Patent Application
20140235013
The present invention relates to so-called organic electronic components, and more particularly to issues due to the localizing of an active organic layer on forming of electronic components or the like. The invention more specifically relates to a method of structuring an active organic layer deposited on a substrate, and to the step of chemically etching said active layer, on manufacturing of an organic diode.
In the field of microelectronics, that is, of micrometric-scale electronic components, said electronic components have been initially developed from inorganic materials such as silicon or gallium arsenide (GaAs), particularly to form the so-called active layer of the components, the latter being formed of a stack of such inorganic layers.
Such inorganic electronic components have the disadvantage of being expensive to manufacture and of being rigid, and accordingly of being fragile and impossible to use for certain applications.
Thus, the active layers of electronic components are now more and more frequently made of organic materials, such as polymers, for example, which have the advantage of being easy to manufacture at a large scale, of having a good mechanical and/or thermal behavior, of having a flexible structure and of being easy to recycle. Further, polymers being soluble in a solvent, the latter may advantageously be deposited in a layer by low-cost and easy-to-implement deposition methods such as, particularly, spin coating, inkjet deposition, or silk-screening deposition.
This is why displays based on so-called OLED or Organic Light-Emitting Diodes or based on so-called OTFT or Organic Thin-Film Transistors can now currently be encountered. Such electronic components are usually formed of a stack of organic and/or inorganic layers where the so-called active layer is made of an organic material.
However, such a stack of organic and/or inorganic layers raises a number of issues, particularly on forming of organic diodes, which requires a highly-homogeneous deposition of an organic active layer, the stacking of the layers of an organic diode usually being as follows: a substrate made of glass, plastic, silicon, etc., a so-called local conductive layer made of indium-tin oxide or ITO, metal, a conductive polymer, etc., a so-called injector layer made of poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) or PEDOT:PSS, for example, an active layer made of a mixture of n- and p-type semiconductor called bulk heterojunction, and a local conductive layer made of metal or a conductive polymer, for example.
Indeed, in the manufacturing of an organic diode, the deposition of the active organic layer is the critical step. Such an organic layer should be very homogeneous and with no defect capable of causing an electric leakage between the two conductive layers of the diode. The active organic layer is usually deposited by a spin coating method, which provides film-forming deposits. However, spin coating does not enable to structure the active organic layer. To structure said active layer, after its deposition on the substrate, several techniques are used, including subtractive etching, also called direct etching, and lift-off.
Subtractive etching, for example illustrated in
Such a subtractive etching is particularly described in document WO 2011/004198.
Subtractive etching has the disadvantage of deteriorating the active layer, as can be seen in
The second structuring technique, called lift-off, comprises, referring to
This type of so-called “lift-off” structuring method is especially described in documents US 2005/0048414 and US 2011/0012097.
The lift-off technique also has the disadvantage of deteriorating active layer 1. Indeed, active layer 1 is damaged by the action of the acetone bath during the dissolution of the sacrificial layer, the acetone bath lasting for approximately 20 minutes. Such an acetone bath weakens active layer 1, resulting in poorly-defined pattern edges and pittings, as can be seen in
One of the aims of the invention thus is to overcome such disadvantages by providing a method of structuring an organic active layer deposited on a substrate, easy to implement and of low cost, and providing defect-free active layer patterns.
For this purpose, and according to the invention, a method of structuring an active organic layer deposited on a substrate is provided, comprising:
It should be understood that, conversely to prior art methods, the protective polymer layer deposited in the pattern of the sacrificial resist layer covers the active layer deposited in said pattern and protects it on removal of the resist by projection of a solvent. Further, the mechanical effect of the solvent projection enables to decrease the duration of the solvent contact with the different component layers, the contact time being shorter than 1 minute, conversely to prior art methods where the solvent remains in contact with the layers for a duration of approximately 20 minutes, and to avoid the redeposition of particles on the active layer.
The step of creating patterns on the resist comprises at least the steps of:
The resist is made of a so-called negative resin, for which ultraviolet radiation induces a polymerization of the exposed areas and/or of a so-called positive resin, for which the ultra-violet radiation induces a chemical transformation of the macromolecules of said resin, and/or of a so-called reversible resin, which has the property of changing polarity in a so-called reversion anneal step.
Further, the step of removing the sacrificial resist layer comprises projecting a solvent on said sacrificial resist layer for a period in the range from 5 to 60 seconds, said solvent being for example made of acetone.
The step of depositing an active organic layer comprises depositing by spin coating a mixture of organic p- and n-type semiconductor molecules or polymers.
Said mixture of organic p- and n-type semiconductor molecules or polymers may for example be made of a mixture of poly(3-hexyl-thiophene) (P3HT) and of 1-(3-methoxy-carbonyl)propyl-1-phenyl-(6,6)C-61 (PCBM) in o-dichlorobenzene, or of a mixture of poly(3-octylthiophene-2,5-diyl) (P3OT) and (6,6)-phenyl C71 butyric acid ester (PC71BM).
The step of depositing an organic polymer protective layer in the pattern of the sacrificial resist layer comprises at least the steps of:
The foregoing and other features and advantages will be discussed in detail in the following non-limiting description of an alternative execution of the method of structuring of an active layer deposited on a substrate according to the invention, in connection with the accompanying drawings, among which:
For clarity, in the following description, the same elements have been designated with the same reference numerals in the different drawings. Further, the various cross-section views are not necessarily drawn to scale.
In this specific embodiment, the etching of an active layer on a substrate to form so-called OLED organic diodes will be described. However, it should be obvious that the method according to the invention may be used to form any type of organic electronic components, such as OTFT-type transistors, for example, without for all this departing from the framework of the invention.
Referring to
Resist 4 is for example a so-called positive resin, sold under reference Microposit® S1818® by Rohm and Haas Electronic Materials LLC. It has a thickness in the range from 1 to 4 micrometers.
Substrate 2 is for example made of glass, covered with so-called ITO indium-tin oxide.
Substrate 2 may however be made of plastic material, for example, of polyethylene naphthalate (PEN) or of polyethylene terephthalate (PET), and have on its upper surface a thin layer of metal, such as gold (Au), silver (Ag), palladium (Pd), aluminum (Al), etc . . . having a thickness in the range from 10 nanometers and 500 nanometers or a thin conductive polymer layer, such as a layer of poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) called PEDOT:PSS, having a thickness in the range from 50 to 2,000 nanometers or a thin inorganic conductor layer, such as indium-tin oxide (ITO) or gallium zinc oxide (GZO) for example, between 50 and 500 nanometers.
Further, resist S1818® used in this embodiment is a so-called positive resin for which the UV radiation induces a chemical transformation of the macromolecules of said resin, causing an increased solubility of the exposed areas in the developer. The resist can thus be made of any positive resin, such as resin AZ® 9260 commercialized by AZ electronic materials GmbH, or the resin commercialized under reference Microposit® SJR 5740® by Rohm and Haas Electronic Materials, for example.
Sacrificial layer 4 may also be made of a so-called negative resist, for which the ultraviolet radiation induces a polymerization of the exposed areas, thus giving these areas a specific resistance to the developing solvent, while the non-illuminated portions selectively disappear in said solvent. Such a negative resin is for example commercialized under reference SU-8 by MicroChem Corp.
Sacrificial layer 4 may finally be made of a so-called reversible resin, which has the property of changing polarity during a so-called reversion anneal step. Such a reversible resin is for example commercialized under reference AZ® 5214 by AZ electronic materials GmbH, or is the resin commercialized under reference T109XR®.
At a step 1b, at least one pattern 5, also called “diode pixel”, is created. For this purpose, sacrificial resist layer 4 is annealed at a temperature in the range from 100 to 130° C. for from 1 to 5 minutes, and preferably at a 115° C. temperature for 3 minutes. Then, the resist is illuminated, that is, exposed to ultraviolet rays (UV) through a mask comprising at least said pattern, the mask being not shown in
After this step of creation of a pattern 5 in sacrificial resist layer 4, the method according to the invention comprises a step 1c of deposition of an active organic layer 1 on sacrificial layer 4 and in said pattern 5.
The step of depositing an active organic layer 1 comprises depositing a thickness in the range from 10 to 300 nanometers of a mixture of organic p- and n-type semiconductor molecules or polymers.
Said mixture of organic p- and n-type semiconductor molecules or polymers is for example formed of a mixture of poly(3-hexyl-thiophene) (P3HT) and of 1-(3-methoxy-carbonyl)propyl-1-phenyl-(6,6)C-61 (PCBM) in o-dichlorobenzene. It may also be made of a mixture of poly(3-octylthiophene-2,5-diyl)(P3OT) and of (6,6)-phenyl C71 butyric acid ester (PC71BM). It may further be made of any other appropriate mixture well known by those skilled in the art.
Active organic layer 1 may be deposited by spin coating or by any other method providing an appropriate homogeneous deposition such as, for example, a deposition by spreading, a silk-screen deposition, or a printing deposition.
Then, at a step 1d, a so-called protective layer 3 made of organic polymer is deposited on active layer 1 and in pattern 5 of sacrificial resin layer 4.
This step of depositing a protective layer 3 comprises depositing by silk-screening by a thickness in the range from 100 to 5,000 nanometers at least one thermocrosslinkable perfluorinated aliphatic polymer such as a perfluorinated polymer commercialized under reference Cytop®. The obtained assembly is then annealed for from 2 to 10 minutes under a temperature in the range from 40 to 80° C., and for 6 minutes under a 60° C. temperature.
At a step 1e, sacrificial resist layer 4 is removed by projection of a solvent on said resin. The removal step comprises spraying a jet of solvent, such as acetone, for example, by any appropriate means, on sacrificial layer 4 for a time in the range from 5 to 60 seconds, and preferably for a time in the range from 10 to 30 seconds. This step of removing sacrificial layer 4 induces the simultaneous removal of active layer 1 and of protective layer 3, except for active layer 1 and protective layer 3 initially deposited in pattern 5.
It can be observed that protective layer 3 deposited in pattern 5 of sacrificial layer 4 covers active layer 1 deposited in said pattern 5 and protects it on removal of the sacrificial layer by projection of a solvent, thus avoiding any surface alteration of said active layer. Further, the mechanical effect of the solvent projection enables to decrease the duration of the contact of the solvent with the different layers of the component, the contact duration being in the order of 20 seconds, and accordingly enables to decrease risks of deterioration of active layer 1. The redeposition of particles on the active is also no longer necessary.
At a last step 1f, protective layer 3 is removed by dissolution of said polymer which forms it in a solvent, such as perfluorotributylamine (FC43). It should be noted that, on removal of protective layer 3, the solvent is only in contact with lateral walls of active layer 1, thus avoiding altering the upper surface of active layer 1.
Thereby, as can be observed in
| Number | Date | Country | Kind |
|---|---|---|---|
| 11.58776 | Sep 2011 | FR | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/FR2012/051649 | Jul 2012 | US |
| Child | 14220261 | US |
