Publications by authors named "Fengming Xie"

Multiple resonance (MR)-type thermally activated delayed fluorescence (TADF) emitters have garnered significant interest due to their narrow full width at half maximum (FWHM) and high electroluminescence efficiency. However, the planar structures and large singlet-triplet energy gaps (ΔEs) characteristic of MR-TADF molecules pose challenges to achieving high-performance devices. Herein, two isomeric compounds, p-TPS-BN and m-TPS-BN, are synthesized differing in the connection modes between a bulky tetraphenylsilane (TPS) group and an MR core.

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  • Blue perovskite light-emitting diodes (PeLEDs) face challenges due to difficult production of high-quality mixed-halide perovskites with wide optical bandgaps, leading to high defect density.
  • A new strategy for nondestructive in-situ halide exchange helps create high-quality blue perovskites with low trap density by using long alkyl chain chloride in chloroform post-treatment.
  • This method improves efficiency in PeLEDs across the blue spectrum, achieving external quantum efficiencies of 23.6% (sky-blue), 20.9% (pure-blue), and 15.0% (deep-blue) emissions.
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  • MR-TADF materials are important for OLEDs because they provide high efficiency and color purity but face issues like emission quenching and spectral changes due to their planar structure.
  • New materials, SBNO and SBNOS, utilize a spiro-carbon bridge to reduce negative intermolecular interactions, resulting in less redshift and broadening in their emission spectra.
  • The enhanced design leads to pure green OLEDs with a CIE y of 0.69 and an impressive EQE of 32.7%, improving upon traditional BNO emitters that exhibit greater spectral shifts and lower efficiency.
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  • Efficient and stable red perovskite light-emitting diodes (PeLEDs) show potential for high-definition displays and biomedical uses, but face issues with stability and efficiency for commercial viability.
  • A new crystallization regulation method using mixed vapors improves perovskite film quality, leading to better structural alignment and reduced surface defects.
  • The resulting red PeLEDs achieve impressive peak external quantum efficiencies (EQEs) of over 30% and longer operational lifetimes, marking significant progress towards their commercialization.
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Despite the rapid development of thermally activated delayed fluorescent (TADF) materials, developing organic light-emitting diodes (OLEDs) with small efficiency roll-off remains a formidable challenge. Herein, we have designed a TADF molecule (mClSFO) based on the spiro fluorene skeleton. The highly twisted structure and multiple charge-transfer channels effectively suppress aggregation-caused quenching (ACQ) and endow mClSFO with excellent exciton dynamic properties to reduce efficiency roll-off.

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  • Intramolecular exciplex systems with thermally activated delayed fluorescence (TADF) are gaining popularity in OLED technology, but organic sandwich exciplexes are still rare due to structural and synthetic difficulties.
  • *The study introduces a new rigid donor-acceptor-donor (A-D-A) complex called dSFQP, which utilizes two sp C-locking moieties and shows promising TADF properties through an effective charge-transfer mechanism.
  • *OLEDs using dSFQP as a dopant achieved an impressive external quantum efficiency (EQE) of 28.5% and maintained high efficiency even at elevated brightness levels, signaling a significant advancement in organic charge-transfer complex design.
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Thermally activated delayed fluorescence (TADF) emitters based on multiple resonance (MR) effects are promising for high-definition organic light-emitting diodes (OLEDs) with narrowband emission and high efficiency. However, they still face the challenges of aggregation-caused quenching (ACQ) and spectral broadening. Solution-processable MR-TADF emitters with an external quantum efficiency (EQE) of >20% and a full width at half-maximum (fwhm) of <30 nm have rarely been reported.

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Organic materials featuring intramolecular through-space charge transfer (TSCT) excited states are advantageous for efficient thermally activated delayed fluorescence (TADF), although the realization of multiple TSCT systems remains challenging. Herein, a rigid molecule with a three-dimensional dislocated sandwich acceptor-donor-acceptor configuration has been developed by a linking biphenazine (2PXZ) donor and 2,4,6-triphenyl-1,3,5-triazine (TRZ) acceptor through the twin-locking of two spiro-fluorene bridges. The twin-locking construction with multiple TSCT effects suppresses the intramolecular rotations of various segments in 2PXZ-2TRZ, leading to a small singlet-triplet energy difference, a fast reverse intersystem crossing process, and high photoluminescence quantum yield.

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Highly flexible and environmentally adaptive soft robots have received considerable attention. There remains a demand for soft robots to realize the stiffness modulation and variable workspace for robust and versatile manipulations. This article presents a compact soft gripper with a polylactic acid-based variable stiffness module (VSM) and a rigid retractable mechanism to achieve soft-rigid hybrid actuation.

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While tremendous progress has recently been made in perovskite light-emitting diodes (PeLEDs), large-area blue devices feature inferior performance due to uneven morphologies and vast defects in the solution-processed perovskite films. To alleviate these issues, a facile and reliable interface engineering scheme is reported for manipulating the crystallization of perovskite films enabled by a multifunctional molecule 2-amino-1,3-propanediol (APDO)-triggered "anchoring effect" at the grain-growth interface. Sky-blue perovskite films with large-area uniformity and low trap states are obtained, showing the distinctly improved radiative recombination and hole-transport capability.

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Although perovskite light-emitting diodes (PeLEDs) are promising for next-generation displays and lighting, their efficiency is still considerably below that of conventional inorganic and organic counterparts. Significant efforts in various aspects of the electroluminescence process are required to achieve high-performance PeLEDs. Here, we present an improved flexible PeLED structure based on the rational interface engineering for energy-efficient photon generation and enhanced light outcoupling.

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White organic light-emitting diodes (WOLEDs) using thermally activated delayed fluorescence (TADF)-based single emissive layer (SEL) have attracted enormous attention because of their simple device structure and full exciton utilization potential for high efficiency. However, WOLEDs made of an all-TADF SEL usually exhibit serious efficiency roll-off and poor color stability due to serious exciton-annihilation and unbalanced radiative decays of different TADF emitters. Herein, a new strategy is proposed to manipulate the TADF-sensitized fluorescence process by combining dual-host systems of high triplet energy with a conventional fluorescent emitter of complementary color.

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Thermally activated delayed fluorescence (TADF) provides great potential for the realization of efficient and stable organic light-emitting diodes (OLEDs). However, it is still challenging for blue TADF emitters to simultaneously achieve high efficiency, high brightness, and low Commission Internationale de l'Eclairage (CIE) coordinate (CIE) value. Here, the design and synthesis of two new benzonitrile-based TADF emitters (namely 2,6-di(9-carbazol-9-yl)-3,5-bis(3,6-diphenyl-9-carbazol-9-yl)benzonitrile (2PhCz2CzBn) and 2,6-di(9-carbazol-9-yl)-3,5-bis(3,6-di--butyl-9-carbazol-9-yl)benzonitrile (2tCz2CzBn)) with a symmetrical and rigid heterodonor configuration are reported.

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The design and synthesis of highly efficient thermally activated delayed fluorescence (TADF) emitters with an electroluminescence wavelength beyond 600 nm remains a great challenge for organic light-emitting diodes (OLEDs). To solve this issue, three TADF molecules, DMAC-BP ( = 1, 2, 3), are developed in combination with the rigid planar dibenzo[,]phenazine (BP) acceptor core and different numbers of 9,9-dimethylacridan (DMAC) donors. All these emitters possess stable internal charge transfer and a large dihedral angle between the donors and planar BP core.

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Two novel D-A bipolar blue phosphorescent host materials based on phenothiazine-5,5-dioxide: 3-(9-carbazol-9-yl)-10-ethyl-10-phenothiazine-5,5-dioxide (CEPDO) and 10-butyl-3-(9-carbazol-9-yl)-10-phenothiazine-5,5-dioxide (CBPDO) were synthesized and characterized. The photophysical, electrochemical and thermal properties were systematically investigated. CEPDO and CBPDO not only have a high triplet energy but also show a bipolar behavior.

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