and Xiangxing Kong

Bio: and Xiangxing Kong is an academic researcher from University of Washington. The author has contributed to research in topics: Trimer & Fluorenone. The author has an hindex of 1, co-authored 1 publications receiving 207 citations.

Fluorenone-Containing Polyfluorenes and Oligofluorenes: Photophysics, Origin of the Green Emission and Efficient Green Electroluminescence†

Abstract: A series of four new statistical copolymers of 9,9-dihexylfluorene and 9-fluorenone with well-defined structures and a new fluorene−fluorenone−fluorene trimer model compound were synthesized and used to investigate the photophysics, origin of the green emission, and electroluminescence of this class of light-emitting materials. We show that the new oligofluorene trimer with a central fluorenone moiety is an excellent model of the green-emitting chromophore in polyfluorenes. From systematic studies of the steady-state photoluminescence (PL) and PL decay dynamics of solutions of the fluorenone-containing copolymers and oligomer and thin films of the copolymers, we show that the controversial 535-nm green emission band originates from the fluorenone defects in single-chain polyfluorenes and not from intermolecular aggregates or excimers. The green emission, centered at 535 nm, was observed in dilute toluene solutions of all fluorenone-containing copolymers and oligomer; it was long-lived with a single-expone...

Synthesis of Light-Emitting Conjugated Polymers for Applications in Electroluminescent Devices

Abstract: A review was presented to demonstrate a historical description of the synthesis of light-emitting conjugated polymers for applications in electroluminescent devices. Electroluminescence (EL) was first reported in poly(para-phenylene vinylene) (PPV) in 1990 and researchers continued to make significant efforts to develop conjugated materials as the active units in light-emitting devices (LED) to be used in display applications. Conjugated oligomers were used as luminescent materials and as models for conjugated polymers in the review. Oligomers were used to demonstrate a structure and property relationship to determine a key polymer property or to demonstrate a technique that was to be applied to polymers. The review focused on demonstrating the way polymer structures were made and the way their properties were controlled by intelligent and rational and synthetic design.

Blue-light-emitting oligoquinolines: Synthesis, properties, and high-efficiency blue-light-emitting diodes

Abstract: The synthesis, photophysics, cyclic voltammetry, and highly efficient blue electroluminescence of a series of four new n-type conjugated oligomers, 6,6′-bis(2,4-diphenylquinoline) (B1PPQ), 6,6′-bis(2-(4-tert-butylphenyl)-4-phenylquinoline) (BtBPQ), 6,6′-bis(2-p-biphenyl)-4-phenylquinoline) (B2PPQ), and 6,6′-bis((3,5-diphenylbenzene)-4-phenylquinoline) (BDBPQ) is reported. The oligoquinolines have high glass-transition temperatures (Tg ≥ 133 °C), reversible electrochemical reduction, and high electron affinities (2.68–2.81 eV). They emit blue photoluminescence with 0.73–0.94 quantum yields and 1.06–1.42 ns lifetimes in chloroform solutions. High-performance organic light-emitting diodes (OLEDs) with excellent blue chromaticity coordinates are achieved from all the oligoquinolines. OLEDs based on B2PPQ as the blue emitter give the best performance with a high brightness (19 740 cd m–2 at 8.0 V), high efficiency (7.12 cd A–1 and 6.56 % external quantum efficiency at 1175 cd m–2), and excellent blue color purity as judged by the Commission Internationale de L'Eclairage (CIE) coordinates (x = 0.15,y = 0.16). These results represent the best efficiency of blue OLEDs from neat fluorescent organic emitters reported to date. These results demonstrate the potential of oligoquinolines as emitters and electron-transport materials for developing high-performance blue OLEDs.

Electrospun Nanofibers of Blends of Conjugated Polymers: Morphology, Optical Properties, and Field-Effect Transistors

Abstract: Electrospun nanofibers of two series of binary blends of poly[2-methoxy-5-(2-ethylhexoxy)-1,4-phenylenevinylene] (MEH−PPV) with regioregular poly(3-hexylthiophene) (PHT) and with poly(9,9-dioctylfluorene) (PFO) were prepared, and their morphology and optical and electrical properties were characterized. Morphological and photophysical studies showed that the phase-separated domains in MEH−PPV/PHT nanofibers (30−50 nm) are much smaller as compared to blend thin films (100−150 nm), and efficient energy transfer was observed in these blend nanofibers. The MEH−PPV/PFO blend nanofibers had cocontinuous or core−shell structures, and significant energy transfer was absent in these blend nanofibers as compared to bulk thin films. Field-effect transistors based on MEH−PPV/PHT blend nanofibers showed exponential dependence of hole mobility on blend composition. The hole mobility decreased from 1 × 10-4 cm2/(V s) in 20 wt % MEH−PPV blend nanofibers to 5 × 10-6 cm2/(V s) at 70 wt %. If corrected for the reduced chann...