WO1991009422A1 - Method of making crack-free insulating films with sog interlayer - Google Patents

Method of making crack-free insulating films with sog interlayer Download PDF

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Publication number
WO1991009422A1
WO1991009422A1 PCT/CA1990/000448 CA9000448W WO9109422A1 WO 1991009422 A1 WO1991009422 A1 WO 1991009422A1 CA 9000448 W CA9000448 W CA 9000448W WO 9109422 A1 WO9109422 A1 WO 9109422A1
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Prior art keywords
layer
deposited
sog
dielectric
spin
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PCT/CA1990/000448
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French (fr)
Inventor
Luc Ouellet
Abdellah Azelmad
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Mitel Corporation
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Publication of WO1991009422A1 publication Critical patent/WO1991009422A1/en

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L23/00Details of semiconductor or other solid state devices
    • H01L23/52Arrangements for conducting electric current within the device in operation from one component to another, i.e. interconnections, e.g. wires, lead frames
    • H01L23/522Arrangements for conducting electric current within the device in operation from one component to another, i.e. interconnections, e.g. wires, lead frames including external interconnections consisting of a multilayer structure of conductive and insulating layers inseparably formed on the semiconductor body
    • H01L23/532Arrangements for conducting electric current within the device in operation from one component to another, i.e. interconnections, e.g. wires, lead frames including external interconnections consisting of a multilayer structure of conductive and insulating layers inseparably formed on the semiconductor body characterised by the materials
    • H01L23/5329Insulating materials
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B6/00Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
    • G02B6/02Optical fibres with cladding with or without a coating
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • H01L21/70Manufacture or treatment of devices consisting of a plurality of solid state components formed in or on a common substrate or of parts thereof; Manufacture of integrated circuit devices or of parts thereof
    • H01L21/71Manufacture of specific parts of devices defined in group H01L21/70
    • H01L21/768Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics
    • H01L21/76801Applying interconnections to be used for carrying current between separate components within a device comprising conductors and dielectrics characterised by the formation and the after-treatment of the dielectrics, e.g. smoothing
    • H01L21/76819Smoothing of the dielectric
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L2924/00Indexing scheme for arrangements or methods for connecting or disconnecting semiconductor or solid-state bodies as covered by H01L24/00
    • H01L2924/0001Technical content checked by a classifier
    • H01L2924/0002Not covered by any one of groups H01L24/00, H01L24/00 and H01L2224/00

Definitions

  • This invention relates to method of making crack-free insulating films comprising a Spin-on glass (SOG) layer, and insulating films made thereby.
  • SOG Spin-on glass
  • SOG Spin-on glasses
  • monomers are polymerized by condensation and release water, solvent, and alcohol.
  • the condensed material is a thin solid film having mechanical, chemical and electrical properties which depend on the starting composition, and the coating and curing process. A good starting solution can give bad results if the coating and curing sequence is not optimized.
  • Siloxanes methyl-, ethyl-, phenyl-, butyl-, doped or undoped
  • Planarization is the filling in of the trenches and crevices formed when a plurality of layers, some of which might be subsequently etched back, are deposited on a substrate. Planarization is used over polysilicon, refractory metals, polycides, suicides, aluminum and aluminum alloys, copper, and gold or otehr conductive materials. The main goal is to smooth/eliminate steps and enhance step coverage by the dielectrics and interconnects. Planarization technology becomes increasingly important when the scale of integrated circuits is in the micron and submicron region. Of the many dielectric planarization techniques, SOG planarization is a particularly attractive method; it is relatively simple, economical and is capable of high throughput.
  • the quasi-inorganic siloxane SOGs have a more flexible structure due to the presence of organic radicals, which prevent complete cross-linking of the SiOxCyHz matrix under condensation, the organic radicals are not stable at high temperatures and are not compatible with oxygen plasma photoresist strippers (which tend to transform the quasi- inorganic SOG to a purely inorganic SOG by burning the organic bonds and producing volatile species like H 2 0, C ⁇ OyH z , and silanol Si-OH) .
  • These two drawbacks limit the use of the quasi-inorganic siloxanes as an alternative to the silicates.
  • SOG planarization can take three forms:
  • Total etchback and partial etchback processes for planarization of dielectrics over aluminum use photoresist, polyimide, or flexible quasi-inorganic SOGs. In those two cases, cracking of the dielectric sandwich does not occur since most of the planarizing material is removed from the wafer.
  • Non-etchback silicate SOG planarization of dielectrics over polysilicon, polycides, refractory metals or silicides has been used for about three years. This technique is not particularly demanding on the dielectric sandwich because the coefficient of thermal expansion of the materials is much lower than for aluminum and aluminum alloys. The dielectric sandwich does not normally crack over those materials.
  • Non-etchback SOG planarization of dielectrics over aluminum alloys is an extremely new process in the semiconductor industry.
  • purely inorganic SOG form dielectric sandwiches which are prone to very bad cracking. Consequently, more flexible quasi-organic SOGs have been tried, but this approach has proved to be questionable because of a serious field inversion problem due to the effect of the hydrogen contained in the organic bonds of the quasi-inorganic SOGs on the characteristics of CMOS semiconductor devices.
  • SOG film properties are of prime importance. Since SQG is generally a more porous material, when compared to LPCVD, APCVD, LACVD, PACVD or PECVD oxides, it is more prone to water absorption. This water absorption reduces the bulk resistivity of the SOG and increases the power consumption of the semiconductor device due to current leakage between adjacent tracks of interconnect. For this reason, among others, SOG must not come into direct contact with the tracks and must be sandwiched between two denser LPCVD, APCVD, LACVD, PACVD or PECVD dielectric films.
  • the present invention provides in a method of fabricating a composite insulating film comprising first and second layers with intermediate spin-on glass zones acting as a planarization interlayer for said first layer, at least said first layer being a dielectric layer, the improvement wherein the first layer is formed under compression to prevent cracking in the composite film during subsequent heat treatment.
  • the second layer can either be a second dielectric layer, or where, in the case of semiconductor fabrication, an interconnect layer is applied directly over the first and SOG layers, the second layer can be the interconnect layer.
  • the method may be applied to the fabrication of a semiconductor device wherein a first dielectric layer is applied over an interconnect layer having tracks defining a conductive pattern and made of material having a high coefficient of expansion, the first dielectric layer forming valleys between the tracks of the interconnect layer, spin-on glass is applied over said first layer to planarize it by forming spin-on glass zones in the valleys defined by the first dielectric layer, and a second layer is applied to the planarized first layer, whereby said first and second layers and said spin-on glass zones form a composite multi-layer film.
  • the first layer is formed under compression to prevent cracking in the composite multi ⁇ layer film during subsequent heat treatment.
  • Figures la to lh illustrate the steps in the manufacture of a composite insulating film with a SOG interlayer.
  • a layer of aluminum interconnect material 1 (Fig. la) is deposited on a substrate and then patterned using photolithography (Fig. lb) .
  • a first layer of dielectric 2 is deposited over the etched interconnect tracks (Fig. lc) and a an inorganic (silicate) spin-on glass (SOG) layer 3 is applied (with or without etchback) to fill the valleys and crevices (Fig. Id) .
  • the SOG is a proprietary composition and can be obtained from a number of sources such as Allied Signal Inc, Milpitas, California. Being liquid, the SOG is almost absent over the peaks la and provides good planarization for the first dielectric layer 2.
  • a second dielectric layer 4 is then applied over the first layer 2 and SOG interlayer 3 (Fig., le) . Contacts holes are then etched away to reach the tracks of the first layer of interconnect material 1 (fig. If) .
  • a second level of interconnect material 5 is deposited over the etched second layer 4 (fig If) and is patterned using photolithography to form the desired conductive tracks 5a (Fig. lh) .
  • Such dielectric sandwiches containing dense purely inorganic (silicate) SOG crack during the subsequenet heat treatments which are needed to cure and stabilize the SOG and the aluminum alloys.
  • Thin film stress can be compressive or tensile.
  • a compressive stress when too excessive, results in delamination, formation of waves and ripples.
  • a film in compression does not crack. In fact, a film in compression stops the propagation of cracks.
  • a tensile stress when too excessive, results in crack formation and propagation.
  • a stressed film When a stressed film is deposited on a substrate, it induces a mechanical bow of that substrate.
  • the bow direction and its magnitude is related to the stress type (tensile or compressive) , and its intensity. If the film is in tension, the substrate bows in such a way that the film is present on the concave face. Similarly, if the film is under compression the substrate bows in such a way that the film is present on the convex face.
  • the stress nature of a given thin film can then be measured by the change of curvature induced in a (100) Si single crystal wafer, due to the deposited film.
  • the wafer can be scanned before and after the deposition to obtain the net change or wafer radius of curvature.
  • the film stress " ⁇ " is calculated using the following expression:
  • M E is the Young's modulus of Si (100) wafer
  • rr is its Poisson's ratio
  • t is the wafer thickness
  • r is the measured net radius of curvature
  • r is the film thickness
  • the SOG stress obtained is not excessively high but the obtained material is very rigid. Although it was not possible to measure the actual coefficient of thermal expansion of the obtained SOG, the appearance of cracks at high temperature in the dielectric sandwich PSG/SOG/PSG (PSG stands for a 4.0 wt% phosphorus doped LPCVD Si0 film which is under a tensile stress of 0.5 - 3.0 x 10 9 dyne/cm 2 , up to four times higher than SOG), deposited over metal tracks of the first level of interconnect, and the absence of cracks in the dielectric sandwich PSG/PSG deposited over equivalent metal tracks, indicates that the SOG has a much smaller coefficient of thermal expansion than PSG.
  • the dielectric sandwich cracking has been substantially eliminated with a special combination of film stresses.
  • the first dielectric layer 1 deposited over the aluminum and under the SOG film must be under compressive stress. In this case, the heat treatments that cause expansion of the aluminum will tend to bring the dielectric under tension. But since the dielectric is already in compression, its stress will stabilize at an almost negligible value. A stress of about 5 x 10 8 to 3 x 10 9 dyne/cm 2 is preferred and its exact value depends on the difference of the coefficient of thermal expansion between the aluminum alloy and the dielectrics used in the sandwich.
  • the SOG layer has a stress that is slightly tensile at about 6 - 8 x 10 8 dynes/cm 2 .
  • the last dielectric layer 4 deposited over the SOG layer 3 and under the second interconnect layer 5 can be under compressive or tensile stress, but a tensile stress is preferred to compensate for the wafer bow generated by the first dielectric.
  • a stress of about 5 x 10 8 to 3 x 10 9 dyne/cm 2 is preferred.
  • the described method is very important because it permits a non-etchback high quality purely inorganic SOG process to be applied to high coefficient of thermal expansion materials, such as aluminum alloys.
  • PECVD Plasma Enhanced Chemical Vapour Deposition
  • LACVD Laser Assisted Chemical Vapour Deposition
  • the deposited compressive material under the SOG can be:
  • the layer 4 over the SOG layer 3 need not be under tension but also can be under compression.
  • the SOG can be of many types.
  • the crack prevention effect is much more pronounced with low coefficient of thermal expansion inorganic (silicates) SOGs.
  • the interconnect material under the SOG can be other than aluminum or aluminum alloy.
  • it can be a metal such as W, Mo, Ta, Co, Ti; or a reacted metal such as Ti x Ny, Ti x Wy, Ti x 0 v Z 2 , Ti x W v N 2 .
  • It can also be a suicide of W, Mo, Ta, Co, Ti, Pt.
  • the upper part of the dielectric sandwich can be omitted and the second metal layer 5 directly deposited over the SOG layer 3 and first dielectric layer 2.
  • the described process has many applications. In particular, it can be applied to other steps in the manufacture of integrated circuits, such as:
  • the process may be useful in the fabrication of:

Abstract

A method of fabricating a semiconductor device is disclosed characterized in that a first dielectric layer is applied over an interconnect layer having tracks defining a conductive pattern, the first dielectric layer forming valleys between the tracks of the interconnect layer, spin-on glass is applied over said first layer to planarize it by forming spin-on glass zones in the valleys defined by the first dielectric layer, and a second layer is applied to the planarized first layer, whereby the first and second layers and said spin-on glass zones form a composite multi-layer film. The first layer is formed such that it has compressive stress at room temperature to prevent cracking in the composite multi-layer film during subsequent heat treatment. The second layer can be another dielectric layer or a further interconnect layer applied directly to the first layer and SOG planarization layer. The method can also be applied to other fields, such as the manufacture of optical fibers, emission diodes and the like.

Description

METHOD OF MAKING CRACK-FREE INSULATING FILMS WITH SOG
INTERLAYER
This invention relates to method of making crack-free insulating films comprising a Spin-on glass (SOG) layer, and insulating films made thereby.
Spin-on glasses (SOG) are proprietary liguid solutions containing siloxane or silicate based monomers diluted in various kinds of solvents or alcohols. During coating and curing, monomers are polymerized by condensation and release water, solvent, and alcohol. The condensed material is a thin solid film having mechanical, chemical and electrical properties which depend on the starting composition, and the coating and curing process. A good starting solution can give bad results if the coating and curing sequence is not optimized.
There are more than one hundred different SOG solutions on the market. They are classified into two major families:
1) Siloxanes (methyl-, ethyl-, phenyl-, butyl-, doped or undoped) .
2) Silicates (doped or undoped).
Planarization is the filling in of the trenches and crevices formed when a plurality of layers, some of which might be subsequently etched back, are deposited on a substrate. Planarization is used over polysilicon, refractory metals, polycides, suicides, aluminum and aluminum alloys, copper, and gold or otehr conductive materials. The main goal is to smooth/eliminate steps and enhance step coverage by the dielectrics and interconnects. Planarization technology becomes increasingly important when the scale of integrated circuits is in the micron and submicron region. Of the many dielectric planarization techniques, SOG planarization is a particularly attractive method; it is relatively simple, economical and is capable of high throughput.
Unfortunately, the purely inorganic silicate SOGs are prone to cracking. This has limited their usefulness in semiconductor and similar applications, especially where they have to undergo subsequent heat treatment. While the quasi-inorganic siloxane SOGs have a more flexible structure due to the presence of organic radicals, which prevent complete cross-linking of the SiOxCyHz matrix under condensation, the organic radicals are not stable at high temperatures and are not compatible with oxygen plasma photoresist strippers (which tend to transform the quasi- inorganic SOG to a purely inorganic SOG by burning the organic bonds and producing volatile species like H20, CχOyHz, and silanol Si-OH) . These two drawbacks, among others, limit the use of the quasi-inorganic siloxanes as an alternative to the silicates.
SOG planarization can take three forms:
1) complete etchback.
2) Partial etchback.
3) Non etchback.
Total etchback and partial etchback processes for planarization of dielectrics over aluminum use photoresist, polyimide, or flexible quasi-inorganic SOGs. In those two cases, cracking of the dielectric sandwich does not occur since most of the planarizing material is removed from the wafer.
Major manufacturing restrictions of the complete/partial etchback techniques impose the non- etchback approach as the preferred technique in a production environment. In this approach, the SOG becomes a permanent part of the dielectric. Non-etchback silicate SOG planarization of dielectrics over polysilicon, polycides, refractory metals or silicides has been used for about three years. This technique is not particularly demanding on the dielectric sandwich because the coefficient of thermal expansion of the materials is much lower than for aluminum and aluminum alloys. The dielectric sandwich does not normally crack over those materials.
Non-etchback SOG planarization of dielectrics over aluminum alloys is an extremely new process in the semiconductor industry. Unfortunately, purely inorganic SOG form dielectric sandwiches which are prone to very bad cracking. Consequently, more flexible quasi-organic SOGs have been tried, but this approach has proved to be questionable because of a serious field inversion problem due to the effect of the hydrogen contained in the organic bonds of the quasi-inorganic SOGs on the characteristics of CMOS semiconductor devices.
SOG film properties are of prime importance. Since SQG is generally a more porous material, when compared to LPCVD, APCVD, LACVD, PACVD or PECVD oxides, it is more prone to water absorption. This water absorption reduces the bulk resistivity of the SOG and increases the power consumption of the semiconductor device due to current leakage between adjacent tracks of interconnect. For this reason, among others, SOG must not come into direct contact with the tracks and must be sandwiched between two denser LPCVD, APCVD, LACVD, PACVD or PECVD dielectric films.
Interconnections between upper and lower tracks by the use of contacts or vias are necessary, and the SOG is then in direct contact with the interconnects at those locations. If too much water is present in the SOG (or if water is generated in the quasi-inorganic SOG during photoresist stripping, after vias/contact patterning) , problems such as via poisoning can occur. One way to prevent via poisoning is to use a dense and purely inorganic SOG, which is not degraded by photoresist strippers. For this reason as well silicate SOGs are preferred, but the formation of microcracks discussed above, especially during subsequent heat treatments, has limited their usefulness.
It has previously been thought that the formation of microcracks in the inorganic SOG layer was an unavoidable consequence of the brittle nature of the SOG material. For example. Japanese patent publication no. 63-021837 seeks to avoid the cracking that occurs in the SOG film during the vitrifying step by coating with SOG under reduced pressure. JP 62-046533 seeks to avoid cracking in the SOG film by pressing the SOG solution with a heating plate during solidification of the SOG layer. There has thus been a tendency to abandon altogether SOGs for planarization purposes despite their otherwise attractive properties in terms of simplicity, economy and high throughput.
It has now been discovered in accordance with the invention that the cracking that occurs in insulating films with SOG planarization interlayers is not mainly due to cracking in the SOG layer, as previously thought, but rather primarily due to the different coefficients of expansion of the SOG, dielectric layers, and interconnect materials.
Accordingly the present invention provides in a method of fabricating a composite insulating film comprising first and second layers with intermediate spin-on glass zones acting as a planarization interlayer for said first layer, at least said first layer being a dielectric layer, the improvement wherein the first layer is formed under compression to prevent cracking in the composite film during subsequent heat treatment.
The second layer can either be a second dielectric layer, or where, in the case of semiconductor fabrication, an interconnect layer is applied directly over the first and SOG layers, the second layer can be the interconnect layer.
The method may be applied to the fabrication of a semiconductor device wherein a first dielectric layer is applied over an interconnect layer having tracks defining a conductive pattern and made of material having a high coefficient of expansion, the first dielectric layer forming valleys between the tracks of the interconnect layer, spin-on glass is applied over said first layer to planarize it by forming spin-on glass zones in the valleys defined by the first dielectric layer, and a second layer is applied to the planarized first layer, whereby said first and second layers and said spin-on glass zones form a composite multi-layer film.
In the above method the first layer is formed under compression to prevent cracking in the composite multi¬ layer film during subsequent heat treatment.
The invention will now be described in more detail, by way of example only, with reference to the accompanying drawings in which:-
Figures la to lh illustrate the steps in the manufacture of a composite insulating film with a SOG interlayer.
First a layer of aluminum interconnect material 1 (Fig. la) is deposited on a substrate and then patterned using photolithography (Fig. lb) . A first layer of dielectric 2 is deposited over the etched interconnect tracks (Fig. lc) and a an inorganic (silicate) spin-on glass (SOG) layer 3 is applied (with or without etchback) to fill the valleys and crevices (Fig. Id) . The SOG is a proprietary composition and can be obtained from a number of sources such as Allied Signal Inc, Milpitas, California. Being liquid, the SOG is almost absent over the peaks la and provides good planarization for the first dielectric layer 2.
A second dielectric layer 4 is then applied over the first layer 2 and SOG interlayer 3 (Fig., le) . Contacts holes are then etched away to reach the tracks of the first layer of interconnect material 1 (fig. If) . A second level of interconnect material 5 is deposited over the etched second layer 4 (fig If) and is patterned using photolithography to form the desired conductive tracks 5a (Fig. lh) .
Such dielectric sandwiches containing dense purely inorganic (silicate) SOG crack during the subsequenet heat treatments which are needed to cure and stabilize the SOG and the aluminum alloys.
These cracks in the dielectric sandwiches cause the device to fail due to electrical shorts between adjacent tracks of the same level of interconnect (intralevel short) , or between tracks of two independent levels of interconnect (interlevel shorts) . This property has limited the use of the purely inorganic SOGs (silicates) and some quasi-inorganic SOGs (siloxanes) for dielectric planarization applications.
Thin film stress can be compressive or tensile. A compressive stress, when too excessive, results in delamination, formation of waves and ripples. A film in compression does not crack. In fact, a film in compression stops the propagation of cracks. A tensile stress, when too excessive, results in crack formation and propagation.
When a stressed film is deposited on a substrate, it induces a mechanical bow of that substrate. The bow direction and its magnitude is related to the stress type (tensile or compressive) , and its intensity. If the film is in tension, the substrate bows in such a way that the film is present on the concave face. Similarly, if the film is under compression the substrate bows in such a way that the film is present on the convex face. The stress nature of a given thin film can then be measured by the change of curvature induced in a (100) Si single crystal wafer, due to the deposited film.
Using a laser optical lever, the wafer can be scanned before and after the deposition to obtain the net change or wafer radius of curvature. The film stress "σ" is calculated using the following expression:
σ = [Et2]/[6(l-τr)rτ]
where ME" is the Young's modulus of Si (100) wafer, "rr" is its Poisson's ratio, "t" is the wafer thickness, "r" is the measured net radius of curvature, and "r" is the film thickness.
Such stress measurements have been performed on various purely inorganic (silicates) SOGs. A (6-8) x lθ8 dyne/cm2 tensile stress was measured. This tensile stress is the result of the solid phase volumetric shrink of the SOG during its condensation:
SiOt(OC2H5)u(OH)v + WH20 -> SiOxHy + ZH20 + bC2H50H Water (H20) and ethanol (C2H5OH) by-products are released and contribute to an increase of the internal stress.
The SOG stress obtained is not excessively high but the obtained material is very rigid. Although it was not possible to measure the actual coefficient of thermal expansion of the obtained SOG, the appearance of cracks at high temperature in the dielectric sandwich PSG/SOG/PSG (PSG stands for a 4.0 wt% phosphorus doped LPCVD Si0 film which is under a tensile stress of 0.5 - 3.0 x 109 dyne/cm2, up to four times higher than SOG), deposited over metal tracks of the first level of interconnect, and the absence of cracks in the dielectric sandwich PSG/PSG deposited over equivalent metal tracks, indicates that the SOG has a much smaller coefficient of thermal expansion than PSG.
It is not, as previously thought, a high stress in the SOG which causes the appearance of cracks, but rather its lower coefficient of thermal expansion The cracks appear in the dielectric sandwich around and over the metal I tracks and propagate easily through the dielectric layers, which are already in tensile stress. Since aluminum inherently has a very high coefficient of thermal expansion, when compared to PSG and particularly SOG, the problem is important, especially in view of the subsequent heat treatments that are required.
In accordance with the invention, the dielectric sandwich cracking has been substantially eliminated with a special combination of film stresses.
The first dielectric layer 1 deposited over the aluminum and under the SOG film must be under compressive stress. In this case, the heat treatments that cause expansion of the aluminum will tend to bring the dielectric under tension. But since the dielectric is already in compression, its stress will stabilize at an almost negligible value. A stress of about 5 x 108 to 3 x 109 dyne/cm2 is preferred and its exact value depends on the difference of the coefficient of thermal expansion between the aluminum alloy and the dielectrics used in the sandwich.
The SOG layer has a stress that is slightly tensile at about 6 - 8 x 108 dynes/cm2. The last dielectric layer 4 deposited over the SOG layer 3 and under the second interconnect layer 5 can be under compressive or tensile stress, but a tensile stress is preferred to compensate for the wafer bow generated by the first dielectric. A stress of about 5 x 108 to 3 x 109 dyne/cm2 is preferred.
Stress measurements have been performed on various different dielectrics to find one that has the required compressive stress. A specially designed undoped LPCVD SiOxHv (SG) gives the desired behaviour, namely a compressive stress of 2 x 109 dyne/cm2. A sandwich composed of 600 nm SG/200 nm SOG/600 nm PSG can theoretically be crack free.
Example
An experiment was performed to compare a standard PSG/SOG/PSG sandwich with a SG/SOG/PSG sandwich fabricated in accordance with the invention. For the experiment, an equal number of blanket aluminum deposited wafers and real patterned device wafers were used to deposit 600 nm of PSG or 600 nm of the special SG. Then, all the wafers were coated with SOG and heat treated. Finally, another 600 nm of PSG was deposited on the top of the SOG, and heat treatments were performed to check for cracking. All wafers with PSG/SOG/PSG sandwich were badly cracked. The PSG/SOG/PSG covered blanket aluminum deposited silicon wafers were randomly cracked. The PSG/SOG/PSG covered wafers with patterns showed cracks that were limited to the area over the aluminum lines of the first level of interconnect, indicating that the coefficient of thermal expansion of SOG is really the underlying cause of the dielectric sandwich cracking.
All wafers with SG/SOG/PSG sandwich were completely crack-free. Even the SG/SOG/PSG covered blanket aluminum deposited silicon wafers were absolutely crack-free. This proves the effectiveness of having a compressive pre- stressed film under the SOG to compensate for its low coefficient of thermal expansion.
The described method is very important because it permits a non-etchback high quality purely inorganic SOG process to be applied to high coefficient of thermal expansion materials, such as aluminum alloys.
There are a number of ways of achieving the desired compressive stress. Examples are as follows:
• Low Pressure Chemical Vapour Deposition (LPCVD)
• Plasma Enhanced Chemical Vapour Deposition (PECVD)
• Laser Assisted Chemical Vapour Deposition (LACVD)
• Photochemical Chemical Vapour Deposition (PhCVD) • Atmospheric Pressure Chemical Vapour Deposition
(APCVD)
• Bias Sputtering (BS)
• Thermal oxidation
Spin-on deposition Electron Cyclotron Resonance (ECRf, biased or otherwise. The deposited compressive material under the SOG can be:
• Silicon nitride, stochiometric or not, with or without H, Cl, F • Polyimide or other mechanically deposited organic dielectric
• silicon dioxide, oxynitride, stochiometric or not, with or without H, Cl, F
• Above-mentioned materials doped/alloyed with As, P, B,
Pb, or other metallic elements, or their combinations.
The layer 4 over the SOG layer 3 need not be under tension but also can be under compression.
The SOG can be of many types. The crack prevention effect is much more pronounced with low coefficient of thermal expansion inorganic (silicates) SOGs.
The interconnect material under the SOG can be other than aluminum or aluminum alloy. For example, it can be a metal such as W, Mo, Ta, Co, Ti; or a reacted metal such as TixNy, TixWy, Tix0vZ2, TixWvN2. It can also be a suicide of W, Mo, Ta, Co, Ti, Pt.
The upper part of the dielectric sandwich can be omitted and the second metal layer 5 directly deposited over the SOG layer 3 and first dielectric layer 2.
The described process has many applications. In particular, it can be applied to other steps in the manufacture of integrated circuits, such as:
• Planarization • Diffusion source Dielectric layer
Diffusion barrier
Encapsulation
Adhesion layer
Buffer layer
Antireflective layer
Corrosion protection layer Etc.
It can also be applied to other semiconductor devices, such as:
• Emission diodes
• Liquid crystal displays
• Electro chromic displays
• Photodetectors
• Solar batteries • Sensors
In other fields, the process may be useful in the fabrication of:
• Optical fibers
• Corrosion protection • Adhesion promoters
• Friction reduction coatings
• Optical/thermal reflectance adjustment coatings

Claims

Claims
1. A method of fabricating a composite insulating film comprising first and second layers with intermediate spin-on glass zones acting as a planarization SOG interlayer for said first layer, at least said first layer being a dielectric layer, characterized in that the first layer is formed under compression to prevent cracking in the composite film during subsequent heat treatment.
2. A method as claimed in claim 1, characterized in that said first layer is formed under a compressive stress of about 5 x 108 to 5 x 109 dynes/cm2.
3. A method as claimed in claim 2 , characterized in that said SOG interlayer is formed under a slightly tensile stress of about 3 x 108 dynes/cm2.
4. A method as claimed in claim 3, characterized in that said second layer is formed under a compressive stress of about 5 x 108 to 5 x 109 dynes/cm2.
5. A method as claimed in claim 4, characterized in that said first layer comprises siOxHy (SG) .
6. A method as claimed in claim 5, characterized in that said second layer comprises PSG.
7. A method as claimed in claim 6, characterized in that said first layer and/or second layer is deposited by LPCVD (Low Pressure Chemical Vapour Deposition) .
8. A method as claimed in claim 6, characterized in that said first layer and/or second layer is deposited by Plasma Enhanced Chemical Vapour Deposition (PECVD) .
9. A method as claimed in claim 6, characterized in that said first layer and/or second layer is deposited by Laser Assisted Chemical Vapour Deposition (LACVD) .
10. A method as claimed in claim 6, characterized in that said first layer and/or second layer is deposited by
Photochemical Chemical Vapour Deposition (PhCVD) .
11. A method as claimed in claim 6, characterized in that said first layer and/or second layer is deposited by Atmospheric Pressure Chemical Vapour Deposition (APCVD) .
12. A method as claimed in claim 6, characterized in that said first layer is deposited by Bias Sputtering (BS) .
13. A method as claimed in claim 6, characterized in that said first layer and/or second layer is deposited by Spin-on deposition.
14. A method as claimed in claim 6, characterized in that said first layer and/or second layer is deposited by Electron Cyclotron Resonance (ECR) , biased or otherwise.
15. A method as claimed in claim 4, characterized in that said first layer and/or second layer comprises silicon nitride, stochiometric or not, with or without H, Cl, F.
16. A method as claimed in claim 4, characterized in that said first layer and/or second layer comprises polyimide or other mechanically deposited organic dielectric.
17. A method as claimed in claim 4, characterized in that said first layer and/or second layer comprises silicon dioxide, oxynitride, stochiometric or otherwise, with or without H, Cl, F.
18. A method as claimed in claim 4, characterized in that said first layer and/or second layer comprises materials as claimed in any of claims 15 to 18 doped/alloyed with As, P, B, Pb, or other metallic elements, combinations thereof.
19. A method of fabricating a semiconductor device characterized in that a first dielectric layer is applied over an interconnect layer having tracks defining a conductive pattern and made of material having a high coefficient of expansion, the first dielectric layer forming valleys between the tracks of the interconnect layer, spin-on glass is applied over said first layer to planarize it by forming spin-on glass zones in the valleys defined by the first dielectric layer, and a second layer is applied to the planarized first layer, whereby said first and second layers and said spin-on glass zones form a composite multi-layer film, characterized in that said first layer is formed under compression to prevent cracking in the composite multi-layer film during subsequent heat treatment.
20. A method as claimed in claim 19, characterized in that said second layer is a dielectric layer.
21. A method as claimed in claim 19, characterized in that said second layer is an interconnect layer deposited directly onto said first layer planarized with said SOG interlayer.
22. A method as claimed in claim 19, characterized in that said SOG interlayer is formed under a slightly tensile stress of about 5 x 108 dynes/cm2.
23. A method as claimed in claim 22, characterized in that said second layer is formed under a compressive stress of about 5 x 108 to 3 x 109 dynes/cm2.
24. A method as claimed in claim 23, characterized in that said first layer comprises SiOxHy (SG) .
25. A method as claimed in claim 23, characterized in that said second layer comprises PSG.
26. A method as claimed in claim 25, characterized in that said first layer is deposited by LPCVD (Low Pressure Chemical Vapour Deposition) .
27. A method as claimed in claim 25, characterized in that said first layer is deposited by Plasma Enhanced Chemical Vapour Deposition (PECVD) .
28. A method as claimed in claim 19, characterized in that said tracks are made of aluminum or aluminum alloy.
29. A method as claimed in claim 19, characterized in that said tracks are made of material selected from the group consisting of: W, Mo, Ta, Co, Ti; or a reacted metal such as TixNy, TixWy, Tix0vZ2, TixWvN2; or a suicide of W, Mo, Ta, Co, Ti, Pt.
30. A composite insulating film comprising first and second layers with intermediate spin-on glass zones acting as a planarization SOG interlayer for said first layer, at least said first layer being a dielectric layer, characterized in that the first layer is formed under compression to prevent cracking in the composite structure during subsequent heat treatment.
31. A composite insulating film as claimed in claim 30, characterized in that said first layer comprises SiOxHy (SG).
32. A composite insulating film as claimed in claim 30, characterized in that said first layer comprises silicon nitride, stochiometric or otherwise, with or without H, Cl, F.
33. A composite insulating film as claimed in claim 30, characterized in that said first layer comprises polyimide or other mechanically deposited organic dielectric.
34. A composite insulating film as claimed in claim 30, characterized in that said first layer comprises silicon dioxide, oxynitride, stochiometric or otherwise, with or without H, Cl, F.
35. A composite insulating film as claimed in claim 30, characterized in that said first layer comprises materials as claimed in any of claims 31 to 34 doped/alloyed with As, P, B, Pb, or other metallic elements, combinations thereof.
PCT/CA1990/000448 1989-12-20 1990-12-19 Method of making crack-free insulating films with sog interlayer WO1991009422A1 (en)

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CA 2006174 CA2006174A1 (en) 1989-12-20 1989-12-20 Method of making crack-free insulating films with sog interlayer
CA2,006,174 1989-12-20

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Cited By (8)

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Publication number Priority date Publication date Assignee Title
WO1993004501A1 (en) * 1991-08-14 1993-03-04 Mitel Corporation High performance passivation for semiconductor devices
US5364818A (en) * 1990-05-29 1994-11-15 Mitel Corporation Sog with moisture resistant protective capping layer
US5371046A (en) * 1993-07-22 1994-12-06 Taiwan Semiconductor Manufacturing Company Method to solve sog non-uniformity in the VLSI process
EP0655776A1 (en) * 1993-11-30 1995-05-31 STMicroelectronics S.r.l. Autoplanarizing process for the passivation of an integrated circuit
EP0678914A3 (en) * 1994-04-18 1997-02-19 Advanced Micro Devices Inc Method for planarizing an integrated circuit topography.
EP0851480A2 (en) * 1996-12-25 1998-07-01 Canon Sales Co., Inc. Stress-adjusted insulating film forming method, semiconductor device and method of manufacturing the same
KR100914443B1 (en) * 2007-09-04 2009-08-28 후지쯔 마이크로일렉트로닉스 가부시키가이샤 Semiconductor device and process for producing the same
JP2016061718A (en) * 2014-09-19 2016-04-25 株式会社デンソー Semiconductor physical quantity sensor and manufacturing method thereof

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EP0046059A2 (en) * 1980-08-08 1982-02-17 Fujitsu Limited Method of plasma enhanced chemical vapour deposition of films
WO1987002828A1 (en) * 1985-11-04 1987-05-07 Motorola, Inc. Glass intermetal dielectric

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EP0046059A2 (en) * 1980-08-08 1982-02-17 Fujitsu Limited Method of plasma enhanced chemical vapour deposition of films
WO1987002828A1 (en) * 1985-11-04 1987-05-07 Motorola, Inc. Glass intermetal dielectric

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5364818A (en) * 1990-05-29 1994-11-15 Mitel Corporation Sog with moisture resistant protective capping layer
WO1993004501A1 (en) * 1991-08-14 1993-03-04 Mitel Corporation High performance passivation for semiconductor devices
US5541445A (en) * 1991-08-14 1996-07-30 Mitel Corporation High performance passivation for semiconductor devices
US5371046A (en) * 1993-07-22 1994-12-06 Taiwan Semiconductor Manufacturing Company Method to solve sog non-uniformity in the VLSI process
EP0655776A1 (en) * 1993-11-30 1995-05-31 STMicroelectronics S.r.l. Autoplanarizing process for the passivation of an integrated circuit
EP0678914A3 (en) * 1994-04-18 1997-02-19 Advanced Micro Devices Inc Method for planarizing an integrated circuit topography.
EP0851480A2 (en) * 1996-12-25 1998-07-01 Canon Sales Co., Inc. Stress-adjusted insulating film forming method, semiconductor device and method of manufacturing the same
EP0851480A3 (en) * 1996-12-25 1998-07-29 Canon Sales Co., Inc. Stress-adjusted insulating film forming method, semiconductor device and method of manufacturing the same
KR100914443B1 (en) * 2007-09-04 2009-08-28 후지쯔 마이크로일렉트로닉스 가부시키가이샤 Semiconductor device and process for producing the same
JP2016061718A (en) * 2014-09-19 2016-04-25 株式会社デンソー Semiconductor physical quantity sensor and manufacturing method thereof

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