1. Field
The present invention generally relates to semiconductor devices, and more particularly to field effect transistor (FET) devices including FinFET structures having enhanced channel mobility, and a method for making the same.
2. Background of the Disclosure
Complementary Metal-oxide-semiconductor (CMOS) technology is commonly used for fabricating field effect transistors (FETs) as part of advanced integrated circuits (IC), such as CPUs, memory, storage devices, and the like. At the core of planar FETs, a channel region is formed in an n-doped or p-doped semiconductor substrate on which a gate structure is formed. Depending whether the on-state current is carried by electrons or holes, the FET comes as an n-FET or a p-FET. The overall fabrication process is well known in the art, and includes forming a gate structure over a channel region connecting a source and a drain region within the substrate on opposite ends of the gate, typically with some vertical overlap between the gate and the source and drain region. As integrated circuits continue to scale downward in size, fin field effect transistors (FinFETs) or tri-gate structures are becoming more widely used, primarily because FinFETs offer better performance than planar FETs at the same power budget. FinFETs are three dimensional (3-D), fully depleted metal-oxide semiconductor field effect transistor (MOSFET) devices having a fin structure formed from the semiconductor substrate material. The fins extent between the device source and drain enfolding the channel region forming the bulk of the semiconductor device. The gate structure is located over the fins covering the channel region. Such architecture allows for a more precise control of the conducting channel by the gate, significantly reducing the amount of current leakage when the device is in off state.
A common technique used in planar FETs manufacturing to enhance carrier mobility in the channel region is channel straining. Channel straining in planar FETs is usually achieved by filling source and drain recesses with a stressor material in order to induce a compressive or tensile strain to the channel region. In FinFET devices conventional channel straining methods are more difficult to apply mostly due to the small dimensions of FinFET elements. For example, in FinFET devices the fin structure cannot be recessed to form an embedded source and drain region as in planar FETs. Factors such as scaling of FinFET devices, FinFETs manufacturing materials and 3-D topography may impact effective channel straining if conducted using traditional straining techniques.
According to an embodiment of the present invention, a method of forming a semiconductor structure includes: growing an epitaxial doped layer over a exposed portion of a plurality of fins, the epitaxial doped layer combines the exposed portion of the fins to form a merged source and drain region, implanting the fins through the epitaxial doped layer to change the crystal lattice of the fins to form amorphized fins, depositing a nitride layer over the semiconductor structure, the nitride layer covers the merged source and drain regions, annealing the semiconductor structure to re-crystallize the amorphized fins to form re-crystallized fins where the re-crystallized fins, the epitaxial doped layer and the nitride layer form a strained source and drain region which induces stress to a channel region.
According to another embodiment of the present invention, a semiconductor structure includes: a gate on a top surface of a semiconductor substrate, a plurality of fins on the top surface of the semiconductor substrate, the gate on top of the plurality of fins, a portion of the plurality of fins not covered by the gate defining a source and drain region, an epitaxial doped layer located over the portion of the fins not covered by the gate forming a merged source and drain region and a remaining portion of a nitride layer located on top and sidewalls of the merged source and drain region forming a strained source and drain region inducing stress to a channel region.
The present disclosure recognizes a problem with previously known techniques for forming semiconductor devices including when the ion implantation is performed sequentially in each region of the device, immediately following the formation of p-FET and/or n-FET doped epitaxial layers using the corresponding p-type or n-type dopants. The device can exhibit problems in the epitaxial layer implanted first due to over enhancement of dopant diffusion under the amorphized source and drain region. Ion implantation just after each epitaxial growth involves lattice amorphization and additional thermal budget of second epitaxial layer growth and re-crystallization annealing. This causes unintended dopant diffusion of amorphized fin areas. This in turn increases undesirable short channel effects in the device such as drain induced barrier lowering (DIBL) and leakage.
The following detailed description, given by way of example and not intended to limit the invention solely thereto, will best be appreciated in conjunction with the accompanying drawings, in which:
The drawings are not necessarily to scale. The drawings are merely schematic representations, not intended to portray specific parameters of the invention. The drawings are intended to depict only typical embodiments of the invention. In the drawings, like numbering represents like elements.
Exemplary embodiments now will be described more fully herein with reference to the accompanying drawings, in which exemplary embodiments are shown. This disclosure may, however, be embodied in many different forms and should not be construed as limited to the exemplary embodiments set forth herein. Rather, these exemplary embodiments are provided so that this disclosure will be thorough and complete and will fully convey the scope of this disclosure to those skilled in the art. In the description, details of well-known features and techniques may be omitted to avoid unnecessarily obscuring the presented embodiments.
Referring to
The sequence of figures from
The semiconductor structure 500 may further include a semiconductor on insulator (SOI) substrate. The SOI substrate employed in the present disclosure may include a base substrate 12, a buried oxide (BOX) layer 14 formed on top of the base substrate 12 and a SOI layer (not shown) formed on top of the BOX layer 14. The BOX layer 14 isolates the SOI layer from the base substrate 12. The base substrate 12 may be made from any of several known semiconductor materials such as, for example, silicon, germanium, silicon-germanium alloy, silicon carbide, silicon-germanium carbide alloy, and compound (e.g. III-V and II-VI) semiconductor materials. The base substrate 12 may include a thickness ranging from about 700 μm to about 900 μm.
The BOX layer 14 may be formed from any known dielectric material. Non-limiting examples include: oxides, nitrides and oxynitrides of silicon. Oxides, nitrides and oxynitrides of other elements are also envisioned. In addition, the BOX layer 14 may include crystalline or non-crystalline dielectric materials. Moreover, the BOX layer 14 may be formed using any method known in the art, for example, ion implantation, thermal or plasma oxidation or nitridation methods, chemical vapor deposition (CVD) and physical vapor deposition (PVD). In one embodiment of the present disclosure, the BOX layer 14 may include a thickness ranging from about 10 nm to about 200 nm.
The SOI layer may include any of the several semiconductor materials included in the base substrate 12. In general, the base substrate 12 and the SOI layer may include the same semiconductor materials with respect to chemical composition, dopant concentration and crystallographic orientation. The SOI layer may be formed by any method known in the art including, but not limited to: separation by implantation of oxygen (SIMOX), wafer bonding and epitaxial layer transfer (ELTRAN®). In one embodiment of the present disclosure, the SOI layer may include a thickness ranging from about 10 nm to about 100 nm.
The initial semiconductor structure 500 may include a plurality of fins 10, the n-FET gate 106 and the p-FET gate 206. Both the n-FET gate 106 and the p-FET gate 206 may be formed over a portion of the fins 10. The fins 10 may be etched from the SOI substrate using typical photolithography techniques. The fins 10 may be primarily formed from the SOI layer of the SOI substrate. In some cases the SOI layer may be entirely consumed during the process of forming the fins. In one embodiment, the fins 10 may include a height of about 4 nm to about 40 nm, and a width of about 2 nm to about 20 nm.
The n-FET gate 106 and the p-FET gate 206 may include a gate dielectric layer 18 which may be formed by any method known in the art. The gate dielectric 18 may include a high-k dielectric material having a dielectric constant greater than, for example, 3.9, which is the dielectric constant of silicon oxide. The n-FET gate 106 and the p-FET gate 206 may be separated from the fins by the gate dielectric layer 18. The width of either the n-FET gate 106 or the p-FET gate 206 may determine the effective channel length of either the n-FET device or the p-FET device, respectively.
In another embodiment of the present invention, the n-FET gate 106 and the p-FET gate 206 may be formed using a gate last process where the initial gate structure may comprise a dummy polysilicon gate or dummy gate. A pair of device spacers can be disposed on opposite sidewalls of the dummy gate. The dummy gate and the pair of device spacers may then be surrounded by an inter-layer dielectric. Later, the dummy gate may be removed from between the pair of device spacers, as by, for example, an anisotropic vertical etch process, such as, a reactive ion etch (RIE). This creates an opening between the pair of device spacers where a metal gate may then be formed between the pair of device spacers. Optionally, a gate dielectric may be configured below the metal gate to separate the metal gate from the fins.
Referring to
Referring now to
First, a blanket layer of dielectric material may be deposited on top of the semiconductor structure 500 to form the first spacer material 32. The first spacer material 32 may cover the fins 10, the n-FET gate 106, and the p-FET gate 206. The first spacer material 32 may be deposited by any technique known in the art, for example, by chemical vapor deposition (CVD), atomic layer deposition (ALD), physical vapor deposition (PVD), or plasma enhanced chemical vapor deposition (PECVD). The first spacer material 32 may be made from an oxide, nitride, oxynitride, or any combination thereof. In one embodiment, the first spacer material 32 may have a thickness ranging from about 3 nm to about 20 nm. In one embodiment, the first spacer material 32 may include an iRAD nitride deposited using a CVD technique. The first spacer material 32 may untimely function as an offset sidewall spacer or first gate spacer for the p-FET device in the p-FET region 200.
Referring now to
The first gate spacer 208 may generally include the same material and have a similar thickness to the dielectric spacer material 32 described above. In one embodiment, the first gate spacer 208 may have a thickness of approximately 8 nm.
Referring now to
Next, formation of the merged source and drain region 212 may include selectively growing an in-situ doped epitaxial layer 210 on the exposed surfaces of the fins 10 in the p-FET region 200. The epitaxial layer 210 may be doped in-situ with a p-type dopant. The fins 10 may have the proper crystalline characteristics for accepting the epitaxial layer 210. The epitaxial layer 210 may merge the fins 10 to form a merged source and drain region 212 in the p-FET region 200 of the semiconductor structure 500.
Epitaxial growth is a known technique in the art. The structural consequence of epitaxial growth may be that a grown material and a host material, at their common interface, may include the same symmetry and crystalline orientation. Selective epitaxial growth may include epitaxial growth only on the exposed surfaces that may have proper crystalline qualities for accepting the growth material.
In the present case, only the fins 10 in the p-FET region 200 have the proper crystalline qualities to allow the epitaxial layer 210 to be grown. Similarly, epitaxial layer 210 may not be grown on the fins 10 of the n-FET region 100 because they are protected or covered by the first spacer material 32.
The epitaxial layer 210 may be grown by any suitable technique known in the art. A suitable technique may include for example, molecular beam epitaxy (MBE), CVD, ultra high vacuum CVD (UHCVD), and rapid thermal CVD (RTCVD).
In one embodiment, for example, the epitaxial layer 210 used to form the merged source and drain region 212 in the p-FET region 200 may include a silicon-germanium (SiGe) material, where the atomic concentration of germanium (Ge) may range from about 10% to about 80%. In another embodiment, the concentration of germanium (Ge) may range from about 25 to about 50%. The epitaxial layer 210 may have a larger lattice constant relative to the lattice constant of silicon (Si). By having a larger lattice constant, the epitaxial layer 210 may induce a compressive strain on the channel region of the p-FET device which may enhance carrier mobility and increase drive current. The p-type dopant may include any known dopant use in the fabrication of a p-FET, such as, for example, boron. In one embodiment, the dopant concentration may range from about 1×1019 cm−3 to about 2×1021 cm−3, and more preferably from about 1×1020 cm−3 to about 1×1021 cm3.
Referring now to
Referring now to
The second gate spacer 108 may generally include the same material and have a similar thickness to the first spacer material 32 and second spacer material 34 described above. In one embodiment, the second gate spacer 108 may have a thickness of approximately 6 nm.
Referring now to
Next, formation of the merged source and drain region 112 may include selectively growing an in-situ doped epitaxial layer 110 on the exposed surfaces of the fins 10 in the n-FET region 100. The epitaxial layer 110 may be doped in-situ with an n-type dopant. The fins 10 may have the proper crystalline characteristics for accepting the epitaxial layer 110. The epitaxial layer 110 may merge the fins 10 to form a merged source and drain region 112 in the n-FET region 100 of the semiconductor structure 500.
In the present case, only the fins 10 in the n-FET region 100 have the proper crystalline qualities to allow the epitaxial layer 110 to be grown. Similarly, epitaxial layer 110 may not be grown on the fins 10 of the p-FET region 200 because they are protected or covered by the second spacer material 34.
The epitaxial layer 110 may be grown by any suitable technique known in the art. A suitable technique may include for example, molecular beam epitaxy (MBE), CVD, ultra high vacuum CVD (UHCVD), and rapid thermal CVD (RTCVD).
In one embodiment, for example, the epitaxial layer 110 used to form the merged source and drain region 112 in the n-FET region 100 may include a carbon-doped silicon (Si:C) material, where the atomic concentration of carbon (C) may range from about 0.2-3.0%. The epitaxial layer 110 may have a smaller lattice constant relative to the lattice constant of silicon (Si). By having a smaller lattice constant, the epitaxial layer 110 may induce a tensile strain on the channel region of the n-FET device which may enhance carrier mobility and increase drive current. The n-type dopant may include any known dopant use in the fabrication of an n-FET, such as, for example, phosphorus or arsenic. In one embodiment, the dopant concentration may range from about 1×1019 cm3 to about 2×1021 cm−3, and more preferably from about 1×1020 cm−3 to about 1×1021 cm−3.
At this point of the manufacturing process, the second dielectric spacer material 34 may be removed from the p-FET region 200 by any method known in the art. In the processing steps described in
Referring now to
For example, for both the n-FET region 100 and the p-FET region 200, the neutral dopants may comprise germanium (Ge) or argon (Ar) ions. The dopant concentration of germanium (Ge) to achieve amorphization may range from about 1×1012 ions/cm2 to about 9×1012 ions/cm2 with a tilt angle ranging from about 0 degrees to about 20 degrees and an implantation energy ranging from about 0.5 keV to about 5 keV. Furthermore, the dopant concentration of argon (Ar) to achieve amorphization may range from about 1×1012 ions/cm2 to about 9×1012 ions/cm2 with a tilt angle ranging from about 0 degrees to about 20 degrees and an implantation energy ranging from about 0.5 keV to about 5 keV.
The ion implantation process may alter the crystal lattice of the fins resulting in amorphized fins 114, 214 (shown in
The amorphization process may cause a crystalline disorder in the fins 10 area, resulting in an amorphous state for the fins 10 (instead of an orderly crystal state). After amorphization of the fins 10 due to implant damage, silicon atoms may re-arrange itself after annealing, according to an incorporated strain force as described below in
Advantages of the present disclosure may be derived from the method as described herein, including discouraging dopant diffusion of amorphized fin areas, and thereby reducing short channel effect in the device.
Referring now to
The first nitride layer 124 may be first deposited in the n-FET region 100 while a photoresist may be applied to the p-FET region 200 to delineate the nitride layer. Then the second nitride layer 224 may be deposited in the p-FET region 200 while a photoresist may be applied to the n-FET region 100 to delineate the nitride layer. The reverse deposition scheme may also be considered.
For example, for the n-FET region 100, the first nitride layer 124 may include a high tensile silicon nitride where the tensile strength may range from about 0.5-2.8 GPa. In an embodiment of the present disclosure, the applied tensile strength may be approximately 1.2 GPa. In such cases, the first nitride layer 124 may exert a high tensile strain on the amorphized fins 114.
For example, for the p-FET region 200, the second nitride layer 224 may include a high compressive silicon nitride where the compressive strength may range from about 2.0-4.0 GPa. In an embodiment of the present disclosure, the applied compressive strength may be approximately 3.0 GPa. In such cases, the second nitride layer 224 may exert a high compressive strain on the amorphized fins 214.
The first nitride layer 124 (n-FET region 100) and the second nitride layer 224 (p-FET region 200) may include a thickness in the range of about 30 nm to about 50 nm.
After deposition of the first nitride layer 124 in the n-FET region 100 and second nitride layer 224 in the p-FET region 200, the semiconductor structure 500 may be thermally treated in order to re-crystallize the amorphized fins 114, 214 forming re-crystallized fins (not shown). The thermal treatment may be conducted by any method known in the art, for example, rapid thermal annealing (RTA) of the semiconductor structure 500. In an embodiment of the present disclosure, the annealing temperature may range from about 800° C. to about 1100° C. The re-crystallization of the amorphized fins 114, 214 may lead to stacking fault formation in the fins, where the re-crystallized fins, the epitaxial doped layer and the nitride layer form strained source and drain regions 116, 216 (
Referring now to
The steps previously described may provide a method for integration of FinFET devices including improved channel mobility as well as enhanced source and drain region resistance.
After removal of the first and second nitride layers 124, 224 (
After the metal layer is formed, the semiconductor structure 500 may be subjected to a thermal annealing process, using conventional processes such as, but not limited to, RTA. During the thermal annealing process, the metal layer reacts with the silicon present in the substrate to form a metal silicide. After the annealing process, an etching process may be carried out to remove substantially all un-reacted metal or metal alloy of the remaining portion of the metal layer. The etching process may comprise a wet etching method.
The descriptions of the various embodiments of the present invention have been presented for purposes of illustration, but are not intended to be exhaustive or limited to the embodiments disclosed. Many modifications and variations will be apparent to those of ordinary skill in the art without departing from the scope and spirit of the described embodiments. The terminology used herein was chosen to best explain the principles of the embodiment, the practical application or technical improvement over technologies found in the marketplace, or to enable others of ordinary skill in the art to understand the embodiments disclosed herein.
Number | Name | Date | Kind |
---|---|---|---|
6395587 | Crowder et al. | May 2002 | B1 |
8334185 | Kronholz et al. | Dec 2012 | B2 |
8435845 | Ning et al. | May 2013 | B2 |
20040219722 | Pham et al. | Nov 2004 | A1 |
20060284255 | Shin et al. | Dec 2006 | A1 |
20100072553 | Xu et al. | Mar 2010 | A1 |
20100117159 | Lindsay | May 2010 | A1 |
20100127327 | Chidambarrao | May 2010 | A1 |
20100308381 | Luning et al. | Dec 2010 | A1 |
20110042744 | Cheng et al. | Feb 2011 | A1 |
20110068375 | Jakschik et al. | Mar 2011 | A1 |
20110079855 | Chan et al. | Apr 2011 | A1 |
20110084336 | Luning et al. | Apr 2011 | A1 |
20110097881 | Vandervorst et al. | Apr 2011 | A1 |
20110151652 | Sssaki et al. | Jun 2011 | A1 |
20110169085 | Xu et al. | Jul 2011 | A1 |
20110212601 | Moroz et al. | Sep 2011 | A1 |
20110266622 | Luning et al. | Nov 2011 | A1 |
20110272763 | Sasaki et al. | Nov 2011 | A1 |
20120001197 | Liaw et al. | Jan 2012 | A1 |
20120018730 | Kanakasabapathy et al. | Jan 2012 | A1 |
20120070947 | Basker et al. | Mar 2012 | A1 |
20120171832 | Toh et al. | Jul 2012 | A1 |
20120276695 | Cheng et al. | Nov 2012 | A1 |
20130023103 | Yang et al. | Jan 2013 | A1 |
20130093019 | Ando et al. | Apr 2013 | A1 |
20130187234 | Kanakasabapathy et al. | Jul 2013 | A1 |
20130200468 | Cai et al. | Aug 2013 | A1 |
20130319613 | Basker et al. | Dec 2013 | A1 |
20140035141 | Cheng et al. | Feb 2014 | A1 |
20140151814 | Giles et al. | Jun 2014 | A1 |
Number | Date | Country | |
---|---|---|---|
20150041911 A1 | Feb 2015 | US |