Effect of (Ce,Dy) co-doping on the microstructural,optical, and photoluminescence characteristics of solution combustion synthesized ZnO nanoparticles

Solution combustion synthesized ZnO nanoparticles that were Ce doped, Dy doped or co-doped at varying dopant concentrations were characterized for their microstructural, optical, and photoluminescence (PL) characteristics. The synthesized nanoparticles matched the standard hexagonal wurtzite structure of ZnO. The lattice fringes in the high-resolution transmission electron micrographs and the bright spotty rings in the selected area electron diffraction patterns authenticated the high crystallinity of the nanoparticles. The diffuse reflectance spectroscopy resolved the energy bandgap for the undoped ZnO as 3.18 eV, which decreased upon doping and co-doping. A sharp narrow ultraviolet emission peak at ~398 nm that originated from excitonic recombination was found in the PL spectra of the nanoparticles. The visible emission peaks in the PL spectra were assigned to the f–d and f–f electron transitions of Ce³⁺ and Dy³⁺ ions, respectively, in addition to different native defects in ZnO. The visible emissions (blue, yellow, and red) improved upon (Ce, Dy) co-doping, therefore (Ce, Dy) co-doped ZnO nanoparticles can be considered a promising luminescent material for the development of energy-saving light sources.     

Probing the optical properties and luminescence mechanism of a UV‐emitting SrBPO5:Ce3+ phosphor

Ce‐doped (1 × 10^?5 to 3.0 mol%) SrBPO₅ phosphors were synthesized using a conventional solid‐state reaction route at 1273 K in an air atmosphere. Phase and morphology of the samples were studied from powder X‐ray diffraction (XRD) patterns and scanning electron microscope (SEM) micrographs, respectively. The band gap energies of the pure and Ce‐doped SrBPO₅ phosphors were calculated from the recorded diffuse reflectance spectra. Photoluminescence (PL) and Ce³⁺ lifetime were recorded at 300 and 77 K. Photoluminescence lifetime measurements revealed two‐lifetime values for Ce³⁺ at both 300 K (17 and 36 nsec) and 77 K (12 and 30 nsec), suggesting the presence of two different environments around Ce³⁺. Time‐resolved emission spectroscopy (TRES) studies confirmed the presence of Ce³⁺ in two different environments. In addition, SrBPO₅:Ce exhibited intense UV emission, signifying its possible use as an efficient sensitizer for solid‐state lighting applications. The effect of γ‐irradiation on PL was also determined. Thermally stimulated luminescence (TSL) glow curves of the γ‐irradiated phosphor, along with trap parameters, dose–response, and the possible TSL mechanism were also investigated. Positron annihilation lifetime spectroscopy was carried out to probe defects present in undoped and Ce‐doped SrBPO₅.     

Luminescence investigation of a cerium‐doped yttrium vanadate phosphor

Cerium (Ce³⁺)‐doped (1, 3, and 7 mol%) yttrium vanadate phosphors were prepared using a co‐precipitation technique. The structural and optical properties of the synthesized samples were studied using X‐ray diffraction (XRD), Fourier transform infrared spectroscopy, scanning electron microscopy (SEM), high‐resolution transmission electron microscopy (HR‐TEM), optical absorption, and photoluminescence (PL) spectroscopy techniques. The tetragonal structure and the formation of the nanosized crystallites in the YVO₄:Ce phosphor were confirmed using XRD analysis. HR‐TEM morphology showed rod‐like nanoparticles of different sizes. Optical absorption spectra demonstrated strong absorption bands at 268 and 276 nm. PL spectra showed strong peaks at 546, 574, and 691 nm following excitation at 300 nm. The calculated CIE chromaticity coordinates demonstrated that YVO₄:Ce could be used as a novel phosphor for the development of light‐emitting diode lamps.     

Microwave‐assisted sintering synthesis of greenish‐yellow emitting Sr2SiO4:Eu2+ phosphors

Europium ion (Eu²⁺) doped Sr₂SiO₄ phosphors with greenish‐yellow emission were synthesized using microwave‐assisted sintering. The phase structure and photoluminescence (PL) properties of the obtained phosphor samples were investigated. The PL excitation spectra of the Sr₂SiO₄:Eu²⁺ phosphors exhibited a broad band in the range of 260 nm to 485 nm with a maximum at 361 nm attributed to the 5f‐4d allowed transition of the Eu²⁺ ions. Under an excitation at 361 nm, the Sr₂SiO₄:Eu²⁺ phosphor exhibited a greenish‐yellow emission peak at 541 nm with an International‐Commission‐on‐Illumination (CIE) chromaticity of (0.3064, 0.4772). The results suggest that the microwave‐assisted sintering method is promising for the synthesis of phosphors owing to the decreased sintering time without the use of additional reductive agents.     

Effect of capping agent concentration on thermoluminescence and photoluminescence of copper‐doped zinc sulfide nanoparticles

Copper‐doped zinc sulfide (ZnS:Cu) nanoparticles with varying concentrations of capping agent were prepared using a chemical route technique. These particles were characterized by scanning electron microscopy (SEM), transmission electron microscopy and X‐ray diffraction (XRD). Optical absorption studies showed that the absorption edge shifted towards the blue region as the concentration of the capping agent increased. Using effective mass approximation, calculation of the nanoparticle size indicated that effective band gap energy increases with decreasing particle size. The thermoluminescence (TL) properties of sodium hexameta phosphate (SHMP)‐passivated ZnS:Cu nanoparticles were investigated after UV irradiation at room temperature. The TL glow curve of capped ZnS:Cu showed variations in TL peak position and intensity with the change in capping agent concentration. The photoluminescence (PL) spectra of ZnS:Cu nanoparticles excited at 254 nm exhibited a broad green emission band peaking around 510 nm, which confirmed the characteristic feature of Zn²⁺ as well as Cu²⁺ ions as the luminescent centres in the lattice. The PL spectra of ZnS:Cu nanoparticles with increasing capping agent concentrations revealed that the emission becomes more intense and shifted towards shorter wavelengths as the sizes of the samples were reduced. Copyright © 2014 John Wiley & Sons, Ltd.     

Novel red colour emitting Ca0.995Mg2(SO4)3:0.5Eu2+ phosphor under ultraviolet,blue, and green excitation for plant growth LEDs

In the recent few years, Eu²⁺- and Mn⁴⁺-activated phosphors are widely used as potential colour converters for indoor plant cultivation lighting application due to their marvellous luminescence characteristics as well as low cost. In this investigation, we synthesized novel red colour-emitting Ca_(2−x)Mg₂(SO₄)₃:xmol% Eu²⁺ (x = 0–1.0 mol%) phosphors via a solid-state reaction method in a reducing atmosphere. The photoluminescence (PL) excitation spectra of synthesized phosphors exhibited a broad excitation band with three excitation bands peaking at 349 nm, 494 nm, and 554 nm. Under these excitations, emission spectra exhibited a broad band in the red colour region at ~634 nm. The PL emission intensity was measured for different concentrations of Eu²⁺. The maximum Eu²⁺ doping concentration in the Ca₂Mg₂(SO₄)₃ host was observed for 0.5 mol%. According to Dexter theory, it was determined that dipole–dipole interaction was responsible for the concentration quenching. The luminous red colour emission of the sample was confirmed using Commission international de l'eclairage colour coordinates. The results of PL excitation and emission spectra of the prepared phosphors were well matched with excitation and emission wavelengths of phytochrome P_R. Therefore, from the entire investigation and obtained results it was concluded that the synthesized Ca_0.995Mg₂(SO₄)₃:0.5mol%Eu²⁺ phosphor has huge potential for plant cultivation application.     

Rapid,controllable, one‐pot and room‐temperature aqueous synthesis of ZnO:Cu nanoparticles by pulsed UV laser and its application for photocatalytic degradation of methyl orange

Zinc oxide (ZnO) and ZnO:Cu nanoparticles (NPs) were synthesized using a rapid, controllable, one‐pot and room‐temperature pulsed UV‐laser assisted method. UV‐laser irradiation was used as an effective energy source in order to gain better control over the NPs size and morphology in aqueous media. Parameters effective in laser assisted synthesis of NPs such as irradiation time and laser shot repetition rate were optimized. Photoluminescence (PL) spectra of ZnO NPs showed a broad emission with two trap state peaks located at 442 and 485 nm related to electronic transition from zinc interstitial level (I_Zn) to zinc vacancy level (V_Zn) and electronic transition from conduction band to the oxygen vacancy level (V_O), respectively. For ZnO:Cu NPs, trap state emissions disappeared completely and a copper (Cu)‐related emission appeared. PL intensity of Cu‐related emission increased with the increase in concentration of Cu²⁺, so that for molar ratio of Cu:Zn 2%, optimal value of PL intensity was obtained. The photocatalytic activity of Cu‐doped ZnO revealed 50 and 100% increasement than that of undoped NPs under UV and visible irradiation, respectively. The enhanced photocatalytic activity could be attributed to smaller crystal size, as well as creation of impurity acceptor levels (T₂) inside the ZnO energy band gap.     

Synthesis and effect of Ce and Mn co‐doping on photoluminescence characteristics of Ca6AlP5O20:Eu novel phosphors

A series of Ca₆AlP₅O₂₀ doped with rare earths (Eu and Ce) and co‐doped (Eu, Ce and Eu,Mn) were prepared by combustion synthesis. Under Hg‐free excitation, Ca₆AlP₅O₂₀:Eu exhibited Eu²⁺ (486 nm) emission in the blue region of the spectrum and under near Hg excitation (245 nm), Ca₆AlP₅O₂₀:Ce phosphor exhibited Ce³⁺ emission (357 nm) in the UV range. Photoluminescence (PL) peak intensity increased in Ca₆AlP₅O₂₀:Eu,Ce and Ca₆AlP₅O₂₀:Eu, Mn phosphors due to co‐activators of Ce³⁺ and Mn²⁺ ions. As a result, these ions played an important role in PL emission in the present matrix. Ca₆AlP₅O₂₀:Eu, Ce and Ca₆AlP₅O₂₀:Eu, Mn phosphors provided energy transfer mechanisms via Ce³⁺ → Eu²⁺ and Eu²⁺ → Mn²⁺, respectively. Eu ions acted as activators and Ce ions acted as sensitizers. Ce emission energy was well matched with Eu excitation energy in the case of Ca₆AlP₅O₂₀:Eu, Ce and Eu ions acted as activators and Mn ions acted as sensitizers in Ca₆AlP₅O₂₀:Eu, Mn. This study included synthesis of new and efficient phosphate phosphors. The impact of doping and co‐doping on photoluminescence properties and energy transfer mechanisms were investigated and we propose a feasible interpretation. Copyright © 2012 John Wiley & Sons, Ltd.     

Thermoluminescence and photoluminescence studies on γ‐ray‐irradiated Ce3+,Tb3+‐doped potassium chloride single crystals

Single crystals of KCl doped with Ce³⁺,Tb³⁺ were grown using the Bridgeman–Stockbarger technique. Thermoluminescence (TL), optical absorption, photoluminescence (PL), photo‐stimulated luminescence (PSL), and thermal‐stimulated luminescence (TSL) properties were studied after γ‐ray irradiation at room temperature. The glow curve of the γ‐ray‐irradiated crystal exhibits three peaks at 420, 470 and 525 K. F‐Light bleaching (560 nm) leads to a drastic change in the TL glow curve. The optical absorption measurements indicate that F‐ and V‐centres are formed in the crystal during γ‐ray irradiation. It was attempted to incorporate a broad band of cerium activator into the narrow band of terbium in the KCl host without a reduction in the emission intensity. Cerium co‐doped KCl:Tb crystals showed broad band emission due to the d–f transition of cerium and a reduction in the intensity of the emission peak due to ⁵D₃–⁷F_j (j = 3, 4) transition of terbium, when excited at 330 nm. These results support that energy transfer occurs from cerium to terbium in the KCl host. Co‐doping Ce³⁺ ions greatly intensified the excitation peak at 339 nm for the emission at 400 nm of Tb³⁺. The emission due to Tb³⁺ ions was confirmed by PSL and TSL spectra. Copyright © 2015 John Wiley & Sons, Ltd.     

5d–4f transition in new phosphate‐based phosphors

The preparation of Ce³⁺‐doped Sr₆AlP₅O₂₀ and Ba₆AlP₅O₂₀ by a combustion method is described. Formation of compounds was confirmed by X‐ray diffraction (XRD) analysis. The photoluminescence (PL) emission spectra were observed at 355 nm when excited at 307 nm for the various concentrations. The PL emission spectra of phosphors showed strong Ce³⁺ emission due to the 5 d → 4f transition of Ce³⁺ ions. The Ce³⁺ emission intensity in Sr₆AlP₅O₂₀:Ce phosphor was higher than that in Ba₆AlP₅O₂₀:Ce and it may be useful for scintillation applications. Copyright © 2011 John Wiley & Sons, Ltd.     

Photo and thermoluminescence of KMgSO4F: Ce and :Mn phosphors

KMgSO₄F:Ce and KMgSO₄F:Mn phosphors were prepared by a wet chemical method and studied for their photoluminescence (PL) and thermoluminescence (TL) characteristics. PL emission of KMgSO₄F:Ce peaked at around 440 nm for the excitation at 377 nm due to 5d → 4f transition, while KMgSO₄F:Mn had a peak at 540 nm for an excitation at 363 nm and 247 nm due to ⁴T_1g → ⁶A_1g transition. The phosphors also showed good thermoluminescence characteristics when they were exposed to γ‐rays at a 5 Gy dose at the rate of 0.36 kGyh^?1. KMgSO₄F:Ce exhibited a single thermoluminescence (TL) peak at around 167 °C and KMgSO₄F:Mn also exhibited a single TL peak at around 177 °C. Possible trapping parameters such as order of kinetics (b), the geometrical factor (μ_g), the frequency factor (s) and the activation energy were also evaluated by Chen's half width method. This article discusses fundamental PL and TL characteristics in inorganic fluoride material activated by Ce³⁺ and Mn²⁺ ions and prepared by a wet chemical method. Copyright © 2014 John Wiley & Sons, Ltd.     

Characterization and luminescence properties of CaMgSi2O6:Eu2+ blue phosphor

A blue CaMgSi₂O₆:Eu²⁺ phosphor was prepared by the solid‐state reaction method and the phosphor characterized in terms of crystal structure, particle size, photoluminescence (PL), thermoluminescence (TL) and mechanoluminescence (ML) properties using X‐ray diffraction (XRD), transmission electron microscopy (TEM), PL spectroscopy, TLD reader and ML impact technique. The XRD result shows that phosphor is formed in a single phase and has a monoclinic structure with the space group C2/c. Furthermore, the PL excitation spectra of Eu²⁺‐doped CaMgSi₂O₆ phosphor showed a strong band peak at 356 nm and the PL emission spectrum has a peak at 450 nm. The depths and frequency factors of trap centers were calculated using the TL glow curve by deconvolution method in which the trap depths were found to be 0.48 and 0.61 eV. The formation of CaMgSi₂O₆:Eu²⁺ phosphor was confirmed by Fourier transform infrared spectroscopy. The ML intensity increased linearly with the impact velocity of the piston used to deform the phosphor. It was shown that the local piezoelectricity‐induced electron bombardment model is responsible for the ML emission. Finally, the optical properties of CaMgSi₂O₆:Eu²⁺ phosphors are discussed. Copyright © 2015 John Wiley & Sons, Ltd.     

Luminescence study on Mn,Ni co‐doped zinc sulfide nanocrystals

Zinc sulfide (ZnS) doped with transition metal has been used as phosphor for various optoelectronic applications. In the present report, ZnS:Mn doped and ZnS:Mn,Ni co‐doped were prepared using chemical co‐precipitation method using polyvinyl pyrolidone as a surfactant. The structural studies were carried out using an X‐ray diffraction technique; optical studies have been performed using ultraviolet–visible light absorption and photoluminescence (PL) spectroscopy. The presences of functional groups were confirmed using Fourier transform infrared spectroscopy. The X‐ray diffraction study and Reitveld analysis confirms the formation of cubic phase with crystalline size 2–3 nm for undoped and doped ZnS nanoparticles. A novel and enhanced luminescence characteristic have been observed in PL spectra. The luminescence intensity of Mn,Ni co‐doped ZnS in the blue region is much higher of that of ZnS. The PL results indicate that the doping of Ni creates shallow trap states or luminescence centres in the forbidden energy gap, which quenches the Mn states emission. Concentration quenching has been observed in Mn‐doped ZnS nanoparticles. From CIE coordinates, it is seen that the yellow and blue light emission of ZnS:Mn,Ni co‐doped nanophosphor may be a promising candidate for display devices and phosphor converted light‐emitting diode applications.     

Novel Na+ doped Alq3 hybrid materials for organic light‐emitting diode (OLED) devices and flat panel displays

Pure and Na⁺‐doped Alq₃ complexes were synthesized by a simple precipitation method at room temperature, maintaining a stoichiometric ratio. These complexes were characterized by X‐ray diffraction, Fourier transform infrared (FTIR), UV/Vis absorption and photoluminescence (PL) spectra. The X‐ray diffractogram exhibits well‐resolved peaks, revealing the crystalline nature of the synthesized complexes, FTIR confirms the molecular structure and the completion of quinoline ring formation in the metal complex. UV/Vis absorption and PL spectra of sodium‐doped Alq₃ complexes exhibit high emission intensity in comparison with Alq₃ phosphor, proving that when doped in Alq₃, Na⁺ enhances PL emission intensity. The excitation spectra of the synthesized complexes lie in the range 242–457 nm when weak shoulders are also considered. Because the sharp excitation peak falls in the blue region of visible radiation, the complexes can be employed for blue chip excitation. The emission wavelength of all the synthesized complexes lies in the bluish green/green region ranging between 485 and 531 nm. The intensity of the emission wavelength was found to be elevated when Na⁺ is doped into Alq₃. Because both the excitation and emission wavelengths fall in the visible region of electromagnetic radiation, these phosphors can also be employed to improve the power conversion efficiency of photovoltaic cells by using the solar spectral conversion principle. Thus, the synthesized phosphors can be used as bluish green/green light‐emitting phosphors for organic light‐emitting diodes, flat panel displays, solid‐state lighting technology – a step towards the desire to reduce energy consumption and generate pollution free light. Copyright © 2014 John Wiley & Sons, Ltd.     

Optical properties of CaAl(SO4)2Br:RE (RE = Dy,Eu, Ce) novel phosphors

A new phosphor CaAl(SO₄)₂Br doped with Dy, Ce and Eu is reported. Rare earth (Dy, Eu and Ce)‐doped polycrystalline CaAl(SO₄)₂Br phosphors were prepared using a wet chemical reaction method and studied for X‐ray diffraction and photoluminescence (PL) characteristics. Dy³⁺ emission in the CaAl(SO₄)₂Br lattice was observed at 484 and 574 nm in the blue and yellow regions of the spectrum, which are assigned to ⁴ F_9/2 → ⁶H_15/2 and ⁴ F_9/2 → ⁶H_13/2 transitions of the Dy³⁺ ion, respectively. While the PL emission spectra of CaAl(SO₄)₂Br:Ce phosphor showed Ce³⁺ emission at 347 nm due to 5d → 4f transition of the Ce³⁺ ion. In a CaAl(SO₄)₂Br:Eu lattice, Eu³⁺ emissions were observed at 593 and 617 nm, coming from the ⁵D₀ → ⁷ F₁ and ⁵D₀ → ⁷ F₂ electron transitions, respectively. The PL study showed that the intensity of electric dipole transition at 617 nm dominates over that of magnetic dipole transition at 590 nm. The maximum PL intensity was obtained for a 1 mol% concentration of Eu³⁺ in CaAl(SO₄)₂Br host lattice. The results showed that the material may be a promising candidate as a blue‐, yellow‐ and red‐emitting phosphor. Copyright © 2013 John Wiley & Sons, Ltd.     

Structural characterization of Er3+,Yb3+‐doped Gd2O3 phosphor,synthesized using the solid‐state reaction method,and its luminescence behavior

We report the synthesis and structural characterization of Er³⁺,Yb³⁺‐doped Gd₂O₃ phosphor. The sample was prepared using the conventional solid‐state reaction method, which is the most suitable method for large‐scale production. The prepared phosphor sample was characterized using X‐ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), thermoluminescence (TL), photoluminescence (PL) and CIE techniques. For PL studies, the excitation and emission spectra of Gd₂O₃ phosphor doped with Er³⁺ and Yb³⁺ were recorded. The excitation spectrum was recorded at a wavelength of 551 nm and showed an intense peak at 276 nm. The emission spectrum was recorded at 276 nm excitation and showed peaks in all blue, green and red regions, which indicate that the prepared phosphor may act as a single host for white light‐emitting diode (WLED) applications, as verified by International de I'Eclairage (CIE) techniques. From the XRD data, the calculated average crystallite size of Er³⁺ and Yb³⁺‐doped Gd₂O₃ phosphor is ~ 38 nm. A TL study was carried out for the phosphor using UV irradiation. The TL glow curve was recorded for UV, beta and gamma irradiations, and the kinetic parameters were also calculated. In addition, the trap parameters of the prepared phosphor were also studied using computerized glow curve deconvolution (CGCD). Copyright © 2015 John Wiley & Sons, Ltd.     

An alternative pathway of light-induced transmembrane electron transfer in photosynthetic reaction centers of <Emphasis Type="Italic">Rhodobacter sphaeroides</Emphasis>

In the absorption spectrum of Rhodobacter sphaeroides reaction centers, a minor absorption band was found with a maximum at 1053 nm. The amplitude of this band is ~10,000 times less and its half-width is comparable to that of the long-wavelength absorption band of the primary electron donor P₈₇₀. When the primary electron donor is excited by femtosecond light pulses at 870 nm, the absorption band at 1053 nm is increased manifold during the earliest stages of charge separation. The growth of this absorption band in difference absorption spectra precedes the appearance of stimulated emission at 935 nm and the appearance of the absorption band of anion-radical B_A ^– at 1020 nm, reported earlier by several researchers. When reaction centers are illuminated with 1064 nm light, the absorption spectrum undergoes changes indicating reduction of the primary electron acceptor Q_A, with the primary electron donor P₈₇₀ remaining neutral. These photoinduced absorption changes reflect the formation of the long-lived radical state PB_AH_AQ_A ^–.     

Photoluminescence of Dy3+ activator sensitized by Ce3+ in KNaSO4 microphosphor

The KNaSO₄ microphosphor doped with Ce or Ce and Dy prepared by a wet chemical method was studied by scanning electron microscopy (SEM) and characterized by photoluminescence (PL). KNaSO₄ has a 5‐µm particle size detected by SEM. The KNaSO₄:Ce³⁺ spectrum shows a single emission band at 327 nm for an excitation of 269 nm due to 5d → 4f transition of the Ce³⁺ ion, indicating weak spin orbiting coupling of the Ce³⁺ ground state. Efficient energy transfer takes place from Ce³⁺ → Dy³⁺ sublattices indicating that Ce³⁺ could effectively sensitize Dy³⁺ (orange emission) and that the Ce³⁺ emission weakens significantly in KNaSO₄. The powder form of prepared KNaSO₄ show negligible change in morphologies and hence no effect on the particle size. The characteristics of this powder could provide improved luminescence properties. The development and understanding of this photoluminescence and the effect of Dy³⁺ on KNaSO₄: Ce³⁺ are discussed. Copyright © 2014 John Wiley & Sons, Ltd.     

Luminescence characteristics of Na3Ca2(SO4)3F: Ce3+ fluoride material

A new Na₃Ca₂(SO₄)₃F: Ce³⁺ phosphor synthesized by a solid state diffusion method is reported. The photoluminescence study showed a single high intensity emission peak at 307 nm wavelength when excited by UV light of wavelength 278 nm. An unresolved peak of comparatively less intensity was also observed at 357 nm along with the main peak. The characteristic emission of dopant Ce in Na₃Ca₂(SO₄)₃F phosphor clearly indicated that it resides in the host lattice in trivalent form. The emission peak can be attributed to 5d → 4f transition of rare earth Ce³⁺. The prepared sample is also characterized for its thermoluminescence properties. The TL glow curve of prepared sample showed a single broad peak at 147°C. The trapping parameters are also evaluated by Chen's method. The values of trap depth (E) and frequency factor (s) were found to be 0.64 ± 0.002 eV and 1.43 × 10⁷ s^–1 respectively. The study of PL and TL along with evaluation of trapping parameters has been undertaken and discussed for the first time. Copyright © 2014 John Wiley & Sons, Ltd.     

Synthesis and characterization of pure and Li+ activated Alq3 complexes for green and blue organic light emitting diodes and display devices

Pure and Li⁺‐doped Alq₃ complexes were synthesized by simple precipitation method at room temperature, maintaining the stoichiometric ratio. These complexes were characterized by X‐ray diffraction, ultraviolet‐visible absorption and Fourier transform infrared and photoluminescence (PL) spectra. X‐ray diffraction analysis reveals the crystalline nature of the synthesized complexes, while Fourier transform infrared spectroscopy confirm the molecular structure, the completion of quinoline ring formation and presence of quinoline structure in the metal complex. Ultraviolet‐visible and PL spectra revealed that Li⁺ activated Alq₃ complexes exhibit the highest intensity in comparison to pure Alq₃ phosphor. Thus, Li⁺ enhances PL emission intensity when doped into Alq₃ phosphor. The excitation spectra lie in the range of 383–456 nm. All the synthesized complexes other than Liq give green emission, while Liq gives blue emission with enhanced intensity. Thus, he synthesized phosphors are the best suitable candidates for green‐ and blue‐emitting organic light emitting diode, PL liquid‐crystal display and solid‐state lighting applications. Copyright © 2013 John Wiley & Sons, Ltd.