US20090239161A1 - Applications of semiconductor nano-sized particles for photolithography - Google Patents

Applications of semiconductor nano-sized particles for photolithography Download PDF

Info

Publication number
US20090239161A1
US20090239161A1 US12/415,013 US41501309A US2009239161A1 US 20090239161 A1 US20090239161 A1 US 20090239161A1 US 41501309 A US41501309 A US 41501309A US 2009239161 A1 US2009239161 A1 US 2009239161A1
Authority
US
United States
Prior art keywords
nano
sized particles
semiconductor nano
light
cuin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/415,013
Inventor
Zhiyun Chen
Erin F. Fleet
Gregory Cooper
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Pixelligent Technologies LLC
Original Assignee
Pixelligent Technologies LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Pixelligent Technologies LLC filed Critical Pixelligent Technologies LLC
Priority to US12/415,013 priority Critical patent/US20090239161A1/en
Publication of US20090239161A1 publication Critical patent/US20090239161A1/en
Priority to US13/189,143 priority patent/US9207538B2/en
Priority to US14/636,433 priority patent/US20150168842A1/en
Priority to US14/848,104 priority patent/US20150380239A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/20Exposure; Apparatus therefor
    • G03F7/2041Exposure; Apparatus therefor in the presence of a fluid, e.g. immersion; using fluid cooling means
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y30/00Nanotechnology for materials or surface science, e.g. nanocomposites
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F1/00Originals for photomechanical production of textured or patterned surfaces, e.g., masks, photo-masks, reticles; Mask blanks or pellicles therefor; Containers specially adapted therefor; Preparation thereof
    • G03F1/62Pellicles, e.g. pellicle assemblies, e.g. having membrane on support frame; Preparation thereof
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials
    • G03F7/09Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers
    • G03F7/091Photosensitive materials characterised by structural details, e.g. supports, auxiliary layers characterised by antireflection means or light filtering or absorbing means, e.g. anti-halation, contrast enhancement
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/20Exposure; Apparatus therefor
    • G03F7/2002Exposure; Apparatus therefor with visible light or UV light, through an original having an opaque pattern on a transparent support, e.g. film printing, projection printing; by reflection of visible or UV light from an original such as a printed image
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F7/00Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
    • G03F7/004Photosensitive materials

Definitions

  • This technology herein relates to photolithography, and more particularly to applications of semiconductor nano-sized particles in photolithography, and even more particularly to applications of semiconductor nano-sized particles as highly refractive media in immersion lithography, as anti-reflection coating, as pellicle, and as sensitizer in UV photoresists.
  • lithography is used to transfer a specific pattern onto a surface.
  • Lithography can be applied to transfer a variety of patterns including, for example, painting, printing, and the like.
  • lithographic techniques have become widespread for use in “microfabrication”—a major (but non-limiting) example of which is the manufacture of integrated circuits such as computer chips.
  • lithography is used to define patterns for miniature electrical circuits.
  • Lithography defines a pattern specifying the location of metal, insulators, doped regions, and other features of a circuit printed on a silicon wafer or other substrate.
  • the resulting circuit can perform any of a number of different functions. For example, an entire computer can be placed on a chip.
  • a primary lithography system includes a wafer stepper, a photomask and photoresist.
  • a wafer stepper generally consists of a ultraviolet (UV) light source, a photomask holder, an optical system for projecting and demagnifying the image of the mask onto a photoresist-coated wafer, and a stage to move the wafer.
  • Conventional lithography also generally requires a photomask—a quartz substrate with chrome patterns on one surface. The chrome patterns form a perfect master of the pattern to be inscribed on one layer of a chip. Also it requires photoresist to receive the light pattern generated by the mask.
  • Improvements in lithography have been mainly responsible for the explosive growth of computers in particular and the semiconductor industry in general.
  • the major improvements in lithography are mainly a result of a decrease in the minimum feature size (improvement in resolution).
  • This improvement allows for an increase in the number of transistors on a single chip (and in the speed at which these transistors can operate).
  • the computer circuitry that would have filled an entire room in 1960's technology can now be placed on a silicon “die” the size of a thumbnail.
  • a device the size of a wristwatch can contain more computing power than the largest computers of several decades ago.
  • d is the minimum feature size
  • is the wavelength
  • NA is the numerical aperture of the optical system
  • k 1 is a constant determined by a specific system. For a certain wavelength and a certain optical design, the only way to improve the resolution is to increase the numerical aperture.
  • the numerical aperture is defined as:
  • n is the refraction index of the relative medium and ⁇ is the half angle of the cone of rays received by the entrance pupil.
  • High NA indicates high light collecting or light focusing power. It is rather straightforward to see that the resolution is proportional the refractive index of the medium.
  • Nano-sized particles are loosely defined as powders with small diameters for example ranging from a few hundred nanometers or less down to a few angstroms. Since they have generally only been the focus of research in the last two decades, there is little standardization, and they take many different names including quantum dot, quantum sphere, quantum crystallite, nano-crystal, micro-crystal, colloidal particle, nano-cluster, Q-particle or artificial atom. Due to their small size, they often possess dramatically different physical properties compared to their bulk counterparts. Nano-sized particles have a wide range of applications including metallurgy, chemical sensors, pharmaceuticals, painting, and cosmetics.
  • Nano-sized particles with sizes less than 5 nm have been synthesized from a variety of semiconductors, examples include C, Si, Ge, CuCl, CuBr, CuI, AgCl, AgBr, AgI, Ag 2 S, CaO, MgO, ZnO, ZnS, HgS, ZnSe, CdS, CdSe, CdTe, HgTe, PbS, BN, AlN, GaN, GaP GaAs, GaSb, InP, InAs, In x Ga 1 ⁇ x As, SiC, Si 1 ⁇ x Ge x , Si 3 N 4 , ZrN, CaF 2 , YF 3 , Al 2 O 3 , SiO 2 , TiO 2 , Cu 2 O, Zr 2 O 3 , SnO 2 , YSi 2 , GaInP 2 , Cd 3
  • bandgaps Semiconductor materials have the so called bandgaps.
  • the electron band below the bandgap is call valence band (VB) and the electron band above the bandgap is called conduction band (CB).
  • VB valence band
  • CB conduction band
  • the manifestation of a bandgap in optical absorption is that only photons with energy larger than the bandgap are absorbed. A photon with sufficient energy excites an electron from the top of valence band to the bottom of conduction band, leaving an empty state, a hole, at the top of the valence band.
  • the bandgap of semiconductor nano-sized particles can be tailored by their size. In a certain range the smaller the size, the larger the bandgap. The bandgap determines the working wavelength.
  • the refractive index can be very high near the bandgap.
  • some semiconductors have the highest refractive indices.
  • wurzite TiO 2 has a refractive index of 2.4
  • wurzite GaN has a refractive index about 2.6 near the bandgap.
  • the refractive indices of common optical materials such as fused silica and quartz used in the UV lithography are around 1.5. This high refractive index is desirable for highly refractive medium immersion lithography and optical coating.
  • nano-sized particles can be easily coated onto optics or wafers in the form of a thin film. They are, therefore, very simple to handle and produce much less contamination. Because of the polycrystalline nature of nano-sized particle films, there is less concern about matching the thermal expansion coefficients between the coating and the optics. Applying nano-sized particles by coating provides least disturbance to the existing lithography system.
  • semiconductors nano-sized particles can reach sizes much smaller than the working wavelength.
  • a large number of semiconductors can be fabricated into nano-sized particles smaller than 5 nm in diameter.
  • the scattering from the nanoparticles is negligible and size fluctuation of nano-sized particles does not affect the final scattered and transmitted light.
  • semiconductors can possess bandgaps as high as 12 eV, corresponding to a wavelength of 100 nm. For 157 nm lithography and beyond, few materials can withstand the radiation except certain semiconductors. Nano-sized particles offer a solution for the optics in these wavelengths.
  • FIG. 1 shows an exemplary illustrative non-limiting optical structure to achieve high resolution by inserting a layer of high refractive index semiconductor nano-sized particle layer between the photomask and the next optics in a projection photolithography system;
  • FIG. 2 shows an exemplary illustrative non-limiting optical structure to achieve high resolution by inserting a thin layer of high refractive index containing semiconductor nano-sized particle between the final optics and the photoresist in a projection photolithography system;
  • FIG. 3 shows an exemplary illustrative non-limiting antireflection coating for optical lens with a thickness of the coating of ⁇ /4 n for maximum transmission;
  • FIG. 4 a is an exemplary illustrative non-limiting photoresist with semiconductor nano-sized particles as sensitizer
  • FIG. 4 b shows the exemplary physical process in which photo-generated electron or hole are transferred out of the particle via surface bonded acceptor or donor;
  • FIG. 4 c demonstrates the exemplary illustrative physical process, i.e. Auger photo-ionization, in which electrons or holes are ejected out the particle as a result of the incoming photon.
  • Nano-sized particles could offer much higher refractive indices. Therefore, nano-sized particles, or mixtures of nano-sized particles with certain liquid, polymer, gel or solid material can improve the resolution in both liquid and solid immersion lithography.
  • FIG. 1 A first exemplary illustrative non-limiting application of nano-sized particle as highly refractive medium in lithography is demonstrated in FIG. 1 .
  • a layer containing nano-sized particles is inserted between the photomask and the immediate next lens. This layer can be coated onto either the photomask or the lens itself.
  • this layer may comprise ZnO or GaN nano-sized particles.
  • it may comprise Mg x Zn 1 ⁇ x O or AlN or BN nano-sized particles.
  • the highly refractive layer has more efficiency in collecting the light transmitted through the photomask.
  • Numerical aperture, as defined by NA n sin ⁇ , describes the light-gathering power of a lens.
  • NA cannot be larger than 1, while with this coating NA can easily exceed 1.
  • the final NA is 1.3.
  • FIG. 2 Another exemplary illustrative implementation is shown in FIG. 2 .
  • the high refractive index nano-sized particle containing layer is applied at the wafer end of the lithography system.
  • a layer containing nano-sized particle is inserted between the photoresist and the exit of the projection optical system.
  • This layer may be simply deposited or spun on top of the photoresist.
  • This layer may also be formed by immersing the space between the final optics and photoresist with nano-sized particle containing highly refractive liquid, polymer or gel.
  • This layer may also be formed by continuously flowing highly refractive liquid or gel through the space between the final optics and the photoresist.
  • the highly refractive liquid may contain nano-sized particles and water. Again, as indicated by the Rayleigh equation, the resolution of the system is increased by a factor of n. For semiconductor nano-sized particles with refractive index bigger than 2.5, this can be a significant improvement.
  • Another exemplary illustrative non-limiting arrangement is to coat the numerical aperture limiting optics.
  • the numerical aperture is usually limited by the entrance optics.
  • the numerical aperture may be limited by some intermediated optics.
  • the specific optics may be coated with highly refractive semiconductor nano-sized particles containing material.
  • Another exemplary illustration is to fill the entire optical system with semiconductor nano-sized particles or mixture of nano-sized particle with liquid, polymer, gel or solid. Light spreads more in the low refractive index material than in the high refractive index material, filling up the entire space with high refractive index material confines the light path to a tighter distribution. Therefore, it can reduce the diameter of the optical design further. This is particularly important to the programmable lithography because smaller optics increase the throughput, see “Photolithographic System For Exposing A Wafer Using A Programmable Mask” by G. Cooper et. al., US patent number U.S. Pat. No. 6,291,110 B1.
  • the high refractive index in these semiconductors also offers certain advantages. For example, it will require less thickness to achieve certain optical path, which is defined as refractive index times the thickness. Smaller thickness in turn results in less absorption.
  • Nano-sized particles such as Mg x Zn 1 ⁇ x O, BN, AlN, CaF 2 , MgF 2 , and SiO 2 may be used as the coating material because they all have bandgap larger than the photon energy.
  • AlN, SiO 2 nano-sized particles may be used. Nano-sized particles can be mixed with certain decomposable polymer matrix, spun on to the optics and then the matrix can removed through chemical processes. Nano-sized particles may also be grown directly on the optics by various know growth methods.
  • a pellicle provides protection for a photomask against dust particles.
  • the pellicle itself may be transparent to the light and have certain mechanical strength.
  • nano-sized particles such as Mg x Zn 1 ⁇ x O, BN, AlN, CaF 2 , MgF 2 , SiO 2
  • candidate materials For 193 nm pellicle, nano-sized particles such as Mg x Zn 1 ⁇ x O, BN, AlN, CaF 2 , MgF 2 , SiO 2 , may be used as candidate materials.
  • AlN, SiO 2 nano-sized particles may be used as candidate materials. Few hundred micrometers of close-packed nano-sized particles may be grown on a substrate, such as thin glass plate using suitable methods. High pressure may be applied after the deposition to assure mechanical strength. Then the substrate can be etched away by selective etching, such as HF acid etching, leaving the free standing film as the pellicle.
  • Nano-sized particles with certain bandgap(s) are mixed with certain polymers as seen in the FIG. 4 a.
  • the resulted electron or hole may be transferred out of the nano-sized particle into surrounding polymers via surface states or surface bonded acceptor or donor.
  • the transferred electrons or holes can then break or form bonds in the polymer and alter its solubility of the polymer to developers.
  • This type of photoresist can be used at wavelength shorter than 193 nm where it is difficult to find conventional photoresists.
  • Auger photo-ionization can be significant.
  • a photon in an Auger process, a photon generates a pair of electron and hole, when the pair recombines, it transfer its energy and momentum to another electron or hole.
  • Auger effects occur simultaneously, some of electrons or holes can gain enough energy to be ejected out of the particle into the surrounding environment.
  • This process is described in the publication entitled “Fluorescence Intermittency In Single Cadmium Selenide Nanocrystals” to M. Nirmal et. al., Nature, 1996, 383, pp. 802-804.
  • the ejected energetic electrons lose their energy by breaking chemical bonds of the polymers. The broken bonds in turn alter the solubility of the polymer to developer.

Abstract

Semiconductor nano-sized particles possess unique optical properties, which make them ideal candidates for various applications in the UV photolithography. In this patent several such applications, including using semiconductor nano-sized particles or semiconductor nano-sized particle containing materials as highly refractive medium in immersion lithography, as anti-reflection coating in optics, as pellicle in lithography and as sensitizer in UV photoresists are described.

Description

    CROSS-REFERENCES TO RELATED APPLICATIONS
  • This application claims the benefit of priority from provisional application No. 60/451,240 filed Mar. 4, 2003, incorporated herein by reference.
  • This application is related to US patent No. U.S. Pat. No. 6,291,110 B1, Cooper et al. entitled “Photolithographic System For Exposing A Wafer Using A Programmable Mask”; and commonly-assigned provisional application No. ______,filed ______ entitled “Programmable photolithographic mask and reversible photo-bleachable materials based on nano-sized semiconductor particles and their applications” to Z. Chen et. al.
  • FIELD
  • This technology herein relates to photolithography, and more particularly to applications of semiconductor nano-sized particles in photolithography, and even more particularly to applications of semiconductor nano-sized particles as highly refractive media in immersion lithography, as anti-reflection coating, as pellicle, and as sensitizer in UV photoresists.
  • STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT
  • Not applicable.
  • BACKGROUND AND SUMMARY Lithography
  • Generally, lithography is used to transfer a specific pattern onto a surface. Lithography can be applied to transfer a variety of patterns including, for example, painting, printing, and the like. More recently, lithographic techniques have become widespread for use in “microfabrication”—a major (but non-limiting) example of which is the manufacture of integrated circuits such as computer chips.
  • In a typical microfabrication operation, lithography is used to define patterns for miniature electrical circuits. Lithography defines a pattern specifying the location of metal, insulators, doped regions, and other features of a circuit printed on a silicon wafer or other substrate. The resulting circuit can perform any of a number of different functions. For example, an entire computer can be placed on a chip.
  • A primary lithography system includes a wafer stepper, a photomask and photoresist. A wafer stepper generally consists of a ultraviolet (UV) light source, a photomask holder, an optical system for projecting and demagnifying the image of the mask onto a photoresist-coated wafer, and a stage to move the wafer. Conventional lithography also generally requires a photomask—a quartz substrate with chrome patterns on one surface. The chrome patterns form a perfect master of the pattern to be inscribed on one layer of a chip. Also it requires photoresist to receive the light pattern generated by the mask.
  • Improvements in lithography have been mainly responsible for the explosive growth of computers in particular and the semiconductor industry in general. The major improvements in lithography are mainly a result of a decrease in the minimum feature size (improvement in resolution). This improvement allows for an increase in the number of transistors on a single chip (and in the speed at which these transistors can operate). For example, the computer circuitry that would have filled an entire room in 1960's technology can now be placed on a silicon “die” the size of a thumbnail. A device the size of a wristwatch can contain more computing power than the largest computers of several decades ago.
  • The resolution of a photolithography system is described by the Rayleigh equation:

  • d=k 1 λ/NA
  • where d is the minimum feature size, λ is the wavelength, NA is the numerical aperture of the optical system and k1 is a constant determined by a specific system. For a certain wavelength and a certain optical design, the only way to improve the resolution is to increase the numerical aperture. The numerical aperture is defined as:

  • NA=n sin θ
  • where n is the refraction index of the relative medium and θ is the half angle of the cone of rays received by the entrance pupil. High NA indicates high light collecting or light focusing power. It is rather straightforward to see that the resolution is proportional the refractive index of the medium.
  • Semiconductor Nano-sized Particles
  • Nano-sized particles are loosely defined as powders with small diameters for example ranging from a few hundred nanometers or less down to a few angstroms. Since they have generally only been the focus of research in the last two decades, there is little standardization, and they take many different names including quantum dot, quantum sphere, quantum crystallite, nano-crystal, micro-crystal, colloidal particle, nano-cluster, Q-particle or artificial atom. Due to their small size, they often possess dramatically different physical properties compared to their bulk counterparts. Nano-sized particles have a wide range of applications including metallurgy, chemical sensors, pharmaceuticals, painting, and cosmetics. As a result of the rapid development in synthesis methods in the last two decades, they have now entered into microelectronic and optical applications. Nano-sized particles with sizes less than 5 nm have been synthesized from a variety of semiconductors, examples include C, Si, Ge, CuCl, CuBr, CuI, AgCl, AgBr, AgI, Ag2S, CaO, MgO, ZnO, ZnS, HgS, ZnSe, CdS, CdSe, CdTe, HgTe, PbS, BN, AlN, GaN, GaP GaAs, GaSb, InP, InAs, InxGa1−xAs, SiC, Si1−xGex, Si3N4, ZrN, CaF2, YF3, Al2O3, SiO2, TiO2, Cu2O, Zr2O3, SnO2, YSi2, GaInP2, Cd3P2, Fe2S, Cu2S, CuIn2S2, MoS2, In2S3, Bi2S3, CuIn2Se2, In2Se3, HgI2, PbI2, Lanthanoids oixides, etc. They have revealed very interesting optical properties.
  • Semiconductor materials have the so called bandgaps. The electron band below the bandgap is call valence band (VB) and the electron band above the bandgap is called conduction band (CB). The manifestation of a bandgap in optical absorption is that only photons with energy larger than the bandgap are absorbed. A photon with sufficient energy excites an electron from the top of valence band to the bottom of conduction band, leaving an empty state, a hole, at the top of the valence band.
  • There are several major advantages of using semiconductor nano-sized particles in photolithography. First, the bandgap of semiconductor nano-sized particles can be tailored by their size. In a certain range the smaller the size, the larger the bandgap. The bandgap determines the working wavelength.
  • Second, the refractive index can be very high near the bandgap. Actually some semiconductors have the highest refractive indices. For example wurzite TiO2 has a refractive index of 2.4, and wurzite GaN has a refractive index about 2.6 near the bandgap. The refractive indices of common optical materials such as fused silica and quartz used in the UV lithography are around 1.5. This high refractive index is desirable for highly refractive medium immersion lithography and optical coating.
  • Third, nano-sized particles can be easily coated onto optics or wafers in the form of a thin film. They are, therefore, very simple to handle and produce much less contamination. Because of the polycrystalline nature of nano-sized particle films, there is less concern about matching the thermal expansion coefficients between the coating and the optics. Applying nano-sized particles by coating provides least disturbance to the existing lithography system.
  • Fourth, semiconductors nano-sized particles can reach sizes much smaller than the working wavelength. Currently, a large number of semiconductors can be fabricated into nano-sized particles smaller than 5 nm in diameter. Hence the scattering from the nanoparticles is negligible and size fluctuation of nano-sized particles does not affect the final scattered and transmitted light.
  • Fifth, in a broad sense semiconductors can possess bandgaps as high as 12 eV, corresponding to a wavelength of 100 nm. For 157 nm lithography and beyond, few materials can withstand the radiation except certain semiconductors. Nano-sized particles offer a solution for the optics in these wavelengths.
  • Lastly, many semiconductor nano-sized particles can be produced rather inexpensively. Therefore, the overall cost will likely be lower than conventional methods.
  • We propose several applications of semiconductor nano-sized particles in lithography. Such as highly refractive medium in immersion lithography, optical coating, pellicle material, and sensitizer in photoresists.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • These and other features and advantages will be better and more completely understood by referring to the following detailed description of presently preferred illustrative embodiments in conjunction with the drawings, of which:
  • FIG. 1 shows an exemplary illustrative non-limiting optical structure to achieve high resolution by inserting a layer of high refractive index semiconductor nano-sized particle layer between the photomask and the next optics in a projection photolithography system;
  • FIG. 2 shows an exemplary illustrative non-limiting optical structure to achieve high resolution by inserting a thin layer of high refractive index containing semiconductor nano-sized particle between the final optics and the photoresist in a projection photolithography system;
  • FIG. 3 shows an exemplary illustrative non-limiting antireflection coating for optical lens with a thickness of the coating of λ/4 n for maximum transmission;
  • FIG. 4 a is an exemplary illustrative non-limiting photoresist with semiconductor nano-sized particles as sensitizer;
  • FIG. 4 b shows the exemplary physical process in which photo-generated electron or hole are transferred out of the particle via surface bonded acceptor or donor; and
  • FIG. 4 c demonstrates the exemplary illustrative physical process, i.e. Auger photo-ionization, in which electrons or holes are ejected out the particle as a result of the incoming photon.
  • DETAILED DESCRIPTION OF PRESENTLY PREFERRED EXAMPLE ILLUSTRATIVE NON-LIMITING IMPLEMENTATIONS
  • It is shown in the Rayleigh equation that the resolution of a lithography system is proportionally dependant on the refractive index of the relevant medium. There are several examples of achieving high resolution by immersion in high refractive index liquid materials. However, the fact that all liquids used in the liquid immersion lithography have refractive index smaller than 1.5 limits the final achievable resolution. Solid immersion lithography has been proposed to achieve higher refractive index.
  • Nano-sized particles, as mentioned before, could offer much higher refractive indices. Therefore, nano-sized particles, or mixtures of nano-sized particles with certain liquid, polymer, gel or solid material can improve the resolution in both liquid and solid immersion lithography.
  • A first exemplary illustrative non-limiting application of nano-sized particle as highly refractive medium in lithography is demonstrated in FIG. 1. In projection lithography, a layer containing nano-sized particles is inserted between the photomask and the immediate next lens. This layer can be coated onto either the photomask or the lens itself. For 365 nm lithography, this layer may comprise ZnO or GaN nano-sized particles. For 193 nm lithography, it may comprise MgxZn1−xO or AlN or BN nano-sized particles. The highly refractive layer has more efficiency in collecting the light transmitted through the photomask. Numerical aperture, as defined by NA=n sin θ, describes the light-gathering power of a lens. In FIG. 1, by inserting a high refractive layer between the mask and the first lens, the numerical aperture is increased by a factor of n, comparing to air. In air, NA cannot be larger than 1, while with this coating NA can easily exceed 1. For example if TiO2 nano-sized particles are used, even with a NA=0.5 in air, the final NA is 1.3.
  • This high light collecting efficiency offers great advantages to the lithography system. First, if the geometry of the entire optical system is kept the same, this added layer will increase the final resolution by a factor of n. If the numerical aperture, i.e. the resolution, is kept the same, then the diameter of the optical system can be reduced by a factor of n and therefore the overall cost of the system can be reduced. In particularly, in programmable lithography, reduced size of optics means increase in the throughput by roughly n2 (see “Photolithographic System For Exposing A Wafer Using A Programmable Mask” by G. Cooper et. al., US patent number U.S. Pat. No. 6,291,110 B1).
  • Another exemplary illustrative implementation is shown in FIG. 2. In this non-limiting example the high refractive index nano-sized particle containing layer is applied at the wafer end of the lithography system. A layer containing nano-sized particle is inserted between the photoresist and the exit of the projection optical system. This layer may be simply deposited or spun on top of the photoresist. This layer may also be formed by immersing the space between the final optics and photoresist with nano-sized particle containing highly refractive liquid, polymer or gel. This layer may also be formed by continuously flowing highly refractive liquid or gel through the space between the final optics and the photoresist. The highly refractive liquid may contain nano-sized particles and water. Again, as indicated by the Rayleigh equation, the resolution of the system is increased by a factor of n. For semiconductor nano-sized particles with refractive index bigger than 2.5, this can be a significant improvement.
  • Another exemplary illustrative non-limiting arrangement is to coat the numerical aperture limiting optics. In an imaging system the numerical aperture is usually limited by the entrance optics. In some systems, the numerical aperture may be limited by some intermediated optics. To improve the overall NA, the specific optics may be coated with highly refractive semiconductor nano-sized particles containing material.
  • Another exemplary illustration is to fill the entire optical system with semiconductor nano-sized particles or mixture of nano-sized particle with liquid, polymer, gel or solid. Light spreads more in the low refractive index material than in the high refractive index material, filling up the entire space with high refractive index material confines the light path to a tighter distribution. Therefore, it can reduce the diameter of the optical design further. This is particularly important to the programmable lithography because smaller optics increase the throughput, see “Photolithographic System For Exposing A Wafer Using A Programmable Mask” by G. Cooper et. al., US patent number U.S. Pat. No. 6,291,110 B1.
  • For certain wavelengths in lithography such as 193 nm and 157 nm, few materials can withstand the highly energetic radiation except some wide bandgap semiconductors such as MgO and AlN. The high refractive index in these semiconductors also offers certain advantages. For example, it will require less thickness to achieve certain optical path, which is defined as refractive index times the thickness. Smaller thickness in turn results in less absorption.
  • An exemplary illustration of applying semiconductor nano-sized particles for optical coating is the anti-reflection coating of optical lenses, as demonstrated in FIG. 3. Anti-reflection coating has an optical path of a quarter of the wavelength, so the reflection is minimized. Of course, the coating material itself has to cause little or no absorption at the working wavelength. For optics working at 193 nm, Nano-sized particles such as MgxZn1−xO, BN, AlN, CaF2, MgF2, and SiO2 may be used as the coating material because they all have bandgap larger than the photon energy. For 157 nm lithography, AlN, SiO2 nano-sized particles may be used. Nano-sized particles can be mixed with certain decomposable polymer matrix, spun on to the optics and then the matrix can removed through chemical processes. Nano-sized particles may also be grown directly on the optics by various know growth methods.
  • Another exemplary illustration is to use the semiconductor nano-sized particles as pellicle materials. A pellicle provides protection for a photomask against dust particles. The pellicle itself may be transparent to the light and have certain mechanical strength. For 193 nm pellicle, nano-sized particles such as MgxZn1−xO, BN, AlN, CaF2, MgF2, SiO2, may be used as candidate materials. For 157 nm lithography, AlN, SiO2 nano-sized particles may be used as candidate materials. Few hundred micrometers of close-packed nano-sized particles may be grown on a substrate, such as thin glass plate using suitable methods. High pressure may be applied after the deposition to assure mechanical strength. Then the substrate can be etched away by selective etching, such as HF acid etching, leaving the free standing film as the pellicle.
  • An exemplary illustration of applying semiconductor nano-sized particles as a sensitizer in photoresist is shown in FIG. 4. Nano-sized particles with certain bandgap(s) are mixed with certain polymers as seen in the FIG. 4 a. Upon absorption of a photon, the resulted electron or hole may be transferred out of the nano-sized particle into surrounding polymers via surface states or surface bonded acceptor or donor. The transferred electrons or holes can then break or form bonds in the polymer and alter its solubility of the polymer to developers. This type of photoresist can be used at wavelength shorter than 193 nm where it is difficult to find conventional photoresists.
  • If nano-sized particles are small enough, multi-body interactions such as Auger photo-ionization can be significant. As depicted in FIG. 4 b, in an Auger process, a photon generates a pair of electron and hole, when the pair recombines, it transfer its energy and momentum to another electron or hole. When multiple Auger effects occur simultaneously, some of electrons or holes can gain enough energy to be ejected out of the particle into the surrounding environment. This process is described in the publication entitled “Fluorescence Intermittency In Single Cadmium Selenide Nanocrystals” to M. Nirmal et. al., Nature, 1996, 383, pp. 802-804. The ejected energetic electrons lose their energy by breaking chemical bonds of the polymers. The broken bonds in turn alter the solubility of the polymer to developer.
  • While the technology herein has been described in connection with exemplary illustrative non-limiting embodiments, the invention is not to be limited by the disclosure. The invention is intended to be defined by the claims and to cover all corresponding and equivalent arrangements whether or not specifically disclosed herein.

Claims (33)

1-8. (canceled)
9. A method of creating an anti-reflection coating on optics comprising; applying, on said at least one optic, at least a thin layer containing semiconductor nano-sized particles.
10. A method of claim 9 wherein the said semiconductor nano-sized particles are selected from the group consisting of C, Si, Ge, CuCl, CuBr, CuI, AgCl, AgBr, AgI, Ag2S, CaO, MgO, ZnO, MgxZn1−xO, ZnS, HgS, ZnSe, CdS, CdSe, CdTe, HgTe, PbS, BN, AlN, GaN, AlxGa1−xN, GaP GaAs, GaSb, InP, InAs, InxGa1−xAs, SiC, Si1−xGex, Si3N4, ZrN, CaF2, YF3, Al2O3, SiO2, TiO2, Cu2O, Zr2O3, ZrO2, SnO2, YSi2, GaInP2, Cd3P2, Fe2S, Cu2S, CuIn2S2, MoS2, In2S3, Bi2S3, CuIn2Se2, In2Se3, HgI2, PbI2, Lanthanoids oxides, etc, and their various alloys.
11. A method of creating pellicle comprising;
having at least a thin layer containing semiconductor nano-sized particles.
12. A method of claim 11 wherein the said semiconductor nano-sized particles are selected from the group consisting of C, Si, Ge, CuCl, CuBr, CuI, AgCl, AgBr, AgI, Ag2S, CaO, MgO, ZnO, MgxZn1−xO, ZnS, HgS, ZnSe, CdS, CdSe, CdTe, HgTe, PbS, BN, AlN, GaN, AlxGa1−xN, GaP GaAs, GaSb, InP, InAs, InxGa1−xAs, SiC, Si1−xGex, Si3N4, ZrN, CaF2, YF3, Al2O3, SiO2, TiO2, Cu2O, Zr2O3, ZrO2, SnO2, YSi2, GaInP2, Cd3P2, Fe2S, Cu2S, CuIn2S2, MoS2, In2S3, Bi2S3, CuIn2Se2, In2Se3, HgI2, PbI2, Lanthanoids oxides, etc, and their various alloys.
13. A method of using semiconductor nano-sized particles as sensitizer in a photoresist.
14. A method of claim 13 wherein the said semiconductor nano-sized particles are selected from the group consisting of C, Si, Ge, CuCl, CuBr, CuI, AgCl, AgBr, AgI, Ag2S, CaO, MgO, ZnO, MgxZn1−xO, ZnS, HgS, ZnSe, CdS, CdSe, CdTe, HgTe, PbS, BN, AlN, GaN, AlxGa1−xN, GaP GaAs, GaSb, InP, InAs, Inx,Ga1−xAs, SiC, Si1−xGex, Si3N4, ZrN, CaF2, YF3, Al2O3, SiO2, TiO2, Cu2O, Zr2O3, ZrO2, SnO2, YSi2, GaInP2, Cd3P2, Fe2S, Cu2S, CuIn2S2, MoS2, In2S3, Bi2S3, CuIn2Se2, In2Se3, HgI2, PbI2, Lanthanoids oxides, etc, and their various alloys.
15. A method of performing photolithography comprising:
projecting light along an optical path to form a light pattern on a substrate comprising a wafer that is at least in part coated with a layer comprising photoresist, at least a portion of said light passing through (a) at least one photomask with at least one pattern, (b) a medium having semiconductor nano-sized particles dispersed therein, and (c) at least an immediate next lens;
said semiconductor nano-sized particle dispersed medium is inserted between said photomask and said immediate next lens;
collecting, on said photoresist, a portion of said light passing through said at least one photomask, said semiconductor nano-sized particle dispersed medium and said immediate next lens; and
changing the solubility of said photoresist at least in part in response to said collected light pattern.
16. The method of claim 15 wherein said medium comprises a liquid, polymer, or a gel.
17. The method of claim 16 wherein said medium comprises water.
18. The method of claim 15 wherein said nano-sized particle dispersed medium is flowed continuously through the space between said photomask and said immediate next lens.
19. The method of claim 18 wherein said medium comprises water.
20. The method of claim 15 wherein said nano-sized particle dispersed medium is coated on said photomask.
21. The method of claim 15 wherein said nano-sized particle dispersed medium is coated on said immediate next lens.
22. The method of claim 15 wherein the said semiconductor nano-sized particles are selected from the group consisting of C, Si, Ge, CuCl, CuBr, CuI, AgCl, AgBr, AgI, Ag2S, CaO, MgO, ZnO, MgxZn1−xO, ZnS, HgS, ZnSe, CdS, CdSe, CdTe, HgTe, PbS, BN, AlN, GaN, AlxGa1−xN, GaP GaAs, GaSb, InP, InAs, Inx,Ga1−xAs, SiC, Si1−xGex, Si3N4, ZrN, CaF2, MgF2, YF3, Al2O3, SiO2, TiO2, Cu2O, Zr2O3, ZrO2, SnO2, YSi2, GaInP2,Cd3P2, Fe2S, Cu2S, CuIn2S2, MoS2, In2S3, Bi2S3, CuIn2Se2, In2Se3, HgI2, PbI2, Lanthanoids oxides, and their various alloys.
23. The method of claim 15 wherein said semiconductor nano-sized particles have bandgaps.
24. The method of claim 15 wherein said nano-sized particles are transparent at least at one of lithographic wavelengths.
25. The method of claim 15 wherein said nano-sized particles comprise nanocrystals.
26. The method of claim 15 wherein said light has a wavelength of 193 nm.
27. The method of claim 15 wherein said light has a wavelength of 157 nm.
28. The method of claim 15 wherein said light has a wavelength of 248 nm.
29. The method of claim 15 wherein said light has a wavelength of 365 nm.
30. The method of claim 15 wherein said nano-sized particle medium fill up space between said photomask and said immediate next lens.
31. The method of claim 15 wherein said photolithography is immersion photolithography.
32. The method of claim 15 wherein said semiconductor nano-sized particles have a refractive index higher than said medium.
33. The method of claim 32 wherein the said semiconductor nano-sized particles are selected from the group consisting of C, Si, Ge, CuCl, CuBr, CuI, AgCl, AgBr, AgI, Ag2S, CaO, MgO, ZnO, MgxZn1−xO, ZnS, HgS, ZnSe, CdS, CdSe, CdTe, HgTe, PbS, BN, AlN, GaN, AlxGa1−xN, GaP GaAs, GaSb, InP, InAs, InxGa1−xAs, SiC, Si1−xGex, Si3N4, ZrN, CaF2, MgF2, YF3, Al2O3, SiO2, TiO2, Cu2O, Zr2O3, ZrO2, SnO2, YSi2, GaInP2, Cd3P2, Fe2S, Cu2S, CuIn2S2, MoS2, In2S3, Bi2S3, CuIn2Se2, In2Se3, HgI2, PbI2, Lanthanoids oxides, and their various alloys.
34. The method of claim 32 wherein said semiconductor nano-sized particles have bandgaps.
35. The method of claim 32 wherein said nano-sized particles are transparent at least at one of lithographic wavelengths.
36. The method of claim 32 wherein said nano-sized particles comprise nanocrystals.
37. The method of claim 32 wherein said light has a wavelength of 193 nm.
38. The method of claim 32 wherein said light has a wavelength of 157 nm.
39. The method of claim 32 wherein said light has a wavelength of 248 nm.
40. The method of claim 32 wherein said light has a wavelength of 365 nm.
US12/415,013 2003-03-04 2009-03-31 Applications of semiconductor nano-sized particles for photolithography Abandoned US20090239161A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
US12/415,013 US20090239161A1 (en) 2003-03-04 2009-03-31 Applications of semiconductor nano-sized particles for photolithography
US13/189,143 US9207538B2 (en) 2003-03-04 2011-07-22 Applications of semiconductor nano-sized particles for photolithography
US14/636,433 US20150168842A1 (en) 2003-03-04 2015-03-03 Block co-polymer photoresist
US14/848,104 US20150380239A1 (en) 2003-03-04 2015-09-08 Block co-polymer photoresist

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US45124003P 2003-03-04 2003-03-04
US10/792,377 US7524616B2 (en) 2003-03-04 2004-03-04 Applications of semiconductor nano-sized particles for photolithography
US12/415,013 US20090239161A1 (en) 2003-03-04 2009-03-31 Applications of semiconductor nano-sized particles for photolithography

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US10/792,377 Division US7524616B2 (en) 2003-03-04 2004-03-04 Applications of semiconductor nano-sized particles for photolithography

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US13/189,143 Division US9207538B2 (en) 2003-03-04 2011-07-22 Applications of semiconductor nano-sized particles for photolithography

Publications (1)

Publication Number Publication Date
US20090239161A1 true US20090239161A1 (en) 2009-09-24

Family

ID=34375180

Family Applications (3)

Application Number Title Priority Date Filing Date
US10/792,377 Expired - Fee Related US7524616B2 (en) 2003-03-04 2004-03-04 Applications of semiconductor nano-sized particles for photolithography
US12/415,013 Abandoned US20090239161A1 (en) 2003-03-04 2009-03-31 Applications of semiconductor nano-sized particles for photolithography
US13/189,143 Expired - Fee Related US9207538B2 (en) 2003-03-04 2011-07-22 Applications of semiconductor nano-sized particles for photolithography

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US10/792,377 Expired - Fee Related US7524616B2 (en) 2003-03-04 2004-03-04 Applications of semiconductor nano-sized particles for photolithography

Family Applications After (1)

Application Number Title Priority Date Filing Date
US13/189,143 Expired - Fee Related US9207538B2 (en) 2003-03-04 2011-07-22 Applications of semiconductor nano-sized particles for photolithography

Country Status (6)

Country Link
US (3) US7524616B2 (en)
EP (1) EP1606670A4 (en)
JP (1) JP2006523383A (en)
KR (1) KR20050109967A (en)
CN (1) CN1799004A (en)
WO (1) WO2005029180A2 (en)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8993221B2 (en) 2012-02-10 2015-03-31 Pixelligent Technologies, Llc Block co-polymer photoresist
JP4522840B2 (en) * 2004-12-22 2010-08-11 独立行政法人科学技術振興機構 Photomask, exposure apparatus and exposure method
WO2007140012A2 (en) * 2006-05-26 2007-12-06 Massachusetts Institute Of Technology Immersion fluids for lithography
JP2009543159A (en) * 2006-07-10 2009-12-03 ピクセリジェント・テクノロジーズ・エルエルシー Lithographic resist
US8134684B2 (en) * 2008-02-22 2012-03-13 Sematech, Inc. Immersion lithography using hafnium-based nanoparticles
JP2010016259A (en) * 2008-07-04 2010-01-21 Panasonic Corp Pattern forming method
KR101813185B1 (en) 2016-06-30 2018-01-30 삼성전자주식회사 Pellicle for photomask and exposure apparatus including the pellicle
KR101813186B1 (en) 2016-11-30 2017-12-28 삼성전자주식회사 Pellicle for photomask, reticle including the same and exposure apparatus for lithography
KR102330943B1 (en) * 2017-03-10 2021-11-25 삼성전자주식회사 Pellicle for photomask, reticle including the same and exposure apparatus for lithography
KR102532602B1 (en) * 2017-07-27 2023-05-15 삼성전자주식회사 Pellicle composition for photomask, pellicle for photomask formed therefrom, preparing method thereof, reticle including the pellicle, and exposure apparatus for lithography including the reticle
JP7169350B2 (en) 2017-10-20 2022-11-10 マジック リープ, インコーポレイテッド Configuration of optical layers in imprint lithography process
JP6971834B2 (en) * 2017-12-26 2021-11-24 三菱マテリアル電子化成株式会社 Powder for forming a black light-shielding film and its manufacturing method

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5121256A (en) * 1991-03-14 1992-06-09 The Board Of Trustees Of The Leland Stanford Junior University Lithography system employing a solid immersion lens
US20030047816A1 (en) * 2001-09-05 2003-03-13 Rensselaer Polytechnic Institute Passivated nanoparticles, method of fabrication thereof, and devices incorporating nanoparticles
US20030071983A1 (en) * 2001-10-12 2003-04-17 Chi-Yuan Hung Method for improving resolution limits of a stepper
US20030227249A1 (en) * 2002-06-07 2003-12-11 Lumileds Lighting, U.S., Llc Light-emitting devices utilizing nanoparticles
US20040075895A1 (en) * 2002-10-22 2004-04-22 Taiwan Semiconductor Manufacturing Co., Ltd. Apparatus for method for immersion lithography
US6927002B2 (en) * 2000-12-28 2005-08-09 Renesas Technology Corp. Photomask, the manufacturing method, a patterning method, and a semiconductor device manufacturing method

Family Cites Families (36)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4253728A (en) * 1979-07-23 1981-03-03 Bell Telephone Laboratories, Incorporated Multimode electrically switched optical port
ATE1462T1 (en) * 1979-07-27 1982-08-15 Werner W. Dr. Tabarelli OPTICAL LITHOGRAPHY PROCESS AND DEVICE FOR COPYING A PATTERN ONTO A SEMICONDUCTOR DISC.
SU948994A1 (en) * 1980-01-29 1982-08-07 Институт теплофизики СО АН СССР Liquid for optical investigations
SU1204623A1 (en) * 1983-11-16 1986-01-15 Новосибирский государственный университет Liquid for optical investigations
US4517337A (en) * 1984-02-24 1985-05-14 General Electric Company Room temperature vulcanizable organopolysiloxane compositions and method for making
FR2655434B1 (en) * 1989-12-05 1992-02-28 Thomson Csf OPTICAL DEVICE WITH QUANTUM WELLS AND METHOD FOR PRODUCING THE SAME.
CA2061796C (en) * 1991-03-28 2002-12-24 Kalluri R. Sarma High mobility integrated drivers for active matrix displays
DE4219287A1 (en) * 1992-06-12 1993-12-16 Merck Patent Gmbh Inorganic fillers and organic matrix materials with refractive index adjustment
RU2051940C1 (en) * 1993-06-22 1996-01-10 Производственное объединение "Новосибирский приборостроительный завод" Immersion liquid
JPH07220990A (en) * 1994-01-28 1995-08-18 Hitachi Ltd Pattern forming method and exposure apparatus therefor
WO1997010527A1 (en) * 1995-09-14 1997-03-20 The Regents Of The University Of California Structured index optics and ophthalmic lenses for vision correction
JPH1010301A (en) * 1996-04-12 1998-01-16 Nikon Corp Photochromic plastic lens and its production
JP3776980B2 (en) * 1996-06-17 2006-05-24 大日本印刷株式会社 Antireflection film and method for producing the same
JP3817836B2 (en) * 1997-06-10 2006-09-06 株式会社ニコン EXPOSURE APPARATUS, ITS MANUFACTURING METHOD, EXPOSURE METHOD, AND DEVICE MANUFACTURING METHOD
US6291110B1 (en) * 1997-06-27 2001-09-18 Pixelligent Technologies Llc Methods for transferring a two-dimensional programmable exposure pattern for photolithography
US6005707A (en) * 1997-11-21 1999-12-21 Lucent Technologies Inc. Optical devices comprising polymer-dispersed crystalline materials
DE19823732A1 (en) * 1998-05-27 1999-12-02 Inst Neue Mat Gemein Gmbh Process for the production of optical multilayer systems
GB9815271D0 (en) * 1998-07-14 1998-09-09 Cambridge Display Tech Ltd Particles and devices comprising particles
WO2000006495A1 (en) * 1998-07-30 2000-02-10 Minnesota Mining And Manufacturing Company Nanosize metal oxide particles for producing transparent metal oxide colloids and ceramers
JP2001057329A (en) * 1999-08-18 2001-02-27 Toshiba Corp Super-resolution exposure filter, and pattern forming method
JP2001067723A (en) * 1999-08-25 2001-03-16 Toshiba Corp Optical recording medium, optical recording and reproducing method and optical recording and reproducing device
US6440637B1 (en) * 2000-06-28 2002-08-27 The Aerospace Corporation Electron beam lithography method forming nanocrystal shadowmasks and nanometer etch masks
WO2002007338A1 (en) * 2000-07-04 2002-01-24 Linkair Communications, Inc. Method of converting spread spectrum multiple address code in a code division multiple access system
EP1235108A1 (en) * 2001-02-22 2002-08-28 Infineon Technologies SC300 GmbH & Co. KG Antireflective coating material and semiconductor product with an ARC layer
US7008749B2 (en) * 2001-03-12 2006-03-07 The University Of North Carolina At Charlotte High resolution resists for next generation lithographies
WO2003001869A2 (en) * 2001-06-29 2003-01-09 California Institute Of Technology Method and apparatus for use of plasmon printing in near-field lithography
DE10135114A1 (en) 2001-07-19 2003-02-13 Univ Muenchen L Maximilians Electrically controllable light modulator with a material composition based on nanoparticles embedded in electro-optical media
US6819845B2 (en) * 2001-08-02 2004-11-16 Ultradots, Inc. Optical devices with engineered nonlinear nanocomposite materials
US7067072B2 (en) * 2001-08-17 2006-06-27 Nomadics, Inc. Nanophase luminescence particulate material
WO2003044597A1 (en) * 2001-11-19 2003-05-30 Pixelligent Technologies Llc Method and apparatus for exposing photoresists using programmable masks
US6642295B2 (en) * 2001-12-21 2003-11-04 Eastman Kodak Company Photoresist nanocomposite optical plastic article and method of making same
US6718277B2 (en) * 2002-04-17 2004-04-06 Hewlett-Packard Development Company, L.P. Atmospheric control within a building
WO2004009505A1 (en) * 2002-07-23 2004-01-29 Shell Internationale Research Maatschappij B.V. Hydrophobic surface treatment composition and method of making and using same
EP1576419A4 (en) * 2002-12-09 2006-07-12 Pixelligent Technologies Llc Programmable photolithographic mask and reversible photo-bleachable materials based on nano-sized semiconductor particles and their applications
US20050161644A1 (en) * 2004-01-23 2005-07-28 Peng Zhang Immersion lithography fluids
TWI259319B (en) * 2004-01-23 2006-08-01 Air Prod & Chem Immersion lithography fluids

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5121256A (en) * 1991-03-14 1992-06-09 The Board Of Trustees Of The Leland Stanford Junior University Lithography system employing a solid immersion lens
US6927002B2 (en) * 2000-12-28 2005-08-09 Renesas Technology Corp. Photomask, the manufacturing method, a patterning method, and a semiconductor device manufacturing method
US20030047816A1 (en) * 2001-09-05 2003-03-13 Rensselaer Polytechnic Institute Passivated nanoparticles, method of fabrication thereof, and devices incorporating nanoparticles
US20030071983A1 (en) * 2001-10-12 2003-04-17 Chi-Yuan Hung Method for improving resolution limits of a stepper
US20030227249A1 (en) * 2002-06-07 2003-12-11 Lumileds Lighting, U.S., Llc Light-emitting devices utilizing nanoparticles
US20040075895A1 (en) * 2002-10-22 2004-04-22 Taiwan Semiconductor Manufacturing Co., Ltd. Apparatus for method for immersion lithography

Also Published As

Publication number Publication date
US20110281221A1 (en) 2011-11-17
WO2005029180A3 (en) 2006-02-02
US9207538B2 (en) 2015-12-08
JP2006523383A (en) 2006-10-12
KR20050109967A (en) 2005-11-22
US20090081594A1 (en) 2009-03-26
CN1799004A (en) 2006-07-05
WO2005029180A2 (en) 2005-03-31
EP1606670A4 (en) 2009-08-05
US7524616B2 (en) 2009-04-28
EP1606670A2 (en) 2005-12-21

Similar Documents

Publication Publication Date Title
US9207538B2 (en) Applications of semiconductor nano-sized particles for photolithography
US7510818B2 (en) Reversible photobleachable materials based on nano-sized semiconductor particles and their optical applications
JP2007133102A (en) Optical element having reflection preventing film, and exposure apparatus having the same
JP2005191381A (en) Exposure method and system thereof
US20150185616A1 (en) Resists for lithography
US10353285B2 (en) Pellicle structures and methods of fabricating thereof
US11307504B2 (en) Humidity control in EUV lithography
US20230375924A1 (en) EUV Metallic Resist Performance Enhancement Via Additives
TW201728992A (en) Pellicle apparatus for semiconductor lithography process
US6692894B1 (en) Photolithographic pattern-forming material and method for formation of fine pattern therwith
US6317274B1 (en) Optical element
TW202242554A (en) Lithography system and methods
US9454086B2 (en) Programmable photolithography
US20070019173A1 (en) Photolithography arrangement
Hibbs et al. 193-nm lithography at MIT Lincoln lab
JP2001057329A (en) Super-resolution exposure filter, and pattern forming method
US20060194142A1 (en) Immersion lithography without using a topcoat
US20230305396A1 (en) Euv Photoresist With Low-Activation-Energy Ligands Or High-Developer-Solubility Ligands
Raza et al. Advances, Application and Challenges of Lithography Techniques
Sood Design and Fabrication of Nanostructure for Mid-IR Antireflection coating applications
JP2006179630A (en) Multilayer reflector and euv exposure device
JP2001028330A (en) Exposure mask, exposure method, and manufacture of exposure mask
JP2001004817A (en) Diffraction optical element and manufacture thereof
Mobrhan-Shafiee Developing an efficient approach to fabricate electric contacts on nanowires
Macdowell Extreme ultraviolet lithography at the NSLS

Legal Events

Date Code Title Description
STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION