The present disclosure generally relates to vehicle lighting systems, and more particularly, to vehicle lighting systems employing one or more photoluminescent structures.
Illumination arising from the use of photoluminescent structures offers a unique and attractive viewing experience. It is therefore desired to implement such structures in automotive vehicles for various lighting applications.
According to one aspect of the present invention, an illumination assembly for a vehicle is disclosed. The illumination assembly includes one or more decorative elements each having a substrate and a film attached thereto. A light source is configured to emit an excitation light. The light source is disposed within a tail-light assembly and the excitation light exits the tail-light assembly through a light transmissive portion towards the decorative element. A first photoluminescent structure is disposed within the decorative element and is configured to convert the excitation light emitted from the light source into a converted light of a different wavelength.
According to another aspect of the present invention, an illuminable decorative element for a vehicle is disclosed. The illuminable decorative element includes a film having a base layer, a decorative layer, and a protective layer. A substrate is integrally attached to the base layer of the film. The substrate includes a photoluminescent structure configured to emit a converted light in response to receiving an excitation light emitted from a light source. An adhesive coating is disposed between the substrate and a vehicle body panel.
According to another aspect of the present invention, a vehicle is disclosed. The vehicle includes an illumination assembly including one or more decorative elements. Each decorative element includes a photoluminescent structure configured to emit a converted light in response to receiving an excitation light. The vehicle further includes a vehicle lighting assembly having one or more light sources therein. A first portion of excitation light is emitted through a lens in the lighting assembly. A second portion of excitation light is emitted through a transmissive portion towards the illumination assembly.
These and other aspects, objects, and features of the present invention will be understood and appreciated by those skilled in the art upon studying the following specification, claims, and appended drawings.
In the drawings:
As required, detailed embodiments of the present invention are disclosed herein. However, it is to be understood that the disclosed embodiments are merely exemplary of the invention that may be embodied in various and alternative forms. The figures are not necessarily to a detailed design and some schematics may be exaggerated or minimized to show function overview. Therefore, specific structural and functional details disclosed herein are not to be interpreted as limiting, but merely as a representative basis for teaching one skilled in the art to variously employ the present invention.
As used herein, the term “and/or,” when used in a list of two or more items, means that any one of the listed items can be employed by itself, or any combination of two or more of the listed items can be employed. For example, if a composition is described as containing components A, B, and/or C, the composition can contain A alone; B alone; C alone; A and B in combination; A and C in combination; B and C in combination; or A, B, and C in combination.
The following disclosure describes an illumination assembly for a vehicle. The illumination assembly may include one or more independently illuminated decorative elements. The decorative elements may include one or more photoluminescent structures configured to convert excitation light received from an associated light source to a converted light at a different wavelength typically found in the visible spectrum.
Referring to
At the most basic level, a given photoluminescent structure 10 includes an energy conversion layer 16 that may include one or more sub layers, which are exemplarily shown through broken lines in
Light emitted by a light source 82 (
The energy conversion layer 16 may be prepared by dispersing the photoluminescent material 18 in a polymer matrix to form a homogenous mixture using a variety of methods. Such methods may include preparing the energy conversion layer 16 from a formulation in a liquid carrier medium 14 and coating the energy conversion layer 16 to a desired substrate 12. The energy conversion layer 16 may be applied to a substrate 12 by painting, screen printing, spraying, slot coating, dip coating, roller coating, and bar coating. Alternatively, the energy conversion layer 16 may be prepared by methods that do not use a liquid carrier medium 14. For example, the energy conversion layer 16 may be rendered by dispersing the photoluminescent material 18 into a solid state solution (homogenous mixture in a dry state) that may be incorporated in a polymer matrix, which may be formed by extrusion, injection molding, compression molding, calendaring, thermoforming, etc. The energy conversion layer 16 may then be integrated into a substrate 12 using any methods known to those skilled in the art. When the energy conversion layer 16 includes sub layers, each sub layer may be sequentially coated to form the energy conversion layer 16. Alternatively, the sub layers can be separately prepared and later laminated or embossed together to form the energy conversion layer 16. Alternatively still, the energy conversion layer 16 may be formed by coextruding the sub layers.
In some embodiments, the converted light 26 that has been down converted or up converted may be used to excite other photoluminescent material(s) 18 found in the energy conversion layer 16. The process of using the converted light 26 outputted from one photoluminescent material 18 to excite another, and so on, is generally known as an energy cascade and may serve as an alternative for achieving various color expressions. With respect to either conversion principle, the difference in wavelength between the excitation light 24 and the converted light 26 is known as the Stokes shift and serves as the principle driving mechanism for an energy conversion process corresponding to a change in wavelength of light. In the various embodiments discussed herein, each of the photoluminescent structures 10 may operate under either conversion principle.
Referring back to
Additional information regarding the construction of photoluminescent structures 10 is disclosed in U.S. Pat. No. 8,232,533 to Kingsley et al., entitled “PHOTOLYTICALLY AND ENVIRONMENTALLY STABLE MULTILAYER STRUCTURE FOR HIGH EFFICIENCY ELECTROMAGNETIC ENERGY CONVERSION AND SUSTAINED SECONDARY EMISSION,” filed Nov. 8, 2011, the entire disclosure of which is incorporated herein by reference. For additional information regarding fabrication and utilization of photoluminescent materials to achieve various light emissions, refer to U.S. Pat. No. 8,207,511 to Bortz et al., entitled “PHOTOLUMINESCENT FIBERS, COMPOSITIONS AND FABRICS MADE THEREFROM”; U.S. Pat. No. 8,247,761 to Agrawal et al., entitled “PHOTOLUMINESCENT MARKINGS WITH FUNCTIONAL OVERLAYERS”; U.S. Pat. No. 8,519,359 B2 to Kingsley et al., entitled “PHOTOLYTICALLY AND ENVIRONMENTALLY STABLE MULTILAYER STRUCTURE FOR HIGH EFFICIENCY ELECTROMAGNETIC ENERGY CONVERSION AND SUSTAINED SECONDARY EMISSION”; U.S. Pat. No. 8,664,624 B2 to Kingsley et al., entitled “ILLUMINATION DELIVERY SYSTEM FOR GENERATING SUSTAINED SECONDARY EMISSION”; U.S. Patent Publication No. 2012/0183677 to Agrawal et al., entitled “PHOTOLUMINESCENT COMPOSITIONS, METHODS OF MANUFACTURE AND NOVEL USES”; U.S. Pat. No. 9,057,021 to Kingsley et al., entitled “PHOTOLUMINESCENT OBJECTS”; and U.S. Patent Publication No. 2014/0103258 A1 to Agrawal et al., entitled “CHROMIC LUMINESCENT COMPOSITIONS AND TEXTILES,” all of which are incorporated herein by reference in their entirety.
According to one embodiment, the photoluminescent material 18 may include organic or inorganic fluorescent dyes including rylenes, xanthenes, porphyrins, phthalocyanines. Additionally, or alternatively, the photoluminescent material 18 may include phosphors from the group of Ce-doped garnets such as YAG:Ce and may be a short persistence photoluminescent material 18. For example, an emission by Ce3+ is based on an electronic energy transition from 5d1 to 4f1 as a parity allowed transition. As a result of this, a difference in energy between the light absorption and the light emission by Ce3+ is small, and the luminescent level of Ce3+ has a ultra-short lifespan, or decay time, of 10−8 to 10−7 seconds (10 to 100 nanoseconds). The decay time may be defined as the time between the end of excitation from the excitation light 24 and the moment when the light intensity of the converted light 26 emitted from the photoluminescent structure 10 drops below a minimum visibility of 0.32 mcd/m2. A visibility of 0.32 mcd/m2 is roughly 100 times the sensitivity of the dark-adapted human eye, which corresponds to a base level of illumination commonly used by persons of ordinary skill in the art.
According to one embodiment, a Ce3+ garnet may be utilized, which has a peak excitation spectrum that may reside in a shorter wavelength range than that of conventional YAG:Ce-type phosphors. Accordingly, Ce3+ has short persistence characteristics such that its decay time may be 100 milliseconds or less. Therefore, in some embodiments, the rare earth aluminum garnet type Ce phosphor may serve as the photoluminescent material 18 with ultra-short persistence characteristics, which can emit the converted light 26 by absorbing purple to blue excitation light 24 emitted from a light source 82. According to one embodiment, a ZnS:Ag phosphor may be used to create a blue converted light 26. A ZnS:Cu phosphor may be utilized to create a yellowish-green converted light 26. A Y2O2S:Eu phosphor may be used to create red converted light 26. Moreover, the aforementioned phosphorescent materials may be combined to form a wide range of colors, including white light. It will be understood that any short persistence photoluminescent material known in the art may be utilized without departing from the teachings provided herein. Additional information regarding the production of short persistence photoluminescent materials is disclosed in U.S. Pat. No. 8,163,201 to Kingsley et al., entitled “PHOTOLYTICALLY AND ENVIRONMENTALLY STABLE MULTILAYER STRUCTURE FOR HIGH EFFICIENCY ELECTROMAGNETIC ENERGY CONVERSION AND SUSTAINED SECONDARY EMISSION,” the entire disclosure of which is incorporated herein by reference.
Additionally, or alternatively, the photoluminescent material 18, according to one embodiment, disposed within the photoluminescent structure 10 may include a long persistent phosphorescent material that emits the converted light 26, once charged by the excitation light 24. The excitation light 24 may be emitted from any excitation source (e.g., any natural and/or artificial light source). The long persistent phosphorescent material may be defined as having a long decay time due to its ability to store the excitation light 24 and release the converted light 26 gradually, for a period of several minutes or hours, once the excitation light 24 is no longer present.
The long persistent phosphorescent material, according to one embodiment, may be operable to emit light at or above an intensity of 0.32 mcd/m2 after a period of 10 minutes. Additionally, the long persistent phosphorescent material may be operable to emit light above or at an intensity of 0.32 mcd/m2 after a period of 30 minutes and, in some embodiments, for a period substantially longer than 60 minutes (e.g., the period may extend 24 hours or longer, and in some instances, the period may extend 48 hours). Accordingly, the long persistent phosphorescent material may continually illuminate in response to excitation from a plurality of light sources that emit the excitation light 24, including, but not limited to, natural light sources (e.g., the sun) and/or any artificial light source 82. The periodic absorption of the excitation light 24 from any excitation source may provide for a substantially sustained charge of the long persistent phosphorescent material to provide for consistent passive illumination. In some embodiments, a light sensor may monitor the illumination intensity of the photoluminescent structure 10 and actuate an excitation source when the illumination intensity falls below 0.32 mcd/m2, or any other predefined intensity level.
The long persistent phosphorescent material may correspond to alkaline earth aluminates and silicates, for example doped di-silicates, or any other compound that is capable of emitting light for a period of time once the excitation light 24 is no longer present. The long persistent photoluminescent material 18 may be doped with one or more ions, which may correspond to rare earth elements, for example, Eu2+, Tb3+ and/or Dy3. According to one non-limiting exemplary embodiment, the photoluminescent structure 10 includes a phosphorescent material in the range of about 30% to about 55%, a liquid carrier medium in the range of about 25% to about 55%, a polymeric resin in the range of about 15% to about 35%, a stabilizing additive in the range of about 0.25% to about 20%, and performance-enhancing additives in the range of about 0% to about 5%, each based on the weight of the formulation.
The photoluminescent structure 10, according to one embodiment, may be a translucent white color, and in some instances reflective, when unilluminated. Once the photoluminescent structure 10 receives the excitation light 24 of a particular wavelength, the photoluminescent structure 10 may emit any color light (e.g., blue or red) therefrom at any desired brightness. According to one embodiment, a blue emitting phosphorescent material may have the structure Li2ZnGeO4 and may be prepared by a high temperature solid-state reaction method or through any other practicable method and/or process. The afterglow may last for a duration of two to eight hours and may originate from the excitation light 24 and d-d transitions of Mn2+ ions.
According to an alternate non-limiting exemplary embodiment, 100 parts of a commercial solvent-borne polyurethane, such as Mace resin 107-268, having 50% solids polyurethane in Toluene/Isopropanol, 125 parts of a blue green long long persistent phosphor, such as Performance Indicator PI-BG20, and 12.5 parts of a dye solution containing 0.1% Lumogen Yellow F083 in dioxolane may be blended to yield a low rare earth mineral photoluminescent structure 10. It will be understood that the compositions provided herein are non-limiting examples. Thus, any phosphor known in the art may be utilized within the photoluminescent structure 10 without departing from the teachings provided herein. Moreover, it is contemplated that any long persistent phosphor known in the art may also be utilized without departing from the teachings provided herein.
Additional information regarding the production of long persistent photoluminescent materials is disclosed in U.S. Pat. No. 8,163,201 to Agrawal et al., entitled “HIGH-INTENSITY, PERSISTENT PHOTOLUMINESCENT FORMULATIONS AND OBJECTS, AND METHODS FOR CREATING THE SAME,” the entire disclosure of which is incorporated herein by reference. For additional information regarding long persistent phosphorescent structures, refer to U.S. Pat. No. 6,953,536 to Yen et al., entitled “LONG PERSISTENT PHOSPHORS AND PERSISTENT ENERGY TRANSFER TECHNIQUE”; U.S. Pat. No. 6,117,362 to Yen et al., entitled “LONG-PERSISTENT BLUE PHOSPHORS”; and U.S. Pat. No. 8,952,341 to Kingsley et al., entitled “LOW RARE EARTH MINERAL PHOTOLUMINESCENT COMPOSITIONS AND STRUCTURES FOR GENERATING LONG-PERSISTENT LUMINESCENCE,” all of which are incorporated herein by reference in their entirety.
Referring to
Referring to
The film 44, according to one embodiment, includes a base layer 46 that may be formed from a soft thermoplastic resin, such as, but not limited to, polypropylene, polystyrene, polyethylene, polyester, acrylic, and/or any combination thereof.
A decorative layer 48 is disposed on the base layer 46. The decorative layer 48 may include a polymeric material or any other suitable material and is configured to control or modify an appearance of the film 44. For example, the decorative layer 48 may be configured to confer a metallic appearance to the viewable portion 40. The metallic appearance can be disposed on the base layer 46 and/or within the base layer 46 through any method known in the art, including, but not limited to, sputter deposition, vacuum deposition (vacuum evaporation coating), electroplating, or directly printed on to the base layer 46 by a computer printer after preparation of the desired pattern through a computer. The metallic appearance may be chosen from a wide range of reflective materials and/or colors, including, but not limited to, silver, chrome, copper, bronze, gold, or any other metallic surface. Additionally, an imitator of any metallic material may also be utilized without departing from the teachings provided herein.
In other embodiments, the decorative layer 48 may be tinted any color to complement the vehicle structure on which the decorative element 38 is to be received. In any event, the decorative layer 48 should be at least partially light transmissible such that the converted light 26 is not prevented from illuminating the viewable portion 40 whenever an energy conversion process is underway.
A protective layer 50 may be disposed over the decorative layer 48. The protective layer 50 may protect the decorative layer 48 and/or base layer 46 from physical and chemical damage arising from environmental exposure. The protective layer 50 may have viscoelasticity (i.e. having both viscosity and elasticity), a low Young's modulus, and/or a high failure strain so that the film 44 may be formed through various manufacturing process, including, but not limited to, thermoforming, vacuum forming, and/or in-mold decorating.
According to one embodiment, the film 44 is attached to a substrate 52 that may be formed by extrusion, injection molding, compression sealing, calendaring, thermoforming, etc. The substrate 52 may be formed from a polymeric material that includes one or more photoluminescent structures 10 therein and/or thereon. Furthermore, the substrate 52 material may be made of a ultraviolet (UV) stable material, such as an acrylic, or may have a UV stabilizer added thereto.
As illustrated in
An adhesive coating 60 may be disposed on a bottom surface 62 of the substrate 52. The adhesive coating 60 can be any adhesive known in the art. According to one embodiment, the thickness of the adhesive coating 60 may be between 0.0002 to 0.02 inches according to one embodiment. Additionally, or alternatively, the decorative element 38 may include a magnetic layer that temporarily adheres to ferrous exterior body panels of the vehicle 32. The decorative element 38 may also include any permanent adhesive backing or fixing apparatus for permanent application to the vehicle 32.
Referring to
Next, a male mold member 68 is closed onto the female mold member 64 to force the mold block 70 of the male mold member 68 against the film 44 and towards the cavity 66 of the female mold member 64. The pressing of the male mold member 68 may press the film 44 into the correct shape. Alternatively, the film 44 may be vacuum formed against the female mold member 64.
A molten plastic material 72, having one or more photoluminescent structures 10 therein, is then filled through the male mold member 68 into the cavity 66 of the female mold member 64 for enabling the applied molten plastic material 72 to be molded on to the film 44, as shown in
Next, the male mold member 68 is separated from the female mold member 64, as shown in
Referring to
The vehicle 32 also includes at least one light sources 82, which may be within any lighting assembly disposed on and/or within the vehicle 32. For example, the light source may be disposed within the tail-light assembly 74 and may emit excitation light 24 that may be directed towards the illumination assembly 28. Alternatively, the light source 82 may be disposed within and/or on any trim component, body panel, or any other surface of the vehicle 32 without departing from the teachings provided herein. Alternatively still, any number of the decorative elements 38 may be disposed on the component having the light source 82 therein to backlight any of the decorative elements 38.
According to one embodiment, the light source 82 emitting the excitation light 24 may be configured as a light emitting diode (LED) that emits a wavelength of light that is characterized as ultraviolet light (˜10-400 nanometers in wavelength), violet light (˜380-450 nanometers in wavelength), blue light (˜450-495 nanometers in wavelength), and/or infrared light (IR) (˜700 nm-1 mm in wavelength) to take advantage of the relative low cost attributable to those types of LEDs. Additionally, the light source 82 may include LEDs that are printed onto an interior surface of the tail-light assembly 74. Additional information regarding the construction of vehicle components incorporating printed LEDs therein is disclosed in U.S. patent application Ser. No. 14/851,726 to Salter et al., entitled “ILLUMINATED STEERING ASSEMBLY,” filed Sep. 11, 2015, the entire disclosure of which is hereby incorporated herein by reference.
In operation, the photoluminescent material 18 is formulated to become excited upon receiving excitation light of a specific wavelength from the light source 82. As a result, the excitation light 24 undergoes an energy conversion process and is re-emitted at a different wavelength. According to one embodiment, the photoluminescent material 18 may be formulated to convert the excitation light 24 into a longer wavelength light, otherwise known as down conversion. Alternatively, the photoluminescent material 18 may be formulated to convert the excitation light 24 into a shorter wavelength light, otherwise known as up conversion. Under either approach, light converted by the photoluminescent material 18 may be immediately outputted from the photoluminescent structure 10 or otherwise used in an energy cascade, wherein the converted light 26 serves as the excitation light 24 to excite another formulation of photoluminescent material 18 located within the energy conversion layer 16, whereby the subsequent the converted light 26 may then be outputted from the photoluminescent structure 10 or used as the excitation light 24, and so on. With respect to the energy conversion processes described herein, the difference in wavelength between the excitation light 24 and the converted light 26 is known as the Stokes shift and serves as the principle driving mechanism for an energy conversion process corresponding to a change in wavelength of light.
The light source(s) 82 may emit the excitation light 24 at a first and/or a second wavelength, thereby exciting the first and/or the second photoluminescent structures 10, 58. The converted light 26 emitted from the first and/or the second photoluminescent structures 10, 58 may blend thereby emitting an outputted light in a wide range of colors. For example, a substantially white light may be outputted from the illumination assembly 28. In an alternative embodiment, the first and second photoluminescent structures 10, 58 may blend in any color necessary to remove any natural color hue of the illumination assembly 28 based on the material used to create the illumination assembly 28. For example, plastics such as polycarbonate may naturally have a yellowish hue. However, this hue may be masked through the use of the first and/or the second photoluminescent structures 10, 58 thereby making the illumination assembly 28 illuminate and appear in any desired color. Alternatively, any type of light source, multicolored or unicolored, may be utilized to make the illumination assembly 28 illuminate in any desired color without the utilization of the first and/or the second photoluminescent structures 10, 58.
The tail-light assembly 74 may extend vehicle side-to-side along the rear portion 30 of the vehicle 32 and may be bordered by body panels of the vehicle 32 such as the truck lid 34, rear fenders 76 and 78, and/or a bumper assembly 80. As illustrated, a single tail-light assembly 74 extends laterally across a substantial portion of the rear portion 30 of the vehicle 32. However, in alternate embodiments, the tail-light assembly 74 may be of any other size, and the vehicle 32 may include any number of lighting assemblies that together form the tail-light assembly 74 without departing from the teachings provided herein.
The tail-light assembly 74 includes one or more light sources 82. The light sources 82 may be configured as any type of light source and may be configured to confer a plurality of vehicular conditions to proximately located vehicles. For example, the light sources 82 may illuminate when the vehicle 32 is running at night, braking, turning a particular direction, etc.
Referring to
As shown in
With respect to the embodiment shown in
The excitation light 24 emitted through the light transmissive portion 96 is directed towards the one or more decorative element(s) 38. The photoluminescent structure 10 within each decorative element 38 emits the converted light 26 in response to receiving the excitation light 24. Accordingly, the decorative element(s) 38 may illuminate in conjunction with, or independently of, the tail-light assembly 74.
Referring to
According to one embodiment, the light source 82 may be configured as a laser diode. As illustrated in
According to one embodiment, the excitation light 24 emitted from the light source(s) 82 is converted by the photoluminescent structure 10 into light of a longer wavelength and outputted therefrom. The converted light 26 corresponds to a visible light, which includes the portion of the electromagnetic spectrum that can be detected by the human eye (˜390-700 nanometers in wavelength) and may be expressed in a variety of colors defined by a single wavelength (e.g., red, green, blue) or a mixture of multiple wavelengths (e.g., white). Thus, it should be understood that the photoluminescent structure 10 may be configured such that the converted light 26 outputted therefrom is capable of being expressed as unicolored or multicolored light. According to one embodiment, the light sources 82 are configured to emit blue light and the photoluminescent structure 10 is configured to convert the blue light into a neutral white light having a color temperature of approximately 4000K to 5000K. The converted light 26 escapes from the illumination assembly 28 via the viewable portion 40. According to one embodiment, the photoluminescent structure 10 is substantially Lambertian, that is, the apparent brightness of the photoluminescent structure 10 is substantially constant regardless of an observer's angle of view. As a consequence, the converted light 26 may be emitted outwardly from the decorative element 38 in numerous directions in a substantially uniform manner.
Referring to
In operation, the first and/or the second photoluminescent structures 10, 58 receive the excitation light 24 and, in response, emits the converted light 26 therefrom. The first and/or the second photoluminescent structure(s) 10, 58 may contain a short persistent phosphorescent material such that the photoluminescent structure 10, 58 emits the converted light 26 while the excitation light 24 is present, and shortly returns to a unilluminated state thereafter. For example, according to one embodiment, the first and/or the second photoluminescent structure 10, 58 may emit light for 100 milliseconds after the removal of the excitation light 24.
In an alternate embodiment, the light source 82 emits the excitation light 24 at predefined times, such as when the vehicle brakes are initiated, to re-excite the phosphorescent material disposed within the first and/or the second photoluminescent structures 10, 58. Additionally, or alternatively, the light source 82 may emit the excitation light 24 in conjunction with vehicle running lights such that the illumination assembly 28 is illuminated whenever the running lights are illuminated.
The photoluminescent structure(s) 10, 58 may exhibit periodic unicolor or multicolor illumination. For example, the controller 118 may prompt the light source 82 to periodically emit only the first wavelength of excitation light 24 to cause the first photoluminescent structure 10 to periodically illuminate in the first color. Alternatively, the controller 118 may prompt the light source 82 to periodically emit only the second wavelength of excitation light 24 to cause the second photoluminescent structure 58 to periodically illuminate in the second color. Alternatively, the controller 118 may prompt the light source 82 to simultaneously and periodically emit the first and second wavelengths of excitation light 24 to cause the first and second photoluminescent structures 10, 58 to simultaneously illuminate in a third color defined by an additive light mixture of the first and second colors. Alternatively still, the controller 118 may prompt the light source 82 to alternate between periodically emitting the first and second wavelengths of excitation light 24 to cause the first and second photoluminescent structures 10, 58 to periodically illuminate by alternating between the first and second colors. The controller 118 may prompt the light source 82 to periodically emit the first and/or the second wavelengths of excitation light 24 at a regular time interval and/or an irregular time interval.
In another embodiment, the illumination assembly 28 may include a user interface 128. The user interface 128 may be configured such that a user may control the wavelength of excitation light 24 that is emitted by the light source 82. Such a configuration may allow a user to control the illumination patterns of the illumination assembly 28.
With respect to the above examples, the controller 118 may modify the intensity of the emitted first and second wavelengths of excitation light 24 by pulse-width modulation or current control. Also, the controller 118 may vary power to each light source 82 from 1 to 5 times steady state current to vary the color and brightness of each illumination. The controller 118 may also illuminate multiple colors within a single multicolored light source 82 concurrently, thereby producing additional color configurations.
In some embodiments, the controller 118 may be configured to adjust a color of the emitted light by sending control signals to adjust an intensity or energy output level of the light source 82. For example, if the light source(s) 82 are configured to emit the excitation light 24 at a low level, substantially all of the excitation light 24 may be converted to the converted light 26 by the first and/or the second photoluminescent structures 10, 58. In this configuration, a color of light corresponding to the converted light 26 may correspond to the color of the emitted light from the illumination assembly 28. If the light source(s) 82 are configured to emit the excitation light 24 at a high level, only a portion of the excitation light 24 may be converted to the converted light 26 by the first and/or the second photoluminescent structures 10, 58. In this configuration, a color of light corresponding to mixture of the excitation light 24 and the converted light 26 may be output as the emitted light. In this way, the controller 118 may control an output color of the emitted light.
Though a low level and a high level of intensity are discussed in reference to the excitation light 24, it shall be understood that the intensity of the excitation light 24 may be varied among a variety of intensity levels to adjust a hue of the color corresponding to the emitted light from the illumination assembly 28. The variance in intensity may be manually altered, or automatically varied by the controller 118 based on pre-defined conditions. According to one embodiment, a first intensity may be output from the illumination assembly 28 when a light sensor senses daylight conditions. A second intensity may be output from the illumination assembly 28 when the light sensor determines the vehicle 32 is operating in a low light environment.
As described herein, the color of the converted light 26 may be significantly dependent on the particular photoluminescent materials 18 utilized in the first and second photoluminescent structures 10, 58. Additionally, a conversion capacity of the first and second photoluminescent structures 10, 58 may be significantly dependent on a concentration of the photoluminescent material 18 utilized in the photoluminescent structures 10, 58. By adjusting the range of intensities that may be output from the light source(s) 82 the concentration, types, and proportions of the photoluminescent materials 18 in the photoluminescent structures 10, 58 discussed herein may be operable to generate a range of color hues of the emitted light by blending the excitation light 24 with the converted light 26. Moreover, the first and second photoluminescent structures 10, 58 may include a wide range of photoluminescent materials 18 that are configured to emit the converted light 26 for varying lengths of time.
Accordingly, an illuminating assembly for a vehicle has been advantageously described herein. The badge provides various benefits including an efficient and cost-effective means to produce illumination that may function as a distinct styling element that increases the refinement of a vehicle, or any other product that may have an illumination assembly disposed thereon.
It is also important to note that the construction and arrangement of the elements of the disclosure as shown in the exemplary embodiments are illustrative only. Although only a few embodiments of the present innovations have been described in detail in this disclosure, those skilled in the art who review this disclosure will readily appreciate that many modifications are possible (e.g., variations in sizes, dimensions, structures, shapes and proportions of the various elements, values of parameters, mounting arrangements, use of materials, colors, orientations, etc.) without materially departing from the novel teachings and advantages of the subject matter recited. For example, elements shown as integrally formed may be constructed of multiple parts or elements shown in multiple parts may be integrally formed, the operation of the interfaces may be reversed or otherwise varied, the length or width of the structures and/or members or connectors or other elements of the system may be varied, the nature or number of adjustment positions provided between the elements may be varied. It should be noted that the elements and/or assemblies of the system might be constructed from any of the wide variety of materials that provide sufficient strength or durability, in any of the wide variety of colors, textures, and combinations. Accordingly, all such modifications are intended to be included within the scope of the present innovations. Other substitutions, modifications, changes, and omissions may be made in the design, operating conditions, and arrangement of the desired and other exemplary embodiments without departing from the spirit of the present innovations.
It will be understood that any described processes or steps within described processes may be combined with other disclosed processes or steps to form structures within the scope of the present disclosure. The exemplary structures and processes disclosed herein are for illustrative purposes and are not to be construed as limiting.
It is to be understood that variations and modifications can be made on the aforementioned structure without departing from the concepts of the present disclosure, and further it is to be understood that such concepts are intended to be covered by the following claims unless these claims by their language expressly state otherwise.
Number | Name | Date | Kind |
---|---|---|---|
5053930 | Benavides | Oct 1991 | A |
5709453 | Krent et al. | Jan 1998 | A |
5839718 | Hase et al. | Nov 1998 | A |
5920150 | Crary et al. | Jul 1999 | A |
6031511 | DeLuca et al. | Feb 2000 | A |
6117362 | Yen et al. | Sep 2000 | A |
6299338 | Levinson et al. | Oct 2001 | B1 |
6419854 | Yocom et al. | Jul 2002 | B1 |
6494490 | Trantoul | Dec 2002 | B1 |
6577073 | Shimizu et al. | Jun 2003 | B2 |
6729738 | Fuwausa et al. | May 2004 | B2 |
6737964 | Samman et al. | May 2004 | B2 |
6773129 | Anderson, Jr. et al. | Aug 2004 | B2 |
6820888 | Griffin | Nov 2004 | B1 |
6851840 | Ramamurthy et al. | Feb 2005 | B2 |
6859148 | Miller | Feb 2005 | B2 |
6871986 | Yamanaka et al. | Mar 2005 | B2 |
6953536 | Yen et al. | Oct 2005 | B2 |
6990922 | Ichikawa et al. | Jan 2006 | B2 |
7161472 | Strumolo et al. | Jan 2007 | B2 |
7213923 | Liu et al. | May 2007 | B2 |
7216997 | Anderson, Jr. | May 2007 | B2 |
7264366 | Hulse | Sep 2007 | B2 |
7264367 | Hulse | Sep 2007 | B2 |
7441914 | Palmer et al. | Oct 2008 | B2 |
7501749 | Takeda et al. | Mar 2009 | B2 |
7575349 | Bucher et al. | Aug 2009 | B2 |
7635212 | Seidler | Dec 2009 | B2 |
7745818 | Sofue et al. | Jun 2010 | B2 |
7753541 | Chen et al. | Jul 2010 | B2 |
7834548 | Jousse et al. | Nov 2010 | B2 |
7845839 | Collier | Dec 2010 | B2 |
7862220 | Cannon et al. | Jan 2011 | B2 |
7937865 | Li et al. | May 2011 | B2 |
7987030 | Flores et al. | Jul 2011 | B2 |
8016465 | Egerer et al. | Sep 2011 | B2 |
8022818 | la Tendresse et al. | Sep 2011 | B2 |
8066416 | Bucher | Nov 2011 | B2 |
8071988 | Lee et al. | Dec 2011 | B2 |
8097843 | Agrawal et al. | Jan 2012 | B2 |
8136425 | Bostick | Mar 2012 | B2 |
8163201 | Agrawal et al. | Apr 2012 | B2 |
8178852 | Kingsley et al. | May 2012 | B2 |
8197105 | Yang | Jun 2012 | B2 |
8203260 | Li et al. | Jun 2012 | B2 |
8207511 | Bortz et al. | Jun 2012 | B2 |
8232533 | Kingsley et al. | Jul 2012 | B2 |
8247761 | Agrawal et al. | Aug 2012 | B1 |
8286378 | Martin et al. | Oct 2012 | B2 |
8408766 | Wilson et al. | Apr 2013 | B2 |
8415642 | Kingsley et al. | Apr 2013 | B2 |
8421811 | Odland et al. | Apr 2013 | B2 |
8466438 | Lambert et al. | Jun 2013 | B2 |
8519359 | Kingsley et al. | Aug 2013 | B2 |
8519362 | Labrot et al. | Aug 2013 | B2 |
8552848 | Rao et al. | Oct 2013 | B2 |
8585263 | Shipman | Nov 2013 | B2 |
8606430 | Seder et al. | Dec 2013 | B2 |
8624716 | Englander | Jan 2014 | B2 |
8631598 | Li et al. | Jan 2014 | B2 |
8664624 | Kingsley et al. | Mar 2014 | B2 |
8683722 | Cowan | Apr 2014 | B1 |
8724054 | Jones | May 2014 | B2 |
8754426 | Marx et al. | Jun 2014 | B2 |
8773012 | Ryu et al. | Jul 2014 | B2 |
8846184 | Agrawal et al. | Sep 2014 | B2 |
8876352 | Robbins et al. | Nov 2014 | B2 |
8952341 | Kingsley et al. | Feb 2015 | B2 |
9006751 | Kleo et al. | Apr 2015 | B2 |
9018833 | Lowenthal et al. | Apr 2015 | B2 |
9057021 | Kingsley et al. | Jun 2015 | B2 |
9065447 | Buttolo et al. | Jun 2015 | B2 |
9187034 | Tarahomi et al. | Nov 2015 | B2 |
9299887 | Lowenthal et al. | Mar 2016 | B2 |
20020159741 | Graves et al. | Oct 2002 | A1 |
20020163792 | Formoso | Nov 2002 | A1 |
20030167668 | Fuks et al. | Sep 2003 | A1 |
20030179548 | Becker et al. | Sep 2003 | A1 |
20040213088 | Fuwausa | Oct 2004 | A1 |
20040244247 | Bolta | Dec 2004 | A1 |
20060087826 | Anderson, Jr. | Apr 2006 | A1 |
20060097121 | Fugate | May 2006 | A1 |
20070032319 | Tufte | Feb 2007 | A1 |
20070285938 | Palmer et al. | Dec 2007 | A1 |
20070297045 | Sakai et al. | Dec 2007 | A1 |
20090219730 | Syfert et al. | Sep 2009 | A1 |
20090251920 | Kino et al. | Oct 2009 | A1 |
20090260562 | Folstad et al. | Oct 2009 | A1 |
20090262515 | Lee et al. | Oct 2009 | A1 |
20110012062 | Agrawal et al. | Jan 2011 | A1 |
20120001406 | Paxton et al. | Jan 2012 | A1 |
20120055055 | Kunowski | Mar 2012 | A1 |
20120104954 | Huang | May 2012 | A1 |
20120138874 | Yuan et al. | Jun 2012 | A1 |
20120183677 | Agrawal et al. | Jul 2012 | A1 |
20120280528 | Dellock et al. | Nov 2012 | A1 |
20130335994 | Mulder et al. | Dec 2013 | A1 |
20140029281 | Suckling et al. | Jan 2014 | A1 |
20140065442 | Kingsley et al. | Mar 2014 | A1 |
20140103258 | Agrawal et al. | Apr 2014 | A1 |
20140240999 | Roberts et al. | Aug 2014 | A1 |
20140264396 | Lowenthal et al. | Sep 2014 | A1 |
20140266666 | Habibi | Sep 2014 | A1 |
20140373898 | Rogers et al. | Dec 2014 | A1 |
20150046027 | Sura et al. | Feb 2015 | A1 |
20150047238 | Shipman | Feb 2015 | A1 |
20150109602 | Martin et al. | Apr 2015 | A1 |
20150138789 | Singer et al. | May 2015 | A1 |
20150267881 | Salter et al. | Sep 2015 | A1 |
20160016506 | Collins et al. | Jan 2016 | A1 |
20160236613 | Trier | Aug 2016 | A1 |
Number | Date | Country |
---|---|---|
101337492 | Jan 2009 | CN |
201169230 | Feb 2009 | CN |
201193011 | Feb 2009 | CN |
204127823 | Jan 2015 | CN |
4120677 | Jan 1992 | DE |
29708699 | Jul 1997 | DE |
10319396 | Nov 2004 | DE |
1793261 | Jun 2007 | EP |
2778209 | Sep 2014 | EP |
2000159011 | Jun 2000 | JP |
2007238063 | Sep 2007 | JP |
20060026531 | Mar 2006 | KR |
2006047306 | May 2006 | WO |
2014068440 | May 2014 | WO |