Publications by authors named "Ji-Hua Tan"

A new aggregation-induced emission (AIE) luminogen is obtained by dimerizing acridin-9(10H)-one (Ac), an aggregation-caused quenching (ACQ) effect monomer via an N─N bond and forming 9H,9'H-[10,10'-biacridine]-9,9'-dione (DiAc) with D symmetry. The quenching of DiAc in solution is ascribed to the enhanced basicity promoting hydrogen bonding and then a hydrogen abstraction (HA) reaction and/or an unallowed transition in frontier orbitals with the same symmetry facilitating intersystem crossing. It is found that emissive Ac is one product of the non-emissive DiAc solution in the HA reaction activated by UV irradiation.

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Constructing J-aggregated organic dyes represents a promising strategy for obtaining biomedical second near-infrared (NIR-II) emissive materials, as they exhibit red-shifted spectroscopic properties upon assembly into nanoparticles (NPs) in aqueous environments. However, currently available NIR-II J-aggregates primarily rely on specific molecular backbones with intricate design strategies and are susceptible to fluorescence quenching during assembly. A facile approach for constructing bright NIR-II J-aggregates using prevalent donor-acceptor (D-A) molecules is still lacking.

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Article Synopsis
  • Multi-resonance thermally activated delayed fluorophores are being researched for high-resolution applications due to their color purity, but face performance issues due to inefficient spin-flip processes.
  • This study presents two novel pure-blue emitters using an organoboron multi-resonance core with a flexible donor, which enhances excited state density without losing color quality.
  • By modifying the electronic structure through different phosphorus motifs, the emitters achieve a 20-fold increase in spin-flip efficiency, resulting in high-performance organic light-emitting diodes with a quantum efficiency of 37.6% and minimized efficiency roll-offs.
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Molecular fluorophores with the second near-infrared (NIR-II) emission hold great potential for deep-tissue bioimaging owing to their excellent biocompatibility and high resolution. Recently, J-aggregates are used to construct long-wavelength NIR-II emitters as their optical bands show remarkable red shifts upon forming water-dispersible nano-aggregates. However, their wide applications in the NIR-II fluorescence imaging are impeded by the limited varieties of J-type backbone and serious fluorescence quenching.

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Rationally tuning the emission position and narrowing the full width at half-maximum (FWHM) of an emitter is of great importance for many applications. By synergistically improving rigidity, strengthening the resonant strength, inhibiting molecular bending and rocking, and destabilizing the HOMO energy level, a deep-blue emitter (CZ2CO) with a peak wavelength of 440 nm and an ultranarrow spectral FWHM of 16 nm (0.10 eV) was developed via intramolecular cyclization in a carbonyl/N resonant core (QAO).

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Simultaneously realizing improved carrier mobility and good photoluminescence (PL) efficiency in red thermally activated delayed-fluorescence (TADF) emitters remains challenging but important. Herein, two isomeric orange-red TADF emitters, PDM and PDM, with the same basic donor-acceptor backbone but a pyrimidine () attachment at different positions are designed and synthesized. The two emitters show similarly good PL properties, including narrow singlet-triplet energy offsets (0.

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The development of photoinduced luminescent radicals with dynamic emission color is still challenging. Herein we report a novel molecular radical system (TBIQ) that shows photo-controllable luminescence, leading to a wide range of ratiometric color changes via light excitation. The conjugated skeleton of TBIQ is decorated with steric-demanding tertiary butyl groups that enable appropriate intermolecular interaction to make dynamic intermolecular coupling possible for controllable behaviors.

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To achieve high-efficiency deep-blue electroluminescence satisfying Rec.2020 standard blue gamut, two thermally activated delayed fluorescent (TADF) emitters are developed: 5-(2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracen-7-yl)-10,10-diphenyl-5,10-dihydrodibenzo[b,e][1,4]azasiline (TDBA-PAS) and 10-(2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracen-7-yl)-9,9-diphenyl-9,10-dihydroacridine (TDBA-DPAC). Inheriting from their parented organoboron multi-resonance core, both emitters show very promising deep-blue emissions with relatively narrow full width at half-maximum (FWHM, ≈50 nm in solution), high photoluminescence quantum yield (up to 92.

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Upon fusing the pyrazinyl pyrazole entity in giving pyrazolo[3,4-f]quinoxaline chelate, the corresponding Os(II) based NIR emitter exhibited "invisible" and efficient electroluminescence with a peak maximum at 811 nm. A maximum external quantum efficiency of 0.97 % and a suppressed efficiency roll-off till a current density of 300 mA cm was also exhibited.

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Enhancing the reverse intersystem crossing (RISC) process of thermally activated delayed fluorescent (TADF) emitters is an effective approach to realize efficient organic light-emitting diodes (OLEDs) with low efficiency roll-off. In this work, we designed two novel TADF emitters, SAT-DAC and SATX-DAC, via a spiro architecture. Efficient maximum external quantum efficiencies (EQEs) of 22.

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This study assesses the chemical characteristics of As in aerosol PM samples that were collected from July 2011 to May 2012 in Beijing, China. Total As, As(Ⅲ), and As(Ⅴ) were analyzed by inductively coupled plasma mass spectrometry (ICP-MS), high performance liquid chromatography (HPLC), and hydride generation atomic fluorescence (HG-AFS), respectively. The average concentrations of total As, As(Ⅲ) and As(Ⅴ) over the entire sampling period were (21.

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Samples of particulate matter from coal-fired boilers of different tons were collected in Lanzhou city, and the water-soluble inorganic ions, carbonaceous species, water-soluble organic compounds (WSOC) and polycyclic aromatic hydrocarbons (PAHs) were analyzed. The results showed that SO, Cl, and Ca were the most important water-soluble ions in the coal-fired boiler samples, accounting for 35.13%, 23.

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A recent breakthrough in the discovery of thermally activated delayed fluorescence (TADF) emitters characterized by small single-triplet energy offsets (Δ) offers a wealth of new opportunities to exploit high-performance metal-free photosensitizers. In this report, two intrinsically cancer-mitochondria-targeted TADF emitters-based nanoparticles (TADF NPs) have been developed for two-photon-activated photodynamic therapy (PDT) and fluorescence imaging. The as-prepared TADF NPs integrate the merits of (1) high O quantum yield of 52%, (2) sufficient near-infrared light penetration depth due to two-photon activation, and (3) excellent structure-inherent mitochondria-targeting capabilities without extra chemical or physical modifications, inducing remarkable endogenous mitochondria-specific reactive oxygen species production and excellent cancer-cell-killing ability at an ultralow light irradiance.

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In order to investigate the chemical characteristics and sources of atmospheric heavy metals, PM samples were collected every three days during the summer of 2011 and summer of 2012. The samples were analyzed for Li, V, Cr, Mn, Co, Cu, Zn, As, Se, Ti, Ga, Ni, Sr, Cd, In, Ba, Tl, Pb, Bi, and U by ICP-MS, with an emphasis on seven major heavy metal elements (Zn, Pb, Mn, Cu, As, V, and Cr). The concentrations of Zn, Pb, Mn, Cu, As, V, and Cr were (331.

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Simultaneous collections of non-methane hydrocarbons (NMHCs) were carried out at 15 sampling sites including urban, suburb and potential pollution areas in Cangzhou City in spring 2015. The results showed that NMHCs were generally higher in urban areas than those in suburb and rural areas; the highest concentration of NMHCs was observed at Cangzhou High-tech zone (urban area); the concentrations of NMHCs were significantly lower at rural sites than in most urban sites except Hejian site; vehicular emissions were the main sources of NMHCs in Cangzhou; Cangzhou chemical fertilizer plant and Cangzhou oil refinery had no significant influence on urban NMHCs during their shutdown period; Dagang Oilfield, with better oil and gas recovery systems, did not have a significant impact on urban NMHCs. In general, alkanes, alkenes and aromatics accounted for 65%, 16% and 19% of NMHCs in Cangzhou City, respectively; xylene (19%), ethylene (14%), toluene(11%), propylene (5%), isopentane (5%) and isopentene (5%) were the most dominant contributors to ozone formation potential; aerosol formation potential was mainly derived from toluene (28%), pinene (28%), xylene(16%), ethylbenzene (9%) and benzene (9%).

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Thirty non-methane hydrocarbons(NMHCs) samples were collected and analyzed in Foshan City during winter 2014 and summer 2015. The concentrations of NMHCs during the sampling period were 122.30 μg·m and 56.

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In order to investigate the influence of the emission reduction measure during the Beijing APEC on the concentrations and pollution characteristics of humic-like substances (HULIS) in atmospheric fine particles, PM₂.₅ samples were collected and analyzed for OCEC, WSOC, HULIS and water-soluble ions. The concentration of HULIS in PM₂.

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Polycyclic aromatic hydrocarbons (PAHs) are a group of important toxic compounds. In order to detect the pollutional characteristics of atmospheric PAHs in Fine Particulate Matter (PM), a total of 60 PM samples were collected in Lanzhou City during the winter of 2012 and summer of 2013. The GC/MS measurement results of the samples demonstrated the averagely total mass concentrations of the most significant 16 homologues of PAHs were (191.

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Pollution characteristic and variation trend of atmospheric carbonyls were investigated in November during the 2014 Beijing APEC. Formaldehyde, acetaldehyde and acetone were the dominant carbonyls, accounting for 82.66% of total carbonyls, and especially, formaldehyde accounted for 40.

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Foshan is a ceramics manufacturing center in the world and the most polluted city in the Pearl River Delta (PRD) in southern China measured by the levels of atmospheric heavy metals. PM2.5 samples were collected in Foshan in winter 2008.

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NMHCs and NOx samples were simultaneously collected and analyzed in six urban and suburban representative sampling sites (Sihuan, Tian'anmen, Pinguoyuan, Fatou, Beijing Airport and Miyun) during a typical haze period in winter 2005, Beijing. The concentrations of NMHCs during the sampling period in descending order were: Sihuan (1101.29 microg x m(-3)) > Fatou (692.

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Benzene, toluene, ethylbenzene and dimethylbenzene are typical anthropogenic emitted organics in the atmosphere, which not only endanger human health but also actively participate in photochemical reactions, generating O3 and secondary organic aerosols. In order to investigate the pollution level and its ozone formation potentials, concentrations of BTEX and O3 were parallel measured by the passive sampler and analyzed using GC-MS and ICS-90 during 2008-2010 in urban Beijing. The results show that toluene was the most abundant compound (8.

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Total suspended particles (TSP), collected during a typical haze period in Guangzhou, were analyzed for the fatty acids (C12-C30) and low molecular weight dicarboxylic acids (C3-C9) using gas chromatography/mass spectrometry (GC/MS). The results showed that the concentration of total fatty and carboxylic acids was pretty high during the haze episode. The ratios of fatty acids and carboxylic acids in haze to those in normal days were 1.

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Volatile Organic Compounds (VOCs) in Foshan City were investigated in December 6 to 30 2008. The concentrations of VOCs in haze days were significantly higher than those in no-haze days. Toluene (68.

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An intercomparison of organic carbon (OC) and elemental carbon (EC) measurements was conducted based on ambient aerosol samples collected during four seasons in Beijing, China. Dependence of OC and EC values on the temperature protocol and the charring correction method is presented and influences of aerosol composition are investigated. EC was found to decrease with the peak inert mode temperature (T(peak)) such that EC determined by the IMPROVE (the Interagency Monitoring of Protected Visual Environments)-A protocol (T(peak) was 580 °C) was 2.

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