Synthesis of Highly Photoluminescent All-Inorganic CsPbX3 Nanocrystals via Interfacial Anion Exchange Reactions.

All-inorganic cesium lead halide perovskite CsPbX3 (X = Cl, Br, I) nanocrystals (NCs) have attracted significant attention owing to their fascinating electronic and optical properties. However, researchers still face challenges to achieve highly stable and photoluminescent CsPbX3 NCs at room temperature by the direct-synthesis method. Herein, we synthesize CsPbX3 NCs by a facile and environmentally friendly method, which uses an aqueous solution of metal halides to react with Cs4PbBr6 NCs via interfacial anion exchange reactions and without applying any pretreatment. This method produces monodisperse and air-stable CsPbX3 NCs with tunable spectra covering the entire visible range, narrow photoluminescence emission bandwidth, and high photoluminescence quantum yield (PL QY, 80%). In addition, the chemical transformation mechanism between Cs4PbBr6 NCs and CsPbX3 NCs was investigated. The Cs4PbBr6 NCs were converted to CsPbBr3 NCs first by stripping CsBr, and then, the as-prepared CsPbBr3 NCs reacted with metal halides to form CsPbX3 NCs. This work takes advantage of the chemical transformation mechanism of Cs4PbBr6 NCs and provides an efficient and environmentally friendly way to synthesize CsPbX3 NCs.

Investigating the transformation of CsPbBr3 nanocrystals into highly stable CsPbBr3/Cs4PbBr6 nanocrystals using ethyl acetate in a microchannel reactor.

The nanocrystals (NCs) of inorganic perovskites CsPbX3 and Cs4PbX6 (X = Cl, Br, I) are showing a great development potential due to their versatility of crystal structure. Here, we used a microchannel reactor to synthesize both CsPbBr3 NCs (CsPbBr3 NCs) and Cs4PbBr6 NCs with embedded CsPbBr3 (CsPbBr3/Cs4PbBr6 NCs). Via speed control of the precursor, ligands around the surface of NCs were effectively regulated by ethyl acetate, allowing the transformation from CsPbBr3 NCs to CsPbBr3/Cs4PbBr6 NCs in a short time, an outstanding stability of NCs, and a better crosslinking between NCs and polymer for the application of LEDs. Without any protection, the CsPbBr3/Cs4PbBr6 NCs, with a production rate of 28 mg min-1, retain more than 90% of the PL intensity after 84 d. Finally, the CsPbBr3/Cs4PbBr6 NCs were used to produce an LED device, and a wide color gamut of 122.8% NTSC or 91.7% Rec 2020 was attained.

Highly Photoluminescent and Stable N-Doped Carbon Dots as Nanoprobes for Hg2+ Detection.

We developed a microreactor with porous copper fibers for synthesizing nitrogen-doped carbon dots (N-CDs) with a high stability and photoluminescence (PL) quantum yield (QY). By optimizing synthesis conditions, including the reaction temperature, flow rate, ethylenediamine dosage, and porosity of copper fibers, the N-CDs with a high PL QY of 73% were achieved. The PL QY of N-CDs was two times higher with copper fibers than without. The interrelations between the copper fibers with different porosities and the N-CDs were investigated using X-ray photoelectron spectroscopy (XPS) and Fourier Transform infrared spectroscopy (FTIR). The results demonstrate that the elemental contents and surface functional groups of N-CDs are significantly influenced by the porosity of copper fibers. The N-CDs can be used to effectively and selectively detect Hg2+ ions with a good linear response in the 0~50 µM Hg2+ ions concentration range, and the lowest limit of detection (LOD) is 2.54 nM, suggesting that the N-CDs have great potential for applications in the fields of environmental and hazard detection. Further studies reveal that the different d orbital energy levels of Hg2+ compared to those of other metal ions can affect the efficiency of electron transfer and thereby result in their different response in fluorescence quenching towards N-CDs.

Regulating the Emission Spectrum of CsPbBr3 from Green to Blue via Controlling the Temperature and Velocity of Microchannel Reactor.

The ability to precisely obtain tunable spectrum of lead halide perovskite quantum dots (QDs) is very important for applications, such as in lighting and display. Herein, we report a microchannel reactor method for synthesis of CsPbBr3 QDs with tunable spectrum. By adjusting the temperature and velocity of the microchannel reactor, the emission peaks of CsPbBr3 QDs ranging from 520 nm to 430 nm were obtained, which is wider than that of QDs obtained in a traditional flask without changing halide component. The mechanism of photoluminescence (PL) spectral shift of CsPbBr3 QDs was investigated, the result shows that the supersaturation control enabled by the superior mass and heat transfer performance in the microchannel is the key to achieve the wide range of PL spectrum, with only a change in the setting of the temperature controller required. The wide spectrum of CsPbBr3 QDs can be applied to light-emitting diodes (LEDs), photoelectric sensors, lasers, etc.

Efficient synthesis of highly fluorescent carbon dots by microreactor method and their application in Fe3+ ion detection.

Rapidly obtaining strong photoluminescence (PL) of carbon dots with high stability is crucial in all practical applications of carbon dots, such as cell imaging and biological detection. In this study, we proposed a rapid, continuous carbon dots synthesis technique by using a microreactor method. By taking advantage of the microreactor, we were able to rapidly synthesized CDs at a large scale in less than 5min, and a high quantum yield of 60.1% was achieved. This method is faster and more efficient than most of the previously reported methods. To explore the relationship between the microreactor structure and CDs PL properties, Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) were carried out. The results show the surface functional groups and element contents influence the PL emission. Subsequent ion detection experiments indicated that CDs are very suitable for use as nanoprobes for Fe3+ ion detection, and the lowest detection limit for Fe3+ is 0.239µM, which is superior to many other research studies. This rapid and simple synthesis method will not only aid the development of the quantum dots industrialization but also provide a powerful and portable tool for the rapid and continuous online synthesis of quantum dots supporting their application in cell imaging and safety detection.