US20170170006A1 - Manufacturing method of semiconductor device - Google Patents
Manufacturing method of semiconductor device Download PDFInfo
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- US20170170006A1 US20170170006A1 US14/968,923 US201514968923A US2017170006A1 US 20170170006 A1 US20170170006 A1 US 20170170006A1 US 201514968923 A US201514968923 A US 201514968923A US 2017170006 A1 US2017170006 A1 US 2017170006A1
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- photoresist
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/027—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34
- H01L21/0271—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/027—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34
- H01L21/0271—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers
- H01L21/0273—Making masks on semiconductor bodies for further photolithographic processing not provided for in group H01L21/18 or H01L21/34 comprising organic layers characterised by the treatment of photoresist layers
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31127—Etching organic layers
- H01L21/31133—Etching organic layers by chemical means
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02041—Cleaning
- H01L21/02057—Cleaning during device manufacture
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/26—Bombardment with radiation
- H01L21/263—Bombardment with radiation with high-energy radiation
- H01L21/265—Bombardment with radiation with high-energy radiation producing ion implantation
- H01L21/266—Bombardment with radiation with high-energy radiation producing ion implantation using masks
Definitions
- a photoresist layer is applied on a substrate and patterned so that some areas of the substrate are exposed. The exposed areas are then implanted with dopants.
- the implantation process may chemically change an outer portion of the photoresist layer so that the outer portion includes tough polymers with inter-molecular bonds. The chemically changed outer portion of the photoresist layer may make the photoresist layer more difficult to remove using conventional techniques.
- FIG. 1 is a flowchart showing a manufacturing method of an integrated circuit in accordance with some embodiments.
- FIG. 2A through FIG. 2E are schematic views showing a manufacturing method of an integrated circuit in accordance with some embodiments.
- FIG. 3A through FIG. 31 are schematic views showing a manufacturing method of an integrated circuit in accordance with some embodiments.
- first and first features are formed in direct contact
- additional features may be formed between the second and first features, such that the second and first features may not be in direct contact
- present disclosure may repeat reference numerals and/or letters in the various examples. This repetition is for the purpose of simplicity and clarity and does not in itself dictate a relationship between the various embodiments and/or configurations discussed.
- spatially relative terms such as “top,” “below,” “lower,” “above,” “upper” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures.
- the spatially relative tell is intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures.
- the apparatus may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein may likewise be interpreted accordingly.
- FIG. 1 is a flowchart showing a manufacturing method of a semiconductor device in accordance with some embodiments.
- FIG. 2A through FIG. 2E are schematic views showing a manufacturing method of a semiconductor device in accordance with some embodiments.
- a photoresist layer 110 is formed over a substrate 102 .
- the substrate 102 is a semiconductor substrate, such as a silicon substrate, a silicon-on-insulator (SOI) substrate, a silicon germanium substrate, or a substrate formed of other suitable semiconductor materials.
- the substrate 102 may be a P-type substrate or an N-type substrate and may have doped regions (e.g., n-wells and p-wells) formed therein.
- the substrate 102 has one or more layers (e.g., insulating layers, conductive layers, etc.) formed thereon.
- a structure 108 is formed over the substrate 102 .
- the structure 108 is any component of the semiconductor device, which is susceptible to damage during performing process on other components or the substrate 102 of the semiconductor device.
- the structure 108 is a conductive pattern such as a conductive line or a dielectric pattern such as an inter-metal dielectric (IMD) layer.
- a material of the structure 108 is a conductive material such as metal, metal alloy, metal silicide, polysilicon or a combination thereof, or a dielectric material such as silicon oxide, silicon nitride, silicon oxynitride or a combination thereof.
- the photoresist layer 110 is applied to the substrate 102 and patterned to have the shape shown in FIG. 2A . In some embodiments, the photoresist layer 110 is applied to protect the structure 108 during other processing steps that might damage or alter the structure 108 , such as etching, implantation, and the like. In some embodiments, the photoresist layer 110 may be formed using a spin-on coating process. In some embodiments, the photoresist layer 110 has a thickness ranging from 0.01 um to 10 um. In some embodiments, the photoresist layer 110 is a negative or positive type photoresist of any suitable composition.
- the negative type photoresist includes a photosensitive composition, such as polyisoprene, diazonaphthoquinone (DNQ) or the like.
- the positive type photoresist includes a photosensitive composition, such as phenol-formaldehyde resin, epoxy resin or the like.
- the photoresist may be soft baked after its deposition. After the photoresist is baked, an exposure process is performed on the photoresist. The exposure process patterns the photoresist. In some embodiments, the exposure process may include introducing a radiation beam to the substrate 102 .
- the radiation beam may be ultraviolet and/or can be extended to include other radiation beams such as ion beam, x-ray, extreme ultraviolet, deep ultraviolet, or other proper radiation energy.
- the exposure process may be part of an immersion lithography process, electron-beam writing, ion-beam writing, maskless photolithography, molecular imprint, and/or other suitable patterning processes.
- a post-exposure bake (PEB) may be performed to allow the exposed photoresist polymers to cleave.
- the exposed photoresist is developed (e.g., a developer is applied to the patterned photoresist to remove the soluble portions of the photoresist).
- the substrate 102 and the exposed photoresist including the cleaved polymer are transferred to a developing chamber to remove portions of the photoresist (e.g., the exposed photoresist) that is soluble to an aqueous developer.
- the developer is tetra-methyl ammonium hydroxide (TMAH).
- TMAH tetra-methyl ammonium hydroxide
- other suitable compositions now known or later developed are used.
- a surfactant may also be included.
- the surfactant may selected from surfactants such as, 3M Novec fluid HFE-7000, HFE-7100, HFE-7200, HFE-7500, HFE-71IPA. 3M Fluorinert FC-72, FC-84, FC-77, FC-3255, FC-3283, FC-40, FC-43, FC-70. 3M Novec 4200, 3M Novec 4300, 3M FC-4432. 3M FC-4430, 3M FC-4434 and/or other surfactants known in the art.
- the developer may be applied by a puddling process, immersion, spray, and/or other suitable methods. After the development process, an etching process is performed to remove a portion of the photoresist. Then, as shown in FIG.
- the photoresist layer 110 is formed and has been patterned to have the shape.
- the photoresist layer 110 exposes a portion of the substrate 102 aside the structure 108 and protects the structure 108 over the substrate 202 .
- a layer for promoting adherence of the photoresist layer 110 is formed over the substrate 102 before forming the photoresist layer 110 .
- the layer for promoting adherence of the photoresist layer 110 is, for example, a hexamethyldisilazane (HMDS) layer.
- HMDS hexamethyldisilazane
- a portion of the photoresist layer 110 is chemically changed to a photoresist crust 112 .
- an implantation process 120 is performed on the photoresist layer 110 .
- the implantation process 120 is used to change the conductivity or remove a portion of the substrate 102 or other components of the semiconductor device while the photoresist layer 110 is used as a masking element to protect the structure 108 from being damaged or altered.
- an energy of the implantation process 120 ranges from 0.5 KeV to 2000 KeV.
- a dose of the dopants ranges from 1e13/cm 2 to 1e16/cm 2 .
- a portion of the photoresist layer 110 may be changed chemically to the photoresist crust 112 due the chemicals and heat to which it is exposed.
- an outer surface of the photoresist layer 110 has been changed to the photoresist crust 112 , and an inner of the photoresist layer 110 remains unchanged and is referred to a photoresist bulk 114 .
- M + ion is doped into the photoresist layer 110 , wherein M is, for example, such as boron (B), phosphorus (P) or arsenic (As).
- M is, for example, such as boron (B), phosphorus (P) or arsenic (As).
- B boron
- P phosphorus
- As arsenic
- some of the polymers in the photoresist layer 110 are highly cross-linked, and changed into the polymers forming the photoresist crust 112 .
- the photoresist crust 112 is formed over a top portion or side portions of the photoresist bulk 114 .
- the photoresist crust 112 is relatively more difficult to be removed than the photoresist bulk 114 .
- the photoresist crust 112 has to be removed by a photoresist stripper at a higher temperature, or a plasma ashing process in a longer time while causing a loss of a portion of the substrate 102 .
- the photoresist layer 110 may include deep ultraviolet (DUV) photoresist, such as a photoresist for 248 nm exposure by a Krypton Fluoride (KrF) Excimer Laser.
- DUV deep ultraviolet
- KrF Krypton Fluoride
- the photoresist crust 112 may be resistant to plasma ashing and may further lead to increased residue after the plasma ashing process.
- a plasma etching process may also chemically change a portion of the photoresist layer 110 to the photoresist crust 112 .
- Step S 20 a cryogenic process 130 is performed on the photoresist layer 110 .
- the photoresist crust 112 is exposed to the cryogenic process 130 , and the photoresist crust 112 becomes fragile.
- the photoresist crust 112 becomes fragile due to inter-molecular bonds in the polymers of the photoresist crust 112 being broken.
- microcracks 116 are formed in the photoresist crust 112 and the photoresist crust 112 of the photoresist layer 110 is substantially broken into several fragments with the microcracks 116 therebetween.
- a temperature of the cryogenic process 130 is, for example, from ⁇ 210° C. to ⁇ 272° C.
- the cryogenic process 130 is performed by using a low temperature liquid gas such as liquid nitrogen, liquid oxygen, liquid argon or the like.
- the cryogenic process 130 is a batch wafer processing or single wafer processing, and performed by an immersion method, a spray method, or the like. In the batch wafer processing, 1 to 25 pieces of wafers are simultaneously immersed in a can supplying with a low temperature liquid gas at a flow rate of 10 ml/min to 1000 ml/min.
- one wafer is sprayed with a low temperature liquid gas at a flow rate of 500 ml/min to 2500 ml/min.
- the photoresist crust 112 shown in FIG. 2B the photoresist crust 112 processed with the cryogenic process 130 and having the microcracks 116 therein is easier to be removed.
- the microcracks 116 expose a portion of the photoresist bulk 114 of the photoresist layer 110 .
- Step S 30 after performing the cryogenic process 130 , a cleaning process 140 is performed on the photoresist layer 110 to remove the photoresist layer 110 .
- the cleaning process 140 is performed by supplying a photoresist stripper to the photoresist layer 110 .
- the photoresist stripper is an ozone liquid, which is formed by mixing ozone gas and a deionized water.
- the ozone liquid includes between approximately 15 ppm and 200 ppm of ozone.
- the ozone is made with an ozone generator, and there is very little or no O 2 in the process.
- the deionized water is supplied to the substrate 102 .
- the deionized water has a temperature less than a temperature of the substrate 102 . In some embodiments, the temperature of the deionized water is about 15° C. or less.
- the deionized water lowers the substrate temperature which mitigates thermal shock or other damage to the substrate 102 while enhancing stripping capabilities of the ozone liquid.
- an activator such as an ultraviolet activator or a hydrogen peroxide activator, is supplied to the ozone liquid to create the activated ozone liquid.
- the photoresist stripper is a sulfuric acid hydrogen peroxide mixture (SPM), which is formed by mixing sulfuric acid and hydrogen peroxide immediately before using.
- SPM sulfuric acid hydrogen peroxide mixture
- concentration of sulfuric acid is generally between 95% to 98%, and a temperature thereof is 60° C. to 200° C.
- concentration of hydrogen peroxide is generally between 25% to 33%, and a temperature thereof is 20° C. to 30° C.
- concentration of sulfuric acid is 98%, and concentration of hydrogen peroxide is 30%.
- a volume ratio of sulfuric acid and hydrogen peroxide is 1:1 to 12:1.
- the cryogenic process 130 and the cleaning process 140 are performed in different chambers.
- the photoresist layer 110 is processed by the cryogenic process 130 before removed by the cleaning process 140 .
- the photoresist crust 112 becomes fragile and forms the microcracks therein after processed by the cryogenic process 130 , and therefore the photoresist layer 110 including the photoresist crust 112 is easily removed by the cleaning process 140 . Accordingly, gentle photoresist stripper may be used in the cleaning process 140 and the photoresist layer 110 can be removed more quickly, and the structure 108 or the substrate 102 susceptible to damage during removal of the photoresist layer 110 is prevented from being damage.
- FIG. 3A through FIG. 31 are schematic views showing a manufacturing method of a semiconductor device in accordance with some embodiments.
- a photoresist layer 110 is formed over a substrate 102 .
- the substrate 102 includes a first region 102 a for one or more semiconductor components (e.g., FET) and a second region 102 b for one or more semiconductor components (e.g., FET).
- shallow trench isolation (STI) features 104 are formed in the substrate 102 .
- the formation of the STI features 104 includes etching a trench in the substrate 102 and filling the trench by one or more insulator materials such as silicon oxide, silicon nitride, or silicon oxynitride.
- the filled trench may have a multi-layer structure such as a thermal oxide liner layer with silicon nitride filling the trench.
- the STI feature 104 is created using a process sequence such as: growing a pad oxide, forming a low pressure chemical vapor deposition (LPCVD) nitride layer, patterning an STI opening using photoresist and mask, etching a trench in the substrate, optionally growing a thermal oxide trench liner to improve the trench interface, filling the trench with CVD oxide, using chemical mechanical planarization (CMP) to etch back, and using nitride stripping to leave the STI feature 104 .
- a doped region 106 is formed therein.
- the substrate 102 is a P-type substrate, and the doped region 106 is an n-well, for example. In alternative embodiments, the substrate 102 is an N-type substrate, and the doped region 106 is p-well, for example.
- structures 108 a , 108 b are respectively formed in the first and second regions 102 a , 102 b .
- the structures 108 a , 108 b are, for example, gate structures.
- a material of the structure 108 a , 108 b is a conductive material, such as metal, metal alloy, metal silicide, polysilicon or a combination thereof.
- a dielectric layer 107 is formed between the substrate 102 and the structure 108 a , 108 b .
- a material of the dielectric layer 107 is silicon oxide, a high dielectric constant (high-k) material or a combination thereof.
- the high-k material has a dielectric constant of greater than about 4 or even greater than about 10.
- the high-k material includes metal oxide, such as titanium oxide (TiO 2 ), zirconium oxide (ZrO 2 ), hafnium oxide (HfO 2 ), tantalum oxide (Ta 2 O 5 ), and barium and strontium titanium oxide ((Ba,Sr)TiO 3 ) or a combination thereof.
- spacers are formed on a sidewall of the structure 108 a , 108 b.
- a photoresist layer 110 is applied to the second region 102 b of the substrate 102 to cover the structure 108 b .
- the photoresist layer 110 is used as a masking element to protect the structure 108 b from being damaged or altered.
- an implantation process 120 is performed in the first region 102 a of the substrate 102 to form doped regions 122 a .
- the implantation process 120 is performed by using n-type dopants such as phosphorus, arsenic, and antimony.
- the doped regions 122 a are formed aside the structure 108 a by using the structure 108 a as a mask.
- the substrate 102 is a P-type substrate, and the doped regions 122 a are n-type source and drain regions, for example.
- a portion of the photoresist layer 110 is chemically changed to a photoresist crust 112 , and the other portion of the photoresist layer 110 is unchanged and refers to a photoresist bulk 114 .
- a cryogenic process 130 is performed on the photoresist layer 110 .
- microcracks 116 are formed in the photoresist crust 112 of the photoresist layer 110 and further extended into the photoresist bulk 114 of the photoresist layer 110 .
- the photoresist crust 112 becomes fragile and is easy to be removed.
- a cleaning process 140 is performed on the photoresist layer 110 to remove the photoresist layer 110 .
- the photoresist crust 112 with the microcracks 116 and the photoresist bulk 114 of the photoresist layer 110 are removed.
- a photoresist stripper is contact with the photoresist bulk 114 through the microcracks 116 .
- a photoresist layer 110 is applied to the first region 102 a of the substrate 102 to cover the structure 108 a . Then, an implantation process 120 is performed in the second region 102 b of the substrate 102 to form doped regions 122 b .
- the photoresist layer 110 is used as a masking element to protect the structure 108 a from being damaged or altered.
- the implantation process 120 is performed by using p-type dopants such as boron, indium, aluminum, and gallium.
- the doped regions 122 b are formed aside the structure 108 b in the doped region 106 by using the structure 108 b as a mask.
- the doped region 106 is an n well, and the doped regions 122 b are p-type source and drain regions, for example.
- a portion of the photoresist layer 110 is chemically changed to a photoresist crust 112 , and the other portion of the photoresist layer 110 is unchanged and refers to a photoresist bulk 114 .
- a cryogenic process 130 is performed on the photoresist layer 110 .
- microcracks 116 are formed in the photoresist crust 112 of the photoresist layer 110 and further extended into the photoresist bulk 114 of the photoresist layer 110 .
- the photoresist crust 112 becomes fragile and is easy to be removed.
- a cleaning process 140 is performed on the photoresist layer 110 to remove the photoresist layer 110 .
- the photoresist crust 112 with the microcracks 116 and the photoresist bulk 114 of the photoresist layer 110 are removed.
- a photoresist stripper is contact with the photoresist bulk 114 through the microcracks 116 .
- the photoresist layer including the outer crust is removed by the cryogenic process and the cleaning process sequentially.
- the cryogenic process the photoresist layer is processed with the low-temperature liquid gas by the immersion method or the spraying method, and thus the photoresist crust including the cross-linked polymers becomes fragile and forms mirocracks therein.
- the gentle photoresist stripper may penetrates the broken photoresist crust and dissolves the photoresist bulk, and thus the photoresist is removed easily.
- the photoresist layer including the crust and the bulk is removed easily and completely, and thus the photoresist may be removed at low temperature and by using gentle chemicals such as ozone-based chemical.
- the structure covering by the photoresist layer is prevented from being damaged. Accordingly, the cost for removing the photoresist is lower, the method for removing the photoresist becomes more environmental friendly, and the semiconductor device has better performance.
- a manufacturing method of a semiconductor device includes the following.
- a photoresist layer is formed over a substrate.
- a cryogenic process is performed on the photoresist layer.
- a cleaning process is performed on the photoresist layer to remove the photoresist layer.
- a manufacturing method of a semiconductor device includes the following.
- a patterned photoresist layer is formed over a substrate to cover a structure.
- An implantation process is performed in the substrate, wherein the implantation process chemically changes a first portion of the patterned photoresist layer.
- a cryogenic process is performed on the patterned photoresist layer. After the cryogenic process, a cleaning process is performed on the patterned photoresist layer to remove the photoresist layer.
- a method for manufacturing a semiconductor device includes the following.
- a photoresist layer is formed over a substrate, wherein the photoresist layer includes a photoresist crust.
- a cryogenic process is performed on the photoresist layer, thereby causing microcracks in the photoresist crust.
- a cleaning process is performed on the photoresist layer to remove the photoresist layer.
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Abstract
Description
- In one example conventional process, a photoresist layer is applied on a substrate and patterned so that some areas of the substrate are exposed. The exposed areas are then implanted with dopants. However, the implantation process may chemically change an outer portion of the photoresist layer so that the outer portion includes tough polymers with inter-molecular bonds. The chemically changed outer portion of the photoresist layer may make the photoresist layer more difficult to remove using conventional techniques.
-
FIG. 1 is a flowchart showing a manufacturing method of an integrated circuit in accordance with some embodiments. -
FIG. 2A throughFIG. 2E are schematic views showing a manufacturing method of an integrated circuit in accordance with some embodiments. -
FIG. 3A throughFIG. 31 are schematic views showing a manufacturing method of an integrated circuit in accordance with some embodiments. - The following disclosure provides many different embodiments, or examples, for implementing different features of the provided subject matter. Specific examples of components and arrangements are described below to simplify the present disclosure. These are, of course, merely examples and are not intended to be limiting. For example, the formation of a second feature over or on a first feature in the description that follows may include embodiments in which the second and first features are formed in direct contact, and may also include embodiments in which additional features may be formed between the second and first features, such that the second and first features may not be in direct contact. In addition, the present disclosure may repeat reference numerals and/or letters in the various examples. This repetition is for the purpose of simplicity and clarity and does not in itself dictate a relationship between the various embodiments and/or configurations discussed.
- Further, spatially relative terms, such as “top,” “below,” “lower,” “above,” “upper” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. The spatially relative tell is are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. The apparatus may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein may likewise be interpreted accordingly.
-
FIG. 1 is a flowchart showing a manufacturing method of a semiconductor device in accordance with some embodiments.FIG. 2A throughFIG. 2E are schematic views showing a manufacturing method of a semiconductor device in accordance with some embodiments. - Referring to
FIGS. 1 and 2A , in Step S10, aphotoresist layer 110 is formed over asubstrate 102. In some embodiments, thesubstrate 102 is a semiconductor substrate, such as a silicon substrate, a silicon-on-insulator (SOI) substrate, a silicon germanium substrate, or a substrate formed of other suitable semiconductor materials. Depending on the requirements of design, thesubstrate 102 may be a P-type substrate or an N-type substrate and may have doped regions (e.g., n-wells and p-wells) formed therein. In alternative embodiment, thesubstrate 102 has one or more layers (e.g., insulating layers, conductive layers, etc.) formed thereon. - In some embodiments, a
structure 108 is formed over thesubstrate 102. Thestructure 108 is any component of the semiconductor device, which is susceptible to damage during performing process on other components or thesubstrate 102 of the semiconductor device. In some embodiments, thestructure 108 is a conductive pattern such as a conductive line or a dielectric pattern such as an inter-metal dielectric (IMD) layer. In some embodiments, a material of thestructure 108 is a conductive material such as metal, metal alloy, metal silicide, polysilicon or a combination thereof, or a dielectric material such as silicon oxide, silicon nitride, silicon oxynitride or a combination thereof. - In some embodiments, the
photoresist layer 110 is applied to thesubstrate 102 and patterned to have the shape shown inFIG. 2A . In some embodiments, thephotoresist layer 110 is applied to protect thestructure 108 during other processing steps that might damage or alter thestructure 108, such as etching, implantation, and the like. In some embodiments, thephotoresist layer 110 may be formed using a spin-on coating process. In some embodiments, thephotoresist layer 110 has a thickness ranging from 0.01 um to 10 um. In some embodiments, thephotoresist layer 110 is a negative or positive type photoresist of any suitable composition. In some embodiments, the negative type photoresist includes a photosensitive composition, such as polyisoprene, diazonaphthoquinone (DNQ) or the like. In some embodiments, the positive type photoresist includes a photosensitive composition, such as phenol-formaldehyde resin, epoxy resin or the like. The photoresist may be soft baked after its deposition. After the photoresist is baked, an exposure process is performed on the photoresist. The exposure process patterns the photoresist. In some embodiments, the exposure process may include introducing a radiation beam to thesubstrate 102. In some embodiments, the radiation beam may be ultraviolet and/or can be extended to include other radiation beams such as ion beam, x-ray, extreme ultraviolet, deep ultraviolet, or other proper radiation energy. The exposure process may be part of an immersion lithography process, electron-beam writing, ion-beam writing, maskless photolithography, molecular imprint, and/or other suitable patterning processes. A post-exposure bake (PEB) may be performed to allow the exposed photoresist polymers to cleave. - In some embodiments, after PEB, the exposed photoresist is developed (e.g., a developer is applied to the patterned photoresist to remove the soluble portions of the photoresist). The
substrate 102 and the exposed photoresist including the cleaved polymer are transferred to a developing chamber to remove portions of the photoresist (e.g., the exposed photoresist) that is soluble to an aqueous developer. In some embodiment, the developer is tetra-methyl ammonium hydroxide (TMAH). In alternative embodiment, other suitable compositions now known or later developed are used. In alternative embodiment, a surfactant may also be included. The surfactant may selected from surfactants such as, 3M Novec fluid HFE-7000, HFE-7100, HFE-7200, HFE-7500, HFE-71IPA. 3M Fluorinert FC-72, FC-84, FC-77, FC-3255, FC-3283, FC-40, FC-43, FC-70. 3M Novec 4200, 3M Novec 4300, 3M FC-4432. 3M FC-4430, 3M FC-4434 and/or other surfactants known in the art. In some embodiments, the developer may be applied by a puddling process, immersion, spray, and/or other suitable methods. After the development process, an etching process is performed to remove a portion of the photoresist. Then, as shown inFIG. 2A , thephotoresist layer 110 is formed and has been patterned to have the shape. In some embodiments, thephotoresist layer 110 exposes a portion of thesubstrate 102 aside thestructure 108 and protects thestructure 108 over the substrate 202. In alternative embodiments, a layer for promoting adherence of thephotoresist layer 110 is formed over thesubstrate 102 before forming thephotoresist layer 110. The layer for promoting adherence of thephotoresist layer 110 is, for example, a hexamethyldisilazane (HMDS) layer. - Referring to
FIGS. 1 and 2B , in some embodiments, a portion of thephotoresist layer 110 is chemically changed to aphotoresist crust 112. In some embodiments, after thephotoresist layer 110 is formed over thestructure 108, animplantation process 120 is performed on thephotoresist layer 110. In some embodiments, theimplantation process 120 is used to change the conductivity or remove a portion of thesubstrate 102 or other components of the semiconductor device while thephotoresist layer 110 is used as a masking element to protect thestructure 108 from being damaged or altered. In some embodiments, an energy of theimplantation process 120 ranges from 0.5 KeV to 2000 KeV. In some embodiments, a dose of the dopants ranges from 1e13/cm2 to 1e16/cm2. During theimplantation process 120, a portion of thephotoresist layer 110 may be changed chemically to thephotoresist crust 112 due the chemicals and heat to which it is exposed. In some embodiments, an outer surface of thephotoresist layer 110 has been changed to thephotoresist crust 112, and an inner of thephotoresist layer 110 remains unchanged and is referred to aphotoresist bulk 114. In some embodiments, during theimplantation process 120, M+ ion is doped into thephotoresist layer 110, wherein M is, for example, such as boron (B), phosphorus (P) or arsenic (As). Thus, some of the polymers in thephotoresist layer 110 are highly cross-linked, and changed into the polymers forming thephotoresist crust 112. In some embodiments, thephotoresist crust 112 is formed over a top portion or side portions of thephotoresist bulk 114. Thephotoresist crust 112 is relatively more difficult to be removed than thephotoresist bulk 114. For example, compared with thephotoresist bulk 114, thephotoresist crust 112 has to be removed by a photoresist stripper at a higher temperature, or a plasma ashing process in a longer time while causing a loss of a portion of thesubstrate 102. - In alternative embodiments, the
photoresist layer 110 may include deep ultraviolet (DUV) photoresist, such as a photoresist for 248 nm exposure by a Krypton Fluoride (KrF) Excimer Laser. In this example, after theimplantation process 120, some of the polymers in thephotoresist layer 110 have been chemically changed to microcrystalline graphite and long, single carbon chains and form thephotoresist crust 112. In alternative embodiments, compared with thephotoresist bulk 114, thephotoresist crust 112 may be resistant to plasma ashing and may further lead to increased residue after the plasma ashing process. In alternative embodiments, a plasma etching process may also chemically change a portion of thephotoresist layer 110 to thephotoresist crust 112. - Referring to
FIGS. 1 and 2C , in Step S20, acryogenic process 130 is performed on thephotoresist layer 110. In some embodiments, thephotoresist crust 112 is exposed to thecryogenic process 130, and thephotoresist crust 112 becomes fragile. In some embodiments, thephotoresist crust 112 becomes fragile due to inter-molecular bonds in the polymers of thephotoresist crust 112 being broken. In some embodiments,microcracks 116 are formed in thephotoresist crust 112 and thephotoresist crust 112 of thephotoresist layer 110 is substantially broken into several fragments with themicrocracks 116 therebetween. In some embodiments, themicrocracks 116 are, for example, further extended into thephotoresist bulk 114. In some embodiments, a temperature of thecryogenic process 130 is, for example, from −210° C. to −272° C. In some embodiments, thecryogenic process 130 is performed by using a low temperature liquid gas such as liquid nitrogen, liquid oxygen, liquid argon or the like. In some embodiments, thecryogenic process 130 is a batch wafer processing or single wafer processing, and performed by an immersion method, a spray method, or the like. In the batch wafer processing, 1 to 25 pieces of wafers are simultaneously immersed in a can supplying with a low temperature liquid gas at a flow rate of 10 ml/min to 1000 ml/min. In the single wafer processing, one wafer is sprayed with a low temperature liquid gas at a flow rate of 500 ml/min to 2500 ml/min. Compared with thephotoresist crust 112 shown inFIG. 2B , thephotoresist crust 112 processed with thecryogenic process 130 and having themicrocracks 116 therein is easier to be removed. In addition, in some embodiments, themicrocracks 116 expose a portion of thephotoresist bulk 114 of thephotoresist layer 110. - Referring to
FIGS. 1 and 2D , in Step S30, after performing thecryogenic process 130, acleaning process 140 is performed on thephotoresist layer 110 to remove thephotoresist layer 110. In some embodiments, thecleaning process 140 is performed by supplying a photoresist stripper to thephotoresist layer 110. In some embodiments, the photoresist stripper is an ozone liquid, which is formed by mixing ozone gas and a deionized water. In some embodiments, the ozone liquid includes between approximately 15 ppm and 200 ppm of ozone. In some embodiments, the ozone is made with an ozone generator, and there is very little or no O2 in the process. In some embodiments, the deionized water is supplied to thesubstrate 102. The deionized water has a temperature less than a temperature of thesubstrate 102. In some embodiments, the temperature of the deionized water is about 15° C. or less. The deionized water lowers the substrate temperature which mitigates thermal shock or other damage to thesubstrate 102 while enhancing stripping capabilities of the ozone liquid. In some embodiments, an activator, such as an ultraviolet activator or a hydrogen peroxide activator, is supplied to the ozone liquid to create the activated ozone liquid. - In alternative embodiments, the photoresist stripper is a sulfuric acid hydrogen peroxide mixture (SPM), which is formed by mixing sulfuric acid and hydrogen peroxide immediately before using. In alternative embodiments, concentration of sulfuric acid is generally between 95% to 98%, and a temperature thereof is 60° C. to 200° C. In alternative embodiments, concentration of hydrogen peroxide is generally between 25% to 33%, and a temperature thereof is 20° C. to 30° C. In alternative embodiments, concentration of sulfuric acid is 98%, and concentration of hydrogen peroxide is 30%. In alternative embodiments, a volume ratio of sulfuric acid and hydrogen peroxide is 1:1 to 12:1. In some embodiment, the
cryogenic process 130 and thecleaning process 140 are performed in different chambers. - In some embodiments, the
photoresist layer 110 is processed by thecryogenic process 130 before removed by thecleaning process 140. In some embodiments, thephotoresist crust 112 becomes fragile and forms the microcracks therein after processed by thecryogenic process 130, and therefore thephotoresist layer 110 including thephotoresist crust 112 is easily removed by thecleaning process 140. Accordingly, gentle photoresist stripper may be used in thecleaning process 140 and thephotoresist layer 110 can be removed more quickly, and thestructure 108 or thesubstrate 102 susceptible to damage during removal of thephotoresist layer 110 is prevented from being damage. -
FIG. 3A throughFIG. 31 are schematic views showing a manufacturing method of a semiconductor device in accordance with some embodiments. Referring toFIG. 3A , aphotoresist layer 110 is formed over asubstrate 102. In some embodiments, thesubstrate 102 includes afirst region 102 a for one or more semiconductor components (e.g., FET) and asecond region 102 b for one or more semiconductor components (e.g., FET). In some embodiments, shallow trench isolation (STI) features 104 are formed in thesubstrate 102. The formation of the STI features 104 includes etching a trench in thesubstrate 102 and filling the trench by one or more insulator materials such as silicon oxide, silicon nitride, or silicon oxynitride. The filled trench may have a multi-layer structure such as a thermal oxide liner layer with silicon nitride filling the trench. In alternative embodiment, theSTI feature 104 is created using a process sequence such as: growing a pad oxide, forming a low pressure chemical vapor deposition (LPCVD) nitride layer, patterning an STI opening using photoresist and mask, etching a trench in the substrate, optionally growing a thermal oxide trench liner to improve the trench interface, filling the trench with CVD oxide, using chemical mechanical planarization (CMP) to etch back, and using nitride stripping to leave theSTI feature 104. In some embodiments, a dopedregion 106 is formed therein. In some embodiments, thesubstrate 102 is a P-type substrate, and the dopedregion 106 is an n-well, for example. In alternative embodiments, thesubstrate 102 is an N-type substrate, and the dopedregion 106 is p-well, for example. - In some embodiments,
structures second regions structures structure dielectric layer 107 is formed between thesubstrate 102 and thestructure dielectric layer 107 is silicon oxide, a high dielectric constant (high-k) material or a combination thereof. In some embodiments, the high-k material has a dielectric constant of greater than about 4 or even greater than about 10. In some embodiments, the high-k material includes metal oxide, such as titanium oxide (TiO2), zirconium oxide (ZrO2), hafnium oxide (HfO2), tantalum oxide (Ta2O5), and barium and strontium titanium oxide ((Ba,Sr)TiO3) or a combination thereof. In alternative embodiments, spacers are formed on a sidewall of thestructure - In some embodiment, a
photoresist layer 110 is applied to thesecond region 102 b of thesubstrate 102 to cover thestructure 108 b. In some embodiments, thephotoresist layer 110 is used as a masking element to protect thestructure 108 b from being damaged or altered. - Referring to
FIG. 3B , animplantation process 120 is performed in thefirst region 102 a of thesubstrate 102 to form dopedregions 122 a. In some embodiments, theimplantation process 120 is performed by using n-type dopants such as phosphorus, arsenic, and antimony. In some embodiments, the dopedregions 122 a are formed aside thestructure 108 a by using thestructure 108 a as a mask. In some embodiments, thesubstrate 102 is a P-type substrate, and the dopedregions 122 a are n-type source and drain regions, for example. In some embodiments, during theimplantation process 120, a portion of thephotoresist layer 110 is chemically changed to aphotoresist crust 112, and the other portion of thephotoresist layer 110 is unchanged and refers to aphotoresist bulk 114. - Referring to
FIG. 3C , acryogenic process 130 is performed on thephotoresist layer 110. In some embodiments,microcracks 116 are formed in thephotoresist crust 112 of thephotoresist layer 110 and further extended into thephotoresist bulk 114 of thephotoresist layer 110. In some embodiments, thephotoresist crust 112 becomes fragile and is easy to be removed. - Referring to
FIGS. 3D and 3E , after performing thecryogenic process 130, acleaning process 140 is performed on thephotoresist layer 110 to remove thephotoresist layer 110. In some embodiments, thephotoresist crust 112 with themicrocracks 116 and thephotoresist bulk 114 of thephotoresist layer 110 are removed. In some embodiments, a photoresist stripper is contact with thephotoresist bulk 114 through themicrocracks 116. - Referring to
FIG. 3F , aphotoresist layer 110 is applied to thefirst region 102 a of thesubstrate 102 to cover thestructure 108 a. Then, animplantation process 120 is performed in thesecond region 102 b of thesubstrate 102 to form dopedregions 122 b. In some embodiment, thephotoresist layer 110 is used as a masking element to protect thestructure 108 a from being damaged or altered. In some embodiments, theimplantation process 120 is performed by using p-type dopants such as boron, indium, aluminum, and gallium. In some embodiments, the dopedregions 122 b are formed aside thestructure 108 b in the dopedregion 106 by using thestructure 108 b as a mask. In some embodiments, the dopedregion 106 is an n well, and the dopedregions 122 b are p-type source and drain regions, for example. In some embodiments, during theimplantation process 120, a portion of thephotoresist layer 110 is chemically changed to aphotoresist crust 112, and the other portion of thephotoresist layer 110 is unchanged and refers to aphotoresist bulk 114. - Referring to
FIG. 3G , acryogenic process 130 is performed on thephotoresist layer 110. In some embodiments,microcracks 116 are formed in thephotoresist crust 112 of thephotoresist layer 110 and further extended into thephotoresist bulk 114 of thephotoresist layer 110. In some embodiments, thephotoresist crust 112 becomes fragile and is easy to be removed. - Referring to
FIGS. 3H and 31 , after performing thecryogenic process 130, acleaning process 140 is performed on thephotoresist layer 110 to remove thephotoresist layer 110. In some embodiments, thephotoresist crust 112 with themicrocracks 116 and thephotoresist bulk 114 of thephotoresist layer 110 are removed. In some embodiments, a photoresist stripper is contact with thephotoresist bulk 114 through themicrocracks 116. - In some embodiments, the photoresist layer including the outer crust is removed by the cryogenic process and the cleaning process sequentially. In the cryogenic process, the photoresist layer is processed with the low-temperature liquid gas by the immersion method or the spraying method, and thus the photoresist crust including the cross-linked polymers becomes fragile and forms mirocracks therein. Thereafter, in the cleaning process, the gentle photoresist stripper may penetrates the broken photoresist crust and dissolves the photoresist bulk, and thus the photoresist is removed easily. In some embodiments, the photoresist layer including the crust and the bulk is removed easily and completely, and thus the photoresist may be removed at low temperature and by using gentle chemicals such as ozone-based chemical. Moreover, the structure covering by the photoresist layer is prevented from being damaged. Accordingly, the cost for removing the photoresist is lower, the method for removing the photoresist becomes more environmental friendly, and the semiconductor device has better performance.
- A manufacturing method of a semiconductor device includes the following. A photoresist layer is formed over a substrate. A cryogenic process is performed on the photoresist layer. After the cryogenic process, a cleaning process is performed on the photoresist layer to remove the photoresist layer.
- A manufacturing method of a semiconductor device includes the following. A patterned photoresist layer is formed over a substrate to cover a structure. An implantation process is performed in the substrate, wherein the implantation process chemically changes a first portion of the patterned photoresist layer. A cryogenic process is performed on the patterned photoresist layer. After the cryogenic process, a cleaning process is performed on the patterned photoresist layer to remove the photoresist layer.
- A method for manufacturing a semiconductor device includes the following. A photoresist layer is formed over a substrate, wherein the photoresist layer includes a photoresist crust. A cryogenic process is performed on the photoresist layer, thereby causing microcracks in the photoresist crust. After the cryogenic process, a cleaning process is performed on the photoresist layer to remove the photoresist layer.
- The foregoing outlines features of several embodiments so that those skilled in the art may better understand the aspects of the present disclosure. Those skilled in the art should appreciate that they may readily use the present disclosure as a basis for designing or modifying other processes and features for carrying out the same purposes and/or achieving the same advantages of the embodiments introduced herein. Those skilled in the art should also realize that such equivalent constructions do not depart from the spirit and scope of the present disclosure, and that they may make various changes, substitutions, and alterations herein without departing from the spirit and scope of the present disclosure.
Claims (20)
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US14/968,923 US9685330B1 (en) | 2015-12-15 | 2015-12-15 | Manufacturing method of semiconductor device |
TW105139067A TWI719083B (en) | 2015-12-15 | 2016-11-28 | Manufacturing method of semiconductor device |
CN201611078060.0A CN107068547A (en) | 2015-12-15 | 2016-11-30 | Method for manufacturing semiconductor device |
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US5451295A (en) * | 1994-04-12 | 1995-09-19 | Micron Technology, Inc. | Process for removing film from a substrate |
JPH11162805A (en) * | 1997-12-02 | 1999-06-18 | Nitto Denko Corp | Resist removal method |
US20070089761A1 (en) * | 2005-10-21 | 2007-04-26 | Souvik Banerjee | Non-plasma method of removing photoresist from a substrate |
DE102005056879A1 (en) * | 2005-11-28 | 2007-05-31 | Christian-Albrechts-Universität Zu Kiel | Nano-connection producing method for use in industrial manufacturing process, involves covering defined area with strip, and producing crack pattern comprising crack lines by inducing stress in strip, such that nano-connections are formed |
US7947605B2 (en) * | 2006-04-19 | 2011-05-24 | Mattson Technology, Inc. | Post ion implant photoresist strip using a pattern fill and method |
KR20110059761A (en) * | 2008-09-12 | 2011-06-03 | 스미또모 가가꾸 가부시키가이샤 | Resist processing method and use of positive resist composition |
US20170301567A9 (en) * | 2012-11-20 | 2017-10-19 | Tokyo Electron Limited | System of controlling treatment liquid dispense for spinning substrates |
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