Chemical mechanical polishing method for tungsten

Abstract

A process for chemical mechanical polishing a substrate containing tungsten is disclosed to reduce corrosion rate and inhibit dishing of the tungsten and erosion of underlying dielectrics. The process includes providing a substrate; providing a polishing composition, containing, as initial components: water; an oxidizing agent; a thiolalkoxy compound; a dicarboxylic acid, a source of iron ions; a colloidal silica abrasive; and, optionally a pH adjusting agent; providing a chemical mechanical polishing pad, having a polishing surface; creating dynamic contact at an interface between the polishing pad and the substrate; and dispensing the polishing composition onto the polishing surface at or near the interface between the polishing pad and the substrate; wherein some of the tungsten (W) is polished away from the substrate, corrosion rate is reduced, dishing of the tungsten (W) is inhibited as well as erosion of dielectrics underlying the tungsten (W).

Claims

1. A method of chemical mechanical polishing tungsten, comprising: providing a substrate comprising tungsten and a dielectric; providing a chemical mechanical polishing composition, comprising, as initial components: water; an oxidizing agent; a thiolalkoxy compound; a colloidal silica abrasive; a dicarboxylic acid, a source of iron (III) ions; and, optionally, a pH adjusting agent; providing a chemical mechanical polishing pad, having a polishing surface; creating dynamic contact at an interface between the chemical mechanical polishing pad and the substrate; and dispensing the chemical mechanical polishing composition onto the polishing surface of the chemical mechanical polishing pad at or near the interface between the chemical mechanical polishing pad and the substrate to remove at least some of the tungsten.

2. The method of claim 1, wherein the thiolalkoxy compound of the chemical mechanical polishing composition has a formula: ##STR00002## wherein R.sub.1 comprise hydrogen, hydroxyl, thiol, carboxyl, or linear or branched (C.sub.1-C.sub.4)alkyl; R.sub.2 and R.sub.3 can be the same or different and comprise hydrogen, or linear or branched (C.sub.1-C.sub.4)alkyl; m, n and q are integers wherein m is an integer of 1 to 4, n is an integer of 1 to 6 and q is an integer of 1 to 2.

3. The method of claim 1, wherein the chemical mechanical polishing composition provided has a tungsten removal rate of 1,000 /min with a platen speed of 80 revolutions per minute, a carrier speed of 81 revolutions per minute, a chemical mechanical polishing composition flow rate of 125 mL/min, a nominal down force of 21.4 kPa on a 200 mm polishing machine; and, wherein the chemical mechanical polishing pad comprises a polyurethane polishing layer containing polymeric hollow core microparticles and a polyurethane impregnated non-woven subpad.

4. The method of claim 1, wherein the chemical mechanical polishing composition, provided comprises, as initial components: the water; 0.01 to 10 wt % of the oxidizing agent, wherein the oxidizing agent is hydrogen peroxide; 50 to 1000 ppm of the thiolalkoxy compound; 0.01 to 10 wt % of the colloidal silica abrasive; 1 to 2,600 ppm of the dicarboxylic acid; 100 to 1,000 ppm of the source of iron (III) ions, wherein the source of iron (III) ions is ferric nitrate nonahydrate; and, optionally, the pH adjusting agent; wherein the chemical mechanical polishing composition has a pH of 1 to 7.

5. The method of claim 4, wherein the chemical mechanical polishing composition provided has a tungsten removal rate of 1,000 /min with a platen speed of 80 revolutions per minute, a carrier speed of 81 revolutions per minute, a chemical mechanical polishing composition flow rate of 125 mL/min, a nominal down force of 21.4 kPa on a 200 mm polishing machine; and, wherein the chemical mechanical polishing pad comprises a polyurethane polishing layer containing polymeric hollow core microparticles and a polyurethane impregnated non-woven subpad.

6. The method of claim 1, wherein the chemical mechanical polishing composition, provided comprises, as initial components: the water; 0.1 to 5 wt % of the oxidizing agent, wherein the oxidizing agent is hydrogen peroxide; 50 to 800 ppm of the thiolalkoxy compound; 0.05 to 7.5 wt % of the colloidal silica abrasive; 100 to 1,400 ppm of the dicarboxylic acid; 150 to 750 ppm of the source of iron (III) ions, wherein the source of iron (III) ions is ferric nitrate; and, optionally, the pH adjusting agent; wherein the chemical mechanical polishing composition has a pH of 1.5 to 4.5.

7. The method of claim 6, wherein the chemical mechanical polishing composition provided has a tungsten removal rate of 1,000 /min with a platen speed of 80 revolutions per minute, a carrier speed of 81 revolutions per minute, a chemical mechanical polishing composition flow rate of 125 mL/min, a nominal down force of 21.4 kPa on a 200 mm polishing machine; and, wherein the chemical mechanical polishing pad comprises a polyurethane polishing layer containing polymeric hollow core microparticles and a polyurethane impregnated non-woven subpad.

8. The method of claim 1, wherein the chemical mechanical polishing composition, provided comprises, as initial components: the water; 0.1 to 3 wt % of the oxidizing agent, wherein the oxidizing agent is hydrogen peroxide; 50 to 300 ppm of the thiolalkoxy compound; 0.1 to 5 wt % of the colloidal silica abrasive; 120 to 1,350 ppm of the dicarboxylic acid, wherein the dicarboxylic acid is malonic acid; 200 to 500 ppm of the source of iron (III) ions, wherein the source of iron (III) ions is ferric nitrate; and, optionally, the pH adjusting agent; wherein the chemical mechanical polishing composition has a pH of 1.5 to 3.5.

9. The method of claim 8, wherein the chemical mechanical polishing composition provided has a tungsten removal rate of 1,000 /min with a platen speed of 80 revolutions per minute, a carrier speed of 81 revolutions per minute, a chemical mechanical polishing composition flow rate of 125 mL/min, a nominal down force of 21.4 kPa on a 200 mm polishing machine; and, wherein the chemical mechanical polishing pad comprises a polyurethane polishing layer containing polymeric hollow core microparticles and a polyurethane impregnated non-woven subpad.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) As used throughout this specification the following abbreviations have the following meanings, unless the context indicates otherwise: C.=degrees Centigrade; g=grams; L=liters; mL=milliliters; =m=microns; kPa=kilopascal; A=angstroms; mV=millivolts; DI=deionized; ppm=parts per million=mg/L; mm=millimeters; cm=centimeter; min=minute; rpm=revolutions per minute; lbs=pounds; kg=kilograms; W=tungsten; S=sulfur atom; HO=hydroxyl; ICP-OES=inductively coupled plasma optical emission spectroscopy; wt %=percent by weight; PS=polishing slurry; CS=control slurry; and RR=removal rate.

(2) The term chemical mechanical polishing or CMP refers to a process where a substrate is polished by means of chemical and mechanical forces alone and is distinguished from electrochemical-mechanical polishing (ECMP) where an electric bias is applied to the substrate. The term TEOS means the silicon dioxide formed from tetraethyl orthosilicate (Si(OC.sub.2H.sub.5).sub.4). The term thiolalkoxy means an aliphatic organic compound having at least one thiol group or moiety, i.e., CSH or RSH a sulfhydryl bonded to a carbon where R represents an alkyl or other organic substituent, and at least one alkoxy or ether functionality, such as an ethoxy functionality: (CH.sub.2CH.sub.2O) in the molecule. The term ether means organic compounds where oxygen is joined to two alkyl groups: ROR. The term alkyl means an organic group with a general formula: C.sub.nH.sub.2n+1 where n is an integer and the yl ending means a fragment of an alkane formed by removing a hydrogen. The term moiety means a part or a functional group of a molecule. The terms a and an refer to both the singular and the plural. All percentages are by weight, unless otherwise noted. All numerical ranges are inclusive and combinable in any order, except where it is logical that such numerical ranges are constrained to add up to 100%.

(3) The method of polishing a substrate of the present invention uses a chemical mechanical polishing composition containing an oxidizing agent; a thiolalkoxy compound; a colloidal silica abrasive; a dicarboxylic acid or salt thereof; a source of iron (III) ions; and, optionally, a pH adjusting agent to provide for the removal of tungsten from the substrate surface while inhibiting dishing of the tungsten, erosion of underlying dielectric materials and reducing corrosion rate.

(4) Preferably, the thiolalkoxy compounds of the present invention have a general formula:

(5) ##STR00001##
wherein R.sub.1 comprise hydrogen, hydroxyl, thiol, carboxyl, or linear or branched (C.sub.1-C.sub.4)alkyl; R.sub.2 and R.sub.3 can be the same or different and comprise hydrogen, or linear or branched (C.sub.1-C.sub.4)alkyl; m, n and q are integers wherein m is an integer of 1 to 4, n is an integer of 1 to 6 and q is an integer of 1 to 2. Preferably R.sub.1 is hydroxyl or thiol, more preferably R.sub.1 is thiol. Preferably R.sub.2 and R.sub.3 can be the same or different and are hydrogen or (C.sub.1-C.sub.2)alkyl, more preferably, R.sub.2 and R.sub.3 are the same and are both hydrogen. Preferably m is an integer of 1 to 3, more preferably m is an integer of 1 to 2, most preferably m is 2. Preferably, n is an integer of 1 to 3, more preferably n is an integer of 1 to 2, most preferably n is 2. Preferably q is 2.

(6) Examples of the thiolalkoxy compound having formula (I) are polyethyleneglycol dithiol; 3-oxa-1,5-pentanedithiol; 3,6-dioxa-1,8-octanedithiol (triethyleneglycol dithiol); tetra(ethyleneglycol)dithiol, poly(ethylene glycol)methyl ether thiol; 2-[2-[2-(2-mercaptoethoxy)] ethoxy] ethanol; 2-[2-[2-(2-mercaptoethoxy) ethoxy] ethoxy] acetic acid; and 2-mercaptoethoxy ethanol. Preferably the thiolalkoxy compounds are 3-oxa-1,5-pentanedithiol and 3,6-dioxa-1,8-octanedithiol. Most preferably the thiolalkoxy compound is 3,6-dioxa-1,8-octanedithiol.

(7) The thiolalkoxy compounds may be prepared by methods known in the art and in the literature. Many of the thiolalkoxy compounds can be commercially obtained such as from SIGMA-ALDRICH.

(8) It is preferred that the chemical mechanical polishing compositions of the present invention are free of inhibitors of tungsten corrosion having nitrogen moieties or heterocyclic structure.

(9) Preferably, the method of polishing a substrate of the present invention, comprises: providing the substrate, wherein the substrate comprises tungsten and a dielectric; providing a chemical mechanical polishing composition, comprising, preferably, consisting of, as initial components: water; an oxidizing agent, preferably in amounts of at least 0.01 wt % to 10 wt %, more preferably in amounts of 0.1 wt % to 5 wt %, still more preferably from 1 wt % to 3 wt %; a thiolalkoxy compound, preferably having formula (I), in amounts of at least 50 ppm, preferably 50 ppm to 1000 ppm, more preferably from 50 ppm to 800 ppm, even more preferably from 50 ppm to 300 ppm, still more preferably from 50 ppm to 275 ppm, most preferably from 50 ppm to 250; a colloidal silica abrasive, preferably in amounts of 0.01 wt % to 10 wt %, more preferably from 0.05 wt % to 7.5 wt %, even more preferably from 0.1 wt % to 5 wt %, still more preferably from 0.2 wt % to 2 wt %; a dicarboxylic acid, salt thereof or mixtures thereof, preferably in amounts of 100 ppm to 1400 ppm, more preferably from 120 ppm to 1350 ppm; a source of iron (III) ions, preferably, wherein the source of iron (III) ions is ferric nitrate nonahydrate; and, optionally, a pH adjusting agent; preferably, wherein the chemical mechanical polishing composition has a pH of 1 to 7; more preferably, of 1.5 to 4.5; still more preferably, of 1.5 to 3.5; still even more preferably, of 2 to 3, most preferably, of 2 to 2.5; providing a chemical mechanical polishing pad, having a polishing surface; creating dynamic contact at an interface between the chemical mechanical polishing pad and the substrate; and dispensing the chemical mechanical polishing composition onto the polishing surface of the chemical mechanical polishing pad at or near the interface between the chemical mechanical polishing pad and the substrate; wherein at least some of the tungsten is polished away from the substrate.

(10) Preferably, in the method of polishing a substrate of the present invention, the substrate comprises tungsten and a dielectric. More preferably, the substrate provided is a semiconductor substrate comprising tungsten and a dielectric. Most preferably, the substrate provided is a semiconductor substrate comprising tungsten deposited within at least one of holes and trenches formed in a dielectric such as TEOS.

(11) Preferably, in the method of polishing a substrate of the present invention, the water contained, as an initial component, in the chemical mechanical polishing composition provided is at least one of deionized and distilled to limit incidental impurities.

(12) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, an oxidizing agent, wherein the oxidizing agent is selected from the group consisting of hydrogen peroxide (H.sub.2O.sub.2), monopersulfates, iodates, magnesium perphthalate, peracetic acid and other per-acids, persulfate, bromates, perbromate, persulfate, peracetic acid, periodate, nitrates, iron salts, cerium salts, Mn (III), Mn (IV) and Mn (VI) salts, silver salts, copper salts, chromium salts, cobalt salts, halogens, hypochlorites and a mixture thereof. More preferably, the oxidizing agent is selected from hydrogen peroxide, perchlorate, perbromate; periodate, persulfate and peracetic acid. Most preferably, the oxidizing agent is hydrogen peroxide.

(13) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, 0.01 to 10 wt %, more preferably, 0.1 to 5 wt %; most preferably, 1 to 3 wt % of an oxidizing agent.

(14) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a source of iron (III) ions. More preferably, in the method of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a source of iron (III) ions, wherein the source of iron (III) ions is selected from the group consisting iron (III) salts. Most preferably, in the method of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a source of iron (III) ions, wherein the source of iron (III) ions is ferric nitrate nonahydrate, (Fe(NO.sub.3).sub.3.9H.sub.2O).

(15) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a source of iron (III) ions sufficient to introduce 1 to 200 ppm, preferably, 5 to 150 ppm, more preferably, 7.5 to 125 ppm, most preferably, 10 to 100 ppm of iron (III) ions to the chemical mechanical polishing composition. It is particularly preferred to include a source of iron (III) ions sufficient to introduce 10 to 150 ppm of iron (III) ions to the chemical mechanical polishing composition.

(16) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a source of iron (III) ions. More preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, 100 to 1,000 ppm, preferably, 150 to 750 ppm, more preferably, 200 to 500 ppm and most preferably, 250 to 400 ppm of a source of iron (III) ions. Most preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, 100 to 1,000 ppm, preferably, 150 to 750 ppm, more preferably, 200 to 500 ppm, most preferably, 250 to 400 ppm of a source of iron (III) ions, wherein the source of iron (III) ions is ferric nitrate nonahydrate, (Fe(NO.sub.3).sub.3.9H.sub.2O).

(17) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a thiolalkoxy compound, preferably having formula (I). Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, at least 50 ppm, preferably 50 ppm to 1000 ppm, more preferably from 50 ppm to 800 ppm, even more preferably from 50 ppm to 300 ppm, still more preferably from 50 ppm to 275 ppm, most preferably from 50 ppm to 250 ppm. When the colloidal silica abrasive has a permanent positive zeta potential, it is preferred that a thiolalkoxy compound, preferably having formula (I), is included in the chemical mechanical polishing composition, as an initial component, in an amount of 500 ppm to 1000 ppm, more preferably from 600 ppm to 1000 ppm, even more preferably from 600 ppm to 800 ppm.

(18) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains a colloidal silica abrasive having a positive or a negative zeta potential. More preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains a colloidal silica abrasive having a permanent negative zeta potential, wherein the chemical mechanical polishing composition has a pH of 1 to 7, preferably, of 1.5 to 4.5; more preferably, of 1.5 to 3.5; still more preferably, of 2 to 2.5. Still more preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains a colloidal silica abrasive having a permanent negative zeta potential, wherein the chemical mechanical polishing composition has a pH of 1 to 7, preferably, of 1.5 to 4.5; more preferably, of 1.5 to 3.5; still more preferably, of 2 to 3 and most preferably, of 2 to 2.5 as indicated by a zeta potential from 0.1 mV to 20 mV.

(19) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a colloidal silica abrasive, wherein the colloidal silica abrasive has an average particle size 100 nm, preferably, 5 to 100 nm; more preferably, 10 to 60 nm; most preferably, 20 to 60 nm as measured by dynamic light scattering techniques.

(20) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains 0.01 to 10 wt %, preferably 0.05 to 7.5 wt %, more preferably, 0.1 to 5 wt %, even more preferably, 0.2 to 5 wt %, most preferably, 0.2 to 2 wt % of a colloidal silica abrasive. Preferably the colloidal silica abrasive has a negative zeta potential.

(21) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a dicarboxylic acid, wherein the dicarboxylic acid includes, but is not limited to malonic acid, oxalic acid, succinic acid, adipic acid, maleic acid, malic acid, glutaric acid, tartaric acid, salts thereof or mixtures thereof. More preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, a dicarboxylic acid, wherein the dicarboxylic acid is selected from the group consisting of malonic acid, oxalic acid, succinic acid, tartaric acid, salts thereof and mixtures thereof. Still more preferably the chemical mechanical polishing composition provided contains, as an initial component, a dicarboxylic acid, wherein the dicarboxylic acid is selected from the group consisting of malonic acid, oxalic acid, succinic acid, salts thereof and mixtures thereof. Most preferably in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, the dicarboxylic acid malonic acid or salts thereof.

(22) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, 1 to 2,600 ppm, preferably, 100 to 1,400 ppm, more preferably, 120 to 1,350 ppm, still more preferably, 130 to 1,100 ppm, of a dicarboxylic acid, wherein the dicarboxylic acid includes, but is not limited to malonic acid, oxalic acid, succinic acid, adipic acid, maleic acid, malic acid, glutaric acid, tartaric acid, salts thereof or mixtures thereof. More preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component, 1 to 2,600 ppm of malonic acid, salt thereof or mixtures thereof. Most preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided contains, as an initial component 100 to 1,400 ppm, more preferably, 120 to 1,350 ppm, still more preferably, 130 to 1,350 ppm, the dicarboxylic acid malonic acid or salts thereof.

(23) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided has a pH of 1 to 7. More preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided has a pH of 1.5 to 4.5. Even more preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided has a pH of 1.5 to 3.5. Still more preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided has a pH of 2 to 3. Most preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided has a pH of 2 to 2.5.

(24) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided optionally contains a pH adjusting agent. Preferably, the pH adjusting agent is selected from the group consisting of inorganic and organic pH adjusting agents. Preferably, the pH adjusting agent is selected from the group consisting of inorganic acids and inorganic bases. More preferably, the pH adjusting agent is selected from the group consisting of nitric acid and potassium hydroxide. Most preferably, the pH adjusting agent is potassium hydroxide.

(25) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing pad provided can by any suitable polishing pad known in the art. One of ordinary skill in the art knows to select an appropriate chemical mechanical polishing pad for use in the method of the present invention. More preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing pad provided is selected from woven and non-woven polishing pads. Still more preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing pad provided comprises a polyurethane polishing layer. Most preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing pad provided comprises a polyurethane polishing layer containing polymeric hollow core microparticles and a polyurethane impregnated non-woven subpad. Preferably, the chemical mechanical polishing pad provided has at least one groove on the polishing surface.

(26) Preferably, in the method of polishing a substrate of the present invention, the chemical mechanical polishing composition provided is dispensed onto a polishing surface of the chemical mechanical polishing pad provided at or near an interface between the chemical mechanical polishing pad and the substrate.

(27) Preferably, in the method of polishing a substrate of the present invention, dynamic contact is created at the interface between the chemical mechanical polishing pad provided and the substrate with a down force of 0.69 to 34.5 kPa normal to a surface of the substrate being polished.

(28) Preferably, in the method of polishing a substrate of the present invention, wherein the chemical mechanical polishing composition provided has a tungsten removal rate 1,000 /min; preferably, 1,500 /min; more preferably, 2,000 /min. More preferably, in the method of polishing a substrate of the present invention, wherein the chemical mechanical polishing composition provided has a tungsten removal rate of 1,000 /min; preferably, 1,500 /min; more preferably, 2,000 /min; and a W/TEOS selectivity of 3. Still more preferably, in the method of polishing a substrate of the present invention, wherein the tungsten is removed from the substrate at a removal rate of 1,000 /min; preferably, 1,500 /min; more preferably, 2,000 /min; and a W/TEOS selectivity of 3 to 60. Most preferably, in the method of polishing the substrate of the present invention, wherein the tungsten is removed from the substrate at a removal rate of 1,000 /min; preferably, 1,500 /min; more preferably, 2,000 /min; and a W/TEOS selectivity of 5 to 30 and with a platen speed of 80 revolutions per minute, a carrier speed of 81 revolutions per minute, a chemical mechanical polishing composition flow rate of 125 mL/min, a nominal down force of 21.4 kPa on a 200 mm polishing machine; and, wherein the chemical mechanical polishing pad comprises a polyurethane polishing layer containing polymeric hollow core microparticles and a polyurethane impregnated non-woven subpad.

(29) As is illustrated in the following Examples, the thiolalkoxy compound CMP methods of the present invention inhibit tungsten dishing in combination with inhibiting erosion of underlying TEOS and further inhibits corrosion rate.

Example 1

Slurry Formulations

(30) The chemical mechanical polishing compositions of this Example were prepared by combining the components in the amounts listed in Table 1 with the balance being DI water and adjusting the pH of the compositions to the final pH listed in Table 1 with 45 wt % potassium hydroxide.

(31) TABLE-US-00001 TABLE 1 Thiolalkoxy Malonic Abrasive.sup.1 DODT.sup.2 Fe(NO.sub.3).sub.3 Acid H.sub.2O.sub.2 Slurry # (wt %) (ppm) (ppm) (ppm) (wt %) pH CS-1 2 362 1320 2 2.3 PS-1 2 50 362 1320 2 2.3 PS-2 2 250 362 1320 2 2.3 PS-3 2 1000 362 1320 2 2.3 .sup.1KLEBOSOL 1598-B25 () zeta potential abrasive slurry manufactured by AZ Electronics Materials, available from The Dow Chemical Company; and .sup.23,6-dioxa-1,8-octanedithiol from SIGMA-ALDRICH.

Example 2

Corrosion Rate Performance of 3,6-Dioxa-1,8-Octanedithiol CMP Slurries

(32) The corrosion tests were carried out by immersing W blanket wafers (1 cm4 cm) in 15 g slurry samples. The W wafers were removed from tested slurries after 10 min. The solutions were subsequently centrifuged for 20 min at 9,000 rpm to remove slurry particles. The supernatant was analyzed by ICP-OES to determine the amount of tungsten by weight. The corrosion rate (A/min) was converted from the W mass assuming an etching wafer surface area of 4 cm.sup.2. The results of the corrosion tests are in Table 2.

(33) TABLE-US-00002 TABLE 2 Slurry # W Corrosion Rate (/min) CS-1 28 PS-1 26 PS-2 24 PS-3 24

(34) The results of the corrosion rate tests showed that the chemical mechanical polishing slurries containing the 3,6-dioxa-1,8-octanedithiol effectively reduced the corrosion on W containing wafers better than the control slurry (CS-1).

Example 3

Chemical Mechanical PolishingDishing and Erosion Performance of 3,6-Dioxa-1,8-Octanedithiol CMP Slurry

(35) The polishing experiments were performed on 200 mm blanket wafers installed on an Applied Materials 200 mm MIRRA polishing machine. The polishing removal rate experiments were performed on 200 mm blanket 15 k-thick TEOS sheet wafers plus W, Ti, and TiN blanket wafers available from Silicon Valley Microelectronics. All polishing experiments were performed using an IC1010 polyurethane polishing pad paired with an SP2310 subpad (commercially available from Rohm and Haas Electronic Materials CMP Inc.) with a typical down pressure of 21.4 kPa (3.1 psi), a chemical mechanical polishing composition flow rate of 125 mL/min, a table rotation speed of 80 rpm and a carrier rotation speed of 81 rpm unless specified otherwise. A Kinik PDA33A-3 diamond pad conditioner (commercially available from Kinik Company) was used to dress the polishing pad. The polishing pad was broken in with the conditioner using a down force of 9.0 lbs (4.1 kg) for 15 minutes and 7.0 lbs (3.2 kg) for 15 minutes at 80 rpm (platen)/36 rpm (conditioner). The polishing pad was further conditioned ex-situ prior to polishing using a down force of 7 lbs (3.2 kg) for 24 seconds. The TEOS erosion depths were determined by measuring the film thickness before and after polishing using a KLA-Tencor FX200 metrology tool. The W removal and dishing rates were determined using a KLA-Tencor RS100C metrology tool. The wafers had varying standard line width features as shown in Tables 3A and 3B. In the tables of this example the numerator refers to W and the denominator refers to TEOS.

(36) TABLE-US-00003 3A 100/100 m 100/100 m dishing erosion 50/50 m 50/50 m 10/10 m 10/10 m Slurry # () () dishing () erosion () dishing () erosion () CS-1 1350 26 1180 44 653 242 PS-1 980 41 1002 6.3 576 232

(37) TABLE-US-00004 3B 0.25/0.25 m 0.25/0.25 m 7/3 m 7/3 m 9/1 m 9/1 m dishing erosion Slurry # dishing () erosion () dishing () erosion () () () CS-1 409 647 352 1077 129 357 PS-1 347 550 249 951 34 334

(38) Overall the slurry which included the 3,6-dioxa-1,8-octanedithiol showed improved performance over the slurry which excluded the 3,6-dioxa-1,8-octanedithiol. The 3,6-dioxa-1,8-octanedithiol slurry showed overall reduced dishing of W and reduced erosion of TEOS.

Example 4

W, TEOS Removal Rate and W, TEOS Maximum Polishing Temperature

(39) The polishing experiments for W and TEOS removal rates were performed substantially as described in Example 3 using the same apparatus and parameters. The wafers were from Silicon Valley Microelectronics. The results are in Table 4.

(40) TABLE-US-00005 TABLE 4 W RR TEOS RR W/TEOS W Temp. TEOS Temp. Slurry # (/min) (/min) Selectivity ( C.) ( C.) CS-1 1802 178 10.1 34.6 PS-l 1993 249 8 38.1 34 PS-2 1602 286 5.6 34.3 33.5

(41) The chemical mechanical polishing compositions of the present invention showed good W RR of greater than 1600 /min and good W/TEOS selectivity greater than 5.

Example 5

Slurry Formulations

(42) The chemical mechanical polishing compositions of this Example were prepared by combining the components in the amounts listed in Table 5 with the balance being DI water and adjusting the pH of the compositions to the final pH listed in Table 5 with 45 wt % potassium hydroxide.

(43) TABLE-US-00006 TABLE 5 Thiolalkoxy Malonic Abrasive.sup.3 DODT.sup.4 Fe(NO.sub.3).sub.3 Acid H.sub.2O.sub.2 Slurry # (wt %) (ppm) (ppm) (ppm) (wt %) pH CS-2 0.6 362 1320 2 2.3 PS-4 0.6 50 362 1320 2 2.3 PS-5 0.6 250 362 1320 2 2.3 PS-6 0.6 1000 362 1320 2 2.3 .sup.3FUSO HL-3 (+) zeta potential abrasive slurry manufactured by Fuso Chemical Co., LTD; and .sup.43,6-dioxa-1,8-octanedithiol from SIGMA-ALDRICH.

Example 6

Corrosion Rate Performance of 3,6-Dioxa-1,8-Octanedithiol CMP Slurries

(44) The corrosion tests were carried out by immersing W blanket wafers (1 cm4 cm) in 15 g slurry samples. The W wafers were removed from tested slurries after 10 min. The solutions were subsequently centrifuged for 20 min at 9,000 rpm to remove slurry particles. The supernatant was analyzed by ICP-OES to determine the amount of tungsten by weight. The corrosion rate (A/min) was converted from the W mass assuming an etching wafer surface area of 4 cm.sup.2. The results of the corrosion tests are in Table 6.

(45) TABLE-US-00007 TABLE 6 Slurry # W Corrosion Rate (/min) CS-2 38 PS-4 31 PS-5 32 PS-6 28

(46) The results of the corrosion rate tests showed that the chemical mechanical polishing slurries containing the 3,6-dioxa-1,8-octanedithiol effectively reduced the corrosion on W containing wafers better than the control slurry (CS-2).

Example 7

Slurry Formulations

(47) The chemical mechanical polishing compositions of this Example were prepared by combining the components in the amounts listed in Table 7 with the balance being DI water and adjusting the pH of the compositions to the final pH listed in Table 7 with 45 wt % potassium hydroxide.

(48) TABLE-US-00008 TABLE 7 Thiolalkoxy Malonic Abrasive.sup.3 DODT.sup.4 Fe(NO.sub.3).sub.3 Acid H.sub.2O.sub.2 Slurry # (wt %) (ppm) (ppm) (ppm) (wt %) pH CS-2 0.6 362 1320 2 2.3 PS-7 0.6 750 362 1320 2 2.3 .sup.3FUSO HL-3 (+) zeta potential abrasive slurry manufactured by Fuso Chemical Co., LTD; and .sup.43,6-dioxa-1,8-octanedithiol from SIGMA-ALDRICH.

Example 8

Chemical Mechanical PolishingDishing and Erosion Performance of 3,6-Dioxa-1,8-Octanedithiol CMP Slurry

(49) The polishing experiments were performed on 200 mm blanket wafers installed on an Applied Materials 200 mm MIRRA polishing machine. The polishing removal rate experiments were performed on 200 mm blanket 15 k-thick TEOS sheet wafers plus W, Ti, and TiN blanket wafers available from Silicon Valley Microelectronics. All polishing experiments were performed using an IC1010 polyurethane polishing pad paired with an SP2310 subpad (commercially available from Rohm and Haas Electronic Materials CMP Inc.) with a typical down pressure of 21.4 kPa (3.1 psi), a chemical mechanical polishing composition flow rate of 125 mL/min, a table rotation speed of 80 rpm and a carrier rotation speed of 81 rpm unless specified otherwise. A Kinik PDA33A-3 diamond pad conditioner (commercially available from Kinik Company) was used to dress the polishing pad. The polishing pad was broken in with the conditioner using a down force of 9.0 lbs (4.1 kg) for 15 minutes and 7.0 lbs (3.2 kg) for 15 minutes at 80 rpm (platen)/36 rpm (conditioner). The polishing pad was further conditioned ex-situ prior to polishing using a down force of 7 lbs (3.2 kg) for 24 seconds. The TEOS erosion depths were determined by measuring the film thickness before and after polishing using a KLA-Tencor FX200 metrology tool. The W removal and dishing rates were determined using a KLA-Tencor RS100C metrology tool. The wafers had varying standard line width features as shown in Tables 8A and 8B. In the tables of this example the numerator refers to W and the denominator refers to TEOS.

(50) TABLE-US-00009 8A 100/100 m 100/100 m dishing erosion 50/50 m 50/50 m 10/10 m 10/10 m Slurry # () () dishing () erosion () dishing () erosion () CS-2 1350 26 1180 44 653 242 PS-7 980 41 1002 6.3 576 232

(51) TABLE-US-00010 8B 0.25/0.25 m 0.25/0.25 m 7/3 m 7/3 m 9/1 m 9/1 m dishing erosion Slurry # dishing () erosion () dishing () erosion () () () CS-2 409 647 352 1077 129 357 PS-7 347 550 249 951 34 334

(52) Overall the slurry which included the 3,6-dioxa-1,8-octanedithiol showed improved performance over the slurry which excluded the 3,6-dioxa-1,8-octanedithiol. The 3,6-dioxa-1,8-octanedithiol slurry showed overall reduced dishing of W and reduced erosion of TEOS.

Example 9

W, TEOS Removal Rate and W, TEOS Maximum Polishing Temperature

(53) The polishing experiments for W and TEOS removal rates were performed substantially as described in Example 8 using the same apparatus and parameters. The wafers were from Silicon Valley Microelectronics. The results are in Table 9.

(54) TABLE-US-00011 TABLE 9 W RR TEOS RR W/TEOS Slurry # (/min) (/min) Selectivity CS-2 2532 397 6.4 PS-5 1802 178 10.1 PS-7 2761 105 26.2

(55) The chemical mechanical polishing compositions of the present invention showed good W RR of greater than 1800 /min and good W/TEOS selectivity greater than 10.