Yellow‐Emitting Y3Si6N11: Ce3+ Phosphors for White Light–Emitting Diodes (LEDs)

A novel Y_3?xSi₆N₁₁: xCe³⁺ yellow phosphor was synthesized using the carbothermal reduction and nitridition method at 1550°C for 16 h in this letter. Photoluminescence spectra indicated that the phosphor showed broad excitation spectrum and had strong absorption in range of 350–450 nm. It also gave a broad emission band (Full width at half maximum = 153 nm) centered at 575 nm under 425‐nm excitation. With increasing Ce³⁺ concentration, the strongest emission intensity was obtained at 5 mol% Ce³⁺ doping amount and a systematic redshift was observed as the Ce³⁺ concentration increased. The results indicate that this novel yellow phosphor is a promising candidate for using in blue‐chip‐excited white light–emitting diodes (LEDs).     

Eu3+‐doped glass as a color rendering index enhancer in phosphor‐in‐glass

A new method for improving color rendering index (CRI) and low correlated color temperature (CCT) in high‐power white‐light‐emitting diodes (WLEDs) is proposed. We used a configuration of phosphor‐in‐glass (PIG) and studied light output changes with the increment in concentration of yellow‐emitting Y₃Al₅O₁₂:Ce³⁺ (YAG:Ce³⁺) phosphor. The PIG was coupled on the top of blue‐light‐emitting diodes (LED) chip (465 nm). To compensate the lack of red emission in the phosphor, Eu³⁺‐doped tellurium glass with different europium content was employed as a red emitter. The suitable contents of YAG:Ce³⁺ and Eu³⁺ were 7.5 weight percent (wt%) and 3 mol percent (mol%), respectively. The CRI value went from 72 to 82, whereas the CCT was reduced from 24 933 to 6434 K. The proposed structure can improve CCT as well as CRI of WLEDs just by placing a glass on top.     

Ce3+‐ and Dy3+‐Doped Oxyfluoride Borosilicate Glasses with Near White Luminescence

A series of Ce³⁺/Dy³⁺‐doped oxyfluoride borosilicate glasses prepared by melt‐quenching method are investigated for light‐emitting diodes applications. These glasses are studied via X‐ray diffraction (XRD), optical absorption, photoluminescence (PL), color coordinate, and Fourier transform infrared (FT‐IR) spectra. We find that the absorption and emission bands of Ce³⁺ ions move to the longer wavelengths with increasing Ce³⁺ concentrations and decreasing B₂O₃ and Al₂O₃ contents in the glass compositions. We also discover the emission behavior of Ce³⁺ ions is dependent on the excitation wavelengths. The glass structure variations with changing glass compositions are examined using the FT‐IR spectra. The influence of glass network structure on the luminescence of Ce³⁺/Dy³⁺ codoped glasses is studied. Furthermore, the near‐ideal white light emission (color coordinate x = 0.32, y = 0.32) from the Ce³⁺/Dy³⁺ codoped glasses excited at 350 nm UV light is realized.     

Cooperative cation substitution facilitated construction of garnet oxynitride MgY2Al3Si2O11N:Ce3+ for white LEDs

Structural modification is an important means to induce redshift of Ce³⁺ emission in garnet phosphor. We intend to design and synthesize garnet oxynitride compounds which combine attributes of rigidity inherited from garnet structure and of high covalence characteristic of oxynitride compounds. However, impurity phase usually occurs in the nitridation of garnet phosphor, due to the low solubility of nitrogen in oxides. We herein exploit the cooperative cation substitution strategy to facilitate the incorporation of nitrogen in Y₃Al₅O₁₂. It is found that partial substitution of Y³⁺‐Al_tet³⁺ pairs by Mg²⁺‐Si⁴⁺ pairs can diminish the phase instability caused by the replacement of Al_tet³⁺‐O^2? by Si⁴⁺‐N^3?. A novel pure garnet phase oxynitride phosphor MgY₂Al₃Si₂O₁₁N:Ce³⁺ with a higher substitution content of N has been obtained and the successful incorporation of N in the garnet phosphor is confirmed by the Rietveld refinements of XRD, XPS, and TEM. The emission and excitation spectra indicate that the blue‐light‐excitable MgY₂Al₃Si₂O₁₁N:Ce³⁺ phosphor exhibited a bright yellow‐orange emission peaking at 570 nm, which is redshifted by 28 nm when compared to YAG:Ce³⁺. The garnet oxynitride phosphor exhibit excellent thermal stability with high quantum efficiency and is a promising candidate for warm white LED.     

Dy3+/Ce3+ Codoped YAG Transparent Ceramics for Single‐Composition Tunable White‐Light Phosphor

Superior optical, thermal, and mechanical properties of transparent ceramics are very important in the applications of solid lasers, solid‐state lighting, and transparent armors. Herein, a series of (Dy_0.03Ce_xY_0.97?x)₃Al₅O₁₂ transparent ceramics were fabricated using vacuum reactive sintering method. Importantly, these Dy³⁺/Ce³⁺ codoped yttrium aluminum garnet (YAG) transparent ceramics served as single‐composition tunable white‐light phosphors for UV‐LEDs is developed for the first time. By combining with commercially available UV‐LEDs directly, the optimal chromaticity coordinates and correlated color temperature (CCT) are (x = 0.33, y = 0.35) and 5609 K, respectively. Notably, the codoping of Ce³⁺ enhances the luminescent intensity of Dy³⁺ ions while excited at 327 nm. The emission color of YAG transparent ceramics can be tuned from white to yellow through energy transfer between Dy³⁺ and Ce³⁺. These new phosphors, possessing of pure CIE chromaticity and environmentally friendly nature, are promising for applications in white UV‐LEDs.     

The Investigations of the Pr,Gd, Si–N Doping,and Phosphor Curvature Effects on the Performances of YAG‐Based WLEDs

The effect of the phosphor curvature in the range 0.1766–0.2589 mm^?1 on the luminous efficacy of Y_2.95Al₅O₁₂:0.05Ce³⁺ (YAG)‐based white‐light‐emitting diodes (WLEDs) was investigated at the similar correlated color temperature (CCT) of ~6300 K by tuning the concentration of YAG phosphors in the phosphor layer ranging from 7.5 to 15 wt%. It was found that both the luminous efficacy and luminous power increased monotonically with the increasing curvature. The luminous efficacy (=82.4 lm/W) and luminous power (=297.85 mW) of the YAG‐based WLED at the preferable phosphor curvature of 0.2589 mm^?1 were 19.44% and 17.36%, respectively, higher than those at the curvature of 0.1766 mm^?1 under 350 mA. This finding reveals that the surface curvature of phosphor layers is a critical factor which cannot be ignored for the investigation of the light output of phosphor‐converted WLEDs. Moreover, the color rendering index (CRI) enhancement of YAG‐based WLED with substitution of Y_2.94Al₅O₁₂:0.05Ce³⁺, 0.01Pr³⁺ (YPrAG), Y_2.45Gd_0.5Al₅O₁₂:0.05Ce³⁺ (YGdAG), and Y_2.95Al_4.8Si_0.2O_11.8N_0.2:0.05Ce³⁺ (YAlSiON) for YAG were assessed under the same phosphor curvature of 0.2589 mm^?1 and the similar CCT ~6350 K. Taking the luminous efficacy, preparation cost of phosphors, and CRI into consideration, we suggest that the YGdAG is a preferable candidate for replacing the YAG for use in WLEDs among the four kinds of phosphors. Compared with the YAG (7.5 wt%)‐based WLED, the YGdAG (7 wt%)‐based WLED exhibited an improved CRI, less preparation cost of phosphors, and the acceptable reduction in luminous efficacy under 350 mA.     

Crystal Structure and Optical Performance of Al3+ and Ce3+ Codoped Ca3Sc2Si3O12 Green Phosphors for White LEDs

Ca₃Sc₂Si₃O₁₂:Ce³⁺ (CSS:Ce) green phosphors used for white light‐emitting diodes (LEDs) are synthesized and codoped with Al³⁺ via a solid‐state reaction method. The crystal structure and vibrational modes are analyzed by X‐ray diffraction, Fourier transform infrared spectroscopy, and Raman scattering spectroscopy. The energy transfer behavior and optical performance are characterized by photoluminescence and excitation spectra, quantum efficiency, and time‐resolved photoluminescence. The incorporation of Al³⁺ into CSS:Ce can inhibit the formation of the impurity phases Sc₂O₃ and CeO₂, improve crystallinity, and enhance the photoluminescence intensity as well as quantum efficiency. The substitution of Sc³⁺ with Al³⁺ increased the crystal field splitting of Ce³⁺ and resulted in the red shift of photoluminescence. The results show that Ca₃Sc_2?xAl_xSi₃O₁₂:Ce³⁺ has high quantum efficiency, making it a promising green phosphor that can be collocated with a commercial 450 nm blue LED and a red phosphor for solid‐state lighting applications.     

Impact of Eu3+ Dopants on Optical Spectroscopy of Ce3+: Y3Al5O12‐Embedded Transparent Glass‐Ceramics

Transparent glass‐ceramics containing Ce³⁺: Y₃Al₅O₁₂ phosphors and Eu³⁺ ions were successfully fabricated by a low‐temperature co‐sintering technique to explore their potential application in white light‐emitting diodes (WLEDs). Microstructure of the sample was studied using a scanning electron microscope equipped with an energy dispersive X‐ray spectroscopy. The impact of co‐sintering temperature, Ce³⁺: Y₃Al₅O₁₂ crystal content and Eu³⁺ doping content on optical properties of glass‐ceramics were systematically studied by emission, excitation spectra, and decay curves. Notably, the spatial separation of these two different activators in the present glass‐ceramics, where Ce³⁺ ions located in YAG crystalline phase while the Eu³⁺ ones stayed in glass matrix, is advantageous to the realization of both intense yellow emission assigned to Ce³⁺: 5d→4f transition and red luminescence originating from Eu³⁺: 4f→4f transitions. As a result, the quantum yield of the glass‐ceramic reached as high as 93%, and the constructed WLEDs exhibited an optimal luminous efficacy of 122 lm/W, correlated color temperature of 6532 K and color rendering index of 75.     

Structure and Photoluminescence of A Blue‐Green‐Emitting Phosphor for Near‐UV White LEDs

A series of phosphors Ca_12(0.97?x)Al₁₄O₃₂F₂: 0.03Ce³⁺, xTb³⁺ have been prepared by a hightemperature solid‐state reaction using boric acid as flux. These oxyfluorides crystallize in cubic structure, space group. Under the near ultraviolet excitation within wavelength range 310–390 nm, Ca_12(0.97?x)Al₁₄O₃₂F₂: 0.03Ce³⁺, xTb³⁺ phosphors exhibit an intense emission covering a broad band of 370–500 nm derived from the 5d→4f transitions of Ce³⁺ and a characteristic emission at 544 nm of Tb³⁺. The emission can be tuned from blue to green by altering the relative ratio of Ce³⁺ to Tb³⁺ in the composition. The energy‐transfer mechanism from Ce³⁺ to Tb³⁺ is investigated based on the site occupancy of the luminescence center in the crystal structure of the Ca₁₂Al₁₄O₃₂F₂ host. More importantly, when a certain amount of boric acid is added as flux in the synthesis, the fluorescence intensity of the phosphors increases about 65%. Because of its broad excitation and efficiently tunable blue to green luminescence, the Ca_12(0.97?x)Al₁₄O₃₂F₂: 0.03Ce³⁺, xTb³⁺ phosphors may find promising application as a near UV‐convertible phosphor for white‐light‐emitting diodes.     

Multicolor Emission in a Single‐Phase Phosphor Ca3Al2O6:Ce3+,Li+: Luminescence and Site Occupancy

A single‐phase multicolor emitting phosphor, Ca₃Al₂O₆:Ce³⁺,Li⁺, was prepared by a solid‐state reaction. When the Ce³⁺ concentration is lower than 0.030 (molar ratio in Ca₃Al₂O₆), yellow and greenish blue emissions can be observed under the excitation by a blue and a near UV light, respectively. The yellow‐emitting phosphor possesses an internal quantum efficiency of 89%. Additional purplish blue emission turns up when Ce³⁺ concentrations are higher than 0.040. Tunable emission bands are originated from Ce³⁺ ions on different Ca sites in Ca₃Al₂O₆. Although the emission band of purplish blue or greenish blue overlaps the excitation band of yellow emission, and the distances between the unlike Ce³⁺ ions are in the range of electric dipole–dipole interaction, no energy transfer is observed. Furthermore, emission wavelengths for the yellow, greenish blue, and purplish blue emission show little change upon increasing Ce³⁺ concentrations.     

Synthesis and photoluminescent properties of high-efficient color-tunable Ba3Y2B6O15: Ce3+, Tb3+ phosphors

High-efficient Ce³⁺/Tb³⁺ co-doped Ba₃Y₂B₆O₁₅ phosphors with multi color-emitting were firstly prepared, and their structural and luminescent properties were studied by XRD Rietveld refinement, emission/excitation spectra, fluorescence lifetimes as well as temperature-variable emission spectra. Upon 365?nm excitation, the characteristic blue Ce³⁺ band along with green Tb³⁺ peaks were simultaneously found in the emission spectra. Moreover, by increasing concentration of Tb³⁺, a blue-to-green tunable emitting color could be realized by effective Ce³⁺→Tb³⁺ energy transfer. Furthermore, all Ba₃Y₂B₆O₁₅: Ce³⁺, Tb³⁺ phosphors exhibit high internal quantum efficiency of ~?90%, while the temperature-variable emission spectra reveal that the phosphors possess impressive color stability as well as good thermal stability (T₅₀ =?~?120?°C). The results indicate that these efficient color-tuning Ba₃Y₂B₆O₁₅: Ce³⁺, Tb³⁺ might be candidate as converted phosphor for UV-excited light-emitting diodes.     

Overcoming the cyan gap for full-spectrum lighting using cation-substitution-induced rigid Ca2YZr2Al3O12:Ce3+

Mixing multicolor phosphors for simulating the full spectrum of sunlight illumination is a popular solution to obtain high-quality white light. However, there is still a need to overcome the cyan gap in the emission spectrum. In this work, a series of garnet Ca₂Y_0.94–xLu_xZr_2–yHf_yAl₃O₁₂:6%Ce³⁺ (abbreviated as CY_0.94–xLu_xZr_2–yHf_yA:Ce³⁺) cyan phosphors are designed and prepared by substituting Y³⁺ and Zr⁴⁺ in Ca₂YZr₂Al₃O₁₂:6%Ce³⁺ with Lu³⁺ and Hf⁴⁺ with smaller ionic radius and larger mass. Under 405 nm violet light excitation, the optimized Ca₂Y_0.88Lu_0.06Hf₂Al₃O₁₂:6%Ce³⁺ (CY_0.88Lu_0.06Hf₂A:Ce³⁺) shows a bright cyan emission band in the range of 430–750 nm with the peak at 477 nm. Importantly, the emission intensity and thermal stability properties of CY_0.88Lu_0.06Hf₂A:Ce³⁺ were significantly improved by 58% and 47% compared to those of pure Ca₂YZr₂Al₃O₁₂:Ce³⁺. Small and heavy cation substitution could induce highly stable rigid structure, thus enhancing emission intensity and stability. The color rendering index increases from 84.5 to 92.0 after supplementing CY_0.88Lu_0.06Hf₂A:Ce³⁺ phosphor in white light-emitting diode devices combining commercial red, green, and blue phosphors with a violet chip, indicating its practical application in full-spectrum lighting. The present study provides promising strategies for the design and development of efficient cyan materials for high-quality full visible spectrum light-emitting diode lighting.     

Partial cation substitution of tunable blue-cyan-emitting Ba2B2O5:Ce3+ for near-UV white LEDs

In this study, Sr²⁺, Ca²⁺, Zn²⁺, and Mg²⁺ ions act to tune the emission band to the blue-cyan region in Ba_xSr_yB₂O₅:Ce³⁺ (BSBO), Ba_xCa_zB₂O₅:Ce³⁺ (BCBO), Ba_xZn_uB₂O₅:Ce³⁺ (BZBO), and Ba_xMg_vB₂O₅:Ce³⁺ (BMBO) phosphors. A red shift occurs with the increase of Sr²⁺, Ca²⁺, Zn²⁺, and Mg²⁺ concentration, and a blue shift occurs when the concentrations of Sr²⁺, Ca²⁺, Zn²⁺, and Mg²⁺ exceed the critical value. The emission color can be tuned from deep blue (0.15, 0.12) to cyan (0.16, 0.27) upon 365 nm UV lamp excitation due to the crystal field splitting and centroid shifts. The excitation band shift to long wavelength by introducing ions, so that the synthesized phosphor can be better matched with the n-UV chip. The emission intensity slowly decreases with the temperature increasing. Therefore, the BMBO:Ce³⁺, BZBO:Ce³⁺, BCBO:Ce³⁺, and BSBO:Ce³⁺ phosphors with relatively good thermal stability were synthesized, which could have potential applications in the n-UV white LEDs.     

Al2O3–Ce:YAG composite phosphor ceramics for white laser lighting: Novel preparation and regulatable properties

In this work, a series of Al₂O₃–Ce:YAG phosphor powders were synthesized by regulating the excess Al³⁺ of (Y,Ce)₃Al₅O₁₂ via coprecipitation method for the first time, where Al³⁺, Ce³⁺, and Y³⁺ elements were uniformly distributed. With the increase of Al³⁺ content, the morphology of the powders changed from wormlike shapes to flaky shapes, and Y₃Al₅O₁₂ phases had a tendency to convert to YAlO₃ phases. The x wt.% Al₂O₃–(Y_0.999Ce_0.001)₃Al₅O₁₂ (x = 20, 30, 40, 50, 60, and 70) composite phosphor ceramics (CPCs) were obtained by vacuum sintering (1775°C × 10 h), where Al₂O₃ and Ce:YAG phases were also well-distributed. When the Al₂O₃ content was 30–40 wt.%, the average grain size of Al₂O₃ was close to that of Ce:YAG. A solid-state laser lighting device was constructed by a 450 nm laser source and CPCs in a reflection mode. By adjusting the laser power, the correlated color temperature (CCT) values of white laser diodes (LDs) were achieved close to the standard white light of 6500 K. Impressively, the white LDs equipped with the 40 wt.% Al₂O₃-containing CPCs showed the optimum CCT of 6498 K (color coordinates: 0.31 and 0.38), as well as a high luminous flux of 1169 lm and efficiency of 166 lm/W at the LD power of 7.05 W. This work has provided a potential idea to optimize the composition uniformity of Al₂O₃–Ce:YAG CPCs as also to explore their excellent performance in the application of white laser lighting.     

NaBaY(BO3)2:Ce3+,Tb3+: A novel sharp green‐emitting phosphor used for WLED and FEDs

A new borate phosphor NaBaY(BO₃)₂: Ce³⁺, Tb³⁺ (NBY:Ce³⁺, Tb³⁺) was successfully synthesized under low temperature designed to put into application in the fields of ultraviolet (UV)‐excited light emitting diodes (LEDs) and field emission displays (FEDs). The structure distortion between Ce³⁺, Tb³⁺ single‐ and co‐doping NBY was discussed by X‐ray powder diffraction Rietveld refinement, high‐resolution transmission electron microscopy (HRTEM) and spectra. NBY: Ce³⁺, Tb³⁺ presents a wide absorption band ranging from 310 to 400 nm and efficient green emission (λ_max = 542 nm) with a full‐width at half‐maximum of 3.3 nm. The remarkable thermal stability has also been tested, indicating that the intensity at 200°C is still beyond 70% of the original intensity. In addition, a white LED device was manufactured by connecting a 370 nm UV chip with a blend of BaMaAl₁₀O₁₇: Eu²⁺ (BAM: Eu²⁺), NBY: Ce³⁺, Tb³⁺ and CaAlSiN₃: Eu²⁺. The color coordinate, correlated color temperature and color rendering index of the manufactured LED device were (0.335, 0.347), 5511 K and 80.16, respectively. Meanwhile, the cathodoluminescence (CL) spectra under the various conditions of probe currents and accelerating voltages were also analyzed. Through successive excitation of low‐voltage electron‐beam, the wonderful performances of degradation property and color stability were obtained. These results suggest that the green‐emitting NBY: Ce³⁺, Tb³⁺ phosphor has the prospect of becoming applications in white UV LEDs and FEDs.     

Highly efficient yellow-orange emission and superior thermal stability of Ba2YAl3Si2O12:Ce3+ for high-power solid lighting

With great economic benefits, white LEDs (w-LEDs) have aroused worldwide attention. For phosphor-converted w-LED, highly efficient emission and good thermal stability of phosphor are significant parameters in practical application. Here, a yellow-orange garnet-structural phosphor, Ba₂YAl₃Si₂O₁₂:xCe³⁺ (x = 0-0.1) (BYAS:xCe³⁺) was developed by solid solution design. The broad emission spectrum of the as-synthesized phosphor could guarantee the effective increase of the color rendering index when it is combined with the InGaN blue chip. Benefiting from the garnet-type highly rigid framework, BYAS:xCe³⁺ exhibits an excellent thermal stability (50%@673K of the initial integrated intensity at 280 K) as well as high absolute quantum efficiency (80.4%@460 nm excitation light). Utilizing the approach of “phosphor-in-glass” (PiG), a high-power warm w-LED is achieved based on a blue LED plus PiG and the illuminance of this w-LED device can be as high as 4227 lx.     

Color conversion properties of various thick-film phosphor-in-glasses depending on structural design for white LEDs

Thick-film phosphor-in-glasses (PiGs) were fabricated via a screen-printing method with various phosphor layer structures, to compose a white light emitting diode (LED). Green (Lu₃Al₅O₁₂:Ce³⁺) and red (CaAlSiN₃:Eu²⁺) phosphors were mixed, layered, and patterned on a glass substrate. The chromaticity of each structured PiG was tuned to achieve a white LED by varying phosphor content and thickness. The emission spectra and the related various color conversion properties, including color coordinates, correlated color temperature (CCT), color rendering index (CRI), luminous efficacy (LE) and the color gamut of the mounted PiGs with different phosphor layer structures were examined and compared. Time-resolved photoluminescence (TRPL) measurements of the white LEDs with various phosphor layer structural designs were also obtained and compared. It was observed that spectral variation depended on the PiG layer structure. A proper PiG layer structural design was discussed for practical applications.     

Fabrication of Ce:YAG,Ce,Cr:YAG and Ce:YAG/Ce,Cr:YAG dual-layered composite phosphor ceramics for the application of white LEDs

(Ce_0.001Y_0.999)₃Al₅O₁₂ and (Ce_0.001Y_0.999)₃(Cr_xAl_1−x)₅O₁₂ (x=0.001−0.005) transparent ceramics were synthesized by the solid state reaction and vacuum sintering and their optical properties were measured. High quality white light was obtained when the Ce:YAG/Ce,Cr:YAG dual-layered composite ceramic was directly combined with commercial blue LED chip. A maximum luminous efficacy exceeding 76 lm/W at a low correlated color temperature of 4905 K was obtained. The color temperature can be controlled by variations of Cr³⁺ concentration and the ceramic thickness. Hence, the Ce:YAG/Ce,Cr:YAG dual-layered composite phosphor ceramic may be a promising candidate for white LEDs.     

Dual effect synergistically triggered Ce:(Y,Tb)3(Al,Mn)5O12 transparent ceramics enabling a high color-rendering index and excellent thermal stability for white LEDs

Ce:Y₃Al₅O₁₂ transparent ceramics (TCs) with appropriate emission light proportion and high thermal stability are significant to construct white light emitting diode devices with excellent chromaticity parameters. In this work, strategies of controlling crystal-field splitting around Ce³⁺ ion and doping orange-red emitting ion, were adopted to fabricate Ce:(Y,Tb)₃(Al,Mn)₅O₁₂ TCs via vacuum sintering technique. Notably, 85.4 % of the room-temperature luminescence intensity of the TC was retained at 150 °C, and the color rendering index was as high as 79.8. Furthermore, a 12 nm red shift and a 16.2 % increase of full width at half maximum were achieved owing to the synergistic effects of Tb³⁺ and Mn²⁺ ions. By combining TCs with a 460 nm blue chip, a warm white light with a low correlated color temperature of 4155 K was acquired. Meanwhile, the action mechanism of Tb³⁺ ion and the energy transfer between Ce³⁺ and Mn²⁺ ions were verified in prepared TCs.     

Processing thin,dense, transparent Ce:Y3Al5O12 films from flame made nanopowders for white light applications

Flame made metal oxide nanopowders enable processing of dense, transparent thin (< 50 μm) films of Ce³⁺ doped Y₃Al₅O₁₂ for white light applications. The addition of very small amounts of SiO₂ (0.14 wt. %) and the use of a final 95:5 N₂:H₂ atmosphere sintering step permits nearly complete removal of pores from films originally sintered in O₂. Furthermore, the introduction of this final step allows reduction in processing temperatures needed to effect Ce⁴⁺ reduction to Ce³⁺ by several hundred degrees below typical temperatures of >1600 °C. At 20–50 μm, the reported films are also much thinner than previously reported for the same materials normally produced by solid state reactions of micron size powders. Spectrofluorometric measurements of the dense transparent films exhibit excitation spectra centered around 450 nm and broad emission spectra in the 470–750 nm range with two peaks centered at 537 and 570 nm, confirming their applicability as a phosphor for white light emitting diodes.