Chemical-Mechanical Polishing Compositions Containing Aspartame And Methods Of Making And Using The Same

a technology of compositions and polishing methods, applied in the field of compositions and compositions of chemical mechanical polishing and methods of making and using the same, can solve the problems of reducing the manufacturing throughput of shallow trench isolation structures, affecting the removal rate of silicon nitride, and severe topography variations, and achieve the effect of maintaining the extremely low silicon nitride ra

Inactive Publication Date: 2008-12-25
FERRO CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented technology allows for better removal of materials during manufacturing processes such as semiconductor device fabrication. It uses certain types of aminosilane with specific properties like Alaphatic Acid Bases (“AAbs") attached onto its backbone through different linkers. These special groups can be used together to enhance their effectiveness at removing material while also being able to prevent damage caused by other layers formed over it's surfaces. Overall this new process improves efficiency and quality control in various industries including electronic devices production.

Problems solved by technology

Technologies related to this patented technical issue: The present inventions described in previous researches involve improving the efficiency and effectiveness of various techniques like thermal stress relief formation and shallown channel isolations in advanced electronic devices called SOFIs. These improvements require precise control over the removal rates of SiO2 and silicate nitrides, but existing methods cannot achieve desired results due to their limitations in achieving specific levels of separation without sacrificially removing silica.

Method used

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  • Chemical-Mechanical Polishing Compositions Containing Aspartame And Methods Of Making And Using The Same

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0027]CMP Slurry Compositions A1, A2 and A3 were prepared as shown in weight percent in Table 1 below.

TABLE 1SlurryCeO2AspartameDI-H2OpHA11%  0%  99%4.32A21%0.3%98.7%4.32A31%0.5%98.5%4.32

[0028]The “CeO2” used in each CMP Slurry Composition was a calcined cerium oxide derived from a cerium carbonate precursor that had a Dmean secondary particle size of 140 nm. A quantity of HNO3 was added to each CMP Slurry Composition sufficient to adjust the pH to 4.32. CMP Slurry Composition A1 was a control in that it did not contain any Aspartame.

[0029]CMP Slurry Compositions A1, A2 and A3 were separately used to polish blanket thermally grown silicon dioxide (“TOX”) and silicon nitride wafers (“Nitride”). The polisher used in each case was an Applied Materials Mirra system. For all test runs, the polishing conditions were 3.0 psi membrane pressure, 3.5 psi retaining ring pressure, 3.0 psi inner tube pressure, 93 rpm head speed and 87 rpm table speed. The flow rate of the CMP Slurry Compositions wa

example 2

[0031]CMP Slurry Compositions B1, B2 and B3 were prepared as shown in weight percent in Table 3 below.

TABLE 3SlurryCeO2AspartameDI-H2OpHB13%  0%  97%4.04B23%0.3%96.7%4.04B33%0.5%96.5%4.04

[0032]The “CeO2” used in each CMP Slurry Composition was the same as used in Example 1. A quantity of HNO3 was added to each CMP Slurry Composition sufficient to adjust the pH to 4.04. CMP Slurry Composition B1 was a control in that it did not contain any Aspartame.

[0033]CMP Slurry Compositions B1, B2 and B3 were separately used to polish blanket thermally grown silicon dioxide and silicon nitride wafers using the equipment and polishing conditions described in Example 1. The removal rate of each material in Å / min and silicon dioxide to silicon nitride selectivity is set forth in Table 4:

TABLE 4SlurryTOX RRNitride RRSelectivityB11936.91439.11B22852.418.0158B32562.210.9235

[0034]Example 2 shows that at 3% ceria and at pH of about 4.0, the selectivity increases with Aspartame additions and even has an i

example 3

[0035]CMP Slurry Compositions C1, C2 and C3 were prepared as shown in weight percent in Table 5 below.

TABLE 5SlurryCeO2AspartameWaterpHC110993.9C210.198.94.4C310.498.64.0

[0036]The “CeO2” used in each CMP Slurry Composition was the same as used in Example 1. CMP Slurry Composition C1 was a control in that it did not contain any Aspartame.

[0037]CMP Slurry Compositions C1, C2 and C3 were separately used to polish patterned high density plasma (HDP) silicon dioxide films using the equipment and polishing conditions described in Example 1. The amount of up area removed (active removal rate, ACT Removed) of each material removed in Å for different polish times is set forth in Table 6 and further illustrated in FIG. 1:

TABLE 6C1C2C3TimeACT RemovedACT RemovedACT Removed000060840130916427511023919245490139445375019105164457565962

[0038]Example 3 shows that at 1% ceria and at a pH of about 4.0, the silicon dioxide step height removal rate is increased with Aspartame additions.

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Abstract

The present invention provides an aqueous CMP slurry composition that comprises abrasive particles and Aspartame. The CMP slurry composition according to the invention is selective for polishing silicon dioxide in preference to silicon nitride from a surface of an article by chemical mechanical planarization. Furthermore, as more Aspartame is added to the slurry, the silicon dioxide rate is either not greatly affected or increases and the silicon nitride rate stays extremely low. In addition to offering selectivity of silicon dioxide to silicon nitride polishing, the present invention provides a method of using Aspartame as a polish accelerant in silicon dioxide polishing.

Description

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Claims

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Application Information

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Owner FERRO CORP
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