GB2366766A - Reactive ion etching a magnetic material - Google Patents

Reactive ion etching a magnetic material Download PDF

Info

Publication number
GB2366766A
GB2366766A GB0128508A GB0128508A GB2366766A GB 2366766 A GB2366766 A GB 2366766A GB 0128508 A GB0128508 A GB 0128508A GB 0128508 A GB0128508 A GB 0128508A GB 2366766 A GB2366766 A GB 2366766A
Authority
GB
United Kingdom
Prior art keywords
ion etching
alloy
mask
magnetic material
etching
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
GB0128508A
Other versions
GB2366766B (en
GB2366766B8 (en
GB2366766A8 (en
Inventor
Isao Nakatani
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Japan Science and Technology Agency
National Research Institute for Metals
Original Assignee
National Research Institute for Metals
Japan Science and Technology Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from JP09256636A external-priority patent/JP3131595B2/en
Priority claimed from JP09256635A external-priority patent/JP3131594B2/en
Application filed by National Research Institute for Metals, Japan Science and Technology Corp filed Critical National Research Institute for Metals
Priority claimed from GB9820639.4A external-priority patent/GB2331273B8/en
Publication of GB2366766A publication Critical patent/GB2366766A/en
Publication of GB2366766B publication Critical patent/GB2366766B/en
Application granted granted Critical
Publication of GB2366766B8 publication Critical patent/GB2366766B8/en
Publication of GB2366766A8 publication Critical patent/GB2366766A8/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y25/00Nanomagnetism, e.g. magnetoimpedance, anisotropic magnetoresistance, giant magnetoresistance or tunneling magnetoresistance
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y40/00Manufacture or treatment of nanostructures
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F41/00Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
    • H01F41/14Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying magnetic films to substrates
    • H01F41/30Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying magnetic films to substrates for applying nanostructures, e.g. by molecular beam epitaxy [MBE]
    • H01F41/302Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying magnetic films to substrates for applying nanostructures, e.g. by molecular beam epitaxy [MBE] for applying spin-exchange-coupled multilayers, e.g. nanostructured superlattices
    • H01F41/308Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying magnetic films to substrates for applying nanostructures, e.g. by molecular beam epitaxy [MBE] for applying spin-exchange-coupled multilayers, e.g. nanostructured superlattices lift-off processes, e.g. ion milling, for trimming or patterning
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F41/00Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
    • H01F41/32Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying conductive, insulating or magnetic material on a magnetic film, specially adapted for a thin magnetic film
    • H01F41/34Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for applying conductive, insulating or magnetic material on a magnetic film, specially adapted for a thin magnetic film in patterns, e.g. by lithography
    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B5/00Recording by magnetisation or demagnetisation of a record carrier; Reproducing by magnetic means; Record carriers therefor
    • G11B5/127Structure or manufacture of heads, e.g. inductive
    • G11B5/31Structure or manufacture of heads, e.g. inductive using thin films
    • G11B5/3163Fabrication methods or processes specially adapted for a particular head structure, e.g. using base layers for electroplating, using functional layers for masking, using energy or particle beams for shaping the structure or modifying the properties of the basic layers

Abstract

The invention provides a method for reactive-ion etching a magnetic material with a plasma of a mixed gas of carbon monoxide and a nitrogen-containing compound e.g. NH<SB>3</SB>, the method comprising exposing a multilayered film comprising a magnetic material thin film having thereon a resist film formed on a substrate to an electron beam and then developed, to form a pattern on the resist film, vacuum depositing a mask material, dissolving the resist to form a mask, and removing a part of the magnetic material thin film that is not covered with the mask by reactive ion etching with a plasma of a mixed gas of carbon monoxide and a nitrogen-containing compound, to form a pattern on the magnetic material thin film.

Description

<Desc/Clms Page number 1> METHOD FOR REACTIVE ION ETCHING FIELD OF THE INVENTION The present invention relates to a method for reactive ion etching. More specifically, the invention relates to a novel method for reactive ion etching using a novel mask material, which is characterized by a dry etching method for @a magnetic material, which is useful for producti on of a magnetic head for read-wri to of a magnetic di sk, a microtrans former or a microinductor installed in a magnetic integrated circuit, a magnetic sensor, various quantum magnetic devices, such as a spin scattering magnetoresistance effect device, a spin valve device, a ferromagnetic tunneling device, a spin diode and a spin transistor, and a constitutional part of a micromachine, such as a thin film magnet and a magnetostrictive actuator.
BACKGROUND OF THE INVENTION A microsemiconductor device such as a VLSI and a micromagnetic device are generally produced by a combination of two processes, i.e., a lithography technique and an etching technique.
The lithograph technique is a technique of producing fine patterns on a photosensitive film such as a resist film coated on a surface of a material to be processed, such as a thin film
<Desc/Clms Page number 2>
of a semiconductor and a thin film of a magnetic material, which includes a photolithography technique where exposure is conducted with an ultraviolet ray, an electron beam lithography technique where exposure is conducted with an electron beam, and an ion beam lithography technique where exposure is conducted with an ion beam.
The etching technique is a technique of producing a device by transferring the resist pattern produced by the lithography to the material to be processed, such as a thin film of a semiconductor and a thin film of a magnetic material.
The etching technique includes a wet etching method, an argon ion milling method and a reactive ion etching method. Among these etching methods, the reactive ion etching method is the most excellent method because the pattern produced by the lithography can be transferred in the most precise manner, it is most suitable for fine working, and the etching rate is the largest. LSIs of semiconductors and semiconductor memory devices are actually produced by this method.
In the reactive ion etching method, a material to be processed is placed in a plasma of a reactive gas with applying an electric field, and atoms on the surface of the material to be processed is chemically and physically removed by an ion beam incident normally onto the surface of the material to be processed, by which an anisotropic working is possible, where a part not covered with the mask is vertically cut along the
<Desc/Clms Page number 3>
edge of the mask. Accordingly, a fine and sharp feature can be transferred by the reactive ion etching method. In the reactive ion etching method, chemical active species such as an ion and a radical of the reactive gas generated in the plasma are adsorbed on the surface of the material to be processed, to chemically react with the material to be processed, and a surface reactive layer having a lower bond energy. The surface of the material to be processed is exposed to the impact of cations accelerated by the electric field in the plasma, and thus the surface reactive layer having a lower bond energy is removed by the sputtering effect by ions or the evaporation effect of itself. That is, the reactive ion etching method is a process, which proceeds with a chemical action and a physical action simultaneously. As a result, the selectivity of etching only a specific material, and the anisotropy of vertically etching the surface of the material to be processed can be realized.
However, an effective reactive ion etching method has not been developed for a magnetic material for a long time. The wet etching method or the argon ion milling is actually used for a magnetic material, to produce a thin film magnetic head, a magnetic sensor and a microtrans former.
Under the circumstances with respect to a magnetic material, the tendencies of the miniaturization and the high density integration of a magnetic material is considerably
<Desc/Clms Page number 4>
delayed, which becomes a difficulty of development of these devices.
The reason why the reactive ion etching of a magnetic material is difficult is as follows. While the magnetic material mainly composed of a transition metal element can react with most of etching gases having been developed for etching semiconductor materials (e.g., CF4, CC14, CC12F2, CClF3, CBrF3, C12, C2F6, C3F8, C4Fzo, CHF3, C2H2, SF6, SiF4, BC13, PC13, SiC14, HC1 and CHClF2), only a reaction product having a far larger bond energy than the reaction product of the semiconductor material is produced. Therefore, it cannot be removed by the sputtering or the evaporation, and etching cannot proceed.
Under the circumstances, an investigation of a novel reactive ion etching process has been investigated that is not analogical inference of the existing technique for semiconductors , and recently a method using a plasma of a mixed gas of carbon monoxide (CO) and ammonia gas (NH3) has been developed by the inventor of the invention. The principal of this method is that a carbonyl compound of a transition metal (e.g., Fe (CO) 5, Ni (CO) 4, Cot (CO) e, Mn2 (CO) lo, Cr (CO) 6, V (CO) 6, MO(CO)6 and W(CO)6) is formed on the surface of the magnetic material mainly composed of a transition metal element as a material to be processed by an active radial of CO, which is then removed by the evaporation or the sputtering of an ion in vacuum, to proceed etching. The carbonyl compound of a
<Desc/Clms Page number 5>
transition metal is the compound having the smallest bond energy among the transition metal compounds. However, since CO is decomposed to C02 and C through a disproportionation reaction, an introduced CO gas does not contribute to the reaction, and the free C atom reacts with the transition metal element to form a stable transition metal carbide, and therefore an etching reaction does not proceed in general. The NH3 gas plays a role of delaying the disproportionation reaction in the presence of the transition metal element, and the objective reactive ion etching can proceed in the plasma of a gas obtained by mixing the substantially same amounts of CO gas and NH3 gas.
By a method according to this principal, it has been confirmed that magnetic materials, such as a permalloy (Fe-Ni alloy) , a Co-Cr alloy and Fe, can be subjected to the reactive ion etching. As a result of the development of such an excellent reactive ion etching method for a magnetic material, further technical development of the method has been expected. However, this method involves a problem in that the etching rate is not so large, for example, 34 nm/min, although working of fine patterns and anisotropic shapes can be realized.
Furthermore, in the conventional etching method using the CO-NH3 mixed gas plasma, an Si02 film produced by a sputtering method has been used as a mask material that is difficult to suffer the etching reaction, and there is a problem in that the working precision and productivity of the Si02 film are limited.
<Desc/Clms Page number 6>
Figure 2 shows a schematic flow diagram of the conventional process.
In step (a) of Figure 2, on a substrate material such as Corning 7059 glass substrate 1, a ferromagnetic thin film to be processed such as a permalloy (Fe-Ni alloy) 2 is formed by a sputtering method, a quartz (Si02) thin film 3 as a mask material and a conductive material such as an amorphous carbon film 4 are formed in this order by a sputtering method, and a resist 5 as an electron beam-sensitive film is coated, for example, by a spin coating method. The amorphous carbon film 4 is a conductive layer necessary for not charging the material to be processed on electron beam exposure, which becomes necessary since the quartz (SiO2) film 3 is an insulating material. In step (b) of Figure 2, a desired pattern is formed on the resist by electron beam writing and development. The amorphous carbon layer is etched by oxygen-ion etching with using the resist pattern as a mask, to expose the Si02 film along with the pattern (step (c) in Figure 2) . The Si02 film is then etched with carbon tetrafluoride (CF4), for example, to transfer the pattern onto the Si02 film. The ion etching with CF4 is effective only to the SiO2 film, and the permalloy as the objective material to be processed is not changed (step (d) of Figure 2).
The pattern transferred to the Si02 film is then transferred onto the permalloy with using the patterned Si02
<Desc/Clms Page number 7>
as a mask by the reactive ion etching method using the CO-NH3 mixed gas plasma described above. The resist film and the amorphous carbon film are also removed through the reactive-ion etching, and the Si02 remains on the patterned permalloy, to complete the transfer of the pattern (step (e) of Figure 2). The fine working with reactive-ion etching of a magnetic material, such as a permalloy (Fe-Ni alloy) , a Co-Cr alloy and Fe, has been conducted according to this conventional process.
However, the conventional process involves a problem in that not only the process is complicated with deteriorated productivity, but also since the transfer is twice performed, high precision of a transferred pattern cannot be obtained. In the conventional process, a pattern corresponding to the part that is has not been exposed to an electron beam finally remains, and as a result, the inverted pattern of the pattern exposed to an electron beam, i.e., a negative pattern, is provided. However, in the course of the production of a complicated and fine structure of a magnetic material, it is also necessary to provide a pattern corresponding to the part that has been exposed to an electron beam, i.e., a positive pattern.
SUMMARY OF THE INVENTION An-object of the invention is to solve the problems associated with the conventional techniques, and to provide a novel method using a novel mask material
<Desc/Clms Page number 8>
that realizes effective reactive ion etching of a magnetic material with a large etching rate, etching with ease and a high resolution and precision, and provision of a positive pattern.
The invention relates to a method for reactive ion etching a magnetic material with a plasma of a mixed gas of carbon monoxide and a nitrogen-containing compound, the method comprising a step, in which a multilayered film comprising a magnetic material thin film having thereon a resist film formed on a substrate is exposed to an electron beam and then developed, to form a pattern on the resist film, a step, in which a mask material is vacuum deposited, a step, in which the resist is dissolved, to form a mask, and a step, in which a part of the magnetic material thin film that is not covered with the mask is removed by reactive-ion etching with a plasma of a mixed gas of carbon monoxide and a nitrogen-containing compound, to form a pattern on the magnetic material thin film, and thus obtaining the magnetic material thin film finely worked.
In the method for reactive-ion etching of the invention described above, the mask used in the reactive ion etching may comprise at least one member selected from the group consisting of titanium, magnesium, aluminum, germanium, platinum,
<Desc/Clms Page number 9>
palladium, an alloy comprising at least one of them as a main component, and a compound thereof.
In the method for reactive-ion etching of the invention, the mask used in the reactive-ion etching may comprise silicon or an alloy comprising silicon as a main component.
In the method for reactive-ion etching of the invention, the mask used in the reactive-ion etching may comprise a compound of silicon, and may be disposed on the pattern formed on the resist film and formed into the mask by a lift-off method.
The invention also relates to an apparatus for reactive ion etching comprising a reaction chamber and metallic parts contained in the reaction chamber, the whole or a part of which comprises at least one metallic material selected from the group consisting of titanium, aluminum, and an alloy comprising at least one of them as a main component.
In the apparatus for reactive ion etching of the invention described above, a surface layer of the whole or a part of the reaction chamber and metallic parts contained in the reaction chamber comprises the at least one metallic material.
In the apparatus for reactive-ion etching of the invention, a susceptor for supporting a material to be etched comprises at least one metallic material described above. In the apparatus for reactive ion etching of the invention, at least one of a high frequency electrode, a high frequency antenna, an ground electrode, a zero potential shield and a
<Desc/Clms Page number 10>
protective plate comprises the at least one metallic material described above.
BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 is a schematic flow diagram of a fine working of a magnetic material according to one embodiment of the invention.
Figure 2 is a schematic flow diagram of a fine working of a magnetic material according to the conventional process. Figure 3 is a schematic cross sectional view of an apparatus for reactive-ion etching of a parallel flat plates type according to one embodiment of the invention.
Figure 4 is a schematic cross sectional view of an apparatus for reactive ion etching of an inductive coupling type according to one embodiment of the invention.
Figure 5 is a schematic cross sectional view of an apparatus for reactive ion etching of an electron cyclotron resonance type according to one embodiment of the invention.
Figures 6A, 6B and 6C are electron micrographs showing etch features of magnetic materials.
DESCRIPTION OF THE PREFERRED EMBODIMENTS The invention relates to a method for reactive ion etching of a magnetic material with a plasma of a mixed gas of carbon monoxide and a
<Desc/Clms Page number 11>
nitrogen-containing compound, and an apparatus for reactive-ion etching.
The invention is described in detail below. (a) Mask for Reactive Ion-Etching A mask substance having been generally used in the semiconductor technique is a resist itself, which is a polymer material. However, the various polymer resists cannot be used as a mask in a CO-NH3 gas plasma due to its large loss. Metallic elements, such as Cr, W, Mo, Mn, Nb, Ta, Fe, Ru, Os, Co, Rh, Ir, Ni, Cu, Ag, Au, Ga, In and Sn, and an alloy or compound comprising them as a main component are not suitable as the mask material because they react with the CO-NH3 gas plasma and themselves are etched by the sputtering action to be worn out. Metallic elements, such as Zn, Cd and Pb, and an alloy or compound comprising them as a main component are also not suitable because they are poor in resistance in vacuo. On the other hand, it has been found from experimental results that Ti, Mg, Al, Si, Ge, Pt, Pd, an alloy comprising at least one of them as a main component, and a compound thereof are suitable as the mask material because they are difficult to react with the CO-NH3 gas plasma. Among these, the most preferred are Ti and an alloy or a compound comprising Ti as a main component in view of the requirements of chemical stability, dense packing of crystalline grains, and difficulty of generation of pinholes.
<Desc/Clms Page number 12>
In the invention, the mask may comprise at least one member selected from the group consisting of Ti, Mg, Al, Ge, Pt, Pd, an alloy comprising at least one of them as a main component, and a compound thereof. For example, the mask comprises at least one of a single metal of Ti, Mg, A-1, Ge, Pt or Pd, a Ti alloy, a Mg alloy, an Al alloy, a Ge alloy, a Pt alloy, a Pd alloy, a Ti-Mg alloy, a Ti-A1 alloy, a Ti-Ge alloy, a Ti-Pt alloy, a Ti-Pd alloy, a Mg-A1 alloy, a Mg-Ge alloy, a Mg-Pt alloy, a Mg-Pd alloy, an Al-Ge alloy, an Al-Pt alloy, an Al-Pd alloy, a Ge-Pt alloy, a Ge-Pd alloy, a Ti-Mg-A1 alloy, a Ti-Al-Ge alloy, a Ti-Mg-Ge alloy, a Ti-Mg-Pt alloy, a TiAl-Pd alloy, a Mg-Al-Ge alloy, Ti02, Mgo, MgF2, A1203, TiN, A1N, MgN, Ge02 and PdO. The term "at least one" used herein means that the whole mask may comprise only one member of them, and the mask may comprise plural kinds of them, which may constitute part by part of the mask, may constitute a laminated structure, or may constitute the exposed surface layer of the mask.
In the invention, the mask may also comprise silicon or an alloy comprising silicon as a main component, as well as a compound of silicon, such as Si02 and Si3N4. Preferred example of the alloy of silicon include those comprises silicon and the above-described metallic elements, e. g., Ti, Mg, Al and Ge,such as a Ti-Si alloy, a Si-A1 alloy, a Si-Ge alloy, a Si-Pt alloy, a Si-Pd alloy, a Ti-Si-Al alloy, a Ti-Mg-Si alloy and an Al-Mg-Si alloy.
<Desc/Clms Page number 13>
While Si02 has been considered as a material for a mask, it has been used in the method in which the pattern is twice transferred. In the invention, on the other hand, it is used as a novel mask by using the lift-off method.
The mask can be formed by various methods, such as vacuum deposition, sputtering, ion plating or ion-beam deposition. Figure 1 shows one embodiment of a schematic flow diagram of the fine working with respect to the method of the invention. In step (a) of Figure 1, a magnetic material thin film 2 as a material to be subjected to the fine working is formed on a substrate material 1 such as Corning 7059 glass, and a resist film 5 is coated thereon, for example, by a spin coating method. The resulting multilayer is exposed to an electron beam, and then developed, to form a desire pattern 6 on the resist film 5 (step (b) of Figure 1). A mask material 7 such as Ti is vapor deposited (step (c) of Figure 1) , and a Ti mask 8 is formed by a lift-off method, i. e. dissolution of the polymer resist (step (d) of Figure 1) . Apart of the magnetic material thin film that is not covered with the Ti mask is removed by reactive-ion etching with a CO-NH3 mixed gas plasma, to form a pattern on the magnetic material thin film, and thus obtaining the magnetic material thin film 9 finely worked (step (e) of Figure 1). The Ti mask remains as not removed in this stage. The remaining Ti mask is removed, if necessary, for example,
<Desc/Clms Page number 14>
by a conventional reactive etching method using a CC14 gas plasma (step (f) of Figure 1) .
In any embodiment of the invention, no redeposition layers or a contamination on the surface of the etched feature are observed, and etching with a sharp and a precise shape can be realized. Representative example of the material to be etched in the invention is a magnetic material including a magnetic material comprising a transition metal as a main component, such as permalloy, Fe, Ni, Co, a Co-Cr alloy, a sendust alloy, Mo, a rare earth element, an alloy or a compound of these elements.
As the resist film used for forming the mask pattern, various organic polymer films utilizing the conventional exposure-development system may be used. It may be formed by direct formation of the mask pattern. As the plasma gas for etching, a mixed gas of CO and a nitrogen-containing compound, such as NH3 or an amine, is used for etching a magnetic material.
(b) Apparatus for Reactive Ion Etching An apparatus for reactive ion etching used in the fine working process of the invention at the step (e) of Figure 1, i . e . the reactive ion etching using the CO-NH3 mixed gas plasma, is described.
In the conventional apparatus for reactive ion etching, the reaction chamber and constitutional parts contained in the
<Desc/Clms Page number 15>
reaction chamber are composed of stainless steel. Stainless steel is an alloy comprising iron, nickel and chromium, which are transition metals, and thus has a composition similar to a magnetic material. Therefore, if the reactive ion etching to a magnetic alloy mainly composed of a transition metal with the mixed gas plasma of CO and NH3 is conducted by using the conventional apparatus for reactive-ion etching, not only the material to be etched but also the reaction chamber, an electrode, a susceptor supporting the material to be etched, and other peripheral parts exposed to the plasma are subjected to the action of the ion etching. Accordingly, a problem arises in that the interior of the reaction vessel is corroded, and.. at the same time, the whole of the reactive gas plasma cannot be effectively used for etching of the material to be etched. This also becomes a factor of contamination of the material to be etched and brings about various unfavorable results such as reduction in etching rate.
In the invention, to solve the problems described above, titanium (Ti) , a Ti alloy, aluminum (Al) , an aluminum alloy or a Ti-Al alloy is used for at least a part of the reaction chamber and constitutional parts contained in the reaction chamber instead of stainless steel used in the conventional apparatus.
The term "a part" used herein means, in view of the object of the invention, a portion or a part that is liable to receive the etching action of a plasma of a mixed gas of CO and NH3 or
<Desc/Clms Page number 16>
a mixed gas of CO and a nitrogen -containing compound, such as an amine, and adversely affects on the reactive ion etching. Therefore, it can be understood in the practical constitution of the apparatus that the whole or a part of the main body of the reaction chamber, its inner surface, an inlet system and an exhaust system of the gas, and various parts disposed in the chamber are made of the above-described metals, with taking the system of generation and introduction of the plasma and the species and the size of the material to be etched into consideration.
For example, Figures 3, 4 and 5 show embodiments of the apparatus of the invention, which are a parallel flat plates type plasma apparatus, an inductive coupling type plasma apparatus, and an electron cyclotron resonance type plasma apparatus, respectively. In these apparatuses, the portions and the parts described below are composed of Ti, Al, a Ti alloy, an Al alloy or an Ti-Al alloy, except for a non-metallic part such as glass or cooling water.
In Figures 3, 4 and 5, numeral 10 denotes a reaction chamber, 11 denotes a protective plate, 12 denotes a ground electrode, 13 denotes a supporting plate, 14 denotes a high frequency electrode, 15 denotes a zero potential shield, 16 denotes a conductance adjusting valve, 17 denotes a window flange or a feed-through flange, 18 denotes an inlet of a reaction gas, 19 denotes a view port, 20 denotes a high frequency
<Desc/Clms Page number 17>
power source, 21 denotes cooling water, 22 denotes a coil antenna, 23 denotes a quartz window, 24 denotes a solenoid coil, and 25 denotes a microwave waveguide.
As a result of actual experiments with respect to Ti, Al, Cu and the conventional stainless steel, in the case where all the metallic parts contained in the reaction chamber, e.g. a susceptor supporting the material to be etched, a high frequency electrode, a zero potential shield, and a ground electrode, as well as struts, shutters, bolts and nuts, were composed of Ti, the most excellent function of the invention was obtained. That is, in the process of reactive ion etching, the ratio of the loss of these parts made of Ti due to corrosion was as small as it cannot be observed in comparison to stainless steel, and the etching rates of a permalloy (80%Ni-Fe alloy) and a l0%Cr-Co alloy as a material to be etched were 120 nm/min and 140 nm/min, respectively, which were 4 times larger than that of the conventional apparatus using stainless steel. Furthermore, no redeposition layers on the surface of the etched feature observed, and etching with a sharp and precise profile could be realized. The parts that exhibit the most considerable influence on the function of the invention are a susceptor supporting the material to be etched, and a ground electrode. In order to constitute these parts, Ti is preferred from the standpoint of its excellent resistance in vaccum, mechanical strength, weldability and workability of bending and cutting.
<Desc/Clms Page number 18>
In addition to pure Ti, various Ti alloys that satisfy the conditions above can be used in the invention. Preferred examples of the Ti alloy include a Ti-Pd alloy, a Ti-Ta alloy, a Ti-Al-Sn alloy, a Ti-Al-V-Mo alloy, a Ti-Al-Sn-Zr-Mo-Si alloy, a Ti-Al-Zr-MO-Sn alloy, a Ti-Al-V alloy, a Ti-Al-Sn-Zr-MO alloy, a Ti-Al-V-Sn alloy and a Ti-V-Cr-A1 alloy.
While pure Al also exhibit the similar function, it should be carefully handled with respect to the weldability and the strength in comparison to Ti. In addition to pure A1, the same function can be obtained by using alloys, such as an AI-Cu-Xl alloy (where X1 is an additive element, e.g. Si, Mn and Mg), an Al-Mn-X2 alloy (where XZ is an additive element, e.g. Mg and Si) , an Al-Mg-X3 alloy (where X3 is Zn, Si, Cr, Mn or Mg) , and an Al-Si-X4 alloy (where X4 is an additive element, e.g. Mg, Cu and Cr).
Pure Cu and alloys composed of Cu as a main component do not exhibit any notable function in comparison to stainless steel.
In the invention, according to the constitution described in the foregoing, a novel method using a novel mask material is provided, that realizes effective reactive-ion etching of a magnetic material with a large etching rate, etching with ease and high resolution and precision, and provision of an positive pattern. The constitution and function of the invention is described in
<Desc/Clms Page number 19>
more detail referring to the following examples, but the invention is not construed as being limited thereto. EXAMPLE 1 Fine Workina of Fe Thin Film using Ti Mask Reactive ion etching was conducted according to the process shown in Figure 1 using the apparatus for reactive ion etching of the invention. In the apparatus, the reaction chamber and a11 the parts contained therein are made of pure Ti.
An Fe thin film having a thickness of 450 nm was formed as. a ferromagnetic material thin film 2 on Corning 7059 glass substrate 1 by a sputtering method. After forming a resist film 5, a pattern 6 of the resist film was formed by electron beam lithography. By using Ti as a mask material 7 formed on the pattern 6, a mask 8 composed of a number of small Ti pads was formed by a lift off method. The resulting sample was placed on 'a lower electrode cooled by water, powered by a high frequency of 13.56 MHz. The distance between the high frequency electrode and a ground electrode was set to 35 mm. With supplying a CO gas and an NH3 gas into the reaction chamber at flow rates of 6.3 cc/min and 6.8 cc/min, respectively, the pressure of the reaction gas in the chamber was maintained at a pressure of 5. 7 x 10-3 Torr by evacuating with a turbo-molecular pump. A high frequency of 3.7 W/ =2 was applied to the lower
<Desc/Clms Page number 20>
electrode supporting the sample, to generate a glow-discharge plasma of the CO-NH3 mixed gas, and thus reactive-ion etching was conducted. The time of etching process was 4.0 minutes.
After the etching was conducted according to the above-described process, step heights between the part covered with the Ti pad used as the mask 8 and the part not covered with it were measured by a multiple-beam reflection interferometer, to obtain an etching rate. The features formed by etching were observed with an electron-beam microscope, to evaluate the etching for flatness and sharpness of the steps, and a contamination or a redeposition layer. As a result of etching, a patterned Fe thin film was obtained as a finely worked magnetic material 9. The etching rate for the Fe thin film was 90 nm/min. The etching feature having a sharpness with a radius of curvature of about 0.1 pun and a depth of 400 nm was obtained.
Figures 6A, 68 and 6c are electron-beam micrographs showing the results of etching of the following thin films with using the Ti mask.
Figure 6A: Fe thin film; Figure 6B: Co-9.8%Cr thin film; Figure 6C: Ni-20%Fe thin film.
It can be understood from the micrographs that excellent working precision can be obtained.
<Desc/Clms Page number 21>
EXAMPLE 2 Fine Working of Permalloy (Ni-20$Fe alloV) Thin Film using Mask The reactive ion etching of an Ni-20%Fe alloy was possible under the same conditions as in Example 1. The etching rate was 120 nm/min and the shape obtained by etching was excellent. EXAMPLE 3 Fine Working of Co-9.8%Cr alloy Thin Film using Ti Mask The reactive ion etching of a Co-9. B%Cr alloy was possible under the same conditions as in Example 1. The etching rate was 140 nm/min and the shape obtained by etching was excellent. EXAMPLE 4 Fine Working of Ni-20%Fe alloy Thin Film using A1 Mask Aluminum was vacuum deposited and an A1 mask was formed by a lift off method under the same conditions as in Example 1. The reactive ion etching of a Ni-20%Fe alloy was possible under the same conditions as in Example 1. The etching rate was 120 nm/min and the shape obtained by etching was excellent. EXAMPLE 5 Fine Working of Co-9.8%Cr alloy Thin Film using Si Mask Silicon was vacuum deposited and an Si mask was formed by a lift off method under the same conditions as in Example 1. The reactive ion etching of a Co-9.8$Cr alloy was possible under the same conditions as in Example 1. The etching rate was 140 nm/min and the shape obtained by etching was excellent.
<Desc/Clms Page number 22>
EXAMPLE 6 Fine Working of CO-9.8%Cr alloy Thin Film using Ge Mask Germanium was vacuum deposited and a Ge mask was formed by a lift-off method under the same conditions as in Example 1. The reactive-ion etching of a Co-9.8%Cr alloy was possible under the same conditions as in Example 1. The etching rate was 140 nm/min and the shape obtained by etching was excellent.
As described in detail in the foregoing, the reactive ion etching of a magnetic material using a CO-NH3 mixed gas plasma can be more effectively conducted by using the apparatus for reactive-ion etching according to the invention, in comparison to the case using the conventional reactive ion etching apparatus. That is, the etching rate can be increased by about 4 times under the same conditions, to contribute to the working efficiency. Furthermore, the material to be etched is not contaminated during the etching process, and the redeposition layer removed by the etching can be reduced to the level that does not bring about a problem.
According to the function described in the foregoing, the production of a micro magnetic head, a microtrans former, a micro magnetic device, a magnetic sensor, a magnetoresistance device, a spin diode, a spin transistor, a spin valve device, a spin valve magnetic memory and a magnetoresistance tunneling effect device can be possible. The production of a patterned
<Desc/Clms Page number 23>
magnetic recording medium of a high density magnetic recording medium that is being developed can also be possible.
<Desc/Clms Page number 24>

Claims (4)

  1. WHAT IS CLAIMED IS 1. A method for reactive ion etching a magnetic material with a plasma of a mixed gas of carbon monoxide and a nitrogen-containing compound, said method comprising a step, in which a multilayered film comprising a magnetic material thin film having thereon a resist film formed on a substrate is exposed to an electron beam and then developed, to form a pattern on said resist film, a step, in which a mask material. is vacuum deposited, a step, in which said resist is dissolved, to form a mask, and a step, in which a part of said magnetic material thin film that is not covered with said mask is removed by reactive ion etching with a plasma of a mixed gas of carbon monoxide and a nitrogen-containing compound, to form a pattern on said magnetic material thin film, and thus obtaining said magnetic material thin film finely worked.
  2. 2. A method for reactive ion etching as claimed in claim 1, wherein said mask used in said reactive ion etching comprises at least one member selected from the group consisting of titanium, magnesium, aluminum, germanium, platinum, palladium, an alloy comprising at least one of them as.a main component, and a compound thereof.
    <Desc/Clms Page number 25>
  3. 3. A method for reactive-ion etching as claimed in claim 1, wherein said mask used in said reactive-ion etching comprises silicon or an alloy comprising silicon as a main component.
  4. 4. A method for reactive-ion etching as claimed in claim 1, wherein said mask used in said reactive ion etching comprises a compound of silicon, and is disposed on said pattern formed on said resist film and formed into said mask by a lift off method.
GB0128508.9A 1997-09-22 1998-09-22 Method for reactive ion etching Expired - Fee Related GB2366766B8 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP09256636A JP3131595B2 (en) 1997-09-22 1997-09-22 Mask for reactive ion etching
JP09256635A JP3131594B2 (en) 1997-09-22 1997-09-22 Reactive ion etching equipment
GB9820639.4A GB2331273B8 (en) 1997-09-22 1998-09-22 Method for reactive-ion etching and apparatus therefor

Publications (4)

Publication Number Publication Date
GB2366766A true GB2366766A (en) 2002-03-20
GB2366766B GB2366766B (en) 2002-05-15
GB2366766B8 GB2366766B8 (en) 2016-06-22
GB2366766A8 GB2366766A8 (en) 2016-06-22

Family

ID=27269487

Family Applications (1)

Application Number Title Priority Date Filing Date
GB0128508.9A Expired - Fee Related GB2366766B8 (en) 1997-09-22 1998-09-22 Method for reactive ion etching

Country Status (1)

Country Link
GB (1) GB2366766B8 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08253881A (en) * 1995-03-15 1996-10-01 Natl Res Inst For Metals Dry etching method

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08253881A (en) * 1995-03-15 1996-10-01 Natl Res Inst For Metals Dry etching method

Also Published As

Publication number Publication date
GB2366766B (en) 2002-05-15
GB2366766B8 (en) 2016-06-22
GB2366766A8 (en) 2016-06-22

Similar Documents

Publication Publication Date Title
US6669807B2 (en) Method for reactive ion etching and apparatus therefor
JP3433721B2 (en) Dry etching method and fine processing method
JP5554465B2 (en) Design process kits to reduce particle generation
US7591641B2 (en) Mold and process of production thereof
WO2021044890A1 (en) Multilayer reflective film-attached substrate, reflective mask blank, reflective mask, and method for producing semiconductor device
JPH02208601A (en) Optical window member and its manufacture
US20050138803A1 (en) Stamper for pattern transfer and manufacturing method thereof
JP2677321B2 (en) Dry etching method
JPH1192971A (en) Mask for reactive ion etching
JP3131594B2 (en) Reactive ion etching equipment
JP2001274143A (en) Dry etching method, micromachining method and mask for dry etching
GB2366766A (en) Reactive ion etching a magnetic material
KR20150066456A (en) Sputter deposition method, sputtering system, manufacture of photomask blank, and photomask blank
JP4495855B2 (en) Titanium sputtering target and manufacturing method thereof
US4599737A (en) X-ray mask with Ni pattern
EP0361516B1 (en) Method of making X-ray mask structure
US5958627A (en) X-ray mask blank and method of manufacturing the same
WO2005015308B1 (en) Fabrication process for high resolution lithography masks using evaporated or plasma assisted electron sensitive resists with plating image reversal
JP2002069627A (en) Sputtering target and sputtering apparatus using the same
CA1322684C (en) Mask repair
JP2003007590A (en) Stencil mask, its manufacturing method and exposing method
JPH03173116A (en) X-ray mask and manufacture thereof
JPH0692791A (en) Method for selectively form diamond
JPH11236686A (en) Dry etching method and production of x-ray mask
HUDSON Nonpropulsive applications of ion beams

Legal Events

Date Code Title Description
S117 Correction of errors in patents and applications (sect. 117/patents act 1977)

Free format text: REQUEST FILED; REQUEST FOR CORRECTION UNDER SECTION 117 FILED ON 18 APRIL 2016.

S117 Correction of errors in patents and applications (sect. 117/patents act 1977)

Free format text: CORRECTIONS ALLOWED; REQUEST FOR CORRECTION UNDER SECTION 117 FILED ON 18 APRIL 2016, ALLOWED ON 15 JUNE 2016.

PCNP Patent ceased through non-payment of renewal fee

Effective date: 20160922