Cheuk-Lam Ho

Functional metallophosphors for effective charge carrier injection/transport: new robust OLED materials with emerging applications

Organic light-emitting diodes (OLEDs) show great promise of revolutionizing display technologies in the scientific community. One successful approach for improved device efficiency has been to maximize the electron-hole recombination using dopants that emit from the triplet excited state. In this context, heavy transition metal complexes have recently gained tremendous academic and industrial research interest for fabricating highly efficient phosphorescent OLEDs by taking advantage of the 1:3 exciton singlet/triplet ratio predicted by simple spin statistics. Traditional room-temperature phosphorescent dyes are monofunctional materials working only as light-emitting centres but other key issues including charge generation and transport remain to be addressed in the electroluminescence. This Feature Article highlights recent and current advances in developing new synthetic strategies for multifunctional organometallic phosphors, which integrate both luminescent and charge carrier injection/transport functions into the same molecules so that they perform most, if not all, of the necessary functional roles (viz. photoexcitation, charge injection and transport as well as recombination) for achieving high-efficiency devices. Considerable focus is placed on the design concepts towards the tuning capability of charge-transport characteristics and phosphorescence emission colour of this prominent class of metallophosphors. In particular, the latest research endeavor in accomplishing novel triplet emitters with enhanced charge injection/charge transport of both hole and electron carriers is criticially discussed, which can provide good implications regarding their possible routes for future research development in the field.

Organometallic Photovoltaics: A New and Versatile Approach for Harvesting Solar Energy Using Conjugated Polymetallaynes

Energy remains one of the worlds great challenges. Growing concerns about limited fossil fuel resources and the accumulation of CO(2) in the atmosphere from burning those fuels have stimulated tremendous academic and industrial interest. Researchers are focusing both on developing inexpensive renewable energy resources and on improving the technologies for energy conversion. Solar energy has the capacity to meet increasing global energy needs. Harvesting energy directly from sunlight using photovoltaic technology significantly reduces atmospheric emissions, avoiding the detrimental effects of these gases on the environment. Currently inorganic semiconductors dominate the solar cell production market, but these materials require high technology production and expensive materials, making electricity produced in this manner too costly to compete with conventional sources of electricity. Researchers have successfully fabricated efficient organic-based polymer solar cells (PSCs) as a lower cost alternative. Recently, metalated conjugated polymers have shown exceptional promise as donor materials in bulk-heterojunction solar cells and are emerging as viable alternatives to the all-organic congeners currently in use. Among these metalated conjugated polymers, soluble platinum(II)-containing poly(arylene ethynylene)s of variable bandgaps (∼1.4-3.0 eV) represent attractive candidates for a cost-effective, lightweight solar-energy conversion platform. This Account highlights and discusses the recent advances of this research frontier in organometallic photovoltaics. The emerging use of low-bandgap soluble platinum-acetylide polymers in PSCs offers a new and versatile strategy to capture sunlight for efficient solar power generation. Properties of these polyplatinynes--including their chemical structures, absorption coefficients, bandgaps, charge mobilities, accessibility of triplet excitons, molecular weights, and blend film morphologies--critically influence the device performance. Our group has developed a novel strategy that allows for tuning of the optical absorption and charge transport properties as well as the PSC efficiency of these metallopolyynes. The absorbance of these materials can also be tuned to traverse the near-visible and near-infrared spectral regions. Because of the diversity of transition metals available and chemical versatility of the central spacer unit, we anticipate that this class of materials could soon lead to exciting applications in next-generation PSCs and other electronic or photonic devices. Further research in this emerging field could spur new developments in the production of renewable energy.

White Polymer Light‐Emitting Devices for Solid‐State Lighting: Materials, Devices, and Recent Progress

White polymer light-emitting devices (WPLEDs) have become a field of immense interest in both scientific and industrial communities. They have unique advantages such as low cost, light weight, ease of device fabrication, and large area manufacturing. Applications of WPLEDs for solid-state lighting are of special interest because about 20% of the generated electricity on the earth is consumed by lighting. To date, incandescent light bulbs (with a typical power efficiency of 12-17 lm W(-1) ) and fluorescent lamps (about 40-70 lm W(-1) ) are the most widely used lighting sources. However, incandescent light bulbs convert 90% of their consumed power into heat while fluorescent lamps contain a small but significant amount of toxic mercury in the tube, which complicates an environmentally friendly disposal. Remarkably, the device performances of WPLEDs have recently been demonstrated to be as efficient as those of fluorescent lamps. Here, we summarize the recent advances in WPLEDs with special attention paid to the design of novel luminescent dopants and device structures. Such advancements minimize the gap (for both efficiency and stability) from other lighting sources such as fluorescent lamps, light-emitting diodes based on inorganic semiconductors, and vacuum-deposited small-molecular devices, thus rendering WPLEDs equally competitive as these counterparts currently in use for illumination purposes.

High‐Efficiency Single Emissive Layer White Organic Light‐Emitting Diodes Based on Solution‐Processed Dendritic Host and New Orange‐Emitting Iridium Complex

An extremely high-efficiency solution-processed white organic light-emitting diode (WOLED) is successfully developed by simultaneously using an ideal dendritic host material and a novel efficient orange phosphorescent iridium complex. The optimized device exhibits forward-viewing efficiencies of 70.6 cd A(-1) , 26.0%, and 47.6 lm W(-1) at a luminance of 100 cd m(-2) , respectively, promising the low-cost solution-processed WOLEDs a bright future as the next generation of illumination sources.

Simultaneous optimization of charge-carrier balance and luminous efficacy in highly efficient white polymer light-emitting devices.

The use of white organic light-emitting devices (WOLEDs) for solid-state lighting applications is becoming increasingly attractive, [ 1 − 5 ] given that legislation in more countries is banning the use of ineffi cient incandescent lamps. Moreover, since fl uorescent lamps involve the use of mercury and its disposal represents a great challenge, many scientists have been working aggressively to make the replacement of the fl uorescent light sources by WOLEDs a reality. Indeed, the effi ciency of multilayer vacuum-evaporated WOLEDs based on small molecules has been greatly improved in the past several years [ 6 − 10 ] and has already exceeded that of fl uorescent lamps. [ 11 ] In contrast, despite many unique advantages, such as low-cost manufacturing using solution-processing techniques, easy processability over large-areas by spin-coating or ink-jet printing, compatibility with fl exible substrates, a relatively small amount of wasted material, and precise control of the doping level, the application of white polymer light-emitting diodes (WPLEDs) is still severely hindered by the relatively low device effi ciency. [ 3 , 12 − 16 ]

Metallophosphors of platinum with distinct main-group elements: a versatile approach towards color tuning and white-light emission with superior efficiency/color quality/brightness trade-offs

A new series of phosphorescent platinum(II) cyclometalated complexes with distinct electronic structures has been developed by simple tailoring of the phenyl ring of ppy (Hppy = 2-phenylpyridine) with various main-group moieties in [Pt(ppy-X)(acac)] (X = B(Mes)2, SiPh3, GePh3, NPh2, POPh2, OPh, SPh, SO2Ph substituted at the para position). Their distinctive electronic characters, resulting in improved hole-injection/hole-transporting or electron-injection/electron-transporting features, have confined/consumed the electrons in the emission layer of organic light-emitting diodes (OLEDs) to achieve good color purity and high efficiency of the devices. The maximum external quantum efficiency of 9.52%, luminance efficiency of 30.00 cd A−1 and power efficiency of 8.36 lm W−1 for the OLEDs with Pt-B (X = B(Mes)2) as the emitter, 8.50%, 29.74 cd A−1 and 19.73 lm W−1 for the device with Pt-N (X = NPh2), 7.92%, 22.06 cd A−1 and 13.64 lm W−1 for the device with Pt-PO (X = POPh2) as well as 8.35%, 19.59 cd A−1 and 7.83 lm W−1 for the device with Pt-SO2 (X = SO2Ph) can be obtained. By taking advantage of the unique electronic structures of the Pt-Ge (X = GePh3) and Pt-O (X = OPh) green emitters and the intrinsic property of blue-emitting hole-transport layer of 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (NPB), single-dopant white OLEDs (WOLEDs) can be developed. These simple WOLEDs emit white light of very high quality (CIE at (0.354, 0.360), CRI of ca. 97 and CCT at 4719 K) even at high brightness (>15000 cd m−2) and the present work represents significant progress to address the bottle-neck problem of WOLEDs for the efficiency/color quality/brightness trade-off optimization that is necessary for pure white light of great commercial value.

Small-molecular blue phosphorescent dyes for organic light-emitting devices

Organic light-emitting devices (OLEDs) are on the lips of most electronic manufacturers currently. With good progress made in terms of production cost, efficiency and color output, OLEDs have found more applications recently as compared to those some years ago. Because of the possibility of obtaining long-lasting, durable and energy-efficient OLEDs, researchers devote much time and effort towards the improvement of OLED technology and development of advanced OLED products. Blue light-emitting materials, especially blue phosphorescent materials, are indispensable for full-color displays and white OLED lighting. Compared with green and red light-emitting materials and devices, the blue-emitting counterparts show a relatively inferior performance in terms of color purity, luminescence efficiency and device durability. In this perspective article, we highlight the recent progress and current challenges of blue-emitting metallophosphors based on small molecules and their applications in phosphorescent OLEDs.

Phosphorescence color tuning by ligand, and substituent effects of multifunctional iridium(III) cyclometalates with 9-arylcarbazole moieties.

The synthesis, isomeric studies, and photophysical characterization of a series of multifunctional cyclometalated iridium(III) complexes containing a fluoro- or methyl-substituted 2-[3-(N-phenylcarbazolyl)]pyridine molecular framework are presented. All of the complexes are thermally stable solids and highly efficient electrophosphors. The optical, electrochemical, photo-, and electrophosphorescence traits of these iridium phosphors have been studied in terms of the electronic nature and coordinating site of the aryl or pyridyl ring substituents. The correlation between the functional properties of these phosphors and the results of density functional theory calculations was made. Arising from the propensity of the electron-rich carbazolyl group to facilitate hole injection/transport, the presence of such a moiety can increase the highest-occupied molecular orbital levels and improve the charge balance in the resulting complexes relative to the parent phosphor with 2-phenylpyridine ligands. Remarkably, the excited-state properties can be manipulated through ligand and substituent effects that allow the tuning of phosphorescence energies from bluish green to deep red. Electrophosphorescent organic light-emitting diodes (OLEDs) with outstanding device performance can be fabricated based on these materials, which show a maximum current efficiency of approximately 43.4 cd A(-1), corresponding to an external quantum efficiency of approximately 12.9 % ph/el (photons per electron) and a power efficiency of approximately 33.4 Lm W(-1) for the best device. The present work provides a new avenue for the rational design of multifunctional iridium-carbazolyl electrophosphors, by synthetically tailoring the carbazolyl pyridine ring that can reveal a superior device performance coupled with good color-tuning versatility, suitable for multicolor-display technology.

High-efficiency and color-stable white organic light-emitting devices based on sky blue electrofluorescence and orange electrophosphorescence

Highly efficient and color-stable two-wavelength white organic light-emitting devices (WOLEDs) combining an orange phosphor [Ir(Cz–CF3)] and a sky blue fluorescent dye BUBD-1 are fabricated where the host singlet is resonant with the fluorophore singlet state and the host triplet is resonant with the phosphor triplet level. A thin layer of 1,3,5-tris[N-(phenyl)benzimidazole]benzene between the phosphorescent and the fluorescent regions confines both singlet and triplet excitons efficiently and suppress Dexter transfer of the phosphor excitons to the nonradiative triplet state of BUBD-1. The best device reaches peak efficiencies of 19.3cd∕A and 11.1lm∕W which are superior to common two-color all-fluorescent or all-phosphor WOLEDs.

A Polyferroplatinyne Precursor for the Rapid Fabrication of L1 0 -FePt-type Bit Patterned Media by Nanoimprint Lithography

A polyferroplatinyne polymer can be patterned on the surface of Si wafer in ordered nanoline or nanodot shapes with PDMS molds through nanoimprint lithography (NIL), and subsequent thermal treatment gives rise to the nanopatterned arrays of L1(0) -FePt nanoparticles with the same periodicities. The method offers excellent potential to be utilized in the simple and rapid fabrication of bit patterned media for magnetic data recording.