Publications by authors named "Yanju Luo"

Deep-blue organic light-emitting diodes (OLEDs) with narrow emission spectra and high efficiency, meeting the Rec.2020 standard, hold significant promise in the realm of 4K/8K ultrahigh-definition displays. However, the development of light-emitting materials exhibiting both narrowband emission and high efficiency, particularly in the realm of deep-blue thermally activated delayed fluorescence (TADF), confronts substantial challenges.

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A novel deep-blue thermally activated delayed fluorescence molecule of SAC-BOC was reported. The SAC-BOC-based device exhibits a narrow full width at half maximum of 57 nm, an impressive maximum external quantum efficiency (EQE) of 15.3% and CIE coordinates of (0.

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Annularly 1,3-localized singlet diradicals are energetic and homolytic intermediates, but commonly too short-lived for widespread utilization. Herein, we describe a direct observation of a long-lived and seven-membered singlet diradical, oxepine-3,6-dione-2,7-diyl (OXPID), spectroscopic experiments and also theoretical evidence from computational studies, which is generated photo-induced ring-expansion of 2,3-diaryl-1,4-naphthoquinone epoxide (DNQO). The photo-generated OXPID reverts to the thermally stable σ-bonded DNQO with in the μs level, thus constituting a novel class of T-type molecular photoswitches with high light-energy conversion efficiency ( = 7.

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Although long-lived triplet charge-transfer ( CT) state with high energy level has gained significant attention, the development of organic small molecules capable of achieving such states remains a major challenge. Herein, by using the through-space electronic coupling effect, we have developed a compound, namely NIC-DMAC, which has a long-lived CT state at the single-molecule level with a lifetime of 210 ms and a high energy level of up to 2.50 eV.

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Although molecular self-assembled porous materials capable of ratiometric fluorescence probing and recycling of metal ions are both economically and environmentally attractive, very few current efforts have been devoted. Herein, we demonstrated a three-dimensional pure organic cage, namely 4-cage, which can serve as a fluorescent probe for simultaneous ratiometric detection and recycling of Ag ion. Taking advantage of the promising emission behavior of its rigidified tetraphenylethylene scaffolds and the chelating ability of its dynamically reversible imine moieties, on one hand, upon the addition of Ag , 4-cage undergoes coordination to form a stable but poorly soluble fluorescent complex, Ag @4-cage, accompanied by a fluorescence color change from bluish-green to yellowish-green.

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Article Synopsis
  • The article in question has been corrected to address previously identified issues.
  • The correction pertains to the original research findings and may impact interpretations or conclusions drawn from the study.
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Real-time acquisition of the morphological information of nanomaterials is crucial to achieving morphological controllable synthesis, albeit being challenging. A novel device was designed, which integrated dielectric barrier discharge (DBD) plasma synthesis and simultaneous spectral monitoring of the formation of metal-organic frameworks (MOFs). Important dynamic luminescence behaviors such as coordination induced emission (CIE), antenna effect (AE), and red-blue shift were continuously captured to reveal the spectral emission mechanism and energy transfer progress and verify the correlation with the morphological evolution of the MOFs.

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Introduction: Sugarcane is one of the most important sugar crops worldwide, however, sugarcane production is seriously limited by sugarcane red rot, a soil-borne disease caused by . YC89 was isolated from sugarcane leaves and can significantly inhibited red rot disease caused by .

Methods: In this study, the genome of YC89 strain was sequenced, its genome structure and function were analyzed using various bioinformatics software, and its genome was compared with those of other homologous strains.

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γCbPhAP, a D-A dyad with γ-carboline as the D unit and 3-phenylacenaphtho[1,2-]pyrazine-8,9-dicarbonitrile as the A moiety and phosphorescence core, was designed and synthesized. The doping system of 1 wt% γCbPhAP in PMMA shows red ambient phosphorescence-dominated afterglow with long lifetime of 0.5 s and decent efficiency over 12%.

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Accurate quantification on the quantum yields (φ) of both the prompt fluorescence (PF) and the delayed fluorescence (DF) species is quite essential for the clarification of molecular design rationales for thermally activated delayed fluorescence (TADF) luminogens. Currently, most φ and φ data of TADF fluorophores were acquired through time-correlated single-photon counting (TCSPC) lifetime measurement systems. However, because of their equal-time-channel working manner, so far all the commercially available TCSPC systems cannot render accurate measurement on φ of TADF materials due to the lack of enough valid data points in the faster decay region of the corresponding photoluminescence (PL) decay curves.

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The harvesting of 'hot' triplet excitons through high-lying reverse intersystem crossing mechanism has emerged as a hot research issue in the field of organic light-emitting diodes. However, if high-lying reverse intersystem crossing materials lack the capability to convert 'cold' T excitons into singlet ones, the actual maximum exciton utilization efficiency would generally deviate from 100%. Herein, through comparative studies on two naphthalimide-based compounds CzNI and TPANI, we revealed that the 'cold' T excitons in high-lying reverse intersystem crossing materials can be utilized effectively through the triplet-triplet annihilation-mediated high-lying reverse intersystem crossing process if they possess certain triplet-triplet upconversion capability.

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By taking advantage of the slight difference in the acidity of DO and HO, we report a novel DO optical sensor, namely Cy, with integrated great water-solubility, absorption/fluorescence dual-channel ratiometric response and even RGB visual sensing application. This work puts forward a facile method for distinguishing DO from HO with high sensitivity and high accuracy.

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The observation and discovery of lysosome dynamic alterations will greatly contribute to the in-depth understanding of lysosome biology and the development of new cancer therapeutics. To visualize lysosomal dynamics, here we have developed a lysosome-targetable fluorescent probe of showing integrated high selectivity, high photostability, and low cytotoxicity. With the aid of the excellent spatial and temporal imaging capability of , three different types of motion of lysosomes were defined, and perinuclear accumulation of lysosomes in response to the pro-inflammatory cytokine stimulus was observed in various cells.

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A novel system was designed, which integrated spectral monitoring with facile synthesis of lanthanide metal-organic frameworks in dielectric barrier discharge (DBD) plasma. It features miniaturization, cost-effectiveness and universality, for spectral information of scattering and luminescence to gain insight into the reactive processes.

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DO plays important roles in a variety of fields (such as the nuclear industry and bioorganic analysis), and thus its isotopic purity (HO contents) is highly concerned. Due to its highly similar physical properties to HO and large excess amounts of HO over DO, it is challenging to distinguish DO from HO. On the basis of the characteristic NIR-II phosphorescence of singlet oxygen (O), and the fact that HO is a more efficient quencher for O than DO, here, we proposed to simply use the 1275 nm emission of O for the analysis of the isotopic purity of DO.

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Owing to the difficulty in acquiring compounds with combined high energy bandgaps and lower-lying intramolecular charge-transfer excited states, the development of ultraviolet (UV) thermally activated delayed fluorescence (TADF) materials is quite challenging. Herein, through interlocking of the diphenylsulfone (PS) acceptor unit of a reported deep-blue TADF emitter (CZ-PS) by a dimethylmethylene bridge, CZ-MPS, a UV-emissive TADF compound bearing a shallower LUMO energy level and a more rigid structure than those of CZ-PS is achieved. This represents the first example of a UV-emissive TADF compound.

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Owing to the quite similar chemical properties of H O and D O, rational molecular design of D O optical sensors has not been realized so far. Now purely organic chromophores bearing OH groups with appropriate pK values are shown to display distinctly different optical responding properties toward D O and H O owing to the slight difference in acidity between D O and H O. This discovery is a new and facile strategy for the construction of D O optical sensors.

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Twisted intramolecular charge-transfer (TICT) fluorogens bearing highly pretwisted geometries and readily-fine-tuned charge-transfer characters are quite promising sensor and electroluminescence (EL) materials. In this study, by using 4-aryloxy-1,8-naphthalimide derivatives as the molecular framework, it is demonstrated for the first time that a CO bond could serve as the central bond to construct new TICT D-A systems. Photophysical and quantum chemical studies confirm that rotation around central CO bonds is responsible for the formation of a stable TICT state in these compounds.

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