Aqueous cleaning composition containing copper-specific corrosion inhibitor for cleaning inorganic residues on semiconductor substrate

Information

  • Patent Grant
  • 9109188
  • Patent Number
    9,109,188
  • Date Filed
    Tuesday, October 23, 2012
    11 years ago
  • Date Issued
    Tuesday, August 18, 2015
    8 years ago
Abstract
A semiconductor wafer cleaning formulation, including 1-35% wt. fluoride source, 20-60% wt. organic amine(s), 0.1-40% wt. nitrogenous component, e.g., a nitrogen-containing carboxylic acid or an imine, 20-50% wt. water, and 0-21% wt. metal chelating agent(s). The formulations are useful to remove residue from wafers following a resist plasma ashing step, such as inorganic residue from semiconductor wafers containing delicate copper interconnecting structures.
Description
FIELD OF THE INVENTION

The present invention relates generally to chemical formulations useful in semiconductor manufacturing and particularly to chemical formulations that are utilized to remove residue from wafers following a resist plasma ashing step. More specifically, the present invention relates to cleaning formulations for removal of inorganic residue from semiconductor wafers containing delicate copper interconnecting structures.


DESCRIPTION OF THE PRIOR ART

The prior art teaches the utilization of various chemical formulations to remove residues and clean wafers following a resist ashing step. Some of these prior art chemical formulations include alkaline compositions containing amines and/or tetraalkyl ammonium hydroxides, water and/or other solvents, and chelating agents. Still other formulations are based on acidic to neutral solutions containing ammonium fluoride.


The various prior art formulations have drawbacks that include unwanted removal of metal or insulator layers and the corrosion of desirable metal layers, particularly copper or copper alloys features. Some prior art formulations employ corrosion inhibiting additives to prevent undesirable copper metal corrosion during the cleaning process. However, conventional corrosion-inhibiting additives typically have detrimental effects on the cleaning process because such additives interact with the residue and inhibit dissolution of such residue into the cleaning fluid. Moreover, conventional additives do not easily rinse off the copper surface after completion of the cleaning process. Such additives therefore remain on the surface sought to be cleaned, and result in contamination of the integrated circuits. Contamination of the integrated circuit can adversely increase the electrical resistance of contaminated areas and cause unpredictable conducting failure within the circuit.


The formulation of post CMP cleaners for advanced integrated circuit manufacturing such as copper and tungsten interconnect materials, includes slurry removal and residue dissolution components that accelerate the physical cleaning process. However, these conventional additives typically have detrimental effects on the metal surface by increasing resistance and corrosion sensitivity.


It is therefore one object of the present invention to provide chemical formulations that effectively remove residue following a resist ashing step, and which do not attack and potentially degrade delicate structures intended to remain on the wafer.


It is another object of the present invention to replace conventional additives with an improved corrosion inhibitor for protection of copper structures on the semiconductor substrate.


It is another object of the invention to provide an improved corrosion inhibitor, which is easily rinsed off the substrate by water or other rinse medium after the completion of the residue-removal process, thereby reducing contamination of the integrated circuit.


Other objects and advantages of the invention will become fully apparent from the ensuing disclosure and appended claims.


SUMMARY OF THE INVENTION

The present invention relates generally to chemical formulations useful in semiconductor manufacturing for removing residue from wafers following a resist plasma ashing step.


In one aspect, the invention relates to a method of removing residue from a wafer following a resist plasma ashing step on such wafer, comprising contacting the wafer with a cleaning formulation, including (i) a fluoride source, (ii) at least one organic amine, (iii) a nitrogen-containing carboxylic acid or an imine, (iv) water, and optionally at least one metal chelating agent.


Another aspect of the invention relates to a wafer cleaning formulation, including (i) a fluoride source, (ii) at least one organic amine, (iii) a nitrogen-containing carboxylic acid or an imine, (iv) water, and optionally at least one metal chelating agent.


In a further aspect, the invention relates to a semiconductor wafer cleaning formulation for use in post plasma ashing semiconductor fabrication, comprising the following components in the percentage by weight (based on the total weight of the formulation) ranges shown:















a fluoride source, eg., ammonium fluoride and/or
  1-35%


derivative(s) thereof



organic amine(s)
 20-60%


a nitrogenous component selected from nitrogen-containing
0.1-40%


carboxylic acids and imines



water
 20-50%


metal chelating agent(s)
  0-21%


TOTAL
   100%









In a still further aspect, the invention relates to a formulation useful for post chemical mechanical polishing (CMP) cleaning, which is a dilute version of the wafer cleaning formulation outlined hereinabove, wherein the dilute formulation comprises: (i) a fluoride source, (ii) at least one organic amine, (iii) 70% to 98% water, and optionally at least one metal chelating agent and optionally a nitrogen-containing carboxylic acid or an imine.


Such formulations of the invention effectively remove inorganic residues following a plasma ashing and/or CMP step.


Such formulations also effectively remove metal halide and metal oxide residues following plasma ashing, and effectively remove slurry particles of aluminum oxides and other oxides remaining after CMP (chemical mechanical polishing).


The formulations of the present invention provide better stripping performance with less corrosivity than formulations containing either ammonium fluoride or amines. Formulations in accordance with the invention also provide better stripping performance at lower processing temperatures than conventional amine-containing formulations.


The formulations of the invention utilize a chelating agent, which may be a single-component chelating agent or a multicomponent-chelating agent, to prevent metal corrosion and increase stripping effectiveness.


Other features and advantages of the present invention will be from the ensuing disclosure and appended claims.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a schematic representation of a copper-specific corrosion inhibitor useful in the broad practice of the present invention, which forms a protective layer on the copper metal to prevent corrosion;



FIG. 2 is a schematic representation of the copper-specific corrosion inhibitor being rinsed away from the copper surface by deionized water;



FIG. 3 depicts cleaning components of the present invention interacting with a surface;



FIG. 4 illustrates that formulations of the present invention may be used to remove residues and particles;



FIG. 5 provides a SEM representing results obtained from an immersion process; and



FIG. 6 illustrates the material etch rate on interconnect materials.





DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The formulations of the present invention are suitable for stripping inorganic wafer residues deriving from high-density plasma etching followed by ashing with oxygen-containing plasmas. Such formulations, in dilute form, are also suitable for removing slurry particles of aluminum oxides and other oxides remaining after CMP (chemical mechanical polishing).


The formulations advantageously contain (i) a fluoride source, such as ammonium fluoride and/or derivative(s) of ammonium fluoride, (ii) an amine or mixture of amines, (iii) a nitrogen-containing carboxylic acid or imine, (iv) water, and, optionally and preferably, (v) one or more metal chelating agents.


As used herein, a fluoride source refers to a compound or a mixture of compounds that in the aqueous cleaning formulation provides fluorine anions.


The preferred formulations for post etch removal include the following components in the percentage by weight (based on the total weight of the formulation) ranges shown:















fluoride source
  1-35%


organic amine(s)
 20-60%


a nitrogenous component selected from nitrogen containing
0.1-40%


carboxylic acids and imines



water
 20-50%


metal chelating agent(s)
  0-21%


TOTAL
   100%









The preferred formulations for post CMP cleaning include the following components in the percentage by weight (based on the total weight of the formulation) ranges shown:















fluoride source
 0.1-5%


organic amine(s)
  1-15%


a nitrogenous component selected from nitrogen containing
  0-10%


carboxylic acids and imines



water
 70-98%


metal chelating agent(s)
  0-5%


TOTAL
   100%









The components of the formulation as described above can be of any suitable type or species, as will be appreciated by those of ordinary skill in the art. Specific illustrative and preferred formulation components for each of the ingredients of the formulation are described below.


Particularly preferred amines include one or more of the following:

  • diglycolamine (DGA),
  • methyldiethanolamine (MDEA),
  • pentamethyldiethylenetriamine (PMDETA),
  • triethanolamine (TEA), and
  • triethylenediamine (TEDA).


Other amines that are highly advantageous include:

  • hexamethylenetetramine,
  • 3,3-iminobis (N,N-dimethylpropylamine),
  • monoethanolamine
  • 2-(methylamino)ethanol,
  • 4-(2-hydroxyethyl)morpholine
  • 4-(3-aminopropyl)morpholine, and
  • N,N-dimethyl-2-(2-aminoethoxy)ethanol.


Fluoride sources useful in the present invention include any combination of ammonia gas or ammonium hydroxide and hydrogen fluoride gas or hydrofluoric acid. Specific preferred fluoride sources include, but are not limited to one or more of the following:

  • ammonium fluoride, and
  • ammonium bifluoride


Other fluoride sources that are highly advantageous include:

  • triethanolammonium fluoride (TEAF);
  • diglycolammonium fluoride (DGAF);
  • methyldiethanolammonium fluoride (MDEAF)
  • tetramethylammonium fluoride (TMAF); and
  • triethylamine tris (hydrogen fluoride) (TREAT-HF).


Specific preferred nitrogen-containing carboxylic acids and imines include one or more of the following:

  • iminodiacetic acid (IDA);
  • glycine;
  • nitrilotriacetic acid (NTA);
  • 1,1,3,3-tetramethylguanidine (TMG); and
  • hydroxyethyliminodiacetic acid
  • ethylenediaminetetracetic acid (EDTA).


Other nitrogen-containing carboxylic acids or imines advantageously utilizable in formulations of the invention include:

  • CH3C(═NCH2CH2OH)CH2C(O)N(CH3)2
  • CH3C(═NCH2CH2OCH2CH2OH)CH2C(O)N(CH3)2
  • CH3C(═NH)CH2C(O)CH3
  • (CH3CH2)2NC(═NH)N(CH3CH2)2
  • HOOCCH2N(CH3)2
  • HOOCCH2N(CH3)CH2COOH


Specific preferred metal chelating agents include:

  • acetoacetamide;
  • ammonium carbamate;
  • ammonium pyrrolidinedithiocarbamate (APDC);
  • dimethyl malonate;
  • methyl acetoacetate;
  • N-methyl acetoacetamide;
  • 2,4-pentanedione;
  • tetramethylammonium thiobenzoate;
  • 1,1,1,5,5,5-hexafluoro-2,4-pentanedione H (hfac);
  • 2,2,6,6-tetramethyl-3,5-heptanedione H (thd);
  • tetramethylammonium trifluoroacetate;
  • tetramethylthiuram disulfide (TMTDS);
  • trifluoracetic acid;
  • lactic acid;
  • ammonium lactate;
  • malonic acid
  • formic acid,
  • acetic acid,
  • propionic acid,
  • gamma-butyrolactone,
  • methyldiethanolammonium trifluoroacetate, and
  • trifluoroacetic acid.


The combination of ammonium fluoride or a substituted fluoride source, as described above, with an amine (other than an amine present as a surfactant in an amount of 1% or less) provides better stripping performance with less corrosivity than formulations containing either ammonium fluoride or amines alone. In addition, the resulting alkaline solutions are effective at lower processing temperatures (e.g., 21°-40° C.) than conventional amine-containing formulations.


The presence of nitrogen-containing carboxylic acids and/or imines enables formulations of the invention to be remarkably effective in stripping residues from semiconductor substrate surfaces containing delicate copper structures.


The nitrogen-containing carboxylic acids or imines provide functional groups that are specifically attracted to free copper atoms. As shown schematically in FIG. 1, the copper-specific corrosion inhibiting-agent C, which contacts the copper surface during the residue-removal process, will attach to the copper surface and form a protective layer to prevent the copper surface being corroded by cleaning agents A+ and X.


Moreover, as shown by FIG. 2, such copper-specific corrosion-inhibiting agent C can be easily rinsed off by deionized water or other solutions and therefore leaves very little contamination on the copper surface after the cleaning operation.


The use of 1,3-dicarbonyl compounds as chelating agents and to prevent metal corrosion is a preferred feature of the inventive formulations, to increase their effectiveness.


In various prior art formulations, amines are present in amounts of 1% or less of the formulation as surfactants, or otherwise are not utilized as formulation ingredients at all. Additionally, the prior art formulations are acidic (pH<7) in character. In preferred formulations of the present invention, the amines are present as major components of the formulation, are highly effective in stripping action, and yield formulations of a basic pH character (pH>7).


The formulations of the invention may include a wide variety of organic amines, substituted ammonium fluorides, and nitrogen-containing carboxylic acids, other than those specifically exemplified. Particular substituted ammonium fluorides of suitable character include those of the general formula, R1R2R3R4NF in which each of the respective R species is independently selected from hydrogen and aliphatic groups. Suitable nitrogen-containing carboxylic acids include those of the general structure COOH—CH2—NRR′, wherein R and R′ are each independently selected from the group consisting of hydrogen, alkyl, aryl, and carboxylic acid moieties. Suitable metal chelating agents include 1,3-dicarbonyl compounds of the general structure X—CHR—Y. In compounds of such formula, R is either a hydrogen atom or an aliphatic group, e.g., C1-C8 alkyl, aryl, alkenyl, etc. X and Y may be the same as or different from one another, and are functional groups containing multiply-bonded moieties with electron-withdrawing properties, as for example CONH2, CONHR′, CN, NO2, SOR′, or SO2Z, in which R′ represents a C1-C8 alkyl group and Z represents another atom or group, e.g., hydrogen, halo or C1-C8 alkyl.


Other chelating agent species useful in the compositions of the invention include amine trifluoroacetates of the general formula, R1R2R3R4N+ −O2CCF3 in which each of the R groups is independently selected from hydrogen and aliphatic groups, e.g., C1-C8 alkyl, aryl, alkenyl, etc.


The formulations of the invention optionally may also include such components as surfactants, stabilizers, corrosion inhibitors, buffering agents, and co-solvents, as useful or desired in a given end use application of formulations of the invention.


Formulations in accordance with the present invention are particularly useful on wafers that have been etched with chlorine- or fluorine-containing plasmas, followed by oxygen plasma ashing. The residues generated by this type of processing typically contain metal oxides. Such residues are often difficult to dissolve completely without causing corrosion of metal and titanium nitride features required for effective device performance. Also, metal oxide and silicon oxide slurry particles remaining after CMP will also be effectively removed by formulations in accordance with the present invention.


The features and advantages of the invention are more fully shown by the following non-limiting examples.


EXAMPLE 1

Copper-specific corrosion inhibitors including either hydrogen-containing carboxylic acids or imines were tested in two different types of alkaline cleaning formulations, with the following components and characteristics.













TABLE 1









Copper




Temp.,

Etch Rate



Components
° C.
pH
(Å/min)



















Formulation
dimethylacetoacetamide,
70
6.2
17.4


1
amine, and water





Formulation
ammonium fluoride,
40
8.6
7.5


2
triethanolamine,






pentamethdiethylenetriamine,






and water









The copper etch rate was determined by a standard four-point probe technique. Addition of corrosion inhibitors in accordance with the present invention significantly slowed down the copper etch rate, as shown by the following table, and effectively prevented undesirable corrosion during the cleaning process:















TABLE 2










Copper








Etch
Reduction of



Temp.
Formulation
Concentration
pH of
Rate
Etch Rate


Corrosion Inhibitor
(° C.)
Used
(%)
solution
(Å/min)
(%)





















Iminodiacetic Acid
40
2
1.5
8.0
1-2
−73.3~86.7


Glycine
40
2
1.5
9.2
3.6
−52.0


Nitrilotriacetic Acid
40
2
1.5
8.2
3.6
−52.0


1,1,3,3-tetramethylguanidine
40
2
1.5
8.7
3.4
−54.7


CH3C(═NCH2CH2OH)CH2C(O)N(CH3)2
70
1
24
10.9
6.2
−64.4


CH3C(═NCH2CH2OCH2CH2OH)CH2C(O)N(CH3)2
70
1
36
10.7
0.32
−98.2


CH3C(═NH)CH2C(O)CH3
40
2
13.68
7.9
4.4
−41.3









EXAMPLE 2

A contamination test was carried out on Formulation 2 containing iminodiacetic acid inhibitor. The semiconductor wafer to be cleaned contained copper and silicon films. After the completion of the cleaning operation, the wafer was rinsed by deionized water at 25° C. for about 15 minutes. The Secondary Ion Mass Spectrometry data (SIMS) obtained are as follows:

















Cu (atoms/cm2)
F (atoms/cm2)
C (atoms/cm2)
CuxO (Å)







Uncleaned
1.6 × 1010
3.3 × 1013
7.5 × 1013
42


Wafer






Cleaned
8.5 × 109 
5.1 × 1013
1.5 × 1013
15


Wafer









The foregoing results show that the copper oxide CuxO has been effectively removed by the cleaning process, while carbon contamination, which is mainly caused by the organic corrosion inhibitors in the cleaning formulation, has been greatly reduced.


The present invention employs dilute alkaline fluoride in compositions for post CMP cleaning of silicon oxide or aluminum oxide particles from metallic surfaces such as copper or tungsten. FIG. 3 depicts how the cleaning components of the present invention interact with the surface. Specially, FIG. 3 depicts that Alkaline Fluoride 30 and chelating agents 32 dissolving inorganic oxide residues 34 after a CMP process.



FIG. 4 illustrates that the formulations taught by the present invention may be used to remove residues 40 and particles 42 for a copper surface 44. In FIG. 4 particles 42 and residues 40 adhere to metal surface 44 as well as dielectric surface 46. Particles 42 and residues 40 may remain following a CMP process. The chemical solutions of the present invention degrade the attractive forces between the residue and the surface as well as dissolve copper and tungsten oxides and oxy-halides.


Formulations that have been found to be effective in cleaning residue and slurry particles from metal surfaces may have a pH value in a range for from about 3 to 11, but typically have pH values between about 7 and about 9. These formulations generally are aqueous solutions that comprise a fluoride source, an organic amine, and metal chelating agent. The individual constituents typically constitute a fluoride source and/or a derivative thereof as about 0.1 to about 5.0% of the formulation, wherein the fluoride may be one of many such fluoride sources known to those skilled in the art including one or more of:

  • any combination of ammonia gas or ammonium hydroxide and hydrogen fluoride gas or hydrofluoric acid;
  • ammonium fluoride,
  • ammonium bifluoride;
  • triethanolammonium fluoride (TEAF);
  • diglycolammonium fluoride (DGAF);
  • methyldiethanolammonium fluoride (MDEAF)
  • tetramethylammonium fluoride (TMAF);
  • triethylamine tris (hydrogen fluoride) (TREAT-HF).


The organic amine or mixture of two amines typically comprises between about 1% and about 15% of the formulation of the present invention, wherein the organic amine can be one of many such organic amines known to those skilled in the art including:

  • diglycolamine (DGA),
  • methyldiethanolamine (MDEA),
  • pentamethyldiethylenetriamine (PMDETA),
  • triethanolamine (TEA),
  • triethylenediamine (TEDA),
  • hexamethylenetetramine,
  • 3,3-iminobis (N,N-dimethylpropylamine),
  • monoethanolamine
  • 2-(methylamino)ethanol,
  • 4-(2-hydroxyethyl)morpholine
  • 4-(3-aminopropyl)morpholine, and
  • N,N-dimethyl-2-(2-aminoethoxy)ethanol.


The nitrogenous component of the mixture typically comprises 0 to about 10% of the mixture. wherein the nitrogenous component may be one of many such nitrogenous component sources known to those skilled in the art including one or more of:

  • iminodiacetic acid (IDA),
  • glycine,
  • nitrilotriacetic acid (NTA),
  • hydroxyethyliminodiacetic acid,
  • 1,1,3,-tetramethylguanidine (TMG),
  • ethylenediaminetetracetic acid (EDTA),
  • CH3C(═NCH2CH2OH)CH2C(O)N(CH3)2,
  • CH3C(═NCH2CH2OCH2CH2OH)CH2C(O)N(CH3)2,
  • CH3C(═NH)CH2C(O)CH3,
  • (CH3CH2)2NC(═NH)N(CH3CH2)2,
  • HOOCCH2N(CH3)2, and
  • HOOCCH2N(CH3)CH2COOH.


The metal chelating agent or mixture of chelating agents typically comprises about 0 to about 5.0% of the formulation. Typical metal chelating agent may be one of many such metal chelating agents known to those skilled in the art including:

  • acetoacetamide;
  • ammonium carbamate;
  • ammonium pyrrolidinedithiocarbamate (APDC);
  • dimethyl malonate;
  • methyl acetoacetate;
  • N-methyl acetoacetamide;
  • 2,4-pentanedione;
  • 1,1,1,5,5,5-hexafluoro-2,4-pentanedione H (hfac);
  • 2,2,6,6-tetramethyl-3,5-heptanedione H (thd);
  • tetramethylammonium thiobenzoate;
  • tetramethylammonium trifluoroacetate;
  • tetramethylthiuram disulfide (TMTDS);
  • trifluoracetic acid;
  • lactic acid;
  • ammonium lactate;
  • malonic acid
  • formic acid,
  • acetic acid,
  • propionic acid,
  • gamma-butyrolactone,
  • methyldiethanolammonium trifluoroacetate, and
  • trifluoroacetic acid.


Several representative examples of formulations are:


















Triethanolamine
    4.5%



Ammonium Fluoride
    0.5%



Water
     95%



PMDETA
 3.8-4.5%



Ammonium Fluoride
    0.5%



2,4-Pentanedione
     1%



Water
 94-94.7%



TEA
    1.7%



PMDETA
    1.5%



TEAHF
     2%



Iminodiacetic Acid
    0.4%



Ammonium Bifluoride
    0.5%



Water
   93.9%



TEA
    3.5%



PMDETA
    1.5%



2,4-Pentanedione
   1.35%



Ammonium Fluoride
    1.2%



Water
   92.45%



TEA
     7%



PMDETA
     3%



2,4-Pentanedione
    2.7%



Ammonium Fluoride
    2.4%



Water
   84.9%










Wafers can be immersed in chemical solutions or chemicals can be applied to the wafer surface by spray or through a brush scrubbing system. FIG. 5 depicts a SEM representing the results obtained with a standard immersion process. Specifically FIG. 5 depicts Tungsten plugs after alumina slurry CMP and immersion in formula c for 10 min at 30° C. Furthermore, selectivity to exposed materials may be illustrated by etch rate data. FIG. 6 and table 3 illustrate the material etch rate on interconnect materials including an electroplated copper film.












TABLE 3







Material
Etch Rate, Å/min for 21° C. @ 30 min



















Copper
~1



Tantalum Nitride
<0.1



Titanium
<0.1



Titanium Nitride
1.0



Tungsten
0.2



TEOS
1.5



BPSG
4.5










While the invention has been described herein with reference to specific features, aspects, and embodiments, it will be appreciated that the invention is not thus limited. The invention therefore may correspondingly embodied in a wide variety of compositions, with corresponding variations of ingredients, and end-use applications. The invention therefore is to be understood as encompassing all such variations, modifications and alternative embodiments, within the spirit and scope of the invention as hereafter claimed.

Claims
  • 1. A cleaning formulation comprising (i) a fluoride source, (ii) at least one organic amine, (iii) a nitrogen-containing carboxylic acid or an imine, (iv) water, and optionally at least one metal chelating agent, wherein the nitrogen-containing carboxylic acid or imine is selected from the group consisting of: iminodiacetic acid (IDA),glycine,1,1,3,3-tetramethylguanidine (TMG),CH3C(═NCH2CH2OH)CH2C(O)N(CH3)2,CH3C(═NCH2CH2OCH2CH2OH)CH2C(O)N(CH3)2,CH3C(═NH)CH2C(O)CH3,(CH3CH2)2NC(═NH)N(CH3CH2)2,HOOCCH2N(CH3)2, andHOOCCH2N(CH3)CH2COOH.
  • 2. The cleaning formulation of claim 1, wherein the wafer cleaning composition has a pH greater than 7.
  • 3. The cleaning formulation of claim 1, wherein the amount of nitrogen-containing carboxylic acid or imine is 0.1-40 weight percent, based on the total weight of the composition.
  • 4. The cleaning formulation of claim 1, wherein the fluoride source comprises a fluoride species selected from the group consisting of: any combination of ammonia gas or ammonium hydroxide and hydrogen fluoride gas or hydrofluoric acid,ammonium bifluoride,ammonium fluoride,triethanolammonium fluoride (TEAF),diglycolammonium fluoride (DGAF),tetramethylammonium fluoride (TMAF),methyldiethanolammonium fluoride (MDEAF), andtriethylamine tris(hydrogen fluoride) (TREAT-HF).
  • 5. The cleaning formulation of claim 1, wherein the amount of fluoride source is 1-35% weight percent, based on the total weight of the composition.
  • 6. The cleaning formulation of claim 1, wherein the organic amine(s) comprise an amine(s) selected from the group consisting of: diglycolamine (DGA),methyldiethanolamine (MDEA),pentamethyldiethylenetriamine (PMDETA),triethanolamine (TEA),triethylenediamine (TEDA),hexamethylenetetramine,3,3-iminobis (N,N-dimethylpropylamine),monoethanolamine,2-(methylamino)ethanol,4-(2-hydroxyethyl)morpholine,4-(3-aminopropyl)morpholine, andN,N-dimethyl-2-(2-aminoethoxyl)ethanol.
  • 7. The cleaning formulation of claim 1, wherein the amount of organic amine(s) is 20-60% weight percent, based on the total weight of the composition.
  • 8. The cleaning formulation of claim 1, wherein the amount of water is 20-50% weight percent, based on the total weight of the composition.
  • 9. The cleaning formulation of claim 1, wherein the wafer cleaning formulation further comprises at least one metal chelating agent selected from the group consisting of: acetoacetamide,ammonium carbamate,ammonium pyrrolidinedithiocarbamate (APDC),dimethyl malonate,methyl acetoacetate,N-methyl acetoacetamide,2,4-pentanedione,1,1,1,5,5,5-hexafluoro-2,4-pentanedione H (hfac),2,2,6,6-tetrammethyl-3,5-heptanedione H (thd),tetramethylammonium thiobenzoate,tetramethylammonium trifluoroacetate,tetramethylthiuram disulfide (TMTDS),trifluoracetic acid,lactic acid,ammonium lactate,malonic acid,formic acid,acetic acid,propionic acid,gamma-butyrolactone,iminodiacetic acid,methyldiethanolammonium trifluoroacetate, andtrifluoroacetic acid.
  • 10. The cleaning formulation of claim 1, wherein the amount of at least one metal chelating agent is 0-21% weight percent, based on the total weight of the composition.
  • 11. The cleaning formulation of claim 1, wherein said fluoride source comprises a compound having the general formula R1R2R3R4NF in which each of the R groups is independently selected from hydrogen atoms, C1-C8 alkyl, aryl and alkenyl groups, and wherein said formulation includes a metal chelating agent of the formula: X—CHR—Yin which R is either hydrogen, C1-C8 alkyl, aryl or alkenyl group and X and Y are functional groups containing multiply bonded moieties having electron-withdrawing properties.
  • 12. The cleaning formulation of claim 11, wherein each of X and Y is independently selected from CONH2, CONHR′, CN, NO2, SOR′, and SO2Z in which R′ is C1-C8 alkyl and Z is hydrogen, halo, or C1-C8 alkyl.
  • 13. The cleaning formulation of claim 1, wherein the nitrogen-containing carboxylic or imine comprises iminodiacetic acid.
RELATED APPLICATIONS

This application is a continuation application claiming benefit of U.S. patent application Ser. No. 12/581,843 filed Oct. 19, 2009, now U.S. Pat. No. 8,263,694, which is a continuation application claiming benefit of U.S. patent application Ser. No. 11/135,892 filed May 24, 2005, now U.S. Pat. No. 7,605,113, which is a continuation application claiming benefit of U.S. patent application Ser. No. 10/047,554 filed Oct. 23, 2001, now U.S. Pat. No. 6,896,826, which claims the benefit of U.S. patent application Ser. No. 09/818,073 filed Mar. 27, 2001 now U.S. Pat. No. 6,755,989, which in turn claims priority of U.S. patent application Ser. No. 08/924,021 filed on Aug. 29, 1997, now U.S. Pat. No. 6,224,785, which in turn claims the priority of U.S. Provisional Patent Application 60/044,824 filed Apr. 25, 1997 and U.S. Provisional Patent Application 60/034,194 filed Jan. 9, 1997, all of which are incorporated by reference herein in their entirety.

US Referenced Citations (80)
Number Name Date Kind
4087367 Rioult et al. May 1978 A
4113551 Bassous et al. Sep 1978 A
4165295 Vander Mey Aug 1979 A
4215005 Vander Mey Jul 1980 A
4349411 Okinaka Sep 1982 A
4371443 Keeney Feb 1983 A
4529450 Panayappan Jul 1985 A
4569722 Maury et al. Feb 1986 A
4582624 Enjo et al. Apr 1986 A
4599175 Yamamizu et al. Jul 1986 A
4765844 Merrem et al. Aug 1988 A
4785137 Samuels Nov 1988 A
4795582 Ohmi et al. Jan 1989 A
4863563 Scardera et al. Sep 1989 A
4871422 Scardera et al. Oct 1989 A
4921572 Roche May 1990 A
4964919 Payne Oct 1990 A
5051212 Culshaw et al. Sep 1991 A
5091103 Dean et al. Feb 1992 A
5094701 Norman et al. Mar 1992 A
5219484 Krulik Jun 1993 A
5241118 Saxton et al. Aug 1993 A
5277835 Ohmi et al. Jan 1994 A
5308745 Schwartzkopf May 1994 A
5320709 Bowden et al. Jun 1994 A
5334332 Lee Aug 1994 A
5421906 Borah Jun 1995 A
5453401 Grivna et al. Sep 1995 A
5466389 Ilardi et al. Nov 1995 A
5498293 Ilardi et al. Mar 1996 A
5509970 Shiramizu Apr 1996 A
5512201 Singh et al. Apr 1996 A
5556833 Howe Sep 1996 A
5560857 Sakon et al. Oct 1996 A
5561105 Honda Oct 1996 A
5571447 Ward et al. Nov 1996 A
5618645 Nakano et al. Apr 1997 A
5630904 Aoyama et al. May 1997 A
5645628 Endo et al. Jul 1997 A
5662769 Schonauer et al. Sep 1997 A
5669980 McNeil et al. Sep 1997 A
5698503 Ward et al. Dec 1997 A
5709756 Ward et al. Jan 1998 A
5733377 Howe Mar 1998 A
5780406 Honda et al. Jul 1998 A
5856062 Hoshi Jan 1999 A
5885362 Morinaga et al. Mar 1999 A
5962385 Maruyama et al. Oct 1999 A
5972862 Torii et al. Oct 1999 A
5989353 Skee et al. Nov 1999 A
6030932 Leon et al. Feb 2000 A
6080709 Ishikawa et al. Jun 2000 A
6136714 Schutz Oct 2000 A
6224785 Wojtczak et al. May 2001 B1
6235693 Cheng et al. May 2001 B1
6255266 Gupta et al. Jul 2001 B1
6280651 Wojtczak et al. Aug 2001 B1
6323168 Kloffenstein et al. Nov 2001 B1
6344432 Wojtczak et al. Feb 2002 B1
6383410 Wojtczak et al. May 2002 B1
6387821 Aoki May 2002 B1
6391794 Chen et al. May 2002 B1
6420329 Callaghan et al. Jul 2002 B1
6440856 Bessho et al. Aug 2002 B1
6465403 Skee Oct 2002 B1
6492311 Lee et al. Dec 2002 B2
6531071 Bedge Mar 2003 B1
6537381 Mikhaylich et al. Mar 2003 B1
6566315 Wojtczak et al. May 2003 B2
6660700 Wojtczak et al. Dec 2003 B2
6755989 Wojtczak et al. Jun 2004 B2
6896826 Wojtczak et al. May 2005 B2
6967169 Wojtczak et al. Nov 2005 B2
7605113 Wojtczak et al. Oct 2009 B2
7662762 Wojtczak et al. Feb 2010 B2
7807613 Rovito et al. Oct 2010 B2
20010006936 Lee et al. Jul 2001 A1
20010008141 Lee Jul 2001 A1
20020034874 Aoki Mar 2002 A1
20020066465 Gotoh et al. Jun 2002 A1
Foreign Referenced Citations (15)
Number Date Country
153308 Dec 1981 DE
0317542 Mar 1995 EP
680078 Nov 1995 EP
812011 Dec 1997 EP
2287827 Sep 1995 GB
07-297158 Nov 1995 JP
8250461 Sep 1996 JP
08306651 Nov 1996 JP
09-062013 Mar 1997 JP
2001064688 Jan 2001 JP
2001051429 Feb 2001 JP
2002050607 Feb 2002 JP
2002299300 Oct 2002 JP
9800244 Jan 1998 WO
0066697 Nov 2000 WO
Non-Patent Literature Citations (3)
Entry
Noguchi, et al.; “Kinki Aruminyumu Hyomen Shori Kenkyuaki Kaishi,” 1996, 179, 3-8, See Abstract.
Chinese State Intellectual Property Office, Second Office Action, Oct. 13, 2010, Chinese Patent Application No. 200810178886.3.
Japan Patent Office, Office Action, Nov. 22, 2010.
Related Publications (1)
Number Date Country
20130072411 A1 Mar 2013 US
Provisional Applications (2)
Number Date Country
60044824 Apr 1997 US
60034194 Jan 1997 US
Continuations (3)
Number Date Country
Parent 12581843 Oct 2009 US
Child 13658415 US
Parent 11135892 May 2005 US
Child 12581843 US
Parent 10047554 Oct 2001 US
Child 11135892 US
Continuation in Parts (2)
Number Date Country
Parent 09818073 Mar 2001 US
Child 10047554 US
Parent 08924021 Aug 1997 US
Child 09818073 US