Green Synthesis of Carbon Dots and Their Integration into Nylon-11 Nanofibers for Enhanced Mechanical Strength and Biocompatibility.

Carbon dots (CDs) have been extensively explored to show good optical features, low toxicity, and good biocompatibility. Herein, we report the new synthesis of forsythia-derived CDs (F-CDs) and their incorporation into Nylon-11 nanofibers for improved mechanical properties and biocompatibility. F-CDs are prepared from a Chinese herb forsythia via a magnetic hyperthermia method in 90 s without the use of any organic solvents. The as-prepared F-CDs with rich surface functional groups can be well embedded into Nylon-11 nanofibers via electrospinning, providing Nylon-11/F-CD nanofiber mats with remarkably enhanced mechanical properties. With the incorporation of F-CDs at 10 wt% into the Nylon-11 nanofiber mats, the tensile strength increases from 7.5 to 16.6 MPa, and the elongation ratio at break increases from 39% to 125%. Moreover, the Nylon-11/F-CD nanofiber mats exhibit excellent cytocompatibility towards L929 fibroblast cells with cell viability of 96%. These findings may guide the development of various CD-embedded nanofiber mats with good mechanical properties and biocompatibility potentially useful for biomedical applications, such as tissue engineering scaffolds or wound dressing.

Microfluidic fluorescent platform for rapid and visual detection of veterinary drugs.

The overuse of veterinary drugs and veterinary drug residues is increasingly becoming an obstacle to sustainable development worldwide. It is therefore imperative to establish a quantitative, sensitive and efficient method for the detection of veterinary drugs. Herein, we developed a visual microfluidic detection platform for rapid and sensitive detection of veterinary drugs using CdTe quantum dots (QDs) with three different ligands as the sensing units. Green-emissive 3-mercaptopropionic acid (MPA)-CdTe QDs, yellow-emissive thioglycolic acid (TGA)-CdTe QDs and orange-emissive N-acetyl-l-cysteine (NAC)-CdTe QDs were synthesized by a sulfhydryl aqueous phase method. These CdTe QDs show selective rapid fluorescence response to pefloxacin (PEF), malachite green (MG), and 1-aminohydantoin hydrochloride (AHD). With the concentration of veterinary drugs increasing, the CdTe QDs reveals a fluorescence color variation from bright to dark until quenched and the response degree of CdTe QDs with different ligands to veterinary drugs is different. Specifically, the limits of detection (LODs) of MPA-CdTe, TGA-CdTe and NAC-CdTe QDs probes for PEF were 7.57 µM, 1.75 µM and 2.90 µM, respectively, and the response was complete in a few seconds, realizing the sensitive and rapid detection of PEF. The three kinds of CdTe QDs could also be used in the detection of other veterinary drugs such as MG and AHD. Finally, a microfluidic detection platform was constructed for visual sensing and rapid detection towards veterinary drugs. The sensor platform holds the advantages of simple operation, low cost, rapid sensing and good sensitivity, and is potentially useful for visual quantitative detection of veterinary drug residues in aquatic products and the environment.

Large-Scale Production of Ligand-Engineered Robust Lead Halide Perovskite Nanocrystals by a Droplet-Based Microreactor System.

Cesium lead halide perovskite nanocrystals (CLHP NCs) have a wide range of potential applications benefited from the properties of high photoluminescence quantum yield (PLQY), wide luminous gamut, and narrow half peak width. However, due to the ionic nature and sensitivity to moisture, oxygen, or heat, perovskite nanocrystals are too fragile to maintain their crystal structure and optical properties. This work proposes solutions to two key issues in the development of CLHP NCs. First, a productive droplet-based microreactor system is designed to accomplish the scale-up production of CLHP NCs, obtaining sub-gram high-purity nanocrystal powders in a single production process. Second, CLHP NCs which are stable in polar solvents, air environment, and high temperature by using 3-aminopropyl triethoxysilane (APTES) as basic ligand are obtained. Wrapped with Si-O-Si generated by APTES, the CLHP NCs exhibit a longer fluorescence lifetime and higher quantum yield. Especially, the PLQY of CsPbBr3 @APTES can be stable at higher than 90% for more than 10 days. The Si-O-Si protective layer can also suppress the anion exchange between CsPbBr3 and CsPbI3 , maintaining the monochromaticity of nanocrystal luminescence. Eventually, full-spectrum quantum light-emitting diode (QLED) beads with robust nanocrystals are fabricated. The gamut of CsPbX3 @APTES encompasses 140% of the NTSC color gamut standard.

Facile synthesis of red dual-emissive carbon dots for ratiometric fluorescence sensing and cellular imaging.

Recently, widespread attention has been paid to red emissive carbon dots (CDs) which have desirable optical properties, low toxicity, and biocompatibility. Despite great efforts, the facile preparation of red dual-emissive CDs useful for ratiometric detection and bioimaging remains challenging. Here, we report a facile synthesis of red dual-emissive CDs and their potential for ratiometric fluorescence sensing and cellular imaging. Derived from the hydrothermal treatment of dicyandiamide and o-phenylenediamine in dilute sulfuric acid, the CDs are surface-tailored with nitrogen-, oxygen-, and sulfur-containing functional groups. The as-prepared CDs show various good features, including good water solubility, biocompatibility, excitation-independent dual-emission with two photoluminescence (PL) peaks centered at 630 and 680 nm, and an absolute quantum yield (QY) of 30.2% in water. The CDs exhibit a selective, sensitive, rapid, and stable ratiometric fluorescence response toward methyl blue, giving a linear relationship in the range of 0.5-300 µM with a correlation coefficient (R2) of 0.997. We also study ratiometric fluorescence sensing for the accurate detection of pH. Moreover, the CDs possess good cellular imaging ability, indicating their promising applicability for biomedical applications. These results pave a way toward the fabrication of red dual-emissive carbon-based nanomaterials useful for both ratiometric sensing and bioimaging.

Fiber-Spinning-Chemistry Method toward In Situ Generation of Highly Stable Halide Perovskite Nanocrystals.

All-inorganic halide perovskite nanocrystals (PNCs) have drawn increasing attention owing to their splendid optical properties. However, such nanomaterials suffer from intrinsic instability, greatly limiting their practical application. Meanwhile, environmental regulation has restricted the emissions of volatile organic compounds (VOCs), initiating a search for alternative approaches to PNC synthesis and film forming. Herein, fiber-spinning chemistry (FSC) is proposed for easy-to-perform synthesis of highly stable PNC fibrous films. The FSC process utilizes spinning fibers as reactors, reducing the generation of VOCs. This method enables the fabrication of CsPbX3 (X = Cl, Br, I) PNCs/poly(methyl methacrylate)/thermoplastic polyurethanes fibrous films at room temperature in one step, exhibiting tunable emission between 450 and 660 nm. Significantly, the in situ generation of PNCs in hydrophobic core-shell nanofibers results in highly improved fluorescence stability. PNCs/polymer fibrous films keep constant in photoluminescence (PL) after storage at atmosphere for 90 d and retain 82% PL after water immersion for 120 h (vs fluorescence quenching in 10 d in air or 5 h in water for pristine PNCs). The PNCs/polymer fibrous films endowed with superior optical stability and great flexibility show promising potentials in flexible optoelectronic applications. This work paves a facile way toward high-performance nanoparticles/polymer fibrous films.