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    • 专利摘要:
    PURPOSE: An effective method for aligning a substrate and laser beams independent of thermal expansion of the substrate is provided to reduce the utmost the number of alignment processes necessary for appropriately aligning the laser and the substrate. CONSTITUTION: In a method for aligning a substrate for manufacturing an organic luminescent display device with laser generating beams transferring an organic material from a donor element to the substrate, at least one calibration mark(42) is installed on the substrate(10). The substrate(10) is arranged to the laser(100), and the substrate is relatively moved until the laser beams hit to the calibration mark between the substrate and the laser and the laser beams. A period of time when the laser beams fit to the calibration mark(42) is detected to determine the position and orientation of the substrate.
    公开号:KR20040020004A
    申请号:KR1020030059968
    申请日:2003-08-28
    公开日:2004-03-06
    发明作者:투트리더블유；베드지크마크디
    申请人:이스트맨 코닥 캄파니；
    IPC主号:
    专利说明:

    USING FIDUCIAL MARKS ON A SUBSTRATE FOR LASER TRANSFER OF ORGANIC MATERIAL FROM A DONOR TO A SUBSTRATE}
    [9] The present invention relates to a method of manufacturing an organic light emitting device (OLED) for transferring an organic material from a donor to a substrate.
    [10] In color or fully color organic electroluminescent (EL) displays with arrays of color pixels, such as red, green and blue pixels (commonly referred to as RGB pixels), precise patterns of color-generating organic EL media are required to produce RGB pixels. Upset is required. Basic EL devices typically have an anode, a cathode, and an organic EL medium located between the anode and the cathode. The organic EL medium may consist of one or more layers of organic thin films, one of which is mainly responsible for luminescence or electroluminescence. This particular layer is generally referred to as the light emitting layer of the organic EL medium. Other organic layers present in the organic EL medium can primarily provide electron transport functions and are referred to as hole transport layers (for hole transport) or electron transport layers (for electron transport). In forming RGB pixels in a full color organic EL display panel, a method of precisely patterning the light emitting layer of the organic EL medium or the entire organic EL medium needs to be devised.
    [11] Typically, electroluminescent pixels are formed on a display by shadow masking techniques, such as those set forth in US Pat. No. 5,742,129. Although this method is effective, there are some disadvantages. It is difficult to achieve high resolution pixel size using shadow masking. It is also difficult to align the substrate and the shadow mask so that the pixels are formed at appropriate locations. If it is desired to increase the substrate size, it is more difficult to manipulate the shadow mask as part of the alignment process to form properly positioned pixels. A further disadvantage of the shadow mask method is that over time, mask holes can become blocked. If the holes in the mask are blocked, the pixels on the EL display will not function properly, resulting in unwanted results.
    [12] There is a further problem with the shadow mask method, which is particularly noticeable when manufacturing an EL device having a dimension larger than a few inches on one side. It is very difficult to produce larger shadow masks with the precision required to form the EL device accurately.
    [13] A method of patterning a high resolution organic EL display is disclosed in US Pat. No. 5,851,709 to Grande et al. The method comprises the steps of: 1) providing a substrate having opposing first and second surfaces; 2) forming a light-transmissive heat-insulating layer over the first surface of the substrate; 3) forming a light-absorption layer over the heat-insulating layer; 4) providing the substrate with an array of openings extending from the second surface to the heat-insulating layer; 5) providing a transferable color-forming organic donor layer formed on the light-absorbing layer; 6) precisely aligning the donor substrate with the display substrate in an oriented relationship between the opening of the substrate and the corresponding color pixel of the device; And 7) allowing the organic layer on the donor substrate to be transferred to the display substrate using an irradiation source to generate sufficient heat in the light-absorbing layer above the opening. A problem with the method of Grand et al. Is that the array of openings on the donor substrate must be patterned. This results in many of the same problems as in the shadow mask method, including the need for precise mechanical alignment between the donor substrate and the display substrate. A further problem is that the donor pattern is fixed and cannot easily be changed.
    [14] The use of unpatterned donor sheets and precision light sources (such as lasers) can eliminate some of the difficulties found in patterned donors. In a series of patents (Wolk et al. (US Pat. Nos. 6,114,088; 6,140,009; 6,214,520; and 6,221,553), a light emitting layer of an EL device is heated from a donor sheet to a substrate by heating selected donor portions with laser light. It teaches how to deliver. Work and the like describe that the use of light may be a desirable heat transfer modality in that precise registration required to manufacture large scale devices is possible. Although precisely tailored by laser heat transfer, it is essential to align and orient the light beam so that the correct area of the substrate receives the transferred donor material. Other heat transfer means also depend on precise alignment means between the substrate and the heat transfer means.
    [15] It is an object of the present invention to provide a more effective method of aligning a substrate with a laser beam regardless of the thermal expansion of the substrate.
    [16] Another object of the present invention is to minimize the number of alignment steps required to properly align the laser and the substrate.
    [1] 1A is a top view of an OLED substrate constructed in accordance with the present invention.
    [2] 1B is a cross sectional view illustrating the positioning of a substrate relative to a laser.
    [3] 2 is a partially enlarged top view of a substrate showing the position and reference marks of the photodetector and the laser spot.
    [4] 3 illustrates an embodiment of a device that provides relative movement to enable the method of the present invention.
    [5] 4A is a cross-sectional view of a laser that irradiates a substrate / donor element combination fixed with a light beam in accordance with the present invention.
    [6] 4B is a cross-sectional view of an OLED substrate and donor elements suitably positioned relative to the substrate in the practice of the present invention.
    [7] 5 is a block diagram of an electro-optic subsystem used to process signals and detect and determine the location of reference marks.
    [8] 6 is a block diagram showing the overall steps in detecting the position of the reference mark.
    [17] This object is a method of aligning a substrate for use in the manufacture of an OLED display by a laser that generates a beam that transfers an organic material from a donor element to the substrate, comprising: (a) providing one or more fiducial marks on the substrate; (b) positioning the substrate relative to the laser and providing relative motion between the laser beam and the laser and the substrate until the laser beam impinges upon the fiducial mark; And determining when the laser beam impinges on the fiducial mark to determine the position and orientation of the substrate.
    [18] An advantage of the present invention is that by providing a fiducial mark on the substrate, an effective method of determining the position and orientation of the substrate can be achieved prior to the delivery of the organic material. A further advantage of the present invention is that the same laser beam used to transfer from the donor element to the substrate can also be used to determine the position and orientation of the substrate relative to the laser. The alignment according to the invention is very accurate and provided by the direct detection of the reference mark. Another advantage of the present invention is that very accurate alignment information can appear in a minimum number of steps. Another advantage of the present invention is that the material can be transferred to different pixel areas by automatic alignment of the laser beam.
    [19] The term "display" or "display panel" is used to refer to a screen capable of electronically displaying a video picture or text. The term “pixel” is used in the art for its recognized use in referring to areas of the display panel that can be stimulated to emit light regardless of other areas. The term " OLED device " or " OLED display " is used in the meaning recognized in the art to be a display device comprising an organic light emitting diode as a pixel. Color OLED devices emit light of one or more colors. The term "multicolor" is used to describe a display panel capable of emitting light of different colors in different areas. In particular, it is used to describe a display panel capable of displaying images of different colors. These regions do not necessarily need to be contiguous. The term "full color" is used to describe multicolor display panels that can emit in the red, green and blue regions of the visible light spectrum and can display images in any color or combination of colors. Red, green, and blue make up the three primary colors, which can be produced by mixing the three primary colors properly. The term "color" refers to the intensity profile of luminescence in the visible light spectrum, with different colors representing a visually discernible color difference. Pixels or subpixels are generally used to indicate the smallest unit that can be addressed in a display panel. In the case of monochrome displays, there is no distinction between pixels or subpixels. The term "subpixel" is used in a multicolor display panel and is used to denote any part of a pixel that can be independently addressed to emit a particular color. For example, a blue subpixel is a portion of a pixel that can be addressed to emit blue light. In full color displays, pixels typically include three primary color subpixels, namely blue, green and red. The term "pitch" is used to indicate the distance apart of two pixels or subpixels in a display panel. Thus, the subpixel pitch refers to the spacing between two subpixels.
    [20] 1A is a top view of an OLED substrate 10 constructed in accordance with the present invention. OLED substrate 10 includes an array of pixel portions 12. These pixel portions 12 are each connected to an electrode and are part of a so-called passive display having overlapping columns and rows of electrodes, or active with conventional anodes and individual thin-film transistors (TFTs). (active) may be part of the display. Each pixel portion 12 may be a pixel (for monochrome display) or a subpixel (for full color display). It may be desirable for the distance between individual pixels or subpixels to be less than 100 μm in such devices.
    [21] The substrate 10 may be an organic solid, an inorganic solid or a combination of an organic solid and an inorganic solid that provides a surface for receiving a luminescent material from the donor. Substrate 10 may be rigid or flexible and may be processed as a separate individual piece, such as a sheet or wafer, or as a continuous roll. Typical substrate materials include glass, plastics, metals, ceramics, semiconductors, metal oxides, semiconductor oxides, semiconductor nitrides, or combinations thereof. Substrate 10 may be a homogeneous mixture of materials, a composite of materials, or a multilayer of materials. Substrate 10 may be an OLED substrate, for example, an active-matrix low temperature polysilicon TFT substrate, which is a substrate commonly used to make OLED displays. Substrate 10 may be light depending on the intended direction of recognition detection and emission. It may be permeable or opaque. The light transmissivity is desirable for viewing the EL emission through the substrate and for viewing the laser spot through the substrate. Transparent glass or plastic is commonly used in this case. For applications in which EL emission is viewed through the top electrode, the transmissive properties of the bottom support are not critical and therefore can be light transmissive, light absorbing or light reflective. Substrates for use in this case include, but are not limited to, glass, plastic, semiconductor materials, ceramics, and circuit board materials. For the present invention, the substrate 10 is preferably an OLED substrate, and the terms "substrate" and "OLED substrate" will be used interchangeably.
    [22] 1A also shows reference marks 40 and 42 on the substrate 10. The reference mark can be detected by any means, for example optically, and the substrate 10 used to determine the position and orientation of the substrate 10 for properly depositing the light emitting layer with respect to the pixel portion 12 by means of obvious means. ) Feature. The feature, which is a reference mark, may have other purposes, for example, may be part of an active or passive matrix. One or more reference marks are formed at a known location on the substrate 10. Reference marks 40 and 42 are preferably external mass transfer regions 14, which are regions in which organic materials are transferred to substrate 10 to form one or more OLED displays. Reference marks 40 and 42 are designed to enable identification of specific points on substrate 40 and may be used to define crosshairs, triangles, crosshairs, circles, squares, intersecting triangles, “X” shapes, or one point. It may have a particular form, which may include any other form present. The reference mark should not be infinite rotational symmetry (eg, circle or bull's eye) if the second reference mark cannot be used. A single reference mark may be partly rotationally symmetric, causing significant substrate alignment errors that are apparent to the naked eye (eg, crosshairs that are rotationally symmetrical at intervals of 90 °). Although it has been appreciated that any non-limiting or restrictive rotational symmetry mark can determine the rotational position, the reference mark 40 is cross-shaped in a preferred embodiment. More precisely, a preferred embodiment is to provide two reference marks 40 and 42, each of which has a particular shape, such as a cross, on the substrate 10 and at a distance of at least 50% of the length of the substrate 10. Away. Reference marks are located above the photodetectors, respectively.
    [23] FIG. 1B is a cross sectional view showing the position of the substrate 10 relative to the laser 100 generating the laser beam 74. In this aspect, the substrate 10 may be configured to provide a laser beam 74 and a relative motion between the substrate 10 and the laser 100 so that the laser beam 74 can impinge on the fiducial mark 42. Located between 100 and photodetector 22. The photo detector 22 may detect when the laser beam 74 collides with the reference mark 42.
    [24] 2 is a partially enlarged top view of the substrate 10 showing the position of the photodetector 22 and the laser spot 20 and the reference mark 40. The photo detector 22 may be a photodetector, for example. The photo detector 22 includes a photo detector active region 24 that is part of the photo detector 22 that is sensitive to impinging light as provided by the laser spot 20. In this particular aspect, the photo detector 22 is positioned below the substrate 10, and the substrate 10 is sufficiently transparent so that sufficient light passes through the substrate and is detected by the photo detector 22. By providing relative motion between the substrate 10, the laser 100 and the laser beam 74, the position and orientation of the fiducial mark 40 can be detected. Relative motion refers to the movement of one or more portions of the device such that the positions of the laser spot 20, the substrate 10 and the photo detector 22 can change relative to each other. This may be accomplished by a variety of methods, such as moving the laser spot 20, moving the movable substrate 10, moving the laser spot 20 and the photo detector 22, and the like. An image of the reference mark 40 can be made by providing a relative motion in the raster scanning method, which is a two-dimensional order of scanning lines. In a preferred embodiment where the reference mark is crosswise, the angular rotation of the reference mark can be inferred from the angle between the horizontal line and the scan line of the plus signal.
    [25] In a preferred embodiment using two reference marks 40 and 42, the angle of rotation alignment error can be determined more accurately than when using a single reference mark due to the increased distance between the two reference marks. This is accomplished by measuring the center of the reference marks 40 and 42 and calculating the angle formed by the laser spot scan 48 and the line between the reference marks. This angle can be compared with the desired orientation and appropriate adjustments made. Knowing the center of the fiducial mark can yield x and y displacements relative to the desired position and proper translation of the substrate, or can be obtained to alter the image file so that the image placement is corrected both rotationally and translationally. .
    [26] Other embodiments are also possible. For example, the photo detector 22 and the laser spot 20 can both be located on the same side, ie above the substrate 10. In this case, the substrate 10 need not be transparent, and the photodetector 22 detects the reflected light from the surface of the substrate 10.
    [27] 2 also shows the relative intensity of the photo detector signal strength 50 in relation to the relative photo detector position 46. The relative movement causes a change in the apparent position of the laser spot 20 such that the laser beam 74 collides with the fiducial mark 40 at multiple positions, as indicated by the laser spot scan 48. The photodetector signal strength 50, as measured by the signal strength 44, is strong near the photodetector active region 24 when not reduced by the reference mark 40. The photo detector 22 may detect when the laser beam 74 collides with the reference mark 40 by the change in the photo detector signal intensity 50. Information such as photo detector signal strength 50 for relative photo detector position 46 may be recorded or estimated from detection of a reference mark such as 40. Thus, the position of the recognition center 26 in the first direction can be determined. By a technique such as further laser spot scanning, it is possible to determine the position of the center of the fiducial mark 40 in the second vertical direction. The recorded information can be used to calculate the orientation and position of the substrate 10.
    [28] 3 shows one aspect of a laser beam 74 that enables the method described herein and an apparatus 18 that provides relative motion between the laser 100 and the substrate 10. The device 18 is a device for moving the substrate 10, i.e. a rotation with a y-axis translation stage 30, an x-axis translation stage 32 and a hold-down platen 36. And a stage 34. Hold-down platen 36 includes a photo detector 22 (not explicitly shown). The laser 100, not shown, is located in a fixed position over the hold-down platen 36 and the substrate 10.
    [29] The substrate 10 may move laterally and angularly to a selected position to provide relative motion between the laser spot 20 and the substrate 10 in a manner described below. Substrate 10 is mounted on hold-down platen 36, which may be a vacuum hold-down device, for example. The laser spot 20 may for example come from a laser printhead. The X-axis translation stage 32 may move and position the substrate 10 laterally at micrometer order resolution. X-axis translation stage 32 is commercially available from manufacturers such as Dover Instruments Corp. The X-axis translation stage 32 can be adjusted with lateral displacement in one direction, thus allowing the substrate 10 to be moved laterally to adjust the position of the laser spot 20 relative to the substrate 10. have.
    [30] The X-axis translation stage 32 is mounted on the Y-axis translation stage 30. The Y-axis translation stage 30 is arranged in a manner similar to, but perpendicular to, the X-axis translation stage 32, and thus can move the X-axis translation stage 32 and by the elongate substrate 10, In the vertical direction, the resolution may be on the order of micrometers.
    [31] The rotary end 34 is mounted on the X-axis parallel moving end 32. Rotating end 34 allows angle adjustment of hold-down platen 36 and substrate 10, thus moving the substrate 10 angularly.
    [32] 4A is a cross-sectional view of a laser 100 for irradiating a fixed substrate / donor element combination with a light beam in accordance with the present invention. Laser 100 is a multichannel laser that emits a controlled multichannel linear laser light beam. The translation stage is not clearly shown. The donor element 16 is positioned in a transfer relationship with the substrate 10 between the laser 100 and the substrate 10. That is, donor element 16 is positioned in contact with substrate 10 (not shown) or maintained at a controlled distance from substrate 10. The donor element 16 is held in place by the pressing means 96. The pressurizing means 96 may be a transparent support or may be a chamber pressurized with gas to fix the donor element 16 in intimate relationship with the substrate 10.
    [33] The laser 100 emits a laser beam 74 which may be multichannel (ie, referring to a number of controlled channels of a linear laser light beam through the print lens 94). The laser beam 74 is shown as a series of lines to emphasize that it may in fact be multichannel as a number of individual addressable channels of laser light for clarity. It will be appreciated that these channels are contiguous and may behave upon irradiation as a continuous band of laser light. The laser beam 74 can be directed towards the donor element 16 through the pressing means 96 which is transparent and attacks the non-transferring surface of the donor element 16. The desired pattern can be obtained by adjusting the laser beam 74 while providing relative motion between the laser 100 and the substrate 10.
    [34] 4B is a cross sectional view showing an OLED substrate and donor elements suitably positioned relative to the substrate in practicing the present invention. Donor element 16 and substrate 10 are in a transfer relationship. That is, donor element 16 is located on or adjacent to substrate 10. The donor element 16 comprises a support 68, an energy absorbing layer 70 and a layer 72 of organic material. Donor element 16 is not patterned. In other words, the energy absorbing layer 70 and the organic material 72 are uniformly coated on the surface of the support 68. Non-transmissive surface 76 of donor element 16 by light beam 74, which is absorbed by a selected portion of energy absorbing material 70 and heats the selected portion of organic material 72 by heating the portion. Is selectively irradiated to transfer the organic material 72 from the transfer surface 78 of the donor element 16 to the substrate 10. Selective irradiation provides a relative motion between the laser beam 74 and the substrate 10 and activates the laser beam 74 in accordance with the determined position and orientation of the substrate 10 to produce the desired position, for example a pixel portion. Achieved by transferring organic material 72 from donor element 16 to substrate 10 at 12. The laser beam 74 can be activated over time or position. Selected portions of organic material 72 are evaporated or sublimed into organic layer 82 upon delivery to substrate 10.
    [35] The energy absorbing layer 70 does not allow the laser beam 74 to pass through the substrate 10. In one aspect, substrate 10 alignment may be performed prior to placing donor element 16 on substrate 10. In another embodiment, the donor element 16 does not include an energy absorbing layer 70 near the reference marks 40 and 42, so that the donor element 16 passes through sufficient light to cause the reference marks 40 and 42 to pass through. It is sufficiently transparent near reference marks 40 and 42 to impinge upon and enable the method herein. In this case, the donor element 16 may be positioned on the substrate 10 before performing the alignment process.
    [36] The support 68 can be made of any of several materials that meet at least the following conditions. The donor support must be flexible enough to withstand the precoating step and roll-to-roll or laminated sheet transport in the practice of the present invention and have adequate tensile strength. The support 68 must be able to maintain structural integrity during the light-to-heat-induced delivery step while being pressurized on one side and during any preheating step considered to remove volatile components such as water vapor. In addition, the support 68 must be able to be accommodated on one surface of a relatively thin coating of organic material and be capable of retaining this coating without deterioration for the expected storage period of the coated support. Support materials that meet these requirements include, for example, metal foils, certain plastic foils that exhibit glass transition temperature values higher than the support temperature values expected to cause delivery of the deliverable organic material of the coating on the support, and fiber-reinforced materials. Plastic foil. Suitable support materials can be selected according to known engineering methods, but it will be further appreciated that certain embodiments of the selected support materials are also considered when arranged as donor supports useful in the practice of the present invention. For example, the support material may require a multi-step cleaning and surface preparation process before it is previously coated with the deliverable organic material. If the support material is a radiation-transmissive material, incorporating the radiation-absorbing material into or on the surface of the support makes the donor support more effective when using radiation flash from a suitable flash lamp or laser light from a suitable laser. It may be advantageous to correspondingly enhance the transfer of the heated and transferable organic donor material from the support to the substrate.
    [37] The energy absorbing layer 70 may generate heat by absorbing radiation in certain portions of the spectrum. The energy absorbing layer can be a dye, such as a dye as commonly described in US Pat. No. 5,578,416, a pigment such as carbon, or a metal such as nickel, chromium, titanium, or the like.
    [38] Typical OLED devices typically contain layers in the following order: anode, hole injection layer, hole transport layer, light emitting layer, electron transport layer, cathode. Any of these layers, or both, may include an organic material 72 to form an organic layer. The organic material 72 may be a hole injection material, a hole transport material, an electron transport material, a light emitting material, a host material or a combination of these materials.
    [39] Hole Injection (HI) Substances
    [40] Although not necessary, it is often useful for a hole injection layer to be provided in an organic light emitting display. The hole injection material can act to improve the deposition properties of subsequent organic layers and to facilitate the injection of holes into the hole transport layer. Suitable materials for use in the hole injection layer include, but are not limited to, porphyrinic compounds as described in US Pat. No. 4,720,432 and plasma deposited fluorocarbon polymers as described in US Pat. No. 6,208,075. Other hole injection materials reported to be useful in organic EL devices are described in EP 0 891 121 A1 and EP 1,029,909 A1.
    [41] Hole Transport (HT) Material
    [42] Hole transport materials useful as the organic material 72 are well known to include compounds such as aromatic tertiary amines, wherein the aromatic tertiary amine is one or more trivalent nitrogen atoms bonded to only carbon atoms (one or more of them) Is a member of an aromatic ring). In one form, the aromatic tertiary amine may be an arylamine, for example monoarylamine, diarylamine, triarylamine or polymeric arylamine. Examples of monomeric triarylamines are illustrated in US Pat. No. 3,180,730 to Klupfel et al. Other suitable triarylamines substituted with one or more vinyl radicals and / or comprising one or more active hydrogen containing groups are disclosed in US Pat. Nos. 3,567,450 and 3,658,520 to Brantley et al.
    [43] A more preferred class of aromatic tertiary amines are amines comprising two or more aromatic tertiary amine moieties, as described in US Pat. Nos. 4,720,432 and 5,061,569. Such compounds include compounds of Formula 1
    [44]
    [45] Where
    [46] Q 1 and Q 2 are independently selected aromatic tertiary amine residues;
    [47] G is a linking group such as an arylene, cycloalkylene or alkylene group of a carbon-carbon bond.
    [48] In one embodiment, at least one of Q 1 or Q 2 contains a polycyclic fused ring structure, such as naphthalene. When G is an aryl group, it is conveniently a phenylene, biphenylene or naphthalene moiety.
    [49] A useful class of triarylamines that satisfy Formula 1 above and contain two triarylamine residues are the compounds of Formula 2:
    [50]
    [51] Where
    [52] R 1 and R 2 are each independently a hydrogen atom, an aryl group or an alkyl group, or R 1 and R 2 together are an atom which completes a cycloalkyl group;
    [53] R 3 and R 4 are each independently an aryl group substituted with a diaryl substituted amino group of the formula:
    [54]
    [55] Where
    [56] R 5 and R 6 are independently selected aryl groups.
    [57] In one embodiment, at least one of R 5 or R 6 contains a polycyclic fused ring structure, for example naphthalene.
    [58] Another class of aromatic tertiary amines are tetraaryldiamines. Preferred tetraaryldiamines include two diarylamino groups such as Formula 3, linked through an arylene group. Useful tetraaryldiamines include compounds of the formula
    [59]
    [60] Where
    [61] Are are each independently selected arylene groups such as phenylene or anthracene residues;
    [62] n is an integer from 1 to 4;
    [63] Ar, R 7 , R 8 and R 9 are independently selected aryl groups.
    [64] In a typical embodiment, at least one of Ar, R 7 , R 8 and R 9 is a polycyclic fused ring structure, for example naphthalene.
    [65] The various alkyl, alkylene, aryl and arylene moieties of the above formulas (1), (2), (3) and (4) may each be substituted in practice. Typical substituents include alkyl groups, alkoxy groups, aryl groups, aryloxy groups, and halogens such as fluoride, chloride and bromide. Various alkyl and alkylene moieties typically contain about 1 to 6 carbon atoms. Cycloalkyl moieties contain 3 to about 10 carbon atoms, but may typically contain 5, 6 or 7 ring carbon atoms, such as cyclopentyl, cyclohexyl and cycloheptyl ring structures. Aryl and arylene moieties are generally phenyl and phenylene moieties.
    [66] The hole transport layer may be formed of a single aromatic tertiary amine compound or a mixture of such aromatic tertiary amine compounds. Specifically, triarylamine such as triarylamine satisfying Formula 2 may be used together with the tetraaryldiamine of Formula 4. When triarylamine is used with tetraaryldiamine, tetraaryldiamine is located as a layer interposed between triarylamine and the electron injection and transport layer. Examples of useful aromatic tertiary amines are as follows:
    [67] 1,1-bis (4-di- p- tolylaminophenyl) cyclohexane;
    [68] 1,1-bis (4-di- p- tolylaminophenyl) -4-phenylcyclohexane;
    [69] 4,4'-bis (diphenylamino) quadriphenyl;
    [70] Bis (4-dimethylamino-2-methylphenyl) -phenylmethane;
    [71] N, N, N-tri ( p- tolyl) amine;
    [72] 4- (di-p-tolylamino) -4 '-[4 (di- p- tolylamino) -styryl] stilbene;
    [73] N, N, N ', N'-tetra- p -tolyl-4,4'-diaminobiphenyl;
    [74] N, N, N ', N'-tetraphenyl-4,4'-diaminobiphenyl;
    [75] N-phenylcarbazole;
    [76] Poly (N-vinylcarbazole);
    [77] N, N'-di-1-naphthalenyl-N, N'-diphenyl-4,4'-diaminobiphenyl;
    [78] 4,4'-bis [N- (1-naphthyl) -N-phenylamino] biphenyl;
    [79] 4,4 "-bis [N- (1-naphthyl) -N-phenylamino] -p-terphenyl;
    [80] 4,4'-bis [N- (2-naphthyl) -N-phenylamino] biphenyl;
    [81] 4,4'-bis [N- (3-acenaphthenyl) -N-phenylamino] biphenyl;
    [82] 1,5-bis [N- (1-naphthyl) -N-phenylamino] naphthalene;
    [83] 4,4'-bis [N- (9-anthryl) -N-phenylamino] biphenyl;
    [84] 4,4 "-bis [N- (1-antryl) -N-phenylamino] -p -terphenyl;
    [85] 4,4'-bis [N- (2-phenanthryl) -N-phenylamino] biphenyl;
    [86] 4,4'-bis [N- (8-fluoroantenyl) -N-phenylamino] biphenyl;
    [87] 4,4'-bis [N- (2-pyrenyl) -N-phenylamino] biphenyl;
    [88] 4,4'-bis [N- (2-naphthacenyl) -N-phenylamino] biphenyl;
    [89] 4,4'-bis [N- (2-perylenyl) -N-phenylamino] biphenyl;
    [90] 4,4'-bis [N- (1-coroneyl) -N-phenylamino] biphenyl;
    [91] 2,6-bis (di- p -tolylamino) naphthalene;
    [92] 2,6-bis [di- (1-naphthyl) amino] naphthalene;
    [93] 2,6-bis [N- (1-naphthyl) -N- (2-naphthyl) amino] naphthalene;
    [94] N, N, N ', N'-tetra (2-naphthyl) -4,4 "-diamino- p -terphenyl;
    [95] 4,4'-bis {N-phenyl-N- [4- (1-naphthyl) -phenyl] amino} biphenyl;
    [96] 4,4'-bis [N-phenyl-N- (2-pyrenyl) amino] biphenyl;
    [97] 2,6-bis [N, N-di (2-naphthyl) amine] fluorene; And
    [98] 1,5-bis [N- (1-naphthyl) -N-phenylamino] naphthalene.
    [99] Another class of useful hole transport materials includes polycyclic aromatic compounds as described in EP 1 009 041. In addition, poly (N-vinylcarbazole) (PVK), polythiophene, polypyrrole, polyaniline, and poly (3,4-ethylenedioxythiophene) / poly (4-styrenesulfonate), also referred to as PEDOT / PSS Polymeric hole transport materials such as copolymers such as these may be used.
    [100] Light emitting material
    [101] Luminescent materials useful as organic materials 72 are well known. As described in more detail in US Pat. Nos. 4,769,292 and 5,935,721, the light emitting layer (LEL) of the organic EL device comprises a luminescent or fluorescent material, and as a result of electron-hole pair recombination within this zone Electroluminescence is produced. The emissive layer may consist of a single material, but more typically consists of a guest material or a host material doped with compounds, wherein the light emission mainly occurs from the dopant and may be of any color. The host material in the light emitting layer can be an electron transport material as defined below, a hole transport material as defined above, or another material that supports hole-electron recombination. In general, dopants are selected from solid fluorescent dyes, but are phosphorescent compounds, for example WO 98/55561, WO 00/18851, WO 00/57676 and WO 00/70655. Also useful are transition metal complexes as described in. Dopants are typically coated in amounts of 0.01 to 10% by weight onto the host material.
    [102] An important relationship in selecting dyes as dopants is the comparison of the bandgap potential, defined as the energy difference between the orbital with the highest energy among the filled orbitals and the orbital with the lowest energy among the empty molecular orbitals. Is in. For effective energy transfer from the host to the dopant molecule, an essential condition is that the bandgap of the dopant must be less than the bandgap of the host material.
    [103] Host and release molecules known to be used include US Pat. No. 4,768,292; No. 5,141,671; 5,150,006; 5,150,006; 5,151,629; 5,294,870; 5,405,709; 5,405,709; No. 5,484,922; 5,593,788; 5,593,788; 5,645,948; 5,645,948; No. 5,683,823; 5,755,999; 5,755,999; 5,928,802; 5,928,802; No. 5,935,720; 5,935,721; And those disclosed in US Pat. No. 6,020,078.
    [104] Metal complexes of 8-hydroxyquinoline and similar derivatives (Formula 5 below) constitute one class of useful host compounds capable of supporting electroluminescence and have wavelengths longer than 500 nm, for example green, yellow, orange and red. Particularly suitable for the emission of:
    [105]
    [106] Where
    [107] M is a metal;
    [108] n is an integer from 1 to 3;
    [109] Z is in each case an atom that independently completes a nucleus having two or more fused aromatic rings.
    [110] From the foregoing, it is apparent that the metal may be monovalent, divalent or trivalent metal. Such metals include, for example, alkali metals such as lithium, sodium or potassium; Alkaline earth metals such as magnesium or calcium; Or an earth metal such as boron or aluminum. In general, any monovalent, divalent or trivalent metal known as a useful chelating metal can be used.
    [111] Z completes a heterocyclic nucleus containing two or more fused aromatic rings, at least one of which is an azole or azine ring. If desired, additional rings including both aliphatic and aromatic rings can be fused to the two essential rings. In order to avoid the addition of molecular bulk without improving function, the number of ring atoms is generally kept below 18.
    [112] Examples of useful chelated oxynoid compounds are as follows:
    [113] CO-1: aluminum trisoxine (aka tris (8-quinolinolato) aluminum (III));
    [114] CO-2: magnesium bisoxine [aka bis (8-quinolinolato) magnesium (II)];
    [115] CO-3: bis [benzo {f} -8-quinolinolato] zinc (II);
    [116] CO-4: bis (2-methyl-8-quinolinolato) aluminum (III) -μ-oxo-bis (2-methyl-8-quinolinolato) aluminum (III);
    [117] CO-5: indium trisoxine [aka tris (8-quinolinolato) indium];
    [118] CO-6: aluminum tris (5-methyloxine) [aka tris (5-methyl-8-quinolinolato) aluminum (III)];
    [119] CO-7: lithium auxin [aka, (8-quinolinolato) lithium (I)].
    [120] Derivatives of 9,10-di- (2-naphthyl) anthracene (Formula 6) constitute one class of useful hosts capable of supporting electroluminescence, wavelengths longer than 400 nm, for example blue, green, yellow Especially suitable for emitting orange or red light:
    [121]
    [122] Where
    [123] R 1 , R 2 , R 3 , R 4 , R 5 and R 6 represent one or more substituents on each ring, wherein each of these substituents is individually selected from the following groups:
    [124] Group 1: hydrogen or alkyl having 1 to 24 carbon atoms;
    [125] Group 2: aryl or substituted aryl having 5 to 20 carbon atoms;
    [126] Group 3: 4 to 24 carbon atoms necessary to complete the fused aromatic ring of anthracenyl, pyrenyl or perillynyl;
    [127] Group 4: heteroaryl or substituted heteroaryl having 5 to 24 carbon atoms which is essential for completing a fused heteroaromatic ring of furyl, thienyl, pyridyl, quinolinyl or other heterocyclic systems;
    [128] Group 5: alkoxylamino, alkylamino or arylamino having 1 to 24 carbon atoms; And
    [129] Group 6: fluorine, chlorine, bromine or cyano.
    [130] Benzazole derivatives (Formula 7) constitute another class of useful hosts capable of supporting electroluminescence and are particularly suitable for light emission of wavelengths longer than 400 nm, for example blue, green, yellow, orange or red. :
    [131]
    [132] Where
    [133] n is an integer from 3 to 8;
    [134] Z is O, NR or S;
    [135] R 'is hydrogen; Alkyl having 1 to 24 carbon atoms such as propyl, t-butyl, heptyl and the like; Aryl or heteroatom substituted aryl having 5 to 20 carbon atoms such as phenyl and naphthyl, furyl, thienyl, pyridyl, quinolinyl and other heterocyclic systems; Or halo such as chloro, fluoro; Or an atom necessary to complete a fused aromatic ring;
    [136] L is a linking unit consisting of alkyl, aryl, substituted alkyl, or substituted aryl which connects multiple benzazoles conjugated or unconjugated together.
    [137] Examples of useful benzazoles are 2,2 ', 2 "-(1,3,5-phenylene) tris [1-phenyl-1H-benzimidazole].
    [138] Preferred fluorescent dopants include anthracene, tetracene, xanthene, perylene, rubrene, coumarin, rhodamine, quinacridone, dicyanomethylenepyrane compound, thiopyrane compound, polymethine compound, pyryllium and thiaryryllium compound and Derivatives of carbostyryl compounds are included. Examples of useful dopants include, but are not limited to:
    [139]
    [140]
    [141]
    [142]
    [143] Other organic light emitting materials such as polyphenylenevinylene derivatives, dialkoxy-polyphenylenevinylene, poly, as taught in commonly assigned US Pat. No. 6,194,119 B1 and in the references cited herein. -Para-phenylene derivatives and polyfluorene derivatives can be polymeric substrates.
    [144] Electron transport (ET) materials
    [145] Preferred electron transport materials for use in the organic EL device of the present invention are metal chelated oxynoid compounds, including chelates of auxin itself (also commonly referred to as 8-quinolinol or 8-hydroxyquinoline). . These compounds aid in the injection and transport of electrons, all exhibit high levels of performance, and are readily manufactured in the form of thin films. Examples of oxynoid compounds contemplated are those which satisfy the above formula (5).
    [146] Other electron transport materials include various butadiene derivatives as disclosed in US Pat. No. 4,356,429 and various heterocyclic optical brighteners as described in US Pat. No. 4,539,507. Benzazoles satisfying Formula 7 above are also useful electron transport materials.
    [147] Other electron transport materials, for example polyphenylenevinylene derivatives, poly-para-phenylene derivatives, polyfluorenes, as taught in the commonly assigned U.S. Patent No. 6,221,553 B1 described above and in the references cited herein. Derivatives, polythiophenes, polyacetylenes and other conductive polymeric organic materials can be polymeric substrates.
    [148] In some cases, a single layer can function to support both luminescence and electron transport, and thus comprise a luminescent material and an electron transport material.
    [149] Anode material
    [150] The conductive anode layer is formed over the substrate and should be transparent or substantially transparent to the emission of interest when EL light emission is viewed through the anode layer. Common transparent anode materials used in the present invention include indium-tin oxide and tin oxide, or other metal oxides including but not limited to aluminum or tin doped zinc oxide, magnesium-indium oxide, and nickel-tungsten oxide. . In addition to the oxides, metal nitrides such as gallium nitride, and metal selenides such as zinc selenide, and metal sulfides such as zinc sulfide can be used as the anode material. When the EL emission is viewed through the upper electrode, any conductive material that is transparent, opaque or reflective can be used since the transmission property of the anode material is not important. Examples of conductors for such use include, but are not limited to, gold, iridium, molybdenum, palladium and platinum. Preferred anode materials (permeable or non-permeable) have a work function of 4.1 eV or greater. The desired anode material may be deposited by any suitable means such as evaporation, sputtering, chemical vapor deposition or electrochemical means. The anode material can be patterned by well known photolithographic processes.
    [151] Cathode material
    [152] When light emission is through the anode, the cathode material may consist of any conductive material. Preferred materials have good deposition properties that ensure good contact with the underlying organic layer, promote electron injection at low voltages and have good stability. Useful cathode materials often contain low work function metals (<4.0 eV) or metal alloys. One preferred cathode material consists of an Mg: Ag alloy, where the percentage of silver is 1 to 20% as described in US Pat. No. 4,885,221. Another suitable class of cathode materials includes two layers consisting of a thin layer of low work function metal or metal salt capped with a thick layer of conductive metal. This cathode consists of a thin layer of LiF followed by a thick layer of Al as described in US Pat. No. 5,677,572. Other useful cathode materials include, but are not limited to, those disclosed in US Pat. Nos. 5,059,861, 5,059,862, and 6,140,763.
    [153] If luminescence is viewed through the cathode, the cathode should be transparent or nearly transparent. In such applications, the metal must be thin or transparent conductive oxides or combinations of these materials must be used. Optically transparent cathodes are described in more detail in US Pat. No. 5,776,623. The cathode material may be deposited by evaporation, sputtering or chemical vapor deposition. In some cases, patterning is achieved through a number of well known methods, including through-mask deposition as described in US Pat. No. 5,276,380 and EP 0 732 868. , Integrated shadow masking, laser ablation, and selective chemical vapor deposition.
    [154] 5 shows a block diagram of one aspect of an electro-optic subsystem used to process a signal and detect the location of a fiducial mark. This subsystem includes a host PC 102, an image processor 104, and movement control electronics 106. It may be a separate unit or the image processor 104 or the mobile control electronics 106 or both may be incorporated into the host PC 102. The host PC 102 is in communication with the image processor 104 and can measure the amount of light incident on the photo detectors 22 and 23 with the host PC. The image processor 104 amplifies the signal 108 provided by the photo detector 22 and amplifies the signal 110 provided by the photo detector 23. The image processor 104 provides this amplified signal to the host PC 102. The host PC 102 can use this amplified signal to calculate information from reference mark detection, such as 40, to determine the position and orientation of the substrate 10. The host PC 102 is also connected to a movement control electronics 106 which controls the movement and position of the translational and rotational stages comprising the device 18. This provides a laser spot scan 48 on the substrate 10 by providing relative motion between the laser 100 and the substrate 10. By providing this relative motion, the laser beam 74 can be scanned over a portion of the substrate 10 including the fiducial mark 40 and the photo detector 22. The relative motion can be provided in a direction perpendicular to the laser spot scan 48 and the process can be repeated. During this time, the output from the photo detector 22 can be monitored and associated with the location information from the movement control electronics 106. In this way, the image processor 104 can produce a raster image of the position of the reference mark 40. By a similar process, a raster image of the position of the reference mark 42 can be obtained at the photo detector 23.
    [155] FIG. 6 is a block diagram showing the overall steps in substrate alignment for use in the manufacture of OLED displays and the position detection of reference marks using these two marks. This process begins by placing a substrate having a reference mark on the translational / rotational stage (step 122). Relative motion is provided such that the laser is scanned in a first direction relative to the photo detector area where the fiducial mark is approximately positioned (step 124). The incident intensity can be measured by the image processor 104 and the host PC 102 to obtain the intensity versus position along the scan as shown in FIG. 2 (detection step 130). The host PC 102 determines whether the scan is the last scan for the photo detector (step 132). If the last scan has not been reached, the translational stage advances perpendicular to the scan direction (step 134) and the process is repeated. Once the scanning of the photo detector is complete (step 132), the host PC determines if there are more reference marks to be scanned (step 138). If there are more reference marks, relative motion is provided to move the laser beam to the beginning of the next recognition (step 140) to repeat the scan (step 124 and subsequent steps). When the last recognition is scanned, the host PC 102 determines the absolute translation and angular position of the reference mark.
    [156] For example, the position and orientation of the substrate 10 may be determined based on information calculated from the detection of reference marks such as (40) and (42). If there is any misalignment, the rotation and translation stages are adjusted using the known position of the reference mark, the image file is adjusted, the start of the image is adjusted or some combination of these actions is performed so that the image is in the correct position. Allow laser delivery (step 142). Such actions may include mechanical or digital translation, mechanical or digital rotation, and mechanical or digital stretching of the image being transferred. Such methods are well known in the art. The transfer positions the donor sheet in a transfer relationship with respect to the substrate 10, provides a relative motion between the laser beam 74 and the substrate 10, and according to the determined position and orientation of the substrate 10. May be activated to transfer organic material 72 from donor element 16 to substrate 10 at a desired location, for example pixel portion 12. The laser beam 74 may be activated over time or position (step 144). A method of transferring material from a donor to a substrate. The process then ends (step 148).
    [157] An advantage of the present invention is that by providing a fiducial mark on the substrate, an effective method of determining the position and orientation of the substrate can be achieved prior to the delivery of the organic material. A further advantage of the present invention is that the same laser beam used to transfer from the donor element to the substrate can also be used to determine the position and orientation of the substrate relative to the laser. The alignment according to the invention is very accurate and provided by the direct detection of the reference mark. Another advantage of the present invention is that very accurate alignment information can appear in a minimum number of steps. Another advantage of the present invention is that the material can be transferred to different pixel areas by automatic alignment of the laser beam.
    权利要求:
    Claims (3)
    [1" claim-type="Currently amended] (a) providing one or more fiducial marks on the substrate;
    (b) positioning the substrate relative to the laser and providing relative motion between the laser beam and the laser and the substrate until the laser beam impinges upon the fiducial mark; And
    (c) detecting when the laser beam impinges upon the fiducial mark and determining the position and orientation of the substrate,
    A method of aligning a substrate for use in the manufacture of an OLED display with a laser that produces a beam that transfers organic material from the donor element to the substrate.
    [2" claim-type="Currently amended] (a) providing one or more fiducial marks on the substrate;
    (b) positioning the substrate relative to the laser and providing relative motion between the laser beam and the laser and the substrate until the laser beam impinges upon the fiducial mark;
    (c) detecting when the laser beam impinges upon the fiducial mark and determining the position and orientation of the substrate; And
    (d) providing a relative motion between the laser beam and the substrate and activating the laser beam in accordance with the determined position and orientation of the substrate to transfer organic material from the donor element to the substrate,
    A method of aligning a substrate and manufacturing an OLED display using a laser that generates a beam that transfers organic material from the donor element to the substrate.
    [3" claim-type="Currently amended] (a) providing at least two reference marks each having a particular shape on the substrate;
    (b) positioning the substrate relative to the laser and providing relative motion between the laser beam and the laser and the substrate until the laser beam impinges upon the fiducial mark;
    (c) detecting when the laser beam impinges on the reference mark, and determining the position and orientation of the substrate based on information calculated from the detection of the reference mark; And
    (d) providing relative motion between the laser beam and the substrate, and activating the laser beam in accordance with the determined position and orientation of the substrate to transfer organic material from the donor element to the substrate,
    A method of aligning a substrate and manufacturing an OLED display using a laser that generates a beam that transfers organic material from the donor element to the substrate.
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    同族专利:
    公开号 | 公开日
    TW200403157A|2004-03-01|
    JP2011077046A|2011-04-14|
    CN1309580C|2007-04-11|
    TWI299308B|2008-08-01|
    EP1394872A3|2009-04-01|
    EP1394872A2|2004-03-03|
    CN1490169A|2004-04-21|
    US6811938B2|2004-11-02|
    EP1394872B1|2015-09-23|
    US20040048173A1|2004-03-11|
    JP2004095555A|2004-03-25|
    KR100995824B1|2010-11-23|
    JP4892094B2|2012-03-07|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2002-08-29|Priority to US10/230,934
    2002-08-29|Priority to US10/230,934
    2003-08-28|Application filed by 이스트맨 코닥 캄파니
    2004-03-06|Publication of KR20040020004A
    2010-11-23|Application granted
    2010-11-23|Publication of KR100995824B1
    优先权:
    申请号 | 申请日 | 专利标题
    US10/230,934|2002-08-29|
    US10/230,934|US6811938B2|2002-08-29|2002-08-29|Using fiducial marks on a substrate for laser transfer of organic material from a donor to a substrate|
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