WO1996027212A1 - An improved laser ablateable material - Google Patents
An improved laser ablateable material Download PDFInfo
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- WO1996027212A1 WO1996027212A1 PCT/US1996/002920 US9602920W WO9627212A1 WO 1996027212 A1 WO1996027212 A1 WO 1996027212A1 US 9602920 W US9602920 W US 9602920W WO 9627212 A1 WO9627212 A1 WO 9627212A1
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- WIPO (PCT)
- Prior art keywords
- pdp
- plasma
- gas
- chamber
- integrated circuit
- Prior art date
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- 239000000463 material Substances 0.000 title description 37
- 238000000034 method Methods 0.000 claims abstract description 54
- 229920000642 polymer Polymers 0.000 claims abstract description 15
- 230000005855 radiation Effects 0.000 claims abstract description 10
- 239000007789 gas Substances 0.000 claims description 48
- 239000000758 substrate Substances 0.000 claims description 25
- 238000005530 etching Methods 0.000 claims description 15
- 238000000151 deposition Methods 0.000 claims description 14
- 229910052751 metal Inorganic materials 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 14
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 10
- 229910052786 argon Inorganic materials 0.000 claims description 5
- 230000005684 electric field Effects 0.000 claims description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 4
- 150000002430 hydrocarbons Chemical class 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 150000002894 organic compounds Chemical class 0.000 claims description 4
- 238000001020 plasma etching Methods 0.000 claims description 2
- 230000003213 activating effect Effects 0.000 claims 2
- 238000000576 coating method Methods 0.000 abstract description 5
- 239000011248 coating agent Substances 0.000 abstract description 4
- 210000002381 plasma Anatomy 0.000 description 26
- 238000002679 ablation Methods 0.000 description 9
- 230000008569 process Effects 0.000 description 9
- 230000008021 deposition Effects 0.000 description 7
- 239000002245 particle Substances 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 229910021417 amorphous silicon Inorganic materials 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 238000002161 passivation Methods 0.000 description 4
- 238000005520 cutting process Methods 0.000 description 3
- 238000004880 explosion Methods 0.000 description 3
- 238000011049 filling Methods 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000005137 deposition process Methods 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 238000005459 micromachining Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- XPDICGYEJXYUDW-UHFFFAOYSA-N tetraarsenic tetrasulfide Chemical compound S1[As]2S[As]3[As]1S[As]2S3 XPDICGYEJXYUDW-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- FSIJKGMIQTVTNP-UHFFFAOYSA-N bis(ethenyl)-methyl-trimethylsilyloxysilane Chemical compound C[Si](C)(C)O[Si](C)(C=C)C=C FSIJKGMIQTVTNP-UHFFFAOYSA-N 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 150000001875 compounds Chemical group 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- ZQBFAOFFOQMSGJ-UHFFFAOYSA-N hexafluorobenzene Chemical compound FC1=C(F)C(F)=C(F)C(F)=C1F ZQBFAOFFOQMSGJ-UHFFFAOYSA-N 0.000 description 1
- NEXSMEBSBIABKL-UHFFFAOYSA-N hexamethyldisilane Chemical compound C[Si](C)(C)[Si](C)(C)C NEXSMEBSBIABKL-UHFFFAOYSA-N 0.000 description 1
- UQEAIHBTYFGYIE-UHFFFAOYSA-N hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000000608 laser ablation Methods 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000004377 microelectronic Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- UHUUYVZLXJHWDV-UHFFFAOYSA-N trimethyl(methylsilyloxy)silane Chemical compound C[SiH2]O[Si](C)(C)C UHUUYVZLXJHWDV-UHFFFAOYSA-N 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 238000009834 vaporization Methods 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02109—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates
- H01L21/02112—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer
- H01L21/02118—Forming insulating materials on a substrate characterised by the type of layer, e.g. type of material, porous/non-porous, pre-cursors, mixtures or laminates characterised by the material of the layer carbon based polymeric organic or inorganic material, e.g. polyimides, poly cyclobutene or PVC
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L29/00—Semiconductor devices specially adapted for rectifying, amplifying, oscillating or switching and having potential barriers; Capacitors or resistors having potential barriers, e.g. a PN-junction depletion layer or carrier concentration layer; Details of semiconductor bodies or of electrodes thereof ; Multistep manufacturing processes therefor
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/02104—Forming layers
- H01L21/02107—Forming insulating materials on a substrate
- H01L21/02225—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer
- H01L21/0226—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process
- H01L21/02263—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase
- H01L21/02271—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition
- H01L21/02274—Forming insulating materials on a substrate characterised by the process for the formation of the insulating layer formation by a deposition process deposition from the gas or vapour phase deposition by decomposition or reaction of gaseous or vapour phase compounds, i.e. chemical vapour deposition in the presence of a plasma [PECVD]
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L21/00—Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
- H01L21/02—Manufacture or treatment of semiconductor devices or of parts thereof
- H01L21/04—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer
- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
- H01L21/30—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26
- H01L21/31—Treatment of semiconductor bodies using processes or apparatus not provided for in groups H01L21/20 - H01L21/26 to form insulating layers thereon, e.g. for masking or by using photolithographic techniques; After treatment of these layers; Selection of materials for these layers
- H01L21/3105—After-treatment
- H01L21/311—Etching the insulating layers by chemical or physical means
- H01L21/31105—Etching inorganic layers
Definitions
- the present invention relates to materials which are ablateable by lasers of visual light and more particular ⁇ ly to methods of using such materials in the fabrication and customization of integrated circuits.
- Integrated circuits are usually manufactured in large runs. However it is frequently desirable to make small runs of a specific integrated circuit, typically for prototyping.
- US Patent 4,924,287 the disclosure of which is incorporated herein by reference, describes a customizable integrated circuit. Methods for customizing of such integrated circuits are shown in US Patent 5,329,152, the disclosure of which is also incorporated herein by reference.
- Customizable integrated circuits typically have predetermined portions which are adapted for modification before being supplied to the end user.
- modifications include, inter alia:
- Customization by cutting of conductor links is preferred since this method does not require extra cir ⁇ cuitry on the integrated circuit as do electrically programmable logic devices. Furthermore, pre-produced links can carry a higher current density than created links.
- Two methods are mainly used to selectively cut links.
- One method is to cut each link directly with a laser beam.
- direct cutting with a laser may require high laser energy densities.
- Application of large amounts of laser energy to integrated circuit surfaces may damage the integrated circuit.
- a preferred method of customizing such circuits is to coat them with a layer of laser sensitive ablative material and to ablate the material at selected locations using a relatively small amount of laser radiation. After such ablation, the integrated circuit is etched using an etchant or other etching method that does not remove the ablative material, for example, by chlorine plasma etch ⁇ ing. Thus, only areas previously ablated by the laser are etched.
- Customizable areas typically include metal links so that etching the links modifies the interconnections, and therefore the function, of the integrated circuit.
- An efficient laser ablative material should be capable of absorbing a large portion of the laser energy and in response thereto be transformed directly and immediately to gas. Laser ablation sometimes causes the material to explode. Explosion transforms part of the material to gas, however, some of the material is also blown away as particles. Some of these particles may fall back on the chip and cover-up previously uncovered areas, counteracting the ablation/explosion at these areas. An effective laser ablative material should not form many particles. The term ablation means that the material is turned directly to gas, and very few particles are formed.
- the resultant ablation pattern be as close as possible to the irradiation pat ⁇ tern and that only small amounts of energy leak into the surrounding area and into the integrated circuit.
- the definition of the geometry will be poor and the integrated circuit may be damaged.
- the material should adhere well to substrates and provide good coverage of step geometries used in microelectronic circuits. Since the purpose of the coating is to protect coated areas while etching the uncoated areas, it is important that the material be resistant to at least one method of etching, preferably a metal etching method.
- Arsenic Sulfide An example of a material which has some but not all of the previous properties is Arsenic Sulfide.
- Arsenic Sulfide has most of the abovementioned properties, howev ⁇ er, since it does not cover uneven surfaces very well it is not as useful as other materials.
- Visible light is preferred to ultra violet light because laser technology supplies more efficient and less expensive lasers in visible light wavelengths.
- US Patent 5,329,152 discloses the use of amorphous silicon as a visible light laser ablative coating materi ⁇ al.
- Amorphous silicon is ablated by visible light lasers and is partially resistant to etching by chlorine plas ⁇ ma, which is used to etch metals.
- chlorine plas ⁇ ma which is used to etch metals.
- an integrated circuit with exposed metal links can be customized by using amorphous silicon as the ablative material.
- PDP Plasma deposited polymers
- PDPs are typically manufactured as follows:
- a substrate is placed in a plasma chamber.
- the chamber is then filled with a gas, such as methane, at a low pressure, typically on the order of 1 torr.
- Plasma is then created in the chamber, typically using a radio frequency (RF) electric field which ion ⁇ izes the gas. Consequently, a polymer layer is continual ⁇ ly deposited on the substrate.
- RF radio frequency
- a PDP is not a direct polymer of the gas used in the process. It is believed that the gas breaks down in the plasma and gas precursors and their compounds form the PDP which is then deposited on the substrate (and on the walls of the chamber) .
- the deposition process is a combination of two processes, one in which molecules hit the substrate and cling, and another in which they do not cling, and may even cause some material to be etched off the substrate.
- the temper ⁇ ature of the substrate dictates the types of molecules which are likely to cling to the substrate and the manner in which they will be attached to the PDP already deposi ⁇ ted.
- the gas usually flows through the chamber at a rate which determines the types of molecules that form in the plasma and, consequently, the type of PDP deposited.
- the gas used is typically an organic compound. However, some inert gases, such as argon, may be added in order to speed up the deposition process. It has also been observed that similar polymers can be created from different starting materials.
- the inventors have discovered a method of depositing a Plasma Deposited Polymer (PDP) which is laser-ablative by laser light having a wavelength longer than ultra ⁇ violet light, such as visible light.
- PDP Plasma Deposited Polymer
- the PDP is deposited in the following manner:
- an inactive gas such as argon is added to the active gas at a ratio between 3:7 and 7:3, prefer ⁇ ably, at a ratio between 4:6 and 6:4; most preferably, at a 1:1 ratio.
- the gas mixture is introduced through the anode and turned into a plasma in the cham ⁇ ber.
- the gas is first turned into a plasma and then introduced into the chamber.
- the inactive gas may be added before or after the active gas is turned into a plasma.
- the substrate is preferably maintained at a tempera ⁇ ture below 70 ⁇ C.
- a pressure of between 0.1 and 2 torr is maintained, preferably, between 0.5 and 1.5 torr.
- the inventors have found that a pressure of about 1 torr is most preferred.
- the active gas used is preferably organ ⁇ ic, preferably, a hydro-carbon; typically, ethylene is used.
- the gas is introduced into the chamber at a flow rate between 1 seem and 50 seem, preferably between 10 and 35 seem and most preferably, about 20 seem. Prefera ⁇ bly, .
- Ionization of the gas is achieved with an RF power density between 0.15 Watt*cm and 1 Watt*cm ⁇ 2 ; most preferably, the power density is between 0.24 Watt*cm ⁇ 2 and 0.48 Watt*cm ⁇ .
- the RF radiation is continuous at 13.6MHz.
- other methods of applica ⁇ tion of RF enegry may be used, such as pulsed RF radia ⁇ tion at a frequency of 400MHz.
- the cathode is 8" in diameter. The distance between the cathode and the anode is between 1.5 and 10 cm, preferably 3 cm.
- a typical deposition time of approximately 10 minutes will produce a polymer of a typically desired thickness of approximately l ⁇ .
- a PDP deposited under the abovementioned conditions has one or more of the following properties:
- the material when ablated by laser, preferably a visible light laser, the material absorbs enough of the incident laser energy directed at it so that underlying layers are not damaged by laser energy;
- the material is ablative, i.e., it vaporizes rather than explodes, so that very little debris is formed on the substrate when the material is ablated;
- the material has good filling qualities, so that it can be deposited evenly over non leveled geometries;
- the material is insulative
- the material adheres well to the substrate; (i) the material is resistant to at least some forms of metal etching;
- the material is etchable by some means, which preferably do not etch the structure of the underlying integrated circuit.
- a PDP having a selected absorption coefficient can be deposited by properly selecting the power density used to generate said plasma.
- a method of customizing integrated circuits providing an integrated circuit; depositing a PDP on the integrated circuit; and ablating the PDP at preselected locations using a laser beam, preferably a visible light laser beam.
- the integrated circuit is then etched, preferably by reactive ion etching, at locations underly ⁇ ing said ablated locations.
- Also provided in accordance with a preferred embodi ⁇ ment of the invention is an integrated circuit coated with a PDP ablateable by visible light.
- Fig. 1 is a schematic of a vapor deposition chamber as used in forming an ablative layer in accordance with a preferred embodiment of the invention
- Figs. 2A-2C show an integrated circuit customized in accordance with a preferred embodiment of the invention.
- Figs. 3A-3D show an integrated circuit customized in accordance with an alternative preferred embodiment of the invention.
- Fig. 1 shows a plasma vacuum chamber 1 suitable for depositing a Plasma Deposited Polymer (PDP) on a sub ⁇ strate, for example, a Plasma-Therm model 790 vacuum chamber.
- PDP Plasma Deposited Polymer
- a substrate 3, to be coated with a PDP is placed in chamber 1, preferably on a cathode 4.
- the temperature of substrate 3 may be controlled by a heater/cooler 5 such that during deposition the substrate is maintained at a substantially constant temperature.
- the substrate is maintaining at 20 ⁇ C while the walls of the chamber are heated.
- a pump 2 reduces the gas pressure in chamber 1.
- the pressure in the chamber during the deposition is approximately 1 torr, however, pres ⁇ sures between 0.1 and 2 torr are useful in carrying out the invention.
- a gas is supplied to chamber 1, preferably through a plurality of nozzles 8 formed in an anode 6.
- the gas is typically a mixture of an active gas, preferably an organic compound such as ethylene or another hydro-carbon and an inactive gas such as argon.
- the ratio between the active gas and the inactive gas is between 7:3 and 3:7, preferably, at a ratio of about 1:1.
- the rate at which the gas mixture is supplied is called the "flow rate" and is preferably between 1 seem and 50 seem, preferably 20 seem.
- the power output of RF generator 6 is typically between 25W and 500W, preferably, between 75W and 150W.
- anode 6 and (the walls of) chamber 1 are grounded and a voltage differential appears between them and cathode 4.
- the distance between anode 6 and cathode 4 is between 1.5 and 10 cm, preferably, 3 cm.
- the active gas is turned into a plasma in a separate compartment within the chamber.
- the inactive gas may be added to the active gas before or after it is turned into a plasma.
- a layer of PDP is continuously deposited on substrate 3.
- a layer having a thickness of about 0.6 ⁇ is deposit ⁇ ed within less than 15 minutes.
- a PDP deposited according to the abovementioned configuration will be ablateable by visible laser light and will have some or all of the following properties:
- a PDP depos ⁇ ited according to a preferred embodiment of the invention has an evenly monotonicly decreasing absorption coeffi ⁇ cient in the visible light range. Thus, it is easily ablateable by ultraviolet light lasers and also ablate ⁇ able by laser light in the near infra red.
- FIGs. 2A - 2C show customization of an integrated circuit in accordance with the present invention.
- Fig 2A shows an integrated circuit which includes a metal layer 901, separated from a second metal layer 902 by an insulation layer 904.
- Layer 902 is also covered by a second insula ⁇ tion layer 905, and another metal layer 903 covers layer 905.
- the entire top of the integrated circuit is prefera ⁇ bly covered with a passivation layer 436.
- customi- zation preferably includes disconnecting metal links in layers 902 and/or 903, a plurality of apertures 422 are preferably formed through passivation layer 436 and through any intervening layers down to a metal link 438 that is to be disconnected.
- a first step of the customization process includes depositing a layer 900 of PDP over the integrated circuit.
- the layer is l ⁇ thick. Since PDP layer 900 is preferably stable at ambi ⁇ ent room conditions, the coated integrated circuit is preferably manufactured in large runs and stored until needed.
- a second step of the customization process includes ablating PDP layer 900 at selected locations. Preferably these locations are over apertures 422.
- a NdYAG frequency doubled laser at 532nm or Nd YLF at 523nm is used for ablating PDP layer 900.
- an Argon laser at 514nm or at 488nm is used.
- the pulses are approximately 100 nano ⁇ seconds long and have an energy density of approximately 4 J/cm .
- the ablations can be performed using a laser micromachining system, preferably, a QS650 available from Chip Express (Israel) LTD.
- a third step of the customization process includes etching the integrated circuit, preferably, using Chlorine plasma.
- the remaining PDP is removed by Oxygen plasma and a passivation layer is formed over the cus ⁇ tomized integrated circuit.
- Figs. 3A-3D show an alternative preferred customiza ⁇ tion process similar to the abovedescribed process.
- the integrated circuit is first coated with a planarization layer 906, preferably silicon diox ⁇ ide or other insulating planerizing materials as well known in the art, before the step of depositing PDP layer 900 thereon (Fig. 3A) .
- Fig. 3B shows the device after layer 900 is ablated at selected locations.
- An additional step of etching planarization layer 906, preferably with CF 4 plasma is preformed (Fig. 3C) before etching the integrated circuit itself (Fig. 3D) .
- the inventors have found that the ablation pattern of the PDP is very similar to the irra ⁇ diation pattern used, so that very precise micromachining of the PDP is possible.
- the depth of the cut is con ⁇ trolled with a precision of 0.3 ⁇ or better.
- the radius of curvature at the corners of rectangular cuts is 0.2 ⁇ or less, even though a wavelength of .532 ⁇ was used. This is attributed to the threshold nature of the ablation proc ⁇ ess and to the properties of imaging with laser coherent light.
- the inventors have found that the PDP is more versatile than using standard photo-resists because it does not need to be developed and washed away. Further ⁇ more, the inventors has discovered that the optical properties of the PDP, in particular absorption, can be controlled by changing the RF power used to ionized the gas, therefore, a PDP layer with the correct absorption can be produced for any chosen laser wavelength and any desirable film thickness. Additionally, the etch resist ⁇ ance properties of the PDP are similar to those of stand ⁇ ard photo-resists.
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- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Manufacturing & Machinery (AREA)
- Chemical & Material Sciences (AREA)
- Plasma & Fusion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Ceramic Engineering (AREA)
- Inorganic Chemistry (AREA)
- Drying Of Semiconductors (AREA)
- Laser Beam Processing (AREA)
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8526446A JPH11502060A (en) | 1995-02-28 | 1996-02-27 | Improved laser ablation material |
US08/894,540 US6255718B1 (en) | 1995-02-28 | 1996-02-27 | Laser ablateable material |
EP96908627A EP0812477A4 (en) | 1995-02-28 | 1996-02-27 | An improved laser ablateable material |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IL11282695A IL112826A (en) | 1995-02-28 | 1995-02-28 | Method for depositing a plasma deposited polymer |
IL112,826 | 1995-02-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996027212A1 true WO1996027212A1 (en) | 1996-09-06 |
Family
ID=11067145
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1996/002920 WO1996027212A1 (en) | 1995-02-28 | 1996-02-27 | An improved laser ablateable material |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP0812477A4 (en) |
JP (1) | JPH11502060A (en) |
KR (1) | KR19980702598A (en) |
CA (1) | CA2214109A1 (en) |
IL (1) | IL112826A (en) |
WO (1) | WO1996027212A1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015034690A1 (en) * | 2013-09-04 | 2015-03-12 | Tokyo Electron Limited | Uv-assisted stripping of hardened photoresist to create chemical templates for directed self-assembly |
GB2529620A (en) * | 2014-08-18 | 2016-03-02 | Flexenable Ltd | Patterning layer stacks for electronic devices |
US9715172B2 (en) | 2013-10-20 | 2017-07-25 | Tokyo Electron Limited | Use of topography to direct assembly of block copolymers in grapho-epitaxial applications |
US9793137B2 (en) | 2013-10-20 | 2017-10-17 | Tokyo Electron Limited | Use of grapho-epitaxial directed self-assembly applications to precisely cut logic lines |
US9947597B2 (en) | 2016-03-31 | 2018-04-17 | Tokyo Electron Limited | Defectivity metrology during DSA patterning |
US10304720B2 (en) | 2016-07-15 | 2019-05-28 | Brewer Science, Inc. | Laser ablative dielectric material |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8268675B2 (en) * | 2011-02-11 | 2012-09-18 | Nordson Corporation | Passivation layer for semiconductor device packaging |
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WO1995006900A1 (en) * | 1993-09-03 | 1995-03-09 | Hitachi, Ltd. | Method and apparatus for pattern formation |
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1995
- 1995-02-28 IL IL11282695A patent/IL112826A/en not_active IP Right Cessation
-
1996
- 1996-02-27 EP EP96908627A patent/EP0812477A4/en not_active Withdrawn
- 1996-02-27 KR KR1019970706003A patent/KR19980702598A/en not_active Application Discontinuation
- 1996-02-27 CA CA002214109A patent/CA2214109A1/en not_active Abandoned
- 1996-02-27 WO PCT/US1996/002920 patent/WO1996027212A1/en not_active Application Discontinuation
- 1996-02-27 JP JP8526446A patent/JPH11502060A/en active Pending
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US4177474A (en) * | 1977-05-18 | 1979-12-04 | Energy Conversion Devices, Inc. | High temperature amorphous semiconductor member and method of making the same |
US4226898A (en) * | 1978-03-16 | 1980-10-07 | Energy Conversion Devices, Inc. | Amorphous semiconductors equivalent to crystalline semiconductors produced by a glow discharge process |
US4517223A (en) * | 1982-09-24 | 1985-05-14 | Sovonics Solar Systems | Method of making amorphous semiconductor alloys and devices using microwave energy |
US5329152A (en) * | 1986-11-26 | 1994-07-12 | Quick Technologies Ltd. | Ablative etch resistant coating for laser personalization of integrated circuits |
US5470661A (en) * | 1993-01-07 | 1995-11-28 | International Business Machines Corporation | Diamond-like carbon films from a hydrocarbon helium plasma |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2015034690A1 (en) * | 2013-09-04 | 2015-03-12 | Tokyo Electron Limited | Uv-assisted stripping of hardened photoresist to create chemical templates for directed self-assembly |
US10490402B2 (en) | 2013-09-04 | 2019-11-26 | Tokyo Electron Limited | UV-assisted stripping of hardened photoresist to create chemical templates for directed self-assembly |
US11538684B2 (en) | 2013-09-04 | 2022-12-27 | Tokyo Electron Limited | UV-assisted stripping of hardened photoresist to create chemical templates for directed self-assembly |
US9715172B2 (en) | 2013-10-20 | 2017-07-25 | Tokyo Electron Limited | Use of topography to direct assembly of block copolymers in grapho-epitaxial applications |
US9793137B2 (en) | 2013-10-20 | 2017-10-17 | Tokyo Electron Limited | Use of grapho-epitaxial directed self-assembly applications to precisely cut logic lines |
GB2529620A (en) * | 2014-08-18 | 2016-03-02 | Flexenable Ltd | Patterning layer stacks for electronic devices |
CN107078027A (en) * | 2014-08-18 | 2017-08-18 | 弗莱克因艾伯勒有限公司 | By the layer stack pattern for electronic installation |
US10541258B2 (en) | 2014-08-18 | 2020-01-21 | Flexenable Limited | Patterning layers stacks for electronic devices |
CN107078027B (en) * | 2014-08-18 | 2021-05-25 | 弗莱克因艾伯勒有限公司 | Patterning layer stacks for electronic devices |
US9947597B2 (en) | 2016-03-31 | 2018-04-17 | Tokyo Electron Limited | Defectivity metrology during DSA patterning |
US10304720B2 (en) | 2016-07-15 | 2019-05-28 | Brewer Science, Inc. | Laser ablative dielectric material |
Also Published As
Publication number | Publication date |
---|---|
KR19980702598A (en) | 1998-08-05 |
IL112826A0 (en) | 1995-05-26 |
EP0812477A4 (en) | 1998-10-07 |
JPH11502060A (en) | 1999-02-16 |
CA2214109A1 (en) | 1996-09-06 |
EP0812477A1 (en) | 1997-12-17 |
IL112826A (en) | 1998-09-24 |
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