Search Results (17)

Perovskite quantum dots (PQDs) based on CsPbX₃ (X = Cl, Br, I) have attracted extensive attention due to their outstanding optoelectronic properties; however, their practical applications are hindered by poor environmental stability. In this work, a sequential surface-modification strategy is developed to address these limitations. First, CsPbBr₃ PQDs are passivated with (3-aminopropyl) triethoxysilane (APTES), which reduces surface defects and enhances the photoluminescence quantum yield (PLQY) from 38.5% to 74.4%. Subsequently, a dense silica shell is constructed via in situ hydrolysis of tetramethyl orthosilicate (TMOS), further improving the PLQY to 95.6% and significantly boosting environmental stability. Structural and optical characterizations confirm effective defect passivation and suppress non-radiative recombination, with carrier lifetimes extended from 2.5 ns to 36.9 ns. Remarkably, the silica-coated PQDs retain over 50% of their initial emission intensity after 100 min of water immersion, far exceeding the stability of uncoated counterparts. Furthermore, when integrated with a commercial K₂SiF₆: Mn⁴⁺ red phosphor and a blue light-emitting diode (LED) chip, the resulting white LED (WLED) exhibits a wide color gamut covering 104% of the National Television System Committee (NTSC) standard and Commission Internationale de l’Éclairage (CIE) coordinates of (0.323, 0.331), closely matching standard white light. Importantly, only the silica-coated PQDs maintain a stable electrically driven device emission spectrum after water exposure. Full article

Perovskite quantum dots (PQDs), with their excellent optical properties, have become a leading semiconductor material in the field of optoelectronics. However, to date, it has been a challenge to achieve the three-dimensional high-resolution patterning of perovskite quantum dots. In this paper, an in situ femtosecond laser-direct-writing technology was demonstrated for three-dimensional high-resolution patterned CsPbBr₃ PQDs using a two-photon photoresist nanocomposite doped with the CsPbBr₃ perovskite precursor. By adjusting the laser processing parameters, the minimum line width of the PQDs material was confirmed to be 98.6 nm, achieving a sub-100 nm PQDs nanowire for the first time. In addition, the fluorescence intensity of the laser-processed PQDs can be regulated by the laser power. Our findings provide a new technology for fabricating high-resolution display devices based on laser-direct-writing CsPbBr₃ PQDs materials. Full article

The ligand engineering of inorganic lead halide perovskite quantum dots (PQDs) is an indispensable strategy to boost their photoluminescence stability, which is pivotal for optoelectronics applications. CsPbX₃ (X = Cl, Br, I) PQDs exhibit exceptional optical properties, including high color purity and tunable bandgaps. Despite their promising characteristics, environmental sensitivity poses a challenge to their stability. This article reviews the solution-based synthesis methods with ligand engineering. It introduces the impact of factors like humidity, temperature, and light exposure on PQD’s instability, as well as in situ and post-synthesis ligand engineering strategies. The use of various ligands, including X- and L-type ligands, is reviewed for their effectiveness in enhancing stability and luminescence performance. Finally, the significant potential of ligand engineering for the broader application of PQDs in optoelectronic devices is also discussed. Full article

Inorganic CsPbX₃ (X = Cl, Br, I) perovskite quantum dots (PQDs) have attracted widespread attention due to their excellent optical properties and extensive application prospects. However, their inherent structural instability significantly hinders their practical application despite their outstanding optical performance. To enhance stability, an in situ electrospinning strategy was used to synthesize CsPbX₃/polyacrylonitrile composite nanofibers. By optimizing process parameters (e.g., halide ratio, electrospinning voltage, and heat treatment temperature), all-inorganic CsPbX₃ PQDs have been successfully grown in a polyacrylonitrile (PAN) matrix. During the electrospinning process, the rapid solidification of electrospun fibers not only effectively constrained the formation of large-sized PQDs but also provided effective physical protection for PQDs, resulting in the improvement in the water stability of PQDs by minimizing external environmental interference. Even after storage in water for over 100 days, the PQDs maintained approximately 93.5% of their photoluminescence intensity. Through the adjustment of halogen elements, the as-obtained composite nanofibers exhibited color-tunable luminescence in the visible light region, and based on this, a series of multicolor anti-counterfeiting patterns were fabricated. Additionally, benefiting from the excellent water stability and optical performance, the CsPbBr₃/PAN composite film was combined with red-emitting K₂SiF₆:Mn⁴⁺ (KSF) on a blue LED (460 nm), producing a stable and efficient WLED device with a color temperature of around 6000 K and CIE coordinates of (0.318, 0.322). These results provide a general approach to synthesizing PQDs/polymer nanocomposites with excellent water stability and multicolor emission, thereby promoting their practical applications in multifunctional optoelectronic devices and advanced anti-counterfeiting. Full article

This work presents a new optical dual sensor based on PtTFPP-containing electrospun fibers and CsPbBr₃ perovskite quantum dots (PQDs) for simultaneous detection of oxygen (O₂) and nitric oxide (NO) gases, wherein PtTFPP-containing electrospun fibers for O₂ sensing was based on electrospinning process fabricated by platinum(II) meso-tetrakis (pentafluorophenyl) porphyrin (PtTFPP) complex immobilized in cellulose acetate (CA) matrix. CsPbBr₃ PQDs were used as NO-sensitive material and coated on the surface of PtTFPP-containing electrospun fibers. Both materials were excited by a UV LED with a central wavelength of 380 nm, and the fluorescence intensities of sensing materials were recorded and analyzed with a spectrometer. The experiment results show that the optical NO and O₂ sensors have linear Stern–Volmer plots, and the sensitivities are around 2.7 and 10.7, respectively. The response and recovery times of the optical NO sensor are 71 and 109 s, respectively. For optical O₂, response and recovery times are 60 and 65 s, respectively. The optical dual sensor with a new method based on fluorescent dye containing electrospun fibers and coated with CsPbBr₃ PQDs has been successfully developed to detect NO and O₂ gases simultaneously. The optical dual gas sensor provides great potential for practical applications with low cost and ease of fabrication. Full article

Metal halide perovskite quantum dots (PQDs) are widely used in the display field due to their excellent photoelectric properties, such as ultra-narrow half-peak widths and ultra-pure luminescence color purity. Inkjet printing, laser direct writing and electrospinning are all common methods for PQDs printing to prepare micropattern displays. In order to produce large-scale and high-resolution PQDs micropatterns, electrohydrodynamic (EHD) printing technology is capable of large-scale deposition of highly oriented nanofibers on rigid or pliable, flat or bent substrates with the advantages of real-time regulation and single control. Therefore, it has a lot of potential in the fabrication of pliable electronic devices for one-dimensional ordered light-emitting fibers. Polycaprolactone (PCL) as an EHD printing technology polymer material has the advantages of superior biocompatibility, a low melting point, saving energy and easy degradation. By synthesizing CsPbBr₃ quantum dots (QDs) and PCL composite spinning stock solution, we used the self-built EHD printing platform to prepare the PCL@CsPbBr₃ composite light-emitting optical fiber and realized the flexible display of high-resolution micropatterns in polydimethylsiloxane (PDMS) packaging. An x-ray diffractometer (XRD), scanning electron microscope (SEM) and photoluminescence (PL) were used to characterize and analyze the fiber’s morphology, phase and spectral characteristics. EHD printing technology may open up interesting possibilities for flexible display applications based on metal halide PQDs. Full article

CsPbX₃ (X = Cl, Br or I) perovskite quantum dots (PQDs) have gained increasing interest due to their superior performance in photoelectric applications. In our work, a series of Mn²⁺ doped CsPbBr₃ PQDs were successfully prepared in glasses by melt quenching and in situ crystallization technique. Due to the ⁴T₁ (⁴G)→⁶A₁ (⁶S) transition of Mn²⁺, a slight red shift from 510 nm to 516 nm was found, with the FWHM expansion from 18 nm to 26 nm. The PQDs@glasses showed excellent thermal stability, and the exciton binding energy reached a high level of 412 meV. The changes of the electronic structure after Mn doping CsPbBr₃ can be demonstrated by first principles. Finally, a contactless electroluminescence device with the PQDs@glasses was designed based on the principle of electromagnetic induction, which is a potential application for detecting distance in sterile and dust−free environments. Full article

In this study, blue perovskite quantum dots (PQDs) were prepared using didodecyldimethylammonium bromide (DDAB), which can passivate surface defects caused by the loss of surface ligands and reduce particle size distribution. After the passivation of DDAB, blue CsPbCl_xBr_3−x PQDs dispersed in n-octane produced a more compact and uniform PQD thin film than the non-passivated ones. The resulting device showed a stabile lifetime, and an EL peak of 470 nm and a maximum EQE of 1.63% were obtained at an operating voltage of 2.6 V and a current density of 0.34 mA/cm². This work aims to provide a simple method to prepare blue-emitting PQDs and high-performance PQD-based light-emitting devices. Full article

The selective control of halide ion exchange in metal halide perovskite quantum dots (PQDs) plays an important role in determining their band gap and composition. In this study, CsPbX₃ (X = Cl⁻, Br⁻, and I⁻) PQDs were self-assembled with PbSO₄-oleate to form a peapod-like morphology to selectively control halide ion exchange. Considering the distinct absorption and bright luminescence characteristics of these PQDs, in situ UV-Vis. absorption and fluorescence spectroscopies were employed to monitor the time-dependent band gap and compositional changes of the PQDs. We determined that the halide exchange in the capped PQDs is hindered—unlike the rapid anion exchange in noncapped PQDs—by a reduction in the halide exchange kinetic rate depending on the extent of coverage of the PQDs. Thus, we tracked the halide ion exchange kinetics between CsPbBr₃ and CsPbI₃ PQDs, depending on the coverage, using in situ UV-Vis. absorption/photoluminescence spectroscopy. We regulated the halide exchange reaction rate by varying the capping reaction temperature of the PQDs. The capping hindered the halide exchange kinetics and increased the activation energy. These results will enable the development of white LEDs, photovoltaic cells, and photocatalysts with alternative structural designs based on the divalent composition of CsPbX₃ PQDs. Full article

Making high-quality raw materials is the key to open the versatile potential of next generation materials. All-inorganic CsPbX₃ (X: Cl⁻, Br⁻, and/or I⁻) perovskite quantum dots (PQDs) have been applied in various optoelectronic devices, such as photocatalysis, hydrogen evolution, solar cells, and light-emitting diodes, due to their outstanding photophysical properties, such as high photoluminescence quantum yield (PLQY), absorption cross-section, efficient charge separation, and so on. Specifically, for further improvement of the PLQY of the PQDs, it is essential to diminish the non-radiative charge recombination processes. In this work, we approached two ways to control the non-radiative charge recombination processes through synthetic and post-synthetic processes. Firstly, we proposed how refinement of the conventional recrystallization process for PbI₂ contributes to higher PLQY of the PQDs. Secondly, after halide exchange from CsPbI₃ PQDs to CsPbBr₃, through an in situ spectroelectrochemical setup, we monitored the positive correlation between bromide deposition of on the surface of the perovskite and photoluminescence improvement of the CsPbBr₃ perovskite film through electrodeposition. These two strategies could provide a way to enhance the photophysical properties of the perovskites for application to various perovskite-based optoelectronic devices. Full article

Nowadays, the excellent performance of metal halide perovskite quantum dots (PQDs) has been demonstrated, but the stability is still a perplexing issue. In this paper, the CsPbBr₃ QDs were assembled into SBA-15 for the first time. The thermal stability and photoluminescence (PL) intensity of SBA-15@CsPbBr₃ QDs were improved. The PL spectra of pure CsPbBr₃ QDs have red-shift (~6 nm) with the increasing temperature. However, that of SBA-15@CsPbBr₃ QDs have almost no red-shift. The PL intensity of SBA-15@CsPbBr₃ QDs decreased slightly after heating and cooling for several times. By comparison, the PL intensity of pure CsPbBr₃ QDs decreased more significantly. The experimental results showed that SBA-15 played a significant role in improving the thermal stability of PQDs, which will have an excellent potential for the application of PQDs in the future. Full article

Photonic devices based on perovskite materials are considered promising alternatives for a wide range of these devices in the future because of their broad bandgaps and ability to contribute to light amplification. The current study investigates the possibility of improving the light amplification characteristics of CsPbBr₃ perovskite quantum dot (PQD) films using the surface encapsulation technique. To further amplify emission within a perovskite layer, CsPbBr₃ PQD films were sandwiched between two transparent layers of poly(methyl methacrylate) (PMMA) to create a highly flexible PMMA/PQD/PMMA waveguide film configuration. The prepared perovskite film, primed with a polymer layer coating, shows a marked improvement in both emission efficiency and amplified spontaneous emission (ASE)/laser threshold compared with bare perovskite films on glass substrates. Additionally, significantly improved photoluminescence (PL) and long decay lifetime were observed. Consequently, under pulse pumping in a picosecond duration, ASE with a reduction in ASE threshold of ~1.2 and 1.4 times the optical pumping threshold was observed for PQDs of films whose upper face was encapsulated and embedded within a cavity comprising two PMMA reflectors, respectively. Moreover, the exposure stability under laser pumping was greatly improved after adding the polymer coating to the top face of the perovskite film. Finally, this process improved the emission and PL in addition to enhancements in exposure stability. These results were ascribed in part to the passivation of defects in the perovskite top surface, accounting for the higher PL intensity, the slower PL relaxation, and for about 14 % of the ASE threshold decrease. Full article

The notable photophysical characteristics of perovskite quantum dots (PQDs) (CsPbBr₃) are suitable for optoelectronic devices. However, the performance of PQDs is unstable because of their surface defects. One way to address the instability is to passivate PQDs using different organic (polymers, oligomers, and dendrimers) or inorganic (ZnS, PbS) materials. In this study, we performed steady-state spectroscopic investigations to measure the photoluminescence (PL), absorption (A), transmission (T), and reflectance (R) of perovskite quantum dots (${\mathrm{CsPbBr}}_3$) and ethylene vinyl acetate/terpene phenol (1%) (EVA-TPR (1%), or EVA) copolymer/perovskite composites in thin films with a thickness of 352 ± 5 nm. EVA is highly transparent because of its large band gap; furthermore, it is inexpensive and easy to process. However, the compatibility between PQDs and EVA should be established; therefore, a series of analyses was performed to compute parameters, such as the band gap, the coefficients of absorbance and extinction, the index of refractivity, and the dielectric constant (real and imaginary parts), from the data obtained from the above investigation. Finally, the optical conductivities of the films were studied. All these analyses showed that the EVA/PQDs were more efficient and stable both physically and optically. Hence, EVA/PQDs could become copolymer/perovskite active materials suitable for optoelectronic devices, such as solar cells and perovskite/polymer light-emitting diodes (PPLEDs). Full article

The current work examines the effects of cesium lead bromide (CsPbBr₃) perovskite quantum dots (PQDs) on the structural and optical properties of conjugated polymer blends of poly[2-methoxy-5-(2′-ethylhexyloxy)-1,4-phenylene vinylene] (MEH–PPV) and poly(9,9-di-n-octylfluorenyl-2,7-diyl) (PFO). MEH–PPV/PFO composite thin-films containing PQDs with weight ratios between 0.5 wt.% and 10 wt.% were prepared via a solution-blending method prior to spin-coating on glass substrates. The MEH–PPV/PFO composites’ crystallinity was improved, and the roughness was dramatically increased with higher PQDs content, as confirmed by X-ray diffraction (XRD) and atomic force microscopy (AFM), respectively. Conversely, a higher PQDs content resulted in a gradual reduction of the Urbach tail and an increase in the steepness parameter, thereby reducing the localized density of the electronic states within the forbidden bandgap of the hybrids. Moreover, a slight reduction in the direct and indirect bandgaps was found in PQDs/(MEH–PPV/PFO) composite films containing a higher PQDs content and provided evidence of the low concentration of the localized states. The incorporation of the PQDs resulted in enhanced non-radiative energy transfer processes in the MEH–PPV/PFO hybrids, which are very important for the development of optimized optoelectronic devices. Full article

The triplet energy transfer mechanism of novel poly(9,9-di-n-octylflourenyl-2,7-diyl) (PFO)/poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV)/CsPbBr₃ perovskite quantum dot (PQD) hybrid thin films was comprehensively investigated. The concentrations of PFO and MEH-PPV in all the specimens were fixed, while the PQD content was varied with various weight ratios and premixed by a solution blending method before it was spin-coated onto glass substrates. The triplet non-radiative Förster resonance energy transfers (FRETs) in the PFO/MEH-PPV/PQDs ternary blend, the dual FRET from PFO to both PQDs and MEH-PPV, and the secondary FRET from PQDs to MEH-PPV were observed. The values of the Förster radius (R_o) of FRET from PFO to MEH-PPV in the presence of various PQD contents (Case I) increased from 92.3 to 104.7 Å, and they decreased gradually from 68.0 to 39.5 Å for FRET from PFO to PQDs in the presence of MEH-PPV (Case II). These R_o values in both cases confirmed the dominance of FRET in ternary hybrid thin films. Upon increasing the PQD content, the distance between the donor and acceptor molecules (R_DA) and the conjugation length (A_π) in both cases gradually decreased. The small values of R_o, R_DA, and A_π with a decrease in the energy transfer lifetime (τ_ET) due to an increase in the PQD contents in both Cases I and II confirmed the efficient FRET in the hybrid. To prevent intermolecular transfer in PFO, the concentrations of MEH-PPV (Case I) and PQDs (Case II) should be decreased to a range of 0.57–0.39 mM and increased in the range of 1.42–7.25 mM. Full article