Excitation power-dependent multicolor upconversion in NaLnF4:Er3+ under 1532†nm irradiation for anti-counterfeiting application.

Upconversion (UC) materials are renowned for their ability to convert low-energy photons into high-energy ones. The manipulation of parameters allows for the observation of multicolored UC luminescence (UCL) within a single material system. While modulation of multicolored UCL commonly relies on excitation at approximately 980 nm, investigation into multicolored UC materials activated by a 1532 nm excitation source remains comparatively scarce. In this work, we introduce NaLnF4:Er3+ as a novel class of smart luminescent materials. When the power density of a 1532 nm laser increases from 0.5 to 20.0 W/cm2, the emission peak positions remain unchanged, but the red-to-green (R/G) ratio decreases significantly from 18.82 to 1.48, inducing a color shift from red to yellow and ultimately to green. In contrast, no color variation is observed when NaLnF4:Er3+ is excited with a 980 nm laser at different power densities. This power-dependent multicolored UCL of NaLnF4:Er3+ excited at 1532 nm can be attributed to the competitive processes of upward pumping and downward relaxation of electrons on the 4I9/2 level of Er3+. By utilizing the unique UC characteristics of NaLnF4:Er3+, its potential utility in anti-counterfeiting applications is demonstrated. Our research highlights the distinctive optical properties of NaLnF4:Er3+ and provides novel insights into the use of luminescent materials in optical anti-counterfeiting technologies.

Efficient Deep-Blue Light-Emitting Diodes from Highly Luminescent Eu2+-Doped Alkali Metal Halide Nanocrystals via Lattice Field Modulation.

Lead-halide perovskite nanocrystals (NCs) are promising for fabricating deep-blue (<460 nm) light-emitting diodes (LEDs), but their development is plagued by low electroluminescent performance and lead toxicity. Herein, the synthesis of 12 kinds of highly luminescent and eco-friendly deep-blue europium (Eu2+)-doped alkali-metal halides (AX:Eu2+; A = Na+, K+, Rb+, Cs+; X = Cl-, Br-, I-) NCs is reported. Through adjustment of the coordination environment, efficient deep-blue emission from Eu-5d → Eu-4f transitions is realized. The representative CsBr:Eu2+ NCs exhibit a high photoluminescence quantum yield of 91.1% at 441 nm with a color coordinate at (0.158, 0.023) matching with the Rec. 2020 blue specification. Electrically driven deep-blue LEDs from CsBr:Eu2+ NCs are demonstrated, achieving a record external quantum efficiency of 3.15% and half-lifetime of ∼1 h, surpassing the reported metal-halide deep-blue NCs-based LEDs. Importantly, large-area LEDs with an emitting area of 12.25 cm2 are realized with uniform emission, representing a milestone toward commercial display applications.

Highly efficient upconversion luminescence in narrow-bandgap Y2Mo4O15.

Lanthanide-doped upconversion (UC) materials have been extensively investigated for their unique capability to convert low-energy excitation into high-energy emission. Contrary to previous reports suggesting that efficient UC luminescence (UCL) is exclusively observed in materials with a wide bandgap, we have discovered in this study that Y2Mo4O15:Yb3+/Tm3+ microcrystals, a narrowband material, exhibit highly efficient UC emission. Remarkably, these microcrystals do not display any four- or five-photon UC emission bands. This particular optical phenomenon is independent of the variation in doping ion concentration, temperature, phonon energy, and excitation power density. Combining theoretical calculations and experimental results, we attribute the vanishing emission bands to the strong interaction between the bandgap of the Y2Mo4O15 host matrix (3.37 eV) and the high-energy levels (1I6 and 1D2) of Tm3+ ions. This interaction can effectively catalyze the UC emission process of Tm3+ ions, which leads to Y2Mo4O15:Yb3+/Tm3+ microcrystals possessing very strong UCL intensity. The brightness of these microcrystals outshines commercial UC NaYF4:Yb3+,Er3+ green phosphors by a factor of 10 and is 1.4 times greater than that of UC NaYF4:Yb3+,Tm3+ blue phosphors. Ultimately, Y2Mo4O15:Yb3+/Tm3+ microcrystals, with their distinctive optical characteristics, are being tailored for sophisticated anti-counterfeiting and information encryption applications.

Tunable and Efficient Photoluminescence of Lanthanide-Doped Cs2NaScCl6 Double Perovskite Single Crystals toward Multifunctional Light-Emitting Diode Applications.

Lead-free halide double perovskite, as one of the promising candidates for lead halide perovskite materials, shows great potential in light-emitting diodes (LEDs), benefiting from its environmental friendliness and high chemical stability. However, the poor regulation of the emission spectra severely limits its application range. Herein, various lanthanide ions were successfully doped in Cs2NaScCl6 double perovskite single crystals (DPSCs) to yield effective and stable emissions spanning from visible to near-infrared (NIR) regions. Notably, efficient energy transfer from the host to the dopants enables tunable emissions with good chromaticity, which is rarely reported in the field of lead-free double perovskite. Moreover, density functional theory calculations reveal that the high local electron density around the [LnCl6]3- octahedron in DPSCs plays a key role in the improvement of photoluminescence quantum yields (PLQYs). The optimal PLQYs are up to 84%, which increases around 3 times over that of the undoped sample. Finally, multicolor and NIR LEDs based on Ln3+-doped Cs2NaScCl6 DPSCs were fabricated and had different application functions. Specifically, the single-composite white LED shows adjustable coordinates and correlated color temperatures, while the NIR LED shows good night vision imaging. This work provides new inspiration for the application of efficient multifunctional LEDs based on lead-free double perovskite materials.

High-Efficiency and Wavelength-Tunable Near-Infrared Emission of Lanthanide Ions Doped Lead-Free Halide Double Perovskite Nanocrystals toward Fluorescence Imaging.

Near-infrared (NIR) fluorescent materials show unique photophysical properties, which make them widely used in optical communication, night vision imaging, biomedicine, and other applications. However, the development of high-efficiency and wavelength-tunable NIR nanomaterials is still a challenge. Herein, a series of lanthanide ions doped Cs2AgIn0.99Bi0.01Cl6 double perovskite nanocrystals (DPNCs) with wavelength-tunable NIR light emission (800-1600 nm) have been synthesized. The optimal photoluminescence quantum yield (PLQY) of the DPNCs reaches 66.7%, which is a record value for DPNCs. It is mainly attributed to the contribution of NIR emission of lanthanide ions doped into DPNCs. More importantly, the series of NIR emission wavelengths of lanthanide ions doped Cs2AgIn0.99Bi0.01Cl6 DPNCs include not only shorter-wavelength NIR light (≤900 nm) but also longer-wavelength NIR light (>900 nm), which are more appropriate for foodstuff analysis and medical diagnosis applications. Furthermore, 11.2% Nd3+ doped Cs2AgIn0.99Bi0.01Cl6 DPNCs with the optimal PLQY were embedded in a polymethyl methacrylate (PMMA) polymer matrix (DPNCs@PMMA), and the stability of DPNCs modified by PMMA has been greatly improved. Finally, the 11.2% Nd3+ ions doped Cs2AgIn0.99Bi0.01Cl6 DPNCs@PMMA based NIR LEDs have demonstrated good night vision and human tissue penetration. This work indicates that lanthanide ions doped DPNCs have a potential in NIR light applications and could inspire future research to explore novel lanthanide ions doped semiconductor NCs based NIR LEDs.

Highly efficient and stable red perovskite quantum dots through encapsulation and sensitization of porous CaF2:Ce,Tb nanoarchitectures.

Lead halide perovskite quantum dots (PQDs) are extremely unstable when exposed to oxygen, water and heat, especially red CsPbBrxI3-x (x = 0, 0.5, 1.2) PQDs. This seriously hinders their practical application. Here, red CsPbBrxI3-x (x = 0, 0.5, 1.2) PQDs have been successfully encapsulated in porous CaF2:Ce,Tb hierarchical nanospheres (HNSs), which not only greatly improved the stability of PQDs, benefitting from the protection of the CaF2 shell, but also maintained the high photoluminescence quantum yield (PLQY) of PQDs, benefitting from the sensitization of Tb3+ ions. More importantly, porous CaF2:Ce,Tb nanoarchitectures can prevent aggregation quenching and anion exchange of PQDs. Therefore, the CaF2:Ce,Tb&CsPbBrxI3-x (x = 0, 0.5, 1.2) composite powder can have high PLQY comparable to that of the PQD powder. In view of this, CaF2:Ce,Tb&CsPbBr1.2I1.8 composite based red light-emitting diodes (LEDs) are prepared, and they are very suitable as a supplementary light source for plant lighting. Furthermore, white LEDs are also prepared by coating the CaF2:Ce,Tb&CsPbBr3 and CaF2:Ce,Tb&CsPbBr1.2I1.8 composite on a 450 nm chip. The optimum luminous efficiency is 61.2 lm W-1, and the color rendering index is 91, which are comparable to the current highest values. This shows that the composite composed of PQDs has great potential in LED lighting.

Double perovskite microcrystals-based white light-emitting diodes without reabsorption of multiphase phosphors.

Here, Tb3+ ions are incorporated into Cs2Ag0.6Na0.4InCl6:Bi double perovskite microcrystals via a re-crystallization method. Tb3+ ions doping not only makes the white light spectrum adjustable, but also maintains the high photoluminescence quantum yield (PLQY). The optimal value of PLQY is 95%. These are comparable to the current highest values. Noteworthy is that, intrinsic emission of Tb3+ ions is attributed to the effective energy transfer from the trapped exciton state of the double perovskite host to Tb3+ ions. Finally, mixing 30% Tb3+ alloyed Cs2Ag0.6Na0.4InCl6:Bi and Cs2NaInCl6:10%Sb phosphors, a series of double-perovskite-based white light-emitting diodes (WLEDs) are prepared. The color coordinates of the best WLEDs are (0.34, 0.32), the lumen efficiency is 42 lm/W, and the color rendering index is 94.3. It is worth mentioning here that there is no blue light loss caused by energy reabsorption between the two phosphors, because the excitation wavelengths of the two phosphors are concentrated in the ultraviolet band. This work provides a new strategy for preparing high-performance WLED.

Ni2+ and Pr3+ Co-doped CsPbCl3 perovskite quantum dots with efficient infrared emission at 1300 nm.

Lead halide perovskite quantum dots (PQDs) show great prospects in the field of optoelectronic applications. Although having high efficiency and narrow-band emission performance in the visible light region, the infrared multicolor luminescence performance of perovskite nanocrystals is still highly desired. In this work, in order to increase the luminescence intensity and extend the infrared multicolor luminescence, transition metal and rare earth ions are co-doped into PQDs. Herein, PQDs emitting at 1300 nm are realized by Pr3+ doping, which has not been reported in previous literature. The luminescence and kinetic process of Ni2+ and Pr3+ co-doped CsPbCl3 PQDs are studied, which exhibit considerably enhanced emission intensity at 400 nm and 1300 nm, with an overall quantum efficiency of photoluminescence (PLQY) of 89% and the highest infrared PLQY of 23%.

Stable and Efficient Upconversion Single Red Emission from CsPbI3 Perovskite Quantum Dots Triggered by Upconversion Nanoparticles.

Here, composites including highly efficient inert shell-modified NaYF4:Yb/Tm@NaYF4 upconversion nanoparticles (UCNPs) and CsPbI3 perovskite quantum dots (PQDs) have been successfully synthesized by the assistance of (3-aminopropyl)triethoxysilane (APTES) as a precursor for a SiO2 matrix. UCNPs and CsPbI3 PQDs in this composite structure show excellent stability in ambient conditions. Importantly, the efficient UC emission of CsPbI3 PQDs was realized, which means that the single red emission of inert shell-modified UCNPs can be easily obtained by depending on these composite structures. Furthermore, the single red emission wavelength can be easily regulated from 705 to 625 nm by introducing appropriate proportion of Br- ions, which is very difficult to achieve for traditional UCNPs. Moreover, benefiting from the efficient downshifting (DS) red emission of CsPbI3 PQDs, the composites possess the dual-wavelength excitation characteristics. So, the excellent dual-mode anticounterfeiting application has been demonstrated. This work will provide a new idea for the development of perovskite-based multifunctional materials.

High-Performance Perovskite Solar Cells Based on NaCsWO3@ NaYF4@NaYF4:Yb,Er Upconversion Nanoparticles.

Extending photoelectric response to the near-infrared (NIR) region using upconversion luminescent (UCL) materials is one promising approach to obtain high-efficiency perovskite solar cells (PSCs). However, challenges remain due to the shortage of highly efficient UCL materials and device structure. NaCsWO3 nanocrystals exhibit near-infrared absorption arising from the local surface plasmon resonance (LSPR) effect, which can be used to boost the UCL of rare-earth-doped upconversion nanoparticles (UCNPs). In this study, using NaCsWO3 as the LSPR center, NaCsWO3@NaYF4@NaYF4:Yb,Er nanoparticles were synthesized and the UCL intensity could be enhanced by more than 124 times when the amount of NaCsWO3 was 2.8 mmol %. Then, such efficient UCNPs were not only doped into the hole transport layer but also used to modify the perovskite film in PSCs, resulting in the highest power conversion efficiency (PCE) reaching 18.89% (that of the control device was 16.01% and the PCE improvement was 17.99%). Possible factors for the improvement of PSCs were studied and analyzed. It is found that UCNPs can broaden the response range of PSCs to the NIR region due to the LSPR-enhanced UCL and increase the visible light reabsorption of PSCs due to the scattering and reflection effect, which generate more photocurrent in PSCs. In addition, UCNPs modify the perovskite film by effectively filling the holes and gaps at the grain boundary and eliminating the perovskite surface defects, which lead to less carrier recombination and then effectively improve the performance of PSC devices.

Strong upconverting and downshifting emission of Mn2+ ions in a Yb,Tm:NaYF4@NaLuF4/Mn:CsPbCl3 core/shell heterostructure towards dual-model anti-counterfeiting.

Herein, a Yb,Tm:NaYF4@NaLuF4/Mn:CsPbCl3 quasi-core/shell heterostructure is synthesized with the assistance of silica. The strong upconverting and downshifting emission of Mn2+ ions was observed in the nanocomposite with a quasi-core/shell structure. The FRET process further improves the energy utilization efficiency of PQDs for UCNPs, which depends on the quasi-core/shell heterostructure. Considering the dual-model fluorescence emission behavior of Mn2+ ions, the stable Yb,Tm:NaYF4@NaLuF4/Mn:CsPbCl3 nanocomposite is used in anti-counterfeiting applications.

Ammonium acetate passivated CsPbI3 perovskite nanocrystals for efficient red light-emitting diodes.

Lead halide perovskite nanocrystals (PNCs) have very recently emerged as promising emitters for their superior optoelectronic properties. However, the defects in perovskite itself make it susceptible to the external environment and internal ion migration, resulting in low photoluminescence quantum yield (PLQY) and poor device efficiency. Herein, we developed a method to reduce the surface defects of PNCs by introducing ammonium acetate in the synthesis of CsPbI3 PNCs. The addition of ammonium acetate can effectively eliminate undesired surface metallic lead cations and dangling bonds, resulting in an enhanced PLQY and stability. The passivated PNCs have an overall up-shift energy level, demonstrating better hole injection efficiency. As a result, the red light-emitting diodes (LEDs) fabricated with the passivated CsPbI3 PNCs achieved an optimal EQE of 10.6% and a maximum brightness of 981 cd m-2, which are 3.1 and 2.4 times that of unpassivated PNCs based devices, respectively.

Bright Blue Light Emission of Ni2+ Ion-Doped CsPbClxBr3-x Perovskite Quantum Dots Enabling Efficient Light-Emitting Devices.

In recent years, significant advances have been achieved in the red and green perovskite quantum dot (PQD)-based light-emitting diodes (LEDs). However, the performances of the blue perovskite LEDs are still seriously lagging behind that of the green and red counterparts. Herein, we successfully developed Ni2+ ion-doped CsPbClxBr3-x PQDs through the room-temperature supersaturated recrystallization synthetic approach. We simultaneously realized the doping of various concentrations of Ni2+ cations and modulated the Cl/Br element ratios by introducing different amounts of NiCl2 solution in the reaction medium. Using the synthetic method, not only the emission wavelength from 508 to 432 nm of Ni2+ ion-doped CsPbClxBr3-x QDs was facially adjusted, but also the photoluminescence quantum yield (PLQY) of PQDs was greatly improved due to efficient removal of the defects of the PQDs. Thus, the blue emission at 470 nm with PLQY of 89% was achieved in 2.5% Ni2+ ion-doped CsPbCl0.99Br2.01 QDs, which increased nearly three times over that of undoped CsPbClBr2 QDs and was the highest for the CsPbX3 PQDs with blue emission, fulfilling the National Television System Committee standards. Benefiting from the highly luminous Ni2+ ion-doped PQDs, the blue-emitting LED at 470 nm was obtained, exhibiting an external quantum efficiency of 2.4% and a maximum luminance of 612 cd/m2, which surpassed the best performance reported previously for the corresponding blue-emitting PQD-based LED.

Impact of Host Composition, Codoping, or Tridoping on Quantum-Cutting Emission of Ytterbium in Halide Perovskite Quantum Dots and Solar Cell Applications.

Recently, various lanthanide ions (Ln3+) have been successfully doped into perovskite quantum dots (PQDs), and the quantum-cutting emission of 2F5/2-2F7/2 for Yb3+with a measurable inner efficiency of more than 100% has been discovered and applied as the luminescent converter of solar cells, which has opened a new branch for the application of PQDs. In this work, to further improve the quantum-cutting efficiency of Yb3+, the codoping and tridoping methods were used to improve the quantum-cutting emission of PQDs. The Yb3+-Ln3+ (Ln = Nd, Dy, Tb, Pr, Ce) pair-doped CsPbClxBryI3-x-y PQDs were fabricated, with all displaying excitonic emission, narrow-band emission of Ln3+ ions, and quantum-cutting emission of Yb3+ ions. It was interesting that Yb3+-Pr3+ as well as Yb3+-Ce3+ pairs could effectively sensitize the emission of Yb3+, owing to Pr3+ and Ce3+ ions offering intermediate energy states close to the exciton transition energy of the PQDs. After host composition optimization and tridoping investigation, overall emissions with a 173% photoluminescence quantum yield (PLQY) were obtained in the Yb3+-Pr3+-Ce3+-tridoped CsPbClBr2 PQDs. Then, the tridoped PQDs were designed as the down-converter for CuIn1-xGaxSe2 (CIGS) as well as the silicon solar cells, which leads to an enhancement of the power conversion efficiency (PCE) of as high as ∼20%. The modified CIGS was further employed to charge the smart mobile phone, which could largely shorten the charging time from 180 to 150 min. This finding is of great significant for expanding the application fields of the impurity-doped PQDs.

Effective blue-violet photoluminescence through lanthanum and fluorine ions co-doping for CsPbCl3 perovskite quantum dots.

All-inorganic CsPbX3 (X = Cl, Br, I) perovskite quantum dots (QDs) have received considerable attention in optoelectronic applications owing to their excellent photoluminescence properties. However, low blue-violet fluorescence emission and instability limit their practical application. Herein, we propose to improve the optical properties of CsPbCl3 QDs by co-doping La3+ and F- ions. The co-doped perovskite QDs were successfully synthesized using the hot injection approach, and they exhibited bright blue-violet emission and a high photoluminescence quantum yield of 36.5%, which is one order higher than that of undoped QDs. Enhanced photoluminescence performance compared to the initial CsPbCl3 QDs could be attributed to efficient modification of defects (Cl vacancy) and increased radiative recombination rate by the introduction of the dopants. Moreover, the as-prepared La3+ and F- ions co-doped CsPbCl3 QDs exhibited potential application for anti-counterfeiting.

Impurity Ions Codoped Cesium Lead Halide Perovskite Nanocrystals with Bright White Light Emission toward Ultraviolet-White Light-Emitting Diode.

White light-emitting diodes (WLEDs) based on all-inorganic perovskite CsPbX3 (X = Cl, Br, I) nanocrystals (NCs) have attracted extensive interests. However, the native ion exchange among halides makes them extremely difficult to realize the white emission. Herein, we demonstrate a novel strategy to obtain WLED phosphors based on the codoping of different metal ion pairs, such as Ce3+/Mn2+, Ce3+/Eu3+, Ce3+/Sm3+, Bi3+/Eu3+, and Bi3+/Sm3+ into stable CsPbCl3 and CsPbCl xBr3- x NCs. Notably, by the typical anion exchange reaction, the highly efficient white emission of Ce3+/Mn2+-codoped all-inorganic CsPbCl1.8Br1.2 perovskite NCs was achieved, with an optimal photoluminescence quantum yield of 75%, which is much higher than the present record of 49% for single perovskite phosphors. Moreover, the WLED with a luminous efficiency of 51 lm/W based on the 365 nm ultraviolet chip and CsPbCl1.8Br1.2:Ce3+/Mn2+ nanophosphor was achieved. This work represents a novel device for perovskite-based phosphor-converted WLEDs.

Considerably enhanced exciton emission of CsPbCl3 perovskite quantum dots by the introduction of potassium and lanthanide ions.

The photoluminescence quantum yield (PLQY) of blue-violet emission of CsPbCl3 quantum dots (QDs) is still low, which has limited their application in multi-colour displays. It is important to search for efficient perovskite phosphors within this wavelength range. In this work, we first considerably enhanced the photoluminescence quantum yield (PLQY) of the CsPbCl3 QDs from 3.2 to 10.3% by the introduction of potassium ions (K+). Then, various lanthanide elements (La, Y, Eu, Lu) were further doped into KxCs1-xPbCl3 QDs. The lanthanide doped KxCs1-xPbCl3 QDs still demonstrated emissions around 408 nm and the PLQY was further improved to 31%. Finally, we carried out anion exchange by gradually substituting chlorine with bromine. Efficient and tunable emissions ranging from 408-495 nm were obtained, with a maximum PLQY of 90%. This work provides a new approach to improve the efficiency of the blue-violet light of perovskite QDs.

Highly stable and water-soluble monodisperse CsPbX3/SiO2 nanocomposites for white-LED and cells imaging.

In spite of the excellent optical properties of all-inorganic halide perovskite quantum dots (PQDs), they still suffer from inherent poor stability even when exposed to moisture from the atmosphere, restricting their applications, especially in white-light-emitting diodes (LEDs) and cells imaging. Here, we proposed a strategy by encapsulating the CsPbX3 (X = Cl, Br, I) PQDs into silica nanoplates to prepare highly stable and water-soluble CsPbX3/SiO2 nanocomposites. First, the 120 nm monodisperse CsPbX3/SiO2 nanocomposites inlayed with several CsPbX3 PQDs were fabricated via the modified Stöber method. After coating, their stability exposed in the air was largely improved for all the CsPbX3 (X = Cl, Br, I) PQDs without changing their emission peaks and full-width at half-maximum, attributed to the suppression of the anion-exchange and decomposition. Moreover, further experiments demonstrated that the CsPbX3/SiO2 nanocomposites were highly water-soluble and stable in the water. Their applications in LEDs and cell imaging demonstrated their ultrastability and high biocompatibility. Therefore, this study shows the possibility of their use in photoelectric devices and biological applications.

All-inorganic perovskite quantum dot/TiO2 inverse opal electrode platform: stable and efficient photoelectrochemical sensing of dopamine under visible irradiation.

CsPbX3 (X = Cl, Br or I) perovskite quantum dots (PQDs) have attracted tremendous attention due to their extraordinarily excellent optical properties. However, there is still an obstacle for their bio-application, which is limited by their water-instability. In this work, we have designed a novel visible light triggered photoelectrochemical (PEC) sensor for dopamine (DA) based on CsPbBr1.5I1.5 PQD immobilized three-dimensional (3D) TiO2 inverse opal photonic crystals (IOPCs). Supported by the TiO2 IOPCs, the water-stability of the PQDs as well as that of the PEC sensor was considerably improved. Furthermore, employed as a photoactive material in PEC sensor, CsPbBr1.5I1.5 PQDs can expand the photocurrent response of the PEC sensor to the whole visible region. In addition, the modulation of the photonic stop band effect of TiO2 IOPCs on the incident light and the emission of PQDs could further enhance the photocurrent response. Such a PEC sensor demonstrates sensitive detection of DA in phosphate buffer saline solution and serum, with a good linear range from 0.1 µM to 250 µM and a low detection limit of approximately 0.012 µM. Our strategy opens an alternative horizon for PQD based PEC sensing, which could be more sensitive, convenient and inexpensive for clinical and biological analysis.

Highly efficient and stable blue-emitting CsPbBr3@SiO2 nanospheres through low temperature synthesis for nanoprinting and WLED.

Inorganic perovskite quantum dots (QDs) have attracted wide attention in display and solid-state lighting because of their easily tunable band-gaps and high photoluminescence quantum yields (PLQY) of green light emission. However, some drawbacks limit their practical applications, including the low PLQY of blue light emission and the instability in the moisture environment. In this work, efficient blue-light emitting CsPbBr3 perovskite QDs with PLQY of 72% were developed through a bandgap engineering approach. The achieved blue-light emitting PLQY is much higher than the values acquired in the inorganic perovskite QDs in the literature. And the emission color of the as-prepared QDs can be facially tuned by only adjusting the reaction temperature. Further, the mono-dispersed perovskite QDs@SiO2 composites were constructed benefiting from the low temperature synthesis. The optical performance of the QDs could be well persisted even in the moisture environment. Finally, the as-prepared QDs@SiO2 composite was fabricated as the QD ink on the anti-counterfeit printing technology, from which the obtained pattern would emit varied color under UV lamp. And the as-prepared composites was also applied for fabricating WLED, with Commission Internationale de l'Eclairage (CIE) color coordinates of (0.33, 0.38) and power efficiency of 32.5 lm W-1, demonstrating their promising potentials in solid-state lighting.