U.S. patent application number 12/283217 was filed with the patent office on 2009-01-22 for forming dual metal complementary metal oxide semiconductor integrated circuits.
Invention is credited to Justin K. Brask, Robert S. Chau, Suman Datta, Mark Doczy, Jack Hwang, Jack Kavalieros, Matthew V. Metz, Mitchell Taylor.
Application Number | 20090020825 12/283217 |
Document ID | / |
Family ID | 35241210 |
Filed Date | 2009-01-22 |
United States Patent
Application |
20090020825 |
Kind Code |
A1 |
Doczy; Mark ; et
al. |
January 22, 2009 |
Forming dual metal complementary metal oxide semiconductor
integrated circuits
Abstract
Complementary metal oxide semiconductor metal gate transistors
may be formed by depositing a metal layer in trenches formerly
inhabited by patterned gate structures. The patterned gate
structures may have been formed of polysilicon in one embodiment.
The metal layer may have a workfunction most suitable for forming
one type of transistor, but is used to form both the n and p-type
transistors. The workfunction of the metal layer may be converted,
for example, by ion implantation to make it more suitable for use
in forming transistors of the opposite type.
Inventors: |
Doczy; Mark; (Beaverton,
OR) ; Taylor; Mitchell; (Lake Oswego, OR) ;
Brask; Justin K.; (Portland, OR) ; Kavalieros;
Jack; (Portland, OR) ; Datta; Suman;
(Beaverton, OR) ; Metz; Matthew V.; (Hillsboro,
OR) ; Chau; Robert S.; (Beaverton, OR) ;
Hwang; Jack; (Portland, OR) |
Correspondence
Address: |
TROP PRUNER & HU, PC
1616 S. VOSS ROAD, SUITE 750
HOUSTON
TX
77057-2631
US
|
Family ID: |
35241210 |
Appl. No.: |
12/283217 |
Filed: |
September 10, 2008 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
10889535 |
Jul 12, 2004 |
7439113 |
|
|
12283217 |
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Current U.S.
Class: |
257/369 ;
257/E27.062 |
Current CPC
Class: |
H01L 21/823842
20130101 |
Class at
Publication: |
257/369 ;
257/E27.062 |
International
Class: |
H01L 27/092 20060101
H01L027/092 |
Claims
1. A semiconductor structure comprising: a transistor of a first
type including a gate electrode; a transistor of a second type
including a gate electrode, said transistor of a second type
including a gate dielectric, a first metal over said gate
dielectric, and a second metal over said first metal, said first
metal having an altered workfunction.
2. The structure of claim 1 wherein the workfunction of said first
metal has been increased.
3. The structure of claim 2 wherein said transistor of a first type
has a metal layer of the same material as the first metal layer of
said transistor of a second type but said first metal layer has a
different workfunction than said metal layer of said transistor of
a first type.
4. The structure of claim 3 wherein said transistor of said first
type is an n-type transistor and said transistor of a second type
is a p-type transistor.
5. The structure of claim 4 wherein said transistors include a gate
dielectric layer having a dielectric constant greater than 10.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a divisional of U.S. patent application
Ser. No. 10/889,535, filed Jul. 12, 2004.
BACKGROUND
[0002] The present invention relates to methods for making
semiconductor devices, in particular, semiconductor devices with
metal gate electrodes.
[0003] MOS field-effect transistors with very thin gate dielectrics
made from silicon dioxide may experience unacceptable gate leakage
currents. Forming the gate dielectric from certain high dielectric
constant (K) dielectric materials, instead of silicon dioxide, can
reduce gate leakage. As used herein, high-k dielectric means having
a dielectric constant higher than 10. When, however, a high-k
dielectric film is initially formed, it may have a slightly
imperfect molecular structure. To repair such a film, it may be
necessary to anneal it at a relatively high temperature.
[0004] Because such a high-k dielectric layer may not be compatible
with polysilicon, it may be desirable to use metal gate electrodes
in devices that include high-k gate dielectrics. When making a CMOS
device that includes metal gate electrodes, it may be necessary to
make the NMOS and PMOS gate electrodes from different materials. A
replacement gate process may be used to form gate electrodes from
different metals. In that process, a first polysilicon layer,
bracketed by a pair of spacers, is removed selectively to a second
polysilicon layer to create a trench between the spacers. The
trench is filled with a first metal. The second polysilicon layer
is then removed, and replaced with a second metal that differs from
the first metal.
[0005] Thus, there is a need for alternate ways to form replacement
metal gate electrodes.
BRIEF DESCRIPTION OF THE DRAWINGS
[0006] FIGS. 1A-1N represent cross-sections of structures that may
be formed when carrying out an embodiment of the method of the
present invention.
[0007] Features shown in these figures are not intended to be drawn
to scale.
DETAILED DESCRIPTION
[0008] FIGS. 1A-1N illustrate structures that may be formed, when
carrying out an embodiment of the method of the present invention.
Initially, high-k gate dielectric layer 170 and a sacrificial metal
layer 169 are formed on substrate 100, generating the FIG. 1A
structure. Substrate 100 may comprise a bulk silicon or
silicon-on-insulator substructure. Alternatively, substrate 100 may
comprise other materials--which may or may not be combined with
silicon--such as: germanium, indium antimonide, lead telluride,
indium arsenide, indium phosphide, gallium arsenide, or gallium
antimonide. Although a few examples of materials from which
substrate 100 may be formed are described here, any material that
may serve as a foundation upon which a semiconductor device may be
built falls within the spirit and scope of the present
invention.
[0009] Some of the materials that may be used to make high-k gate
dielectric layer 170 include: hafnium oxide, hafnium silicon oxide,
lanthanum oxide, lanthanum aluminum oxide, zirconium oxide,
zirconium silicon oxide, tantalum oxide, titanium oxide, barium
strontium titanium oxide, barium titanium oxide, strontium titanium
oxide, yttrium oxide, aluminum oxide, lead scandium tantalum oxide,
and lead zinc niobate. Particularly preferred are hafnium oxide,
zirconium oxide, titanium oxide and aluminum-oxide. Although a few
examples of materials that may be used to form high-k gate
dielectric layer 170 are described here, that layer may be made
from other materials that serve to reduce gate leakage. The layer
170 has a dielectric constant higher than 10 and from 15 to 25 in
one embodiment of the present invention.
[0010] High-k gate dielectric layer 170 may be formed on substrate
100 using a conventional deposition method, e.g., a conventional
chemical vapor deposition ("CVD"), low pressure CVD, or physical
vapor deposition ("PVD") process. Preferably, a conventional atomic
layer CVD process is used. In such a process, a metal oxide
precursor (e.g., a metal chloride) and steam may be fed at selected
flow rates into a CVD reactor, which is then operated at a selected
temperature and pressure to generate an atomically smooth interface
between substrate 100 and high-k gate dielectric layer 170. The CVD
reactor should be operated long enough to form a layer with the
desired thickness. In most applications, high-k gate dielectric
layer 170 may be less than about 60 Angstroms thick, for example,
and, in one embodiment, between about 5 Angstroms and about 40
Angstroms thick.
[0011] A sacrificial metal layer 169 may be formed over the
dielectric layer 170. The sacrificial metal layer 169 may be any
metal that is capable of withstanding high temperatures (greater
than 450.degree. C.) without reaction with overlying materials. As
one example, the sacrificial metal layer 14 may be formed of
titanium nitride. In one embodiment, the layer 169 may be formed by
sputtering. In another embodiment, the layer 169 may be formed by
atomic layer deposition.
[0012] After high-k gate dielectric layer 170 and sacrificial metal
layer 169 are formed on substrate 100, sacrificial layer 171 is
formed on high-k gate dielectric layer 170 as shown in FIG. 1B. In
this embodiment, hard mask layer 172 is then formed on sacrificial
layer 171, generating the FIG. 1B structure. Sacrificial layer 171
may comprise polysilicon and may be deposited on sacrificial metal
layer 169 using a conventional deposition process. Sacrificial
layer 171 may be, for example, between about 100 and about 2,000
Angstroms thick, and, in one embodiment, between about 500 and
about 1,600 Angstroms thick.
[0013] Hard mask layer 172 may comprise silicon nitride between
about 100 and about 1000 Angstroms thick, for example, and between
about 200 and about 350 Angstroms thick in one embodiment. Hard
mask layer 172 may be formed on sacrificial layer 171.
[0014] Sacrificial layer 171 and hard mask layer 172 are then
patterned to form patterned hard mask layers 130, 131, and
patterned sacrificial layers 104, 106, and 169--as FIG. 1C
illustrates. Conventional wet or dry etch processes may be used to
remove unprotected parts of hard mask layer 172, sacrificial metal
layer 169 and sacrificial layer 171. In this embodiment, after
those layers have been etched, exposed part 174 of high-k gate
dielectric layer 170 is removed.
[0015] Although exposed part 174 of high-k gate dielectric layer
170 may be removed using dry or wet etch techniques, it may be
difficult to etch that layer using such processes without adversely
affecting adjacent structures. It may be difficult to etch high-k
gate dielectric layer 170 selectively to the underlying substrate
using a dry etch process, and wet etch techniques may etch high-k
gate dielectric layer 170 isotropically--undercutting overlying
sacrificial layers 104, 106 in an undesirable fashion.
[0016] To reduce the lateral removal of high-k gate dielectric
layer 170, as exposed part 174 of that layer is etched, exposed
part 174 of high-k gate dielectric layer 170 may be modified to
facilitate its removal selectively to covered part 175 of that
layer. Exposed part 174 may be modified by adding impurities to
that part of high-k gate dielectric layer 170 after sacrificial
layer 171 has been etched. A plasma enhanced chemical vapor
deposition ("PECVD") process may be used to add impurities to
exposed part 174 of high-k gate dielectric layer 170. In such a
PECVD process, a halogen or halide gas (or a combination of such
gases) may be fed into a reactor prior to striking a plasma. The
reactor should be operated under the appropriate conditions (e.g.,
temperature, pressure, radio frequency, and power) for a sufficient
time to modify exposed part 174 to ensure that it may be removed
selectively to other materials. In one embodiment, a low power
PECVD process, e.g., one taking place at less than about 200 Watts,
is used.
[0017] In one embodiment, hydrogen bromide ("HBr") and chlorine
("Cl.sub.2") gases are fed into the reactor at appropriate flow
rates to ensure that a plasma generated from those gases will
modify exposed part 174 in the desired manner. Between about 50 and
about 100 Watts wafer bias (for example, about 100 Watts) may be
applied for a sufficient time to complete the desired
transformation of exposed part 174. Plasma exposure lasting less
than about one minute, and perhaps as short as 5 seconds, may be
adequate to cause that conversion.
[0018] After exposed part 174 has been modified, it may be removed.
The presence of the added impurities enables that exposed part to
be etched selectively to covered part 175 to generate the FIG. 1D
structure. In one embodiment, exposed part 174 is removed by
exposing it to a relatively strong acid, e.g., a halide based acid
(such as hydrobromic or hydrochloric acid) or phosphoric acid. When
a halide based acid is used, the acid preferably contains between
about 0.5% and about 10% HBr or HCl by volume--and more preferably
about 5% by volume. An etch process that uses such an acid may take
place at or near room temperature, and last for between about 5 and
about 30 minutes--although a longer exposure may be used if
desired. When phosphoric acid is used, the acid may contain between
about 75% and about 95% H.sub.3PO.sub.4 by volume. An etch process
that uses such an acid may, for example, take place at between
about 140.degree. C. and about 180.degree. C., and, in one
embodiment, at about 160.degree. C. When such an acid is used, the
exposure step may last between about 30 seconds and about 5
minutes--and for about one minute for a 20 Angstrom thick film.
[0019] FIG. 1D represents an intermediate structure that may be
formed when making a complementary metal oxide semiconductor
("CMOS"). That structure includes first part 101 and second part
102 of substrate 100 shown in FIG. 1E. Isolation region 103
separates first part 101 from second part 102. Isolation region 103
may comprise silicon dioxide, or other materials that may separate
the transistor's active regions. First sacrificial layer 104 is
formed on first high-k gate dielectric layer 105, and second
sacrificial layer 106 is formed on second high-k gate dielectric
layer 107. Hard masks 130, 131 are formed on sacrificial layers
104, 106.
[0020] After forming the FIG. 1D structure, spacers may be formed
on opposite sides of sacrificial layers 104, 106. When those
spacers comprise silicon nitride, they may be formed in the
following way. First, a silicon nitride layer of substantially
uniform thickness, for example, less than about 1000 Angstroms
thick--is deposited over the entire structure, producing the
structure shown in FIG. 1E. Conventional deposition processes may
be used to generate that structure.
[0021] In one embodiment, silicon nitride layer 134 is deposited
directly on substrate 100 and opposite sides of sacrificial layers
104, 106--without first forming a buffer oxide layer on substrate
100 and layers 104, 106. In alternative embodiments, however, such
a buffer oxide layer may be formed prior to forming layer 134.
Similarly, although not shown in FIG. 1E, a second oxide may be
formed on layer 134 prior to etching that layer. If used, such an
oxide may enable the subsequent silicon nitride etch step to
generate an L-shaped spacer.
[0022] Silicon nitride layer 134 may be etched using a conventional
process for anisotropically etching silicon nitride to create the
FIG. 1F structure. As a result of that etch step, sacrificial layer
104 is bracketed by a pair of sidewall spacers 108, 109, and
sacrificial layer 106 is bracketed by a pair of sidewall spacers
110, 111.
[0023] As is typically done, it may be desirable to perform
multiple masking and ion implantation steps (FIG. 1G) to create
lightly implanted regions 135a-138a near layers 104, 106 (that will
ultimately serve as tip regions for the device's source and drain
regions), prior to forming spacers 108, 109, 110, 111 on
sacrificial layers 104, 106. Also as is typically done, the source
and drain regions 135-138 may be formed, after forming spacers 108,
109, 110, 111, by implanting ions into parts 101 and 102 of
substrate 100, followed by applying an appropriate anneal step.
[0024] An ion implantation and anneal sequence used to form n-type
source and drain regions within part 101 of substrate 100 may dope
sacrificial layer 104 n-type at the same time. Similarly, an ion
implantation and anneal sequence used to form p-type source and
drain regions within part 102 of substrate 100 may dope sacrificial
layer 106 p-type. When doping sacrificial layer 106 with boron,
that layer should include that element at a sufficient
concentration to ensure that a subsequent wet etch process, for
removing n-type germanium containing layer 104, will not remove a
significant amount of p-type sacrificial layer 106.
[0025] The anneal will activate the dopants that were previously
introduced into the source and drain regions and tip regions and
into sacrificial layers 104, 106. In a preferred embodiment, a
rapid thermal anneal is applied that takes place at a temperature
that exceeds about 1,000.degree. C. and, optimally, that takes
place at 1,080.degree. C. In addition to activating the dopants,
such an anneal may modify the molecular structure of high-k gate
dielectric layers 105, 107 to create gate dielectric layers that
may demonstrate improved performance.
[0026] Because of the imposition of the sacrificial metal layer
169, better performing dielectric layers 170 may result from these
high temperature steps without significant reaction between the
high dielectric constant dielectric layer 170 and the sacrificial
layer 171.
[0027] After forming spacers 108, 109, 110, 111, dielectric layer
112 may be deposited over the device, generating the FIG. 1G
structure. Dielectric layer 112 may comprise silicon dioxide, or a
low-k material. Dielectric layer 112 may be doped with phosphorus,
boron, or other elements, and may be formed using a high density
plasma deposition process. By this stage of the process, source and
drain regions 135, 136, 137, 138, which are capped by silicided
regions 139, 140, 141, 142, have already been formed. Those source
and drain regions may be formed by implanting ions into the
substrate, then activating them. Alternatively, an epitaxial growth
process may be used to form the source and drain regions, as will
be apparent to those skilled in the art.
[0028] Commonly used nitride spacer, source/drain, and silicide
formation techniques to make the FIG. 1G structure. That structure
may include other features--not shown, so as not to obscure the
method of the present invention--that may be formed using
conventional process steps.
[0029] Dielectric layer 112 is removed from hard masks 130, 131,
which are, in turn, removed from patterned sacrificial layers 104,
106, producing the FIG. 1H structure. A conventional chemical
mechanical polishing ("CMP") operation may be applied to remove
that part of dielectric layer 112 and hard masks 130, 131. Hard
masks 130, 131 may be removed to expose patterned sacrificial
layers 104, 106. Hard masks 130, 131 may be polished from the
surface of layers 104, 106, when dielectric layer 112 is
polished--as they will have served their purpose by that stage in
the process.
[0030] After forming the FIG. 1H structure, sacrificial layers 104
or 106 are removed to generate trenches 113, producing the
structure shown in FIG. 1I. A 1% solution of HF may be used for 15
to 30 seconds to remove the chemical oxide formed over the
remaining polysilicon.
[0031] In a second embodiment, a wet etch process that is selective
for layers 104 over sacrificial layer 106 is applied to remove
layers 104 and 169 without removing significant portions of layer
106. When sacrificial layer 104 is doped n-type, and sacrificial
layer 106 is doped p-type (e.g., with boron), such a wet etch
process may comprise exposing sacrificial layer 104 to an aqueous
solution that comprises a source of hydroxide for a sufficient time
at a sufficient temperature to remove substantially all of layer
104. That source of hydroxide may comprise between about 2 and
about 30 percent ammonium hydroxide or a tetraalkyl ammonium
hydroxide, e.g., tetramethyl ammonium hydroxide ("TMAH"), by volume
in deionized water. Any remaining sacrificial layer 104 may be
selectively removed by exposing it to absolution, which is
maintained at a temperature between about 15.degree. C. and about
90.degree. C. (for example, below about 40.degree. C.), that
comprises between about 2 and about 30 percent ammonium hydroxide
by volume in deionized water. During that exposure step, which
preferably lasts at least one minute, it may be desirable to apply
sonic energy at a frequency of between about 10 kHz and about 2,000
kHz, while dissipating at between about 1 and about 10
Watts/cm.sup.2.
[0032] In the second embodiment, sacrificial layer 104, with a
thickness of about 1,350 Angstroms, may be selectively removed by
exposing it at about 25.degree. C. for about 30 minutes to a
solution that comprises about 15 percent ammonium hydroxide by
volume in deionized water, while applying sonic energy at about
1,000 kHz--dissipating at about 5 Watts/cm.sup.2. Such an etch
process should remove substantially all of an n-type sacrificial
layer without removing a meaningful amount of a p-type sacrificial
layer.
[0033] As a third embodiment, sacrificial layer 104 may be
selectively removed by exposing it for at least one minute to a
solution, which is maintained at a temperature between about
60.degree. C. and about 90.degree. C., that comprises between about
20 and about 30 percent TMAH by volume in deionized water, while
applying sonic energy. Removing sacrificial layer 104, with a
thickness of about 1,350 Angstroms, by exposing it at about
80.degree. C. for about 2 minutes to a solution that comprises
about 25 percent TMAH by volume in deionized water, while applying
sonic energy at about 1,000 kHz--dissipating at about 5
Watts/cm.sup.2--may remove substantially all of layer 104 without
removing a significant amount of layer 106. First high-k gate
dielectric layer 105 should be sufficiently thick to prevent the
etchant that is applied to remove sacrificial layer 104 from
reaching the channel region that is located beneath first high-k
gate dielectric layer 105.
[0034] The sacrificial metal layer 169 may also be removed by
selective etching. In some embodiments, the layer 169 may not be
removed. In some embodiments, the dielectric layer 105 may be
removed before forming the replacement metal gate. In such case, a
metal oxide gate dielectric may be formed before forming the
replacement gate.
[0035] In the illustrated embodiment, n-type metal layer 180 is
formed directly on layers 105 and in the trenches 113 to generate
the FIG. 1J structure. N-type metal layer 180 may comprise any
n-type conductive material. N-type metal layer 180 preferably has
thermal stability characteristics that render it suitable for
making a metal NMOS gate electrode for a semiconductor device. In
one embodiment, the layer 180 may be between 30 and 1000 Angstroms
thick and may be deposited by physical vapor deposition or chemical
vapor deposition.
[0036] Materials that may be used to form n-type metal layer 180
include: hafnium, zirconium, titanium, tantalum, aluminum, and
their alloys, e.g., metal carbides that include these elements,
i.e., hafnium carbide, zirconium carbide, titanium carbide,
tantalum carbide, and aluminum carbide. N-type metal layer 180 may
be formed on first high-k gate dielectric layer 105 using well
known PVD or CVD processes, e.g., conventional sputter or atomic
layer CVD processes.
[0037] The p-type side 200 may be masked and an n-type layer 115
may be deposited on the n-type side 202 to form the FIG. 1K
structure. The layer 115 may be the same as the layer 180, in one
embodiment.
[0038] N-type metal layers 115 and 180 may serve as a metal NMOS
gate electrode that has a workfunction that is between about 3.9 eV
and about 4.2 eV, and that is between about 100 Angstroms and about
2,000 Angstroms thick and, in one embodiment, may particularly be
between about 500 Angstroms and about 1,600 Angstroms thick.
Although FIG. 1K represents structures in which n-type metal layers
115, 180 fill all of trench 113, in alternative embodiments, n-type
metal layer 115 may fill only part of trench 113, with the
remainder of the trench being filled with a material that may be
easily polished, e.g., tungsten, aluminum, titanium, or titanium
nitride. Using a higher conductivity fill metal in place of the
workfunction metal may improve the overall conductivity of the gate
stack. In such an alternative embodiment, n-type metal layer 115,
which serves as the workfunction metal, may be between about 50 and
about 1,000 Angstroms thick and, for example, at least about 100
Angstroms thick.
[0039] In embodiments in which trench 113 includes both a
workfunction metal and a trench fill metal, the resulting metal
NMOS gate electrode may be considered to comprise the combination
of both the workfunction metal and the trench fill metal. If a
trench fill metal is deposited on a workfunction metal, the trench
fill metal may cover the entire device when deposited, forming a
structure like the FIG. 1J structure. That trench fill metal must
then be polished back so that it fills only the trench, generating
a structure like the FIG. 1K structure.
[0040] In the illustrated embodiment, after forming n-type metal
layer 115 within trench 113, the masking of p-type side 200 may be
removed and the horizontal portions of the layer 180, as well as
the horizontal portions of the 115, may be polishing off, and
n-type side 202 may be masked. Then a workfunction adjusting
implant I is performed on the p-type side 200 as shown in FIG. 1L.
The implant species may be nitrogen, oxygen, chlorine, fluorine, or
bromine, for example, to increase the workfunction of the n-type
layer 180 to make it more suitable for use in p-type transistors.
Alternatively, the workfunction increasing species may be aided by
plasma enhanced ion implantation, furnace diffusion, or plasma
deposition, to mention a few examples. The species may be added
until the species makes up from about 3 to about 50 atomic percent
of the exposed layer 180. In many cases, between about 5 and about
10 atomic percent may be sufficient doping. If the trenches 113
have a reentrant profile, an angled implant may be used.
[0041] In this embodiment, p-type metal layer 116 is formed
directly on layer 180 to fill trench 115 on the p-type side 200 and
to generate the FIG. 1M structure. P-type metal layer 116 may
comprise any p-type conductive material from which a metal PMOS
gate electrode may be derived. P-type metal layer 116 preferably
has thermal stability characteristics that render it suitable for
making a metal PMOS gate electrode for a semiconductor device.
[0042] Materials that may be used to form p-type metal layer 116
include: ruthenium, palladium, platinum, cobalt, nickel, and
conductive metal oxides, e.g., ruthenium oxide. P-type metal layer
116 may be formed on second high-k gate dielectric layer 107 using
well known PVD or CVD processes, e.g., conventional sputter or
atomic layer CVD processes. As shown in FIG. 1N, p-type metal layer
116 is removed except where it fills trench 113. Layer 116 may be
removed from other portions of the device via a wet or dry etch
process, or an appropriate CMP operation, with dielectric 112
serving as an etch or polish stop.
[0043] P-type metal layer 116 may serve as a metal PMOS gate
electrode with a workfunction that is between about 4.9 eV and
about 5.2 eV, and that is between about 100 Angstroms and about
2,000 Angstroms thick, and more preferably is between about 500
Angstroms and about 1,600 Angstroms thick. Although FIGS. 1M and 1N
represent structures in which p-type metal layer 116 fills all of
trench 150, in alternative embodiments, p-type metal layer 116 may
fill only part of trench 150. As with the metal NMOS gate
electrode, the remainder of the trench may be filled with a
material that may be easily polished, e.g., tungsten, aluminum,
titanium, or titanium nitride. In such an alternative embodiment,
p-type metal layer 116, which serves as the workfunction metal, may
be between about 50 and about 1,000 Angstroms thick. Like the metal
NMOS gate electrode, in embodiments in which trench 150 includes a
workfunction metal and a trench fill metal, the resulting metal
PMOS gate electrode may be considered to comprise the combination
of both the workfunction metal and the trench fill metal.
[0044] After removing metal layer 116, except where it fills trench
113, a capping dielectric layer may be deposited onto dielectric
layer 112, metal NMOS gate electrode 115, and metal PMOS gate
electrode 116, using any conventional deposition process. Process
steps for completing the device that follow the deposition of such
a capping dielectric layer, e.g., forming the device's contacts,
metal interconnect, and passivation layer, are well known to those
skilled in the art and will not be described here.
[0045] While the present invention has been described with respect
to a limited number of embodiments, those skilled in the art will
appreciate numerous modifications and variations therefrom. It is
intended that the appended claims cover all such modifications and
variations as fall within the true spirit and scope of this present
invention.
* * * * *