The present invention relates to the manufacture of semiconductor devices; more specifically, it relates to a method of fabricating a nitrided silicon-oxide gate dielectric.
The trend in integrated circuits is toward higher performance, higher speed and lower cost. Correspondingly, device dimensions and element sizes are shrinking and gate dielectrics must scale accordingly. As physical gate dielectric thickness has decreased, the need for a higher dielectric constant and less leaky gate dielectric has arisen. In advanced metal oxide semiconductor field effect transistors (MOSFETs) silicon oxynitride (SiOxNy) layers are used as a gate dielectric. MOSFET transistors include a channel region formed in a silicon substrate, an N or P doped polysilicon gate formed on top of a thin gate dielectric layer and aligned over the channel region, and source/drain regions formed in the silicon substrate on either side of the channel region.
However, a problem with SiOxNy gate dielectrics is thickness and nitrogen concentration variation across the wafer. Across wafer thickness and nitrogen concentration variation of the gate dielectric leads directly to across wafer threshold voltage variation, especially in P-channel field effect transistors (PFETs), causing variations in performance of individual integrated circuit chips from the same wafer. Therefore, there is a need for a method of fabricating a SiOxNy layer having a relatively uniform across wafer thickness and nitrogen concentration.
A first aspect of the present invention is a method of fabricating a gate dielectric layer, comprising: providing a substrate; forming a silicon dioxide layer on a top surface of the substrate; performing a plasma nitridation in a reducing atmosphere to convert the silicon dioxide layer into a silicon oxynitride layer.
A second aspect of the present invention is a method of fabricating a MOSFET, comprising: providing a semiconductor substrate having at least a uppermost silicon layer; forming a silicon dioxide layer on a top surface of the semiconductor substrate; performing a plasma nitridation in a reducing atmosphere to convert the silicon dioxide layer into a silicon oxynitride layer; forming a polysilicon gate on the silicon oxynitride layer aligned over a channel region in the semiconductor substrate; and forming source/drain regions in the semiconductor substrate, the source drain regions aligned to the polysilicon gate.
The features of the invention are set forth in the appended claims. The invention itself, however, will be best understood by reference to the following detailed description of an illustrative embodiment when read in conjunction with the accompanying drawings, wherein:
The term nitrided silicon dioxide refers to a SiO2 layer into which nitrogen has been introduced to form a silicon oxynitride (SiOxNy). The scope of SiOxNy includes all combinations of integers x and y (or fractions thereof) at which SiOxNy is stable. A reducing atmosphere is defined as a gaseous atmosphere containing species that react with oxygen.
In
In
In
In step 155, a base SiO2 layer is formed, for example, by a thermal oxidation in a furnace in an oxygen-containing atmosphere at about 600 to 800° C. for about 0.5 to 30 minutes, by a RTO in an oxygen-containing atmosphere at about 800 to 1000° C. for about 5 to 60 seconds or by exposing a cleaned silicon surface to air or oxygen. The base SiO2 layer is about 8 to 23 Å thick.
In step 160 a remote plasma nitridation process is performed. In a first example, a mixture of nitrogen and an inert gas such as helium are introduced into the plasma generation port of the remote plasma nitridation tool and a reducing gas such as hydrogen or ammonia is introduced through a second, non plasma generation port while the wafer being processed is rotated in the process chamber (see
In a second example, a mixture of nitrogen, an inert gas such as helium and a reducing gas such as hydrogen or ammonia are introduced into the plasma generation port of the remote plasma nitridation tool while the wafer being processed is rotated in the process chamber (see
In both examples, the nitrogen dose is about 1E14 to 5E15 atom/cm2 and the completed SiOxNy layer contains about 2 to 20% nitrogen.
In step 165, an optional anneal step is performed. Generally annealing is not required since the remote plasma nitridation is done on hot wafers. Either a standard rapid thermal anneal (RTA) or a spike RTA may be performed. A spike anneal is used to increase the mobility without driving the nitrogen to the SiO2/Si interface. A spike anneal is defined as an anneal where the time the wafer is at a maximum wafer temperature is about 60 seconds or less while a standard RTA is defined as an anneal where the time the wafer is at a maximum wafer temperature is greater than about 60 seconds.
The following steps use the nitrided SiO2 dielectric as a gate dielectric for a MOSFET.
In step 170, a polysilicon layer is formed over the nitrided SiO2 using one of a number of deposition processes well known in the art, such as LPCVD or RTCVD. The polysilicon layer may be undoped or doped N-type of P-type. In one example, the polysilicon layer is 1000 to 2000 Å thick.
In step 175, the MOSFET is essentially completed. The polysilicon layer is etched; for example, by a RIE processes to form a gate, spacers are formed on sidewalls of the gate and source/drains are formed in the substrate on either side of the gate (typically by one or more ion-implantation processes). The SiOxNy layer is the gate dielectric of the MOSFET. If the polysilicon layer was not doped during deposition, the gate may be doped N-type or P-type after spacer formation by ion implantation in conjunction with the formation of the source/drains or as a separate step.
In use, wafer 195 having a base SiO2 layer (not shown) on a top surface 230 of the wafer is placed into chamber 185 from a transfer chamber (not shown) and rotated, a pre-selected nitridation gas mixture (in the present example, He/N2) at a pre-selected flow rate is introduced into the chamber via first inlet 210A, a pre-selected reducing gas mixture (in the present example, H2 or NH3) at a pre-selected flow rate is introduced into the chamber via second inlet B and the chamber maintained at a pre-selected pressure via the vacuum pump attached to exhaust port 220. A pre-selected wattage of microwave power is impressed on microwave coils 200 to energize and maintain plasma 205. After a pre-selected time, the microwave power is turned off extinguishing plasma 205, the gas flows are turned off and chamber 185 is brought up to transfer chamber pressure. Plasma 205 is predominantly a nitrogen ion, helium ion, hydrogen neutral plasma.
One example of a suitable tool for practicing the present invention is an AMAT model XE12 chamber manufactured by Applied Materials Corp, Santa Clara, Calif. with a decoupled plasma unit also supplied by Applied Materials Corp.
Secondary ion mass spectrometry (SIMS) profiles of the layer 225 and 230 indicate improvements in nitrogen concentration uniformity tracks very well with improvement in SiOxNy thickness, uniformity as seen by TABLE I. Note there is a one to one correspondence between nitrogen dose and concentration.
In table I, nitrogen concentration varies by over 50% from center to edge in a wafer processed by remote plasma nitridation without a reducing gas present in the chamber. In two examples of a wafer processed by remote plasma nitridation with a reducing gas present in the chamber nitrogen concentration varies by not more than 25% from center to edge in a wafer.
Thus, both the SiOxNy thickness uniformity and nitrogen concentration uniformity improve by factors of about two.
Thus, the need for a method of fabricating a SiOxNy layer having a relatively uniform across wafer thickness has been satisfied by the present invention.
The description of the embodiments of the present invention is given above for the understanding of the present invention. It will be understood that the invention is not limited to the particular embodiments described herein, but is capable of various modifications, rearrangements and substitutions as will now become apparent to those skilled in the art without departing from the scope of the invention. Therefore, it is intended that the following claims cover all such modifications and changes as fall within the true spirit and scope of the invention.
This Application is a division of U.S. patent application Ser. No. 10/604,905 filed on Aug. 26, 2003.
Number | Name | Date | Kind |
---|---|---|---|
4510172 | Ray | Apr 1985 | A |
4621277 | Ito et al. | Nov 1986 | A |
5219773 | Dunn | Jun 1993 | A |
5445999 | Thakur et al. | Aug 1995 | A |
5596218 | Soleimani et al. | Jan 1997 | A |
5648284 | Kusunoki et al. | Jul 1997 | A |
5726087 | Tseng et al. | Mar 1998 | A |
5817549 | Yamazaki et al. | Oct 1998 | A |
5926730 | Hu et al. | Jul 1999 | A |
6027977 | Mogami | Feb 2000 | A |
6114258 | Miner et al. | Sep 2000 | A |
6136654 | Kraft et al. | Oct 2000 | A |
6140024 | Misium et al. | Oct 2000 | A |
6171911 | Yu | Jan 2001 | B1 |
6200651 | Roche et al. | Mar 2001 | B1 |
6228779 | Bloom et al. | May 2001 | B1 |
6254676 | Yang et al. | Jul 2001 | B1 |
6291867 | Wallace et al. | Sep 2001 | B1 |
6335252 | Oishi et al. | Jan 2002 | B1 |
6368923 | Huang | Apr 2002 | B1 |
6380056 | Shue et al. | Apr 2002 | B1 |
6380104 | Yu | Apr 2002 | B1 |
6399445 | Hattangady et al. | Jun 2002 | B1 |
6450116 | Noble et al. | Sep 2002 | B1 |
6555485 | Liu et al. | Apr 2003 | B1 |
6596570 | Furukawa | Jul 2003 | B2 |
6610615 | McFadden et al. | Aug 2003 | B1 |
6667251 | McFadden et al. | Dec 2003 | B2 |
6723663 | Wieczorek et al. | Apr 2004 | B1 |
6821833 | Chou et al. | Nov 2004 | B1 |
6821868 | Cheng et al. | Nov 2004 | B2 |
6906398 | Yeo et al. | Jun 2005 | B2 |
20010044186 | Reinberg | Nov 2001 | A1 |
20020023900 | Mahawili | Feb 2002 | A1 |
20020072177 | Grider | Jun 2002 | A1 |
20020073925 | Noble et al. | Jun 2002 | A1 |
20020109199 | Moore | Aug 2002 | A1 |
20020130377 | Khare et al. | Sep 2002 | A1 |
20020155702 | Aoki et al. | Oct 2002 | A1 |
20040142577 | Sugawara et al. | Jul 2004 | A1 |
20050233599 | Sugawara et al. | Oct 2005 | A1 |
20060246436 | Ohno et al. | Nov 2006 | A1 |
Number | Date | Country |
---|---|---|
0886308 | Dec 1998 | EP |
0973189 | Jan 2000 | EP |
2001-044419 | Feb 2001 | JP |
WO02058130 | Jul 2002 | WO |
Entry |
---|
Merz et al.; IBM Technical Disclosure Bulletin, vol. 28, No. 6, Nov. 1985; Controlled Nitridation of SiO2 for the Formation of Gate Insulators in FET Devices; pp. 2665-2666. |
Haggett et al.; IBM Technical Disclosure Bulletin, vol. 19, No. 4, Sep. 1976; MNOS Reactor Process; p. 1160. |
Dockerty et al.; IBM Technical Disclosure Bulletin, vol. 14, No. 4, Sep. 1971; Transconductance in Silicon Gate Nitride-Oxide IGFET; p. 1098. |
Supplementary European Search Report; Jul. 4, 2008. |
European Patent Office—Office Action dated Jun. 16, 2009; Application No. 04 782 258.-1235. 3 pages. |
Number | Date | Country | |
---|---|---|---|
20080014692 A1 | Jan 2008 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 10604905 | Aug 2003 | US |
Child | 11778238 | US |