Classifications

• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
  • H05K3/00—Apparatus or processes for manufacturing printed circuits
  • H05K3/10—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern
  • H05K3/12—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using thick film techniques, e.g. printing techniques to apply the conductive material or similar techniques for applying conductive paste or ink patterns
  • H05K3/1241—Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using thick film techniques, e.g. printing techniques to apply the conductive material or similar techniques for applying conductive paste or ink patterns by ink-jet printing or drawing by dispensing
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/02—Printing inks
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D11/00—Inks
  • C09D11/30—Inkjet printing inks
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
  • C23C18/02—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition
  • C23C18/08—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by thermal decomposition characterised by the deposition of metallic material
• • C—CHEMISTRY; METALLURGY
  • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
  • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
  • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
  • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
  • C23C18/1601—Process or apparatus
  • C23C18/1603—Process or apparatus coating on selected surface areas
  • C23C18/1607—Process or apparatus coating on selected surface areas by direct patterning
  • C23C18/161—Process or apparatus coating on selected surface areas by direct patterning from plating step, e.g. inkjet
• • G—PHYSICS
  • G02—OPTICS
  • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
  • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
  • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
  • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
  • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
  • G02F1/136—Liquid crystal cells structurally associated with a semi-conducting layer or substrate, e.g. cells forming part of an integrated circuit
  • G02F1/1362—Active matrix addressed cells
• • H—ELECTRICITY
  • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
  • H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
  • H05K2203/00—Indexing scheme relating to apparatus or processes for manufacturing printed circuits covered by H05K3/00
  • H05K2203/01—Tools for processing; Objects used during processing
  • H05K2203/0195—Tool for a process not provided for in H05K3/00, e.g. tool for handling objects using suction, for deforming objects, for applying local pressure

Definitions

• the invention generally relates to (i) a micron-scale, direct-write patterning method using microfabricated (tipless) cantilevers coated with ink, which can be called Cantilever MicroDeposition; and (ii) its application to flat panel display repair and especially TFT LCD (thin film transistor liquid crystal displays) repair.
• TFT LCD thin film transistor liquid crystal displays
• a new contact method for writing conductive metal features has been developed that offers controllable feature sizes from 100 micron to sub-micron dimensions.
• a (microfabricated) cantilever can be loaded with e.g. molecular or nanoparticulate ink which, by contacting a surface, is dispensed in very small quantities in the form of, for example, line and dot patterns.
• both loading of the cantilever and deposition can be performed passively.
• additional systems can inco ⁇ orate active ink delivery.
• the precursor inks can be patterned under ambient environmental conditions and converted to metallic films at relatively low temperatures so that they can be applied to substrates such as, for example, plastics which cannot withstand high temperature processes.
• the invention provides a method for writing, for example, conductive metal or metal precursor comprising: providing a cantilever having a cantilever end, wherein the cantilever can be a tipless cantilever; providing an ink disposed at the cantilever end; providing a substrate surface; and moving the cantilever end or moving the substrate surface so that ink is delivered from the cantilever end to the substrate surface.
• the substrate surface can be moved and the cantilever held stationary, or the substrate surface can be moved and the cantilever held stationary.
• the movement which results ink deliver can result generally in contact between the cantilever and the substrate surface, although their may be possibly be ink between the cantilever and the surface.
• the invention provides a method for writing conductive metal or metal precursor comprising: providing two or more cantilevers each having a cantilever ends, wherein the cantilevers can comprise a tip at the end or can be tipless cantilevers, wherein the cantilevers have a gap between them which is about one micron to about 20 microns; providing an ink disposed in the gap; providing a substrate surface; contacting the two or more cantilevers with the gap and the substrate surface so that ink is delivered from the gap to the substrate surface.
• the invention also provides an ink formulation for microlithography or nanolithography comprising: one or more metal salts and one or more solvents, wherein the concentration of metal salt is about 1 mg/100 ⁇ L to about 500 mg/100 ⁇ L.
• the amount of the metal salt can be adjusted to be sufficiently high to provide suitable dispersion and suitable mass density and a thickness for a given application.
• the invention also provides a method for direct writing conductive metal comprising: providing a cantilever having a cantilever end, wherein the cantilever is a tipless cantilever; providing an ink disposed at the cantilever end, wherein the ink comprises metallic nanoparticles; providing a substrate surface; contacting the cantilever end and the substrate surface so that ink is delivered from the cantilever end to the substrate surface.
• Important advantages of the present invention include ability to operate in a variety of different size regimes for a particular system including, for example, the about one micron to the about 15 micron regime or the about one micron to about 10 micron regime (e.g., single digit) for lateral dimensions such as length and width with excellent control. Problems with clogging in nozzles or pipettes can be avoided in many embodiments. Instrumentation to do this is relatively straightforward and does not require, for example, high vacuum. Registration and versatility are excellent. Mass production and disposability are possible. In addition, a series of numbered embodiments are also provided: 1.
• a method of depositing a conductive coating in a desired pattern onto a substrate comprising: depositing a precursor onto the substrate in the desired pattern by nanolithography with use of a tip coated with the precursor; contacting the precursor with a ligand; applying sufficient energy to transfer electrons from the ligand to the precursor, thereby decomposing the precursor to form a conductive precipitate in the desired pattern and thus forming the conductive pattern directly on the substrate.
• the tip is a nanoscopic tip.
• the tip is a scanning probe microscopic tip.
• the tip is an atomic force microscope tip. 5.
• the coating comprises a metal with a purity of at least about 80%. 6.
• the coating comprises a metal with a thickness of less than about 10 angstroms. 7. The method of 1, wherein the coating comprises a metal with a thickness of at least about 100 angstroms.
• the precursor comprises a salt selected from the group consisting of a carboxylate, a halide, a pseudohalide, and a nitrate. 9. The method of 1, wherein the precursor comprises a carboxylate. 10. The method of 1, wherein the pattern comprises a circuit.
• the ligand comprises a material selected from the group consisting of an amine, an amide, a phosphine, a sulfide, and an ester. 12.
• the method of 1 wherein the ligand is selected from the group consisting of a nitrogen donor, a sulphur donor, and a phosphorous donor. 13.
• the method of 1 wherein the precipitate comprises a metal.
• the method of 1 wherein the precipitate is selected from the group consisting of copper, zinc, palladium, platinum, silver, gold, cadmium, titanium, cobalt, lead, tin, silicon and germanium.
• the method of 1 wherein the precipitate comprises an electrical conductor.
• the method of 1 wherein the precipitate comprises an electrical semiconductor. 17.
• the substrate comprises a non-conductor.
• the substrate comprises at least one of a conductor and a semiconductor. 19.
• the method of 1 wherein the step of applying energy comprises applying heat.
• the step of applying energy comprises applying infra red radiation or UV radiation.
• the method of 1 wherein the step of applying energy comprises applying vibrational energy.
• the precursor comprises a salt selected from the group consisting of a carboxylate, a halide, a pseudo halide, a nitrate, and the ligand comprises a material selected from the group consisting of an amine, an amide, a phosphine, a sulfide and an ester.
• the method of 19, wherein the precipitate is selected from the group consisting of copper, zinc, palladium, platinum, silver, gold, cadmium, titanium, cobalt, lead, tin, silicon and germanium.
• the step of applying energy comprises applying radiant heat.
• a method of printing a conductive metal in a desired pattern onto a substrate comprising: drawing a metal precursor and ligand directly onto the substrate according to the desired pattern using nanolithography with use of a tip coated with a precursor; and decomposing the precursor by applying energy to form the conductive metal in the desired pattern, without removing from the substrate a substantial quantity of the precursor, and without removing from the substrate a substantial quantity of the metal. 26.
• the method of 25, wherein the metal is selected from the group consisting
• a nanolithographic method comprising: depositing a metallic precursor from a tip onto a substrate to form a nanostructure, and subsequently converting the precursor nanostructure to a metallic deposit. 31. The method according to 30, wherein the deposition and conversion is carried out without use of an electrical bias between the tip and substrate. 32. The method according to 30, wherein the deposition and conversion is carried out with use of a chemical agent other than the substrate. 33. The method according to 30, wherein the tip is a nanoscopic tip. 34. The method according to 30, wherein the tip is a scanning probe microscopic tip. 35.
• the method according to 30, wherein the tip is an AFM tip. 36. The method according to 35, wherein the deposition and conversion is carried out without use of an electrical bias between the tip and substrate. 37. The method according to 30, wherein the method is repeated to form a multilayer. 38. The method according to 30, wherein the tip is adapted to not react with the precursor. 39. The method according to 30, wherein the method is used to connect at least one nanowire with another structure. 40. The method according to 30, wherein the method is used to connect at least two electrodes. 41. The method according to 30, wherein the method is used to prepare a sensor. 42. The method according to 30, wherein the method is used to fabricate a lithographic template. 43.
• a nanolithographic method consisting essentially of: depositing an ink composition consisting essentially of a metallic precursor from a nanoscopic tip onto a substrate to form a nanostructure, and subsequently converting the metallic precursor of the nanostructure to a metallic form.
• the method according to 44, wherein the conversion is a thermal conversion without use of a chemical agent. 46. The method according to 44, wherein the conversion is a chemical conversion carried out with use of a reducing agent. 47. The method according to 44, wherein the reducing agent is used in the vapor state to carry out the conversion. 48. The method according to 44, wherein the tip is an AFM tip. 49. The method according to 44, wherein the tip comprises a surface which does not react with the precursor. 50. A method according to 44, wherein the method is repeated a plurality of times to generate a multi-layer structure. 51.
• a method of printing without use of electrochemical bias or reaction between the ink and substrate comprising depositing a metallic precursor ink composition onto a substrate from a tip in the form of a microstructure or nanostructure on the substrate to form an array having discreet objects separated from each other by about one micron or less. 52. The method according to 51, further comprising the step of forming metal from the precursor. 53. The method according to 51, wherein the discreet objects are separated from each other by about 500 nm or less. 54. The method according to 51, wherein the discreet objects are separated from each other by about 100 nm or less. 55.
• a method for writing conductive metal comprising providing a cantilever having a cantilever end, wherein the cantilever can comprise a tip at the end or can be a tipless cantilever; providing an ink disposed at the cantilever end; providing a substrate surface; contacting the cantilever end and the substrate surface so that ink is delivered from the cantilever end to the substrate surface.
• the cantilever is a tipless cantilever.
• the method according to 55, wherein the cantilever comprises a tip at the cantilever end.
• the ink comprises one or more metals.
• the ink comprises one or more metal salts.
• the ink comprises one or more metal nanoparticles.
• the ink comprises one or more hydrophobic nanoparticles.
• the ink comprises one or more hydrophilic nanoparticles.
• the ink comprises one or more metal nanoparticles having an organic shell.
• the ink comprises one or more metal nanoparticles having an insulating shell. 67.
• the method according to 55, wherein the ink is a hydrophobic ink.
• the ink is a hydrophilic ink.
• the method according to 55, wherein the ink is a hydrophobic ink, and the substrate surface is a hydrophobic surface.
• the method according to 55, wherein the ink is a hydrophilic ink, and the substrate surface is a hydrophilic surface..
• the method according to 55, wherein the ink comprises both hydrophobic and hydrophilic agents. 72.
• the ink comprises one or more metal nanoparticles having an average diameter of about 100 nm or less. 73. The method according to 55, wherein the ink comprises one or more biological molecules. 74. The method according to 55, wherein the ink comprises one or more peptides or proteins. 75. The method according to 55, wherein the ink comprises one or more nucleic acids. 76. The method according to 55, wherein the ink comprises one or more sol- gel materials.
• the ink comprises one or more magnetic materials or precursors thereof. 78. The method according to 55, wherein the ink comprises one or more semiconductor materials or precursors thereof. 79. The method according to 55, wherein the ink comprises one or more optical materials or precursors thereof. 80. The method according to 55, wherein the ink comprises one or more solvents having a boiling point over 100°C. 81. The method according to 55, wherein the ink comprises one or more compounds which chemisorb to or covalently bond with the substrate surface. 82. The method according to 55, wherein the ink forms a feature on the substrate surface. 83. The method according to 55, wherein the ink forms metal oxide on the surface.
• the method according to 55 wherein the ink forms a feature on the substrate surface and is subjected to annealing at temperature of about 100°C to about 300°C. 95.
• the method according to 55, wherein the ink is subjected to a reduction reaction on the substrate surface.
• the ink forms a feature on the substrate surface which is made continuous after contacting.
• the ink forms a feature on the substrate surface which is converted to a metallic state which has a resistivity of about 10 microohm*cm or less. 98.
• the method according to 55, wherein the cantilever has a width of about one micron to about 100 microns. 116. The method according to 55, wherein the cantilever has a width of about five microns to about 25 microns. 117. The method according to 55, wherein the cantilever is a straight beam shaped cantilever. 118. The method according to 55, wherein the contacting is carried out with use of force-feedback. 119. The method according to 55, wherein the cantilever has a spring constant of about 0.001 N/m to about 0.50 N/m. 120. The method according to 55, wherein the cantilever has a spring constant of about 0.004 N/m to about 0.20 N/m. 121.
• the method according to 55, wherein the cantilever has a length of about 100 microns to about 400 microns. 122. The method according to 55, wherein the cantilever has a length of about 150 microns to about 300 microns. 123. The method according to 55, wherein the cantilever is one of a plurality of cantilevers which deposit ink in parallel. 124. The method according to 55, wherein the ink is a polyol ink. 125. The method according to 55, wherein the ink comprises metal salts together with one or more alcohols or polyols. 126. The method according to 55, wherein the ink forms features on the substrate surface having a lateral dimension of about one micron to about 15 microns. 127.
• a substrate comprising a substrate surface and an ink thereon prepared by the method of claim 55. 130.
• a method for writing conductive metal comprising: providing two or more cantilevers each having a cantilever ends, wherein the cantilevers can comprise a tip at the end or can be tipless cantilevers, wherein the cantilevers have a gap between them which is about one micron to about 20 microns; providing an ink disposed in the gap; providing a substrate surface; contacting the two or more cantilevers with the gap and the substrate surface so that ink is delivered from the gap to the substrate surface.
• the gap is about one micron to about five microns.
• the gap is about five microns to about ten microns.
• An ink formulation for nanolithography comprising: one or more metal salts and one or more solvents, wherein the concentration of metal salt is about 1 mg/100 ⁇ L to about 500 mg/100 ⁇ L. 135.
• the ink formulation of 134, wherein the formulation further comprises two or more oligomer or polymer additives having different average molecular weight. 138.
• the ink formulation of 134 wherein the formulation further comprises at least one oligomer and at least one polymer.
• a method for direct writing conductive metal comprising: providing a cantilever having a cantilever end, wherein the cantilever can comprise a tip at the end or can be a tipless cantilever; providing an ink disposed at the cantilever end, wherein the ink comprises metallic nanoparticles; providing a substrate surface; contacting the cantilever end and the substrate surface so that ink is delivered from the cantilever end to the substrate surface. 142.
• FIG. 3 Au Nanoparticles deposited between gold electrodes.
• Figure 4. Au Nanoparticles deposited between gold electrodes.
• FIG. 1 Au Nanoparticles deposited between gold electrodes.
• a and B optical images before and after curing of a line formed by drawing a 10 ⁇ m wide FIB cantilever across two electrodes. The measured resistance across the gap for this pattern is 22 Ohms.
• C Topographic AFM image of 11.5 ⁇ m wide line and 80 nm height in the red boxed area in (B).
• D Corresponds to cursor profile of the fabricated line.
• FIG. 6 Au Nanoparticles deposited between gold electrodes.
• (C) and (F) correspond to cursor profile of the fabricated line.
• Figure 7. Au Nanoparticles deposited between gold electrodes.
• FIG. 8 Platinum/gold alloy ink deposited between gold electrodes on silicon oxide using cantilevers. Each line was formed by dipping a cantilever into an ink-filled inkwell and then drawing a line until the cantilever ran out of ink. Note the similarities in line shape and length.
• FIG. 9 Platinum/gold alloy ink deposited between gold electrodes on silicon oxide using adjacent cantilevers.
• Each of the three lines was fabricated using a single cantilever or adjacent cantilevers loaded with ink.
• the line on the left was generated by drawing a single 31 micron wide cantilever across the surface until it ran out of ink
• the widest, middle line was generated using 4 adjacent 31 micron wide cantilevers
• the right line was generated by 2 adjacent 31 micron wide cantilevers. Note that the maximum length of the lines increases with increasing number of writing cantilevers.
• FIG 10. AFM height images of nanoscale palladium patterns on silicon oxide. Palladium acetate dissolved to saturation in 80% ethylene glycol was patterned using a PDMS coated silicon nitride AFM tip. The line scans of the cured patterns reveal a increase in height from 2 nm to 10 nm between the first and second layers.
• Figure 11. AFM height images of nanoscale gold patterns on quartz. Gold nanoparticle ink was patterned by holding an ink-coated conventional silicon nitride AFM cantilever/tip in contact with the surface for 10 s at a constant force.
• the rightmost row of dots (diameter 50 nm, height 3.5 nm) were formed at a force of 0.2 nN, the middle row of dots were formed at a force of 1.5 nN (diameter 65 nm, height 6 nm) and the leftmost row of dots were formed at a force of 4 nN (diameter 85 nm, height 7.5 nm).
• the patterns were imaged immediately after patterning with the coated tip.
• FIG. 12 AFM height images of nanoscale gold patterns on quartz. Gold nanoparticles dissolved in mesitylene (the 'ink') were patterned by translating an ink- coated conventional silicon nitride AFM tip across the surface at a rate of 0.15 microns/s. The line trace indicates that the height and the width of the lines increase with applied force.
• FIG 13 AFM height images of nanoscale gold patterns on quartz. Gold nanoparticles dissolved in mesitylene (the 'ink') were patterned by holding an ink- coated conventional silicon nitride AFM tip in contact with the surface for 10 seconds. The resulting pattern was cured for 10 seconds at 250°C using a heat gun and then imaged. After curing, the height of the particle patterns decreases from around 30 nm to around 15 nm.
• mesitylene mesitylene
• Figure 14 Optical image of a micron scale platinum line drawn with a silicon nitride cantilever across gold electrodes on a silicon oxide wafer.
• the platinum ink comprised platinum chloride dissolved in 80% ethylene glycol (100 mg in 15 microlitres).
• the precursor ink was converted to metal by heating on a hot plate a 200°C for 20 s.
• the width of the line after curing was approximately 5 microns.
• Figure 15 Optical image of a cured micron scale platinum line drawn with a silicon nitride cantilever across chromium electrodes on a glass wafer.
• the platinum ink comprised 100 mg of platinum chloride dissolved in 15 microliter aqueous solution containing 30 mg each of 300 and 10,000 molecular weight polyethylene glycol.
• the precursor ink was converted to metallic platinum by heating with a heat gun at 250 °C for 10 seconds.
• FIG 16. AFM height image of nanoscale gold features drawn between gold electrodes on silicon oxide.
• the gold precursor ink solution comprises 100 mg of gold tetrachloride salt dissolved in 80% ethylene glycol/20% water.
• the large particles are a result of three layers of ink, with each layer cured by heating on a hot plate at 200 °C for 10 seconds. This trace was not conductive.
• Figure 17. Images of platinum-gold alloy patterns generated using AFM cantilevers.
• the alloy precursor ink comprised 100 mg of platinum salt and 50 mg of gold salt co- dissolved in 30 microliters of water containing 60 mg each of 300 and 10,000 MW polyethylene glycol. The traces were cured by heating with a heat gun for 10 seconds at 250 °C.
• (A) A two layer pattern drawn across the 30 micron gap between gold electrodes on a silicon oxide wafer. The resistance of the trace was 90 ohms.
• (B) A six layer pattern drawn between chromium electrodes on a glass wafer. The resistance of the trace was 32 ohms.
• Figure 17(B) was carried out with use of a PDMS DPN stamp tip.
• (C) An AFM image showing the large grainy microstructure of the platinum-gold alloy film; grain sizes were -150 nm.
• FIG 18. An optical micrograph of a large gold feature on glass prepared dropping epoxy/gold precursor ink onto the slide and then curing for two hours at 150 °C.
• the gold precursor ink was prepared by dissolving 85 mg of hydrogen gold tetrachloride in 50 microliters of dimethylformamide and then adding 1 microliter of ethylene glycol and 1 microliter of epoxy mixture to 3 microliters of this salt solution. The resistance of the film was 0.3 ohms.
• Figure 19 An AFM height image of a gold pattern generated by depositing a gold precursor ink onto quartz using a PDMS-coated silicon nitride AFM tip.
• the gold precursor ink was prepared by dissolving 85.5 mg of gold tetrachloride (85.5 mg) in 50 ⁇ L of dimethylformamide. To this solution is added 1 ⁇ L of ethylene glycol and 0.1 mg of thiotic acid. The 4.5 x 4.5 micron square pattern was cured by heating with a hot air gun at 250 °C for 10 seconds. The 1 -layer pattern was 15 nm high after curing (see line trace).
• Figure 20 Direct- writing of silver lines on a silicon nitride substrate using a commercial silver nanoparticle ink.
• FIG. 21 Optical images showing cantilever microdepositions of a commercial silver nanoparticle ink on a glass substrate before and after curing.
• Figure 22 Deposition and low-temperature curing of a commercial silver nanoparticle ink on a glass substrate coated with a chromium thin film. Laser ablation was used to form a gap in the chromium film and expose the underlying glass substrate (in the center of the image).
• FIG. 23 Optical images illustrating the fabrication of multilayered lines by repeated drawing: (IL) One-layer line with a 6 ⁇ m width and 30 nm thickness; (2L) Two-layer line with a 8.6 ⁇ m witdh and 41 nm thickness; (3L) Three-layer line with a 8 ⁇ m width and 70 nm thickness.
• Figure 24 Coating of a tipless cantilever with ink by dipping into a microfabricated reservoir.
• Top-view optical images of a cantilever (A) just above or (B) dipping into a pool of ink in a millimeter- wide circular reservoir (fabricated by deep reactive ion etching in a silicon wafer; bottom part of the image). Note the meniscus around the cantilever in image B.
• Figure 25 Optical images illustrating the repair of a thin film transistor (TFT) flat panel display.
• Figure 26 Schematic diagram of a tipless cantilever with an ink storage slit.
• Figure 27 Diagram illustrating four alternative designs for tipless slit cantilevers.
• Figure 28 Optical image illustrating the deposition of a commercial silver ink on a glass substrate with a slit cantilever.
• Figure 29 Two examples of deposition and curing of lines made of silver nanoparticle ink across a gap between gold electrodes on a glass substrate when using a slit cantilever.
• Figure 30 Line writing with a slit cantilever loaded with a gold nanoparticle / 1,3,5- TEB ink.
• Figure 31 Diagram illustrating an instrument for the repair of flat panel displays and similar objects. It utilizes a cantilever or cantilevered microbrush coated with a metal- precursor ink to repair gaps in conductive traces.
• a XYZ stage controls the cantilever's high-resolution motion.
• An inking mechanism comprising an inkwell and its protective cover supplies the material to the cantilever prior to the touchdown operation.
• a coarse Z- motion stage is provided for inking the cantilever and contacting the surface, while a rotation stage can position it at any angle about the Z axis.
• Monitoring of the brightness of the cantilever (which varies with bending) via video imaging with the included camera system and appropriate image processing software detects the touchdown of the cantilever on the surface when putting it in initial contact with the surface.
• a laser system is provided to (thermally) cure the microdeposited material.
• Figure 32 Schematic diagram illustrating a second instrument for flat panel repair.
• the output of a laser reflective sensor is monitored as it measures the Z position of the cantilever, detecting touchdown of the cantilever on the substrate surface.
• a few-nanometer-resolution XYZ stage provides cantilever motion, and a laser (not shown) cures the deposited material ("ink").
• An inking mechanism supplies the material ("ink") to the cantilever prior to the touchdown operation.
• a large motion Z-stage moves supplies gross Z motion for inking, while the rotation stage can position the cantilever at any angle about the Z axis.
• Figure 33 Alternative design for a FPD repair instrument, in which a confocal distance measurement device detects the touchdown of the cantilever on the substrate surface.
• Figure 34 Optical images illustrating the deposition of conductive Au traces deposited from a 5 ⁇ m tipless cantilever loaded with gold nanoparticle ink across insulating gaps of various widths (10, 20, 40 ⁇ m) between conductive ITO (indium tin oxide) electrodes.
• Figure 35 Diagram illustrating how a gap may be formed near a topography step when drawing a line using a tipless cantilever.
• Figure 36 Diagram illustrating the loading and fabrication of micron-scale
• Figure 37 Diagram illustrating how the line width is controlled by (is proportional to) the cantilever width.
• Figure 38 Experimental results illustrating how the line width is controlled by (is proportional to) the cantilever width.
• A A ten-micron-wide cantilever is shown writing a line of similar width.
• B A two-micron cantilever is shown writing a circa two-micron line. Both images are at the same scale for easier comparison of the line widths.
• Figure 39 Optical and AFM images (A and B respectively) of conductive gold traces deposited across a 200 ⁇ m gap between chromium electrodes.
• a gold nanoparticles / mesitylene / decanol mixture (described in the additional working examples) was used in this experiment.
• the ink was converted to low-resistivity metallic form by performing a high-temperature curing at 250 - 300° C for 7 minutes followed by a lower temperature curing at 120° C for 60 min.
• FIG. 40 Adhesion Tests. Single-layer gold lines were deposited onto glass on three adhesion test samples and cured for -10 seconds at 150 °C. Tape peel tests showed no loss of adhesion to the substrate and the lines withstood chemical cleaning.
• the invention which can for convenience be referred to as "cantilever microdeposition" (CMD) in its preferred embodiments, can be practiced in numerous embodiments, including those described below in the working examples.
• Embodiment 1 Cantilever Microdeposition
• the invention provides a method for fabricating micrometer-scale and submicrometer-scale patterns using a cantilever or microbrush, the method comprising (1) providing a cantilever or microbrush; (2) providing an ink, meaning a chemical compound or a mixture thereof, disposed on said cantilever or microbrush; (3) providing a substrate surface; and (4) contacting the microbrush and the substrate surface so that ink is delivered from the cantilever or microbrush to the substrate surface.
• Figure 36 illustrates the principle of this method.
• the smallest lateral dimension of the resulting pattern (measured parallel to the substrate surface, e.g. the width of a line) ranges from 0.5 micron to 15 microns. Its largest lateral dimension (e.g. the length of a line) exceeds 100 microns and preferably 200 microns, and its height (e.g. measured substantially orthogonally to said local plane) ranges from 1 nm to 2 microns.
• the cantilever or microbrush is a microfabricated device, meaning a microelectromechanical system (MEMS) fabricated using standard microfabrication techniques, including but not limited to photolithography, electron beam lithography, thin film deposition, etching, lift-off and focused ion beam micromachining.
• MEMS microelectromechanical system
• the microbrush may have the shape of a cantilever having a free end and an end bound to a macro- or mesoscopic body or it may be a device comprising a multiplicity of cantilevers.
• the cantilever(s) may be with or without tip(s) protruding out of the principal plane of the cantilever.
• the meso/macroscopic body may be a diced (silicon or glass) wafer. Two or more neighboring cantilevered bodies may form a gap or slit of fixed or variable width that may be used for ink storage or dispensing.
• a microfluidic circuit may be formed on/in the cantilevered bodies and/or the meso- or macroscopic body it is attached to.
• the microfluidic circuit may comprise reservoirs, channels, and vias for ink delivery.
• Channels and reservoirs may be formed by two substantially parallel surfaces (such as the walls of the slits described above) or by three or more surfaces (e.g. forming an open channel or a completely enclosed channel).
• a substantially flat, tipless cantilever is used.
• Many inks may be deposited, including organic and inorganic compounds, including metal salts and complexes, sol-gel precursors, polymers, biomolecules such as nucleic acid (e.g. DNA), peptides and proteins, nanoparticles and solutions or mixtures thereof. Deposition may be preceded or followed by a number of treatments, including substrate cleaning, surface preparation, hole drilling, micromachining with a laser or ion beam, photolithography and curing by application of heat or light.
• Literature useful for practicing the invention Cantilevers, tips, inks, substrate surfaces, and contact methods are known in the art, and one skilled in the art can refer to the following technical literature in the practice of the present invention in its many embodiments including the preferred embodiments and working examples described below. In addition, a list of references is provided later in the specification, and all references in this specification are inco ⁇ orated by reference in their entirety and can be relied upon in general in practicing the invention.
• Cantilever microdeposition is related to but distinct from Dip Pen NanolithographyTM (DPNTM) printing, a technology commercially developed by Nanolnk, Inc.
• DPNTM Dip Pen NanolithographyTM
• a sha ⁇ tip with a nanometer-scale apex is coated with an ink; (2) the ink flows from the tip onto a substrate through a meniscus that naturally condenses at the contact junction.
• the present invention does not require a sha ⁇ tip but rather preferably uses a flat, spatula-like micrometer-sized cantilever or cantilever as the ink application means.
• Cantilever microdeposition is best used for the fabrication of patterns with a critical dimension from the high submicrometer to ten-micron range, while DPN printing is best for very-high-resolution (e.g. nanoscale) patterning.
• the throughput of cantilever microdeposition is higher than that of DPN printing, especially since higher speed (of the cantilever or microbrush relative to the surface) may be used.
• the cantilever used in the present invention does not contact directly the surface of the substrate. Rather, a layer of ink is trapped between the surface and the microbrush or cantilever end.
• the inte ⁇ lay of hydrodynamics and capillary tension in the space between the cantilever and the surface controls ink deposition.
• the pattern height and overall quality (continuity) is sensitive to the pressure applied to the cantilever, while in DPN this is generally not the case.
• the line width is highly correlated to the cantilever width (see Figures 37 and 38, for example) and mostly independent from the patterning speed, while in contrast, with DPN printing, it is controlled by the diffusion rate of the ink from a point source (the tip-sample contact) and the patterning speed.
• DPN printing it is controlled by the diffusion rate of the ink from a point source (the tip-sample contact) and the patterning speed.
• a lot of the technical developments associated with Dip Pen Nanolithography including but limited to inks, ink delivery technology, cantilever/ brush fabrication processes, cantilever position control technology and computer- control design and fabrication algorithms, are highly relevant to cantilever microdeposition.
• a variety of products related to DPN printing can be obtained from Nanolnk including deposition instruments (e.g.
• NSCRIPTORTM platform computer software, environmental chambers, pens, substrates, kits, inks, inkwells, calibration software, alignment software, accessories, and the like.
• Single DPN printing probes, passive multi-probe arrays, A-frame cantilevers, diving-board-shaped cantilevers, as well as AC-mode cantilevers can be obtained from Nanolnk. Also available are sha ⁇ ened and unsha ⁇ ened tips.
• DIP PEN NANOLITHOGRAPHYTM and DPNTM are trademarks for Nanolnk, Inc., Chicago, IL) and are used accordingly herein.
• patent publication number 2002/0063212 Al published May 30, 2002 ("Methods Utilizing Scanning Probe Microscope Tips and Products Therefor or Produced Thereby”).
• U.S. patent publication number 2002/0122873 Al published September 5, 2002 ("Nanolithography Methods and Products Produced Therefor and Produced Thereby”).
• PCT publication number WO 00/41213 Al published July 13, 2000 based on PCT application no.
• PCT/US00/00319 filed January 7, 2000 (“Methods Utilizing Scanning Probe Microscope Tips and Products Therefor or Produced Thereby”).
• PCT publication number WO 01/91855 Al published December 6, 2001 based on PCT application no.
• 2004/0008330 describes patterning of conductive polymers and is hereby inco ⁇ orated by reference in its entirety.
• US regular application 10/442,189 filed May 21, 2003 to Mirkin et al. (“Peptide and Protein Nanoarrays and Direct- Write Nanolithographic Printing of Peptides and Proteins”) is inco ⁇ orated by reference in its entirety and describes a variety of peptides and proteins which can be patterned according to the present invention.
• U.S. patent application serial no. 10/689,547 filed October 21, 2003 to Van Crocker et al. (“Nanometer Scale Engineering Structures") is inco ⁇ orated by reference in its entirety.
• Embodiment 2 Cantilever microdeposition and curing for producing conductive metallic and other patterns
• the invention provides a method for writing conductive metal comprising: (1) providing a cantilever having a cantilever end, wherein the cantilever can comprise a tip at the end or can be a tipless cantilever; (2) providing an inkdisposed at the cantilever end; (3) providing a substrate surface; and (4) contacting the cantilever end and the substrate surface so that ink is delivered from the cantilever end to the substrate surface.
• the deposition is preferably followed by localized heat curing step e.g. by use of a medium-power laser or an infrared gun.
• stamp tips are used to deposit material which are described further below.
• Stamp tips are described in, for example, U.S. provisional patent application 60/544,260 entitled “Direct- Write Nanolithography with Stamp Tip: Fabrication and Applications” to H. Zhang et al. and filed February 13, 2004, and US regular patent application serial no. 11/056,391 filed February 14, 2005 (attny no. 083847-0264) which are hereby inco ⁇ orated by reference in their entirety.
• Cantilevers are known in the art and are available from, for example, MikroMasch USA (Portland, OR). Cantilevers can be coated and functionalized as desired. Tipless cantilevers are also known in the art as described in, for example, U.S. Patent Nos.
• the geometry and shape of the cantilever can be used to control at least one dimension of the features formed on the substrate surfaces from inks.
• the ink is not particularly limited, although a primary embodiment of the invention is metal-based inks, including both metal precursor inks, often using metal salts, and metal nanoparticulates inks. Useful embodiments are described further in patent application no. 16 (conductive patterns) noted above and described further below.
• the three primary ink components include (1) the primary material to be deposited such as, for example, one or more metals or metal salts, (2) one or more solvents, and (3) one or more additives if desired.
• Inks can be fully or partially dried, if desired, on the cantilever or the cantilever tip before delivery to the substrate surface. Inks can be fully or partially dried on the substrate surface after delivery.
• the nanoparticles of the ink are not particularly limited although a primary embodiment of the invention is metal-based inks. Inorganic compounds can be used in the nanoparticles.
• the nanoparticles can be substantially homogeneous or can be heterogeneous.
• Nanoparticles can have a core-shell structure if desired. They can have organic surface coatings or shells if desired. They can be magnetic in nature. They can be semiconductive in nature, whether doped or undoped. Nanoparticles can be electrically insulating or have an insulating shell. The nanoparticles can be hydrophilic or hydrophobic. Nanoparticles can also be precursors to other technologically useful materials including electrical conductors, magnetic materials including ferromagnetic materials, semiconductors, and optical materials. Nanoparticles can exhibit quantum confinement effects and show useful properties such as for example electroluminescent and photoluminescence of various colors. Nanoparticles can be fiinctionalized to chemisorb to or covalently bond to the surface.
• the solvent system is not particularly limited.
• Ink solvents which are high- boiling are generally preferred.
• solvents with boiling points above about 100°C and more particularly above about 150 °C can be used.
• Aromatic hydrocarbons are one kind of high boiling solvent for example.
• the inks can begin drying as desired for form features which are preferably stable over time after, for example, one month.
• the features can be cured and made stable against rinsing with solvents including aggressive solvents and etching systems.
• Features can be subjected to annealing, light, lasers, electric currents, and other stimulations. Often, it is desired to form continuous masses of structures which provide, for example, high electrical conductivity.
• features can be nanostructures or microstructures.
• the height of the feature is not particularly limited as layering can be carried out to build up height.
• Lateral dimensions such as length and width are not particularly limited as the methods described herein can be used to prepare nanoscale and micron scale dimensions.
• dot diameter or line width can be, for example, about 5 nm to about one micron.
• dot diameter or line width can be, for example, about one micron to about 100 microns, or about 5 microns to about 25 microns. Additional references are described throughout the rest of the specification for use in practicing the present invention. No admission is made that any of these references are prior art. The invention is further described by the following non- limiting examples.
• Patterning Micron sized patterns were generated using the translation stages of Thermomicroscopes CP Research instruments or NSCRIPTOR (Nanolnk, Chicago, IL) instruments.
• Cantilevers were coated with different metal precursor inks by using the z-stepper motors to bring the cantilevers into contact with microfabricated inkwells filled with ink.
• the z-motor and x-y translation stage were then used to position the coated cantilevers over the substrate, and to bring the cantilever into contact with the surface.
• the cantilevers were brought into contact at a slight angle (several degrees) so that only the end of the cantilever touched the surface. A slight bending of the flexible cantilever as monitored by optical microscopy indicated that contact has been achieved.
• Ink Deposition A new method for directly writing ink on surfaces was developed that enables line and dot patterns with dimensions of hundreds of microns and as small as sub- micron.
• the ink delivery method involved the following general steps: Ink Loading.
• a flexible cantilever was loaded with an ink.
• the cantilever can have a sha ⁇ tip on the end, or be tipless, and can have various end shapes and widths, from several microns to hundreds of microns.
• Ink loading can be performed passively by bringing the cantilever in contact with a droplet or reservoir of ink and then removing it. The ink wets the underside of the cantilever and adheres through cohesive forces. Passive loading and delivery of ink was demonstrated in the working examples. The methods described by C. Bergaud and collaborators to actively draw up liquid inks and control the deposition via electrowetting and dielectrophoresis can be also used.
• the cantilever can be brought into contact with the surface for patterning. In most cases, a laser force-feedback mechanism is not required, nor is a piezoelectric scanning/positioning mechanism required. Mechanical "Z" stepper motors can be used to bring the cantilever into contact with the surface, and optical microscopy can be used to detect defection of the cantilever when it comes into contact with the surface.
• Line patterns can be formed by drawing the cantilever along the surface.
• NSCRIPTOR and Thermomicroscope CP Research platforms “X” and “Y” stepper motors or fine manual positioning screws can be used to translate the lever along the surface in the form of the desired pattern.
• Commercial high-resolution piezoelectric stage (NPoint, Madison, WI) may be retrofitted in either instrument.
• the NSCRIPTOR platform one can use custom pattern design software to direct the motion of the cantilever..
• the width of the line can be directly related to the width of the end of the cantilever as shown in Figure 1.
• one can control the shape of the lines e.g.
• Figures 1 through 7 show optical images of 60 and 45 micron wide lines.
• Figure 6 shows optical and AFM height images of 5 and 4 micron wide lines, and Figure 7 shows 3 and 2 micron wide lines. Even at the narrowest line widths, the lines are sufficiently continuous to yield resistivities as low as 4 microohm.cm.
• Advanced lithography methods such as focused ion beam can be used to further reduce the dimensions of the cantilever by milling. Note that the process works equivalently when the surface is translated under a stationary cantilever. With current instrumentation, one can fabricate lines as wide as 100 microns and down to less than a micron with a single cantilever pass at a speed of 20 microns/second, although the higher conductivity traces are obtained from writing speeds of 10 microns per second. Feature Height Control. By controlling several patterning variables, one can vary the height of the line traces. In general, the thickness of the line pattern generated by a single pass can be under 1 nm to several hundred nanometers after curing (see following section).
• the cantilever is brought into contact with the surface at an angle greater than several degrees, rather than parallel to the surface.
• One can vary the height of the traces by controlling the distance between the cantilever and surface, the force or bending of the cantilever, and the tip translation speed.
• the height of the patterned traces is decreased.
• the force was approximately controlled by varying the separation between the cantilever and the surface while monitoring the cantilever deflection.
• Qualitative observations have implied that another method of increasing the height of the patterns is to decrease the translation speed of the cantilever during patterning. With slow tip translation, 100 nm high features (after curing) can be generated in a single pass. To form dot patterns the cantilever is brought into contact with the surface, maintained in contact for a fixed time (usually several seconds), and then removed.
• split and Multiple Cantilevers One can increase the maximum ink loading, and thus the maximum line length, by changing the geometry of the cantilever. With single cantilevers that are 50 microns to 200 microns long, one is able to reproducibly obtain lines as long as several hundred microns with a single loading step, as shown in Figure 8 for two different tip geometries. One can greatly improve the total supply of ink (i.e. the volume available from a single dip) by writing with adjacent cantilevers that have a very small gap (microns) between them. The increased ink supply can yield higher patterns or longer line patterns. The slit or gap in between the cantilevers acts as a reservoir to hold ink due to capillary action.
• FIG. 9 is an optical image of patterned lines generated with multiple adjacent cantilevers. Note how the maximum line length (and thus ink loading) obtained increases with the increasing number of cantilevers in the 'pen' (1, 4, 2 adjacent cantilevers). Also note the increase in line width scales with the number of cantilevers in the pen.
• Layering One can increase the height of the line and dot patterns by applying multiple layers. Typically, for metal inks, each layer is first cured by heating before a second layer of the same metal precursor ink is applied. A nanoscale two-layer palladium pattern is shown in the AFM images and line scans in Figure 10. Note the increase in height from 2 nm for the first layer to 10 nm for the second layer.
• the ink used in this experiment was a saturated solution of palladium acetate dissolved in 80% ethylene glycol: 20% water. For other applications it may be necessary to build layered features of dissimilar materials, such as metals, oxide, and semiconductors.
• improved instrumentation could include an energy source that can anneal or sinter ink as it is deposited onto a surface.
• the energy source may be a heated sample stage for thermal curing, a laser or other light source, or a method of applying a current to the substrate to induce conversion of the ink to the final metal or metal oxide form.
• the general method for patterning conductive features comprises the steps of choosing an appropriate precursor ink and dispersant, applying the ink to the surface, for instance using the method described in the previous sections, and finally treating the pattern to convert the precursor material to the final desired material, for example by applying energy, such as heat.
• inks were prepared by dispersing the particles in solvents with high boiling points, such as mesitylene, xylene, and dimethylformamide to reduce evaporation of the inks.
• Nanoparticle Ink Deposition and Conversion to Metal In order to attain inks that are compatible with the substrate of interest, it is generally useful to choose a thiol capping surfactant and solvent that enables the ink to wet the surface.
• a thiol capping surfactant and solvent that enables the ink to wet the surface.
• the nanoparticles are hydrophobic, and disperse well in non-polar solvents such as toluene, mesitylene, and xylene. These inks were very useful for patterning hydrophobic or uncleaned surfaces.
• nanoparticles prepared with thiotic acid or mercaptosuccinic acid disperse in relatively polar solvents, such as alcohols, so they were used to pattern on hydrophilic surfaces including clean glass, quartz, oxidized silicon, silicon, and silicon nitride.
• relatively polar solvents such as alcohols
• the ink When the ink is incompatible with the surface it doesn't form a continuous line, but de-wets from the surface to form droplets.
• Some non-polar solvents such as mesitylene were useful for both hydrophilic and hydrophobic glass surfaces.
• the nanoparticles can be converted into bulk metal using many different sources of energy, including a laser or heated stage, as long as the temperature is sufficient to remove the insulating organic shell.
• optical images show gold traces written between two gold electrodes before and after curing, and an AFM line scans showing average heights of approximately from 12 nm to 90 nm can be obtained with a single layer of ink.
• long chain carbon compounds for example C-5 to C-50, preferably C-10 to C-18, gives improved results.
• the long chain carbon has a boiling point of 200 °C or greater.
• long carbon chain compounds preferably 10 to 18 carbon
• dodecane or pentadecane with boiling point 215 and 270 °C respectively may be used.
• pentadecane we attended 1-2 microliter of pentadecane to the 4 microliter of nanoparticles solution composed of (nanoparticles, mesitelyne and thiotic acid), these long chain carbons will interact and inter-digitate with the carbon chain on the nanoparticles to form a three dimensional structure to form continuous and homogeneous films as shown in the optical images of Figure 3 to 7 in comparison with the optical images of Figure 1 and 2.
• nanoparticles prepared from nanoparticle precursors adhered very well to clean glass surfaces (see Figure 40), although the nature of the capping group can play a significant role in adhesion.
• nanoparticles prepared with acid terminated thiol capping groups such as thiotic acid, formed films on glass that withstood a scotch tape test, where a strip of tape is placed over the pattern, rubbed, and then removed.
• these hydrophilic films on glass were removed by rinsing with water.
• cured films made from hydrophobic gold nanoparticles i.e.
• the ink had excellent writing properties, wetting glass surfaces well during writing, and curing cleanly at 250 °C.
• Evidence of the excellent resistance to scotch tape and rinsing tests is shown in Figures 1 and 2.
• the resulting gold thin films are metallic yellow, approximately 50-100 nm thick as measured by AFM, and exhibit excellent conductivity, as measured by a two-probe configuration.
• traces such as the one shown in Figure 2 that are approximately 250 microns long and 15 microns wide have measured resistances of about 18 ohm. Therefore, a resistivity of 8 microohm.cm was calculated for this particular trace, and resistivities for patterned traces as low as 4 microohm.cm have been measured.
• the bulk resistivity of gold is 2.44 microohm.cm. Similar results can be obtained by preparing inks from nanoparticles that have a ratio of acid-terminated thiols and hydrophobic methyl -terminated thiols. Particles with different ratios of dissimilar thiol capping molecules can be prepared in situ, or tailored using place exchange reactions as described by Hostetler and coworkers (M. J. Hostetler, S. J. Green, J. J. Stokes, and R. W. Murray, J. Am. Chem. Soc.
• the patterning method is generally applicable to any nanoparticle material that can be prepared with capping ligands.
• materials including Cu, Pd, Ag, Ru, Mo, CdSe, Ni, Co, and others.
• Nanoscale patterns with Nanoparticle Inks The nanoparticle-based ink formulations can be patterned using the Dip Pen Nanolithography printing method to yield sub-micron sized patterns.
• hexanethiol-capped gold nanoparticles saturated solution in mesitylene
• tips were coated in nanoparticle ink by contacting the tip with a droplet of nanoparticle ink in a silicon inkwell for several seconds.
• the coated tips were then used to generate line and dot features on a quartz surface. For example, dot patterns were generated by holding the tip in contact with the surface for 10 seconds, as shown in Figure 11.
• the diameters and heights of the dots were varied from 50 nm to 85 nm wide and from 2.5 nm to 7.5 nm high by changing the applied force from 0.2 nN to 4 nN.
• Lines were generated by translating the tip across the surface at a fixed rate (-0.15 microns/second).
• the height and width of the lines can also be varied by changing the applied force, as in Figure 12.
• the nanoscale particle patterns were cured by applying heat (250 oC, 5 s) from a heat gun, and verified by re-imaging, Figure 13.
• Polyol Inks Another method of preparing nanoparticles is to chemically reduce metal salts in the presence of alcohols or polyols with heat. This method was reported by Figlarz et al. as a means of making dispersed nanoparticles (U.S. Patent 4,539,041). The method was improved by Chow et al who reported a similar method to form continuous films. One can creatively and advantageously adapt this polyol process for forming nanoparticles for use as an ink for nanoscale and microscale conductive patterns.
• the general formula for the metal precursor inks comprises alcohol containing matrix and metal salts. After patterning, the salts are transformed in situ into nanoparticles, which coalesce into metal films with increased heat. In preliminary experiments this process has been demonstrated for metals such as Au, Pt, Pd, and Ag, although many other metals and metal alloys (outlined in U.S. patents 5,759,230 and 4,539,041) are also amenable to this process.
• Nanometer Scale Patterns with Polyol Inks Nanoscale features of platinum using a precursor ink consisting of 10 mg/100 ⁇ L hydrogen hexachloroplatinate (IV) hydrate dissolved in 20% Millipore water and 80% ethylene glycol have been written. This ink can be written onto clean glass or silicon oxide substrates using the DPN printing technique. For micron sized patterns a tipless cantilever gives the optimal control over pattern size and thickness, whereas for nanoscale patterns a cantilever with an ultrasha ⁇ tip (e.g. silicon nitride) on the end of a flexible cantilever offers the optimal resolution. After deposition the precursor patterns are converted to metal features by heating with a hot plate or a hot air gun. This curing or conversion reaction occurs rapidly (several seconds) at temperatures around 250 °C. The thickness of the patterns can be increased by adding layers of ink in between curing steps. Figure 10 shows layered nanoscale patterns generated on
• Figure 14 shows a 110 micron long line drawn with the platinum chloride ink by translating an ink-coated cantilever in the direction parallel to its short axis. After curing, the single layer of ink had high resistance, but subsequent layers could be added to increase the height of the pattern, and thus the conductivity.
• Working Example 2 the platinum ink was used to form dot features between micron sized gold electrodes. Dots are formed by bringing a coated tip/cantilever assembly into contact with the surface briefly (several seconds) and then retracting the tip to leave a droplet, as shown in the optical image in Figure 15. The size of the droplet depends on the wetting properties of the ink to the surface, the loading of the tip, and the in some cases the tip-substrate holding time.
• Figure 16 shows an example of a single layer platinum trace drawn between chromium electrodes. After curing, the resistance of the 50 micron long trace was 80 ohms and the trace adhered well to the surface during rinsing and scotch tape peel tests.
• Working Example 4 Gold has a much lower bulk resistivity than platinum. Therefore, to improve the conductivity of metal traces for applications such as repair of metal traces in thin film transistors, a similar metal ink precursor was tested based on a gold salt, hydrogen tetrachloroaurate (III) trihydrate.
• a typical formulation comprises 100 mg of Au salt in 80% ethylene glycol / 20% water.
• the gold precursor inks wet silicon oxide and glass surfaces well during writing, and cured within 5-10 seconds at 200 °C on a hot plate. The resulting films appeared black in an optical micrograph, and according to AFM images, consisted of small isolated particles. Single layer traces were usually non-conductive, and adhered poorly to clean silicon oxide substrates.
• the AFM scan in Figure 17 shows large gold particles that have formed after 3 layers of gold chloride ink deposited on silicon oxide between gold electrodes.
• a useful ink for forming conductive traces on silicon oxide would combine the properties of the gold and platinum precursor inks.
• alloy-forming inks were developed based on gold and platinum.
• one formulation that was very compatible with the patterning method was composed of 100 mg of platinum salt and 50 mg of gold salt co-dissolved in 30 microliters of water containing 60 mg each of 300 and 10,000 MW polyethylene glycol.
• One method of improving the adhesion of polyol inks to glass surfaces is to add small amounts of epoxy to the ink formulation.
• 85 mg of hydrogen gold tetrachloride was dissolved in 50 microliters of dimethylformamide.
• 1 microliter of ethylene glycol and 1 microliter of epoxy mixture were added.
• Two part epoxy purchased from Epotek (377 Epotek) cured in 1 hour at 120 °C in the absence of metal salts, and epoxy purchased from Aldrich (bisphenol-F) cured in 1 minute at 150 °C, although the curing time increased in the presence of the gold salts.
• this ink can be deposited with silicon nitride tips, the reliability of the patterning is improved if PDMS (polydimethylsiloxane) coated tips are used for writing.
• Writing this ink on quartz substrates produces features as high as 15 nm, as demonstrated in the AFM image in Figure 19.
• the precursor ink patterns are cured in an oven at 120 °C for 5 min, and then at 250 °C for 10 s. Importantly, the patterns exhibit excellent stability, resisting water rinsing and two piranha solution washes (3: 1 H 2 SO 4 /H 2 O 2 ) for 10 min each at 120 °C.
• Deposition is performed using:
• Particles are applied to a surface via spin coating, by displacement, ejection technologies (ink jet) transfer techniques (e.g. microcontact printing), or electrostatic patterning.
• ejection technologies ink jet
• microcontact printing e.g. microcontact printing
• electrostatic patterning e.g. electrostatic patterning.
• a modified "pull-down bar” mechanism can be used to deposit these thin films. In this technique a flat rod or wedge is brought in close proximity to the surface to be covered, and then passed over the surface with a pool of the nanoparticle suspension disposed on the side of the direction of travel. The result is the formation of a thin film on the trailing side of the bar.”
• Patent describes a method for synthesizing metal nanoparticles that involves chemical reduction of a metal-ligand complex in the presence of a solvent.
• Duthaler et al Preferred methods for producing electrical circuit elements used to control an electronic display. Ink jet printing of materials to fabricate displays, and various other soft lithography technologies. 4,539,041 Figlarz et al. Process for the reduction of metallic compounds by polyols, and metallic powders obtained by this process.
• the processing of metals can be difficult, and operating at the nanoscale can make matters even more difficult.
• Many methods are limited to micron level manufacturing. Many methods are limited by the need for electrochemical biases or very high temperatures. Moreover, many methods are limited by physical requirements of the deposition process such as ink viscosity. Better methods are needed to fabricate metallic nanostructures by means which provide for, among other things, alignment, ability to layer films and wires, high resolution, and versatility.
• the present invention provides a method of depositing a conductive coating in a desired pattern onto a substrate comprising: (a) depositing a precursor onto the substrate in the desired pattern by nanolithography with use of a tip coated with the precursor; (b) contacting the precursor with a ligand; (c) applying sufficient energy, optionally from an extended radiation source, to transfer electrons from the ligand to the precursor, thereby decomposing the precursor to form a conductive precipitate in the desired pattern and thus forming the conductive pattern directly on the substrate.
• the present invention also provides a method of printing a conductive metal in a desired pattern onto a substrate comprising: (a) drawing a metal precursor and ligand directly onto the substrate according to the desired pattern using nanolithography with use of a tip coated with a precursor; and (b) decomposing the precursor by applying energy, optionally from an extended radiation source, to form the conductive metal in the desired pattern, without removing from the substrate a substantial quantity of the precursor, and without removing from the substrate a substantial quantity of the metal.
• the present invention also provides a nanolithographic method comprising depositing a metallic precursor from a tip onto a substrate to form a nanostructure and subsequently converting the precursor nanostructure to a metallic deposit. The deposition can be carried out without use of an electrical bias between the tip and substrate.
• the present invention also provides a nanolithographic method consisting essentially of: depositing an ink composition consisting essentially of a metallic precursor from a nanoscopic tip onto a substrate to form a nanostructure, and subsequently converting the metallic precursor of the nanostructure to a metallic form.
• a nanolithographic method consisting essentially of: depositing an ink composition consisting essentially of a metallic precursor from a nanoscopic tip onto a substrate to form a nanostructure, and subsequently converting the metallic precursor of the nanostructure to a metallic form.
• Basic and novel aspects of the invention are noted throughout this specification, but these aspects include that stamps and resists are not needed, electrochemical bias is not needed, expensive equipment not readily available for typical research laboratories and production facilities is not needed, and reaction between the substrate and the ink is not needed. Accordingly, compositions and inks can be formulated and patterned without these limitations.
• the present invention also provides a method of printing without use of electrochemical bias or reaction between the ink and substrate comprising depositing a metallic precursor ink composition onto a substrate from a tip in the form of a microstructure or nanostructure on the substrate to form an array having discreet objects separated from each other by about one micron or less, about 500 nm or less, or about 100 nm or less.
• the present invention also provides patterned arrays comprising a substrate and discreet nanoscopic and/or microscopic metal deposits thereon prepared by the methods according to this invention.
• the metal deposits can be, for example, rectangles, squares, dots, or lines.
• the present invention also provides methods of using these methods including, for example, preparing sensors, biosensors, and lithographic templates, as well as other applications described herein.
• Figure 1 in reference 16 illustrates AFM data of palladium structures according to the present invention in Working Example 1.
• Figure 2 in reference 16 illustrates AFM data of palladium structures according to the present invention in Working Example 3.
• Figure 3 in reference 16 illustrates AFM data of platinum structures according to the present invention in Working Example 4.
• Figure 4 in reference 16 illustrates AFM data of palladium structures according to the present invention in Working Example 5.
• Figure 5 in reference 16 illustrates AFM data of palladium structures according to the present invention in Working Example 5.
• Reference 16 claims benefit to provisional applications 60/405,741 to Crocker et al. filed August 26, 2002, and 60/419,781 to Crocker et al. filed October 21, 2002 and inco ⁇ orated herein by reference in its entirety.
• DPNTM and DIP PEN NANOLITHOGRAPHYTM are trademarks of Nanolnk, Inc. and are used accordingly herein (e.g, DPN printing or DIP PEN NANOLITHOGRAPHY printing).
• DPN methods and equipment are generally available from Nanolnk, Inc. (Chicago, IL), including the NScriptorTM which can be used to carry out the nanolithography according to the present invention.
• a protein can be directly patterned onto a substrate by DPN printing, or a template compound can be patterned which is used to bind a protein.
• DPN printing is an enabling nanofabrication/nanolithographic technology which allows one to practice fabrication and lithography at the nanometer level with exceptional control and versatility. This type of nanofabrication and nanolithography can be difficult to achieve with many technologies that are more suitable for micron scale work.
• the tip can be a nanoscopic tip. It can be a scanning probe microscopic tip including an AFM tip. It can be hollow or non-hollow. Ink can pass through the middle of a hollow tip, coating the end of the tip. The tip can be modified to facilitate printing of the precursor ink. In general, it is preferred that the tip does not react with the ink and can be used over extended periods of time.
• the patterns deposited by the nanolithography are not particularly limited by the shape of the pattern. Common patterns include dots and lines and arrays thereof. The height of the pattern can be, for example, about 10 nm or less, and more particularly about 5 nm or less.
• the lines can be, for example, about one micron wide or less, and more particularly, about 500 nm wide or less, and more particularly about 100 nm wide or less.
• dots can be, for example, about one micron wide in diameter or less, and more particularly, about 500 nm wide or less, and more particularly about 100 nm wide or less.
• the nanolithography is preferably carried out to form nanostructures, structures at a micron scale can be also of interest. For example, experiments used to pattern a structure of 1-10 square microns in area, such as a rectangle, square, dot, or line, can be useful in also designing experiments for smaller nanostructures.
• conductive patterns are formed with use of DPN printing with use of the following steps: 1) depositing a precursor such as, for example, a metal salt, onto a substrate in a desired pattern with use of a coated tip, 2) applying an appropriate ligand onto the substrate, wherein for example the ligand comprises a donor atom such as nitrogen, phosphorous, or sulfur, 3) applying sufficient energy to transfer electrons from the ligand to the precursor by, for example, radiant heat, thereby decomposing the precursor to form a precipitate such as, for example, a metal.
• a precursor such as, for example, a metal salt
• the ink solution is generally contemplated herein to include a solvent and solute.
• the solvent can be any material capable of solvating the solute, but is generally contemplated to comprise an inexpensive, readily available, relatively non- toxic material such as water, various alcohols and so forth.
• the solute is generally contemplated to include at least two components which chemically react with one another under the influence of an energy source, such that a metal or other substance precipitates out of the solution.
• one component of the solute comprises a salt
• another component of the solute comprises an appropriate ligand.
• salt means any combination of an acid (A) and a base (B).
• metallic salts such as copper formate, acetate, acrylate, thiocyanate, and iodide.
• non-metallic salts such as ammonium formate and ammonium acrylate.
• the various components of the solution may be deposited on the substrate concurrently or sequentially, or in some combination of the two. Thus, it is contemplated that the salt may be deposited concurrently with the ligand, or separately from the ligand.
• the solvent may itself comprise or contribute one or more aspects of the salt or the ligand.
• ligand refers to any substance which can be thermally activated to displace one or more aspects of the salt in a redox reaction, such that AB+L ⁇ -> AL+B, or AB+L ⁇ ->A+BL.
• preferred ligands are non-crystalline, leave no non-metallic residue, and are stable under normal ambient conditions. More preferred ligands are also capable of taking part in redox reactions with a particular salt being used at reasonable temperatures, which are generally considered to be less than about 300°C.
• a preferred class of ligands are nitrogen donors, including, for example, cyclohexylamine.
• nitrogen donors including, for example, cyclohexylamine.
• Contemplated solutions may include other compounds besides salts and ligands.
• a mixture of copper (II) formate in a nitrogen donor solvent with or without water and an alcohol may be used to facilitate transport from tip to substrate.
• a small amount of a solvent based polymer or a surfactant may also be useful additives for adjusting the rheology of the precursor solution to facilitate transport from tip to substrate, and to impart better film forming properties.
• larger amounts of high boiling solvents and/or additives such as triethylphosphate, Triton XI 00, glycerol, etc., are preferably to be avoided as these have a tendency to contaminate the film produced on account of incomplete pyrolysis over temperature sensitive substrates such as Kapton.TM. or paper.
• the substrate may be worthwhile to treat the substrate with a coupling agent to improve the adhesion of the deposited material to the substrate as a function of the coupling agent's modifying the hydrophobicity or hydrophilicity of the surface of the substrate.
• the salt contains a metal
• all metals are contemplated.
• Preferred metals include conductive elements such as copper, silver and gold, but also include semiconductors such as silicon and germanium.
• metals such as cadmium, chromium, cobalt, iron, lead, manganese, nickel, platinum, palladium, rhodium, silver, tin, titanium, zinc, etc. can be used.
• the term "metal” also includes alloys, metal/metal composites, metal ceramic composites, metal polymer composites, as well as other metal composites.
• the substrate can comprise virtually any substance upon which a compound can be deposited.
• contemplated substrates include metals and non- metals, conductors and non-conductors, flexible and inflexible materials, absorbent and non-absorbent materials, flat and curved materials, textured and non-textured materials, solid and hollow materials, and both large and small objects.
• Particularly preferred substrates are circuit boards, paper, glass, and metal objects. Viewed from another perspective, the wide breadth of contemplated substrates gives some indication of the scope of contemplated objects to which the present teachings may advantageously be applied.
• methods and apparatus taught herein may be used for a variety of applications, including multichip modules, PCMCIA cards, printed circuit boards, silicon wafers, security printing, decorative printing, catalysts, electrostatic shielding, hydrogen transport membranes, functionally gradient materials, production of nanomaterials, battery electrodes, fuel cell electrodes, actuators, electrical contacts, capacitors, and so forth.
• the methods and apparatus can be used as sensors and biosensors.
• the method and apparatus can be used to prepare templates for further lithography such as imprint nanolithography. Using the methods to connect nano wires and nanotubes is of particular interest.
• the substrate is contemplated to represent any suitable substrate, including especially a circuit board, which may or may not be installed in or form part of an electronic device such as a computer, disk drive or other data processing or storage device, a telephone or other communication device, and a battery, capacitor, charger, controller or other energy storage related device.
• Suitable energy sources contemplated herein include any source which is capable of effecting the desired chemical reaction(s) without causing excessive damage to the substrate or the coating.
• particularly preferred energy sources are radiative and convection heat sources, including especially infrared lamps and hot air blowers.
• Other suitable energy sources include electron beams, and radiative devices at non-IR wavelengths including x-ray, gamma ray and ultra-violet.
• Still other suitable energy sources include vibrational sources such as microwave transmitters.
• the various energy sources can be applied in numerous ways.
• the energy source is directed at the precursor/ligand deposited on the substrate.
• a heated ligand could be applied to a cold precursor, or a heated precursor could be applied to a cold ligand.
• Many advantages can be discerned from this invention including, for example, smooth surfaces, good coating adhesion, and control of coating thickness.
• Still another advantage of various embodiments of the present teachings is that coatings can be deposited with a purity of at least 80% by weight.
• the purity of the metal or other material intended to be included in the coating is at least 90%, in still more preferred embodiments the purity is at least 95%, and in most preferred embodiments the purity is at least 97%.
• Still another advantage of various embodiments of the present teachings is that coatings can be deposited with very little waste. In preferred embodiments at least 80% by weight of the material to be deposited on the substrate remains to form the desired pattern. For example, if copper (II) formate is used to produce a copper circuit, then at least 80% of the copper deposited on the substrate can remain to form the desired pattern, and no more than 20% of the copper is removed as "waste".
• the waste is no more than 10%, in still more preferred embodiments the waste is no more than 95%, and in most preferred embodiments the waste is no more than 3%.
• Still another advantage of various embodiments of the present teachings is low temperature operation. Metals, for example, can be deposited in desired patterns at temperatures of less than about 150°C, preferably less than about 100°C, more preferably less than about 75° C, and most preferably at ordinary room temperatures of room temperature (25-30°C).
• the redox or "curing" step can also be performed at relatively low temperatures below about 100°C, more preferably below about 75°C, and even as low as about 50°C. Even lower temperatures are also possible, although below about 50°C. the redox reaction tends to be too slow for most applications.
• inks or patterning compounds are of particular interest for the present invention: copper formate or copper acetate; silver sulfate; silver nitrate; silver tetrafluroborate; palladium chloride, acetate, and acetylacetonate; hexachloroplatinic(IV) acid; ammonium iron citrate; carboxylates, (pseudo-)halides, sulfates, and nitrates of zinc, nickel, cadmium, titanium, cobalt, lead, iron, and tin; metalcarbonyl complexes, including chromium hexacarbonyl; amine bases, including cyclohexylamine, 3- picoline, (iso)quinoline, cyclopentylamine, di
• deposition can be carried out with use of aqueous solutions as ink, wherein the solutions comprise water, metal salt, and a water-soluble polymer such as a polyalkylene oxide polymer having molecular weight of about 50,000 or less.
• Aqueous solutions can be also useful as carriers for the reducing agent.
• deposition of disodium palladium chloride in water with 10% polyethylene oxide (MW 10,000) via DPN printing on amino-silanized glass can be carried out (Schott Glass company), and subsequent chemical reduction to palladium metal using a reducing agent such as, for example, 0.03 M aqueous solution of dimethylamine:borane complex (DMAB).
• a reducing agent such as, for example, 0.03 M aqueous solution of dimethylamine:borane complex (DMAB).
• the concentration of the reducing agent can be varied to determine the best conditions for reduction.
• Atomic force micrographs of the patterns can be obtained before and after reduction.
• AFM imaging can be carried out with the tip which was used to deposit the structure or a different tip. If a different tip is used, the image can be better, particularly if the tip is selected or adapted for imaging rather than deposition.
• polymers which are of commercial use in printing inks can be used in the present invention.
• nanolithographic deposition can be carried out of palladium acetylacetonate (Pd(acac)) via DPN printing on an oxidized silicon substrate, and subsequent reduction by application of (1) a reducing agent, such as a liquid reducing agent like formamide, and (2) heat to the patterned surface.
• a reducing agent such as a liquid reducing agent like formamide
• Another system is palladium acetate in DMF solvent.
• Pd(acac) can be dissolved in an organic solvent including a halogenated solvent such as chloroform to form an ink for use in coating a solid tip or passing through a hollow tip.
• Heat treatment can be sufficient to carry out the reduction including temperatures of, for example, about 100°C to about 300°C or about 150°C.
• the heat time, temperature, and atmospheric conditions can be adjusted to achieve the desired pattern. Generally, a heat time of one to five minutes at 150°C can achieve a desired result.
• the stability of the deposited pattern can be examined by solvent rinsing, and the experimental conditions can be varied to improve the stability.
• Nanolithographic deposition experimental variables, including substrate and ink composition also can be varied to provide better resolution.
• AFM micrographs can be obtained before reduction and after application of heat including use of height scan analysis of the patterns.
• the imaging parameters can be varied to improve image resolution.
• a tip such as a gold coated tip can catalyze reduction of a metal salt directly on the cantilever.
• the tip composition can be varied to prevent this. For example, an aluminum coated probe can be useful to avoid this reduction on the tip.
• the tips are preferably selected and adapted for long term use and avoid catalyzing reaction with the ink.
• the reduction of a nanolithographically patterned metal salt can be also carried out by vapor reduction rather than liquid phase reduction, wherein the reducing agent is converted to vapor form and passed over the patterned substrate.
• Heaters known in the art can be used to heat the reducing agent to a vapor state as needed. In some cases, this type of treatment can improve the preservation of the original pattern during reduction.
• deposition can be carried out for a silver salt emulsion consisting of ferric ammonium chloride, tartaric acid, silver nitrate, and water onto an amino-silanized glass substrate via DPN printing, followed by development by photoreduction under a UV lamp.
• AFM imaging can be carried out to show patterns.
• the reduction step can be carried out with sufficient heat and sufficient time to reduce the metal salt without use of a chemically reducing agent.
• temperatures below about 400°C can be used, or below about 200°C can be used.
• One skilled in the art can select temperatures and experiment accordingly based on a given ink system and pattern.
• the deposition methods according to this invention also can include one or more pre-deposition steps, one or more probe cleaning or chemical modification steps aimed at improving ink coating; and one or more deposition steps, which may use dip pen nanolithography printing technology; one or more post-deposition steps, including cleaning steps and inspection steps.
• Pre-deposition substrate surface treatment steps include but are not limited to (in no particular order):
• chemical cleaning such as, for example, piranha cleaning, basic etching (eg. hydrogen peroxide and ammonium hydroxide);
• Probe cleaning or modification steps include but are not limited to (in no particular order):
• Deposition steps include but are not limited to the deposition of one or more inks e.g.
• Possible inks include but are not limited to precursors, compounds that will form the bulk of the final pattern, catalysts, solvents, small molecule or polymeric carrier agents, host matrix materials, or sacrificial reducing agents, and mixtures of above materials. They may be deposited as thin films or as thick multilayers (formed by multiple deposition steps), with or without variation of the chemical composition from layer to layer. Post-deposition steps include but are not limited to (in no particular order):
• Heating of the substrate for example with a heat lamp, hot air blower, or hot plate,
• Irradiation of the substrate with electromagnetic radiation e.g., IR, visible, and UV light
• charged particles e.g. electrons, ions drawn from a gun or a plasma source. This process may occur in air, vacuum, or in solution, with or without photosensitizing agents,
• the metallic nanostructures can be in the form of conductive nanoscopic grids which can include nanowires.
• crossbar structures can be formed.
• Metallic layers can be formed on top of each other.
• Structures can be included to integrate the nanoscopic conductive patterns with microscopic and macroscopic testing methods. Resistors, capacitors, electrodes, and inductors can be used as desired to form a circuit. Semiconductors and transistors can be used as desired. Formation of multilayers can be carried out to increase the height of the structure. Different metals can be in different layers of the multilayer. The methods of the invention can be used to electrically connect electrodes. In sensor applications, for example, the metallic deposit can have a resistivity which is modified when an analyte of interest binds to the structure. In biosensor applications, for example, antibody- antigen, DNA hybridization, protein adso ⁇ tion, and other molecular recognition events can be used to trigger a change in resistivity.
• U.S. Patent 6,579,742 to Chen describes nanolithographic structures formed by imprinting for nanocomputing and microelectronics applications. Imprinting, however, can suffer from mold stickiness effects. USP 6,579,742 nanocomputing applications and structures can be carried out using the nanolithographic methods described herein, and this patent is inco ⁇ orated by reference in its entirety.
• the substrate can be a protosubstrate as described in, for example, U.S. regular patent application no. 10/444,061 filed May 23, 2003 to Cruchon-Dupeyrat et al "Protosubstrates". This allows electrical conductivity of the printed structure to be examined by macroscopic methods.
• Reference 16's Non-limiting working examples are described below.
• a typical ink formulation can comprise a metal salt (e.g. carboxylate, nitrate, or halide) along with an appropriate organic Lewis base or ligand (amines, phosphines).
• Additives small molecules such as ethyleneglycol, polymers such as polyethyleneoxide, PMMA, polyvinylcarbazol, etc
• additives small molecules such as ethyleneglycol, polymers such as polyethyleneoxide, PMMA, polyvinylcarbazol, etc
• gentle heating in an ambient or inert environment e.g., 40-200 °C
• an ambient or inert environment e.g. 40-200 °C
• This approach enables deposition of a variety of metals or metal oxides including, for example copper, under mild conditions with very little organic contaminant [see, for example, Sharma et al., U.S.
• Patent 5,980,998 the complete disclosure of which is hereby inco ⁇ orated by reference, in particular for the materials deposited].
• Potential pitfalls may occur if the ligand evaporates from the patterned substrate before reaction takes place. In that case, the salt-patterned substrate may be exposed to a ligand in a second step prior to the heating.
• Deposition experiments and AFM imaging can be carried out with a CP Research AFM (Veeco Instruments, Santa Barabara, CA) or an NSCRIPTOR (Nanolnk).
• contact mode can be used including topography or lateral force modes.
• Example 1 One specific example of the use of this method used DPNTM printing or deposition to pattern palladium acetylacetonate dissolved in chloroform (1 mg/microliter; generally, almost saturated solutions of inks are desired) on oxidized silicon, glass, or amino-silanized glass. After patterning of the dots, a droplet (1 microlitre) of formamide was placed on the horizontal substrate and heated to 150°C for 2 min. The resulting metal patterns were stable towards solvent rinsing (including water, alcohols, and other non-polar organics) while the salt patterns prior to reduction were removed by solvent rinsing.
• Fig. 1 shows AFM images and a height scan of the patterns before (Fig. la) and after treatment (Fig.
• the patterned substrate was placed vertically in a conical polyethylene tube and 10 microlitres of formamide liquid was placed in the bottom of the tube.
• the tube was placed on a heating block and heated at 80°C for 30 min. so that the vapor caused reduction of the metal precursor. This method is useful because it preserves the metal pattern on the substrate.
• the resulting metal structures are resistive to solvent rinsing and other common methods of cleaning.
• Reference 16's Palladium nanopatterns deposited by DPN metallized by chemical reduction.
• a DPN ink consisting of disodium palladium chloride in water with 10% polyethyleneoxide (MW 10,000) was patterned onto amino-silanized glass (Schott Glass company) using the DPN technique.
• DMAB dimethylamine:borane complex
• Fig. 2 shows AFM images and a height scan of the patterns before (2a) and after (2b, 2c) treatment with DMAB.
• Reference 16's Example 4 Platinum nanopatterns deposited by DPN metallized by chemical reduction.
• a DPN ink consisting of platinum tetrachloride in water was patterned onto amino- silanized glass (Schott Glass company) using the DPN technique.
• Fig. 3 shows an AFM height scan of platinum nanostructures deposited by DPN and reduced by DMAB.
• Reference 16's Example 5 Palladium patterns deposited by DPN. A DPN ink consisting of palladium acetate in dimethylformamide was patterned onto silicon oxide using the DPN technique. Prior to patterning the substrate was cleaning in piranha solution for 15 min at 80°C. After patterning the substrate was heated using a hot plate in air for at least 1 minute.
• Fig. 4 and Fig. 5 show a desired structure design (left figure) and actual patterns before reduction (center figures) and after thermal reduction (right figures).
• the imaging of these patterns, particularly those patterns already reduced, can be improved by, for example, using clean tips not used for deposition.
• nanolithographic deposition of metallic nanostructures is provided using coated tips for use in microelectronics, catalysis, and diagnostics.
• AFM tips can be coated with metallic precursors and the precursors patterned on substrates. The patterned precursors can be converted to the metallic state with application of heat. This concludes the section on "Additional Description from Reference 16 ("Conductive Patterns”).”
• the gold nanoparticle ink described in the working example above was improved by addition of an alcohol such as, for example decanol CH 3 (CH2) OH.
• decanol improves wetting of hydrophillic substrates and in particular avoids the beading of the deposited ink into droplets onto said hydrophillic substrate, which would result in discontinuous (non-conductive) lines.
• This ink composition was typically prepared by dissolving 1 mg of hexanethiol-capped gold nanoparticles in 1.5 ⁇ L of thiotic acid dissolved in mesitylene (1 mg/mL) and 0.3 ⁇ L of decanol.
• the ink was converted to low-resistivity metallic form by high-temperature curing at 250 - 300 °C for 7 minutes followed by a lower temperature curing at 120 °C for 60 min.
• the gold nanoparticle ink above was further improved by replacing mesitylene and decanol by 1,3,5-triethylbenzene (1,3,5-TEB), a solvent with higher boiling point than mesitylene.
• Ink Composition #3 Commercial Silver Nanoparticle Ink A commercial silver paste (Nanopaste NPS-J obtained from Harima Chemicals, Japan, http://www.harima.co.ip) was used as an ink for flat panel display repair.
• the silver paste comprises monodispersed nanoparticles created by gas evaporation and protected by a dispersing agent.
• the average nanoparticle diameter is about 7 nm.
• this ink acts almost like a liquid even at high metal content. Therefore, it may be necessary to pre- concentrate this ink (by solvent evaporation in air) to reach optimum viscosity. Circuit formation with this ink is known in the art via printing, dispensing, and impregnation. Its sintering temperature is lower than 200 ° C . Similar commercial inks comprising silver, gold (Harima NPG-J) or other types of nanoparticles may be used as well.
• Figures 20, 21, 22 and 39 are illustrations of the successful deposition of the inks disclosed in working example 8 on various substrates.
• Figure 20 illustrates the direct-writing of silver lines on a silicon nitride substrate using the Harima silver nanoparticle ink (composition #3). Observed variations in line width and quality are the result of the increase in the viscosity (increasing concentration) of the ink with time. With time, the ink became too viscous to form continuous lines. All lines were drawn at the same cantilever speed relative to the substrate. Observed striations are an artifact of the stop-and-go motion of the high-precision stage that was used in this experiment.
• Figure 21 illustrates deposition of the same ink on a glass substrate.
• Figure 22 illustrates the deposition and low-temperature curing of a commercial silver nanoparticle ink on a glass substrate coated with a chromium thin film. Laser ablation was used to form a groove in the chromium film and expose the underlying glass substrate (in the center of the image). A tipless cantilever was then used to draw two lines onto the chromium film on each side of the laser-ablated gap and across the gap. While deposition was successful on the chromium film per se, it was not across the gap, because, in this case, the glass substrate left after laser ablation was particularly rough (> 1 micron, higher than the film being deposited).
• Figure 39 illustrate deposition of the ink composition #1 on chromium and glass
• Figure 30 (described in further details below) illustrates the deposition of the gold nanoparticle / 1,3,5-TEB ink.
• FIG. 23 illustrates the fabrication of multilayered lines (with up to 3 layers) using a tipless cantilever coated with the gold nanoparticle/mesitylene ink described above.
• a first layer was deposited on the substrate. After reloading with ink, the cantilever was repositioned at the start of the first-layer line and used to draw a second layer directly on top of the first. Note that, because the quantity of deposited material is small, the solvent in the first layer dries fast enough to allow second-layer drawing without need for an intermediate thermal curing step.
• a third layer was deposited by repeating the same process to form a three-layer line. This process enables the fabrication of thick lines with larger conductivity and improves line continuity. Line broadening was observed as well. However, a fraction of the line broadening is believed to result from limitations of the existing XY stage. Its replacement with a more repeatable stage should result in narrower lines.
• FIG. 24 illustrates the coating of a tipless cantilever (which may be with or without a slit) with ink by dipping into a microfabricated reservoir.
• a microfabricated cantilever was mounted on the scanning head of the NSCRIPTOR instrument (Nanolnk, Inc. Chicago, IL) and placed above a silicon microfabricated inkwell chip with the help of the top-view video microscope and XY motor stage integrated in the instrument.
• the fabrication of this inkwell chip which is normally used to deliver ink to tips for dip-pen nanolithographic printing, has been described in U.S. Application 10/705,776 to Cruchon-Dupeyrat et al. and related art.
• the inkwell comprises microfluidic millimeter-scale reservoirs, in which ink may be deposited using a pipette.
• the cantilever was dipped into the pool of ink in one of the aforementioned reservoirs (bottom part of the image). Note the meniscus around the cantilever in image B.
• the process is easily automated using appropriate (Z-axis) positioning devices and software.
• FIG. 25 illustrates the repair of a thin film transistor (TFT) flat panel display.
• Laser ablation was used to create holes in the insulating (silicon nitride) layer protecting on each side of a defect in the conductive traces forming electronic circuits on the flat panel display.
• a line was drawn between these holes with a gold nanoparticle ink; it was then cured to form an electrical bridge between the left and right parts of the trace, repairing the defect.
• FIG. 26 is the schematic diagram of a tipless cantilever with an ink storage slit or channel. This cantilever can store more ink volume with each dipping which will in turn result in better uniformity over the length of the line, increased line height, better conductivity and better ability to write over high steps.
• Figure 27 illustrates four additional designs for tipless slit cantilevers, which may be triangular or rectangular in shape and may comprise an enlarged portion acting as a reservoir for fluid storage.
• the fabrication technology can be adapted from methods for the fabrication of AFM cantilevers that are known in the art.
• a silicon nitride film is deposited via CVD on a sacrificial silicon substrate. Portions of the silicon nitride is then patterned and then etched to form cantilevers and slits.
• the underlying silicon may be partially anisotropically etched to free the cantilevers.
• the silicon nitride layer may be bonded to a Pyrex glass wafer and the silicon substrate is entirely etched. The wafer is then diced to afford chips terminated with tipless slit cantilevers.
• the cantilevers may be optionally coated with a thin reflective metal layer. The metal coating must be carefully chosen so as not to react with or otherwise affect the ink.
• Figures 28, 29 illustrate the actual deposition with a slit silicon nitride cantilever (fabricated according to the blueprint in Figure 26) of ink composition #3 (silver nanoparticle) on a glass substrate and across a gap between gold electrodes patterned on said glass substrate.
• the resistance between the two gold electrodes in image B was about 100 ohms after heat curing. Note that the ink deposited directly on top of the gold electrodes is not visible after heat-gun curing, the possible result of alloying or dewetting during curing.
• Figure 30 demonstrates the deposition of the gold nanoparticle / 1,3,5-TEB ink composition #2 with the same type of cantilever.
• Embodiment 3 Instrument and method for flat panel display repair using cantilever microdeposition and laser curing
• the invention further provides an instrument for the repair of gaps in open traces on a flat panel display substrate and similar devices, the instrument comprising: (1) a cantilever (or microbrush) adapted to receiving an ink; (2) a cantilever holding and positioning means adapted to contacting and translating said cantilever on the surface of said flat panel display substrate in order to pattern said ink on said substrate in the shape of a repair patch; (3) an inking mechanism that supplies said ink to said cantilever; (4) optionally, a curing system adapted to converting the deposited material into a low-resistivity form adapted to electrical conduction.
• the curing system may comprise a laser and its focusing optics.
• the cantilever positioning means may comprise: (1) a nanometer-resolution stage controlling the motion of said microbrush along the X, Y, Z axes; (2) a coarse long-range Z-stage adapted to contacting said microbrush with said substrate; (3) a rotation stage that can position the microbrush at any angle about the Z axis; (4) optionally, a cantilever contact detection means.
• the said contact detection and cantilever deflection measurement means may be chosen among a group consisting of (1) a video camera, its associated optics, a light source and computing means adapted to measuring the brightness of light reflected by of at least parts of said cantilever; (2) a laser reflective sensor; and (3) a confocal distance measurement system.
• the invention provides an instrument adapted to the repair of flat panel displays and other substantially flat circuitry, such as printed circuit boards.
• the instrument may comprise some or all of the following:
• FIG. 31 shows a first design of this instrument, where the brightness of the cantilever is monitored via video imaging to detect the touchdown of the cantilever on the surface.
• the task of detecting the precise height at which the microbrush or cantilever comes in contact with the substrate is accomplished by computer monitoring of the video image area corresponding to the cantilever for changes in brightness as the nanometer scale XYZ stage moves the cantilever downward. Upon contact and under proper lighting, a dramatic change in brightness occurs (due to cantilever bending) with enough sensitivity to allow detection of contact.
• the nanometer scale XYZ stage can move the cantilever in the XYZ directions, depositing ink on the 2D surface and on 3D surface structures.
• the 360 degree motorized rotation stage allows the cantilever to always be pulled rather than pushed (i.e. in the direction parallel to its length, from its free end to its bound end; see working example below). This avoids cantilever buckling and other problems leading to poor patterning results.
• the cantilever is moved upward by the coarse motorized Z stage until it is above the level of the inkwell rotary stage.
• the inkwell rotating stage then rotates the inkwell to a position directly below the cantilever.
• the cantilever is then lowered into the inkwell and ink coats the cantilever.
• the cantilever is then moved up again, and the inkwell is rotated out of the cantilever area.
• the cantilever is then ready to deposit ink on the substrate.
• the curing laser is activated.
• a mirror and beam splitter or other device that selectively reflects the light from the laser towards the substrate, it directs laser light onto the area where in was deposited. Curing can be viewed as it occurs through the beam splitter to the camera and microscope assembly. The entire assembly may be moved over large distances (meters) to position the assembly over areas of the substrate in need of repair.
• the laser light can be directed downward or at angle, without mirrors, utilized the XY motion of the gantry that can move the entire assembly over large distances (meters) to position the cantilever or the curing laser over repair areas.
• use of direct laser lighting may preclude microscope viewing of the curing process.
• the task of detecting the precise height at which the microbrush or cantilever comes in contact with the substrate is accomplished by computer monitoring of the output of a Z-axis laser reflective sensor (Keyence Co ⁇ ., Japan) focused on the cantilever. Upon contact, a dramatic change in sensor output occurs, with sensitivity that allows detection of contact.
• the nanometer scale XYZ stage can move the cantilever in the XYZ directions, depositing ink on the 2D surface and on 3D surface structures.
• the task of detecting the precise height at which the cantilever comes in contact with the substrate is accomplished by computer monitoring of the output of a confocal distance sensor (again available from Keyence Co ⁇ .) targeted at the cantilever. Laser curing can be viewed as it occurs, as the confocal sensor may inco ⁇ orate a built-in CCD array.
• the invention further provides a method for the additive repair of gaps in open traces on a flat panel display substrate by local deposition of a precursor ink followed by curing of said ink to a conductive form, the method comprising the steps of: providing a cantilever (or microbrush); providing a precursor ink; disposing said ink on said cantilever; providing a substrate surface; contacting said cantilever and said substrate surface so that ink is delivered from the cantilever to the substrate surface; curing the deposited ink.
• Working Example 14 Bidirectional Writing and Cantilever Rotation
• gold traces were deposited from a 5 ⁇ m tipless cantilever loaded with gold nanoparticle ink across an insulating gap between conductive ITO (indium tin oxide) electrodes.
• FIG 35 explains how a gap may be formed near a topography step when drawing a line using a tipless cantilever.
• a cantilever draws a line with ink from right to left on top of two ITO islands on a non- conductive glass substrate, which are separated by a groove (see Figure 34).
• the cantilever end faithfully deposits ink over the right edge, but may be lifted from the bottom of the groove when the cantilever body hits the left edge. That may result in non-conductive lines after curing of the ink.
• a simple remedy to this problem consists of (i) writing a first layer of ink from, say, right to left; (ii) writing a second layer from left to right atop the first layer (a method nicknamed "bidirectional writing").
• the cantilever is rotated 180 degrees before writing the second layer, as best patterning results (narrowest lines) were obtained when moving the cantilever parallel to its length and from its free end towards its bound end. Otherwise, the cantilever may bend or buckle, releasing ink in unwanted areas. This is best achieved by inco ⁇ orating a cantilever rotation stage in the patterning instrument.
• this includes the use of said cantilever for (iii) the fabrication of network of conductive traces on flat panel displays; (ii) the repair or fabrication of other elements of flat panel displays than metallic conductive traces, including but not limited to semiconductive (polysilicon) layers, transparent conductive oxide layers (such as ITO); (iii) especially, the repair of color filters in flat panel displays; (iv) the repair or fabrication of other types of flat or flexible displays; including (v) the repair of organic light- emitting diode (OLED) displays; (vi) the fabrication or repair of the masks used in semiconductor chip manufacturing, including the photomasks used in UV photolithography; (vii) the fabrication or repair of micro- or nanostructured stamps or molds; (vii) the fabrication or repair of thin film resistors or other thick or thin film passive components, as well as (viii) other micron-scale precision deposition applications.
• the fabrication of network of conductive traces on flat panel displays including but not limited to semiconductive (polysilicon) layers, transparent conductive
• the cantilever used for CMD may be modified for better ink retention or deposition capabilities.
• the whole cantilever may be coated with a layer of polymer, such as PDMS (polydimethylsiloxane).
• Cantilevers with integrated actuators e.g. with an integrated heater and thermally driven bimo ⁇ h, may be used to better control patterning.
• Cantilevers adapted for CMD may be combined in the same chip with other devices, for example a Atomic Force Microscopy cantilever with integrated tip for high-resolution imaging or a cantilever with an heated tip for ink curing after deposition.

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• 2005
  • 2005-02-25 KR KR1020067019567A patent/KR101165484B1/ko not_active IP Right Cessation
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