U.S. patent application number 11/185190 was filed with the patent office on 2005-12-08 for low-k dielectric structure and method.
Invention is credited to Kloster, Grant M., Leu, Jihperng, Morrow, Xiarong.
Application Number | 20050272248 11/185190 |
Document ID | / |
Family ID | 32324635 |
Filed Date | 2005-12-08 |
United States Patent
Application |
20050272248 |
Kind Code |
A1 |
Kloster, Grant M. ; et
al. |
December 8, 2005 |
Low-k dielectric structure and method
Abstract
A low-k dielectric sacrificial material is formed within a
microelectronic structure covered with a suitable porous or low
density permeable material. At an appropriate time, the underlying
sacrificial material is decomposed and diffused away through the
overlying permeable material. As a result, at least one void is
created, contributing to desirable dielectric characteristics.
Inventors: |
Kloster, Grant M.; (Lake
Oswego, OR) ; Morrow, Xiarong; (Portland, OR)
; Leu, Jihperng; (Portland, OR) |
Correspondence
Address: |
BLAKELY SOKOLOFF TAYLOR & ZAFMAN
12400 WILSHIRE BOULEVARD
SEVENTH FLOOR
LOS ANGELES
CA
90025-1030
US
|
Family ID: |
32324635 |
Appl. No.: |
11/185190 |
Filed: |
July 19, 2005 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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11185190 |
Jul 19, 2005 |
|
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10301957 |
Nov 21, 2002 |
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Current U.S.
Class: |
438/618 ;
257/E21.581; 257/E23.144; 257/E23.167 |
Current CPC
Class: |
H01L 2924/0002 20130101;
H01L 23/5222 20130101; H01L 2924/0002 20130101; H01L 21/7682
20130101; H01L 23/5329 20130101; H01L 2924/00 20130101 |
Class at
Publication: |
438/618 |
International
Class: |
H01L 021/76 |
Claims
1. A method to make a microelectronic structure comprising: forming
a sacrificial dielectric layer adjacent a substrate layer; forming
a permeable layer upon the sacrificial dielectric layer;
decomposing a portion of the sacrificial dielectric layer to form a
decomposition; diffusing the decomposition through the permeable
layer to form a void in a position previously occupied by a portion
of the sacrificial dielectric layer.
2. The method of claim 1 wherein decomposing a portion of a
sacrificial dielectric layer comprises heating a portion of the
sacrificial dielectric layer above the thermal decomposition
temperature for the sacrificial dielectric layer.
3. The method of claim 1 wherein decomposing a portion of a
sacrificial dielectric layer comprises introducing a solvent to
chemically decompose a portion of the sacrificial dielectric
layer.
4. The method of claim 1 wherein diffusing the decomposition
through the permeable layer comprises introducing a carrier plasma
to the permeable layer to induce diffusion of the decomposition
through the permeable layer to the carrier plasma.
5. The method of claim 1 further comprising forming a conductive
layer across the sacrificial dielectric layer and the permeable
layer before decomposition.
6. The method of claim 1 further comprising forming a conductive
layer across the sacrificial dielectric layer before forming the
permeable layer.
7. The method of claim 6 further comprising forming a shunt layer
over the conductive layer before forming the permeable layer.
8. The method of claim 1 further comprising forming an additional
dielectric layer between the substrate layer and the sacrificial
dielectric layer, the additional dielectric layer comprising a
dielectric material which does not substantially decompose during
decomposing the sacrificial dielectric layer.
9. The method of claim 1 wherein the sacrificial dielectric layer
comprises a polymer.
10. The method of claim 9 wherein the sacrificial dielectric layer
comprises a polymer from the group consisting of polynorbornene,
polycyclohexene, polypropylene oxide, polyethylene oxide,
polystyrene, poly(p-phenylene), polyxylene, cross-linked PMMA,
polyarylene, and poly(aryl ether).
11. The method of claim 1 wherein the permeable layer comprises a
siloxane-based polymer or a carbon doped oxide.
12. The method of claim 5 wherein the permeable layer comprises a
material from the group consisting of silicon dioxide, silicon
nitride, aluminum oxide, aluminum phosphate, boron nitride,
mesoporous silica, aluminosilicate, and fluorinated silicate
glass.
13. A microelectronic structure comprising: substrate layer; a
permeable layer; a sacrificial dielectric layer between the
substrate layer and the permeable layer; and a conductive layer
extending across the sacrificial dielectric layer between the
substrate layer and permeable layer; the permeable layer being
permeable to a decomposition comprising a portion of the
sacrificial dielectric layer.
14. The microelectronic structure of claim 13 wherein the
sacrificial dielectric layer has a lower thermal decomposition
temperature than the permeable layer.
15. The microelectronic structure of claim 13 wherein the
sacrificial dielectric layer is susceptible to a chemically
decomposing agent which is substantially ineffective on the
permeable layer.
16. The microelectronic structure of claim 13 further comprising an
additional dielectric layer between the substrate layer and the
sacrificial dielectric layer, the additional dielectric layer
comprising a dielectric material which does not substantially
decompose during decomposing the sacrificial dielectric layer.
17. The microelectronic structure of claim 13 wherein the
conductive layer is formed across the permeable layer.
18. The microelectronic structure of claim 13 wherein the
conductive layer does not cross the permeable layer, the permeable
layer blanket covering exposed portions of the conductive layer and
sacrificial dielectric layer.
19. The microelectronic structure of claim 18 further comprising a
shunt layer between the permeable layer and exposed portions of the
conductive layers.
20. The microelectronic structure of claim 13 wherein the
sacrificial dielectric layer comprises a polymer.
21. The microelectronic structure of claim 20 wherein the
sacrificial dielectric layer comprises a polymer from the group
consisting of polynorbornene, polycyclohexene, polypropylene oxide,
polyethylene oxide, polystyrene, poly(p-phenylene), polyxylene,
cross-linked PMMA, polyarylene, and poly(aryl ether).
22. The microelectronic structure of claim 13 wherein the permeable
layer comprises a siloxane-based polymer or a carbon doped
oxide.
23. The microelectronic structure of claim 17 wherein the permeable
layer comprises a material from the group consisting of silicon
dioxide, silicon nitride, aluminum oxide, aluminum phosphate, boron
nitride, mesoporous silica, aluminosilicate, and fluorinated
silicate glass.
24. The microelectronic structure of claim 13 wherein the
sacrificial dielectric layer defines one or more voids occupying at
least a portion of the volume occupied by the sacrificial
dielectric layer.
25. The microelectronic structure of claim 24 wherein the one or
more voids occupy more than about 70% of the volume occupied by the
sacrificial dielectric layer.
26. The microelectronic structure of claim 24 wherein the one or
more voids are formed by decomposing a portion of the sacrificial
dielectric layer to form a decomposition, and diffusing the
decomposition away through the permeable layer after forming the
conductive layer.
Description
BACKGROUND OF THE INVENTION
[0001] Low dielectric constant materials are used as interlayer
dielectrics in microelectronic devices, such as semiconductor
devices, to reduce the RC delay and improve device performance. As
device sizes continue to shrink, the dielectric constant of the
material between metal lines must also decrease to maintain the
improvement. Certain low-k materials have been proposed, including
various carbon-containing materials such as organic polymers and
carbon-doped oxides. The eventual limit for a dielectric constant
is k=1, which is the value for a vacuum. Methods and structures
have been proposed to incorporate void spaces or "air gaps" in
attempts to obtain dielectric constants closer to k=1. One major
issue facing air gap technology is how to remove sacrificial
material to facilitate multi-layer structures. Another major issue
facing air gap technology is how to facilitate air gap creation
while providing a structure which can withstand modern processing
steps, such as chemical-mechanical polishing and thermal treatment,
as well as post processing mechanical and thermo-mechanical
rigors.
[0002] Accordingly, there is a need for a microelectronic device
structure incorporating air gaps which has low-k dielectric
properties, can be used in multi-layer structures, and has
acceptable mechanical characteristics during and after
processing.
BRIEF DESCRIPTION OF THE DRAWINGS
[0003] The present invention is illustrated by way of example and
is not limited in the figures of the accompanying drawings, in
which like references indicate similar elements. Features shown in
the drawings are not intended to be drawn to scale, nor are they
intended to be shown in precise positional relationship.
[0004] FIGS. 1A-1J depict cross-sectional views of various aspects
of one embodiment of the present invention incorporating a
permeable layer which functions as a hard mask.
[0005] FIGS. 2A-2B depict two cross sectional views of another
embodiment of the present invention incorporating a permeable layer
which functions as a hard mask, and an additional dielectric layer
between the sacrificial dielectric layer and the substrate
layer.
[0006] FIGS. 3A-3M depict cross-sectional views of various aspects
of another embodiment of the present invention incorporating a
permeable layer which functions as an inter-layer dielectric
layer.
DETAILED DESCRIPTION
[0007] In the following detailed description of embodiments of the
invention, reference is made to the accompanying drawings in which
like references indicate similar elements. The illustrative
embodiments described herein are disclosed in sufficient detail to
enable those skilled in the art to practice the invention. The
following detailed description is therefore not to be taken in a
limiting sense, and the scope of the invention is defined only by
the appended claims.
[0008] This invention involves the integration of decomposable
dielectric materials and permeable layers through which decomposed
portions of the dielectric materials may be effectively diffused,
leaving behind voids or air gaps associated with desirable
dielectric qualities, as well as a permeable layer which may
function as a geometrically efficient, low conductivity platform
for subsequent layers in a multi-layer structure. The use of
permeable layers in hard mask and via inter-layer dielectric
positions may eliminate the need for other intermediate structural
layers between air gap interconnect layers, due to the structural
integrity of the permeable layer which remains intact during
removal of sacrificial material and subsequent multi-layer
construction. In this regard, the permeable layer functions
somewhat like a multi-purpose scaffold to facilitate load bearing,
diffusional transportation of sacrificial material, and dielectric
insulation. The use of permeable layers as described herein may
also eliminate lithographic steps or masks required by other
air-gap dielectric processing techniques for removal of sacrificial
materials, thereby streamlining process requirements. While three
illustrative embodiments are depicted and described in detail,
other variations and modifications will be apparent to those of
ordinary skill in the art, and such variations and modifications
are included within the intended scope of the invention.
[0009] FIG. 1A depicts a multi-layer microelectronic structure
(100) comprising a substrate layer (104), a dielectric layer having
etch selectivity and density such that it functions as a
conventional "etch stop" layer, two conductive layers (110, 112), a
permeable layer (122), and a sacrificial dielectric layer (108)
positioned between the conductive layers (110, 112), and between
the permeable layer and etch stop dielectric layer (106). The
conductive layers (110, 112) are formed across both the permeable
layer (122) and the sacrificial dielectric layer (108). The spacing
between the conductive layers (110, 112) may vary with feature size
of the microelectronic structure as would be apparent to one
skilled in the art, and preferably is between about 10 nanometers
and about 1,000 nanometers. The etch stop dielectric layer (106),
sacrificial dielectric layer (108), conductive layers (110, 112),
and permeable layer (122) are positioned substantially within
planes occupied by the conductive layers (110, 112), which may be
collectively known as the "interconnect layer" (120). The depicted
conductive layers each comprise a line portion (118) and a via
portion (116), as is common conductive layer cross sectional
geometry in some interconnect structures.
[0010] FIG. 1B shows a variation of the structure of FIG. 1A having
similar substrate (104) and interconnect (120) layers, with the
exception that a transformation has occurred at the position
previously occupied by the sacrificial dielectric layer (108) of
FIG. 1A. A portion of the sacrificial dielectric layer has been
"remotely decomposed", or decomposed as other surrounding layers
are left substantially intact, to produce a sacrificial dielectric
layer decomposition (not shown), which has been removed by
diffusion along a diffusion pathway (144) through the permeable
layer (122). The resulting microelectronic structure, shown in FIG.
1B, comprises one or more voids (126) in the volume (128)
previously occupied by the intact sacrificial dielectric layer, the
voids (126) preferably occupying more than about 70% of the volume
(128) previously occupied by the intact sacrificial dielectric
layer. The variation depicted in FIG. 1B may be referred to as the
"transformed" version of the structure of FIG. 1A. This transformed
structure may have more preferable dielectric properties than the
intact structure, and continues to have the structural benefit of
the other surrounding layers, which remain intact and can
contribute to a resistance of forces which may be subsequently
applied during treatments such as chemical mechanical polishing
("CMP").
[0011] In the variation of FIGS. 1A and 1B, the permeable layer
(122) is positioned to protect dielectric layers between it and a
substrate (104) not only from mechanical loads, but also from
environmental factors such as chemicals used to remove subsequent
materials, such as lithography patterning materials. The position
occupied by the permeable layer in FIGS. 1A and 1B may be referred
to as the position often occupied by a "hard mask" layer, which
typically has such a protective functionality for layers between it
and the substrate layer (104), as would be apparent to those
skilled in the art. Specifically, the depicted variation comprises
a permeable layer (122) in the position of a hard mask which is
disposed adjacent both the sacrificial layer (108) and the
conductive layers (110, 112) in a manner wherein the top surface of
the permeable layer (122) hard mask is positioned substantially
within the same plane as the top surface of the conductive layers
(110, 112).
[0012] The material comprising the permeable layer (122) in the
hard mask position is selected for its ability to withstand and
facilitate both remote decomposition of a portion of the material
comprising the sacrificial dielectric layer (108), to produce a
sacrificial dielectric layer decomposition, and removal of the
sacrificial dielectric layer decomposition through the permeable
layer (122), by diffusion, without substantially affecting the
mechanical integrity of the permeable layer (122) or other layers
which surround the sacrificial dielectric layer. The material
comprising the sacrificial dielectric layer (108) is selected for
its ability to not only perform as a low-conductance dielectric
material, but also for its ability to be remotely decomposed and
removed through the permeable layer (122) with which it is matched,
by diffusion.
[0013] Suitable materials for the sacrificial dielectric layer
(108) include but are not limited to polynorbornene-based polymers,
such as that sold under the trade name "Unity400.TM.", distributed
by Promerus LLC; polycyclohexene; the co-polymer of polypropylene
oxide and polyethylene oxide; polystyrene; poly(p-phenylene);
polyxylene; cross-linked polymethylmethacrylate ("PMMA");
polyarylene-based polymeric dielectrics such as that sold under the
trade name "SiLK.TM.", distributed by Dow Chemical Corporation;
poly(aryl ether)-based polymeric dielectrics such as that sold
under the trade name "FLARE.TM.", distributed by Honeywell
Corporation; and polyarylene-based spin-on dielectrics such as that
sold under the trade name "GX-3.TM.", also from Honeywell
Corporation. Depending upon the material selected for this and
other associated layers, such as the conductive layers (110, 112),
the sacrificial dielectric layer (108) may be deposited using
conventional techniques, such as spin-on, chemical vapor deposition
("CVD"), plasma-enhanced chemical vapor deposition ("PECVD"),
evaporative deposition, or physical vapor deposition ("PVD") to
form a layer preferably having a thickness between about 200
nanometers and about 1,500 nanometers. In the case of spin-on or
other deposition techniques, solvent may need to be removed by
evaporative techniques familiar to those skilled in the art.
[0014] Suitable materials for the permeable layer (122) include but
are not limited to silicon dioxide; silicon nitride; silicon
carbide; aluminum oxide; aluminum phosphate; boron nitride; porous
materials known as "zeolites", such as highly-ordered mesoporous
silica and aluminosilicate; a siloxane-based polymer sold under the
trade name "LKD-5109.TM.", distributed by JSR Microelectronics
Corporation, which may be formed into porous layers; fluorinated
silicate glass ("FSG"); porous and nonporous carbon doped oxide
("CDO"), having the molecular structure Si.sub.xO.sub.yR.sub.z, in
which "R" is an alkyl or aryl group, the CDO preferably comprising
between about 5 and about 50 atom % carbon, and more preferably,
about 15 atom % carbon; a CVD-deposited CDO sold under the trade
name "Black Diamond.TM.", distributed by Applied Materials
Corporation; siloxane-based polymers, such as those sold under the
trade names "Nanoglass E.TM." and "Zirkon.TM.", distributed by
Honeywell Corporation and Shipley Corporation, respectively; a
spin-on low-k silicon dioxide variant sold under the trade name
"FOx.TM.", distributed by Dow Corning Corporation; a CVD-deposited
CDO sold under the trade name "Coral.TM.", distributed by Novellus
Corporation; and electron-beam-cured CVD-deposited CDO materials.
It is generally desirable that layers positioned for hard mask
functionality have as small a thickness as possible while still
allowing for reliable etching. Depending upon the etchants and
materials selected for the permeable layer (122) and other
associated layers, such as the conductive layers (110, 112), the
permeable layer (122) may be deposited using conventional
techniques, such as spin-on, CVD, PECVD, evaporative deposition, or
PVD to form a layer having a thickness preferably between about 10
nanometers and about 200 nanometers. Zeolite materials may be
synthesized by an aerogel or xerogel process, spin-coated into
place, or deposited using CVD to form a voided structure upon
deposition.
[0015] The modality for remote decomposition and removal of
sacrificial material without substantial effect upon the permeable
material varies with the materials selected. In one embodiment,
sacrificial material comprising the sacrificial dielectric layer
(108) may be selectively decomposed and removed through the
permeable layer (122) on the basis of differences in thermal
decomposition temperatures between the sacrificial material and
other surrounding materials. For example, several of the
aforementioned suitable sacrificial materials, such as
polynorbornene, polypropylene oxide-polyethylene oxide copolymer,
polystyrene, and cross-linked PMMA may be thermally decomposed at
temperatures not substantially effecting surrounding structures
comprising materials such as silicon dioxide, silicon nitride,
carbon doped oxide, and mesoporous silica, and aluminosilicate. A
pairing of a sacrificial material having a relatively low thermal
decomposition threshold may contribute to selective removal of
thermally decomposed sacrificial material, or sacrificial material
"decomposition", as facilitated or induced, for example, by
introduction of an oxygen or hydrogen rich carrier plasma to carry
away the decomposition, as is known to those skilled in the art as
a standard plasma enhanced carrier technique. Thermally decomposing
the sacrificial material may be accomplished using conventional
equipment, such as a furnace or oven. Depending upon the materials
selected, plasma tools may be appropriate as well, as would be
apparent to one skilled in the art.
[0016] Many of the aforementioned suitable sacrificial materials
also may be selectively chemically decomposed without substantial
decomposition of the aforementioned preferred permeable layer (122)
materials using chemical solvents and agents, such as propylene
glycol monomethyl ether acetate, a versatile solvent used in many
applications, cyclohexanone, a ketone solvent, ketenes such as
1-ene-3-cyclohexanone, hydrogen peroxide, tert-butyl peroxide, and
solutions containing the cerium (IV) ion. In other words,
sacrificial dielectric materials susceptible to a chemically
decomposing agent may be paired with permeable layers comprising
materials upon which such chemically decomposing agent is
substantially ineffective for selective chemical decomposition.
Polymeric sacrificial materials may need functionalization with
polar groups such as hydroxy or alkoxy groups for solvent
compatibility with the selected solvent or agent, as is convention
to those skilled in the art. To clarify the simplified terminology
used herein as associated with the thermal or chemical break-down
of sacrificial materials for subsequent removal, references to
"decompositions" and "decomposing" comprise references to
"dissolving" and "dissolution" as well, or more simply,
"break-down" by thermal or chemical means.
[0017] Once a sacrificial dielectric layer decomposition has been
formed by heating at least a portion of the sacrificial dielectric
material to the appropriate decomposition temperature or
introducing the appropriate chemical agents, the decomposition is
removed by diffusion along a pathway (144) through the permeable
layer (123). Gases comprising broken down, decomposed, or dissolved
sacrificial materials may be diffused through solid materials at
rates in the range of 1.times.10.sup.-8 to 1.times.10.sup.-10 cubic
centimeters per second, and may be diffused through porous
materials even faster, such as rates between 1.times.10.sup.-5 to
1.times.10.sup.-6 cubic centimeters per second or faster, depending
upon the size of the pores or voids. Diffusion of gases into porous
oxide and other materials have been demonstrated in related
technologies and structures, such as with CVD barrier deposition,
plasma treatments, and resist poisoning after etching. Given the
suitable materials and ranges of preferred dimensions for the
various structures, gases comprising broken down, decomposed, or
dissolved sacrificial materials may be diffused away and removed
from an interconnect position within a time between about 20 second
and 300 seconds.
[0018] Diffusion may occur as a byproduct of the decomposition
process, such as the scenario wherein gases carrying portions of
the sacrificial material decomposition may be exhausted away from
the permeable layer (123) given an available lower gradient
pathway, or may occur as facilitated or induced by introduction of
reactive carriers to the area of the decomposition. Preferred
reactive carriers include carrier plasmas such as oxygen and
hydrogen rich plasmas, which are known to actively absorb and
transport materials or portions thereof due to the high reactivity
of oxygen and plasma. Chemical cleaning or etching agents, such as
supercritical carbon dioxide, which are also known to absorb and
transport decomposed materials, may also be used to remove
sacrificial material decompositions. Both the plasma and
supercritical carbon dioxide decomposition modalities require
special process equipment and environments, as is convention to
those skilled in the art.
[0019] Given the variety of suitable materials, many pairings of
permeable layer and sacrificial material may be successfully paired
for selective decomposition and removal, depending upon the mode of
decomposition, surrounding materials, and environmental
limitations. Thermal and chemical modalities for facilitating
selective decomposition and removal of sacrificial materials are
preferred, in part because precise thermal and chemical treatments
are convention in microelectronic device processing. In a preferred
thermal transformation embodiment, the material comprising the
permeable layer (122) has a higher thermal decomposition
temperature, in addition to a high glass transition temperature for
thermo-mechanical stability. With such a pairing, the sacrificial
dielectric layer (108), or a portion thereof, may be heated to a
temperature above the thermal decomposition temperature for the
sacrificial material which is below the thermal decomposition
temperature for the permeable layer (122) and other surrounding
structures, to facilitate removal of the sacrificial material
decomposition before subsequent cooling. In a preferred chemical
transformation embodiment, chemically-enhanced decomposition of the
selected sacrificial material results is substantially no
decomposition of the associated permeable layer material or other
adjacent materials.
[0020] Preferred pairings of permeable and sacrificial materials,
for example, include but are not limited to: a polynorbornene-based
polymer dielectric sacrificial material with a silicon dioxide
permeable layer, wherein the polynorbornene-based polymer
dielectric material is thermally decomposed at a temperature of
between about 400 and about 425 degrees Celsius, without thermally
decomposing the silicon dioxide permeable layer, which has a
thermal decomposition temperature over 500 degrees Celsius; a
polycyclohexene-based polymer dielectric sacrificial material with
a silicon nitride permeable layer, wherein the
polycyclohexene-based polymer dielectric material is thermally
decomposed at a temperature of between about 400 and about 425
degrees Celsius, without thermally decomposing the silicon nitride
permeable layer, which has a thermal decomposition temperature over
500 degrees Celsius; a polystyrene sacrificial dielectric material
with a mesoporous aluminosilicate permeable layer, wherein the
polystyrene sacrificial dielectric material is thermally decomposed
at a temperature of between about 400 and about 425 degrees
Celsius, without thermally decomposing the mesoporous
aluminosilicate permeable layer, which has a thermal decomposition
temperature over 500 degrees Celsius.
[0021] The substrate (104) may be any surface generated when making
an integrated circuit, upon which a conductive layer may be formed.
Substrate (104) thus may comprise, for example, active and passive
devices that are formed on a silicon wafer, such as transistors,
capacitors, resistors, diffused junctions, gate electrodes, local
interconnects, etcetera. Substrate (104) may also comprise
insulating materials (e.g., silicon dioxide, either undoped or
doped with phosphorus or boron and phosphorus; silicon nitride;
silicon oxynitride; or a polymer) that separate active and passive
devices from the conductive layer or layers that are formed
adjacent them, and may comprise other previously formed conductive
layers.
[0022] The structures, methods, and materials associated with the
illustrated embodiments of FIGS. 1A and 1B are further described in
the multiple-layer example depicted in FIGS. 1C-1J which builds
upon the structure depicted in FIG. 1B using similar layers and
materials, and thus serves to not only further describe
single-interconnect-layer methods and structures such as those
depicted in FIGS. 1A and 1B, but also to describe how such
embodiments may be integrated into more complex multi-layer
embodiments of the invention, with previously formed permeable
layers functioning as mechanical platforms to enable formation of
subsequent layers in close proximity to voids resulting from
removed sacrificial materials without mechanical failure.
[0023] Referring to FIG. 1C, an additional etch stop dielectric
layer (131) has been added to the structure depicted in FIG. 1B.
FIG. 1D depicts the microelectronic structure of FIG. 1C with
another sacrificial dielectric layer (109) added adjacent the etch
stop dielectric layer (131). The etch stop dielectric layer (131)
preferably comprises a material, such as silicon nitride other
known etch stop material appropriately matched with the etchability
of adjacent layers, which selectively does not substantially etch
when the layer above (109) is being etched. The etch stop
dielectric layer (131) is deposited using conventional chemical
vapor deposition ("CVD"), plasma enhanced CVD, or low-pressure CVD
techniques, as are well known in the art, at a thickness preferably
between about 10 nanometers and about 200 nanometers. The
sacrificial dielectric layer may comprise a material similar to
that which comprises the sacrificial dielectric layer (108)
depicted in FIG. 1A, such as the aforementioned polymeric
dielectric materials, and may be deposited using conventional
deposition techniques such as spin-on for suitable polymers,
conventional CVD, or physical vapor deposition ("PVD"), at a
thickness depending upon the conductive layer material chosen,
preferably between 200 nanometers and 1,500 nanometers.
[0024] Referring to FIG. 1E, a microelectronic structure similar to
that of FIG. 1D is depicted, the structure of FIG. 1E having two
additional layers deposited adjacent the sacrificial dielectric
layer (109), the two additional layers comprising an additional
permeable dielectric layer (123), and an additional etch stop
dielectric layer (133). Each of these layers may comprise a similar
material and be formed in a similar manner to that with which the
predecessor similar layers (122, 131) were formed, such as by
conventional CVD or spin-on techniques.
[0025] Referring to FIG. 1F, a trench (136) is shown across the
uppermost etch stop layer (133), the adjacent permeable layer
(123), and the sacrificial dielectric layer (109) in an orientation
substantially perpendicular to the plane of the substrate layer, as
is typical convention. The trench (136) is formed using
conventional lithography patterning and etching techniques, in
which the etching may be plasma-enhanced dry etching, or wet
etching using liquid etchants. FIG. 1G shows an expanded trench,
formed using similar conventional lithography patterning and
etching techniques, subsequent to removal of the uppermost etch
stop layer (133 in FIG. 1F) using known techniques such as plasma
ashing or CMP. The resultant enlarged trench (138), having a width
preferably between about 10 nanometers and about 1,000 nanometers
depending upon the materials selected for the conductive layers and
other associated structures, may then be coated with a barrier
layer (not shown) as appropriate given the selected conductive
material. For example, in the case of a copper, a preferred
conductive material which may react adversely with adjacent
dielectric materials and devices, a barrier layer may be formed to
block diffusion of copper or other conductive layer elements into
adjacent layers of dielectric material. Preferable barrier layer
materials for copper conductive layers comprise refractory
materials such as tantalum, tantalum nitride, and titanium nitride,
or other materials that can inhibit diffusion from conductive
layers into dielectric layers. Such barrier layers preferably are
between about 10 and 50 nanometers thick, and preferably are formed
using a conformal CVD process. Known polymeric barrier layers may
also be employed, subject to the requirement that they be selected
from the subgroup of polymer barrier materials which have
relatively good electromigration characteristics.
[0026] Referring to FIG. 1H, a conductive layer (113) is formed
into the geometry defined by the enlarged trench (138) depicted in
FIG. 1G. The conductive layer (113) comprises material
conventionally used to form conductive layers in integrated
circuits, and preferably comprises metals such as copper, aluminum,
and alloys thereof, formed using known techniques such as
electroplating or CVD, or PVD.
[0027] For example, the depicted conductive layer (113) may be
formed using dual damascene techniques, wherein a trench filled
with a conductive material using, for example, known
electroplating, chemical vapor deposition, or physical deposition
techniques. As a result of the deposition process, the trench may
be overfilled with conductive material, resulting in extra
conductive material outside of the trench (114), as depicted in
FIG. 1H. Copper is a preferred conductive material, and copper dual
damascene processing, generally comprising adding a barrier layer
for isolation purposes before electroplating, as discussed above,
is known convention in the art. Alternatively, a conductive layer
(113) may be made from doped polysilicon or a silicide, e.g., a
silicide comprising tungsten, titanium, nickel, or cobalt, using
known techniques. The resultant conductive layer (113) is formed
across both the permeable layer (123) and the sacrificial
dielectric layer (109).
[0028] It is important to note that while a damascene type process
is illustrated, wherein the conductive layer is formed into
trenches using electroplating techniques, the dielectric aspects of
the invention, illustrated in summary fashion with the
transformation from structures like that of FIGS. 1A, 1I, 2A, 3C,
and 3L to structures like those of FIGS. 1B, 1J, 2B, 3D, and 3M,
respectively, may be similarly applied to structures formed using
other conventional techniques for forming conductive layers, such
as subtractive metallization, given that the appropriate materials
are in place as further described herein. As would be apparent to
one skilled in the art, subtractive metallization may involve
formation of adjacent dielectric layers after formation of
conductive layers, and the geometries of conductive layers formed
may vary from those available with electroplating processes such as
dual damascene.
[0029] Referring to FIG. 1I, the extra conductive material outside
of the trench (114) previously seen in FIG. 1G has been removed,
preferably by chemical mechanical polishing of the extra material
until substantially none remains and the conductive layer is
refined to compose a line portion (118) and a via portion (116),
the line portion (118) having a top surface which is substantially
within the same plane as the top surface of the adjacent permeable
layer (123), as shown in FIG. 1I. Since, for illustrative purposes,
the modifications, materials, and processes depicted in FIGS. 1C-1I
and described herein have paralleled those used to develop the
structures of FIGS. 1A and 1B, the top portion of the structure
depicted in FIG. 1I looks very similar to the structure of FIG. 1A,
in that it has a sacrificial dielectric layer (109), between a
permeable layer (123) positioned as a hard mask, and an etch stop
dielectric layer (131), with a conductive layer crossing portions
of the permeable (123), sacrificial dielectric (109), and etch stop
(131) layers.
[0030] Referring to FIG. 1J, and following the description in
reference to the parallel structure of FIG. 1B, the sacrificial
dielectric material has been remotely decomposed using thermal or
chemical techniques, and removed by diffusion (144) through the
permeable layer (123), leaving behind a dielectric layer having one
or more voids (127) in the volume (129) previously occupied by the
intact sacrificial dielectric layer (109) of FIG. 1J, the voids
(127) preferably occupying more than about 70% of the volume
previously occupied by the intact sacrificial dielectric layer
(109).
[0031] Depending upon the selected conductive material, a shunt
layer (not shown) may be subsequently formed over the conductive
layer (113) using conventional techniques and materials, to isolate
the conductive layer from subsequent treatments and materials. With
copper metal conductive layers, a metal shunt layer comprising, for
example, cobalt or tungsten, is effective for isolating the copper.
The shunt material (not shown) preferably is deposited using
conventional selective techniques such as electroless or flash
deposition, at a thickness preferably between about 5 nanometers
and about 100 nanometers. Deposition of the shunt material may
follow a planarization using known techniques such as
chemical-mechanical planarization. As would be apparent to one
skilled in the art, the selectivity of the preferred shunt
deposition procedures generally obviates the need for additional
planarization or etch back to remove shunt material from dielectric
materials adjacent the conductive layers.
[0032] Referring to FIGS. 2A and 2B, an analog of the structure
depicted in FIGS. 1A and 1B is depicted, the variation of FIG. 2
having substantially the same substrate layer (104), etch stop
dielectric layer (106), conductive layers (110, 112), and permeable
layer (122) as included in the structures of FIGS. 1A and 1B, and
having a thinner sacrificial dielectric layer (208) which, in this
embodiment, provides room for an additional dielectric layer (246)
positioned between the etch stop dielectric layer (106) and both
the conductive layers (110, 112) and the sacrificial dielectric
layer (208), as shown in FIG. 2A. In a manner analogous to that of
the structure of FIG. 1, the structure of FIG. 2A is converted to
the structure of FIG. 2B by remote decomposition of at least a
portion of the sacrificial dielectric layer (208) to form a
sacrificial dielectric layer decomposition, and removal of a
portion of the decomposition through the permeable layer (122) by
diffusion along a diffusion pathway (244) away from the volume
(228) now occupied by a dielectric layer defining one or more voids
(226), which provide dielectric property advantages. In the
depicted variation, the dielectric layer (246) comprises a
dielectric material which is not removed during the transformation
of the sacrificial dielectric layer (208), and is in this sense a
"nonsacrificial" dielectric layer. Depending upon the mode of
decomposition of the sacrificial dielectric layer (208), the
nonsacrificial layer may, for example, be selected from dielectric
materials having higher thermal decomposition temperatures than
that of the material comprising the sacrificial dielectric layer
(208), or lower chemical decomposition thresholds when placed in
contact with chemical solvents, for example, which may be used to
selectively chemically decompose the material comprising the
sacrificial dielectric layer (208).
[0033] Suitable materials for the dielectric layer (246) include
but are not limited to siloxane-based polymers, such as those sold
under the trade names "LKD-5109.TM.", "Nanoglass E.TM.", and
"Zirkon.TM.", distributed by JSR Microelectronics Corporation,
Honeywell Corporation, and Shipley Corporation, respectively;
fluorinated silicate glass ("FSG"); porous and nonporous carbon
doped oxide ("CDO"), having the molecular structure
Si.sub.xO.sub.yR.sub.z, in which "R" is an alkyl or aryl group, the
CDO preferably comprising between about 5 and about 50 atom %
carbon, and more preferably, about 15 atom % carbon; a
CVD-deposited CDO sold under the trade name "Black Diamond.TM.",
distributed by Applied Materials Corporation; silicon dioxide; a
spin-on low-k silicon dioxide variant sold under the trade name
"FOx.TM.", distributed by Dow Corning Corporation; a CVD-deposited
CDO sold under the trade name "Coral.TM.", distributed by Novellus
Corporation; electron-beam-cured CVD-deposited CDO materials; and
materials known as "zeolites", such as highly-ordered mesoporous
silica and aluminosilicate.
[0034] Many other dielectric materials known in the art may be
suitable to comprise the dielectric layer (246), as its main
function besides low dielectric constant isolation is mechanical
support for adjacent structures. Other suitable materials for the
dielectric layer (246) include but are not limited to silicon
dioxide (either undoped or doped with phosphorus or boron and
phosphorus); silicon nitride; silicon oxy-nitride; porous oxide; an
organic containing silicon oxide; or a polymer. Silicon dioxide,
silicon nitride, and silicon oxy-nitride preferably have relatively
high mechanical strength characteristics as compared with many
suitable dielectric layer (246) materials. Also preferred are
polymers or carbon doped oxides, as further described above, with a
low dielectric constant: preferably less than about 3.5 and more
preferably between about 1.5 and about 3.0.
[0035] Preferably, the material comprising the dielectric layer
(246) has a thermal decomposition temperature higher than that of
the associated sacrificial material should a thermal decomposition
modality be envisioned; should a chemical decomposition modality be
employed to facilitate removal of the sacrificial material, a
material for the dielectric layer (246) is preferred which is not
substantially decomposed with exposure to the pertinent chemical
agents or solvents. In other words, the material comprising the
dielectric layer (246) preferably does not substantially decompose
during decomposing of the sacrificial dielectric layer (208). The
dielectric layer (246) preferably has a thickness between about 100
nanometers and about 1,200 nanometers and is formed using
conventional techniques appropriate for the selected material, such
as spin-on, CVD, PECVD, evaporative deposition, and PVD.
[0036] In the depicted variation, the dielectric layer (246) is
positioned adjacent the via portions (116) of the conductive layers
and not adjacent to the line portions (118). Such a geometric
configuration may be desirable because it provides support to the
narrowed via portions (116), which may be more susceptible to
undesirable bending or deformation due to their smaller relative
size, while it also leaves the highly-conductive line portions
(118) more likely surrounded by voids resulting from the
decomposition and removal of a portion of the sacrificial
dielectric layer (208).
[0037] Referring to FIGS. 3A and 3J, another illustrative
embodiment of the invention is depicted wherein the permeable layer
(or layers), as first shown in FIG. 3C (324), are located not in
conventional hard mask position, but in the position and function
of a dielectric layer, and more specifically, an interlayer
dielectric or "ILD" layer for a subsequently-formed interconnect
layer. Following the manner in which FIGS. 1A-1B are used above to
introduce concepts further described and expanded in FIGS. 1C-1J,
FIGS. 3A-3D serve an analogous function for FIGS. 3E-3M, which
build upon the concepts introduced with reference to FIGS. 3A-3D,
once again illustrating how such embodiments may be integrated into
more complex multi-layer embodiments of the invention, with
previously formed permeable layers functioning as mechanical
platforms to enable formation of subsequent layers in close
proximity to voids resulting from removed sacrificial materials
without mechanical failure.
[0038] Referring to FIG. 3A, a microelectronic structure (300) is
depicted having a dielectric layer (340) disposed between a
substrate layer (104) and a sacrificial dielectric layer (308), and
two conductive layers (110, 112) positioned across the dielectric
layer (340) and sacrificial dielectric layer (308). The substrate
layer (104) may comprise similarly broad panoply of materials and
compositions as has been described in reference to FIG. 1.
[0039] Depicted adjacent the substrate layer (104) is a dielectric
layer (340), which in the depicted embodiment, comprises a
nonsacrificial material relative to the sacrificial dielectric
layer (308) to which it is adjacent, in that the dielectric layer
(340) is selected to not substantially decompose during remote
decomposition of the sacrificial dielectric layer (308), as
described in further detail below. Depending upon the mode of
decomposition of the sacrificial dielectric layer (308), the
nonsacrificial dielectric layer (340) may, for example, be selected
from dielectric materials having higher thermal decomposition
temperatures than that of the material comprising the sacrificial
dielectric layer (308), or lower chemical decomposition thresholds
when placed in contact with chemical solvents, for example, which
may be used to selectively chemically decompose the material
comprising the sacrificial dielectric layer (208).
[0040] Depending upon process demands associated with the substrate
layer (104), the dielectric layer (340) may comprise almost any
dielectric material used to isolate conductive layers such as those
depicted (110, 112). Suitable materials and formation techniques
are discussed above in reference to the dielectric layer (246) of
FIGS. 2A and 2B. As discussed below in reference to FIG. 3C, in
embodiments wherein a portion of the inter-layer dielectric
material must function as a permeable layer through which a
sacrificial material decomposition shall be diffused, a more narrow
selection of materials is required.
[0041] Preferably, the material comprising the dielectric layer
(340) has a thermal decomposition temperature higher than that of
the associated sacrificial material should a thermal decomposition
modality be envisioned; should a chemical decomposition modality be
employed to facilitate removal of the sacrificial material, a
material for the dielectric layer (340) is preferred which is not
substantially effected by exposure to the pertinent chemical agents
or solvents. The dielectric layer (340) preferably has a thickness
between about 100 nanometers and about 1,200 nanometers and is
formed using conventional techniques for the selected materials,
such as spin-on, CVD, PECVD, evaporative deposition, and PVD.
[0042] In the depicted variation, the dielectric layer (340) is
positioned adjacent the via portions (316) of the conductive layers
and not adjacent to the line portions (318). As with the dielectric
structure of FIGS. 2A and 2B, such a geometric configuration may be
desirable because it provides support to the narrowed via portions
(316), which may be more susceptible to undesirable bending or
deformation due to their smaller relative size, while it also
leaves the highly-conductive line portions (318) more likely
surrounded by voids resulting from the decomposition and removal of
a portion of the sacrificial dielectric layer (308), as described
below.
[0043] A sacrificial dielectric layer (308) is positioned adjacent
the dielectric layer (340) and between the two depicted conductive
layers (110, 112), as shown in FIG. 3A. The material comprising the
sacrificial layer (308), like that of the previously described
sacrificial layers (108, 208), is selected for not only dielectric
properties, but also for relative decomposition threshold and
diffusability through a permeable layer with which is paired. In
other words, the material comprising the sacrificial layer (308)
must have desirable dielectric performance, particularly if any
significant portion of the layer (308) is to remain intact after
some other portion of the layer (308) has been decomposed and
removed; it must be selectively and remotely decomposable without
substantial effect to surrounding structures, such as conductive
layers (110, 112), shunt layers which may partially or completely
encapsulate the conductive layers (342 of FIG. 3B, for example),
the dielectric layer (340), and the permeable layer (324 of FIG.
3C, for example); and when decomposed, must be diffusible through
and away from the permeable layer (324 of FIG. 3C, for example)
material with which is structurally associated.
[0044] Suitable materials for the sacrificial dielectric layer
(308) in the depicted embodiment include but are not limited to
polynorbornene-based polymers, such as that sold under the trade
name "Unity400.TM.", distributed by Promerus LLC; polycyclohexene;
the co-polymer of polypropylene oxide and polyethylene oxide;
polystyrene; poly(p-phenylene); polyxylene; cross-linked
polymethylmethacrylate ("PMMA"); polyarylene-based polymeric
dielectrics such as that sold under the trade name "SiLK.TM.",
distributed by Dow Chemical Corporation; poly(aryl ether)-based
polymeric dielectrics such as that sold under the trade name
"FLARE.TM.", distributed by Honeywell Corporation; and
polyarylene-based spin-on dielectrics such as that sold under the
trade name "GX-3.TM.", also from Honeywell Corporation. Depending
upon the material selected for this and other associated layers,
the sacrificial dielectric layer (308) may be deposited using
conventional techniques, such spin-on, CVD, PECVD, evaporative
deposition, and PVD, to form a layer having a thickness preferably
between about 100 nanometers and about 1,000 nanometers.
[0045] As with the conductive layers (110, 112) described in
association with other embodiments, the conductive layers depicted
in FIGS. 3A-3M may comprise material conventionally used to form
conductive layers in integrated circuits, and preferably comprises
metals such as copper, aluminum, and alloys thereof, formed using
known techniques such as electroplating or CVD, or PVD.
[0046] Referring to FIG. 3B, a shunt layer (342) has been added
adjacent each of the conductive layers (110, 112). A shunt layer
(342) may be formed using conventional techniques and materials, to
isolate material comprising the conductive layers (110, 112) from
subsequent treatments and materials. With copper metal conductive
layers, a metal shunt layer comprising, for example, cobalt or
tungsten, is effective for isolating the copper. The shunt material
preferably may be deposited using conventional selective techniques
such as electroless or flash deposition to form a shunt layer (342)
having a thickness preferably between about 5 nanometers and about
100 nanometers. Deposition of the shunt material may follow a
planarization using known techniques such as chemical-mechanical
planarization. As would be apparent to one skilled in the art, the
selectivity of the preferred shunt deposition procedures generally
obviates the need for additional planarization or etch back to
remove shunt material from dielectric materials adjacent the
conductive layers.
[0047] Referring to FIG. 3C, a permeable layer (324) is shown,
formed adjacent the exposed shunt layer (324) and sacrificial
dielectric layer (308) surfaces. In this embodiment, the conductive
layers (110, 112), in place before the permeable layer (324), are
not formed across the permeable layer (324). The positioning of the
permeable layer (324) over the existing depicted topology may be
known as "blanket" deposition due to the nature of the layer
"blanket" covering, or substantially fully covering, surfaces of
structures which may not be in the same plane, as a traditional
blanket would when positioned over physical topology. Given the
inter-layer dielectric position of the permeable layer (324) as
shown in FIGS. 3J and 3K, for example, the material comprising it
preferably has a low dielectric constant. In addition, such
material is selected and paired with a sacrificial material to
enable remote decomposability via either thermal or chemical means,
and removal of a decomposition of sacrificial material by diffusion
through the permeable layer (324). Further, since the permeable
layer (324) remains intact subsequent to removal of sacrificial
material, materials providing added mechanical integrity to the
integration are preferred.
[0048] Suitable materials for the permeable layer (324) include but
are not limited to porous materials such as siloxane-based
polymers, sold under trade names such as "LKD-5109.TM.",
distributed by JSR Microelectronics Corporation, "Nanoglass E.TM.",
distributed by Honeywell Corporation, "Zirkon.TM.", distributed by
Shipley Corporation, and "MesoELK.TM.", distributed by Air Products
Corporation; and porous carbon doped oxide ("CDO"), having the
molecular structure Si.sub.xO.sub.yR.sub.z, in which "R" is an
alkyl or aryl group, the CDO preferably comprising between about 5
and about 50 atom % carbon, and more preferably, about 15 atom %
carbon. Such materials form porous permeable layers having pores
with average diameters between about 5 angstroms and about 20
angstroms, the term "average diameter", conventionally calculated
as twice the cube root of (0.75*actual pore volume/pi), being in
reference to the fact that the pores generally are not perfectly
spherical in shape. Low density materials such as
electron-beam-cured CVD-deposited carbon doped oxides, also are
suitable. Each of the aforementioned porous and/or low-density
materials has relatively high thermal decomposition temperature,
over 500 degrees Celsius. Depending upon the materials selected for
the permeable layer (324) and other associated layers, such as the
conductive layers (313, 315), the permeable layer (324) may be
deposited using conventional techniques, such as spin-on, CVD,
PECVD, evaporative deposition, and PVD, to form a layer preferably
having a thickness between about 100 nanometers and about 500
nanometers.
[0049] In an analogous fashion to that described in reference to
FIGS. 1A and 1B, and 2A and 2B, the structure depicted in FIG. 3C
may be transformed into the structure of FIG. 3D by remote
decomposition of at least a portion of the sacrificial dielectric
layer (308) using, for example, chemical or thermal means, and
subsequent removal of the sacrificial dielectric decomposition by
diffusion of the decomposition through the permeable layer (324)
along a diffusion pathway (344), as shown in FIG. 3B, leaving
behind one or more voids (326) in the volume (324) previously
occupied by the intact sacrificial dielectric layer (308 of FIG.
3A) which may have both preferred dielectric properties and
structural integrity. The voids preferably occupy more than about
70% of the volume previously occupied by the intact sacrificial
dielectric layer.
[0050] Preferred pairings of permeable and sacrificial materials
include but are not limited to: a polynorbornene-based polymer
dielectric sacrificial material with a porous siloxane-based
polymer permeable layer, wherein the polynorbornene-based polymer
dielectric material is thermally decomposed at a temperature of
between about 400 and about 425 degrees Celsius, without thermally
decomposing the siloxane-based polymer permeable layer, which has a
thermal decomposition temperature over 500 degrees Celsius; and a
polycyclohexene-based polymer sacrificial dielectric material with
a porous carbon doped oxide permeable layer, wherein the
polycyclohexene-based sacrificial dielectric material is thermally
decomposed at a temperature of between about 400 and about 425
degrees Celsius, without thermally decomposing the porous carbon
doped oxide permeable layer, which has a thermal decomposition
temperature over 500 degrees Celsius.
[0051] The structures, methods, and materials associated with the
illustrated embodiments of FIGS. 3A-3D are further described in the
multiple-layer example depicted in FIGS. 3E-3M which builds upon
the structure depicted in FIG. 3D using similar layers and
materials, and thus serves to not only further describe
single-interconnect-layer embodiments such as that depicted in
FIGS. 3A-3D, but also to describe how such embodiments may be
integrated into more complex multi-layer embodiments of the
invention.
[0052] Referring to FIG. 3E, an additional sacrificial dielectric
layer (309) has been deposited adjacent the permeable layer (324)
following the transformation to the structure of FIG. 3D. The
material comprising the sacrificial dielectric layer (309) may be
comprised of similar materials to those comprising the previous
sacrificial layer (308), and may be deposited using conventional
techniques such as spin on or known vapor deposition variations at
thicknesses preferably between about 10 nanometers and 200
nanometers. Referring to FIG. 3F, two additional layers have been
formed adjacent the sacrificial dielectric layer (309), one being a
first hard mask layer (332), the other being a second hard mask
layer (334), the two hard mask layers enabling conventional
multi-phase lithography, as is illustrated in FIGS. 3G and 3H. Dual
layer hard masking is well known in the art of dual damascene
interconnect formation, and conventional pairings of materials for
the two hard mask layers (332, 334), which generally have different
etch selectivities relative to each other, may be employed.
[0053] Referring to FIG. 3G, trenches (336, 337) are formed
substantially perpendicularly to the orientation of the plane of
the substrate layer (104) using patterning followed by etching to
the shunt layer (342), resulting in trenches (336, 337). Referring
to FIG. 3H, subsequent to removal of the second hard mask layer
(334) using conventional techniques, the trenches are enlarged with
further etching to form enlarged trenches (338, 339) to define the
shape of subsequently-formed conductive layers, as shown in FIG.
31, with a width preferably between 10 nanometers and 1,000
nanometers.
[0054] Referring to FIG. 31, conductive layers are formed,
preferably using similar materials and process technologies as
described in reference to FIG. 1H. Barrier layers (not shown) may
also be added to isolate the selected conductive material, as
further described in reference to FIG. 1H. As shown in FIG. 31,
conductive layer formation may result in conductive material
portions (314) extending beyond the main body of the conductive
layers (313, 315) as defined by the previously formed enlarged
trenches (338 and 339 of FIG. 3H). Referring to FIG. 3J, such
extending portions have been removed using standard techniques such
as CMP or etch back.
[0055] Referring to FIG. 3K, a shunt layer (343) is formed adjacent
the conductive layers (313, 315), as described in reference to
analogous structures of FIG. 3B. Subsequently, a permeable layer
(325) is blanket deposited adjacent the exposed portions of the
shunt layer (343) and sacrificial dielectric layer (309), as shown
in FIG. 3L, the materials comprising the permeable layer (325)
being appropriately paired with those of the sacrificial dielectric
layer (309) for decomposition and removal of at least a portion of
the sacrificial dielectric material, as discussed above. As
discussed in reference to FIG. 3C, in this embodiment, the
conductive layers (313, 315), in place before the permeable layer
(325), are not formed across the permeable layer (325). Finally, in
reference to FIG. 3M, a transformation has been made due to the
selective remote decomposition of at least a portion of the
sacrificial dielectric layer (309 of FIG. 3K) and diffusion of such
decomposition through the permeable layer (325) to leave behind one
or more voids (327) in the volume previously occupied (329) by the
intact sacrificial layer (309 of FIG. 3K), the voids preferably
occupying more than about 70% of the volume previously occupied by
the intact sacrificial layer.
[0056] Thus, a novel solution for low-k structure and formation
thereof is disclosed. Although the invention is described herein
with reference to specific embodiments, many modifications therein
will readily occur to those of ordinary skill in the art.
Accordingly, all such variations and modifications are included
within the intended scope of the invention as defined by the
following claims.
* * * * *