Etching composition

Abstract

To provide etching compositions and processes using the etching compositions.SOLUTION: The present disclosure is directed to etching compositions that are useful for, e.g., selectively removing silicon germanium (SiGe) from a semiconductor substrate as an intermediate step in a multistep semiconductor manufacturing process.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present disclosure relates to etching compositions and processes using the etching compositions. In particular, the present disclosure relates to etching compositions capable of selectively etching silicon germanium in the presence of other exposed or underlying materials, such as metallic conductors (e.g., copper), barrier materials, and insulators (e.g., low-k dielectric materials). [Background technology]

[0002] The semiconductor industry is rapidly reducing the dimensions and increasing the density of electronic circuitry and components in microelectronic devices, silicon chips, liquid crystal displays, MEMS (microelectromechanical systems), printed wiring boards, etc., within which integrated circuits are stacked or stacked with ever-decreasing thicknesses of insulating layers between each electronic circuitry layer, resulting in smaller and smaller feature sizes. As feature sizes shrink, patterns become smaller and device performance parameters become more stringent and demanding. As a result, various problems that were previously tolerable due to smaller feature sizes are no longer tolerable or have become greater problems.

[0003] In the production of advanced integrated circuits, both high-k and low-k insulators and matching barrier layer materials are used to minimize density problems and optimize performance.

[0004] Silicon germanium (SiGe) can be utilized as nanowires and / or nanosheets in the production of semiconductor devices, liquid crystal displays, MEMS (microelectromechanical systems), printed wiring boards, etc. For example, it can be used as the gate material in multi-gate devices such as multi-gate field effect transistors (FETs) (e.g., gate-all-around FETs). Summary of the Invention [Problem to be solved by the invention]

[0005] In the fabrication of semiconductor devices, it is often necessary to etch silicon germanium (SiGe). In various SiGe use types and device environments, other layers are in contact with or exposed when this material is being etched. High selectivity in etching SiGe in the presence of these other materials (e.g., metal conductors, dielectrics, and hard masks) is typically required for device yield and longevity. The etching process for SiGe can be a plasma etching process. However, using a plasma etching process on a SiGe layer can result in damage to either or both the gate dielectric and the semiconductor substrate. Furthermore, the etching process can remove portions of the semiconductor substrate by etching the gate dielectric layer exposed near the gate electrode. This can adversely affect the electrical characteristics of the transistor. To avoid such etching damage, additional protective device production steps are sometimes employed, but this comes at a significant cost.

[0006] The present disclosure relates to compositions and processes for selectively etching SiGe relative to hard mask layers, gate materials (e.g., SiN, polysilicon, or SiOx), and low-k dielectric layers (e.g., SiN, polysilicon, SiOx, carbon doped oxide, or SiCO) present in semiconductor devices. In particular, the present disclosure relates to compositions and processes for selectively etching SiGe relative to low-k dielectric layers. [Means for solving the problem]

[0007] In one embodiment, the present disclosure is directed to an etching composition comprising: a) at least one fluorine-containing acid, wherein the fluorine-containing acid comprises hydrofluoric acid or hexafluorosilicic acid; b) at least one oxidizing agent; c) at least one organic acid or anhydride thereof, wherein the organic acid comprises formic acid, acetic acid, propionic acid, or butyric acid; d) at least one polymerized naphthalenesulfonic acid; e) at least one amine, wherein the amine comprises an amine represented by formula (I): N—R1R2R3, wherein R1 is C1-C8 alkyl optionally substituted with OH or NH2, R2 is H or C1-C8 alkyl optionally substituted with OH, and R3 is C1-C8 alkyl optionally substituted with OH; and f) water.

[0008] In another aspect, the present disclosure is directed to a method comprising contacting a semiconductor substrate including a SiGe film with an etching composition described herein, thereby removing the SiGe film.

[0009] In yet another aspect, the present disclosure is directed to an article formed by the above method, wherein the article is a semiconductor device (eg, an integrated circuit). DETAILED DESCRIPTION OF THE INVENTION

[0010] Unless otherwise specified, in this disclosure, all percentages are to be understood as weight percent based on the total weight of the composition. Unless otherwise specified, ambient temperature is defined as about 16 degrees Celsius (°C) to about 27 degrees Celsius (°C).

[0011] In general, the present disclosure describes an etching composition (e.g., an etching composition for selectively removing SiGe) that includes: a) at least one fluorine-containing acid, where the fluorine-containing acid is hydrofluoric acid (HF) or hexafluorosilicic acid (HSiF); b) at least one oxidizing agent, where the oxidizing agent is hydrogen peroxide; c) at least one organic acid, where the organic acid is formic acid, acetic acid, propionic acid, or butyric acid; d) at least one polymerized naphthalenesulfonic acid; e) at least one amine, where the amine comprises an amine of formula (I): N—R—R—R, where R is C—C alkyl optionally substituted with OH or NH; R is H or C—C alkyl optionally substituted with OH; and R is C—C alkyl optionally substituted with OH; and f) water.

[0012] Typically, the etching compositions of the present disclosure can include at least one (e.g., two, three, or four) fluorine-containing acid. The fluorine-containing acid described herein can be an inorganic acid such as HF or H2SiF6. In some embodiments, the at least one fluorine-containing acid is present in an amount of about 0.1 wt% or more (e.g., about 0.2 wt% or more, about 0.4 wt% or more, about 0.5 wt% or more, about 0.6 wt% or more, about 0.8 wt% or more, about 1 wt% or more, about 1.2 wt% or more, about 1.4 wt% or more, or about 1.5 wt% or more) to about 2 wt% or less (e.g., about 1.9 wt% or less, about 1.8 wt% or less, about 1.7 wt% or less, about 1.6 wt% or less, about 1.5 wt% or less, about 1.2 wt% or less, about 1 wt% or less, or about 0.5 wt% or less) of the etching compositions of the present disclosure. Without wishing to be bound by theory, it is believed that the fluorine-containing acid facilitates and accelerates the removal of SiGe on the semiconductor substrate during the etching process.

[0013] The etching compositions of the present disclosure can include at least one (e.g., two, three, or four) oxidizing agent suitable for use in microelectronic applications. Examples of suitable oxidizing agents include, but are not limited to, oxidizing acids and their salts (e.g., nitric acid, permanganate, or potassium permanganate), peroxides (e.g., hydrogen peroxide, dialkyl peroxides, urea peroxide), persulfonic acids (e.g., hexafluoropropanepersulfonic acid, methanepersulfonic acid, trifluoromethanepersulfonic acid, or p-toluenepersulfonic acid) and their salts, ozone, peroxycarboxylic acids (e.g., peracetic acid) and their salts, perphosphoric acid and its salts, persulfuric acid and its salts (e.g., ammonium persulfate or tetramethylammonium persulfate), perchloric acid and its salts (e.g., ammonium perchlorate, sodium perchlorate, or tetramethylammonium perchlorate), and periodic acid and its salts (e.g., periodic acid, ammonium periodate, or tetramethylammonium periodate). These oxidizing agents may be used alone or in combination.

[0014] In some embodiments, the at least one oxidizing agent may be present in an amount of about 5% by weight or more (e.g., about 6% by weight or more, about 7% by weight or more, about 8% by weight or more, about 9% by weight or more, about 10% by weight or more, about 11% by weight or more, about 13% by weight or more, or about 15% by weight or more) to about 20% by weight or less (e.g., about 18% by weight or less, about 16% by weight or less, about 15% by weight or less, about 14% by weight or less, about 12% by weight or less, or about 10% by weight or less) of the etching composition of the present disclosure. Without wishing to be bound by theory, it is believed that the oxidizing agent facilitates and accelerates the removal of SiGe on the semiconductor substrate.

[0015] Typically, the etching compositions of the present disclosure can include at least one (e.g., two, three, or four) organic acid or anhydride thereof. In some embodiments, the organic acid can be formic acid, acetic acid, propionic acid, or butyric acid. In some embodiments, the organic acid anhydride can be formic anhydride, acetic anhydride, propionic acid anhydride, or butyric acid anhydride. In some embodiments, the at least one organic acid or anhydride can be about 30% by weight or more (e.g., about 35% by weight or more, about 40% by weight or more, about 45% by weight or more, about 50% by weight or more, about 55% by weight or more, or about 60% by weight or more) to about 90% by weight or less (e.g., about 85% by weight or less, about 80% by weight or less, about 75% by weight or less, about 70% by weight or less, about 65% by weight or less, about 60% by weight or less, about 55% by weight or less, about 50% by weight or less, about 45% by weight or less, or about 40% by weight or less). Without wishing to be bound by theory, it is believed that the organic acid or anhydride thereof facilitates and accelerates the removal of SiGe on the semiconductor substrate.

[0016] Generally, the etching compositions of the present disclosure can include at least one polymerized naphthalenesulfonic acid (or poly(naphthalenesulfonic acid)), for example as a surfactant or selective inhibitor. In some embodiments, the polymerized naphthalenesulfonic acid can be a sulfonic acid having the following chemical structure:

[0017] [ka] where n is 3, 4, 5, or 6.

[0018] Commercially available examples of such polymerized naphthalenesulfonic acids include the Takesurf A-47 series of products manufactured by Takemoto Oil & Fat Co., Ltd. In some embodiments, the at least one polymerized naphthalenesulfonic acid is present in an amount of about 0.005 wt. % or more (e.g., about 0.01 wt. % or more, about 0.02 wt. % or more, about 0.03 wt. % or more, about 0.04 wt. % or more, about 0.05 wt. % or more, or about 0.1 wt. % or more) to about 0.15 wt. % or less (e.g., about 0.14 wt. % or less, about 0.12 wt. % or less, about 0.1 wt. % or less, about 0.08 wt. % or less, about 0.06 wt. % or less, or about 0.05 wt. % or less) relative to the etching composition of the present disclosure. Without wishing to be bound by any theory, it is believed that polymerized naphthalenesulfonic acid selectively inhibits the removal of SiN, polysilicon, and SiCO when removing SiGe from a semiconductor substrate using the etching composition of the present disclosure.

[0019] Typically, etching compositions of the present disclosure can include at least one (e.g., two, three, or four) amines. In some embodiments, the amine can be an amine of formula (I): N—R1R2R3, where R1 is C1-C8 alkyl optionally substituted with OH or NH2, R2 is H or C1-C8 alkyl optionally substituted with OH, and R3 is C1-C8 alkyl optionally substituted with OH. Suitable examples of amines of formula (I) include diisopropylamine, N-butyldiethanolamine, N-(3-aminopropyl)-diethanolamine, N-octylglucamine, N-ethylglucamine, N-methylglucamine, and 1-[bis(2-hydroxyethyl)amino]-2-propanol.

[0020] In some embodiments, the at least one amine may be present in an amount of from about 0.001 wt. % or more (e.g., about 0.002 wt. % or more, about 0.005 wt. % or more, about 0.008 wt. % or more, about 0.01 wt. % or more, about 0.02 wt. % or more, about 0.05 wt. % or more, or about 0.1 wt. % or more) to about 0.15 wt. % or less (e.g., about 0.14 wt. % or less, about 0.12 wt. % or less, about 0.1 wt. % or less, about 0.08 wt. % or less, about 0.06 wt. % or less, or about 0.05 wt. % or less) of the etching composition of the present disclosure. Without wishing to be bound by theory, it is believed that the amine selectively inhibits the removal of SiN, polysilicon, and SiCO when removing SiGe from a semiconductor substrate using the etching composition of the present disclosure.

[0021] Typically, etching compositions of the present disclosure can include water as a solvent. In some embodiments, the water may be deionized, ultrapure water that is free of organic contaminants and has a minimum resistivity of about 4 to about 17 ohms, or about 17 ohms or greater. In some embodiments, the water may be about 20% by weight or greater (e.g., about 25% by weight or greater, about 30% by weight or greater, about 35% by weight or greater, about 40% by weight or greater, about 45% by weight or greater, about 50% by weight or greater, about 55% by weight or greater, or about 60% by weight or greater) to about 75% by weight or less (e.g., about 70% by weight or less, about 65% by weight or less, about 60% by weight or less, about 55% by weight or less, about 50% by weight or less, about 45% by weight or less, or about 40% by weight or less). Without wishing to be bound by theory, it is believed that an amount of water greater than 75% by weight of the composition may adversely affect the SiGe etch rate, making it more difficult to remove SiGe during the etching process. While not wishing to be bound by theory, it is believed that the etching compositions of the present disclosure should contain a certain level of water (e.g., 20% by weight or more) to keep all other components solubilized and to avoid a decrease in etching performance.

[0022] In some embodiments, the etching composition of the present disclosure can further include at least one (e.g., two, three, or four) organic solvent. In some embodiments, the at least one organic solvent can include an alcohol or an alkylene glycol ether. Examples of suitable organic solvents include propylene glycol, hexylene glycol, 1,3-propanediol, ethylene glycol butyl ether, and 3-methoxy-3-methyl-1-butanol. In some embodiments, the at least one organic solvent can be present in an amount of about 10% by weight or more (e.g., about 15% by weight or more, about 20% by weight or more, about 25% by weight or more, about 30% by weight or more, or about 35% by weight or more) to about 40% by weight or less (e.g., about 35% by weight or less, about 30% by weight or less, about 25% by weight or less, about 20% by weight or less, or about 15% by weight or less) of the etching composition.

[0023] In some embodiments, the etching composition of the present disclosure can further include at least one (e.g., two, three, or four) sugar alcohols (e.g., mannitol or sorbitol). In some embodiments, the at least one sugar alcohol can be present in an amount of about 0.001 wt % or more (e.g., about 0.002 wt % or more, about 0.005 wt % or more, about 0.01 wt % or more, about 0.02 wt % or more, or about 0.05 wt % or more) to about 0.1 wt % or less (e.g., about 0.08 wt % or less, about 0.06 wt % or less, about 0.05 wt % or less, about 0.04 wt % or less, about 0.02 wt % or less, or about 0.01 wt % or less) relative to the etching composition. Without wishing to be bound by theory, it is believed that the inclusion of a sugar alcohol in the etching composition of the present disclosure can inhibit the etching rate of polysilicon.

[0024] In some embodiments, the etching compositions of the present disclosure can further comprise at least one (e.g., two, three, or four) boronic acid. For example, the boronic acid can be of the following formula: RB(OH), where R is C1-C6. 10wherein the aryl or heteroaryl is optionally 1 to 6 (e.g., 1, 2, 3, 4, 5, or 6) C1-C 10 Examples of suitable boronic acids include phenylboronic acid and naphthalene-1-boronic acid.

[0025] In some embodiments, the at least one boronic acid may be present in an amount of about 0.01 wt. % or more (e.g., about 0.02 wt. % or more, about 0.05 wt. % or more, about 0.1 wt. % or more, about 0.2 wt. % or more, or about 0.3 wt. % or more) to about 0.5 wt. % or less (e.g., about 0.4 wt. % or less, about 0.3 wt. % or less, about 0.2 wt. % or less, about 0.1 wt. % or less, about 0.08 wt. % or less, or about 0.05 wt. % or less) of the etching composition. Without wishing to be bound by theory, it is believed that the inclusion of a boronic acid in the etching composition of the present disclosure can inhibit the etching rate of SiOx.

[0026] In some embodiments, the pH value of the etching composition of the present disclosure may be about 1 or greater (e.g., about 1.2 or greater, about 1.4 or greater, about 1.5 or greater, about 1.6 or greater, about 1.8 or greater, about 2 or greater, about 2.2 or greater, about 2.4 or greater, or about 2.5 or greater) and / or about 3 or less (e.g., about 2.8 or less, about 2.6 or less, about 2.5 or less, about 2.4 or less, about 2.2 or less, about 2 or less, or about 1.5 or less). Without wishing to be bound by theory, it is believed that etching compositions with a pH higher than 3 have a significantly greater etch rate for low-k dielectric materials, resulting in insufficient selectivity for SiGe relative to low-k dielectric materials (e.g., SiOx). Furthermore, it is believed that etching compositions with a pH lower than 1 may decompose some components due to their strong acidity.

[0027] Additionally, in some embodiments, the etching compositions of the present disclosure may optionally contain additives such as pH adjusters, preservatives, surfactants, additional organic solvents, biocides, and antifoaming agents. Examples of suitable additives include alcohols (e.g., polyvinyl alcohol), organic acids (e.g., iminodiacetic acid, malonic acid, oxalic acid, succinic acid, and malic acid), and inorganic acids (e.g., boric acid). Examples of suitable antifoaming agents include polysiloxane antifoams (e.g., polydimethylsiloxane), polyethylene glycol methyl ether polymers, ethylene oxide / propylene oxide copolymers, and glycidyl ether-capped acetylene diol ethoxylates (e.g., those disclosed in U.S. Patent 6,717,019, which is incorporated herein by reference). Examples of suitable surfactants may be cationic, anionic, nonionic, or amphoteric.

[0028] Generally, the etching compositions of the present disclosure can have a relatively high SiGe / dielectric material (e.g., SiN, polysilicon, or SiCO) etch selectivity (i.e., a high ratio of the etch rate of SiGe to the etch rate of the dielectric material). In some embodiments, the etching compositions can have a SiGe / dielectric material etch selectivity of about 2 or greater (e.g., about 3 or greater, about 4 or greater, about 5 or greater, about 6 or greater, about 7 or greater, about 8 or greater, about 9 or greater, about 10 or greater, about 15 or greater, about 20 or greater, about 30 or greater, about 40 or greater, or about 50 or greater), and / or about 500 or less (e.g., about 100 or less).

[0029] In some embodiments, the etching compositions of the present disclosure may be free of one or more, or any combination of, additional components selected from the group consisting of polymers, oxygen scavengers, quaternary ammonium salts (including quaternary ammonium hydroxides such as TMAH), amines, alkali bases (such as NaOH, KOH, and LiOH), surfactants other than antifoaming agents, antifoaming agents, fluoride-containing compounds, abrasives, silicates, hydroxycarboxylic acids containing three or more hydroxyl groups, carboxylic or polycarboxylic acids lacking amino groups, silanes (e.g., alkoxysilanes), cyclic compounds (e.g., azoles (e.g., diazoles, triazoles, or tetraazoles), triazines, and cyclic compounds containing two or more rings, such as substituted or unsubstituted naphthalene or substituted or unsubstituted biphenyl ether), buffers, non-azole preservatives, and metal salts (e.g., metal halides).

[0030] The etching compositions of the present disclosure can be prepared by simply mixing the components, or by blending two components in a kit. The first composition in the kit can be an aqueous solution of an oxidizing agent (e.g., HO). The second composition in the kit can contain the remaining components of the etching compositions of the present disclosure in concentrated form in predetermined ratios, allowing the two compositions to be blended to produce the desired etching composition of the present disclosure.

[0031] In some embodiments, the present disclosure provides a method for etching a semiconductor substrate including at least one SiGe film. The method may include contacting the semiconductor substrate including at least one SiGe film with an etching composition of the present disclosure to remove the SiGe film. The method may further include rinsing the semiconductor substrate with a rinsing solvent after the contacting step and / or drying the semiconductor substrate after the rinsing step. In some embodiments, the method does not substantially remove metallic conductors (e.g., copper) or dielectric materials (e.g., SiN, polysilicon, or SiCO) from the semiconductor substrate. For example, the method does not remove more than about 5% by weight (e.g., more than about 3% by weight, or more than about 1% by weight) of metallic conductors or dielectric materials from the semiconductor substrate.

[0032] In some embodiments, a SiGe film on a semiconductor substrate can include about 10% or more (e.g., about 12% or more, about 14% or more, about 15% or more, about 16% or more, about 18% or more, or about 20% or more) and / or about 35% or less (e.g., about 34% or less, about 32% or less, about 30% or less, about 28% or less, about 26% or less, about 25% or less, about 24% or less, about 22% or less, about 20% or less, about 18% or less, about 16% or less, or about 15% or less) of Ge by weight. Without wishing to be bound by theory, it is believed that SiGe films containing about 10% to about 35% by weight of Ge can be more easily removed from a semiconductor substrate by an etching composition than films having a Ge content greater than 35% or less than 10% by weight.

[0033] In some embodiments, the etching method comprises the steps of: (A) Providing a semiconductor substrate including a SiGe film; (B) contacting the semiconductor substrate with an etching composition described herein; (C) rinsing the semiconductor substrate with one or more suitable rinsing solvents; (D) Optionally, drying the semiconductor substrate (eg, by any suitable means that removes the rinse solvent but does not compromise the integrity of the semiconductor substrate).

[0034] The SiGe-containing semiconductor substrates etched by this method may contain organic and metalorganic residues, as well as a range of metal oxides, some or all of which may be removed during the etching process.

[0035] Typically, the semiconductor substrate (e.g., wafer) described herein is composed of silicon, silicon germanium, a III-V compound such as GaAs, or any combination thereof. The semiconductor substrate may further include exposed integrated circuit structures such as interconnect features (e.g., metal lines and dielectric materials). Metals and alloys used in interconnect features include, but are not limited to, aluminum, aluminum alloyed with copper, copper, titanium, tantalum, cobalt, silicon, titanium nitride, tantalum nitride, and tungsten. The semiconductor substrate may also include intermediate layers of interlayer dielectrics, polysilicon, silicon oxide, silicon nitride, silicon carbide, titanium oxide, and carbon-doped silicon oxide.

[0036] The semiconductor substrate can be contacted with the etching composition in any suitable manner, such as by placing the etching composition in a tank and immersing and / or submerging the semiconductor substrate, spraying the etching composition onto the semiconductor substrate, flowing the etching composition onto the semiconductor substrate, or any combination thereof.

[0037] The etching compositions of the present disclosure can be effectively used at temperatures up to about 85°C (e.g., about 20°C to about 80°C, about 55°C to 65°C, or about 60°C to 65°C). As temperatures increase within this range, the etch rate of SiGe increases, and therefore, processes at higher temperatures can be completed in shorter times. Conversely, lower etching temperatures typically require longer etching times.

[0038] Etching times can vary widely depending on the specific etching method, thickness, and temperature used. For immersion batch-type processes, suitable times range, for example, from 10 minutes or less (e.g., from about 1 minute to about 7 minutes, from about 1 minute to about 5 minutes, or from about 2 minutes to about 4 minutes). Etching times for single-wafer processes range from about 30 seconds to about 5 minutes (e.g., from about 30 seconds to about 4 minutes, from about 1 minute to about 3 minutes, or from about 1 minute to about 2 minutes).

[0039] Mechanical agitation can be used to further enhance the etching ability of the etching compositions of the present disclosure. Examples of suitable agitation methods include circulating the etching composition over the substrate, flowing or spraying the etching composition over the substrate, and ultrasonic or megasonic agitation during the etching process. The orientation of the semiconductor substrate relative to the ground surface can be at any angle. Horizontal or vertical orientation is preferred.

[0040] After the etching, the semiconductor substrate may be rinsed with a suitable rinse solvent for about 5 seconds to about 5 minutes, with or without agitation. Multiple rinse steps using different rinse solvents may be performed. Examples of suitable rinse solvents include, but are not limited to, deionized (DI) water, methanol, ethanol, isopropyl alcohol, N-methylpyrrolidone, γ-butyrolactone, dimethyl sulfoxide, ethyl lactate, and propylene glycol monomethyl ether acetate. Alternatively, or in addition, an aqueous rinse having a pH greater than 8 (e.g., dilute aqueous ammonium hydroxide solution) may be used. Examples of rinse solvents include, but are not limited to, dilute aqueous ammonium hydroxide solution, DI water, methanol, ethanol, and isopropyl alcohol. The rinse solvent may be applied by a method similar to that used to apply the etching composition of the present disclosure. The etching composition may be removed from the semiconductor substrate prior to the start of the rinse step, or may still be in contact with the semiconductor substrate at the start of the rinse step. In some embodiments, the temperature used in the rinsing step is between 16°C and 27°C.

[0041] The semiconductor substrate is optionally dried after the rinsing step. Any suitable known drying method can be used. Examples of suitable drying means include spin drying, flowing a drying gas across the semiconductor, or heating the semiconductor with a heating means such as a hot plate or infrared lamp, Marangoni drying, Rotagoni drying, IPA drying, or any combination thereof. Drying times depend on the specific method used, but are typically on the order of 30 seconds to several minutes.

[0042] In some embodiments, the etching methods described herein further include forming a semiconductor device (e.g., an integrated circuit device such as a semiconductor chip) from the semiconductor substrate obtained by the method.

[0043] The present disclosure will be described in more detail with reference to the following examples, which are for illustrative purposes and should not be construed as limiting the scope of the disclosure. [Example]

[0044] All percentages given are by weight (wt%) unless otherwise noted. Controlled stirring during testing was achieved using a 1-inch stirrer at 300 revolutions per minute (rpm) unless otherwise noted.

[0045] <General Step 1: Mixing the Formula> Samples of the etching compositions were prepared by adding the remaining ingredients of the formulation to the calculated amount of solvent while stirring, and after a homogeneous solution was obtained, optional additives, if used, were added.

[0046] <General Procedure 2: Materials and Methods> Blanket film etch rate measurements were performed on films using commercially available, unpatterned 300 mm diameter wafers diced into 0.5 inch x 1.0 inch evaluation test coupons. The primary blanket film materials tested included: 1) a SiGe film deposited to a thickness of approximately 500 Å on a silicon substrate; 2) a SiNx film deposited to a thickness of approximately 600 Å on a silicon substrate; 3) a polysilicon film deposited to a thickness of approximately 1000 Å on a silicon substrate; 4) a SiCO film deposited to a thickness of approximately 200 Å on a silicon substrate; and 5) a SiOx film deposited to a thickness of approximately 1200 Å on a silicon substrate.

[0047] Blanket film test coupons were measured for pre- and post-treatment thickness to determine the blanket film etch rate. Thickness was measured by ellipsometry using a Woollam VASE® for SiGe, SiNx, SiOx, and polysilicon blanket films before and after treatment.

[0048] Patterned Si (3 nm) / Si test coupons were evaluated for material compatibility and / or etch response. The processed test coupons were then evaluated by scanning electron microscopy (SEM). SEM images of the processed coupons were compared with a set of previously captured pre-processing SEM images to evaluate the material compatibility and etch response of each test formulation with the patterned test device features.

[0049] <General Procedure 3: Etching Evaluation by Beaker Test> All blanket film etching tests were performed at room temperature (21-23°C) in a 600 mL glass beaker containing 200 g of sample solution, which was continuously stirred at 250 revolutions per minute (rpm) and had a Parafilm® cover in place at all times to minimize evaporation loss. All blanket test coupons, with one side of the blanket dielectric film exposed to the sample solution, were diamond-scribed to a 0.5 inch x 1.0 inch square test coupon size for beaker-sized testing. Each individual test coupon was held in place using a single 4-inch long plastic locking tweezer clip. The test coupons, held on one side by the locking tweezer clip, were suspended in a 600 mL HDPE beaker and immersed in 200 g of test solution, which was continuously stirred at 250 rpm at room temperature. Immediately after placing each sample coupon into the stirred solution, the top of the 600 mL HDPE beaker was covered with Parafilm® and resealed. The test coupons were then allowed to stand for 10 minutes at a time until the treatment time (General Procedure 3) was reached. A The coupons were held statically in the stirred solution until the treatment time (described in ) had elapsed. After the treatment time in the test solution, the sample coupons were immediately removed from the 600 mL HDPE beaker and rinsed per General Procedure 3A. After the final IPA rinse step, all test coupons were subjected to a filtered nitrogen gas blow-off step using a handheld gas blower, which forcibly removed all traces of IPA to produce a final dry sample for test measurements.

[0050] <General Procedure 3A: Blanket Test Coupon> Immediately after the 2-10 minute treatment period per General Procedure 3, the coupons were immersed in a volume of 300 mL of gently agitated ultrapure deionized (DI) water for 15 seconds, followed by a 15-second immersion in 300 mL of gently agitated isopropyl alcohol (IPA), and a final rinse of 15 seconds in 300 mL of gently agitated isopropyl alcohol (IPA). Treatment was completed per General Procedure 3.

[0051] [Example 1] Prescription example 1 8 (FE-1 through FE-8) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 1.

[0052] [Table 1] JPEG0007789116000003.jpg29141

[0053] As shown in Table 1, FE-1 through FE-3 and FE-5 through FE-8 (including Takesurf A-47Q and various amines described herein) all exhibited relatively high etch selectivities for SiGe25 / SiNx, SiGe25 / polysilicon, and SiGe25 / SiCO. In other words, these recipes were able to effectively remove SiGe films while minimizing the removal of SiNx, polysilicon, and SiCO on the exposed semiconductor substrate during the etching process. While some of these recipes exhibited relatively high SiOx etch rates, a low SiOx etch rate or high SiGe25 / SiOx etch selectivity (albeit preferred) is only part of the objective of the disclosed etch recipes. Even if the disclosed etch recipes exhibit relatively high SiOx etch rates, they may still be satisfactory for their intended purposes.

[0054] Comparative Formulation Examples 1-8 (CFE-1 through CFE-8) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 2.

[0055] [Table 2] JPEG0007789116000005.jpg13144

[0056] As shown in Table 2, CFE-1 did not contain Takesurf A-47Q or amine. This resulted in a relatively high SiNx etch rate. CFE-2 contained Takesurf A-47Q but no amine. This recipe resulted in a significantly reduced SiNx etch rate and a relatively high polysilicon etch rate. CFE-3 was identical to CFE-2, except that Takesurf A-47Q was replaced with another sulfonic acid. This recipe also resulted in a relatively high polysilicon etch rate. CFE-4 contained Takesurf A-47Q, no amine, and an additive (i.e., PVP). This recipe resulted in a relatively low polysilicon etch rate, but a reduced SiGe etch rate. CFE-5 was identical to CFE-4, except that Takesurf A-47Q was replaced with another sulfonic acid. This formulation also resulted in a relatively low SiGe etch rate. CFE-6 and CFE-7 were identical to CFE-1, except that these two formulations contained the amine of formula (I) described herein. Like CFE-1, these two formulations resulted in a relatively high SiNx etch rate. CFE-8 contained no HF, no Takesurf A-47Q, and no amine. This formulation resulted in no etching of SiGe at all, which is the target material to be removed by the etching compositions described herein.

[0057] [Example 2] Formulation Examples 9 and 10 (FE-9 and FE-10) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 3.

[0058] [Table 3]

[0059] FE-9 and FE-10 contained an additive (i.e., sugar alcohol) in their formulations, as shown in Table 3. The results show that both formulations exhibited excellent etch selectivity for SiGe25 / SiNx, SiGe25 / polysilicon, and SiGe25 / SiCO.

[0060] [Example 3] Formulation Examples 11-15 (FE-11 to FE-15) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 4.

[0061] [Table 4]

[0062] As shown in Table 4, FE-11 to FE-15 contained gradually increasing percentages of water and gradually decreasing percentages of HF, H2O2, and acetic acid. These results indicate that as the percentage of water increased, the etching rate of SiGe25 decreased, while the etching rate of SiOx also decreased. In other words, these data indicate that water can suppress the etching rates of SiGe and SiOx in the etching process.

[0063] [Example 4] Formulation Examples 16-21 (FE-16 to FE-21) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 5.

[0064] [Table 5] JPEG0007789116000009.jpg26101

[0065] As shown in Table 5, FE-16 contained no organic solvent, while FE-17 to FE-21 contained different water-soluble organic solvents. The results showed that formulations FE-16 to FE-19 and FE-21 exhibited relatively high etch selectivity for SiGe25 / SiNx, SiGe25 / polysilicon, and SiGe25 / SiCO. Relevant data for FE-20 was not measured. Furthermore, without wishing to be bound by theory, it is believed that propylene glycol, hexylene glycol, 3-methoxy-3-methyl-1-butanol, and 1,3-propanediol can suppress the etch rate of SiOx.

[0066] [Example 5] Formulation Examples 22-31 (FE-22 to FE-31) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 6.

[0067] [Table 6] JPEG0007789116000011.jpg16139

[0068] As shown in Table 6, formulations FE-22 through FE-31 contained different additives. The results indicated that formulations FE-22 through FE-27 and FE-29 through FE-31 had relatively high SiGe25 etch rates and relatively low SiOx etch rates. In particular, the results for formulations FE-28 through FE-31 indicate that as the amount of boric acid increased from 0.01% to 0.25%, both the SiGe25 etch rate and the SiOx etch rate decreased. Formulation FE-28 had low SiGe25 and SiOx etch rates, which is likely due to the high amount of boric acid present (i.e., 0.25%).

[0069] [Example 6] Formulation Examples 32-37 (FE-32 to FE-37) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 7.

[0070] [Table 7] JPEG0007789116000013.jpg8144

[0071] As shown in Table 7, formulations FE-32 to FE-37 contained either phenylboronic acid or naphthalene-1-boronic acid as an additive. The results showed that all formulations exhibited relatively high etch selectivity for SiGe25 / SiNx, SiGe25 / polysilicon, and SiGe25 / SiCO, while the etch rate for SiOx was relatively low.

[0072] [Example 7] Comparative Formulations 9-12 (CFE-9 to CFE-12) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 8.

[0073] [Table 8]

[0074] As shown in Table 8, formulations CFE-9 through CFE-12 did not contain hydrogen hydroxide or acetic acid. The results showed that formulations CFE-9, CFE-11, and CFE-12 had relatively high SiOx etch rates. Formulation CFE-10 had a relatively low SiOx etch rate, but also a relatively low etch rate for removing SiGe, the target material to be removed by the etching composition of the present disclosure.

[0075] [Example 8] Formulation Examples 38-44 (FE-38 to FE-44) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 9.

[0076] [Table 9]

[0077] Formulations FE-38, FE-40, and FE-41 contained a yellow-brown precipitate, which is believed to be Takesurf A-47Q that precipitated from solution due to the relatively low water and organic solvent content of each formulation, while the other four formulations contained no precipitate, indicating that all solutes were dissolved in those formulations.

[0078] As shown in Table 9, all of these recipes (except for FE-42, for which no data was measured) had relatively low SiOx etch rates. Furthermore, recipes FE-38 to FE-40 showed relatively high etch selectivities for SiGe / SiNx, SiGe / polysilicon, and SiGe / SiCO.

[0079] [Example 9] Formulation Examples 45-52 (FE-45 to FE-52) were prepared according to General Procedure 1 and evaluated according to General Procedures 2 and 3A. The formulations and test results are summarized in Table 10.

[0080] [Table 10] JPEG0007789116000017.jpg5129

[0081] As shown in Table 10, formulations FE-45 to FE-52 contained acetic anhydride instead of acetic acid and phenylboronic acid (PBA) as an additive. The results showed that all formulations had relatively high etch rates for SiGe and relatively low etch rates for SiOx. Furthermore, formulations FE-50 and FE-52 showed relatively high etch selectivities for SiGe / SiNx, SiGe / polysilicon, and SiGe / SiCO.

[0082] Although the invention has been described in detail with reference to specific embodiments thereof, it will be understood that modifications and variations are intended to fall within the spirit and scope of what is described and claimed.

[0083] [CROSS-REFERENCE TO RELATED APPLICATIONS] This application claims priority from U.S. Provisional Patent Application No. 62 / 811,600, filed February 28, 2019, and U.S. Provisional Patent Application No. 62 / 774,382, filed December 3, 2018, the contents of which are incorporated herein by reference in their entireties.

[0084] The present disclosure also includes the following aspects. <1> an etching composition comprising: at least one fluorine-containing acid, wherein the at least one fluorine-containing acid comprises hydrofluoric acid or hexafluorosilicic acid; at least one oxidizing agent; at least one organic acid or anhydride thereof, wherein the at least one organic acid comprises formic acid, acetic acid, propionic acid, or butyric acid; at least one polymerized naphthalenesulfonic acid; at least one amine, wherein the at least one amine comprises an amine of formula (I): N-R1R2R3, wherein R1 is C1-C8 alkyl optionally substituted with OH or NH2, R2 is H or C1-C8 alkyl optionally substituted with OH, and R3 is C1-C8 alkyl optionally substituted with OH; and water. <2> The at least one polymerized naphthalenesulfonic acid comprises a sulfonic acid having the following structure: <1> The composition described in [ka] Here, n is 3 to 6. <3> the at least one polymerized naphthalene sulfonic acid is present in an amount of from about 0.005% to about 0.15% by weight of the composition; <1> The composition described in <4> The amine of formula (I) is diisopropylamine, N-butyldiethanolamine, N-(3-aminopropyl)-diethanolamine, N-octylglucamine, N-ethylglucamine, N-methylglucamine, or 1-[bis(2-hydroxyethyl)amino]-2-propanol; <1> The composition described in <5> the at least one amine is present in an amount of from about 0.001% to about 0.15% by weight of the composition; <1> The composition described in <6> the at least one fluorine-containing acid is present in an amount of from about 0.1% to about 2% by weight of the composition; <1> The composition described in <7> the at least one oxidizing agent comprises hydrogen peroxide or peracetic acid; <1> The composition described in <8> the at least one oxidizing agent is present in an amount of about 5% to about 20% by weight of the composition; <1> The composition described in <9> the at least one organic acid or anhydride thereof comprises acetic acid or acetic anhydride; <1> The composition described in <10> the at least one organic acid or anhydride thereof is present in an amount of from about 30% to about 90% by weight of the composition; <1> The composition described in <11> the water is present in an amount of about 20% to about 75% by weight of the composition; <1> The composition described in <12> further comprising at least one organic solvent; <1> The composition described in <13> the at least one organic solvent comprises an alcohol or an alkylene glycol ether; <12> The composition described in <14> the at least one organic solvent comprises propylene glycol, hexylene glycol, 1,3-propanediol, or ethylene glycol butyl ether; <12> The composition described in <15> the at least one organic solvent is present in an amount of from about 10% to about 40% by weight of the composition; <12> The composition described in <16> further comprising at least one sugar alcohol, <1> The composition described in <17> the at least one sugar alcohol comprises mannitol or sorbitol; <16> The composition described in <18> further comprising at least one boronic acid; <1> The composition described in <19> the at least one boronic acid comprises phenylboronic acid or naphthalene-1-boronic acid; <18> The composition described in <20> the at least one boronic acid is present in an amount of about 0.01% to about 0.5% by weight of the composition; <18> The composition described in <21> The pH of the composition is 1 to 3. <1> The composition described in <22> A semiconductor substrate including a SiGe film <1> ~ <21> and substantially removing the SiGe film by contacting the SiGe film with the composition of any one of claims 1 to 5. <23> the SiGe film comprises about 10 wt % to about 25 wt % Ge; <22> The method described below. <24> Further comprising rinsing the semiconductor substrate with a rinsing solvent after the contacting step. <22> The method described below. <25> Further comprising drying the semiconductor substrate after the rinsing step. <24> The method described below. <26> the method does not substantially remove SiN, polysilicon, or SiCO; <22> The method described below. <27> A semiconductor device, <22> 2. An object formed by the method described in claim 1. <28> the semiconductor device is an integrated circuit; <27> The object described in.

Claims

1. An etching composition for selectively etching silicon germanium, comprising: at least one fluorine-containing acid, wherein said at least one fluorine-containing acid comprises hydrofluoric acid or hexafluorosilicic acid; at least one oxidizing agent; at least one organic acid or anhydride thereof, wherein the at least one organic acid comprises formic acid, acetic acid, propionic acid, or butyric acid; at least one polymerized naphthalenesulfonic acid; at least one amine, wherein said at least one amine has the formula (I): N—R １ R ２ R ３ and R １ is optionally OH or NH ２ C substituted with １ ~C ８ is an alkyl of R ２ is H or C optionally substituted with OH １ ~C ８ and R ３ is optionally substituted with OH １ ~C ８ is an alkyl of the formula: water, Including, the at least one organic acid or anhydride thereof is present in an amount of 30% to 90% by weight of the etching composition; 1. An etching composition wherein the at least one amine is present at 0.005% to 0.05% by weight of the etching composition.

2. 2. The etching composition of claim 1, wherein the at least one organic acid or anhydride thereof comprises acetic acid and acetic anhydride, and the combined amount of acetic acid and acetic anhydride is from 30% to 90% by weight of the etching composition.

3. 3. The etching composition of claim 2, wherein the combined amount of acetic acid and acetic anhydride is from 60% to 80% by weight of the etching composition.

4. The etching composition of claim 1 further comprising an inorganic acid.

5. at least one fluorine-containing acid, wherein said at least one fluorine-containing acid comprises hydrofluoric acid or hexafluorosilicic acid, and is present in an amount of 2% or less by weight of said etching composition; at least one oxidizing agent in an amount of 5% to 20% by weight of the etching composition; at least one organic acid or anhydride thereof, wherein the at least one organic acid comprises formic acid, acetic acid, propionic acid, or butyric acid, and is present in an amount of 30% to 90% by weight of the etching composition; at least one polymerized naphthalene sulfonic acid in an amount of 0.005% to 0.15% by weight of the etching composition; at least one amine, wherein said at least one amine has the formula (I): N—R １ R ２ R ３ and present in an amount of 0.005% to 0.05% by weight of the etching composition; １ is optionally OH or NH ２ C substituted with １ ~C ８ is an alkyl of R ２ is H or C optionally substituted with OH １ ~C ８ and R ３ is optionally substituted with OH １ ~C ８ is an alkyl of the formula: water, The etching composition of claim 1 comprising:

6. 6. The etching composition of claim 5, wherein the at least one fluorine-containing acid is present in an amount of 0.5% or less by weight of the etching composition.

7. 6. The etching composition of claim 5, wherein the at least one oxidizing agent is present in an amount of 6% to 10% by weight of the etching composition.

8. 6. The etching composition of claim 5, wherein the at least one organic acid or anhydride thereof comprises acetic acid and acetic anhydride, and the total amount of acetic acid and acetic anhydride is 30% to 90% by weight of the etching composition.

9. 9. The etching composition of claim 8, wherein the combined amount of acetic acid and acetic anhydride is 60% to 80% by weight of the etching composition.

10. 6. The etching composition of claim 5, wherein the at least one polymerized naphthalene sulfonic acid is present in an amount of 0.005% to 0.05% by weight of the etching composition.

11. The etching composition of claim 5 further comprising an inorganic acid.

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