Method for making nanostructure transistors with offset source/drain dopant blocking structures including a superlattice

Information

  • Patent Grant
  • 12142662
  • Patent Number
    12,142,662
  • Date Filed
    Friday, March 22, 2024
    8 months ago
  • Date Issued
    Tuesday, November 12, 2024
    12 days ago
Abstract
A method for making semiconductor device may include forming spaced apart gate stacks on a substrate defining respective trenches therebetween. Each gate stack may include alternating layers of first and second semiconductor materials, with the layers of the second semiconductor material defining nanostructures. The method may further include forming respective source/drain regions within the trenches, forming respective insulating regions adjacent lateral ends of the layers of the first semiconductor material, and forming respective dopant blocking superlattices adjacent lateral ends of the nanostructures and offset outwardly from adjacent surfaces of the insulating regions. Each dopant blocking superlattice may include a plurality of stacked groups of layers, with each group of layers comprising stacked base semiconductor monolayers defining a base semiconductor portion, and at least one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions.
Description
TECHNICAL FIELD

The present disclosure generally relates to semiconductor devices, and, more particularly, to metal oxide semiconductor (MOS) devices including nanostructures and related methods.


BACKGROUND

Structures and techniques have been proposed to enhance the performance of semiconductor devices, such as by enhancing the mobility of the charge carriers. For example, U.S. Patent Application No. 2003/0057416 to Currie et al. discloses strained material layers of silicon, silicon-germanium, and relaxed silicon and also including impurity-free zones that would otherwise cause performance degradation. The resulting biaxial strain in the upper silicon layer alters the carrier mobilities enabling higher speed and/or lower power devices. Published U.S. Patent Application No. 2003/0034529 to Fitzgerald et al. discloses a CMOS inverter also based upon similar strained silicon technology.


U.S. Pat. No. 6,472,685 B2 to Takagi discloses a semiconductor device including a silicon and carbon layer sandwiched between silicon layers so that the conduction band and valence band of the second silicon layer receive a tensile strain. Electrons having a smaller effective mass, and which have been induced by an electric field applied to the gate electrode, are confined in the second silicon layer, thus, an n-channel MOSFET is asserted to have a higher mobility.


U.S. Pat. No. 4,937,204 to Ishibashi et al. discloses a superlattice in which a plurality of layers, less than eight monolayers, and containing a fractional or binary or a binary compound semiconductor layer, are alternately and epitaxially grown. The direction of main current flow is perpendicular to the layers of the superlattice.


U.S. Pat. No. 5,357,119 to Wang et al. discloses a Si—Ge short period superlattice with higher mobility achieved by reducing alloy scattering in the superlattice. Along these lines, U.S. Pat. No. 5,683,934 to Candelaria discloses an enhanced mobility MOSFET including a channel layer comprising an alloy of silicon and a second material substitutionally present in the silicon lattice at a percentage that places the channel layer under tensile stress.


U.S. Pat. No. 5,216,262 to Tsu discloses a quantum well structure comprising two barrier regions and a thin epitaxially grown semiconductor layer sandwiched between the barriers. Each barrier region consists of alternate layers of SiO2/Si with a thickness generally in a range of two to six monolayers. A much thicker section of silicon is sandwiched between the barriers.


An article entitled “Phenomena in silicon nanostructure devices” also to Tsu and published online Sep. 6, 2000 by Applied Physics and Materials Science & Processing, pp. 391-402 discloses a semiconductor-atomic superlattice (SAS) of silicon and oxygen. The Si/O superlattice is disclosed as useful in a silicon quantum and light-emitting devices. In particular, a green electroluminescence diode structure was constructed and tested. Current flow in the diode structure is vertical, that is, perpendicular to the layers of the SAS. The disclosed SAS may include semiconductor layers separated by adsorbed species such as oxygen atoms, and CO molecules. The silicon growth beyond the adsorbed monolayer of oxygen is described as epitaxial with a fairly low defect density. One SAS structure included a 1.1 nm thick silicon portion that is about eight atomic layers of silicon, and another structure had twice this thickness of silicon. An article to Luo et al. entitled “Chemical Design of Direct-Gap Light-Emitting Silicon” published in Physical Review Letters, Vol. 89, No. 7 (Aug. 12, 2002) further discusses the light emitting SAS structures of Tsu.


U.S. Pat. No. 7,105,895 to Wang et al. discloses a barrier building block of thin silicon and oxygen, carbon, nitrogen, phosphorous, antimony, arsenic or hydrogen to thereby reduce current flowing vertically through the lattice more than four orders of magnitude. The insulating layer/barrier layer allows for low defect epitaxial silicon to be deposited next to the insulating layer.


Published Great Britain Patent Application 2,347,520 to Mears et al. discloses that principles of Aperiodic Photonic Band-Gap (APBG) structures may be adapted for electronic bandgap engineering. In particular, the application discloses that material parameters, for example, the location of band minima, effective mass, etc., can be tailored to yield new aperiodic materials with desirable band-structure characteristics. Other parameters, such as electrical conductivity, thermal conductivity and dielectric permittivity or magnetic permeability are disclosed as also possible to be designed into the material.


Furthermore, U.S. Pat. No. 6,376,337 to Wang et al. discloses a method for producing an insulating or barrier layer for semiconductor devices which includes depositing a layer of silicon and at least one additional element on the silicon substrate whereby the deposited layer is substantially free of defects such that epitaxial silicon substantially free of defects can be deposited on the deposited layer. Alternatively, a monolayer of one or more elements, preferably comprising oxygen, is absorbed on a silicon substrate. A plurality of insulating layers sandwiched between epitaxial silicon forms a barrier composite.


Despite the existence of such approaches, further enhancements may be desirable for using advanced semiconductor materials and processing techniques to achieve improved performance in semiconductor devices.


SUMMARY

A method for making semiconductor device may include forming a plurality of spaced apart gate stacks on a substrate defining respective trenches therebetween. Each gate stack may include alternating layers of first and second semiconductor materials, with the layers of the second semiconductor material defining nanostructures. The method may further include forming respective source/drain regions within the trenches, forming respective insulating regions adjacent lateral ends of the layers of the first semiconductor material, and forming respective dopant blocking superlattices adjacent lateral ends of the nanostructures and offset outwardly from adjacent surfaces of the insulating regions. Each dopant blocking superlattice may include a plurality of stacked groups of layers, with each group of layers comprising a plurality of stacked base semiconductor monolayers defining a base semiconductor portion, and at least one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions.


In an example embodiment, the method may further include forming a respective semiconductor buffer layer between each nanostructure and the adjacent dopant blocking superlattice. In some implementations, the method may also include forming a respective lateral bottom dopant blocking superlattice between the substrate and the source/drain regions, with each lateral bottom dopant blocking superlattice comprising a plurality of stacked groups of layers, each group of layers comprising a plurality of stacked base semiconductor monolayers defining a base semiconductor portion, and at least one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions.


By way of example, the first semiconductor material may comprise silicon germanium, and the second semiconductor material may comprise silicon. Also by way of example, the source/drain regions may comprise phosphorus doped silicon (Si:P), the base semiconductor monolayers may comprise silicon, and the non-semiconductor monolayers may comprise oxygen.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a greatly enlarged schematic cross-sectional view of a superlattice for use in a semiconductor device in accordance with an example embodiment.



FIG. 2 is a perspective schematic atomic diagram of a portion of the superlattice shown in FIG. 1.



FIG. 3 is a greatly enlarged schematic cross-sectional view of another embodiment of a superlattice in accordance with an example embodiment.



FIGS. 4A-4E are a series of cross-sectional diagrams illustrating a method of making a nanosheet transistor with superlattice dopant blocking layers in accordance with an example embodiment.



FIGS. 5A-5F are a series of cross-sectional diagrams illustrating another method of making a nanosheet transistor with superlattice dopant blocking layers in accordance with an example embodiment.



FIGS. 6A-6D are a series of cross-sectional diagrams illustrating a conventional method of making a nanosheet transistor in accordance with the prior art.



FIGS. 7A-7H are a series of cross-sectional diagrams illustrating another method of making a nanosheet transistor with superlattice dopant blocking layers and providing enhanced contact area in accordance with an example embodiment.



FIGS. 8A-8C are a series of cross-sectional diagrams illustrating still another method of making a nanosheet transistor providing enhanced contact area in accordance with an example embodiment.



FIGS. 9A-9D are a series of cross-sectional diagrams illustrating yet another method of making a nanosheet transistor providing enhanced contact area in accordance with an example embodiment.



FIGS. 10A-10D are a series of cross-sectional diagrams illustrating another method of making a nanosheet transistor providing enhanced contact area in accordance with an example embodiment.





DETAILED DESCRIPTION

Example embodiments will now be described more fully hereinafter with reference to the accompanying drawings, in which the example embodiments are shown. The embodiments may, however, be implemented in many different forms and should not be construed as limited to the specific examples set forth herein. Rather, these embodiments are provided so that this disclosure will be thorough and complete. Like numbers refer to like elements throughout.


Generally speaking, the present disclosure relates to semiconductor devices having an enhanced semiconductor superlattice therein to provide performance enhancement characteristics. The enhanced semiconductor superlattice may also be referred to as an “MST” layer or “MST technology” in this disclosure.


More particularly, the MST technology relates to advanced semiconductor materials such as the superlattice 25 described further below. In prior work, Applicant theorized that certain superlattices as described herein reduce the effective mass of charge carriers and that this thereby leads to higher charge carrier mobility. See, e.g., U.S. Pat. No. 6,897,472, which is hereby incorporate herein in its entirety by reference.


Further development by Applicant has established that the presence of MST layers may advantageously improve the mobility of free carriers in semiconductor materials, e.g., at interfaces between silicon and insulators like SiO2 or HfO2. Applicant theorizes, without wishing to be bound thereto, that this may occur due to various mechanisms. One mechanism is by reducing the concentration of charged impurities proximate to the interface, by reducing the diffusion of these impurities, and/or by trapping the impurities so they do not reach the interface proximity. Charged impurities cause Coulomb scattering, which reduces mobility. Another mechanism is by improving the quality of the interface. For example, oxygen emitted from an MST film may provide oxygen to a Si—SiO2 interface, reducing the presence of sub-stoichiometric SiOx. Alternately, the trapping of interstitials by MST layers may reduce the concentration of interstitial silicon proximate to the Si—SiO2 interface, reducing the tendency to form sub-stoichiometric SiOx. Sub-stoichiometric SiOx at the Si—SiO2 interface is known to exhibit inferior insulating properties relative to stoichiometric SiO2. Reducing the amount of sub-stoichiometric SiOx at the interface may more effectively confine free carriers (electrons or holes) in the silicon, and thus improve the mobility of these carriers due to electric fields applied parallel to the interface, as is standard practice in field-effect-transistor (“FET”) structures. Scattering due to the direct influence of the interface is called “surface-roughness scattering”, which may advantageously be reduced by the proximity of MST layers followed by anneals or during thermal oxidation.


In addition to the enhanced mobility characteristics of MST structures, they may also be formed or used in such a manner that they provide piezoelectric, pyroelectric, and/or ferroelectric properties that are advantageous for use in a variety of different types of devices, as will be discussed further below.


Referring now to FIGS. 1 and 2, the materials or structures are in the form of a superlattice 25 whose structure is controlled at the atomic or molecular level and may be formed using known techniques of atomic or molecular layer deposition. The superlattice 25 includes a plurality of layer groups 45a-45n arranged in stacked relation, as perhaps best understood with specific reference to the schematic cross-sectional view of FIG. 1.


Each group of layers 45a-45n of the superlattice 25 illustratively includes a plurality of stacked base semiconductor monolayers 46 defining a respective base semiconductor portion 46a-46n and a non-semiconductor monolayer (s) 50 thereon. The non-semiconductor monolayers 50 are indicated by stippling in FIG. 1 for clarity of illustration.


The non-semiconductor monolayer 50 illustratively includes one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions. By “constrained within a crystal lattice of adjacent base semiconductor portions” it is meant that at least some semiconductor atoms from opposing base semiconductor portions 46a-46n are chemically bound together through the non-semiconductor monolayer 50 therebetween, as seen in FIG. 2. Generally speaking, this configuration is made possible by controlling the amount of non-semiconductor material that is deposited on semiconductor portions 46a-46n through atomic layer deposition techniques so that not all (i.e., less than full or 100% coverage) of the available semiconductor bonding sites are populated with bonds to non-semiconductor atoms, as will be discussed further below. Thus, as further monolayers 46 of semiconductor material are deposited on or over a non-semiconductor monolayer 50, the newly deposited semiconductor atoms will populate the remaining vacant bonding sites of the semiconductor atoms below the non-semiconductor monolayer.


In other embodiments, more than one such non-semiconductor monolayer may be possible. It should be noted that reference herein to a non-semiconductor or semiconductor monolayer means that the material used for the monolayer would be a non-semiconductor or semiconductor if formed in bulk. That is, a single monolayer of a material, such as silicon, may not necessarily exhibit the same properties that it would if formed in bulk or in a relatively thick layer, as will be appreciated by those skilled in the art.


Applicant theorizes without wishing to be bound thereto that non-semiconductor monolayers 50 and adjacent base semiconductor portions 46a-46n cause the superlattice 25 to have a lower appropriate conductivity effective mass for the charge carriers in the parallel layer direction than would otherwise be present. Considered another way, this parallel direction is orthogonal to the stacking direction. The band modifying layers 50 may also cause the superlattice 25 to have a common energy band structure, while also advantageously functioning as an insulator between layers or regions vertically above and below the superlattice.


Moreover, this superlattice structure may also advantageously act as a barrier to dopant and/or material diffusion between layers vertically above and below the superlattice 25. These properties may thus advantageously allow the superlattice 25 to provide an interface for high-K dielectrics which not only reduces diffusion of the high-K material into the channel region, but which may also advantageously reduce unwanted scattering effects and improve device mobility, as will be appreciated by those skilled in the art.


It is also theorized that semiconductor devices including the superlattice 25 may enjoy a higher charge carrier mobility based upon the lower conductivity effective mass than would otherwise be present. In some embodiments, and as a result of the band engineering achieved by the present embodiments, the superlattice 25 may further have a substantially direct energy bandgap that may be particularly advantageous for opto-electronic devices, for example.


The superlattice 25 also illustratively includes a cap layer 52 on an upper layer group 45n. The cap layer 52 may comprise a plurality of base semiconductor monolayers 46. The cap layer 52 may have between 2 to 100 monolayers of the base semiconductor, and, more preferably between 10 to 50 monolayers.


Each base semiconductor portion 46a-46n may comprise a base semiconductor selected from the group consisting of Group IV semiconductors, Group III-V semiconductors, and Group II-VI semiconductors. Of course, the term Group IV semiconductors also includes Group IV-IV semiconductors, as will be appreciated by those skilled in the art. More particularly, the base semiconductor may comprise at least one of silicon and germanium, for example.


Each non-semiconductor monolayer 50 may comprise a non-semiconductor selected from the group consisting of oxygen, nitrogen, fluorine, carbon and carbon-oxygen, for example. The non-semiconductor is also desirably thermally stable through deposition of a next layer to thereby facilitate manufacturing. In other embodiments, the non-semiconductor may be another inorganic or organic element or compound that is compatible with the given semiconductor processing as will be appreciated by those skilled in the art. More particularly, the base semiconductor may comprise at least one of silicon and germanium, for example.


It should be noted that the term monolayer is meant to include a single atomic layer and also a single molecular layer. It is also noted that the non-semiconductor monolayer 50 provided by a single monolayer is also meant to include a monolayer wherein not all of the possible sites are occupied (i.e., there is less than full or 100% coverage). For example, with particular reference to the atomic diagram of FIG. 2, a 4/1 repeating structure is illustrated for silicon as the base semiconductor material, and oxygen as the energy band-modifying material. Only half of the possible sites for oxygen are occupied in the illustrated example.


In other embodiments and/or with different materials this one-half occupation would not necessarily be the case as will be appreciated by those skilled in the art. Indeed it can be seen even in this schematic diagram, that individual atoms of oxygen in a given monolayer are not precisely aligned along a flat plane as will also be appreciated by those of skill in the art of atomic deposition. By way of example, a preferred occupation range is from about one-eighth to one-half of the possible oxygen sites being full, although other numbers may be used in certain embodiments.


Silicon and oxygen are currently widely used in conventional semiconductor processing, and, hence, manufacturers will be readily able to use these materials as described herein. Atomic or monolayer deposition is also now widely used. Accordingly, semiconductor devices incorporating the superlattice 25 in accordance with the embodiments may be readily adopted and implemented, as will be appreciated by those skilled in the art.


Referring now additionally to FIG. 3, another embodiment of a superlattice 25′ in accordance with the embodiments having different properties is now described. In this embodiment, a repeating pattern of 3/1/5/1 is illustrated. More particularly, the lowest base semiconductor portion 46a′ has three monolayers, and the second lowest base semiconductor portion 46b′ has five monolayers. This pattern repeats throughout the superlattice 25′. The non-semiconductor monolayers 50′ may each include a single monolayer. For such a superlattice 25′ including Si/O, the enhancement of charge carrier mobility is independent of orientation in the plane of the layers. Those other elements of FIG. 3 not specifically mentioned are similar to those discussed above with reference to FIG. 1 and need no further discussion herein.


In some device embodiments, all of the base semiconductor portions of a superlattice may be a same number of monolayers thick. In other embodiments, at least some of the base semiconductor portions may be a different number of monolayers thick. In still other embodiments, all of the base semiconductor portions may be a different number of monolayers thick.


Turning to FIGS. 4A-4E, a method for making nanosheet transistor devices which incorporate the above-described superlattice structures, such as to advantageously provide dopant blocking between the source/drain and nanosheet channel layers, is now described. A plurality of gate stacks 102 are formed on a silicon substrate 101, followed by source/drain recesses 103 (FIG. 4A). In the illustrated example, each gate stack 102 includes alternating silicon (Si) nanosheets 104 and silicon germanium (SiGe) (e.g., boron-doped SiGe) layers 105, with inner spacers 109 (e.g., SiO2) on the ends of the SiGe layers, although different materials may be used in different embodiments.


In some embodiments, silicon buffers 106a, 106b may optionally be epitaxially grown on the sides of the nanosheets 104 and the substrate 101 within the recess 103, respectively (FIG. 4B). The buffers 106a, 106b may help mitigate any surface roughness prior to formation of the MST superlattice films, which helps to prevent or reduce defects therein. In an example implementation, the buffers 106a, 106b may have a thickness of 2 nm or less, although other thicknesses may be used in different embodiments.


MST film and cap formation may then be performed (FIG. 4C) to define superlattices 125a and cap layers 152a on the buffers 106a, as well as a superlattice 125b and cap layer 152b on the buffer 106b (FIG. 4D), as described above. By way of example, the superlattices 125a, 125b may have two or three non-semiconductor monolayers 50 (e.g., two or three oxygen-inserted monolayers), although other numbers may be used in different embodiments.


Source/drain regions 107 may then be formed within the recesses 103 using a hard mask 108 (FIG. 4D). In the illustrated example, this is done with a Si:P growth, although other source/drain materials may be used in different embodiments. It should be noted that the Si:P growth occurs over the cap layers 152a, 152b in the illustrated example, but in some embodiments these cap layers may be omitted. After removal of the hard mask 108 (FIG. 4E), additional processing steps may be performed to complete the nanosheet transistor, such as removing the SiGe layers 105 and forming a gate-all-around (GAA) structure in which the nanosheets 104 provide a plurality of stacked channels between the source/drain regions 107, as will be appreciated by those skilled in the art. Further details regarding the formation of GAA devices are provided in U.S. Pat Pubs. US2022/0005926, US2022/0005927, US2022/0384600, US2022/0376047, and US2023/0121774, all of which are also assigned to the present Applicant and are hereby incorporated herein in their entireties by reference. It should be noted that other nanostructures besides nanosheets 104 (e.g., nanotubes, etc.) may be used in some configurations.


Referring additionally to FIGS. 5A-5F, another example approach for making nanosheet transistor devices is now described. This approach begins similarly to the one described above, although after the trench 103′ is etched, then a further recess etch is performed on the silicon nanosheets 104′ and substrate 101′ (FIG. 5B). As such, the buffers 106a′ and portions of the buffer 106b′ are recessed laterally inside of the inner spacers 109′ upon formation (FIG. 5C), as are the subsequent MST superlattice films 125a′ and cap layers 152a′, as well as portions of the superlattice 125b′ and cap layer 152b′, as seen in FIG. 5D. The source/drain region 107′ formation (FIGS. 5E-5F) and subsequent processing steps may be similar to those described above.


It should be noted that in some embodiments the buffers 106a′ and/or 106b′ may be omitted, as the additional Si recess etching may provide sufficient surface smoothing without the buffer (s). Furthermore, formation of the cap layer 152b′ may occur as part of the source/drain region 107′ formation (Si:P process), which does not diminish the overall area available for the source/drain region. The cap layer 152′ eventually gets doped with P during this process. Additionally, in some embodiments the cap layers 152a′ and/or 152b′ may optionally be omitted. More particularly, in an example implementation the MST and Si:P formation may both advantageously occur within the same chamber in-situ, in which case MST layers without a cap layer may still provide desired blocking capabilities. The Si:P 107′ may then be etched where exposed through the hard mask 108′, and a metal 120′ deposited thereover (FIG. 5F), followed by silicide formation to define a contact.


While the superlattices 125a′ provide similar dopant blocking capabilities (i.e., blocking the phosphorous in the source/drain regions 107′ from the nanosheet 104 channel layers) to the superlattices 125a described above, the present approach may provide an additional advantage in that the buffers 106a′, superlattices 125a′, and cap layers 152a′ do not protrude into the source/drain regions 107′. By way of example, this configuration may occupy significantly less source/drain area, on the order of 11-25% in some embodiments, whereas the above-described approach may create additional resistance due to the loss of available source/drain surface area, which may be undesirable in certain embodiments.


Turning to FIGS. 6A-6D, a conventional approach for making nanosheet transistor devices is now described. This approach begins with forming a plurality of gate stacks 62 on a silicon substrate 61, followed by source/drain recesses 63 via a hard mask 68 (FIG. 6A), as similarly described above. In the illustrated example, each gate stack 62 includes alternating silicon (Si) nanosheets 64 and silicon germanium (SiGe) layers 65. Source/drain regions 67 and inner spacers 69 may then be formed within the recesses 63 using the hard mask 68 (FIG. 6B). In the illustrated example, this is done with a Si:P growth, although other source/drain materials may be used in different embodiments. A metal layer 70 is formed over the hard mask 68 and the source/drain region 67 (FIG. 6C), followed by silicidation/metal removal (FIG. 6D) to define a source/drain contact 71. The hard mask 68 may then be removed.


A potential drawback of this conventional approach is that there is a relatively small amount of contact area between the contact 70 and the source/drain region 67 (i.e., only at the top of the source/drain region), which may result in relatively high contact resistance. Various example embodiments which provide for enhanced contact area, and therefore lower contact resistance, are now described. One such example embodiment is described with reference to FIGS. 7A-7H. A plurality of gate stacks 202 are formed on a silicon substrate 201, followed by source/drain recesses 203 (FIG. 7A). In the illustrated example, each gate stack 102 includes alternating silicon (Si) nanosheets 204 and silicon germanium (SiGe) layers 205, with inner spacers 209 (e.g., SiO2) on the ends of the SiGe layers, as similarly discussed above.


In some embodiments, silicon buffers 206a, 206b may optionally be epitaxially grown on the sides of the nanosheets 204 and the substrate 201 within the recess 203, respectively (FIG. 7B). As noted above, the buffers 206a, 206b may help mitigate any surface roughness prior to formation of the MST superlattice films, which helps to prevent or reduce defects therein. MST film and cap formation may then be performed (FIG. 7C) to define superlattices 225a, 225b and cap layers 252a, 252b on the buffers 206a, 206b (FIG. 7D), respectively, as similarly described above. Source/drain regions 207 (e.g., Si:P) may then be formed within the recesses 203 using a hard mask 208 (FIG. 7D). Here again, in the illustrated example the Si:P growth occurs over the cap layers 152, but in some embodiments these cap layers may be omitted.


Next, spacers 212 are formed on the inside edges of the hard mask 208, allowing the Si:P to be etched such that a Si:P liner remains within the trench 203 (FIG. 7E). Thereafter, a metal layer 210 may be deposited over the hard mask 208 and filling the trench 203 (FIG. 7F), followed by silicidation and metal removal (FIG. 7G) to define a contact liner 211 along the bottom and sidewalls of the trench 203, which may then be filled with a metal plug 213 to complete the contact structure (FIG. 7H). As discussed further above, the hard mask 208 may then be removed and additional processing steps performed to complete the nanosheet transistor.


Another example embodiment which provides reduced contact resistance is now described with reference to FIGS. 8A-8C. Beginning with the structure shown in FIG. 6B, here spacers 212′ are next formed on the inside edges of the hard mask 208′, allowing the Si:P to be etched such that a Si:P liner remains within the trench 203′ (FIG. 8A). Thereafter, a metal layer 210′ may be deposited over the hard mask 208′ and filling the trench 203′ (FIG. 8B), followed by silicidation/metal removal and metal plug 213′ formation (FIG. 8C), as described above. The resulting structure is similar to that of FIG. 7H, with the exception that MST films 225 and cap layers 252 are omitted in this embodiment. Here again, the hard mask 208′ may then be removed and additional processing steps performed to complete the nanosheet transistor.


Still another example embodiment which provides reduced contact resistance is now described with reference to FIGS. 9A-9D. This approach begins with a structure similar to that of FIG. 7B, but the trench 203″ is then filled with Si:P source/drain material 207″ (FIG. 9A). Spacers 212″ are next formed on the inside edges of the hard mask 208″, allowing the Si:P to be etched such that a Si:P liner remains within the trench 203′ (FIG. 9B). Thereafter, metal deposition followed by silicidation/metal removal (FIG. 9C) and metal plug 213″ formation (FIG. 9D) may be performed, as described above. Here again, the hard mask 208″ may then be removed and additional processing steps performed to complete the nanosheet transistor.


Yet another example embodiment which provides reduced contact resistance is now described with reference to FIGS. 10A-10D. This approach also begins with a structure similar to that of FIG. 7B, but a partial deposition of Si:P source/drain material 207′″ is performed to line (but not completely fill) the trench 203′″ (FIG. 10A). Thereafter, metal 210′″ deposition followed by silicidation/metal removal (FIG. 10C) and metal plug 213′″ formation (FIG. 10D) may be performed, as described above. Here again, the hard mask 208′″ may then be removed and additional processing steps performed to complete the nanosheet transistor. With respect to the partial deposition of Si:P, it should be noted that this approach may also be used in the above-described embodiments (with or without the use of MST layers) rather than fully filling the trench with Si:P. Moreover, in another similar approach to that shown in FIGS. 10A-10D, all of the illustrated steps would be the same except the process would begin with a structure similar to that of FIG. 6A (i.e., where no silicon recess of the nanosheets 203′″ is performed prior to the Si:P partial deposition).


Example dimensions which may be used for one of more of the following embodiments include: gate height=˜63 nm; gate length (Lg)=˜12 nm; SiGe layer thickness=˜12.8 nm; and Si nanosheet thickness=˜5 nm. However, it will be appreciated that other dimensions are possible in different configurations, as will be appreciated by those skilled in the art.


Many modifications and other embodiments of the invention will come to the mind of one skilled in the art having the benefit of the teachings presented in the foregoing descriptions and the associated drawings. Therefore, it is understood that the invention is not to be limited to the specific embodiments disclosed, and that modifications and embodiments are intended to be included within the scope of the appended claims.

Claims
  • 1. A method for making a semiconductor device comprising: forming a plurality of spaced apart gate stacks on a substrate defining respective trenches therebetween, each gate stack comprising alternating layers of first and second semiconductor materials, the layers of the second semiconductor material defining nanostructures;forming respective source/drain regions within the trenches;forming respective insulating regions adjacent lateral ends of the layers of the first semiconductor material; andforming respective dopant blocking superlattices adjacent lateral ends of the nanostructures and offset outwardly from adjacent surfaces of the insulating regions, each dopant blocking superlattice comprising a plurality of stacked groups of layers, each group of layers comprising a plurality of stacked base semiconductor monolayers defining a base semiconductor portion, and at least one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions.
  • 2. The method of claim 1 further comprising forming a respective semiconductor buffer layer between each nanostructure and the adjacent dopant blocking superlattice.
  • 3. The method of claim 1 comprising forming a respective lateral bottom dopant blocking superlattice between the substrate and the source/drain regions, each lateral bottom dopant blocking superlattice comprising a plurality of stacked groups of layers, each group of layers comprising a plurality of stacked base semiconductor monolayers defining a base semiconductor portion, and at least one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions.
  • 4. The method of claim 1 wherein the first semiconductor material comprises silicon germanium.
  • 5. The method of claim 1 wherein the second semiconductor material comprises silicon.
  • 6. The method of claim 1 wherein the source/drain regions comprise phosphorus doped silicon (Si:P).
  • 7. The method of claim 1 wherein the base semiconductor monolayers comprise silicon.
  • 8. The method of claim 1 wherein the non-semiconductor monolayers comprise oxygen.
  • 9. A method for making a semiconductor device comprising: forming a plurality of spaced apart gate stacks on a substrate defining respective trenches therebetween, each gate stack comprising alternating layers of first and second semiconductor materials, the layers of the second semiconductor material defining nanostructures;forming respective source/drain regions within the trenches;forming respective insulating regions adjacent lateral ends of the layers of the first semiconductor material;forming respective dopant blocking superlattices adjacent lateral ends of the nanostructures and offset outwardly from adjacent surfaces of the insulating regions, each dopant blocking superlattice comprising a plurality of stacked groups of layers, each group of layers comprising a plurality of stacked base semiconductor monolayers defining a base semiconductor portion, and at least one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions;forming a respective semiconductor buffer layer between each nanostructure and the adjacent dopant blocking superlattice; andforming a respective lateral bottom dopant blocking superlattice between the substrate and the source/drain regions, each lateral bottom dopant blocking superlattice comprising a plurality of stacked groups of layers, each group of layers comprising a plurality of stacked base semiconductor monolayers defining a base semiconductor portion, and at least one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions.
  • 10. The method of claim 9 wherein the first semiconductor material comprises silicon germanium.
  • 11. The method of claim 9 wherein the second semiconductor material comprises silicon.
  • 12. The method of claim 9 wherein the source/drain regions comprise phosphorus doped silicon (Si:P).
  • 13. The method of claim 9 wherein the base semiconductor monolayers comprise silicon.
  • 14. The method of claim 9 wherein the non-semiconductor monolayers comprise oxygen.
  • 15. A method for making a semiconductor device comprising: forming a plurality of spaced apart gate stacks on a substrate defining respective trenches therebetween, each gate stack comprising alternating layers of first and second semiconductor materials, the layers of the second semiconductor material defining nanostructures;forming respective source/drain regions within the trenches;forming respective insulating regions adjacent lateral ends of the layers of the first semiconductor material; andforming respective dopant blocking superlattices adjacent lateral ends of the nanostructures and offset outwardly from adjacent surfaces of the insulating regions, each dopant blocking superlattice comprising a plurality of stacked groups of layers, each group of layers comprising a plurality of stacked base silicon monolayers defining a base silicon portion, and at least one oxygen monolayer constrained within a crystal lattice of adjacent base silicon portions.
  • 16. The method of claim 15 further comprising forming a respective semiconductor buffer layer between each nanostructure and the adjacent dopant blocking superlattice.
  • 17. The method of claim 15 comprising forming a respective lateral bottom dopant blocking superlattice between the substrate and the source/drain regions, each lateral bottom dopant blocking superlattice comprising a plurality of stacked groups of layers, each group of layers comprising a plurality of stacked base semiconductor monolayers defining a base semiconductor portion, and at least one non-semiconductor monolayer constrained within a crystal lattice of adjacent base semiconductor portions.
  • 18. The method of claim 15 wherein the first semiconductor material comprises silicon germanium.
  • 19. The method of claim 15 wherein the second semiconductor material comprises silicon.
  • 20. The method of claim 15 wherein the source/drain regions comprise phosphorus doped silicon (Si:P).
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. provisional app. nos. 63/507,578 and 63/492,038 filed Jun. 12, 2023 and Mar. 24, 2023, respectively, which are hereby incorporated herein in their entireties by reference.

US Referenced Citations (220)
Number Name Date Kind
4937204 Ishibashi et al. Jun 1990 A
5216262 Tsu Jun 1993 A
5357119 Wang et al. Oct 1994 A
5683934 Candelaria Nov 1997 A
5796119 Seabaugh Aug 1998 A
6376337 Wang et al. Apr 2002 B1
6447933 Wang et al. Sep 2002 B1
6472685 Takagi Oct 2002 B2
6741624 Mears et al. May 2004 B2
6830964 Mears et al. Dec 2004 B1
6833294 Mears et al. Dec 2004 B1
6878576 Mears et al. Apr 2005 B1
6891188 Mears et al. May 2005 B2
6897472 Mears et al. May 2005 B2
6927413 Mears et al. Aug 2005 B2
6952018 Mears et al. Oct 2005 B2
6958486 Mears et al. Oct 2005 B2
6993222 Mears et al. Jan 2006 B2
7018900 Kreps Mar 2006 B2
7033437 Mears et al. Apr 2006 B2
7034329 Mears et al. Apr 2006 B2
7045377 Mears et al. May 2006 B2
7045813 Mears et al. May 2006 B2
7071119 Mears et al. Jul 2006 B2
7105895 Wang et al. Sep 2006 B2
7109052 Mears et al. Sep 2006 B2
7123792 Mears et al. Oct 2006 B1
7148712 Prey, Jr. et al. Dec 2006 B1
7153763 Hytha et al. Dec 2006 B2
7202494 Blanchard et al. Apr 2007 B2
7227174 Mears et al. Jun 2007 B2
7229902 Mears et al. Jun 2007 B2
7265002 Mears et al. Sep 2007 B2
7279699 Mears et al. Oct 2007 B2
7279701 Kreps Oct 2007 B2
7288457 Kreps Oct 2007 B2
7303948 Mears et al. Dec 2007 B2
7402512 Derraa et al. Jul 2008 B2
7432524 Mears et al. Oct 2008 B2
7435988 Mears et al. Oct 2008 B2
7436026 Kreps Oct 2008 B2
7446002 Mears et al. Nov 2008 B2
7446334 Mears et al. Nov 2008 B2
7491587 Rao Feb 2009 B2
7514328 Rao Apr 2009 B2
7517702 Halilov et al. Apr 2009 B2
7531828 Mears et al. May 2009 B2
7531829 Blanchard May 2009 B2
7531850 Blanchard May 2009 B2
7535041 Blanchard May 2009 B2
7586116 Kreps et al. Sep 2009 B2
7586165 Blanchard Sep 2009 B2
7598515 Mears et al. Oct 2009 B2
7612366 Mears et al. Nov 2009 B2
7625767 Huang et al. Dec 2009 B2
7659539 Kreps et al. Feb 2010 B2
7700447 Dukovski et al. Apr 2010 B2
7718996 Dukovski et al. May 2010 B2
7781827 Rao Aug 2010 B2
7812339 Mears et al. Oct 2010 B2
7863066 Mears et al. Jan 2011 B2
7880161 Mears et al. Feb 2011 B2
7928425 Rao Apr 2011 B2
8389974 Mears et al. Mar 2013 B2
9275996 Mears et al. Mar 2016 B2
9406753 Mears et al. Aug 2016 B2
9558939 Stephenson et al. Jan 2017 B1
9716147 Mears Jul 2017 B2
9721790 Mears et al. Aug 2017 B2
9722046 Mears et al. Aug 2017 B2
9899479 Mears et al. Feb 2018 B2
9941359 Mears et al. Apr 2018 B2
9972685 Mears et al. May 2018 B2
10084045 Mears et al. Sep 2018 B2
10107854 Roy Oct 2018 B2
10109342 Roy Oct 2018 B2
10109479 Mears et al. Oct 2018 B1
10170560 Mears Jan 2019 B2
10170603 Mears et al. Jan 2019 B2
10170604 Mears et al. Jan 2019 B2
10191105 Roy Jan 2019 B2
10249745 Mears et al. Apr 2019 B2
10276625 Mears et al. Apr 2019 B1
10304881 Chen et al. May 2019 B1
10355151 Chen et al. Jul 2019 B2
10361243 Mears et al. Jul 2019 B2
10367028 Chen et al. Jul 2019 B2
10367064 Rao Jul 2019 B2
10381242 Takeuchi Aug 2019 B2
10396223 Chen et al. Aug 2019 B2
10410880 Takeuchi Sep 2019 B2
10453945 Mears et al. Oct 2019 B2
10461118 Chen et al. Oct 2019 B2
10468245 Weeks et al. Nov 2019 B2
10529757 Chen et al. Jan 2020 B2
10529768 Chen et al. Jan 2020 B2
10566191 Weeks et al. Feb 2020 B1
10580866 Takeuchi et al. Mar 2020 B1
10580867 Takeuchi et al. Mar 2020 B1
10593761 Takeuchi et al. Mar 2020 B1
10608027 Chen et al. Mar 2020 B2
10608043 Chen et al. Mar 2020 B2
10615209 Chen et al. Apr 2020 B2
10636879 Rao Apr 2020 B2
10727049 Weeks et al. Jul 2020 B2
10741436 Stephenson et al. Aug 2020 B2
10763370 Stephenson Sep 2020 B2
10777451 Stephenson et al. Sep 2020 B2
10797163 Yu et al. Oct 2020 B1
10811498 Weeks et al. Oct 2020 B2
10818755 Takeuchi et al. Oct 2020 B2
10825901 Burton et al. Nov 2020 B1
10825902 Burton et al. Nov 2020 B1
10840335 Takeuchi et al. Nov 2020 B2
10840336 Connelly et al. Nov 2020 B2
10840337 Takeuchi et al. Nov 2020 B2
10840388 Burton et al. Nov 2020 B1
10847618 Takeuchi et al. Nov 2020 B2
10854717 Takeuchi et al. Dec 2020 B2
10868120 Burton et al. Dec 2020 B1
10879356 Stephenson et al. Dec 2020 B2
10879357 Burton et al. Dec 2020 B1
10884185 Stephenson Jan 2021 B2
10937868 Burton et al. Mar 2021 B2
10937888 Burton et al. Mar 2021 B2
11075078 Cody et al. Jul 2021 B1
11094818 Takeuchi et al. Aug 2021 B2
11177351 Weeks et al. Nov 2021 B2
11183565 Burton et al. Nov 2021 B2
11302823 Weeks et al. Apr 2022 B2
11329154 Takeuchi et al. May 2022 B2
11355667 Stephenson Jun 2022 B2
11362182 Shin et al. Jun 2022 B2
11387325 Stephenson et al. Jul 2022 B2
11430869 Weeks et al. Aug 2022 B2
11437486 Burton Sep 2022 B2
11437487 Burton Sep 2022 B2
11469302 Takeuchi et al. Oct 2022 B2
11569368 Takeuchi et al. Jan 2023 B2
11631584 Hytha et al. Apr 2023 B1
11664427 Stephenson et al. May 2023 B2
11664459 Stephenson May 2023 B2
11682712 Hytha et al. Jun 2023 B2
11721546 Hytha et al. Aug 2023 B2
11728385 Hytha et al. Aug 2023 B2
11742202 Takeuchi et al. Aug 2023 B2
11810784 Hytha et al. Nov 2023 B2
11837634 Weeks et al. Dec 2023 B2
11848356 Weeks et al. Dec 2023 B2
11869968 Takeuchi et al. Jan 2024 B2
11923418 Hytha et al. Mar 2024 B2
11923431 Burton Mar 2024 B2
11935940 Burton Mar 2024 B2
11978771 Weeks et al. May 2024 B2
20030034529 Fitzgerald et al. Feb 2003 A1
20030057416 Currie et al. Mar 2003 A1
20040262594 Mears et al. Dec 2004 A1
20040266116 Mears Dec 2004 A1
20050029510 Mears et al. Feb 2005 A1
20050032241 Mears et al. Feb 2005 A1
20050279991 Mears et al. Dec 2005 A1
20050282330 Mears et al. Dec 2005 A1
20060011905 Mears et al. Jan 2006 A1
20060220118 Stephenson et al. Oct 2006 A1
20060223215 Blanchard Oct 2006 A1
20060231857 Blanchard Oct 2006 A1
20060243964 Kreps et al. Nov 2006 A1
20060263980 Kreps et al. Nov 2006 A1
20060267130 Rao Nov 2006 A1
20060273299 Stephenson et al. Dec 2006 A1
20060289049 Rao Dec 2006 A1
20060292765 Blanchard Dec 2006 A1
20070010040 Mears et al. Jan 2007 A1
20070012910 Mears et al. Jan 2007 A1
20070015344 Mears et al. Jan 2007 A1
20070020833 Mears et al. Jan 2007 A1
20070020860 Mears et al. Jan 2007 A1
20070063185 Rao Mar 2007 A1
20070063186 Rao Mar 2007 A1
20070158640 Stephenson et al. Jul 2007 A1
20070166928 Halilov et al. Jul 2007 A1
20070187667 Halilov et al. Aug 2007 A1
20080012004 Huang et al. Jan 2008 A1
20100270535 Halilov et al. Oct 2010 A1
20110215299 Rao Sep 2011 A1
20160163860 Lee Jun 2016 A1
20170213913 Lee et al. Jul 2017 A1
20190058059 Stephenson et al. Feb 2019 A1
20190348539 Yoo Nov 2019 A1
20200135489 Weeks et al. Apr 2020 A1
20200286991 Basler Sep 2020 A1
20210226066 Young et al. Jul 2021 A1
20210367050 Tsai et al. Nov 2021 A1
20220005706 Weeks et al. Jan 2022 A1
20220005927 Weeks et al. Jan 2022 A1
20220139911 Wei et al. May 2022 A1
20220278204 Shin et al. Sep 2022 A1
20220278226 Hall et al. Sep 2022 A1
20220285152 Takeuchi et al. Sep 2022 A1
20220310786 Merchant et al. Sep 2022 A1
20220352322 Hytha et al. Nov 2022 A1
20220359208 Lin et al. Nov 2022 A1
20220367676 Burton Nov 2022 A1
20220376047 Mears et al. Nov 2022 A1
20220384600 Mears et al. Dec 2022 A1
20230006040 Lee et al. Jan 2023 A1
20230040606 Colombeau et al. Feb 2023 A1
20230060784 Liu et al. Mar 2023 A1
20230122723 Weeks et al. Apr 2023 A1
20230290862 Hall et al. Sep 2023 A1
20230352299 Takeuchi et al. Nov 2023 A1
20230361178 Hytha et al. Nov 2023 A1
20230395374 Hytha et al. Dec 2023 A1
20230411491 Hytha et al. Dec 2023 A1
20230411557 Hytha et al. Dec 2023 A1
20240063268 Weeks et al. Feb 2024 A1
20240072095 Takeuchi et al. Feb 2024 A1
20240072096 Takeuchi et al. Feb 2024 A1
20240097003 Burton Mar 2024 A1
20240097026 Takeuchi et al. Mar 2024 A1
Foreign Referenced Citations (1)
Number Date Country
2347520 Jun 2000 GB
Non-Patent Literature Citations (15)
Entry
R. Tsu “Phenomena in silicon nanostructure device” published online Sep. 6, 2000 by Applied Physics and Materials Science & Processing, pp. 391-402.
Xu et al., “MOSFET performance and scalability enhancement by insertion of oxygen layers”, Department of Electrical Engineering and Computer Science, University of California, Berkeley, 2012, pp. 1-4.
Luo et al., “Chemical Design of Direct-Gap Light-Emitting Silicon” published in Physical Review Letters, vol. 89, No. 7; Aug. 12, 2002; 4 pgs.
R. Tsu “Si Based Green ELD: Si-Oxygen Superlattice” ysiwyg://l/http://www3.interscience.wiley.com/cgi-bin/abstract/72512946/start: published online Jul. 21, 2000; 2 pgs. Abstract Only.
Novikov et al. “Silicon-based Optoelectronics” 1999-2003, pp. 1-6.
Mears et al. “Simultaneous Carrier Transport Enhancement and variability reduction in Si MOSFETs by insertion of partial Monolayers of oxygen” IEEE silicon Nanoelectronics Workshop (2012): (Date of conference Jun. 10-11, 2012) pp. 2.
Xu et al. “Extension of planar bulk n-channel MOSFET scaling with oxygen insertion technology” IEEE Transactions on Electron devices, vol. 61, No. 9; Sep. 2014. pp. 3345-3349.
Xu et al. “Effectiveness of Quasi-confinement technology for improving P-chanel Si an Ge MOSSFET performance” Department of Electrical Engineering and Computer Science, University of California, Berkeley, 2012, pp. 2. mearstech.net; retrieved from internet Jan. 18, 2016.
Maurizio Di Paolo Emilio “Quantum-Engineered Material Boosts Transistor Performance” https://www.eetimes. com/quantum-engineered-material-boosts-transistor-performance/# EE Times; retreived from internet Feb. 10, 2022; pp. 3.
U.S. Appl. No. 18/613,401; filed Mar. 22, 2024 Donghun Kang.
U.S. Appl. No. 18/613,435; filed Mar. 22, 2024 Donghun Kang.
U.S. Appl. No. 18/613,476; filed Mar. 22, 2024 Donghun Kang.
U.S. Appl. No. 18/613,509; filed Mar. 22, 2024 Donghun Kang.
U.S. Appl. No. 18/613,557; filed Mar. 22, 2024 Donghun Kang.
Loubet et al. “Stacked nanosheet gate-all-around transistor to enable scaling beyond FinFET” https://www.researchgate.net/publication/319035460; Abstract Only.
Related Publications (1)
Number Date Country
20240322005 A1 Sep 2024 US
Provisional Applications (2)
Number Date Country
63507578 Jun 2023 US
63492038 Mar 2023 US