Publications by authors named "Zhaofeng Wu"

-methylpyrrolidone (NMP) is an excellent advanced solvent that can be easily absorbed by the human body and has the characteristics of flammability and explosion. To reduce the risk, the environmental concentrations of NMP need to be measured. A series of covalent organic frameworks (COF) connected by an imine bond have been successfully prepared at room temperature by changing the synthesis time catalyzed by scandium(III) trifluoromethanesulfonate (Sc(OTf)).

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Ratiometric fluorescent sensing based on dual-emitting fluorescent coordination polymers (FL-CPs) has attracted intense attention due to their sensing accuracy and easy visualization when compared with sensing relying solely on monochromatic FL-CPs. In this work, a series of rare-earth metal-based CPs, formuled as [(CH)NH][Ln(bpdc)] (Ln = Y, Eu and Tb, Hbpdc = biphenyl-4,4'-dicarboxylic acid), are presented, which show dual emission aroused from the Ln ions and the inefficient intermolecular energy transfer from ligands to Ln metals. For clarity, the as-made Ln-CPs are named Eu-bpdc, Tb-bpdc, and Y-bpdc based on the corresponding Ln.

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In this study, biomass-derived carbon material obtained from Lyocell fibers was first utilized as a gas sensor. The impacts of varying pyrolytic carbonization temperatures and pregrinding treatments on the structure, surface morphology, elemental composition, and gas sensitivity of the samples were thoroughly examined. The CL-500 sensor can realize rapid detection of trimethylamine with a high response (12.

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The aim of this research was to investigate the impact of periplocin (PPLN) on oxaliplatin (OXA) resistance in hepatocellular carcinoma (HCC) cells and offer insights for improving clinical treatment of HCC. The IC50 value of HCC cell lines against OXA was detected by the CCK-8 assay, and an OXA-resistant HepG2 cell line (HepG2/OXA) was constructed. THP-1 cells were induced into M1 or M2 macrophages, and M2 macrophage-conditioned medium (M2-CM) was prepared.

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Background: The tumour mutation burden (TMB) is a valuable indicator of the accumulation of somatic mutations, and is thought to be associated with the biological behaviour and prognosis of tumours. However, the related genetic mechanism for these association is still unclear. The aim of the present study was to identify the key gene(s) associated with TMB in hepatocellular carcinoma (HCC) and to investigate its biological functions, downstream transcription factors, and mechanism of action.

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As trimethylamine (TMA) is widely used in agriculture and industry, inhalation of TMA can cause very serious negative effects on human health. However, most of the current gas sensors for detecting TMA are commonly performed at high temperatures and cannot meet market needs. Inspired by this, we prepared imine covalent organic frameworks (TB-COF) synthesized from two monomers, 1,3,5-tris(4-aminophenyl)benzene (TAPB) and 1,3,5-benzotricarboxaldehyde (BTCA), using acetic acid as a catalyst at room temperature.

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Substrate oxidation is inevitable when exposed to ambient atmosphere during semiconductor manufacturing, which is detrimental to the fabrication of state-of-the-art devices. Optimizing the deoxidation process in molecular beam epitaxy (MBE) for random substrates poses a multidimensional challenge and is sometimes controversial. Due to variations in substrates and growth processes, the determination of the deoxidation condition heavily relies on the individual's expertise, yielding inconsistent results.

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The applications of self-assembled InAs/GaAs quantum dots (QDs) for lasers and single photon sources strongly rely on their density and quality. Establishing the process parameters in molecular beam epitaxy (MBE) for a specific density of QDs is a multidimensional optimization challenge, usually addressed through time-consuming and iterative trial-and-error. Here, we report a real-time feedback control method to realize the growth of QDs with arbitrary density, which is fully automated and intelligent.

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Correction for 'The {CuI} cluster bearing metal organic frameworks: crystal structures and fluorescence detecting performances towards cysteine and explosive molecules' by Jiang Jiang , , 2024, , 706-714, https://doi.org/10.1039/d3dt03363e.

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Article Synopsis
  • Recent developments in porous coordination polymers (PCPs) have led to their use as fluorescent sensors, particularly for detecting explosive molecules and toxic ions like chromate and dichromate.
  • Unlike traditional PCP sensors that are insoluble and less accurate due to environmental interference, the Zn-PCP in this study is soluble in organic solvents, providing a clear solution with strong blue fluorescence.
  • This innovative approach allows for more reliable detection, showing a good correlation between fluorescence intensity and the concentration of the target analytes, thus paving the way for improved task-specific PCP sensors.
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The colorless and odorless ethylene glycol is prone to unknowingly causing poisoning, making preventive monitoring of ethylene glycol necessary. In this paper, scandium (III) trifluoromethanesulfonate was used as a catalyst to successfully prepare covalent organic framework (COF) nanospheres linked by imines at room temperature. The COF nanospheres were characterized by XRD, SEM, TEM, FT-IR, UV-Vis and BET.

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Article Synopsis
  • Two new metal organic frameworks (MOFs), Eu-CuI-INA and Sr-K-CuI-INA, were synthesized and characterized, featuring unique 3-D structures.
  • These MOFs incorporate {CuI} clusters coordinated by isonicotinic acid (INA) ligands, along with metal ions like Eu and Sr.
  • Notably, Sr-K-CuI-INA shows promising fluorescence sensing capabilities for detecting cysteine and nitro compounds, suggesting its potential use in applications related to biological and explosive detection.
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Herein, we present a new series of CuI-based hybrid materials with tunable structures and semiconducting properties. The CuI inorganic modules can be tailored into a one-dimensional (1D) chain and two-dimensional (2D) layer and confined/stabilized in coordination frameworks of potassium isonicotinic acid (HINA) and its derivatives (HINA-R, R = OH, NO, and COOH). The resulting CuI-based hybrid materials exhibit interesting semiconducting behaviors associated with the dimensionality of the inorganic module; for instance, the structures containing the 2D-CuI module demonstrate significantly enhanced photoconductivity with a maximum increase of five orders of magnitude compared to that of the structures containing the 1D-CuI module.

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This study reports the synthesis of CdS/WS composites via a green and ultra-low-cost hydrothermal method. By controlling the relative mass ratio between WS and CdS, an n-n type CdS/WS heterostructure, with excellent NH gas-sensitive properties, was developed and investigated at room temperature. Compared with pristine WS and CdS, the CdS/WS-40%wt composite exhibited excellent selectivity of more than 4 orders of magnitude for sensing NH, a very short recovery time of 3 s, and ultrahigh selectivity at room temperature.

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This study aimed to investigate the indocyanine green (ICG) dose in real-time fluorescent cholangiography during laparoscopic cholecystectomy (LC) with a 4K fluorescent system. A randomized controlled clinical trial was conducted in patients who underwent LC for treatment of cholelithiasis. Using the OptoMedic 4K fluorescent endoscopic system, we compared four different doses of ICG (1, 10, 25, and 100 µg) administered intravenously within 30 min preoperatively and evaluated the fluorescence intensity (FI) of the common bile duct and liver background and the bile-to-liver ratio (BLR) of the FI at three timepoints: before surgical dissection of the cystohepatic triangle, before clipping the cystic duct, and before closure.

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Green and economical self-doped nitrogen-containing fluorescent carbon quantum dots (N-CQDs) were synthesized using a one-pot hydrothermal treatment method. The optical and structural properties of the N-CQDs were investigated in detail by UV-vis and fluorescence spectroscopy, X-ray diffraction (XRD) techniques, transmission electron microscopy (TEM), and high-resolution transmission electron microscopy (HRTEM). Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS) spectroscopy, and elemental analysis illustrate the surface function and composition of N-CQDs.

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In this study, chitin fibers (CFs) were combined with molybdenum sulfide (MoS) to develop high-performance sensors, and chitin carbon materials were innovatively introduced into the application of gas sensing. MoS/CFs composites were synthesized via a one-step hydrothermal method. The surface properties of the composites were greatly improved, and the fire resistance effect was remarkable compared with that of the chitin monomer.

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The photoinduced electron-transfer (ET) process plays an irreplaceable role in chemical and biological fields exemplified by enzymatic catalysis, artificial photosystems, solar energy conversion, and so forth. Searching for a new photoinduced ET system is of great importance for the development of functional materials. Herein, a series of host-guest compounds based on a magnesium metal-organic framework (Mg-MOF) as a host and pyridine derivatives as guests have been presented.

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Field-induced nonlinear materials, with extended abilities of manipulating electromagnetic waves, have been widely employed in electromagnetic protection, absorption, and detection. Until now, it was found that the field-induced nonlinearity mainly shows in the optical and terahertz frequency bands. Applying the microwave band into such technical activities is hampered due to a lack of investigations on the nonlinearity caused by microwave electric fields, especially in the ultrawideband and microwave high-frequency bands.

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In this work, a copper iodine module bearing a coordination polymer (CP) with a formula of [(CuI)Ce(INA)(DMF)]·DMF (, HINA = isonicotinic acid, DMF = ,-dimethyl formamide) is presented. The title compound features a three dimensional (3D) structure, in which the {CuI} cluster and {CuI} chain modules are coordinated by N atoms from a pyridine ring in INA ligands, while the Ce ions are bridged by the carboxylic groups of INA ligands. More importantly, compound exhibits an uncommon red fluorescence (FL) with a single emission band maximized at 650 nm belonging to near infrared (NIR) luminescence.

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Recently, the use of semiconductor-based photocatalytic technology as an effective way to mitigate the environmental crisis attracted considerable interest. Here, the S-scheme BiOBr/CdS heterojunction with abundant oxygen vacancies (Vo-BiOBr/CdS) was prepared by the solvothermal method using ethylene glycol as a solvent. The photocatalytic activity of the heterojunction was investigated by degrading rhodamine B (RhB) and methylene blue (MB) under 5 W light-emitting diode (LED) light.

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Exploration of sensitive and selective fluorescence sensors towards toxic metal species is of great importance to solve metal pollution issues. In this work, a three-dimensional (3D) strontium coordination polymer of Sr(tcbpe) (Htcbpe = 1,1,2,2-tetrakis(4-(4-carboxy-phenyl)phenyl)ethene) has been synthesized and developed as a fluorescent sensor to Fe ions. Sr(tcbpe) shows a mechanochromic fluorescence with emission shifting from blue of the pristine to green after being ground.

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Intricate superstructures possess unusual structural features and promising applications. The preparation of superstructures with single-crystalline nature are conducive to understanding the structure-property relationship, however, remains an intriguing challenge. Herein we put forward a new hierarchical assembly strategy towards rational and precise construction of intricate single-crystal superstructures.

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Pursuing novel materials with efficient photothermal conversion under irradiation at the near-infrared region windows (NIR, 750-850 nm; NIR-I and NIR-II, 1000-1320 nm)) is of great importance due to their irreplaceable applications, especially in the biomedical field. Herein, on the basis of a coordination chemistry strategy, an iron-based metal-organic framework (MOF) of [N(CH)][Fe(NDC)]·DMF·3HO (, 1,4-HNDC = 1,4-naphthalenedicarboxylic acid, N(CH) = tetramethyl-ammonium, and DMF = N,N-dimethylformamide) was prepared and characterized. Due to the - transition effect introduced by coordination with the transition-metal ion of iron and the highly conjugated naphthalenic moiety in 1,4-HNDC, guaranteeing an energy transfer between iron and the organic module, shows a remarkable broad absorption, which could be extended into the NIR-II section.

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Waste human hair was carbonized into carbon sheets by a simple carbonization method, which was studied as gas sensing materials for the first time. The effect of carbonization temperature on the structure and gas sensing properties of hair-based carbon sheet was studied by scanning electron microscope, X-ray diffraction, infrared spectrum, Raman spectrum, and gas-sensitive tester. The results showed that the carbonization temperature had a significant effect on the structure and gas sensing performance of carbon sheets, which were doped with K, N, P, and S elements during carbonization.

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