The invention pertains to methods of etching oxide, and to methods of cleaning debris (such as solid-form etch by-products) from within openings. In particular aspects, the invention pertains to methods for reducing roughness induced on surfaces during cleaning of debris, and in some aspects the invention pertains to methods of forming capacitor constructions.
It is common to etch through various oxides during semiconductor processing. Exemplary oxides include silicon dioxide, and doped silicon dioxide (such as, for example, borophosphosilicate glass (BPSG), and phosphosilicate glass (PSG)). Oxides are common in semiconductor processing due to their electrically insulative properties, and due to their ease of formation (for instance, oxides can be formed as spin-on-dielectric materials, or by numerous deposition methods, including, for example, chemical vapor deposition (CVD) methods).
It is common for oxides to be formed over electrically conductive nodes, and for openings to subsequently be etched through the oxides to the electrically conductive nodes to expose the nodes for subsequent processing. The openings are formed with etch chemistry which removes the oxide. In some aspects, the openings can be formed with multiple etch chemistries. For instance, a first etch chemistry can be utilized to create the openings, and a second etch chemistry can be utilized to clean debris that may have been formed by the first etch chemistry.
Problems can occur during formation of openings extending into oxides, in that one or more of the etch chemistries utilized during the formation of the openings can undesirably roughen the exposed oxide surfaces. For instance, substantially planar oxide surfaces may be exposed to the etch chemistry utilized to etch oxide-containing debris from within openings, and such surfaces may be undesirably roughened by such etch chemistry. Accordingly, it is desired to develop new methods for etching oxides.
In one aspect, the invention includes a method for etching an oxide. The oxide is exposed to a mixture which includes an alcohol, fluoride ions, and one or more components of a carboxylic acid having an acidic dissociation constant of at least 1×10−6. For purposes of interpreting this disclosure and the claims that follow, the dissociation constants utilized herein are to be understood as being the dissociation constants which would be measured in water.
In one aspect, the invention includes a method for reducing roughness induced on a silicon-dioxide-containing surface during removal of silicon-dioxide-containing debris with a cleaning solution. The method includes incorporation within the cleaning solution of one or more components of a carboxylic acid having an acidic dissociation constant of at least 1×10−6.
In one aspect, the invention includes a semiconductor processing method. A semiconductor substrate is provided. The substrate supports an oxide. At least one opening is etched to extend at least partially through the oxide. The etching leaves debris within the opening (the debris can be, for example, etch by-products). At least some of the debris is cleaned from within the opening. One or more components of a carboxylic acid having an acidic dissociation constant of at least 1×10−6 are utilized during such cleaning.
In one aspect, the invention includes a method of forming a capacitor construction. A semiconductor construction is provided. The semiconductor construction includes a conductive node and an oxide over the node. The oxide consists essentially of silicon dioxide or doped silicon dioxide. An opening is etched through the oxide to expose the conductive node. The etching leaves debris within the opening (the debris can comprise etch by-products). At least some of the debris is cleaned from within the opening. A solution containing an alcohol, fluoride ions and a carboxylic acid having an acidic dissociation constant of at least 1×10−6 is utilized during such cleaning. After the cleaning, a first capacitor electrode is formed within the opening. A capacitor dielectric is formed over the first capacitor electrode, and a second capacitor electrode is formed over the capacitor dielectric and capacitively coupled with the first capacitor electrode.
Preferred embodiments of the invention are described below with reference to the following accompanying drawings.
This disclosure of the invention is submitted in furtherance of the constitutional purposes of the U.S. Patent Laws “to promote the progress of science and useful arts” (Article 1, Section 8).
Exemplary aspects of the invention are described with reference to
An isolation region 14 is formed within substrate 12. Isolation region 14 can comprise, for example, a shallow trench isolation region. Accordingly, the isolation region 14 can comprise a trench formed within substrate 12 and then filled with suitable dielectric material, such as, for example, silicon dioxide.
A transistor device 16 is supported by substrate 12. The transistor device comprises a gate 18 containing conductive gate material 20 spaced from substrate 12 by gate dielectric 22. The gate dielectric 22 can comprise, consist essentially of, or consist of, silicon dioxide.
The conductive gate material 20 can comprise any suitable composition or combination of compositions, and can, for example, comprise metal, metal compounds and/or conductively-doped semiconductor material such as, for example, conductively-doped silicon.
The gate 18 also comprises a dielectric cap 24 formed over conductive material 20. Cap 24 can comprise, for example, silicon dioxide and/or silicon nitride.
The transistor device 16 comprises source/drain regions 26 and 28 on opposing sides of the gate 18. The shown source/drain regions are conductively-doped diffusion regions extending within substrate 12. Such diffusion regions can comprise p-type doped regions and/or n-type doped regions. The shown regions contain heavily-doped portions 30 and 32, and lightly-doped extensions 34 and 36 which extend between the heavily-doped portions and the edges of gate 18. A channel region 38 is beneath gate 18 and between the source/drain regions 26 and 28. In operation, the source/drain regions are electrically coupled to one another through the channel region when appropriate current passes through the gate.
A conductive pedestal 40 is formed over source/drain region 28 and electrically-coupled to such source/drain region. The conductive pedestal can comprise any suitable electrically conductive composition or combination of compositions. In some aspects, the pedestal will comprise conductively-doped silicon. The conductive pedestal has an uppermost surface 41 which can be referred to as an electrically conductive node in some aspects of the invention.
The exemplary processing described herein ultimately forms a capacitor construction coupled to diffusion region 28 through pedestal 41 to form a dynamic random access memory (DRAM) device comprising transistor 16 and the capacitor. The diffusion region 26 can be electrically coupled to a bitline so that the DRAM device can be incorporated into a DRAM array. Various methodologies for coupling diffusion region 26 to a bitline will be recognized by persons of ordinary skilled in the art, and such methodologies are not discussed in detail in this disclosure. Accordingly, various conductive materials that can be formed over diffusion region 26 for ultimately coupling the diffusion region to the bitline are not described or shown. It is to be understood, however, that a conductive pedestal similar to the pedestal 40 can be formed over diffusion region 26 in some aspects of the invention. It is also to be understood that numerous methods are known for coupling a capacitor to a diffusion region, and that some of the methods eliminate the conductive pedestal 40 and instead couple a storage node of the capacitor directly to the diffusion region. Thus, although the invention is described utilizing the conductive pedestal 40 between a capacitor (described below) and the diffusion region 28, it is to be understood that the invention also encompasses aspects (not shown) in which the conductive pedestal 40 is omitted and the capacitor is instead directly coupled to the diffusion region.
Sidewall spacers 42 are shown formed along sidewalls of gate 18. The sidewall spacers can comprise any suitable electrically insulative composition or combination of compositions, and typically will comprise one or both of silicon nitride and silicon dioxide. The conductive pedestal 40 is electrically isolated from conductive gate material 20 by one of the sidewall spacers.
An electrically insulative material 44 is provided over substrate 12, over transistor construction 16, and over conductive pedestal 40. Material 44 can comprise any suitable composition or combination of compositions. In particular aspects, material 44 will comprise, consist essentially of, or consist of silicon dioxide and/or doped silicon dioxide. For instance, material 44 can comprise BPSG, PSG, and/or silicon dioxide formed from tetra-ethyl-ortho-silicate (TEOS). One or more compositions of material 44 can be formed by chemical vapor deposition, and/or as spin-on-dielectrics. It is to be understood that the insulative material 44 can, in some aspects, comprise a non-oxide insulative composition in addition to one or more oxide insulative compositions. For instance, insulative material 44 can comprise a layer of silicon nitride in addition to one or more layers of silicon-dioxide-containing compositions.
A patterned mask 46 is formed over insulative material 44. Mask 46 can comprise, for example, photolithographically patterned photoresist. Mask 46 has an opening 48 extending therethrough. The opening is directly over the conductive node corresponding to surface 41 of pedestal 40.
Referring next to
Referring next to
Any carboxylic acids can be utilized, provided that the carboxylic acids have the acidic dissociation constant of at least 1×10−6. For instance, the carboxylic acids can be mono-carboxylic acids, di-carboxylic acids, or carboxylic acids having three or more carboxylic acid groups. Ultimately, as discussed below, the carboxylic acids are utilized to reduce roughness on oxide-containing surfaces. It can be preferred to utilize carboxylic acids having more than one carboxylate group for such roughness-reduction, in that such carboxylic acids can, in some aspects, produce a greater roughness-reduction effect than is produced by mono-carboxylic acids.
Exemplary carboxylic acids that can be utilized in accordance with aspects of the present invention are trichloroacetic acid (which has an acidic dissociation constant in water of 1.99×10−1); maleic acid (which has an acidic dissociation constant in water of 1.5×10−2); and citric acid (which as an acidic dissociation constant in water of 6.6×10−4).
In some aspects, a cleaning solution can include a alcohol, fluoride ions and water in addition to the one or more components of at least one carboxylic acid having an acidic dissociation constant of at least 1×10−6. The alcohol can be an alkyl alcohol, and in exemplary aspects can comprise, consist essentially of, or consist of isopropyl alcohol. In some aspects, other organic solvents can be utilized in addition to, or alternatively to, the alcohol. Such other organic solvents can include, for example, ketones, ethers and esters.
Cations can be present in addition to the fluoride ions, and in exemplary aspects, the cations can consist essentially of, or consist of ammonium ions. It is to be understood that ammonium ions are exemplary cations, and that other suitable cations can be utilized either alternatively or additionally to ammonium cations.
An exemplary mixture for cleaning oxide-containing debris can be formed by mixing the following:
The cleaning mixture prepared as described above will typically be a solution rather than other types of mixtures, (with other types of mixtures including, for example, emulsions, and mixtures having undissolved components therein).
The cleaning mixture is utilized to etch oxide-containing debris from within the opening 48. Such etching can be conducted while maintaining the cleaning solution at a temperature of from about 0° C. to about 75° C., under a pressure of anywhere from 0.01 atmospheres to greater than 10 atmospheres, and with a treatment time of from 1 second to about 10 hours. A typical treatment time is from about 1 minute to about 20 minutes.
In light of the dramatic reduction in roughening occurring through incorporation of carboxylic acids having an acidic dissociation constant of 1×10−6 in a cleaning solution during removal of silicon-dioxide-containing debris, such incorporation can be considered to be a method for reducing roughness induced on silicon-dioxide-containing surfaces during such cleaning. This can provide a significant advantage, in that the roughness induced during the cleaning can lead to numerous problems in controlling uniformity of opening dimensions. If uniformity is not adequately controlled, devices ultimately formed within the openings can operate outside of desired tolerances, and devices formed within adjacent openings can short to one another. Also, there can be poor interfaces formed between layers ultimately provided within opening 48 and the sidewalls of the opening if excessive roughening of the sidewalls occurs.
A possible mechanism by which the carboxylic acid can reduce the roughness occurring along the sidewalls of the opening is as follows. By-products may accumulate and aggregate during an etch, and such by-products may reduce an etch rate. The reduction in etch rate may increase the etch duration utilized to completely remove debris, and the increased etch duration may lead to increased roughening of exposed oxide surfaces. The by-products may accumulate because there is insufficient material within the cleaning solution to bind or dissolve the by-products, (for example, due to the coefficient of solubility of the by-products). The addition of carboxylic acids having acidic dissociation constants of 1×10−6 or greater can help in dissolving the by-products. The addition of water can also help in dissolving the by-products, but such addition adversely impacts selectivity of the etch for oxides. In contrast, addition of carboxylic acids having high acidic dissociation constants (i.e., acidic dissociation constants of at least 1×10−6) does not have such adverse impact on the etch selectivity.
The mechanism is provided herein to assist the reader in understanding aspects of the present invention, and is not to limit the claims except to the extent, if any, that such mechanism is expressly recited in the claims.
Referring next to
Referring next to
A bitline 70 is shown electrically coupled with source/drain region 26. Accordingly, the construction of
The shown aspect of the invention is but one of many applications for methodology of the present invention. For instance, the incorporation of one or more of carboxylic acids having an acidic dissociation constant of at least 1×10−6 can be utilized during the initial etch to form an opening (such as, for example, the etch of
In compliance with the statute, the invention has been described in language more or less specific as to structural and methodical features. It is to be understood, however, that the invention is not limited to the specific features shown and described, since the means herein disclosed comprise preferred forms of putting the invention into effect. The invention is, therefore, claimed in any of its forms or modifications within the proper scope of the appended claims appropriately interpreted in accordance with the doctrine of equivalents.
This application is a continuation of U.S. patent application Ser. No. 11/127,944, filed May 11, 2005, which is incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
3717560 | Breslow | Feb 1973 | A |
3835130 | Woodward | Sep 1974 | A |
3917698 | Breslow | Nov 1975 | A |
4165295 | Vander Mey | Aug 1979 | A |
4215005 | Vander Mey | Jul 1980 | A |
4595519 | Takeno et al. | Jun 1986 | A |
6075266 | Yoshitomi | Jun 2000 | A |
6103627 | Robinson et al. | Aug 2000 | A |
6162739 | Sumnitsch et al. | Dec 2000 | A |
6225345 | Fassler et al. | May 2001 | B1 |
6492075 | Templeton et al. | Dec 2002 | B1 |
6492309 | Behr et al. | Dec 2002 | B1 |
6517738 | Torek et al. | Feb 2003 | B1 |
6524974 | Sukharev | Feb 2003 | B1 |
6562735 | Allman et al. | May 2003 | B1 |
6783695 | Torek et al. | Aug 2004 | B1 |
7112506 | Kim et al. | Sep 2006 | B2 |
7244784 | Amick et al. | Jul 2007 | B2 |
20020068685 | Wojtczak et al. | Jun 2002 | A1 |
20020130388 | Stamper | Sep 2002 | A1 |
20030181342 | Seijo et al. | Sep 2003 | A1 |
20030235996 | Leon et al. | Dec 2003 | A1 |
20040171503 | Rovito et al. | Sep 2004 | A1 |
20060237392 | Auger et al. | Oct 2006 | A1 |
Number | Date | Country |
---|---|---|
0782177 | Jul 1997 | EP |
1536291 | Jun 2005 | EP |
455513 | Sep 2001 | TW |
WO2004019134 | Mar 2004 | WO |
Number | Date | Country | |
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20100221916 A1 | Sep 2010 | US |
Number | Date | Country | |
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Parent | 11127944 | May 2005 | US |
Child | 12778043 | US |