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Phosphor

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For the chemical element, see phosphorus.
Example of phosphorescence
Monochrome monitor
Aperture grille CRT phosphors

A phosphor is a substance that exhibits the phenomenon of luminescence; it emits light when exposed to some type of radiant energy. The term is used both for fluorescent or phosphorescent substances which glow on exposure to ultraviolet or visible light, and cathodoluminescent substances which glow when struck by an electron beam (cathode rays) in a cathode-ray tube.

When a phosphor is exposed to radiation, the orbital electrons in its molecules are excited to a higher energy level; when they return to their former level they emit the energy as light of a certain color. Phosphors can be classified into two categories: fluorescent substances which emit the energy immediately and stop glowing when the exciting radiation is turned off, and phosphorescent substances which emit the energy after a delay, so they keep glowing after the radiation is turned off, decaying in brightness over a period of milliseconds to days.

Fluorescent materials are used in applications in which the phosphor is excited continuously: cathode-ray tubes (CRT) and plasma video display screens, fluoroscope screens, fluorescent lights, scintillation sensors, white LEDs, and luminous paints for black light art. Phosphorescent materials are used where a persistent light is needed, such as glow-in-the-dark watch faces and aircraft instruments, and in radar screens to allow the target 'blips' to remain visible as the radar beam rotates. CRT phosphors were standardized beginning around World War II and designated by the letter "P" followed by a number.

Phosphorus, the light-emitting chemical element for which phosphors are named, emits light due to chemiluminescence, not phosphorescence.[1]

Light-emission process

Jablonski diagram shows the energy levels in a fluorescing atom in a phosphor. An electron in the phosphor absorbs a high-energy photon from the applied radiation, exciting it to a higher energy level. After losing some energy in non-radiative transitions, it eventually transitions back to its ground state energy level by fluorescence, emitting a photon of lower energy in the visible light region.

The scintillation process in inorganic materials is due to the electronic band structure found in the crystals. An incoming particle can excite an electron from the valence band to either the conduction band or the exciton band (located just below the conduction band and separated from the valence band by an energy gap). This leaves an associated hole behind, in the valence band. Impurities create electronic levels in the forbidden gap. The excitons are loosely bound electron–hole pairs that wander through the crystal lattice until they are captured as a whole by impurity centers. The latter then rapidly de-excite by emitting scintillation light (fast component). In the case of inorganic scintillators, the activator impurities are typically chosen so that the emitted light is in the visible range or near-UV, where photomultipliers are effective. The holes associated with electrons in the conduction band are independent from the latter. Those holes and electrons are captured successively by impurity centers exciting certain metastable states not accessible to the excitons. The delayed de-excitation of those metastable impurity states, slowed by reliance on the low-probability forbidden mechanism, again results in light emission (slow component).

Phosphors are often transition-metal compounds or rare-earth compounds of various types. In inorganic phosphors, these inhomogeneities in the crystal structure are created usually by addition of a trace amount of dopants, impurities called activators. (In rare cases dislocations or other crystal defects can play the role of the impurity.) The wavelength emitted by the emission center is dependent on the atom itself and on the surrounding crystal structure.

Materials

Phosphors are usually made from a suitable host material with an added activator. The best known type is a copper-activated zinc sulfide (ZnS) and the silver-activated zinc sulfide (zinc sulfide silver).

The host materials are typically oxides, nitrides and oxynitrides,[2] sulfides, selenides, halides or silicates of zinc, cadmium, manganese, aluminium, silicon, or various rare-earth metals. The activators prolong the emission time (afterglow). In turn, other materials (such as nickel) can be used to quench the afterglow and shorten the decay part of the phosphor emission characteristics.

Many phosphor powders are produced in low-temperature processes, such as sol-gel, and usually require post-annealing at temperatures of ~1000 °C, which is undesirable for many applications. However, proper optimization of the growth process allows manufacturers to avoid the annealing.[3]

Phosphors used for fluorescent lamps require a multi-step production process, with details that vary depending on the particular phosphor. Bulk material must be milled to obtain a desired particle size range, since large particles produce a poor-quality lamp coating, and small particles produce less light and degrade more quickly. During the firing of the phosphor, process conditions must be controlled to prevent oxidation of the phosphor activators or contamination from the process vessels. After milling, the phosphor may be washed to remove minor excess of activator elements. Volatile elements must not be allowed to escape during processing. Lamp manufacturers have changed compositions of phosphors to eliminate some toxic elements, such as beryllium, cadmium, or thallium, formerly used.[4]

The commonly quoted parameters for phosphors are the wavelength of emission maximum (in nanometers, or alternatively color temperature in kelvins for white blends), the peak width (in nanometers at 50% of intensity), and decay time (in seconds).

Examples:

  • Calcium sulfide with strontium sulfide with bismuth as activator, (Ca,Sr)S:Bi, yields blue light with glow times up to 12 hours, red and orange are modifications of the zinc sulfide formula. Red color can be obtained from strontium sulfide.
  • Zinc sulfide with about 5 ppm of a copper activator is the most common phosphor for the glow-in-the-dark toys and items. It is also called GS phosphor.
  • Mix of zinc sulfide and cadmium sulfide emit color depending on their ratio; increasing of the CdS content shifts the output color towards longer wavelengths; its persistence ranges between 1–10 hours.
  • Strontium aluminate activated by europium, SrAl2O4:Eu(II):Dy(III), is a material developed in 1993 by Nemoto & Co. engineer Yasumitsu Aoki with higher brightness and significantly longer glow persistence; it produces green and aqua hues, where green gives the highest brightness and aqua the longest glow time.[5][6] SrAl2O4:Eu:Dy is about 10 times brighter, 10 times longer glowing, and 10 times more expensive than ZnS:Cu.[5] The excitation wavelengths for strontium aluminate range from 200 to 450 nm. The wavelength for its green formulation is 520 nm, its blue-green version emits at 505 nm, and the blue one emits at 490 nm. Colors with longer wavelengths can be obtained from the strontium aluminate as well, though for the price of some loss of brightness.

Phosphor degradation

Many phosphors tend to lose efficiency gradually by several mechanisms. The activators can undergo change of valence (usually oxidation), the crystal lattice degrades, atoms – often the activators – diffuse through the material, the surface undergoes chemical reactions with the environment with consequent loss of efficiency or buildup of a layer absorbing either the exciting or the radiated energy, etc.

The degradation of electroluminescent devices depends on frequency of driving current, the luminance level, and temperature; moisture impairs phosphor lifetime very noticeably as well.

Harder, high-melting, water-insoluble materials display lower tendency to lose luminescence under operation.[7]

Examples:

  • BaMgAl10O17:Eu2+ (BAM), a plasma-display phosphor, undergoes oxidation of the dopant during baking. Three mechanisms are involved; absorption of oxygen atoms into oxygen vacancies on the crystal surface, diffusion of Eu(II) along the conductive layer, and electron transfer from Eu(II) to absorbed oxygen atoms, leading to formation of Eu(III) with corresponding loss of emissivity.[8] Thin coating of aluminium phosphate or lanthanum(III) phosphate is effective in creating a barrier layer blocking access of oxygen to the BAM phosphor, for the cost of reduction of phosphor efficiency.[9] Addition of hydrogen, acting as a reducing agent, to argon in the plasma displays significantly extends the lifetime of BAM:Eu2+ phosphor, by reducing the Eu(III) atoms back to Eu(II).[10]
  • Y2O3:Eu phosphors under electron bombardment in presence of oxygen form a non-phosphorescent layer on the surface, where electron–hole pairs recombine nonradiatively via surface states.[11]
  • ZnS:Mn, used in AC thin-film electroluminescent (ACTFEL) devices degrades mainly due to formation of deep-level traps, by reaction of water molecules with the dopant; the traps act as centers for nonradiative recombination. The traps also damage the crystal lattice. Phosphor aging leads to decreased brightness and elevated threshold voltage.[12]
  • ZnS-based phosphors in CRTs and FEDs degrade by surface excitation, coulombic damage, build-up of electric charge, and thermal quenching. Electron-stimulated reactions of the surface are directly correlated to loss of brightness. The electrons dissociate impurities in the environment, the reactive oxygen species then attack the surface and form carbon monoxide and carbon dioxide with traces of carbon, and nonradiative zinc oxide and zinc sulfate on the surface; the reactive hydrogen removes sulfur from the surface as hydrogen sulfide, forming nonradiative layer of metallic zinc. Sulfur can be also removed as sulfur oxides.[13]
  • ZnS and CdS phosphors degrade by reduction of the metal ions by captured electrons. The M2+ ions are reduced to M+; two M+ then exchange an electron and become one M2+ and one neutral M atom. The reduced metal can be observed as a visible darkening of the phosphor layer. The darkening (and the brightness loss) is proportional to the phosphor's exposure to electrons and can be observed on some CRT screens that displayed the same image (e.g. a terminal login screen) for prolonged periods.[14]
  • Europium(II)-doped alkaline earth aluminates degrade by formation of color centers.[7]
  • Y
    2    SiO
    5    :Ce3+ degrades by loss of luminescent Ce3+ ions.[7]
  • Zn
    2    SiO
    4    :Mn (P1) degrades by desorption of oxygen under electron bombardment.[7]
  • Oxide phosphors can degrade rapidly in presence of fluoride ions, remaining from incomplete removal of flux from phosphor synthesis.[7]
  • Loosely packed phosphors, e.g. when an excess of silica gel (formed from the potassium silicate binder) is present, have tendency to locally overheat due to poor thermal conductivity. E.g. InBO
    3    :Tb3+ is subject to accelerated degradation at higher temperatures.[7]

Applications

Lighting

Phosphor layers provide most of the light produced by fluorescent lamps, and are also used to improve the balance of light produced by metal halide lamps. Various neon signs use phosphor layers to produce different colors of light. Electroluminescent displays found, for example, in aircraft instrument panels, use a phosphor layer to produce glare-free illumination or as numeric and graphic display devices. White LED lamps consist of a blue or ultra-violet emitter with a phosphor coating that emits at longer wavelengths, giving a full spectrum of visible light. Unfocused and undeflected cathode-ray tubes have been used as stroboscope lamps since 1958.[15]

Phosphor thermometry

Main article: Phosphor thermometry

Phosphor thermometry is a temperature measurement approach that uses the temperature dependence of certain phosphors. For this, a phosphor coating is applied to a surface of interest and, usually, the decay time is the emission parameter that indicates temperature. Because the illumination and detection optics can be situated remotely, the method may be used for moving surfaces such as high speed motor surfaces. Also, phosphor may be applied to the end of an optical fiber as an optical analog of a thermocouple.

Glow-in-the-dark toys

Main article: Phosphorescence

In these applications, the phosphor is directly added to the plastic used to mold the toys, or mixed with a binder for use as paints.

ZnS:Cu phosphor is used in glow-in-the-dark cosmetic creams frequently used for Halloween make-ups. Generally, the persistence of the phosphor increases as the wavelength increases. See also lightstick for chemiluminescence-based glowing items.

Oxygen sensing

Quenching of the triplet state by O2 (which has a triplet ground state) as a result of Dexter energy transfer is well known in solutions of phosphorescent heavy-metal complexes and doped polymers.[16] In recent years, phosphorescence porous materials(such as Metal–organic frameworks and Covalent organic frameworks) have shown promising oxygen sensing capabilities, for their non-linear gas-adsorption in ultra-low partial pressures of oxygen.[17][18]

Postage stamps

Phosphor banded stamps first appeared in 1959 as guides for machines to sort mail.[19] Around the world many varieties exist with different amounts of banding.[20] Postage stamps are sometimes collected by whether or not they are "tagged" with phosphor (or printed on luminescent paper).

Radioluminescence

Main article: Radioluminescence

Zinc sulfide phosphors are used with radioactive materials, where the phosphor was excited by the alpha- and beta-decaying isotopes, to create luminescent paint for dials of watches and instruments (radium dials). Between 1913 and 1950 radium-228 and radium-226 were used to activate a phosphor made of silver doped zinc sulfide (ZnS:Ag), which gave a greenish glow. The phosphor is not suitable to be used in layers thicker than 25 mg/cm2, as the self-absorption of the light then becomes a problem. Furthermore, zinc sulfide undergoes degradation of its crystal lattice structure, leading to gradual loss of brightness significantly faster than the depletion of radium. ZnS:Ag coated spinthariscope screens were used by Ernest Rutherford in his experiments discovering atomic nucleus.

Copper doped zinc sulfide (ZnS:Cu) is the most common phosphor used and yields blue-green light. Copper and magnesium doped zinc sulfide (ZnS:Cu,Mg) yields yellow-orange light.

Tritium is also used as a source of radiation in various products utilizing tritium illumination.

Electroluminescence

Main article: Electroluminescence

Electroluminescence can be exploited in light sources. Such sources typically emit from a large area, which makes them suitable for backlights of LCD displays. The excitation of the phosphor is usually achieved by application of high-intensity electric field, usually with suitable frequency. Current electroluminescent light sources tend to degrade with use, resulting in their relatively short operation lifetimes.

ZnS:Cu was the first formulation successfully displaying electroluminescence, tested at 1936 by Georges Destriau in Madame Marie Curie laboratories in Paris.

Powder or AC electroluminescence is found in a variety of backlight and night light applications. Several groups offer branded EL offerings (e.g. IndiGlo used in some Timex watches) or "Lighttape", another trade name of an electroluminescent material, used in electroluminescent light strips. The Apollo space program is often credited with being the first significant use of EL for backlights and lighting.[21]

White LEDs

White light-emitting diodes are usually blue InGaN LEDs with a coating of a suitable material. Cerium(III)-doped YAG (YAG:Ce3+, or Y3Al5O12:Ce3+) is often used; it absorbs the light from the blue LED and emits in a broad range from greenish to reddish, with most of its output in yellow. This yellow emission combined with the remaining blue emission gives the "white" light, which can be adjusted to color temperature as warm (yellowish) or cold (bluish) white. The pale yellow emission of the Ce3+:YAG can be tuned by substituting the cerium with other rare-earth elements such as terbium and gadolinium and can even be further adjusted by substituting some or all of the aluminium in the YAG with gallium. However, this process is not one of phosphorescence. The yellow light is produced by a process known as scintillation, the complete absence of an afterglow being one of the characteristics of the process.

Some rare-earth-doped Sialons are photoluminescent and can serve as phosphors. Europium(II)-doped β-SiAlON absorbs in ultraviolet and visible light spectrum and emits intense broadband visible emission. Its luminance and color does not change significantly with temperature, due to the temperature-stable crystal structure. It has a great potential as a green down-conversion phosphor for white LEDs; a yellow variant also exists (α-SiAlON[22]). For white LEDs, a blue LED is used with a yellow phosphor, or with a green and yellow SiAlON phosphor and a red CaAlSiN3-based (CASN) phosphor.[23][24][25]

White LEDs can also be made by coating near-ultraviolet-emitting LEDs with a mixture of high-efficiency europium-based red- and blue-emitting phosphors plus green-emitting copper- and aluminium-doped zinc sulfide (ZnS:Cu,Al). This is a method analogous to the way fluorescent lamps work.

Some newer white LEDs use a yellow and blue emitter in series, to approximate white; this technology is used in some Motorola phones such as the Blackberry as well as LED lighting and the original-version stacked emitters by using GaN on SiC on InGaP but was later found to fracture at higher drive currents.

Many white LEDs used in general lighting systems can be used for data transfer, as, for example, in systems that modulate the LED to act as a beacon.[26]

It is also common for white LEDs to use phosphors other than Ce:YAG, or to use two or three phosphors to achieve a higher CRI, often at the cost of efficiency. Examples of additional phosphors are R9, which produces a saturated red, nitrides which produce red, and aluminates such as lutetium aluminum garnet that produce green. Silicate phosphors are brighter but fade more quickly, and are used in LCD LED backlights in mobile devices. LED phosphors can be placed directly over the die or made into a dome and placed above the LED: this approach is known as a remote phosphor.[27] Some colored LEDs, instead of using a colored LED, use a blue LED with a colored phosphor because such an arrangement is more efficient than a colored LED. Oxynitride phosphors can also be used in LEDs. The precursors used to make the phosphors may degrade when exposed to air.[28]

Cathode-ray tubes

Spectra of constituent blue, green and red phosphors in a common cathode-ray tube

Cathode-ray tubes produce signal-generated light patterns in a (typically) round or rectangular format. Bulky CRTs were used in the black-and-white household television (TV) sets that became popular in the 1950s, as well as first-generation, tube-based color TVs, and most earlier computer monitors. CRTs have also been widely used in scientific and engineering instrumentation, such as oscilloscopes, usually with a single phosphor color, typically green. Phosphors for such applications may have long afterglow, for increased image persistence.

The phosphors can be deposited as either thin film, or as discrete particles, a powder bound to the surface. Thin films have better lifetime and better resolution, but provide less bright and less efficient image than powder ones. This is caused by multiple internal reflections in the thin film, scattering the emitted light.

White (in black-and-white): The mix of zinc cadmium sulfide and zinc sulfide silver, the ZnS:Ag + (Zn,Cd)S:Ag is the white P4 phosphor used in black and white television CRTs. Mixes of yellow and blue phosphors are usual. Mixes of red, green and blue, or a single white phosphor, can also be encountered.

Red: Yttrium oxide-sulfide activated with europium is used as the red phosphor in color CRTs. The development of color TV took a long time due to the search for a red phosphor. The first red emitting rare-earth phosphor, YVO4:Eu3+, was introduced by Levine and Palilla as a primary color in television in 1964.[29] In single crystal form, it was used as an excellent polarizer and laser material.[30]

Yellow: When mixed with cadmium sulfide, the resulting zinc cadmium sulfide (Zn,Cd)S:Ag, provides strong yellow light.

Green: Combination of zinc sulfide with copper, the P31 phosphor or ZnS:Cu, provides green light peaking at 531 nm, with long glow.

Blue: Combination of zinc sulfide with few ppm of silver, the ZnS:Ag, when excited by electrons, provides strong blue glow with maximum at 450 nm, with short afterglow with 200 nanosecond duration. It is known as the P22B phosphor. This material, zinc sulfide silver, is still one of the most efficient phosphors in cathode-ray tubes. It is used as a blue phosphor in color CRTs.

The phosphors are usually poor electrical conductors. This may lead to deposition of residual charge on the screen, effectively decreasing the energy of the impacting electrons due to electrostatic repulsion (an effect known as "sticking"). To eliminate this, a thin layer of aluminium (about 100 nm) is deposited over the phosphors, usually by vacuum evaporation, and connected to the conductive layer inside the tube. This layer also reflects the phosphor light to the desired direction, and protects the phosphor from ion bombardment resulting from an imperfect vacuum.

To reduce the image degradation by reflection of ambient light, contrast can be increased by several methods. In addition to black masking of unused areas of screen, the phosphor particles in color screens are coated with pigments of matching color. For example, the red phosphors are coated with ferric oxide (replacing earlier Cd(S,Se) due to cadmium toxicity), blue phosphors can be coated with marine blue (CoO·nAl
2O
3) or ultramarine (Na
8Al
6Si
6O
24S
2). Green phosphors based on ZnS:Cu do not have to be coated due to their own yellowish color.[7]

Black-and-white television CRTs

The black-and-white television screens require an emission color close to white. Usually, a combination of phosphors is employed.

The most common combination is ZnS:Ag + (Zn,Cd)S:Cu,Al (blue + yellow). Other ones are ZnS:Ag + (Zn,Cd)S:Ag (blue + yellow), and ZnS:Ag + ZnS:Cu,Al + Y2O2S:Eu3+ (blue + green + red – does not contain cadmium and has poor efficiency). The color tone can be adjusted by the ratios of the components.

As the compositions contain discrete grains of different phosphors, they produce image that may not be entirely smooth. A single, white-emitting phosphor, (Zn,Cd)S:Ag,Au,Al overcomes this obstacle. Due to its low efficiency, it is used only on very small screens.

The screens are typically covered with phosphor using sedimentation coating, where particles suspended in a solution are let to settle on the surface.[31]

Reduced-palette color CRTs

For displaying of a limited palette of colors, there are a few options.

In beam penetration tubes, different color phosphors are layered and separated with dielectric material. The acceleration voltage is used to determine the energy of the electrons; lower-energy ones are absorbed in the top layer of the phosphor, while some of the higher-energy ones shoot through and are absorbed in the lower layer. So either the first color or a mixture of the first and second color is shown. With a display with red outer layer and green inner layer, the manipulation of accelerating voltage can produce a continuum of colors from red through orange and yellow to green.

Another method is using a mixture of two phosphors with different characteristics. The brightness of one is linearly dependent on electron flux, while the other one's brightness saturates at higher fluxes—the phosphor does not emit any more light regardless of how many more electrons impact it. At low electron flux, both phosphors emit together; at higher fluxes, the luminous contribution of the nonsaturating phosphor prevails, changing the combined color.[31]

Such displays can have high resolution, due to absence of two-dimensional structuring of RGB CRT phosphors. Their color palette is, however, very limited. They were used e.g. in some older military radar displays.

Color television CRTs

The phosphors in color CRTs need higher contrast and resolution than the black-and-white ones. The energy density of the electron beam is about 100 times greater than in black-and-white CRTs; the electron spot is focused to about 0.2 mm diameter instead of about 0.6 mm diameter of the black-and-white CRTs. Effects related to electron irradiation degradation are therefore more pronounced.

Color CRTs require three different phosphors, emitting in red, green and blue, patterned on the screen. Three separate electron guns are used for color production (except for displays that use beam-index tube technology, which is rare). The red phosphor has always been a problem, being the dimmest of the three necessitating the brighter green and blue electron beam currents be adjusted down to make them equal the red phosphor's lower brightness. This made early color TVs only usable indoors as bright light made it impossible to see the dim picture, while portable black-and-white TVs viewable in outdoor sunlight were already common.

The composition of the phosphors changed over time, as better phosphors were developed and as environmental concerns led to lowering the content of cadmium and later abandoning it entirely. The (Zn,Cd)S:Ag,Cl was replaced with (Zn,Cd)S:Cu,Al with lower cadmium/zinc ratio, and then with cadmium-free ZnS:Cu,Al.

The blue phosphor stayed generally unchanged, a silver-doped zinc sulfide. The green phosphor initially used manganese-doped zinc silicate, then evolved through silver-activated cadmium-zinc sulfide, to lower-cadmium copper-aluminium activated formula, and then to cadmium-free version of the same. The red phosphor saw the most changes; it was originally manganese-activated zinc phosphate, then a silver-activated cadmium-zinc sulfide, then the europium(III) activated phosphors appeared; first in an yttrium vanadate matrix, then in yttrium oxide and currently in yttrium oxysulfide. The evolution of the phosphors was therefore (ordered by B-G-R):

  • ZnS:Ag – Zn2SiO4:Mn – Zn3(PO4)2:Mn
  • ZnS:Ag – (Zn,Cd)S:Ag – (Zn,Cd)S:Ag
  • ZnS:Ag – (Zn,Cd)S:Ag – YVO4:Eu3+ (1964–?)
  • ZnS:Ag – (Zn,Cd)S:Cu,Al – Y2O2S:Eu3+ or Y2O3:Eu3+
  • ZnS:Ag – ZnS:Cu,Al or ZnS:Au,Cu,Al – Y2O2S:Eu3+[31]

Projection televisions

For projection televisions, where the beam power density can be two orders of magnitude higher than in conventional CRTs, some different phosphors have to be used.

For blue color, ZnS:Ag,Cl is employed. However, it saturates. (La,Gd)OBr:Ce,Tb3+ can be used as an alternative that is more linear at high energy densities.

For green, a terbium-activated Gd2O2Tb3+; its color purity and brightness at low excitation densities is worse than the zinc sulfide alternative, but it behaves linear at high excitation energy densities, while zinc sulfide saturates. However, it also saturates, so Y3Al5O12:Tb3+ or Y2SiO5:Tb3+ can be substituted. LaOBr:Tb3+ is bright but water-sensitive, degradation-prone, and the plate-like morphology of its crystals hampers its use; these problems are solved now, so it is gaining use due to its higher linearity.

Y2O2S:Eu3+ is used for red emission.[31]

Standard phosphor types

Standard phosphor types[32][33]
Phosphor Composition Color Wavelength Peak width Persistence Usage Notes
P1, GJ Zn2SiO4:Mn (Willemite) Green 525 nm 40 nm[34] 1-100ms CRT, Lamp Oscilloscopes and monochrome monitors
P2 ZnS:Cu(Ag)(B*) Blue-Green 543 nm – Long CRT Oscilloscopes
P3 Zn8:BeSi5O19:Mn Yellow 602 nm – Medium/13 ms CRT Amber monochrome monitors
P4 ZnS:Ag+(Zn,Cd)S:Ag White 565,540 nm – Short CRT Black and white TV CRTs and display tubes.
P4 (Cd-free) ZnS:Ag+ZnS:Cu+Y2O2S:Eu White – – Short CRT Black and white TV CRTs and display tubes, Cd free.
P5 CaWO4:W Blue 430 nm – Very Short CRT Film
P6 ZnS:Ag+ZnS:CdS:Ag White 565,460 nm – Short CRT
P7 (Zn,Cd)S:Cu Blue with Yellow persistence 558,440 nm – Long CRT Radar PPI, old EKG monitors, early oscilloscopes
P10 KCl green-absorbing scotophor – – Long Dark-trace CRTs Radar screens; turns from translucent white to dark magenta, stays changed until erased by heating or infrared light
P11, BE ZnS:Ag,Cl or ZnS:Zn Blue 460 nm – 0.01-1 ms CRT, VFD Display tubes and VFDs; Oscilloscopes (for fast photographic recording)[35]
P12 Zn(Mg)F2:Mn Orange 590 nm – Medium/long CRT Radar
P13 MgSi2O6:Mn Reddish Orange-Reddish Orange 640 nm – Medium CRT Flying spot scanning systems and photographic applications
P14 ZnS:Ag on ZnS:CdS:Cu Blue with Orange persistence – – Medium/long CRT Radar PPI, old EKG monitors
P15 ZnO:Zn Blue-Green 504,391 nm – Extremely Short CRT Television pickup by flying-spot scanning
P16 CaMgSi2O6:Ce Bluish Purple-Bluish Purple 380 nm – Very Short CRT Flying spot scanning systems and photographic applications
P17 ZnO,ZnCdS:Cu Blue-Yellow 504,391 nm – Blue-Short, Yellow-Long CRT
P18 CaMgSi2O6:Ti, BeSi2O6:Mn white-white 545,405 nm – Medium to Short CRT
P19, LF (KF,MgF2):Mn Orange-Yellow 590 nm – Long CRT Radar screens
P20, KA (Zn,Cd)S:Ag or (Zn,Cd)S:Cu Yellow-green 555 nm – 1–100 ms CRT Display tubes
P21 MgF2:Mn2+ Reddish 605 nm – – CRT, Radar Registered by Allen B DuMont Laboratories
P22R Y2O2S:Eu+Fe2O3 Red 611 nm – Short CRT Red phosphor for TV screens
P22G ZnS:Cu,Al Green 530 nm – Short CRT Green phosphor for TV screens
P22B ZnS:Ag+Co-on-Al2O3 Blue – – Short CRT Blue phosphor for TV screens
P23 ZnS:Ag+(Zn,Cd)S:Ag White 575,460 nm – Short CRT, Direct viewing television Registered by United States Radium Corporation.
P24, GE ZnO:Zn Green 505 nm – 1–10 μs VFD most common phosphor in vacuum fluorescent displays.[36]
P25 CaSi2O6:Pb:Mn Orange-Orange 610 nm – Medium CRT Military Displays - 7UP25 CRT
P26, LC (KF,MgF2):Mn Orange 595 nm – Long CRT Radar screens
P27 ZnPO4:Mn Reddish Orange-Reddish Orange 635 nm – Medium CRT Color TV monitor service
P28, KE (Zn,Cd)S:Cu,Cl Yellow – – Medium CRT Display tubes
P29 Alternating P2 and P25 stripes Blue-Green/Orange stripes – – Medium CRT Radar screens
P31, GH ZnS:Cu or ZnS:Cu,Ag Yellowish-green – – 0.01-1 ms CRT Oscilloscopes and monochrome monitors
P33, LD MgF2:Mn Orange 590 nm – > 1sec CRT Radar screens
P34 – Bluish Green-Yellow Green – – Very Long CRT –
P35 ZnS,ZnSe:Ag Blue White-Blue White 455 nm – Medium Short CRT Photographic registration on orthochromatic film materials
P38, LK (Zn,Mg)F2:Mn Orange-Yellow 590 nm – Long CRT Radar screens
P39, GR Zn2SiO4:Mn,As Green 525 nm – Long CRT Display tubes
P40, GA ZnS:Ag+(Zn,Cd)S:Cu White – – Long CRT Display tubes
P43, GY Gd2O2S:Tb Yellow-green 545 nm – Medium CRT Display tubes, Electronic Portal Imaging Devices (EPIDs) used in radiation therapy linear accelerators for cancer treatment
P45, WB Y2O2S:Tb White 545 nm – Short CRT Viewfinders
P46, KG Y3Al5O12:Ce Green 530 nm – Very short (70ns) CRT Beam-index tube
P47, BH Y2SiO5:Ce Blue 400 nm – Very short CRT Beam-index tube
P53, KJ Y3Al5O12:Tb Yellow-green 544 nm – Short CRT Projection tubes
P55, BM ZnS:Ag,Al Blue 450 nm – Short CRT Projection tubes
ZnS:Ag Blue 450 nm – – CRT –
ZnS:Cu,Al or ZnS:Cu,Au,Al Green 530 nm – – CRT –
(Zn,Cd)S:Cu,Cl+(Zn,Cd)S:Ag,Cl White – – – CRT –
Y2SiO5:Tb Green 545 nm – – CRT Projection tubes
Y2OS:Tb Green 545 nm – – CRT Display tubes
Y3(Al,Ga)5O12:Ce Green 520 nm – Short CRT Beam-index tube
Y3(Al,Ga)5O12:Tb Yellow-green 544 nm – Short CRT Projection tubes
InBO3:Tb Yellow-green 550 nm – – CRT –
InBO3:Eu Yellow 588 nm – – CRT –
InBO3:Tb+InBO3:Eu amber – – – CRT Computer displays
InBO3:Tb+InBO3:Eu+ZnS:Ag White – – – CRT –
(Ba,Eu)Mg2Al16O27 Blue – – – Lamp Trichromatic fluorescent lamps
(Ce,Tb)MgAl11O19 Green 546 nm 9 nm – Lamp Trichromatic fluorescent lamps[34]
BAM BaMgAl10O17:Eu,Mn Blue 450 nm – – Lamp, displays Trichromatic fluorescent lamps
BaMg2Al16O27:Eu(II) Blue 450 nm 52 nm – Lamp Trichromatic fluorescent lamps[34]
BAM BaMgAl10O17:Eu,Mn Blue-Green 456 nm,514 nm – – Lamp –
BaMg2Al16O27:Eu(II),Mn(II) Blue-Green 456 nm, 514 nm 50 nm 50%[34] – Lamp
Ce0.67Tb0.33MgAl11O19:Ce,Tb Green 543 nm – – Lamp Trichromatic fluorescent lamps
Zn2SiO4:Mn,Sb2O3 Green 528 nm – – Lamp –
CaSiO3:Pb,Mn Orange-Pink 615 nm 83 nm[34] – Lamp
CaWO4 (Scheelite) Blue 417 nm – – Lamp –
CaWO4:Pb Blue 433 nm/466 nm 111 nm – Lamp Wide bandwidth[34]
MgWO4 Blue pale 473 nm 118 nm – Lamp Wide bandwidth, deluxe blend component [34]
(Sr,Eu,Ba,Ca)5(PO4)3Cl Blue – – – Lamp Trichromatic fluorescent lamps
Sr5Cl(PO4)3:Eu(II) Blue 447 nm 32 nm[34] – Lamp –
(Ca,Sr,Ba)3(PO4)2Cl2:Eu Blue 452 nm – – Lamp –
(Sr,Ca,Ba)10(PO4)6Cl2:Eu Blue 453 nm – – Lamp Trichromatic fluorescent lamps
Sr2P2O7:Sn(II) Blue 460 nm 98 nm – Lamp Wide bandwidth, deluxe blend component[34]
Sr6P5BO20:Eu Blue-Green 480 nm 82 nm[34] – Lamp –
Ca5F(PO4)3:Sb Blue 482 nm 117 nm – Lamp Wide bandwidth[34]
(Ba,Ti)2P2O7:Ti Blue-Green 494 nm 143 nm – Lamp Wide bandwidth, deluxe blend component [34]
3Sr3(PO4)2.SrF2:Sb,Mn Blue 502 nm – – Lamp –
Sr5F(PO4)3:Sb,Mn Blue-Green 509 nm 127 nm – Lamp Wide bandwidth[34]
Sr5F(PO4)3:Sb,Mn Blue-Green 509 nm 127 nm – Lamp Wide bandwidth[34]
LaPO4:Ce,Tb Green 544 nm – – Lamp Trichromatic fluorescent lamps
(La,Ce,Tb)PO4 Green – – – Lamp Trichromatic fluorescent lamps
(La,Ce,Tb)PO4:Ce,Tb Green 546 nm 6 nm – Lamp Trichromatic fluorescent lamps[34]
Ca3(PO4)2.CaF2:Ce,Mn Yellow 568 nm – – Lamp –
(Ca,Zn,Mg)3(PO4)2:Sn Orange-pink 610 nm 146 nm – Lamp Wide bandwidth, blend component[34]
(Zn,Sr)3(PO4)2:Mn Orange-Red 625 nm – – Lamp –
(Sr,Mg)3(PO4)2:Sn Orange-pinkish white 626 nm 120 nm – Fluorescent lamps Wide bandwidth, deluxe blend component[34]
(Sr,Mg)3(PO4)2:Sn(II) Orange-red 630 nm – – Fluorescent lamps –
Ca5F(PO4)3:Sb,Mn 3800K – – – Fluorescent lamps Lite-white blend[34]
Ca5(F,Cl)(PO4)3:Sb,Mn White-Cold/Warm – – – Fluorescent lamps 2600 to 9900 K, for very high output lamps[34]
(Y,Eu)2O3 Red – – – Lamp Trichromatic fluorescent lamps
Y2O3:Eu(III) Red 611 nm 4 nm – Lamp Trichromatic fluorescent lamps[34]
Mg4(F)GeO6:Mn Red 658 nm 17 nm – High-pressure mercury lamps [34]
Mg4(F)(Ge,Sn)O6:Mn Red 658 nm – – Lamp –
Y(P,V)O4:Eu Orange-Red 619 nm – – Lamp –
YVO4:Eu Orange-Red 619 nm – – High Pressure Mercury and Metal Halide Lamps –
Y2O2S:Eu Red 626 nm – – Lamp –
3.5 MgO · 0.5 MgF2 · GeO2 :Mn Red 655 nm – – Lamp 3.5 MgO · 0.5 MgF2 · GeO2 :Mn
Mg5As2O11:Mn Red 660 nm – – High-pressure mercury lamps, 1960s –
SrAl2O7:Pb Ultraviolet 313 nm – – Special fluorescent lamps for medical use Ultraviolet
CAM LaMgAl11O19:Ce Ultraviolet 340 nm 52 nm – Black-light fluorescent lamps Ultraviolet
LAP LaPO4:Ce Ultraviolet 320 nm 38 nm – Medical and scientific UV lamps Ultraviolet
SAC SrAl12O19:Ce Ultraviolet 295 nm 34 nm – Lamp Ultraviolet
SrAl11Si0.75O19:Ce0.15Mn0.15 Green 515 nm 22 nm – Lamp Monochromatic lamps for copiers[37]
BSP BaSi2O5:Pb Ultraviolet 350 nm 40 nm – Lamp Ultraviolet
SrFB2O3:Eu(II) Ultraviolet 366 nm – – Lamp Ultraviolet
SBE SrB4O7:Eu Ultraviolet 368 nm 15 nm – Lamp Ultraviolet
SMS Sr2MgSi2O7:Pb Ultraviolet 365 nm 68 nm – Lamp Ultraviolet
MgGa2O4:Mn(II) Blue-Green – – – Lamp Black light displays

Various

Some other phosphors commercially available, for use as X-ray screens, neutron detectors, alpha particle scintillators, etc., are:

  • Gd2O2S:Tb (P43), green (peak at 545 nm), 1.5 ms decay to 10%, low afterglow, high X-ray absorption, for X-ray, neutrons and gamma
  • Gd2O2S:Eu, red (627 nm), 850 μs decay, afterglow, high X-ray absorption, for X-ray, neutrons and gamma
  • Gd2O2S:Pr, green (513 nm), 7 μs decay, no afterglow, high X-ray absorption, for X-ray, neutrons and gamma
  • Gd2O2S:Pr,Ce,F, green (513 nm), 4 μs decay, no afterglow, high X-ray absorption, for X-ray, neutrons and gamma
  • Y2O2S:Tb (P45), white (545 nm), 1.5 ms decay, low afterglow, for low-energy X-ray
  • Y2O2S:Eu (P22R), red (627 nm), 850 μs decay, afterglow, for low-energy X-ray
  • Y2O2S:Pr, white (513 nm), 7 μs decay, no afterglow, for low-energy X-ray
  • Zn
    0.5    Cd
    0.4    S:Ag     (HS), green (560 nm), 80 μs decay, afterglow, efficient but low-res X-ray
  • Zn
    0.4    Cd
    0.6    S:Ag     (HSr), red (630 nm), 80 μs decay, afterglow, efficient but low-res X-ray
  • CdWO4, blue (475 nm), 28 μs decay, no afterglow, intensifying phosphor for X-ray and gamma
  • CaWO4, blue (410 nm), 20 μs decay, no afterglow, intensifying phosphor for X-ray
  • MgWO4, white (500 nm), 80 μs decay, no afterglow, intensifying phosphor
  • Y2SiO5:Ce (P47), blue (400 nm), 120 ns decay, no afterglow, for electrons, suitable for photomultipliers
  • YAlO3:Ce (YAP), blue (370 nm), 25 ns decay, no afterglow, for electrons, suitable for photomultipliers
  • Y3Al5O12:Ce (YAG), green (550 nm), 70 ns decay, no afterglow, for electrons, suitable for photomultipliers
  • Y3(Al,Ga)5O12:Ce (YGG), green (530 nm), 250 ns decay, low afterglow, for electrons, suitable for photomultipliers
  • CdS:In, green (525 nm), <1 ns decay, no afterglow, ultrafast, for electrons
  • ZnO:Ga, blue (390 nm), <5 ns decay, no afterglow, ultrafast, for electrons
  • ZnO:Zn (P15), blue (495 nm), 8 μs decay, no afterglow, for low-energy electrons
  • (Zn,Cd)S:Cu,Al (P22G), green (565 nm), 35 μs decay, low afterglow, for electrons
  • ZnS:Cu,Al,Au (P22G), green (540 nm), 35 μs decay, low afterglow, for electrons
  • ZnCdS:Ag,Cu (P20), green (530 nm), 80 μs decay, low afterglow, for electrons
  • ZnS:Ag (P11), blue (455 nm), 80 μs decay, low afterglow, for alpha particles and electrons
  • anthracene, blue (447 nm), 32 ns decay, no afterglow, for alpha particles and electrons
  • plastic (EJ-212), blue (400 nm), 2.4 ns decay, no afterglow, for alpha particles and electrons
  • Zn2SiO4:Mn (P1), green (530 nm), 11 ms decay, low afterglow, for electrons
  • ZnS:Cu (GS), green (520 nm), decay in minutes, long afterglow, for X-rays
  • NaI:Tl, for X-ray, alpha, and electrons
  • CsI:Tl, green (545 nm), 5 μs decay, afterglow, for X-ray, alpha, and electrons
  • 6LiF/ZnS:Ag (ND), blue (455 nm), 80 μs decay, for thermal neutrons
  • 6LiF/ZnS:Cu,Al,Au (NDg), green (565 nm), 35 μs decay, for neutrons
  • Cerium doped YAG phosphor, yellow, used in white LEDs for turning blue to white light with a broad spectrum of light

See also

References

  1. ^ Emsley, John (2000). The Shocking History of Phosphorus. London: Macmillan. ISBN 978-0-330-39005-7.
  2. ^ Xie, Rong-Jun; Hirosaki, Naoto (2007). "Silicon-based oxynitride and nitride phosphors for white LEDs—A review". Sci. Technol. Adv. Mater. 8 (7–8): 588. Bibcode:2007STAdM...8..588X. doi:10.1016/j.stam.2007.08.005.Open access icon
  3. ^ Li, Hui-Li; Hirosaki, Naoto; Xie, Rong-Jun; Suehiro, Takayuki; Mitomo, Mamoru (2007). "Fine yellow α-SiAlON:Eu phosphors for white LEDs prepared by the gas-reduction–nitridation method". Sci. Technol. Adv. Mater. 8 (7–8): 601. Bibcode:2007STAdM...8..601L. doi:10.1016/j.stam.2007.09.003.Open access icon
  4. ^ Kane, Raymond and Sell, Heinz (2001) Revolution in lamps: a chronicle of 50 years of progress, 2nd ed. The Fairmont Press. ISBN 0-88173-378-4. Chapter 5 extensively discusses history, application and manufacturing of phosphors for lamps.
  5. ^ a b Matsuzawa, T.; Aoki, Y.; Takeuchi, N.; Murayama, Y. (1996-08-01). "A New Long Phosphorescent Phosphor with High Brightness, SrAl2O4: Eu2+, Dy3+". Journal of the Electrochemical Society. 143 (8): 2670–2673. Bibcode:1996JElS..143.2670M. doi:10.1149/1.1837067. ISSN 0013-4651.
  6. ^ US5424006A, "Phosphorescent phosphor", issued 1994-02-25 
  7. ^ a b c d e f g Peter W. Hawkes (1 October 1990). Advances in electronics and electron physics. Academic Press. pp. 350–. ISBN 978-0-12-014679-6. Retrieved 9 January 2012.
  8. ^ Bizarri, G; Moine, B (2005). "On phosphor degradation mechanism: thermal treatment effects". Journal of Luminescence. 113 (3–4): 199. Bibcode:2005JLum..113..199B. doi:10.1016/j.jlumin.2004.09.119.
  9. ^ Lakshmanan, p. 171.
  10. ^ Tanno, Hiroaki; Fukasawa, Takayuki; Zhang, Shuxiu; Shinoda, Tsutae; Kajiyama, Hiroshi (2009). "Lifetime Improvement of BaMgAl10O17:Eu2+ Phosphor by Hydrogen Plasma Treatment". Japanese Journal of Applied Physics. 48 (9): 092303. Bibcode:2009JaJAP..48i2303T. doi:10.1143/JJAP.48.092303. S2CID 94464554.
  11. ^ Ntwaeaborwa, O. M.; Hillie, K. T.; Swart, H. C. (2004). "Degradation of Y2O3:Eu phosphor powders". Physica Status Solidi C. 1 (9): 2366. Bibcode:2004PSSCR...1.2366N. doi:10.1002/pssc.200404813.
  12. ^ Wang, Ching-Wu; Sheu, Tong-Ji; Su, Yan-Kuin; Yokoyama, Meiso (1997). "Deep Traps and Mechanism of Brightness Degradation in Mn-doped ZnS Thin-Film Electroluminescent Devices Grown by Metal-Organic Chemical Vapor Deposition". Japanese Journal of Applied Physics. 36 (5A): 2728. Bibcode:1997JaJAP..36.2728W. doi:10.1143/JJAP.36.2728. S2CID 98131548.
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  16. ^ Lehner, P.; Staudinger, C.; Borisov, S. M.; Klimant, l. (2014). "Ultra-sensitive optical oxygen sensors for characterization of nearly anoxic systems". Nature Communications. 5: 4460. Bibcode:2014NatCo...5.4460L. doi:10.1038/ncomms5460. PMC 4109599. PMID 25042041.
  17. ^ Hamzehpoor, E; Ruchlin, C.; Tao, Y.; Liu, C. H.; Titi, H. M.; Perepichka, D. F. (2022). "Efficient room-temperature phosphorescence of covalent organic frameworks through covalent halogen doping". Nature Chemistry. 15 (1): 83–90. doi:10.1038/s41557-022-01070-4. PMID 36302870. S2CID 253183290.
  18. ^ Xie, Z.; Ma, L.; deKrafft, K. E.; Jin, A.; Lin, W. (2010). "Porous phosphorescent coordination polymers for oxygen sensing". J. Am. Chem. Soc. 132 (3): 922–923. doi:10.1021/ja909629f. PMID 20041656.
  19. ^ SEEING PHOSPHOR BANDS on U.K. STAMPS Archived 2015-10-19 at the Wayback Machine.
  20. ^ Phosphor Bands Archived 2017-03-17 at the Wayback Machine.
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  22. ^ XTECH, NIKKEI. "Sharp to Employ White LED Using Sialon". NIKKEI XTECH. Retrieved 2019-01-10.
  23. ^ Youn-Gon Park; et al. "Luminescence and temperature dependency of β-SiAlON phosphor". Samsung Electro Mechanics Co. Archived from the original on 2010-04-12. Retrieved 2009-09-24.
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  36. ^ "VFD｜Futaba Corporation". 27 February 2021.
  37. ^ Lagos C (1974) "Strontium aluminate phosphor activated by cerium and manganese" U.S. patent 3,836,477

Bibliography

Look up phosphor in Wiktionary, the free dictionary.
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