent thermal and solid-state luminescence properties. The amorphous nature permits their application as pure-blue emissive materials in OLEDs. Under nondoped conditions, the device performances observed surpass those for analogous and simple oligophenylenevinylenes known so far; for example, the device based on OPV 2 as an emitting material and structurally analogous Bim-DPAB as a hole-transporting material yields pure-blue electroluminescence with an external quantum efficiency of ca. 4.70% at 20 mA/cm(2), which is higher than those reported for nondoped pure-blue OPV emitters.

Hydroxynaphthyridine-derived group III metal chelates: wide band gap and deep blue analogues of green Alq3 (tris(8-hydroxyquinolate)aluminum) and their versatile applications for organic light-emitting diodes.

A series of group III metal chelates have been synthesized and characterized for the versatile application of organic light-emitting diodes (OLEDs). These metal chelates are based on 4-hydroxy-1,5-naphthyridine derivates as chelating ligands, and they are the blue version analogues of well-known green fluorophore Alq(3) (tris(8-hydroxyquinolinato)aluminum). These chelating ligands and their metal chelates were easily prepared with an improved synthetic method, and they were facially purified by a sublimation process, which enables the materials to be readily available in bulk quantity and facilitates their usage in OLEDs. Unlike most currently known blue analogues of Alq(3) or other deep blue materials, metal chelates of 4-hydroxy-1,5-naphthyridine exhibit very deep blue fluorescence, wide band gap energy, high charge carrier mobility, and superior thermal stability. Using a vacuum-thermal-deposition process in the fabrication of OLEDs, we have successfully demonstrated that the application of these unusual hydroxynaphthyridine metal chelates can be very versatile and effective. First, we have solved or alleviated the problem of exciplex formation that took place between the hole-transporting layer and hydroxynaphthyridine metal chelates, of which OLED application has been prohibited to date. Second, these deep blue materials can play various roles in OLED application. They can be a highly efficient nondopant deep blue emitter: maximum external quantum efficiency eta(ext) of 4.2%; Commision Internationale de L'Eclairage x, y coordinates, CIE(x,y) = 0.15, 0.07. Compared with Alq(3), Bebq(2) (beryllium bis(benzoquinolin-10-olate)), or TPBI (2,2',2''-(1,3,5-phenylene)tris(1-phenyl-1H-benzimidazole), they are a good electron-transporting material: low HOMO energy level of 6.4-6.5 eV and not so high LUMO energy level of 3.0-3.3 eV. They can be ambipolar and possess a high electron mobility of 10(-4) cm(2)/V s at an electric field of 6.4 x 10(5) V/cm. They are a qualified wide band gap host material for efficient blue perylene (CIE(x,y) = 0.14, 0.17 and maximum eta(ext) 3.8%) or deep blue 9,10-diphenylanthracene (CIE(x,y) = 0.15, 0.06 and maximum eta(ext) 2.8%). For solid state lighting application, they are desirable as a host material for yellow dopant (rubrene) in achieving high efficiency (eta(ext) 4.3% and eta(P) 8.7 lm/W at an electroluminance of 100 cd/m(2) or eta(ext) 3.9% and eta(P) 5.1 lm/W at an electroluminance of 1000 cd/m(2)) white electroluminescence (CIE(x,y) = 0.30, 0.35).