Kyushu University · Engineering
Professor Xun Tang's research lab specializes in advanced optoelectronic materials, with a primary focus on organic light-emitting diodes (OLEDs) and next-generation battery technologies. The lab pioneers innovative molecular designs and nanostructured materials to achieve high-efficiency, stable, and color-pure white OLEDs through strategies such as energy transfer engineering, host-dopant modulation, and exciplex formation. In parallel, the lab explores self-healing anode materials for lithium-ion batteries, leveraging low-melting-point metals like gallium in carbon-encapsulated nanostructures to enhance cyclability and structural integrity. The overarching research direction emphasizes the rational design of functional materials at the molecular and nanoscale to address critical challenges in energy storage and display technologies.
Figures are computed from collected data and may differ slightly.
There is a great deal of interest in developing battery systems that can exhibit self-healing behavior, thus enhancing cyclability and stability. Given that gallium (Ga) is a metal that melts near room temperature, we wanted to test if it could be employed as a self-healing anode material for lithium-ion batteries (LIBs). However, Ga nanoparticles (NPs), when directly applied, tended to aggregate upon charge/discharge cycling. To address this issue, we employed carbon-coated Ga<sub>2</sub>O<sub>
Efficient red-green-blue primary luminescence with an extraordinarily narrow band and durability is crucial for advanced display applications. Recently, the emergence of multiple-resonance (MR) from short-range atomic interactions has been shown to induce extremely narrow spectral widths in pure organic emitters. However, achieving wide-range color tuning without compromising color purity remains a persistent challenge for MR emitters. Herein, the concept of electronic donor/acceptor "core-shell
Abstract Implementing rigorous standards for high‐quality white organic light‐emitting diodes (WOLEDs) demands further investigation. Herein, a novel and feasible color remedy strategy (CRS) is proposed in WOLEDs composed of binary‐emitters, to arouse the green‐emission, thereby complementing the spectral deficiency in white‐emission. Thus, the color rendering indexes (CRIs) of binary‐emissive WOLEDs can be boosted from 63 to 80 threshold, and the Commission International de I'Eclairage‐( x , y
Abstract White organic light‐emitting diodes (WOLEDs) composed of conventional fluorophores possess color purity, low efficiency roll‐off, and rare metal absence, but suffer from theoretical limits due to the lack of triplet utilization. Due to the different diffusion distance for singlets and triplets, multiple Förster resonance energy transfer (FRET) channels can be adequately built up. Herein, besides the complementary component, a blue fluorescence layer, hosted by pure hydrocarbon material
How to maintain high power efficiency (PE) and color stability under operating brightness is critical for the white organic light-emitting diodes (WOLEDs). To this end, two novel spiro-type materials STPy3 and STPy4 were designed. These materials could act as a single host and achieve a remarkable external quantum efficiency of 27.5% at 1000 cd m<sup>-2</sup>; to further optimize the PEs of OLEDs, STPy3/4 and PO-T2T were used as co-host-induced exciplexes, which enhanced the PE of green OLED to
Manipulating dynamic behaviours of charge carriers and excitons in organic light-emitting diodes (OLEDs) is essential to simultaneously achieve high colour purity and superior operational lifetime. In this work, a comprehensive transient electroluminescence investigation reveals that incorporating a thermally activated delayed fluorescence assistant molecule with a deep lowest unoccupied molecular orbital into a bipolar host matrix effectively traps the injected electrons. Meanwhile, the behavio
A continuous-wave (CW) organic solid-state laser is highly desirable for spectroscopy, sensing, and communications, but is a significant challenge in optoelectronics. The accumulation of long-lived triplet excitons and relevant excited-state absorptions, as well as singlet-triplet annihilation, are the main obstacles to CW lasing. Here, progress in singlet- and triplet-state utilizations in organic gain media is reviewed to reveal the issues in working with triplets. Then, exciton behaviors that
Green phosphorescent inverted organic light-emitting diodes (IOLEDs) with 1,4,5,8,9,11-hexaazatriphenylene-hexacarbonitrile (HAT-CN)/aluminium/n-doped 4,7-diphenyl-1,10-phenanthroline (Bphen) used as an electron injection layer (EIL) were demonstrated.
Abstract Rationally manipulating the functional substituents plays a crucial role in tuning the luminescence and lasing properties of organic gain media. Herein, a cyanophenyl‐moiety, which exhibits relatively weaker electron affinity, is connected to 2,6‐dicarbonitrile diphenyl‐1λ 5 ‐phosphinine (DCNP) via para ‐linking. Resultantly, the appreciated locally‐excited characteristics ensuring a large oscillator strength and high radiative rate can be reserved in DCNP‐4‐(4‐cyanophenyl) (DCNP‐pCN).
The investigation of organic light-emitting diodes (OLEDs) and organic laser devices with thermally activated delayed fluorescence (TADF) molecules is emerging due to the potential of harnessing triplets. In this work, a boron/nitrogen multiple-resonance TADF polycyclic framework fusing carbazole units (CzBNPh) was proposed. CzBNPh exhibited a narrowband emission (<30 nm), a unity photoluminescence quantum yield, and a fast radiative rate. Consequently, CzBNPh demonstrated a low distributed feed
Experiments are reported to fundamentally understand foaming in ceramic slips. Adsorption of two different types of surfactants, one anionic and another nonionic, onto alumina powders was studied. The most significant observation was that while the anionic surfactant strongly adsorbed onto alumina powders, the nonionic surfactant had essentially no adsorption. A model polymer based on the anionic surfactant was synthesized and compared with a similar polymer prepared with the nonionic surfactant
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