Realization of a green-emitting pyrosilicate-structured Er3+-activated Y2Si2O7 phosphor: a systematic study of opto-electronic characteristics and thermal stability for lighting applications.

A series of green-emitting Y2-x Si2O7:xEr3+ phosphors (x = 1-7 mol%) have been successfully synthesized using a straightforward gel-combustion method facilitated by urea. X-ray diffraction analysis provided specific patterns for samples, confirming a consistent triclinic phase across erbium-doped structures compared to undoped structures. Studies using TEM and EDX were conducted to identify the surface-related characteristics and chemical composition of the synthesized nanophosphor, respectively. The band gap was determined to be 5.55 eV and 5.80 eV for the host material and optimal sample, respectively. The primary peak of excitation, observed at 379 nm, represents the highly sensitive electric dipole transition from the 4I15/2 state to the 4G11/2 level, suggesting that the prepared phosphors could effectively absorb NUV light for activation. The PL profiles of Y2-x Si2O7:xEr3+ (x = 1-7 mol%) phosphors demonstrate characteristic emissions at 409 nm (2H9/2 → 4I15/2), 522 nm (2H11/2 → 4I15/2), 553 nm (4S3/2 → 4I15/2) and 662 nm (4F9/2 → 4I15/2). In accordance with Dexter's theory, luminescence quenching observed at a concentration of 4 mol% Er3+ is attributed to dipole-quadrupole interactions. The optimal sample demonstrates excellent thermal stability, indicated by its luminescence at different temperatures and activation energy of 0.2641 eV. Additionally, the CIE, color purity and CCT values of the fabricated nanomaterials make it ideal for use in lighting applications.

Structural, morphological, and optical characteristics of Gd2 Si2 O7 :Dy3+ nanophosphors for WLEDs.

Yellowish-white light-emitting Gd2-x Si2 O7 :xDy3+ (x = 1-5 mol%) nanophosphors were prepared using a solution combustion synthesis method. Fluorescence spectrophotometry and X-ray diffraction measurements were performed to scrutinize the optical performances and phase recognition of the designated nanophosphors. The outcomes specified that the prepared phosphors were crystallized into a triclinic phase with a P-1 space group. As the concentration of Dy3+ ions was increased, the unit-cell volume decrease proportionally due to the replacement of large-sized Gd3+ by small-sized Dy3+ ions. Under ultraviolet excitation at 349 nm, emission spectra consisted of two pronounced emission lines at ~482 nm (blue line), ~578 nm (yellow line), and a relatively weaker emission at ~670 nm (red line) due to 4 F9/2 →6 H15/2 , 4 F9/2 →6 H13/2 , and 4 F9/2 →6 H11/2 intraconfigurational transitions of Dy3+ ions, respectively. The evidence about the site symmetry around Dy3+ ions was examined by considering the ratio of yellow-to-blue emission intensity. The observed critical distance (Rc ) value was ~20.56 Å (≫5 Å), which signified that energy transfer primarily occurred due to multipolar interaction. The obtained coordinates were close to the white region of the Commission Internationale de l'Éclairage chromaticity diagram, which marked a significant milestone in the development of white light-emitting diodes.

Combustion derived single phase Y4Al2O9:Tb3+ nanophosphor: crystal chemistry and optical analysis for solid state lighting applications.

Cool green light emanating monoclinic Y4-x Al2O9:xTb3+ (x = 1-5 mol%) nanophosphors have been fabricated through gel-combustion method. X-ray diffraction and transmission electron-microscopy data have been utilized to assess their structural and microstructural characteristics, including cell parameters and crystallite size. Uneven aggregation of nanoparticles in the nano-scale with distinctive porosity can be seen in the TEM micrograph. Kubelka-Munk model imitative diffuse reflectance spectra and an optical band gap of 5.67 eV for the Y3.97Al2O9:0.03Tb3+ nanophosphor revealed high optical quality in the samples, which were thought to be non-conducting. The emission (PL) and excitation (PLE) spectra as well as lifetime measurements have been used to determine the luminescence characteristics of the synthesized nanophosphors. The emission spectra show two color i.e. blue color due to 5D3 → 7F J (J = 4 and 5) transitions and green color due to 5D4 → 7F J (J = 3, 4, 5 and 6) transitions. The most dominant transition (5D4 → 7F5) at 548 nm was responsible for the greenish color in focused nanocrystalline samples. Calculated colorimetric characteristics such as CIE, and CCT along with color purity of the synthesized nanocrystalline materials make them the best candidate for the solid-state lighting (SSL).

Crystallographic, morphological and photoluminescent investigations of Tb3+ -doped YAlO3 perovskites for lighting applications.

Terbium(III)-doped yttrium aluminate perovskite (YAP:xTb3+ ) (x = 0.01-0.08 mol) was synthesized using a simple gel-combustion method. Structural elucidations were performed using X-ray diffraction (XRD) and Rietveld analysis. Fourier-transform infrared spectral studies validated the efficient synthesis of designed doped samples. Transmission electron microscopic images showed the agglomerated irregular dimensions of the synthesized nanocrystalline materials. When excited at 251 nm, a strong emissive line attributed to 5 D4 → 7 F5 electronic transition was observed at 545 nm (green emission). The maximum luminescence was found at the optimized concentration (0.05 mol) of Tb3+ ions; this emission was quenched by dipolar-dipolar (d-d) interactions. Chromaticity (x and y) and correlated colour temperature parameters were obtained by analysing the emission profiles. Finally, the colour coordinates of nanophosphors were closer to the National Television Standards Committee green coordinates, which replicates their potency in the design and architecture of R-G-B-based white LEDs.

Luminous LaAlO3 :Dy3+ perovskite nanomaterials: Synthesis, structural, and luminescence characteristics for white light-emitting diodes.

A single-phase perovskite LaAlO3 :Dy3+ phosphor was synthesized using a gel-combustion method at 600°C utilization with hexamethylenetetramine as a fuel. Further calcination of the samples was carried out (800 and 1000°C) to investigate the resultant effect on the crystalline and luminescence behaviour. The crystal structure had a cubic unit cell (space group Pm3̅m) and was examined using the Rietveld refinement and X-ray diffraction data. Additionally, Debye-Scherrer and Williamson-Hall equations were applied to determine other structural features. The particle size and morphology of phosphors were evaluated using transmission electron microscopy. Diffraction measurements were supported by the various metal-oxygen vibration modes studied with the help of Fourier transform infrared spectroscopy. Energy-dispersive X-ray analysis verified the chemical composition of synthesized sample. Luminescence spectra of the LaAlO3 :Dy3+ phosphors exhibited intense bands for 4 F9/2 →6 H15/2 (482 nm, bluish region) and 4 F9/2 →6 H13/2 (574 nm, yellowish region) transitions. Commission Internationale de L'Eclairage and correlated colour temperature data confirmed the cool-white emission of the samples under ultraviolet light excitation. The interesting and advantageous luminescence characteristics of LaAlO3 :Dy3+ phosphors make them potential materials for white light-emitting diodes.

Emerging green light emission of Er3+ -activated single phased GdAlO3 phosphors for lighting applications.

An erbium ion (Er3+ )-activated gadolinium aluminate (GdAlO3 ) nanophosphor was synthesized by utilizing urea assisted gel-combustion method. The crystal structure along with all other crystal parameters was determined by X-ray diffraction (XRD) patterns. The selected samples are of orthorhombic phase with Pnma space group. The agglomerated particles within nanorange have been confirmed by transmission electron microscopy (TEM) micrographs. Elemental investigation was performed by energy dispersive X-ray spectroscopy (EDX). Photoluminescence excitation (PLE) spectrum reveals a strong excitation band corresponding to the gadolinium ion (Gd3+ ) (276 nm) and a band near ultraviolet (UV) absorption for Er3+ (377 nm). Strong excitation band of Gd3+ was evident for the energy transfer between Gd3+ and Er3+ ions. All the doped sampled are excited at 377 nm wavelength. The photoluminescence (PL) spectrum exhibits an intense band at 546 nm (4 S3/2 → 4 I15/2 ) which is responsible for the green emission in the processed samples. The color coordinate values define their color in the green region and correlated color temperature (CCT) values affirm their utility as a cold light source.

Red-emitting ß-diketonate Eu(III) Complexes With Substituted 1,10-phenanthroline Derivatives: Optoelectronic and Spectroscopic Analysis.

A series of europium diketonate complexes with 1-phenyl-1,3-butanedione (PBD) and 1,10-phenanthroline derivatives were synthesized and explored spectroscopically. Photophysical characteristics of synthesized complexes have been investigated experimentally as well as theoretically. Photoluminescence emission spectra of complexes do not contain any peak of ligand revealing efficient transferal of energy from ligand to Eu3+ ion. Presence of peak at 611 nm corresponding to 5D0 → 7F2 transition is responsible for red emanation of ternary europium complexes. Photophysical parameters viz., Judd-Ofelt, quantum efficiency, radiative and non radiative decay rates were also estimated theoretically from LUMPAC software. Geometry optimization of complexes was done via Avogadro software. All synthesized trivalent complexes exhibit red emission which was further sustained by the position of chromaticity coordinates in CIE triangle. These red emanating materials could be utilized in designing electroluminescent display devices.

Synthesis, Optoelectronic and Photoluminescent Characterizations of Green Luminous Heteroleptic Ternary Terbium Complexes.

This article presents four ternary terbium complexes based on fluorinated 2-thenoyltrifluoroacetone (TTFA) and N donor bidentate neutral ligands. The prepared complexes were examined by elemental study, electrochemical analysis, spectroscopically and thermo-gravimetrically. Spectral analysis shows the bonding of Tb3+ ion with oxygen and nitrogen atom of diketone and neutral ligand respectively. Upon excitation in UV region, synthesized terbium complexes show luminescence in green region of electromagnetic spectrum. Photoluminescence emission spectra of complexes do not show any ligand based peak suggesting the effective transferal of energy from ligand to metal ion. Green emanation by terbium complexes is owing to intense peak ~547 nm (5D4 → 7F5). The outcome of emission data and CIE coordinates correlate with each other and affirms the utility of green luminous complexes as potential emissive material for optoelectronic gadgets applied in lighting system.

Photoluminescence and structural analysis of trivalent europium doped MLaAl3 O7 (M = Ba, Ca, Mg and Sr) nanophosphors.

The solution combustion technique was used to synthesize MLaAl3 O7 (M = Ba, Ca, Mg, and Sr) nanophosphors-doped with Eu3+ using metal nitrates as precursors. The photoluminescence (PL) emission spectra exhibited three peaks at 587-591, 610-616, and 653-654 corresponding to 5 D0 →7 F1 , 5 D0 →7 F2 , and 5 D0 →7 F3 transitions, respectively. Upon excitation at 254 nm, these nanophosphors displayed strong red emission with the dominant peak attributed to the 5 D0 →7 F2 transition of Eu3+ . The materials were further heated at 900 and 1050°C for 2 h to examine the consequence of temperature on crystal lattice and PL emission intensity. X-ray diffraction (XRD) analysis proved that all the synthesized materials were of a crystalline nature. CaLaAl3 O7 material has a tetragonal crystal structure with space group P421m. Scherer's equation was used to calculate the crystallite size of synthesized phosphors using XRD data. A Fourier transformation infrared study was used to observe the stretching vibrations of metal-oxygen bonds. Infrared peaks for stretching vibrations corresponding to lanthanum-oxygen and aluminium-oxygen bonds were found at 582 and 777 cm-1 respectively for CaLaAl3 O7 phosphor material. Transmission electron microscopy images were used to determine the size of particles (18-37 nm for the as-prepared materials) and also to analyze the three-dimensional view of these materials. The experimental data indicate that these materials may be promising red-emitting nanophosphors for use in white light-emitting diodes.