Excitation Wavelength Research Articles

Photomodulation of Charge Transfer through Excited‐State Processes: Directing Donor‐Acceptor Binding Dynamics

AbstractModulating charge transfer (CT) interactions between donor and acceptor molecules may give rise to unique dynamic changes in physicochemical properties, exhibiting great importance in supramolecular chemistry and materials science. In this work, we demonstrate the first instance of reversible photomodulation of donor‐acceptor (D−A) CT interaction in the solid state. Pyridinium‐based chromophore featuring π‐conjugated D−A structures can not only function as a good electron acceptor to undergo photoinduced electron transfer (ET) or engage in intermolecular CT interaction, but also exhibit unique dual emission depending on the excitation wavelengths. The rotatable C−C single bonds within D−A pairs enhance the tunability of molecular structure. Through the synergy of a photoinduced ET and an excited‐state conformational change, the intermolecular CT interaction can be switched on and off by alternate light irradiation to enable reversibly modulation of the affinity between donor and acceptor molecules, accompanied by visual color switching and fluorescence on‐off as feedback signals.

Excitation wavelength and time dependent colour tunable room temperature phosphorescence from boron doped carbon nanodots.

Developing metal free room temperature phosphorescence (RTP) materials have received tremendous attention due its potential application in various fields such as sensing, optoelectronics and anticounterfeiting. Herein, we have synthesized an excitation wavelength and time dependent phosphorescent boron doped carbon nanodots (BCNDs) by thermal treatment of ethanolamine and boric acid at 240°C, where boric acid act as both doping and host agents. The obtained BCNDs display blue to orange fluorescence in both aqueous medium and solid state. In addition, the BCNDs display tunable orange-yellow-green phosphorescence in solid state under UV and visible light, lasting upto 10s, visible to naked eye. The boron and nitrogen doping regulates the band gap of the BCNDs, resulting the phosphorescence colour tunability. The average phosphorescence lifetime and quantum yield of BCNDs are found to be 1.27s and 8.61% respectively. Based on the optical properties, the BCNDs are applied as security ink in information encryption and security marking. Hence, this work can promote the development of metal free phosphorescent carbon based materials which may find application in various emerging fields.

An Increase in The Cross-Section of Two-Photon Absorption of Styrene Dye in Supramolecular Complexes with Cucurbituriles

Two-photon absorption cross sections of aqueous solutions of the styryl dye trans-4-[4-(dimethylamino)styryl]-1-methylpyridinium iodide (DASPI) and its inclusion complexes with cucurbit[n]urils (CB[n] n = 6–8) were measured using fluorescence spectroscopy. A nonmonotonic dependence of the cross-section size on the excitation wavelength and on the cavitand cavity size was found. Compared with a free dye, a sevenfold increase in the two-photon absorption cross section was observed in DASPI inclusion complexes with CB[8] at an excitation wavelength of 980 nm.

Multi‐Channel Optical Encryption Film With Strong Circularly Polarized Luminescence and High Quantum Yield

AbstractDeveloping a sustainable security module with multiple optical states is important to deter counterfeits, but is challenging. This work designs a kind of chiral luminescent film through the co‐assembly of the CNCs and d‐glucose, simultaneously doped with the lanthanide complex and organic dye. Superior mechanical performance makes it undertake various deformations, including twist, and tension without breaking. Meanwhile, this film has unique optical characteristics. On the one hand, the chiroptical signals can be manipulated through the matching of the photonic bandgap and fluorescence peak. On the other hand, due to the co‐assembly with two luminophores, the film displays the excitation wavelength (Ex)‐dependent circularly polarized luminescence properties. Under the Ex of 275 nm, the film simultaneously integrates a large dissymmetry factor of −0.3898, a high quantum yield of 69.19%, and a considerable lifetime of 1381 µs, which has exceeded most reported chiral luminescent assemblies. These multimodal and convertible optics endow the film with practical applications in the anti‐counterfeit. It can be designed as a security label or used as a written paper to encrypt the information. Even in humid surroundings, this security effect is still ensured.

Investigating the multifunctionality of Cu2+ doped LaSrMnO3: understanding structural, optical, and magnetic responses

Abstract This study examines the impact of copper ions (Cu2+) on the structural, optical, and magnetic, characteristics of La0.6Sr0.4Mn1-xCuxO3 (LSMCO) manganites. Various techniques, including X-ray diffraction, field emission scanning electron microscopy, Raman spectroscopy, DC magnetization, and photoluminescence measurements were employed for a comprehensive analysis. Structural examinations revealed that all compositions exhibit a single-phase orthorhombic structure. Raman spectroscopy reveals the structural distortion due to the inclusion of Cu at Mn site. The photoluminescence properties of the manganite were found to be influenced by the excitation wavelength, demonstrating energy transfer from Mn ions. Magnetic investigations indicated that the introduction of Cu leads to a reduction in the saturation magnetization of the manganite.

Ultrafast Charge Transfer-Induced Unusual Nonlinear Optical Response in ReSe2/ReS2 Heterostructure.

Ultrafast charge transfer in van der Waals heterostructures can effectively engineer the optical and electrical properties of two-dimensional semiconductors for designing photonic and optoelectronic devices. However, the nonlinear absorption conversion dynamics with the pump intensity and the underlying physical mechanisms in a type-II heterostructure remain largely unexplored, yet hold considerable potential for all-optical logic gates. Herein, two-dimensional ReSe2/ReS2 heterostructure is designed to realize an unusual transition from reverse saturable absorption to saturable absorption (SA) with a conversion pump intensity threshold of approximately 170 GW/cm2. Such an intriguing phenomenon is attributed to the decrease of two-photon absorption (TPA) of ReS2 and the increase of SA of ReSe2 with the pump intensity. Based on the characterization results of X-ray photoelectron spectroscopy, ultraviolet photoelectron spectroscopy, femtosecond transient absorption spectrum, Kelvin probe force microscopy, and density functional theory calculation, a type-II charge-transfer-energy level model is proposed combined with the TPA of ReS2 and SA of ReSe2 processes. The results reveal the critical role of ultrafast interfacial charge transfer in tuning the unusual nonlinear absorption and improving the SA of ReSe2/ReS2 under different excitation wavelengths. Our finding deepens the understanding of nonlinear absorption physical mechanisms in two-dimensional heterostructure materials, which may further diversify the nonlinear optical materials and photonic devices.

Light-modulated van der Waals force microscopy

Atomic force microscope generally works by manipulating the absolute magnitude of the van der Waals force between tip and specimen. This force is, however, less sensitive to atom species than to tip-sample separations, making compositional identification difficult, even under multi-modal strategies or other atomic force microscopy variations. Here, we report the phenomenon of a light-modulated tip-sample van der Waals force whose magnitude is found to be material specific, which can be employed to discriminate heterogeneous compositions of materials. We thus establish a near-field microscopic method, named light-modulated van der Waals force microscopy. Experiments discriminating heterogeneous crystalline phases or compositions in typical materials demonstrate a high compositional resolving capability, represented by a 20 dB signal-to-noise ratio on a MoTe2 film under the excitation of a 633 nm laser of 1.2 mW, alongside a sub-10 nm lateral spatial resolution, smaller than the tip size of 20 nm. The simplicity of the light modulation mechanism, minute excitation light power, broadband excitation wavelength, and diversity of the applicable materials imply broad applications of this method on material characterization, particularly on two-dimensional materials that are promising candidates for next-generation chips.

Short-Wave Infrared Upconverting Nanoparticles.

Optical technologies enable real-time, noninvasive analysis of complex systems but are limited to discrete regions of the optical spectrum. While wavelengths in the short-wave infrared (SWIR) window (typically, 1700-3000 nm) should enable deep subsurface penetration and reduced photodamage, there are few luminescent probes that can be excited in this region. Here, we report the discovery of lanthanide-based upconverting nanoparticles (UCNPs) that efficiently convert 1740 or 1950 nm excitation to wavelengths compatible with conventional silicon detectors. Screening of Ln3+ ion combinations by differential rate equation modeling identifies Ho3+/Tm3+ or Tm3+ dopants with strong visible or NIR-I emission following SWIR excitation. Experimental upconverted photoluminescence excitation (U-PLE) spectra find that 10% Tm3+-doped NaYF4 core/shell UCNPs have the strongest 800 nm emission from SWIR wavelengths, while UCNPs with an added 2% or 10% Ho3+ show the strongest red emission when excited at 1740 or 1950 nm. Mechanistic modeling shows that addition of a low percentage of Ho3+ to Tm3+-doped UCNPs shifts their emission from 800 to 652 nm by acting as a hub of efficient SWIR energy acceptance and redistribution up to visible emission manifolds. Parallel experimental and computational analysis shows rate equation models are able to predict compositions for specific wavelengths of both excitation and emission. These SWIR-responsive probes open a new IR bioimaging window, and are responsive at wavelengths important for vision technologies.

N‐Arylphenothiazines and N,N‐Diarylphenazines as Tailored Organophotoredox Catalysts for the Reductive Activation of Alkenes

AbstractA small library of N‐arylphenothiazines, N‐arylbenzo[b]phenothiazines and N,N‐diarylphenazines has been synthesized as strongly reducing organophotocatalysts without the need for sacrificial reagents or electrochemistry. Their opto‐electronic properties and their suitability as organophotoredox catalysts for the efficient activation of olefins was investigated using the addition of methanol to α‐methylstyrene as a model reaction. The findings were supported by DFT calculations. Three photocatalysts were identified that allowed quantitative yields with 10 mol % catalyst loading and 20 h irradiation by a 365 nm LED. The catalyst loading was gradually reduced to 0.5 mol % and the irradiation time was reduced to only 20 min. These experiments revealed that N,N‐diisobutyl‐4′‐(10H‐phenothiazin‐10‐yl)‐[1,1′‐biphenyl]‐4‐amine is the most efficient photocatalyst among the N‐arylphenothiazines. This chromophore combines high electron density introduced by the diisobutylamino phenyl group with high absorptivity at 365 nm caused by the phenylene bridge to the phenothiazine core. In an attempt to shift the excitation wavelength into the visible light range for selectivity and sustainability purposes (potential use of sunlight as a light source), N‐arylbenzo[b]phenothiazines N,N‐diarylphenazines were designed that exhibit a red‐shifted and broad absorbance shoulder into the visible range, but only N,N‐diarylphenazines allow photocatalysis and the one‐electron activation of alkenes by visible light (450 nm LED).

Exploration of value-added soybean oil cake based carbon quantum dots for in-vitro biomedical applications

Carbon quantum dots (C-dots) enthused the inquisitiveness of investigators in biomedicine due to their distinctive features including minimal toxicity, superior water solubility and biocompatibility. This study uses an environmental friendly hydrothermal approach to create high-fluorescent agricultural residue-derived carbon quantum dots from Soybean Oil Cake (SOC). The synthesized SOCC-Dots were examined by physiochemical techniques such as High-Resolution Transmission Electron Microscopy (HR-TEM), UV–Visible spectroscopy (UV–Vis), Photoluminescence (PL), Fourier Transform Infrared Spectroscopy (FT-IR), X-ray diffraction analysis (XRD), Zeta potential and Raman Spectroscopy. The absorption peak at 275 nm is evident due to the presence of C = O bonds of π→π* transition. The synthesized SOCC-Dots demonstrated the existence of several functional groups OH, C = O, and CO stretching vibration. The particles collected display spherical morphology with an average of 3.25 nm size by HR-TEM analysis spectra. The photoluminescence showed stability against various excitation wavelengths and had a maximum emission peak at 445 nm. Anti-inflammatory activity is tested using a Bovine serum assay displaying significant results of 87.4 % for SOCC-dots at a concentration of 50 µg/mL due to their superior biocompatibility and water solubility. The results of the cytotoxicity evaluation showed an 85 % survival rate among nauplii after 48 h at concentrations of 80 µg/mL, and the antioxidant activity exhibited outstanding performance, achieving an 87 % efficacy rate for SOCC-dots at a concentration of 50 μg/mL

Circular photocurrents in centrosymmetric semiconductors with hidden spin polarization

Centrosymmetric materials with site inversion asymmetries possess hidden spin polarization, which remains challenging to be converted into spin currents because the global inversion symmetry is still conserved. This study demonstrates the spin-polarized circular photocurrents in centrosymmetric transition metal dichalcogenide semiconductors at normal incidence without applying electric bias. The global inversion symmetry is broken by using a spatially-varying circularly polarized light beam, which could generate spin gradient owing to the hidden spin polarization. The dependence of the circular photocurrents on electrode configuration, illumination position, and beam spot size indicates an emergence of circulating electric current under spatially inhomogeneous light, which is associated with the deflection of spin-polarized current through the inverse spin Hall effect. The circular photocurrents is subsequently utilized to probe the spin polarization and the inverse spin Hall effect under different excitation wavelengths and temperatures. The results of this study demonstrate the feasibility of using centrosymmetric materials with hidden spin polarization and non-vanishing Berry curvature for spintronic device applications.

A New approach for simultaneous detection and photocatalytic degradation of imidacloprid and dinotefuran in water using terbium-based fluorometry and mixed-phase TiO2

This study explores a novel method for detecting neonicotinoid insecticides, imidacloprid (IMD) and dinotefuran (DNT), in water using terbium (Tb3+) ions photo probe. The optimal excitation and emission wavelengths for Tb3+ luminescence were identified at 310 nm and 545 nm, respectively. The influence of pH and solvent on Tb-complex fluorescence was investigated. Results indicate a significant enhancement of luminescence intensity at pH 6 for IMD in DMF and pH 7.0 for DNT in DMSO. The fluorescence intensity exhibited a linear relationship with IMD and DNT concentrations ranging from 0.1 to 20 µg/mL (R2 > 0.99). Limits of quantitation (LOQ) were determined as 0.1 µg/mL for IMD and 0.05 µg/mL for DNT. This newly developed photo probe demonstrates the potential for monitoring photolysis and photocatalytic degradation of these neonicotinoids using TiO2 as a catalyst under controlled photoreactor conditions. The method offers a promising alternative for rapidly and sensitively detecting these prevalent insecticides in water samples.

Using Femtosecond Laser Light to Investigate the Concentration- and Size-Dependent Nonlinear Optical Properties of Laser-Ablated CuO Quantum Dots.

In this work, the nonlinear optical (NLO) properties of CuO nanoparticles (CuO NPs) were studied experimentally using the pulsed laser ablation (PLA) technique. A nanosecond Nd: YAG laser was employed as the ablation excitation source to create CuO NPs in distilled water. Various CuO NPs samples were prepared at ablation periods of 20, 30, and 40 min. Utilizing HR-TEM, the structure of the synthesized CuO NPs samples was verified. In addition, a UV-VIS spectrophotometer was used to investigate the linear features of the samples. The Z-scan technique was utilized to explore the NLO properties of CuO NPs samples, including the nonlinear absorption coefficient (β) and nonlinear refractive index (n2). An experimental study on the NLO features was conducted at a variety of excitation wavelengths (750-850 nm), average excitation powers (0.8-1.2 W), and CuO NPs sample concentrations and sizes. The reverse saturable absorption (RSA) behavior of all CuO NPs samples differed with the excitation wavelength and average excitation power. In addition, the CuO NPs samples demonstrated excellent optical limiters at various excitation wavelengths, with limitations dependent on the size and concentration of CuO NPs.

Multiwavelength Surface-Enhanced Raman Scattering Fingerprints of Human Urine for Cancer Diagnosis.

Label-free surface-enhanced Raman spectroscopy (SERS) is capable of capturing rich compositional information from complex biosamples by providing vibrational spectra that are crucial for biosample identification. However, increasing complexity and subtle variations in biological media can diminish the discrimination accuracy of traditional SERS excited by a single laser wavelength. Herein, we introduce a multiwavelength SERS approach combined with machine learning (ML)-based classification to improve the discrimination accuracy of human urine specimens for bladder cancer (BCa) diagnosis. This strategy leverages the excitation-wavelength-dependent SERS spectral profiles of complex matrices, which are mainly attributed to wavelength-related vibrational changes in individual analytes and differences in the variation ratios of SERS intensity across different wavelengths among various analytes. By capturing SERS fingerprints under multiple excitation wavelengths, we can acquire more comprehensive and unique chemical information on complex samples. Further experimental examinations with clinical urine specimens, supported by ML algorithms, demonstrate the effectiveness of this multiwavelength strategy and improve the diagnostic accuracy of BCa and staging of its invasion with SERS spectra from increasing numbers of wavelengths. The multiwavelength SERS holds promise as a convenient, cost-effective, and broadly applicable technique for the precise identification of complex matrices and diagnosis of diseases based on body fluids.

A highly sensitive β-AKBA-Ag-based fluorescent “turn off” chemosensor for rapid detection of abamectin in tomatoes

Abstract This study presents the synthesis of a sensitive AKBA-Based fluorescent “Turn off” chemosensor for rapid detection of abamectin residues in tomatoes. Silver nanoparticles were synthesized by using 3-O-acetyl-11-keto-β-boswellic acid (β-AKBA) by chemical reduction method. The characterization of AKBA-AgNPs was performed by UV–vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), and transmission electron microscopy (TEM). The average particle size of NPs was found to be 46.2 ± 2 nm with lumps of macro-sized particles. TEM data further revealed that nanoparticles were polydispersed and spherical in shape and also show good stability at high temperatures and pH. The biosensing properties of nanoparticles were studied for the detection of abamectin residues in tomato samples. Abamectin a natural product derived from the bacterium Streptomyces avermitilis is effective against a wide range of pests. In sensing protocol 67 organic tomato samples were segregated into 34 (safe group, without a spray of abamectin) and 33 samples (as an unsafe group, sprayed with abamectin insecticide solution). Emission spectra of these sample solutions were measured in the wavelength range of 450–530 nm, excitation wavelength was fixed at 488 nm. The effect of minor wavelength variation for the discrimination and classification of the two groups was investigated by applying two chemometric methods including partial least square discriminant analysis and principal component analysis with projection. The mechanism of its interaction between the AKBA-Ag NPs and abamectin residue was also established through UV/visible, FTIR, and TEM microscopy. This newly synthesized nanoparticle was found to have excellent stability at variables, i.e., temperature, storage period, salt concentration, and pH. Therefore, the synthesized Ag NPs are potential candidates for biosensing applications against abamectin.

Hydrogel-based fluorescence assay kit for simultaneous determination of ceftazidime and avibactam

Monitoring the concentration of antibiotics rapidly and cost-effectively is crucial for accurate clinical medication and timely identification of drug-induced illnesses. Here, we constructed a novel fluorescent assay kit to monitor Zavicefta, an effective antibiotic composed of avibactam (AVI) and ceftazidime (CFZ) to treat carbapenem-resistant gram-negative bacteria infections. AVI can emit fluorescence, but CFZ cannot. To enable simultaneous measurement of both in one kit, we designed molecularly imprinted polymer (MIP) modified quantum dots (QDs) for CFZ determination. MIPs have received significant attention as an artificial antibody due to their exceptional specificity for various targets, particularly drugs with small molecular weight. Under the excitation wavelength of 350 nm, the detection process involves a decrease in QDs’ fluorescence signal at 600 nm owing to the “gate effect” between MIP and CFZ and the internal filtration effect between CFZ and QDs. Simultaneously, a fluorescence emission characteristic peak at 420 nm for AVI emerges. In addition, to simplify the operation procedure and improve determination throughput, the detection agents were incorporated into a hydrogel and placed in a 96-well plate, enabling concurrent quantification of AVI and CFZ within the respective range of 80–1000 μM and 1–1000 μM. The developed assay kit successfully determined AVI and CFZ in human serums and therapeutic drug monitoring in a live rabbit model. Recoveries of AVI and CFZ were 92.7–114%, with relative standard deviations below 6.0%. Moreover, a smartphone was employed to read the fluorescence signals, which was beneficial for cost reduction and out-of-lab analysis. This study will deliver a pragmatic resolution to developing high-throughput assay kits for drug determination.Graphical

Interface induced photoluminescence enhancement from heterojunction BaMoO4/HEAs phosphors: Experiment, theory and anti-counterfeiting application

The BaMoO4/FeCoNiCrMo (BMO/HEA(Mo)), BMO/FeCoNiCrTi (HEA(Ti)) and BMO/FeCoNiCrTiAl (HEA(Al)) phosphors were synthesized by an integrated technology. The structural characterization showed that except the main lattice phase, only the characteristic peak of high-entropy alloys (HEAs) appeared in BMO/HEAs phosphors and the existence of lattice distortion for [MoO4]2- in BMO. The microstructure analysis confirmed that there is a special interface contact between BMO and HEAs, which makes the metal in HEAs easy to have a certain connection with BMO, which causes the lattice distortion of [MoO4]2- to intensify, thus accelerating the recombination rate of charge carriers in BMO/HEAs phosphors. The BMO/HEAs phosphors have a strong emission peak at 445 nm under the excitation wavelength of 285 nm. Theoretical calculations and experiments confirmed that the luminescence of BMO/HEAs phosphor is caused by the lattice distortion of [MoO4]2-, the interface defect of BMO/HEAs and the recombination of charge carriers. The Mo in HEA(Mo) can accelerate the recombination rate of charge carriers between BMO and HEAs, thus enhancing the luminescence performance of BMO/HEA(Mo) phosphor and exhibit dynamic fluorescence anti-counterfeiting applications. However, the Ti in HEA(Ti) and Al in HEA(Al) can easily separate the charge carriers between BMO and HEAs, thus reducing the luminescence of BMO/HEA(Ti) and BMO/HEA(Al) phosphors.

Opto/Thermoresponsive Multimode Luminescence in Eu- and Er-Activated CaF2 Phosphor for High-Security Anticounterfeiting.

As the landscape of information storage and security continues to evolve, the deployment of sophisticated anticounterfeiting strategies with robust security features and multimodal luminescent capabilities becomes imperative. In this work, Eu3+ and Er3+ ions are codoped into CaF2 phosphors to achieve multimodel optical output. The self-reduction of Eu3+ within the CaF2 matrix gives rise to the coexistence of Eu3+ and Eu2+ ions, which manifests as a color transition from orange to blue as the excitation wavelength is varied from 300 to 335 nm. Moreover, the distinct temperature-dependent behaviors of Eu3+ and Eu2+ ions underscore the material's visible temperature-sensitive luminescence properties, characterized by remarkable thermal sensitivity (Sa = 0.0156 K-1, Sr = 0.83%K-1). Additionally, the strategic introduction of Er3+ ions adds an extra dimension, enabling the realization of color-tunable upconversion luminescence through the fine-tuning of Er3+ concentration. This synergistic integration culminates in the establishment of an efficient three-path authentication model within the CaF2 host matrix, facilitating a dynamic multicolor response to changes in the excitation wavelength and temperature. By harnessing these diverse luminescent modalities, the study delivers a versatile and potent anticounterfeiting solution, advancing the frontiers of information security.

Multi-Wavelength Excitable Multicolor Upconversion and Ratiometric Luminescence Thermometry of Yb3+/Er3+ Co-Doped NaYGeO4 Microcrystals.

Excitation wavelength controllable lanthanide upconversion allows for real-time manipulation of luminescent color in a composition-fixed material, which has been proven to be conducive to a variety of applications, such as optical anti-counterfeiting and information security. However, current available materials highly rely on the elaborate core-shell structure in order to ensure efficient excitation-dependent energy transfer routes. Herein, multicolor upconversion luminescence in response to both near-infrared I and near-infrared II (NIR-I and NIR-II) excitations is realized in a novel but simple NaYGeO4:Yb3+/Er3+ phosphor. The remarkably enhanced red emission ratio under 1532 nm excitation, compared with that under 980 nm excitation, could be attributed to the Yb3+-mediated cross-relaxation energy transfers. Moreover, multi-wavelength excitable temperature-dependent (295-823 K) upconversion luminescence realizes a ratiometric thermometry relying on the thermally coupled levels (TCLs) of Er3+. Detailed investigations demonstrate that changing excitation wavelength makes little difference for the performances of TCL-based ratiometric thermometry of NaYGeO4:Yb3+/Er3+. These findings gain more insights to manipulate cross-relaxations for excitation controllable upconversion in single activator doped materials and benefit the cognition of the effect of excitation wavelength on ratiometric luminescence thermometry.

Structural, morphological and photoluminescence studies of Ca7Mg2P6O24:RE3+(RE3+= Tb3+, Dy3+) nanophosphor for solid state illumination

The Ca7Mg2P6O24:RE3+ (RE3+= Tb3+, Dy3+) nanophosphor material was synthesized by traditional wet chemical method. The XRD are used to determine phase and crystallinity of the synthesized sample; further FTIR, SEM, TEM, and PL properties were studied. The XRD pattern of prepared sample match well with standard JCPDS card no 00–020–0348, and it exhibits the rhombohedral structure along with space group R3c (161). The phosphate (PO4)3-group absorption band was observed at 990–1100 cm-1 in FTIR. Surface morphology (TEM analysis) reveals particle sizes in the range of 55–110 nm. The luminescence emission spectra of Ca7Mg2P6O24 phosphor activated by Tb3+ were studied at three different excitations: 352 nm, 370 nm, and 379 nm. The spectra show two emission peaks at 470 nm (blue) and 545 nm (green). These are due to the 5D4 → 7F6 and 5D4 → 7F5 transitions of Tb3+ ions. The highest intensity peak is located at 545 nm. The Ca7Mg2P6O24:Tb3+ phosphor's CIE chromaticity coordinates are (0.040, 0.316) at 491 nm and (0.265, 0.724) at 543 nm. These are in the blue and green areas on the edges of the CIE diagram, respectively. The photoluminescence emission spectra of Dy3+-doped Ca7Mg2P6O24 phosphor show two significant emission peaks located at 482 nm and 574 nm. These are caused by the 4F9/2 → 5H15/2 and 4F9/2 → 6H13/2 transitions of Dy3+ ions, which produce blue and yellow light, respectively, with an excitation wavelength of 350 nm. The sharp peak position at 482 nm produces the strongest emission. The effect of concentration quenching in between the Dy3+-Dy3+ions and Tb3+-Tb3+ ions is due to dipole-dipole interaction. The CIE color coordinate is found to be (0.082, 0.156) at 482 nm and (0.471, 0.527) at 574 nm which lies in blue and yellow border of CIE diagram. The lifespan of Tb3+, Dy3+activated Ca7Mg2P6O24 nanophosphor of highest concentration is found to be 1.917 ms and 0.9985 ms respectively. On investigation, the synthesized Tb3+, Dy3+activated Ca7Mg2P6O24 nanophosphor can be potential for solid lightning devices & other display application.