Yellow fluorosulfide phosphors for light-emitting diode and preparation method thereof

Abstract

A novel yellow phosphor of a fluorosulfide having a chemical formula of (A1-x-yCexBy)2Ca1-zSrzF4S2 and a tetragonal crystal phase is disclosed, wherein A and B are different rare earth metals other than Ce, the values of x, y, z are 0

Description

BACKGROUND

1. Technical Field

The disclosure relates to a yellow phosphor. More particularly, the disclosure relates to a novel fluorosulfide phosphor for solid-state lighting application.

2. Description of Related Art

Since the invention of blue light-emitting InGaN-based chip in the early 20^th century, remarkable progress have been made in the development of commercially realized efficient white light-emitting diodes (WLEDs). By the combination of blue emission from the InGaN-based chips and yellow emission based upon the downconversion of Y₃Al₅O₁₂:Ce³⁺ (YAG:Ce)-based phosphors, the generated white light has already exceeded that of incandescent lamps and is competitive with conventional fluorescent lamps. WLEDs are energy-efficient, life-durable, and environment-friendly in comparison to the conventional light sources. However, the color quality of WLEDs still requires improvement with respect to the white hue tunability, color temperature, and color rendering. In particular, these properties are closely correlated to the general illumination.

For most of the currently applied phosphors in WLEDs system, they do not reach the optimal requirements for white light and show poor color rendition in red spectral region. Therefore, to find a suitable luminescent material for phosphor converted WLEDs (pc-WLEDs) is important to attain the optical requirements for white light.

SUMMARY

In one aspect, the present invention is directed to a yellow phosphor of a fluorosulfide having a chemical formula of (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂ and a tetragonal crystal phase, wherein A and B are different rare earth metals other than Ce, the values of x, y, z are 0<x≦1, 0≦y≦1, and 0≦z≦1, respectively.

According to an embodiment, the rare earth metal is Sc, Y, or a lanthanoid, wherein the Inathanoids is La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, or Lu.

According to another embodiment, the chemical formula is (A_1-xCe_x)₂Ca_1-zSr_zF₄S₂ when y is zero.

According to another embodiment, the chemical formula is (A_1-xCe_x)₂CaF₄S₂ when both y and z are zero.

According to another embodiment, the chemical formula is (A_1-xCe_x)₂SrF₄S₂ when y is zero and z is 1.

According to another embodiment, the chemical formula is (A_1-x-yCe_xB_y)₂CaF₄S₂ when z is zero.

According to another embodiment, the chemical formula is (A_1-x-yCe_xB_y)₂SrF₄S₂ when z is 1.

In another aspect, this invention also directs to a white light emitting diode comprising a blue light phosphor and the yellow phosphor of the fluororsulfide described above.

In light of the forgoing, the novel yellow phosphor based on Ce doped fluorosulfide can serve as a potential candidate for white-light LED, especially for generation of warm white-light.

The above presents a simplified summary of the disclosure in order to provide a basic understanding to the reader. This summary is not an extensive overview of the disclosure and it does not identify key/critical elements of the present invention or delineate the scope of the present invention. Its sole purpose is to present some concepts disclosed herein in a simplified form as a prelude to the more detailed description that is presented later.

Many of the attendant features will be more readily appreciated as the same becomes better understood by reference to the following detailed description considered in connection with the accompanying drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-1D are XRD spectra of Examples 1, 9, 2 and 10, respectively.

FIGS. 2A-2C are excitation and emission spectra of Examples 1, 8 and 9, respectively.

FIGS. 3A-3C are excitation and emission spectra of Examples 12, 18 and 23, respectively.

FIG. 4 shows the temperature dependent photoluminescence intensity of CaS:Ce³⁺, (Y_0.99Ce_0.01)₂CaF₄S₂ and (Y_0.99Ce_0.01)₂SrF₄S₂.

FIG. 5( a) is a visible photoluminescence spectrum of a WLED using the yellow phosphor of (Y_0.99Ce_0.01)₂Ca_0.65Sr_0.55F₄S₂ with 0.1 mm thick and an InGaN LED chip emitting blue light of 460 nm.

FIG. 5( b) shows the variation in CIE chromaticity coordinates as a function of fraction of phosphor used.

DETAILED DESCRIPTION

For most phosphors doped with Ce³⁺, they show a parity allowed 4f-5d emission ranging from ultraviolet to red color depending upon the host lattice and on the basis of the site size, site symmetry and coordination number. In fact, the emission color of Ce³⁺ can also be controlled in the desired region of the spectrum by changing the crystal field strength. For example, the optical iii properties of Ce³⁺ dopant in Ca(Si,Al)N₂:Ce³⁺ (red), (La,Gd)Sr₂AlO₅:Ce³⁺ (yellow), (Ca,Sr)Sc₂O₄:Ce³⁺ (green) phosphors have been investigated.

In recent years, great attentions have been attracted to study the mixed-anion fluoroxide crystals doped with Ce³⁺ and show their potentially applicable to WLEDs assemblies, but there has been no reported study on the photoluminescence (PL) properties of the fluorosulfides/mixed-anions system prior to this present work. The quaternary fluorosulfide Y₂CaF₄S₂ is isostructural with Sm₂CaF₄S₂, which is first announced as a new color pigment. In this compound, the chromatic and chemical properties of rare earth, which is surrounded by fluorine and sulfur ligands, is expected to combine the advantages of sulfides and fluorides.

Yellow Phosphor Material of (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂

Accordingly, in one aspect, this invention directs to a novel fluorosulfide phosphor having a general chemical formula of (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂ for emitting yellow light having a CIE value of (0.30-0.60, 0.30-0.60). The lattice structure of (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂, which is similar to that of Y₂CaF₄S₂, is tetragonal space group (I4/mmm, No. 139), wherein A³⁺, Ce³⁺, and/or B³⁺ are isovalent substitutions for Y³⁺ in Y₂CaF₄S₂, and Sr²⁺ is a isovalent substitution for Ca²⁺ in Y₂CaF₄S₂. Since Ce³⁺ is responsible for emitting yellow light, the value of x is 0<x≦1. The values of y and z are both 0-1. In (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂, both A and B represents different trivalent rare earth elements other than Ce, such as Sc, Y and lanthanoids, wherein the lanthanoids can be La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, or Lu, for example.

When y and/or z are 0 and/or 1, some simplified chemical formulas of the formula (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂ can be obtained. For example, when y is zero, simplified to (A_1-xCe_x)₂Ca_1-zSr_zF₄S₂ is obtained. When z is zero, (A_1-x-yCe_xB_y)₂CaF₄S₂ is obtained. When z is 1, (A_1-x-yCe_xB_y)₂SrF₄S₂ is obtained. When y and z are zero, (A_1-xCe_x)₂CaF₄S₂. When y is zero and z is 1, (A_1-xCe_x)₂SrF₄S₂ is obtained.

Preparation Method of the (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂

In another aspect, this invention directs to a preparation method of the novel fluorosulfide phosphor (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂. First, according to the chemical formula of the desired Ce³⁺ doped fluorosulfide, stoichiometric amounts of at least one sulfide and at least one fluoride of Ce, at least one rare earth metal other than Ce, Ca and/or Sr are weighted. For example, trivalent Y source can be YF₃ or Y₂S₃, and divalent Ca source can be CaS or CaF₂. According to an embodiment of this invention, when (Y_0.99Ce_0.01)₂CaF₄S₂ is synthesized, YF₃, Y₂S₃, CaF₂ and CeF₃ can be used as the reactants, for example.

Next, the weighted sulfides and fluorides are grinded until they are uniformly mixed. Then, the mixture is calcined under a vacuum environment, or under an inert gas or nitrogen at a pressure of about 1 atm, and at a temperature of 900-1100° C. until a pure crystal phase is obtained. The crystal phase of the obtained product can be examined by x-ray powder diffracion (XRD) spectrum.

Embodiment 1: (A_1-xCe_x)₂CaF₄S₂ (y=z=0)

When y=z=0, (A_1-x-yCe_xB_y)₂Ca_1-zSr_zF₄S₂ is simplified to (A_1-xCe_x)₂CaF₄S₂. Examples included that A was Y, La, Sm, Eu, Gd or Tb, and x was 0.01, were prepared according to the preparation method described above.

The XRD spectra of Examples 1 and 2 are shown in FIGS. 1A and 1C. The excitation and emission spectrum of Example 1 is shown in FIG. 2A. The prepared fluorosulfides and photoluminescence properties thereof are listed in Table

Comparing FIGS. 1A and 1C, only the trivalent cations were different, i.e. Y³⁺ in FIG. 1A and La³⁺ in FIG. 1C. The isovalent cation substitution with various sizes was used to change the structural environment for Ce³⁺, and the crystal field splitting of Ce³⁺ 5d level was thus changed. Since Y³⁺ and La³⁺ were compatible with the fluorosulfide host lattice, the substitution may result in different emission efficiency and color rendition.

Firstly from Table 1, it can be seen that the 1 mol % substitution of Ce³⁺ can create wide excitation and emission ranges. Thus, this Ce³⁺-doped fluorosulfide system can use UV-to-blue light as the excitation source to meet the request for the pc-WLED applications.

Second, only a little blueshift or redshift occurred relative to the excitation and emission ranges and CIE value of (Y_0.99Ce_0.01)₂CaF₄S₂. Roughly speaking, the substitution, such as La³⁺ subsutition, that result in the expansion of Ce—S bonds is expected to decerease the emission wavelength, i.e. blueshift. Contrarily, the substitution that result in the contraction of Ce—S bonds is expected to increase the emission wavelength, i.e. redshift. Therefore, the crystal field strengths sensed by the Ce³⁺ ions were changed by the various trivalent rare earth metal ions, and the emission wavelengths were thus blueshifted or redshifted.

However, the excitation, emission ranges, and the CIE values were also relatively unchanged by the various rare earth elements of A. It can be understood that the sizes of these trivalent rare earth metal ions are only a subtle change for the fluorosulfide's lattice. Hence, the tetragonal aspect ratio and the lattice size of the fluorosulfides are slightly affected.

TABLE 1
Photoluminescence properties of (A0.99Ce0.01)2CaF4S2, where A
was Y, La, Sm, Eu, Gd or Tb.
		9-fold	Main	Main
		coordination	Excitation	Emission
		atomic radius	Range	Range	CIE
Examples	(Å)	(peak) (nm)	(peak) (nm)	(x, y)
1	(Y0.99Ce0.01)2CaF4S2	1.075	250-547	500-800	(0.53, 0.46)
			(300, 337, 470)	(590)
2	(La0.99Ce0.01)CaF4S2	1.216	250-542	500-800	(0.50, 0.48)
			(338, 468)	(588)
3	(Sm0.99Ce0.01)2CaF4S2	1.132	250-542	500-800	(0.53, 0.45)
			(341, 470)	(589)
4	(Eu0.99Ce0.01)2CaF4S2	1.12	250-545	503-800	(0.53, 0.45)
			(335, 471)	(591, 623)
5	(Gd0.99Ce0.01)2CaF4S2	1.107	250-545	512-800	(0.54, 0.47)
			(335, 472)	(595)
6	(Tb0.99Ce0.01)2CaF4S2	1.095	250-545	503-800	(0.53, 0.45)
			(335, 471)	(548, 591)

Embodiment 2: Substitution of Ca²⁺ by Sr²⁺ in (A_1-xCe_x)₂CaF₄S₂

Next, the Ca²⁺ in (A_1-xCe_x)₂CaF₄S₂ (y=0 and z=0) was gradually substituted by Sr⁺ until (A_1-xCe_x)₂SrF₄S₂ (y=0 and z=1) was obtained. Examples included that A was Y or La, x was 0.01, and z=0, 0.1, 0.5, 1, were prepared according to the preparation method described above.

The XRD spectra of Examples 1, 9, 2 and 10 are shown in FIGS. 1A-1D. The excitation and emission spectra of Examples 1, 8 and 9 are shown in FIGS. 2A-2C. The prepared fluorosulfides and photoluminescence properties thereof are listed in Table 2.

From FIGS. 1A-1D, it can be seen that the crystal phase of the (A_1-xCe_x)₂CaF₄S₂ was unchanged by the substitution of Ca²⁺ by Sr²⁺ for both Y (examples 1 and 9) and La (examples 2 and 10) series. The crystal phases of these examples were remained the same as Y₂CaF₄S₂ with the tetragonal structure. However, the XRD peaks move to lower angle positions after Ca²⁺ was substituted by Sr²⁺. The results shown in FIGS. 1A-1D are in accordance with the ionic size variation where the atomic radii for 8-fold coordination of Ca²⁺ and Sr²⁺ are 1.12 Å and 1.26 Å, respectively. That means, the lattice volume was expanded by the Sr⁺ substitution.

From FIGS. 2A-2C, it can be seen that both of the excitation and emission spectra were blueshifted. The blue shift phenomena can also be further seen in Table 2 for both Y (examples 1 and 7-9) and La (examples 2 and 10) series. It indicates that the above substitution leads to size expansion of the lattice volume, which is induced by larger Sr²⁺ ionic size. In such cases, the Ce³⁺ ions experience a weaker crystal field splitting due to the expansion of lattice size, and the lowest-lying 5d level is elevated. Therefore, it is reasonable that the blueshifted excitation and emission spectra were observed.

From Table 2, the x value of CIE is decreased as the z value in (A_1-xCe_x)₂Ca_1-zSr_zF₄S₂ increased, and the y value is increased as the z value is increased, since the color of the emitted light moves from orange to green-yellow.

TABLE 2
Photoluminescence properties of (A0.99Ce0.01)2Ca1-zSr2F4S2,
where z = 0, 0.1, 0.5, 1 for Y series and z = 0, 1 for La series.
		Main	Main
		Excitation	Emission
		Range	Range
Examples	(peak) (nm)	(peak) (nm)	CIE(x, y)
1	(Y0.99Ce0.01)2CaF4S2	250-547	500-800	(0.53, 0.46)
		(300, 337,	(590)
		470)
7	(Y0.99Ce0.01)2Ca0.9Sr0.1F4S2	250-545	503-800	(0.52, 0.46)
		(300, 335,	(585)
		467)
8	(Y0.99Ce0.01)2Ca0.5Sr0.5F4S2	250-540	500-800	(0.45, 0.47)
		(331,461)	(576)
9	(Y0.99Ce0.01)2SrF4S2	250-543	480-800	(0.42, 0.53)
		(299, 335,	(553)
		441)
2	(La0.99Ce0.01)2CaF4S2	250-542	500-800	(0.50, 0.48)
		(338, 468)	(588)
10	(La0.99Ce0.01)2SrF4S2	250-539	475-800	(0.40, 0.49)
		(289, 330,	(550)
		439)

Embodiment 3: Substitution of the First Traivalent Rare Earth Metal Ion by a Second Trivalent Rare Earth Metal Ion in (A_1-xCe_x)₂CaF₄S₂

10 mol % of the first trivalent rare earth metal ion, A, in (A_1-xCe_x)₂CaF₄S₂ (y=0 and z=0) was substituted by a second trivalent rare earth metal ion, B, to obtain (A_0.9-xCe_xB_0.1)₂CaF₄S₂ (y=0.1 and z=0). The first trivalent rare earth metal A in (A_0.9-xCe_xB_0.1)₂CaF₄S₂ (y=0.1 and z=0) was Y, and the second trivalent rare earth metal B was Sc, La, Sm, Eu, Gd, or Tb when x was 0.01 were perepared by the prepartaion method described above. The prepared examples and photoluminesecnce properties are listed in Table 3.

Similar to the results of embodiment 1 (Table 1 above), the trend of the excitation spectra, the emission spectra, and the CIE value were the same as the partial substitution of first trivalent rare earth metal ion, A, by the second trivalent rare earth metal ion, B.

TABLE 3
Photoluminesecnce properties of (Y0.89Ce0.01B0.1)2CaF4S2,
where B was Sc, La, Sm, Eu, Gd, or Tb.
		Main	Main
		Excitation	Emission
		Range (peak)	Range (peak)
Examples	(nm)	(nm)	CIE(x, y)
11	(Y0.89C0.01Sc0.1)2CaF4S2	250-537	520-800	(0.50, 0.48)
		(333, 466)	(588)
12	(Y0.89Ce0.01La0.1)2CaF4S2	250-538	520-800	(0.51, 0.48)
		(335, 467)	(588)
13	(Y0.89Ce0.01Sm0.1)2CaF4S2	250-540	510-800	(0.52, 0.48)
		(349, 467)	(589)
14	(Y0.89Ce0.01Eu0.1)2CaF4S2	250-539	514-800	(0.52, 0.45)
		(357, 468)	(589, 624)
15	(Y0.89Ce0.01Gd0.1)2CaF4S2	250-545	511-800	(0.53, 0.47)
		(358, 468)	(594)
16	(Y0.89Ce0.01Tb0.1)2CaF4S2	250-539	520-800	(0.52, 0.46)
		(356, 468)	(548, 589)

Embodiment 4: Substitution of Ca²⁺ Ion by Sr²⁺ Ion in (A_1-x-yCe_xB_y)₂CaF₄S₂

The Ca²⁺ in (Y_0.89Ce_0.01B_0.1)₂CaF₄S₂ of embodiment 3 (examples 11-16) was further substituted by Sr²⁺ to verify the lattice size expansion effect. The results are shown in Table 4, and the excitation and emission spectra of examples 12, 18, and 23 are shown in FIGS. 3A-3C.

From Table 4 and FIGS. 3A-3C, it can be seen that the blue shift of both excitation and emission spectra was not obvious, and the CIE values were also about the same. This result is different from Embodiment 2 above. Comparing Embodiments 1 and 2, it can be known that the divalent cations have greater influence than trivalent cations on the fluorosulfide's lattice size and thus the emission energy. Therefore, the result of this Embodiment 4 implies that the emission energy is not simply determined by the crystal field, but also by some other factors, such as the covalent-ionic percentage of the Ce—S coordination bonds.

TABLE 4
Photoluminesence properties of (Y0.89Ce0.01B0.1)2Ca1-zSrzF4S2,
where B was Sc, La, Sm, Eu, Gd, or Tb, z is 0 and 0.1 for Sc, Sm,
Eu, Gd, and Tb series, and z is 0, 0.1, and 1 for La series.
		Main Excitation	Main Emission
		Range (peak)	Range (peak)
Examples	(nm)	(nm)	CIE(x, y)
11	(Y0.89Ce0.01Sc0.1)2CaF4S2	250-537	520-800	(0.50, 0.48)
		(333, 466)	(588)
17	(Y0.89Ce0.01Sc0.1)2Ca0.9Sr0.1F4S2	250-545	503-800	(0.52, 0.46)
		(300, 334,	(585)
		465)
12	(Y0.89Ce0.01La0.1)2CaF4S2	250-538	520-800	(0.51, 0.48)
		(335, 467)	(588)
18	(Y0.89Ce0.01La0.1)2Ca0.9Sr0.1F4S2	250-546	505-800	(0.52, 0.45)
		(298, 331,	(585)
		467)
23	(Y0.89Ce0.01La0.1)2SrF4S2	250-538	520-800	(0.52, 0.48)
		(365, 473)	(594)
13	(Y0.89Ce0.01Sm0.1)2CaF4S2	250-540	510-800	(0.52, 0.48)
		(349, 467)	(589)
19	(Y0.89Ce0.01Sm0.1)2Ca0.9Sr0.1F4S2	250-546	501-800	(0.53, 0.45)
		(300, 335,	(587)
		468)
14	(Y0.89Ce0.01Eu0.1)2CaF4S2	250-539	514-800	(0.52, 0.45)
		(357, 468)	(589, 624)
20	(Y0.89Ce0.01Eu0.1)2Ca0.9Sr0.1F4S2	250-546	509-800	(0.51, 0.44)
		(299, 332,	(586, 623)
		466)
15	(Y0.89Ce0.01Gd0.1)2CaF4S2	250-545	511-800	(0.53, 0.47)
		(358, 468)	(594)
21	(Y0.89Ce0.01Gd0.1)2Ca0.9Sr0.1F4S2	250-527	506-800	(0.50, 0.49)
		(275, 327,	(587)
		467)
16	(Y0.89Ce0.01Tb0.1)2CaF4S2	250-539	520-800	(0.52, 0.46)
		(356, 468)	(548, 589)
22	(Y0.89Ce0.01Tb0.1)2Ca0.9Sr0.1F4S2	250-527	507-800	(0.51, 0.48)
		(283, 331,	(547, 588)
		463)

Embodiment 5: Temperature Dependent Photoluminescence Intensity for (Y_0.99Ce_0.01)₂CaF₄S₂ and (Y_0.99Ce_0.01)₂SrF₂S₂

In this embodiment 5, the temperature dependent behavior of the photoluminescence (PL) intensity of both (Y_0.99Ce_0.01)₂CaF₄S₂ and (Y_0.99Ce_0.01)₂SrF₄S₂ were examined. FIG. 4 shows the temperature dependent photoluminescence intensity of commercial CaS:Ce³⁺, (Y_0.99Ce_0.01)₂CaF₄S₂ and (Y_0.99Ce_0.01)₂SrF₄S₂ in the range of 25-225° C.

In FIG. 4, the PL intensities in all samples are found to be diminished as compared to that of the same sample observed at room temperature, which may be explained on the basis of the increasing thermal energy is utilized to excite electrons to the lowest state of the conduction band and then ionized. Surprisingly, the thermal stability of fluorosulfides were comparable to or even more stable than that of binary sulfides, CaS:Ce³⁺. The introduction of F atoms into the sulfide host lattice can lower the extent of thermal quenching as a result of the softer phonon modes.

In FIG. 4, the values of ΔE for (Y_0.99Ce_0.01)₂CaF₄S₂ and (Y_0.99Ce_0.01)₂SrF₄S₂ are estimated to be 0.3741 and 0.3829 eV, respectively. The ΔE represents the thermal energy that excites the electrons to the 5d states of Ce³⁺ ions. It can be seen that the (Y_0.99Ce_0.01)₂CaF₄S₂ shows higher activation energy characteristic than that of (Y_0.99Ce_0.01)₂SrF₄S₂, since weaker crystal field strength was experienced by Ce³⁺ ions in (Y_0.99Ce_0.01)₂SrF₄S₂.

Embodiment 6: pc-WLEDs Application of (Y_0.99Ce_0.01)₂Ca_1-zSr_zF₄S₂

To demonstrate the potential of (Y_0.99Ce_0.01)₂Ca_1-zSr_zF₄S₂ for pc-WLEDs application, two phosphors with z values of 0.55 and 0.65 were utilized to fabricate pc-WLEDs with an InGaN LED chip emitting blue light of 460 nm. The typical visible photoluminescence spectrum of this WLED was shown in FIG. 5(a), and the variation in CIE chromaticity coordinates as a function of fraction of phosphor used was shown in FIG. 5(b) as an inset. In FIG. 5, the phosphor of (Y_0.99Ce_0.01)₂Ca_0.65Sr_0.55F₄S₂ was noted as YCSFS-0.55, and the other phosphor of (Y_0.99Ce_0.01)₂Ca_0.55Sr_0.65F₄S₂ was noted as YCSFS-0.65. The whole visible spectral region in FIG. 5 can be obtained when excited by the blue chip and the color rendering index (CRI) Ra of this dichromatic pc-WLEDs was determined to be around 74 to 85.

The Commission International de I′Eclairage (CIE) chromaticity coordinates, the correlating color temperature (CCT) of the pc-WLEDs and the corresponding luminous efficiency are shown in Table 5. In Table 5, compare with the pc-WLEDs using conventional YAG:Ce³⁺ phosphor having Ra values in the range from 70 to 75 and color temperature 6,900K. Therefore, the generated dichromatic white light in this work possess two better properties, higher Ra and lower color temperature.

TABLE 5
Optical and chromaticity parameters for pc-WLEDs with
YCSFS-0.55 and YCSFS-0.65 as the conversion phosphor layer.
	Thickness		CCT	CRI	Luminous
Sample	(nm)	CIE(x, y)	(k)	(Ra)	(Im/W)
YCSFS-0.55	1	(0.31, 0.21)	6,962	83.5	19.8
	2	(0.33, 0.33)	5,320	84.9	16.7
	3	(0.37, 0.37)	4,201	81.6	14.2
YCSFS-0.65	1	(0.30, 0.26)	8,772	83.9	29.18
	2	(0.32, 0.31)	5,812	85	27
	3	(0.41, 0.41)	3,511	74	17.43

According to the disclosure above, the novel yellow phosphor based on Ce doped fluorosulfide can serve as a potential candidate for white-light LED, especially for generation of warm white-light. Moreover, only 1 mol % substitution of Ce³⁺ can create wide excitation and emission ranges. Thus, this Ce³⁺-doped fluorosulfide system can use UV-to-blue light as the excitation source to meet the request for the pc-WLED applications.

The reader's attention is directed to all papers and documents which are filed concurrently with this specification and which are open to public inspection with this specification, and the contents of all such papers and documents are incorporated herein by reference.

All the features disclosed in this specification (including any accompanying claims, abstract, and drawings) may be replaced by alternative features serving the same, equivalent or similar purpose, unless expressly stated otherwise. Thus, each feature disclosed is one example only of a generic series of equivalent or similar features.

Claims

1. A yellow phosphor of a fluorosulfide having a chemical formula of (A1-x-yCexBy)2Ca1-zSrzF4S2 and a tetragonal crystal phase, wherein A and B are different rare earth metals other than Ce, the values of x, y, z are 0<x≦0.01, 0≦y≦1, and 0≦z≦1, respectively.

2. The fluorosulfide of claim 1, wherein the rare earth metal is Sc, Y, or a lanthanoid.

3. The fluorosulfide of claim 2, wherein the Inathanoid is La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, or Lu.

4. The fluorosulfide of claim 1, wherein y is zero and the chemical formula is (A1-xCex)2Ca1-zSrzF4S2.

5. The fluorosulfide of claim 4, wherein z is zero and the chemical formula is (A1-xCex)2CaF4S2.

6. The fluorosulfide of claim 4, wherein z is 1 and the chemical formula is (A1-xCex)2SrF4S2.

7. The fluorosulfide of claim 1, wherein z is zero and the chemical formula is (A1-x-yCexBy)2CaF4S2.

8. The fluorosulfide of claim 1, wherein z is 1 and the chemical formula is (A1-x-yCexBy)2SrF4S2.

9. A white light emitting devise, comprising: a blue light phosphor; anda yellow light phosphor having a chemical formula of (A1-x-yCexBy)2Ca1-zSrzF4S2 and a tetragonal crystal phase, wherein A and B are different rare earth metals other than Ce, the values of x, y, z are 0<x≦1, 0≦y≦1, and 0≦z≦1, respectively.

10. The white light emitting device of claim 9, wherein the rare earth metal is Sc, Y, or a lanthanoid.

11. The white light emitting device of claim 10, wherein the Inathanoid is La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, or Lu.

12. The white light emitting device of claim 9, wherein y is zero and the chemical formula is (A1-xCex)2Ca1-zSrzF4S2.

13. The white light emitting device of claim 12, wherein z is zero and the chemical formula is (A1-xCex)2CaF4S2.

14. The white light emitting device of claim 12, wherein z is 1 the chemical formula is (A1-xCex)2SrF4S2.

15. A preparation method of the fluorosulfide of claim 1, comprising: weighting stoichiometric amounts of at least one sulfide and at least one fluoride of Ce, at least one rare earth metal other than Ce, Ca and/or Sr according to the desired chemical formula in claim 1;uniformly mixing the at least one sulfide and the at least one fluoride by grinding to form a mixture; andcalcining the mixture under a vacuum environment at a temperature of 900-1100° C. until a pure crystal phase is obtained.

16. The preparation method of claim 15, wherein the rare earth metal is Sc, Y, or a lanthanoid.

17. The preparation method of claim 16, wherein the Inathanoid is La, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, or Lu.