METHOD OF SLIMMING RADIATION-SENSITIVE MATERIAL LINES IN LITHOGRAPHIC APPLICATIONS
A method and system for patterning a substrate using a radiation-sensitive material is described. The method and system include forming a layer of radiation-sensitive material on a substrate, exposing the layer of radiation-sensitive material to a pattern of radiation, and then performing a post-exposure bake following the exposing. The imaged layer of radiation-sensitive material is then positive-tone developed to remove a region having high radiation exposure to form radiation-sensitive material lines. An exposure gradient within the radiation-sensitive material lines is then removed, followed by slimming the radiation-sensitive material lines.
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This application is a divisional application of co-pending U.S. patent application Ser. No. 12/751,362 filed Mar. 31, 2010, and entitled METHOD OF SLIMMING RADIATION-SENSITIVE MATERIAL LINES IN LITHOGRAPHIC APPLICATIONS, the disclosure of which is incorporated herein by reference in its entirety as if completely set forth herein below.
FIELD OF THE INVENTIONThe invention relates to methods of patterning a substrate. In particular, the invention relates to methods of decreasing line dimension (slimming) in radiation-sensitive materials.
BACKGROUND OF THE INVENTIONThe need to remain competitive in cost and performance in the production of semiconductor devices has caused a continuous increase in device density of integrated circuits. To accomplish higher integration and miniaturization in a semiconductor integrated circuit, miniaturization of a circuit pattern formed on a semiconductor wafer must also be accomplished.
Design rules define the space tolerance between devices or interconnect lines so as to ensure that the devices or lines do not interact with one another in any unwanted manner. One important layout design rule that tends to determine the overall size and density of the semiconductor device is the critical dimension (CD). A critical dimension of a circuit is defined as the smallest width of a line or the smallest space between two lines. Another critical design rule is minimum pitch, which is defined as the minimum width of a given feature plus the distance to the adjacent feature edge.
Photolithography is a standard technique utilized to manufacture semiconductor wafers by transferring geometric shapes and patterns on a mask to the surface of a semiconductor wafer. The basic photolithographic process includes projecting a patterned light source onto a layer of radiation-sensitive material, such as a photoresist layer, which is then followed by a development step.
To create finely detailed patterns with small critical dimensions and pitch requires projecting a clearly imaged light pattern. But the ability to project a clear image of a small feature onto the semiconductor wafer is limited by the wavelength of the light that is used, and the ability of a reduction lens system to capture enough diffraction orders from the illuminated mask. Current state-of-the-art photolithography tools use deep ultraviolet (DUV) light with wavelengths of 248 or 193 nm, which allow minimum feature sizes down to about 50 nm.
The minimum feature size that a projection system can print is given approximately by:
CD=k1·λ/NA
where CD is the minimum feature size or the critical dimension; k1 is a coefficient that encapsulates process-related factors, and typically equals 0.4 for production; λ is the wavelength of light used; and NA is the numerical aperture of the lens, as seen from the semiconductor wafer. According to this equation, minimum feature sizes can be decreased by decreasing the wavelength and/or by increasing the numerical aperture to achieve a tighter focused beam and a smaller spot size.
A photolithographic process utilizes an exposure tool to irradiate the layer of radiation-sensitive material on a wafer through a mask to transfer the pattern on the mask to the wafer. As the critical dimensions of the pattern layout approach the resolution limit of the lithography equipment, optical proximity effects (OPE) begin to influence the manner in which features on a mask transfer to the layer of radiation-sensitive material such that the mask and actual layout patterns begin to differ. Optical Proximity effects are known to result from optical diffraction in the projection system. The diffraction causes adjacent features to interact with one another in such a way as to produce pattern-dependent variations; the closer together features are, the more proximity effect is seen. Thus, the ability to locate line patterns close together encroaches on optical parameter limitations.
In accordance with the above description, new and improved methods for patterning semiconductor devices are therefore necessary, so as to accomplish the continued miniaturization of a circuit pattern formed on a semiconductor wafer. One non-optical approach is to narrow the line width of the radiation-sensitive material after the imaging, and the first developing are completed. Narrowing of line width is also known as “slimming” or “shrinking”, those terms being used herein synonymously.
As discussed above, patterning of a semiconductor wafer generally involves coating a surface of the wafer (substrate) with a thin film or layer of a radiation-sensitive material, such as a photoresist, and then exposing the layer of radiation-sensitive material to a pattern of radiation by projecting radiation from a radiation source through a mask. Thereafter, a developing process is performed to remove various regions of the radiation-sensitive material. The specific region being removed is dependent upon the tone of the material and the developing chemistry. As an example, in the case of a positive-tone photoresist, the irradiated regions may be removed using a first developing chemistry and the non-irradiated regions may be removed using a second developing chemistry. Conversely, in the case of a negative-tone photoresist, the non-irradiated regions may be removed using a third developing chemistry and the irradiated regions may be removed using a fourth developing chemistry. The removed regions of photoresist expose the underlying wafer surface in a pattern that is ready to be etched into the surface.
As an example for positive-tone pattern development, a typical lithographic patterning technique is shown in
As shown in
One typical method for reducing radiation-sensitive material line width involves plasma-based etching of the unexposed region 106 of the radiation-sensitive material after a positive-tone development conducted at nominal temperature. Plasma-based etching suffers from various issues such as process stability and higher front end costs. Other slimming or shrinking methods include wet methods, such as performing a positive-tone development at elevated temperatures. But wet developing methods may suffer from anisotropic slimming caused by or exacerbated by variations in the photolithographic image, as will be discussed further below.
Additional details of the photolithographic image are provided in
While it would be desirable to produce only two types of image patterns, i.e., exposed and unexposed,
In view thereof, new methods of slimming radiation-sensitive material lines that overcome the problems of the prior art are needed.
SUMMARY OF THE INVENTIONEmbodiments of the invention provide a method of patterning a substrate, wherein the dimensions of radiation-sensitive material lines are decreased. The methods comprise forming a layer of radiation-sensitive material on a substrate; exposing the layer of radiation-sensitive material to a pattern of radiation, wherein the pattern includes: a first region having a high radiation exposure, a second region having a low radiation exposure, and a third region having an exposure gradient ranging from about said high radiation exposure to about said low radiation exposure. The methods further comprise performing a post-exposure bake following the exposing the layer of radiation-sensitive material to the pattern of radiation; performing positive-tone developing of the layer of radiation-sensitive material to remove the first region from the substrate; removing the exposure gradient of the third region by transforming the second region and the third region to a fourth region having a substantially uniform level of radiation exposure or de-protection, or a combination thereof; and slimming the fourth region.
Other embodiments of the invention provide a platform configured for patterning a substrate. The platform comprises a track system configured to coat a substrate with a layer of radiation-sensitive material; a lithography system that includes a pattern exposure system configured to expose the substrate to patterned EM radiation; an exposure gradient removal system that is configured to expose the substrate to an exposure gradient removal treatment; and a transfer system configured to transfer the substrate between the track system, the pattern exposure system, and the exposure gradient removal system.
In the accompanying drawings:
A method and system for patterning a substrate is disclosed in various embodiments. However, one skilled in the relevant art will recognize that the various embodiments may be practiced without one or more of the specific details, or with other replacement and/or additional methods, materials, or components. In other instances, well-known structures, materials, or operations are not shown or described in detail to avoid obscuring aspects of various embodiments of the invention.
Similarly, for purposes of explanation, specific numbers, materials, and configurations are set forth in order to provide a thorough understanding of the invention. Nevertheless, the invention may be practiced without specific details. Furthermore, it is understood that the various embodiments shown in the figures are illustrative representations and are not necessarily drawn to scale.
Reference throughout this specification to “one embodiment” or “an embodiment” or variation thereof means that a particular feature, structure, material, or characteristic described in connection with the embodiment is included in at least one embodiment of the invention, but do not denote that they are present in every embodiment. Thus, the appearances of the phrases such as “in one embodiment” or “in an embodiment” in various places throughout this specification are not necessarily referring to the same embodiment of the invention. Furthermore, the particular features, structures, materials, or characteristics may be combined in any suitable manner in one or more embodiments. Various additional layers and/or structures may be included and/or described features may be omitted in other embodiments.
Additionally, it is to be understood that “a” or “an” may mean “one or more” unless explicitly stated otherwise.
Various operations will be described as multiple discrete operations in turn, in a manner that is most helpful in understanding the invention. However, the order of description should not be construed as to imply that these operations are necessarily order dependent. In particular, these operations need not be performed in the order of presentation. Operations described may be performed in a different order than the described embodiment. Various additional operations may be performed and/or described operations may be omitted in additional embodiments.
Methods for patterning a substrate, including methods to reduce the critical dimension of a pattern that can be transferred onto a substrate for a given lithographic tool and mask, are described herein. Multiple chemical treatments are used to achieve an isotropic reduction in a critical dimension of a radiation-sensitive material line.
Referencing
As described above, the substrate 301 may comprise a film stack having one or more thin films or layers disposed between a base layer and the layer of radiation-sensitive material 302. Each thin film in substrate 301 may comprise a conductive layer, a non-conductive layer, or a semi-conductive layer. For instance, the thin film may include a material layer comprising a metal, metal oxide, metal nitride, metal oxynitride, metal silicate, metal silicide, silicon, poly-crystalline silicon (poly-silicon), doped silicon, silicon dioxide, silicon nitride, silicon carbide, silicon oxynitride, etc. Additionally, for instance, the thin film may comprise a low dielectric constant (i.e., low-k) or ultra-low dielectric constant (i.e., ultra-low-k) dielectric layer having a nominal dielectric constant value less than the dielectric constant of SiO2, which is approximately 4 (e.g., the dielectric constant for thermal silicon dioxide can range from 3.8 to 3.9). More specifically, the thin film may have a dielectric constant of less than 3.7, or a dielectric constant ranging from 1.6 to 3.7.
According to embodiments of the invention, the layer of radiation-sensitive material 302 may comprise, for example, a 248 nm radiation-sensitive material, a 193 nm radiation-sensitive material, a 157 nm radiation-sensitive material, or an extreme ultraviolet radiation-sensitive material, or a combination of two or more thereof. According to another embodiment, the layer of radiation-sensitive material 302 comprises poly(hydroxystyrene)-based resist or a (meth)acrylate-based resist. According to another embodiment, the layer of radiation-sensitive material 302 comprises a material that switches solubility due to a change in polarity upon performing an exposure to radiation of the appropriate wavelength and thereafter performing a first post-exposure bake following the exposure. According to another embodiment, the layer of radiation-sensitive material 302 comprises a material that provides acid-catalyzed de-protection upon performing an exposure to radiation having the appropriate wavelength and thereafter performing a first post-exposure bake following the exposure. According to another embodiment, the layer of radiation-sensitive material 302 comprises a material that provides acid-catalyzed de-protection upon performing a thermal decomposition bake following the exposure to radiation. According to yet another embodiment, the layer of radiation-sensitive material 302 comprises a material that provides acid-catalyzed de-protection upon performing an acid wash and performing a post-acid wash bake.
According to yet another embodiment, the layer of radiation-sensitive material 302 comprises an acid generator, such as a photo acid generator, a thermal acid generator and/or combinations thereof. Reference herein to “an acid generator” should be understood to synonymously refer to “one or more acid generators.” According to yet another embodiment, the layer of radiation-sensitive material 302 comprises a protected polymer that undergoes de-protection upon heating to a temperature equal to or greater than a thermal decomposition temperature of said protected polymer. According to yet another embodiment, the layer of radiation-sensitive material 302 comprises a protected polymer that undergoes de-protection upon heating to a temperature equal to or greater than a thermal decomposition temperature of said protected polymer, after performing an acid wash treatment.
The layer of radiation-sensitive material 302 may be formed using a track system. For example, the track system can comprise a Clean Track ACT 8, ACT 12, or Lithius resist coating and developing system commercially available from Tokyo Electron Limited (TEL). Other systems and methods for forming a layer of radiation-sensitive material on a substrate are well known to those skilled in the art of spin-on resist technology.
Following the application of the layer of radiation-sensitive material 302 to substrate 301, the layer of radiation-sensitive material may be thermally treated in a post-application bake (PAB). For example, a temperature of the substrate may be elevated to between about 50° C. and about 200° C., for a duration of about 30 seconds to about 180 seconds. A track system having post-application substrate heating and cooling equipment may be used to perform the PAB, for example, one of the track systems described above. Other systems and methods for thermally treating an exposed radiation-sensitive material film on a substrate are well known to those skilled in the art of spin-on resist technology.
As shown in
The exposure of the layer of radiation-sensitive material 302 to the pattern of EM radiation may be performed in a dry or wet photo-lithography system. The lithography system may be capable of providing a pattern of EM radiation at wavelengths of 365 nm, 248 nm, 193 nm, 157 nm, and 13 nm, for example. The image pattern can be formed using any suitable conventional stepping lithographic system, or scanning lithographic system. For example, the photo-lithographic system may be commercially available from ASML Netherlands B.V. (De Run 6501, 5504 DR Veldhoven, The Netherlands), or Canon USA, Inc., Semiconductor Equipment Division (3300 North First Street, San Jose, Calif. 95134). The mask 303 can be illuminated, for example, with normal incident light and off-axis illumination light, such as annular illumination, quadrupole illumination, and dipole illumination. These methods of illumination and exposing the layer of radiation-sensitive material 302 to radiation using the mask 303 are known to one of ordinary skill in the art of microelectronic device manufacturing.
A track system, as described above, having post-exposure substrate heating and cooling equipment may be used to perform a post-exposure bake (PEB). Other systems and methods for thermally treating an exposed layer of radiation-sensitive material on a substrate are well known to those skilled in the art of spin-on resist technology.
In further reference to
In one embodiment, the response profile 306 may represent the acid concentration in the layer of radiation-sensitive material 302 that is proportional to radiation exposure profile 305, as shown in
In one embodiment, the upper threshold 308 corresponds to a first threshold of solubility of the layer of radiation-sensitive material 302 when a first developing chemistry is applied. In one embodiment, the lower threshold 309 corresponds to a second threshold of solubility of the layer of radiation-sensitive material 302 when a second developing chemistry is applied.
In one embodiment, the first regions 312 of the layer of radiation-sensitive material 302 that correspond to the transparent regions 304 of the mask 303 and that have high radiation exposure in the radiation exposure profile 305 are selectively removed from the substrate 301 using a first developing chemistry. The second regions 313 of the layer of radiation-sensitive material 302 that have low radiation exposure in the radiation exposure profile 305 may be selectively unaffected or minimally-affected by exposure to the first developing chemistry. The third regions 314 that correspond approximately to the edges of opaque regions 310 and that have intermediate exposure in the radiation exposure profile 305 (i.e., radiation exposure between the upper threshold 308 and the lower threshold 309) may remain on the substrate 301, but may show a selectivity of resistance to the first developing chemistry that would be proportional to the relative level of protection.
Conversely, the second regions 313 of the layer of radiation-sensitive material 302, which have low radiation exposure in the radiation exposure profile 305, may be selectively removed by exposure to the second developing chemistry. The first regions 312 of the layer of radiation-sensitive material 302, which correspond to the transparent regions 304 and have high radiation exposure in the radiation exposure profile 305, may be selectively unaffected or minimally-affected by exposure to the second developing chemistry. The third regions 314, which correspond approximately to the edges of opaque regions 310 and have intermediate exposure in the radiation exposure profile 305 (i.e., radiation exposure between the upper threshold 308 and the lower threshold 309), may remain on the substrate 301 but show a resistance to the second developing chemistry that would be proportional to the relative level of exposure.
In one embodiment, for the first regions 312, the response profile 306 includes a concentration of acid in the layer of radiation-sensitive material 302 that is higher than the upper threshold 308 of acid concentration. In one embodiment, the upper threshold 308 represents an acid level solubility threshold of the layer of radiation-sensitive material 302. For example, if an acid concentration in the layer of radiation-sensitive material 302 is higher than the upper threshold 308 of acid concentration, the layer of radiation-sensitive material 302 becomes soluble when a first developing chemistry is applied.
In one embodiment, for the second regions 313, the response profile 306 includes a concentration of acid in the layer of radiation-sensitive material 302 that is lower than the lower threshold 309 of acid concentration. In one embodiment, the lower threshold 309 represents another acid level solubility threshold of the layer of radiation-sensitive material 302. For example, if acid concentration in the layer of radiation-sensitive material 302 is lower than lower threshold 309 of acid concentration, the layer of radiation-sensitive material 302 becomes soluble when a second developing chemistry is applied.
In one embodiment, the upper threshold 308 of acid concentration ranges from about 30% to about 60% of the clear field acid level and the lower threshold 309 of acid concentration ranges from about 10% to about 25% of the clear field acid concentration. In one embodiment, the clear field acid concentration is defined as the acid level of the radiation-sensitive material completely exposed to radiation. In another embodiment, the clear field acid concentration is defined as the acid concentration when substantially all the acid generator material has reacted with radiation 307 to produce acid species or when substantially all the thermal acid generator has decomposed to produce acid species.
Due to diffraction of radiation 307 by the mask 303, the third regions 314 corresponding to intermediate radiation exposure are created. In one embodiment, the third regions 314 comprise an acid concentration between the upper threshold 308 and the lower threshold 309. The first regions 312 corresponding to high radiation exposure may be selectively removed from the substrate 301 using a first developing chemistry. The second regions 313 corresponding to low radiation exposure may be selectively removed from the substrate 301 using a second developing chemistry. The third regions 314 corresponding to intermediate radiation exposure may substantially remain on substrate 301 during the first and/or second developing chemistries.
Referring still to
A third critical dimension 324 may be related to a positive-tone developing of an imaged radiation-sensitive material. The third critical dimension 324 includes the second region 313 and the adjoining third region(s) 314. A fourth critical dimension 326 may be related to a negative-tone developing of an imaged radiation-sensitive material. The fourth critical dimension 326 includes the first region 312 and the adjoining third region(s) 314.
As used herein, positive-tone developing chemistry refers to a solvent system that selectively removes the first regions 312 having a high radiation exposure and includes a base, e.g., alkali, amines, etc. In one embodiment, the positive-tone developing chemistry to selectively remove the first regions 312 includes tetramethylammonium hydroxide (TMAH). In another embodiment, the positive-tone developing chemistry to selectively remove the first regions 312 includes a base, water, and an optional surfactant.
As used herein, a negative-tone developing chemistry refers to a solvent system that selectively removes the second regions 313, having the low radiation exposure, and may comprise an organic solvent. The negative-tone developing chemistry may further comprise an organic solvent, optionally water, and an optional surfactant.
To better understand the properties of the development chemistries utilized to develop imaged radiation-sensitive materials, the following terms are defined. RMIN is defined as the minimum development rate. RMAX is defined as the maximum development rate. Development rates may be conveniently described in nanometers per second. For positive-tone development, the RMIN is observed at low levels of de-protection, whereas RMAX is observed at high levels of de-protection. In contrast, for negative-tone development, the RMIN is observed at high levels of de-protection, whereas RMAX is observed at low levels of de-protection
An exemplary embodiment comprising a radiation-sensitive material is shown in
As further characterization of the regions 412-414, in one embodiment, the first region 412 may have a high percent conversion of acid generator to acid as a result of the high radiation exposure, the second region 413 may have a low percent conversion of acid generator to acid as a result of the low radiation exposure, and the third region 414 may have an exposure gradient wherein the percent conversion of acid generator to acid ranges from about the high percent conversion to about the low percent conversion as a result of the intermediate radiation exposure that ranges from high to low.
Referring still to
In one embodiment, the first regions 412 corresponding to high radiation exposure receive about 50% or more of radiation 407 incident on substrate 401, the second regions 413 corresponding to low radiation exposure receive less than 15% of the radiation 407 incident on substrate 401, and the third regions 414 corresponding to intermediate radiation exposure receive between about 15% and about 50% of the radiation 407 incident on substrate 401.
In one embodiment, high exposure to radiation 407 increases the concentration of an acid in the first regions 412 to a level higher than an upper acid concentration threshold. The upper acid concentration threshold is a first threshold of solubility of the layer of radiation-sensitive material 402. In one embodiment, when the concentration of the acid in the first regions 412 increases to a level higher than the first threshold of solubility of the layer of radiation-sensitive material 402 (e.g., acid concentration threshold), the first regions 412 become soluble when a first developing chemistry is applied.
In another embodiment, when the chemical concentration of de-protected polymers in the first regions 412 increases to a level higher than the first threshold of solubility of the layer of radiation-sensitive material 402 (e.g., acid concentration threshold), the first regions 412 become soluble when a first developing chemistry is applied.
In the second regions 413 corresponding to low radiation exposure, a concentration of an acid and/or chemical concentration of de-protected polymers is less than a lower threshold of solubility of the layer of radiation-sensitive material 402 (e.g., acid concentration threshold). The second regions 413 become soluble when a second developing chemistry is applied.
Typically, the first solubility threshold and the second solubility threshold are determined by a material property of the layer of radiation-sensitive material 402. The third regions 414 corresponding to an intermediate radiation exposure have an exposure gradient wherein an acid concentration ranges between about the first solubility threshold and the second solubility threshold. That is, the third regions 414 are not readily soluble when either of the first developing chemistry or the second developing chemistry is applied to layer of radiation-sensitive material 402.
Following the exposure of the layer of radiation-sensitive material 402 to EM radiation 407, the exposed layer of radiation-sensitive material 402 may be thermally treated in a first post-exposure bake (PEB). For example, a temperature of the substrate may be elevated to between about 50° C. and about 200° C. for a duration of about 30 seconds to about 180 seconds. The PEB may be performed in a module of the track system.
Referring now to
In one embodiment, substrate 401 having the exposed layer of radiation-sensitive material 402 is brought into contact with a development solution containing the first developing chemistry to remove first regions 412 that are soluble in the first developing chemistry. Thereafter, the substrate 401 is dried. The developing process may be performed for a pre-specified time duration (e.g., about 30 seconds to about 180 seconds), a pre-specified temperature (e.g., room temperature), and a pre-specified pressure (e.g., atmospheric pressure). The developing process can include exposing the substrate to a developing solution in a developing system, such as a track system, for example, the track systems described above.
As shown in
As illustrated in
In reference to
In one embodiment, the fourth regions 430 have a substantially uniform high percent conversion of acid generator to acid which subsequently lead to substantially uniform regions of de-protected polymers. Exemplary methods of affecting the high percent conversion of the acid generator to acid in the third region 414 and the second region 413 to form the fourth region 430 include a flood exposure of radiation, acid wash treatment, performing a bake at an elevated temperature, and combinations thereof. In another aspect of this embodiment, the fourth regions 430 are substantially uniform regions of de-protected polymers. The substantial uniformity of the de-protection level in the fourth regions 430 permits uniform reactivity with a subsequent chemistry, i.e., the uniformity permits isotropic slimming. Thus, after the removal of the exposure gradient, a dimension WO (i.e., the existing critical dimension 424′) may be slimmed to the desired or target critical dimension Wf, as shown in
In reference to
Referring now to
In 530, a post-exposure bake (PEB) is performed, wherein a temperature of the substrate is elevated to a post-exposure temperature. The PEB may comprise setting the post-exposure temperature, a time the substrate is elevated to the post-exposure temperature, a heating rate for achieving the post-exposure temperature, a cooling rate for reducing the post-exposure temperature, a pressure of a gaseous environment surrounding the substrate during the elevation of the substrate to the post-exposure temperature, or a composition of a gaseous environment surrounding the substrate during the elevation of the substrate to the post-exposure temperature, or a combination of two or more thereof. The post-exposure temperature may be ramped, or stepped.
In 540, positive-tone developing of the layer of radiation-sensitive material is performed, wherein the first regions are removed from the substrate using a first developing chemistry. The removal of the first regions may be characterized by a first critical dimension. The positive-tone developing process may comprise setting a composition of the first developing chemistry, time duration for applying the first developing chemistry, or a temperature for applying the first developing chemistry, or any combination of two or more thereof. The first developing chemistry may comprise a base solution. The first developing chemistry may further comprise a base solution, water, and an optional surfactant. Thereafter, what remains is a layer of radiation-sensitive material comprising second regions having low radiation exposure, with third regions having intermediate exposure located immediately adjacent the second regions. It is this combination of second and third regions that form the radiation-sensitive material lines.
In 550, the layer of radiation-sensitive material, which comprises third regions, as well as second regions, are exposed to chemistry and/or conditions that affect a high percent conversion of the acid generator to acid and/or affect a high percent de-protection of the polymer. The exposure gradient removal can be achieved by performing an operation, such as a flood exposure that is followed by a post-flood exposure bake; a thermal decomposition bake, or acid wash that is followed by a post-acid wash bake. These methods of removing the exposure gradient yield a de-protected fourth region, derived from combination of the third regions and the second regions. These methods render the fourth region approximately uniformly de-protected and in-sensitive to radiation.
According to one embodiment of the invention, flood exposure of the layer of radiation-sensitive material may be performed. During the flood exposure, the layer of radiation-sensitive material is exposed to un-patterned radiation. The flood exposure may comprise exposing the substrate to electromagnetic (EM) radiation without a mask or reticle. The EM radiation may possess a wavelength in the visible spectrum, or a wavelength in the ultraviolet spectrum, or a combination thereof. Additionally, the flood exposure may comprise exposing the substrate to continuous EM radiation, pulsed EM radiation, poly-chromatic EM radiation, mono-chromatic EM radiation, broad-band EM radiation, or narrow-band radiation, or a combination thereof.
For example, the flood exposure may comprise exposing the substrate to 436 nm EM radiation, 365 nm EM radiation, 248 nm EM radiation, 193 nm EM radiation, 157 nm EM radiation, or deep ultraviolet (DUV) EM radiation, or any combination of two or more thereof. Additionally, for example, the flood exposure may comprise exposing the substrate to EM radiation at a wavelength capable of creating acid in the layer of radiation-sensitive material.
Subsequent to the flood exposure, a post-flood exposure bake (PFEB) is performed, wherein a temperature of the substrate is elevated to a PEFB temperature. The post-flood exposure bake may comprise setting the PFEB temperature, a time the substrate is elevated to the PFEB temperature, a heating rate for achieving the PFEB temperature, a cooling rate for reducing the PFEB temperature, a pressure of a gaseous environment surrounding the substrate during the elevation of the substrate to the PFEB temperature, or a composition of a gaseous environment surrounding the substrate during the elevation of the substrate to the PFEB temperature, or a combination of two or more thereof.
According to another embodiment of the invention, thermal decomposition bake (TDB) of the layer of radiation-sensitive material may be performed. For a thermal decomposition bake, the TDB temperature may include a temperature at which an acid generator will substantially undergo a thermal decomposition to produce acid and thereby facilitate the acid-catalyzed decomposition of the radiation-sensitive material; or a temperature at which a protected polymer, such as a tert-butyl carbonate (tBOC) protected radiation-sensitive material, will substantially de-protect. In any event, the end result is substantially removing the exposure gradient of the third region, as well as substantially de-protecting/decomposing the previously unexposed second region of the layer of radiation-sensitive material. It should be noted that the baking temperature should not exceed the glass transition temperature (Tg) of the layer of radiation-sensitive material.
According to yet another embodiment of the invention, an acid wash of the layer of radiation-sensitive material may be performed. An acid wash may provide a sufficient quantity of acid to the surface of the layer of radiation-sensitive material that upon heating to a sufficient temperature, it may facilitate or enhance de-protection or thermal decomposition of the radiation-sensitive material. A suitable acid wash may comprise exemplary acidic compounds, such as sulfuric acid and dichloroacetic acid.
In 560, slimming of the fourth region is performed, wherein the dimensions of a radiation-sensitive material line are reduced in a substantially uniform manner. According to embodiments of the present invention, this can be achieved by various methods, as will be discussed further below.
In reference to
In reference to
In reference to
In reference to
According to embodiments of the invention, the developing chemistries may be tailored or adjusted to provide isotropic dissolution rates that enable predictable and reproducible performance simply by controlling the duration of exposure to the developing chemistry. For example, developing chemistries and/or conditions may be modified to establish a dissolution rate ranging from about 0.1 nm/sec to about 5 nm/sec; about 0.2 nm/sec to about 4 nm/sec; or about 0.5 to about 2 nm/sec. In one example, the dissolution rate may be about 1 nm/sec.
In alternative 910, the slimming may be accomplished by performing a negative-tone developing. Negative-tone developing chemistry, while generally selective to removing low de-protection regions, may still provide the desired removal of high de-protection regions but at a much reduced development rate. Negative-tone developing chemistries generally comprise an organic solvent, and may further comprise one or more organic co-solvents, optionally water, and an optional surfactant. Thus, slimming of highly de-protected radiation-sensitive material lines may be affected by negative-tone development at an RMIN. Optimization of the negative-tone development chemistry can be readily achieved by selecting a solvent or solvent mixture to obtain the desired dissolution rate.
In alternatives 920-940, slimming may be accomplished by utilizing a positive-tone developing chemistry. Positive-tone developing chemistry, while generally selective toward highly de-protected radiation-sensitive materials, may still be employed under modified conditions to provide a reduced development rate. The dissolution rate of the positive-tone developing chemistry may be reduced by methods, such as diluting the positive-tone chemistry solution, including a muting agent in the layer of radiation-sensitive material, or performing the positive-tone developing chemistry at an ultra-cold temperature. As stated above, positive-tone developing chemistries generally include a base, e.g., alkali, amines, etc.; water; and an optional surfactant. One exemplary base is tetramethylammonium hydroxide (TMAH).
In alternative 920, slimming may be accomplished by performing a positive-tone developing with a dilute positive-tone developing chemistry solution. For example, the development rate may be reduced by diluting the positive-tone developing chemistry by a factor of 100, 200, 500, or 1000. Optimization of the diluted positive-tone development chemistry can be readily achieved by selecting an appropriate dilution factor to obtain the desired dissolution rate.
In alternative 930, slimming may be accomplished by performing a positive-tone developing with a positive-tone developing chemistry on a muted or inhibited layer of radiation-sensitive material. For example, during the formation of the film stack, a radiation-sensitive material solution may further comprise a muting agent. As such, this process makes use of a positive-tone developing chemistry that at high levels of de-protection develops at or near RMAX, but the presence of the muting agent reduces the effective dissolution rate of the highly de-protected radiation-sensitive material to a desired dissolution rate. One exemplary muting agent is cholic acid.
In alternative 940, the slimming may be accomplished by performing a positive-tone developing with a positive-tone developing chemistry at an ultra-cold temperature. As used herein, ultra-cold temperature is defined as a temperature greater than the freezing point of the developing chemistry and less than room temperature. For example, the ultra-cold temperature may range from about 0° C. to about 20° C.; from about 0° C. to about 15° C.; or from about 5° C. to about 10° C.
Moreover, the foregoing slimming methods may be combined. The slimming step may be accomplished by adjusting the composition of the negative-tone developing chemistry, adjusting the concentration of the positive-tone developing chemistry, adjusting a composition of the layer of radiation-sensitive material; adjusting the duration for applying the negative or positive developing chemistry; adjusting the temperature of developing chemistry, or a combination of two or more thereof.
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Although only certain embodiments of this invention have been described in detail above, those skilled in the art will readily appreciate that many modifications are possible in the embodiments without materially departing from the novel teachings and advantages of this invention. Accordingly, all such modifications are intended to be included within the scope of this invention.
While the present invention has been illustrated by a description of one or more embodiments thereof and while these embodiments have been described in considerable detail, they are intended to restrict or in any way limit the scope of the appended claims to such detail. Additional advantages and modifications will readily appear to those skilled in the art. The invention in its broader aspects is therefore not limited to the specific details, representative apparatus and method, and illustrative examples shown and described. Accordingly, departures may be made from such details without departing from the scope of the general inventive concept.
Claims
1. A platform configured for patterning a substrate, comprising:
- a track system configured to coat a substrate with a layer of radiation-sensitive material;
- a lithography system including a pattern exposure system configured to expose said substrate to patterned EM radiation;
- an exposure gradient removal system configured to expose said substrate to an exposure gradient removal treatment; and
- a transfer system configured to transfer said substrate between said track system, said pattern exposure system, and said exposure gradient removal system.
2. The platform of claim 1, wherein said exposure gradient removal system is integrated with said pattern exposure system within said lithography system.
3. The platform of claim 2, wherein said pattern exposure system comprises a radiation source, a mask imaging system, and a substrate holder.
4. The platform of claim 1, wherein said exposure gradient removal system is a flood exposure system and a post-flood exposure system.
5. The platform of claim 1, wherein said exposure gradient removal system is an acid wash and post-acid wash bake system.
6. The platform of claim 1, wherein said exposure gradient removal system is an temperature control apparatus capable of heating said layer of radiation-sensitive material to a thermal decomposition temperature.
7. The platform of claim 1, wherein said exposure gradient removal system is integrated within said track system.
8. The platform of claim 1, wherein said exposure gradient removal system comprises a stand-alone module separate from said track system and said pattern exposure system, and coupled to said track system or said pattern exposure system or both.
Type: Application
Filed: Dec 20, 2012
Publication Date: May 2, 2013
Applicant: TOKYO ELECTRON LIMITED (Tokyo)
Inventor: Tokyo Electron Limited (Tokyo)
Application Number: 13/722,548
International Classification: G03F 7/26 (20060101);