Deposition of permanent polymer structures for OLED fabrication

Abstract

A light emitting display comprising a first electrode layer on a substrate. The electrode layer is patterned to form a plurality of laterally spaced apart strips in a first direction. A plurality of spacedly disposed light emitting organic elements with a second electrode layer atop are disposed on the first electrode layer in a second direction. An undercut structure made of an undercut pattern transfer layer and an overlaying pattern transfer layer. The undercut structure is disposed between the plurality of spacedly disposed light emitting organic elements. A light emitting display having a color isolation well. The color isolation well is characterized by a first well layer and a second well layer in which the first well layer matches a property of an emissive polymer or small molecule dye held by the well whereas the second well layer does not match the property.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS [0001] This application is a continuation of Ser. No. 10 / 422,212, filed Apr. 23, 2003 which is a continuation-in-part of co-pending application Ser. No. 09 / 875,115 to Maloney, et al., published as US 2002 / 0076495, that was filed Jun. 6, 2001 and is entitled “Method of Making Electronic Materials,” which is hereby incorporated by reference in its entirety.FIELD OF THE INVENTION [0002] The present invention relates to improved organic electroluminescent devices and improved methods for manufacturing organic electroluminescent devices. Organic electroluminescent devices include organic light-emitting diodes and polymer light-emitting diodes. They are used in a number of devices, such as car radios, mobile phones, digital cameras, camcorders, personal digital assistants, and other devices using flexible and non-flexible displays. BACKGROUND OF THE INVENTION [0003] Over the past two decades, new flat panel display technology based on light emission...

AI Technical Summary

Benefits of technology

[0084] An advantage of the present invention is that feature size of structures 580 can be made smaller than the feature size of structures used to perform the same function in the prior art (e.g. undercut pillar 310 of FIG. 3). Referring to FIG. 5K, in some embodiments, undercut structures 580 have a length 553 that is between 100 nm and 500 microns and a width (not shown) that is between 100 nm and 400 microns. In some embodiments, length 553 is between 25 microns and 35 microns whereas and the width is between 15 microns and 25 microns. As referred to herein, the length 553 and width of undercut structures is measured at a top portion of the undercut structure rather than the etched undercut portion of the structure 580. In some embodiments, the thickness 555 (FIG. 5K) of structures 580 (the aggregate thickness of layers 552A and 552B) is between about 0.75 microns and about 4.5 microns. In a more preferred embodiment, the thickness 555 of structures 580 is between about 2 microns and 3 microns.

[0085] This aspect of the present invention provides novel self-aligning dual damascene type methods for making color isolation wells for color matrix OLED display applications. FIG. 7 illustrates an exemplary embodiment in accordance with this aspect of the invention. In FIG. 7A, a substrate 32 is coated with a first well layer 702.

[0086] The exact composition of first well layer 702 is application dependent. In some embodiments, the composition of the material used to form first well layer 702 is chosen such that it has good wetability properties for the predetermined emissive polymer or small molecule dye that will be deposited in the color isolation well once it has been formed. For example, in some embodiments, if the predetermined emissive polymer or small molecule dye is a hydrophobic material, the material used to make first well layer 702 is selected for its hydrophobic properties. In another example, if the predetermined emissive polymer or small molecule dye is a hydrophilic material, the material used to make first well layer 702 is selected for its hydrophilic properties. In still another example, if the predetermined emissive polymer or small molecule dye is a positively charged material, the material used to make first well layer 702 is selected for its ability to present a negatively charged surface area. Those of skill in the art will appreciate that, because the present invention does not require the use of photoresists to make color isolation wells, any material amendable to lithography can be used to make first well layer 702.

[0087] In FIG. 7B, a first precursor layer, e.g., comprising a metal complex, is applied atop first well layer 702. The first precursor layer is equivalent to layer 554 of FIG. 5D. The first precursor layer can be deposited using any of the techniques described in Step E of Section I of the present invention as well as in Section III of the present invention, below. Further, the first precursor layer can b

Problems solved by technology

Attempting to perform the pattern-transfer for each step individually would be very difficult due

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