U.S. patent application number 10/152782 was filed with the patent office on 2003-11-27 for process and composition for removing residues from the microstructure of an object.
Invention is credited to Iijima, Katsuyuki, Masuda, Kaoru, Peters, Darryl W., Yoshikawa, Tetsuya.
Application Number | 20030217764 10/152782 |
Document ID | / |
Family ID | 29400523 |
Filed Date | 2003-11-27 |
United States Patent
Application |
20030217764 |
Kind Code |
A1 |
Masuda, Kaoru ; et
al. |
November 27, 2003 |
Process and composition for removing residues from the
microstructure of an object
Abstract
A process for removing residues from the microstructure of an
object is provided, which comprises steps of preparing a remover
including carbon dioxide, an additive for removing the residues and
a co-solvent dissolving the additive in said carbon dioxide at a
pressurized fluid condition; and bringing the object into contact
with the remover so as to remove the residues from the object. A
composition for removing residues from the microstructure of an
object is also provided.
Inventors: |
Masuda, Kaoru; (Kobe-shi,
JP) ; Iijima, Katsuyuki; (Kobe-shi, JP) ;
Yoshikawa, Tetsuya; (Takasago-shi, JP) ; Peters,
Darryl W.; (Stewartsiville, NJ) |
Correspondence
Address: |
REED SMITH LLP
Suite 1400
3110 Fairview Park Drive
Falls Church
VA
22042
US
|
Family ID: |
29400523 |
Appl. No.: |
10/152782 |
Filed: |
May 23, 2002 |
Current U.S.
Class: |
134/26 |
Current CPC
Class: |
B08B 7/0021 20130101;
C11D 7/3209 20130101; C11D 11/0047 20130101; C11D 7/5022 20130101;
G03F 7/425 20130101; C11D 7/32 20130101; G03F 7/422 20130101 |
Class at
Publication: |
134/26 |
International
Class: |
B08B 003/00 |
Claims
What is claimed is:
1. A process for removing residues from the microstructure of an
object comprising steps of: preparing a remover including carbon
dioxide, an additive for removing the residues, an inhibitor for
suppressing residues and a co-solvent for dissolving said additive
and said inhibitor in said carbon dioxide at a pressurized fluid
condition; and bringing the object into contact with said remover
so as to remove the residues from the object.
2. The process according to claim 1, wherein said additive includes
quaternaryammoniumfluoride.
3. The process according to claim 1, wherein said additive includes
tetramethylammoniumfluoride.
4. The process according to claim 1, wherein the concentration of
said additive is between 0.001 to 0.1 weight percent.
5. The process according to claim 1, wherein said inhibitor
includes polyhydric alcohol.
6. The process according to claim 5, wherein said polyhydric
alcohol is a dihydric alcohol.
7. The process according to claim 5, wherein said dihydric alcohol
is a propylene glycol.
8. A process for removing residues from the microstructure of an
object comprising steps of: preparing a remover including carbon
dioxide, an additive for removing the residues and a co-solvent for
dissolving said additive in said carbon dioxide at a pressurized
fluid condition; and bringing the object into contact with said
remover so as to remove the residues from the object followed by a
rinse step including rinse agent of which dielectric constant at a
temperature and pressure of 25.degree. C. and 1 at m is 78 or
larger.
9. The process according to claim 8, wherein said rinse agent is
selected from at least one of the compounds including water,
formamide, methylformamide and methylacetamide.
10. The process according to claim 8, wherein said remover includes
an inhibitor for suppressing residues.
11. The process according to claim 8, wherein said additive
includes quaternaryammoniumfluoride.
12. The process according to claim 8, wherein said additive
includes tetramethylammoniumfluoride.
13. The process according to claim 8, wherein the concentration of
said additive is between 0.001 to 0.1 weight percent.
14. The process according to claim 10, wherein said inhibitor
includes polyhydric alcohol.
15. The process according to claim 14, wherein said polyhydric
alcohol is a dihydric alcohol.
16. The process according to claim 14, wherein said dihydric
alcohol is a propylene glycol.
17. A composition for removing residue from the microstructure of
an object, comprising: carbon dioxide, a fluoride containing
additive, a co-solvent or mixture of co-solvents capable of
dissolving the fluoride containing additive, and an inhibitor.
18. The composition according to claim 17, wherein the fluoride
containing additive is a quaternary ammonium fluoride.
19. The composition according to claim 18, wherein the quaternary
ammonium fluoride is tetramethylammonium fluoride.
20. The composition according to claim 17, wherein the co-solvent
or mixture of co-solvents is ethanol, methanol, n-propanol,
isopropanol, n-butanol or dimethylacetamide.
21. The composition according to claim 20, wherein the co-solvent
is a mixture of ethanol and dimethylacetamide.
22. The composition according to claim 17, wherein the inhibitor is
propylene glycol.
23. A composition for removing residue from the microstructure of
an object, comprising: carbon dioxide, tetramethylammoniumfluoride,
ethanol, dimethylacetamide, and propylene glycol.
Description
BACKGROUND OF THE INVENTION
[0001] 1. Field of the Invention
[0002] The present invention relates to a process and a composition
for removing residues from the microstructure of an object. The
present invention specifically relates to a process and a
composition for removing residues, such as resists, generated
during a semiconductor manufacturing process from a semiconductor
wafer surface having a fine structure of convex and concave
portions.
[0003] 2. Description of the Related Art
[0004] It is required as one step in manufacturing a semiconductor
wafer to remove residues, such as photoresists, UV-hardened
resists, X-ray hardened resists, ashed resists, carbon-fluorine
containing polymer, plasma etch residues, and organic or inorganic
contaminants from the other steps of the manufacturing process. The
dry and wet removal methods are commonly used In tie wet removal
method, the semiconductor wafer is dipped in an agent, such as a
water solution, including a remover to remove residues from the
surface of semiconductor wafer.
[0005] Recently, supercritical carbon dioxide is used as such an
agent because of its low viscosity and high diffusivity. According
to such properties, cleaning with supercritical carbon dioxide
provide several advances in the treatment of microstructures, such
as high penetration into small areas between microstructures and
successfully drying microstructures because of non liquid-liquid
interface in the supercritical phase
[0006] However, supercritical carbon dioxide is not enough by
itself to remove several residues from the surface of the
semiconductor wafer. To resolve this problem, several additives to
supercritical carbon dioxide are proposed. As described in the
Japanese unexamined patent publication No. 10-125644, methane or
surfactant having CFx group is used as an additive to supercritical
carbon dioxide. In Japanese unexamined patent publication No.
8-191063, dimethylsulfoxide or dimethyl-formamide is used as such
an additive. However, based on the Inventors' studies, these
additives are not always effective for removing residues.
Especially, when the cleaning object is like a wafer which consist
of low dielectric constant materials, the quality of such wafer
decreased after treatments by such process using alkaline compounds
and water. This might be occurred because basic compounds and water
caused damages on low dielectric constant materials, especially on
materials having dielectric constant lower than 4. (hereinafter
referred to as low-k materials) Thus the present invention is
objected to provide a novel and effective cleaning without
significant damage to the low-k materials.
SUMMARY OF THE INVENTION
[0007] An object of the present invention is, therefore, to provide
a process and a composition for effectively removing residues from
the microstructure of an object without significant damages to the
low-k materials.
[0008] According to the present invention, a process is provided
for removing residues from the object, which comprises steps of
preparing a remover including carbon dioxide, an additive for
removing the residues, an inhibitor for protecting low-k damage and
a co-solvent for dissolving said additive in said carbon dioxide at
a pressurized fluid condition, and bringing the object into contact
with said remover so as to remove the residues from the object.
[0009] A composition is further provided for removing residue from
the object, which comprises carbon dioxide, a fluoride containing
additive, a co-solvent or mixture of co-solvents capable of
dissolving the fluoride containing additive, and an inhibitor.
BRIEF DESCRIPTION OF THE DRAWINGS
[0010] The foregoing and additional features and characteristics of
the present invention will become more apparent from the following
detailed description considered with reference to the accompanying
drawings in which like reference numerals designate like elements
and wherein:
[0011] FIG. 1 is a schematic diagram of an apparatus for removing
residues in accordance with the present invention.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0012] The present invention is applied to the microstructure of an
object, e.g., a semiconductor wafer having a fine structure of
convex and concave portions on its surface, and a substrate made of
a metal, plastic or ceramic which forms or remains continuous or
non-continuous layer of materials different therefrom.
[0013] First, said remover used in this invention is described. It
includes carbon dioxide, an additive for removing the residues, an
inhibitor for suppressing residues and a co-solvent for dissolving
said additive and said inhibitor in said carbon dioxide at a
pressurized fluid condition.
[0014] The pressurized carbon dioxide has a high dispersion rate
and enables the dissolved residues to disperse therein. If carbon
dioxide is converted to a supercritical condition, it penetrates
into fine pattern portions of the object more effectively. By this
feature, the additive is conveyed into pores or concave portions on
a surface of the object due to the low viscosity of carbon dioxide.
The carbon dioxide is pressurized to 5 MPa or more, but not less
than 7.1 MPa at a temperature of 31.degree. C. to convert the
carbon dioxide to a supercritical fluid condition.
[0015] Although any additives that can remove residues from
microstructures could be used, it is preferred in the present
invention to use quaternaryammoniumfluorides because of their
effective cleaning ability. The preferred fluoride compounds
includes at least one element selected from the group consisting of
tetramethylammoniumfluoride, tetraethylammoniumfluoride,
tetrapropylammoniumfluoride, tetrabutylammoniumfluoride,
cholinefluoride. Among these compounds, tetramethylammoniumfluoride
(TMAF) is the most preferable one.
[0016] If the concentration of the additive is too low, cleaning of
residues is not sufficient The lower limit of the additive is 0.001
wt %, preferably 0.005 wt %, and more preferably 0.01 wt %.
However, when the concentration is more than 0.1 wt %, low-k
materials are damaged because of excessive etching of low-k
materials. Thus, the upper range of the additive is 0.1 wt %,
preferably 0.05 wt %, and more preferably 0.03 wt %.
[0017] The remover in the present invention also includespolyhydric
alcohol. Polyhydric alcohol act as an inhibitor that protects the
low-k materials from the significant damage from the additives such
as fluorides. During inventors' studies, after some cleaning tests
of microstructures containing of low-k films, there were some
liquid-like residues. These `liquid like residues` were recognized
as byproducts originated from etching reactions between some of the
compounds in the remover and a part of low-k materials. Such
byproducts could not be removed and appeared as liquid-like
residues because such products from low-k materials were not easily
dissolved into supercritical carbon dioxide.
[0018] By further investigations, it was found that the amount of
such liquid-like residues could be reduced when polyhydric alcohols
were used as a component of said remover. Therefore, the present
invention, the remover includes polyhydric alcohols as an inhibitor
to protect low-k materials from the damage. Although the mechanism
of the protection of low-k by polyhydric alcohol is still under
investigations, polyhydric alcohol might adsorb on the surface of
the low-k materials and protect the surface from the attack of the
chemicals.
[0019] Polyhydric alcohols may be dihydric alcohol such as
ethyleneglycol, propyleneglycol, trimethyleneglycol,
diethyleneglycol, dipropyleneglycol, 1,2- , 1,3-, 1,4- or
2,3-butanediol, pentamehyleneglycol, hexyleneglycol, octyleneglycol
or trihydric alcohols such as glycerin, trimethylolpropanae,
1,2,6-hexanetriol, and tetrahydric alcohols such as
pentaelythritol. Also, polyethyleneglycol or polypropyleneglycol
may be used. Among, these compounds, dihydric alcohols are
preferable and ethyleneglycol and propyleneglycol are more
preferable.
[0020] If the concentration of the polyhydric alcohols is too low,
the protection of the low-k is not sufficient and amount of
liquid-like residues increases. The lower range of the polyhydric
alcohols is 0.005 wt %, preferably 0.007 wt %, and more preferably
0.01 wt %. However, when the concentration is higher than 0.1 wt %,
the efficiency of the protection is saturated. Thus, the upper
range of the polyhydric alocholos is 0.1 wt %, preferably 0.07 wt
%, and more preferably 0.05 wt %.
[0021] As the pressurzed carbon dioxide is not enough by itself to
dissolve additives and inhibitors such as TMAF and polyhydric
alcohols, the present invention uses co-solvent to dissolve them
into carbon dioxide. The co-solvent of the present invention is a
compound having an affinity to both carbon dioxide and the
additive. Such a co-solvent dissolves or disperses the additive
homogeneously in the pressurized carbon dioxidein fluid condition.
Although any co-solvent is used if it can make additives and
polyhydric alcohols soluble into pressurized carbon dioxide,
alcohols are preferable. The alcohol may be any alcohol, e.g.
ethanol, methanol, n-propanol, iso-propanol, n-butanol,
iso-butanol, diethyleneglycolmonomethyleter,
diethyleneglycolmonoethyleter, and hexafluoro isopropanol. Among
these alcohols, methanol ethanol and iso-propanol are preferable
because they act as a good co-solvent to wide range of
compounds.
[0022] The kind and amount of the co-solvent are selected depending
on the kind and amount of the additive to carbon dioxide. The
amount of the co-solvent is preferably five times or more than that
of the additive because the remover easily becomes homogeneous and
transparent. Alternatively, the remover may include the co-solvent
in a range of 1 wt. % to 50 wt. %. If more than 50 wt. % of the
co-solvent is added, the penetration rate of the remover decreases
due to less amount of carbon dioxide. It is prefrable to use a
remover including carbon dioxide, alcohol as the co-solvent,
quaternaryammoniumfluoride and/or quaternaryammoniumhydroxide as
the additive because these additives are well dissolved in carbon
dioxide by alcohol and are CQ philic.
[0023] When TMAF is used as an additive, TMAF should be initially
dissolved into said co-solvent because TMAF is a sold at ambient
temperature. At this time, solvents such as dimethylacetamide
(DMAC) or de-ionized water (DIW) could be added to help TMAF to be
dissolved into carbon dioxide more easily. The amount of such
solvents is preferably less than 20 times of TMAF. Especially, a
concentration of DIW should be minimized because of the damages to
the low-k materials.
[0024] The practical procedure will be described using drawings. In
the below description, components of remover other than carbon
dioxide, a mixture of additives, inhibitors, co-solvents is simply
called `cleaning reagents`. FIG. 1 shows a simplified schematic
drawing of an apparatus use for removing residues according to the
present invention. In the figure, 1 is a carbon dioxide cylinder, 2
is a high pressure pump for carbon dioxide, 3 is a storage tank of
cleaning reagents, 4 is a pump for cleaning reagents, 5 is a valve,
6 is a storage tank for rinse reagents, 7 is a pump for rinse
reagents, 8 is a valve, 9 is a high pressure vessel, and 10 is a
thermostat. Firstly, the microstructures, for example,
semiconductor wafer having residues on its surface is introduced to
and placed in a high pressure vessel 9, then carbon dioxide is
supplied from a carbon dioxide cylinder 1 to the high pressure
vessel 9 by a high pressure pump 2. The high pressure vessel 9 is
thermostated at a specific temperature by a thermostat 10 in order
to maintain the pressurized carbon dioxide in the high pressure
vessel 9 at the supercritical condition. High pressure vessel 9 can
be replaced by that having heating unit. Cleaning reagents are
supplied to the high pressure vessel 9 from tanks 3 by high
pressure pumps 4. Cleaning step starts at the time when the
cleaning reagents are fed from tank 3 to the high pressure vessel
9. The feed of the carbon dioxide and cleaning reagents may be
continuous or batch-like.
[0025] The removing process is performed at a temperature in the
range from 31.degree. C. to 120.degree. C., and at a pressure
ranged from 5 M Pa to 30 M Pa, preferably, from 7.1 M Pa to 20 M
Pa. The time required for removing the residues depends on the size
of the object, the kind and amount of the residues, which is
usually in the range from a minute to several ten minutes.
[0026] After a cleaning step, a rinse step follows. Residues
removed from surface during the cleaning step remains in the vessel
9 after the cleaning step finishes. If pure carbon dioxide is fed
into such conditions, some portion of residues will deposit on the
surface of the objects. Therefore, after the cleaning step, the
first rinse step with the mixture of carbon dioxide and rinse
agents is applied. After this first rinse step, the second rinse
step with pure carbon dioxide is applied.
[0027] Preferable rinse agents used in the first rinse step are
those that can remove liquid-like residues. After inventors'
investigations, compounds having specific dielectric constant
similar to water are effective for this purpose. Since the specific
dielectric constant of water is 78 at 25.degree. C. under
atmospheric pressure, compounds having specific dielectric constant
not smaller than 78 are used. The reason why the required specific
dielectric constants are similar to that of water is that the
liquid-like residues as byproducts of low-k etching have high
polarity, resulting in the high affinity to the polar solvents.
[0028] On the other hand, polyhydric alcohols are required in the
present invention as described in the previous section. However, if
the amount of the cleaning reagents is small enough to suppress the
by-production due to damages of low-k materials, rinse agent having
specific dielectric constant not smaller than 78 may be used with a
relative longer treatment time without any addition of polyhydric
alcohols in the cleaning step. However, in order to minimize the
process time of the first rinse step (for example, 5 min. or less),
it is preferable to minimize the by-production of liquid-like
residues with addition of polyhydric alcohols.
[0029] Practically, the first rinse step can be done by stopping
the feed of the cleaning reagents by the valve 5, followed by feed
of carbon dioxide and rinse reagents to the high pressure vessel 9
to get rid of the contents of vessel 9. A flow meter 12 may be used
to control the flow rate. During the first rinse step, it is
preferable to decrease the feed rate of rinse reagents gradually or
in a stepwise manner with valve 8 to replace the contents by pure
carbon dioxide, followed by the second rinse step with pure carbon
dioxide.
[0030] Fluid evacuated from the cleaning step and the first rinse
step can be recycled and reused by the separation into gaseous
carbon dioxide and liquid fractions by a carbon dioxide recycle
process, for example, including a liquid gas separator.
[0031] After the second rinse step, by releasing pressure with a
pressure control valve 11, carbon dioxide vaporize to gaseous
phase. Therefore, microstructures such as semiconductor wafers can
be dried without any water mark and any destructions of the
pattern.
[0032] Hereinafter, the present invention is described with
reference to experiments. Although the present invention has been
fully described by way of example with reference to the
accompanying drawings, it is to be understood that various changes
and modifications will be apparent to those skilled in the art.
Therefore, unless otherwise such changes and modifications depart
from the scope of the present invention, they should be construed
as being included therein.
EXAMPLES
Example 1
[0033] At first, in order to investigate the degree of the damage
of cleaning reagent to the low-k materials, etch rate measurements
of low-k films were carried out. Low-k films were prepared on the
silicon wafer by coating the materials consisting of organic
silicon followed by heating and drying. The film thickness of the
low-k films was about 5000 .ANG. and k-value was in the range of 2
to 3. Using cleaning tools shown in the FIG. 1, a wafer coated by
the low-k film was set into the high pressure vessel 9. After
closing the cover of the vessel 9, carbon dioxide was introduced
from carbon dioxide cylinder 1 through the pump 2. The temperature
of the vessel 9 was maintained at 50.degree. C. with a thermostat
10 and the pressure was controlled by the control valve 11. After
the pressure reached 15 MPa, cleaning reagents were fed into the
vessel 9 from the storage tank 4 through the pump 4. After a 10
minute-treatment, 5 minutes of the first rinse step was applied,
followed by 10 minutes of the second rinse step with a pure carbon
dioxide. A rinse reagent used in the first rinse step was 0.5wt %
of de-ionized water, 4.5 wt % of ethanol and 95 wt % of carbon
dioxide.
[0034] After the second rinse step, the pressure was released by
the pressure control valve 11 and wafer was taken to be provided
for further evaluation. Etch rates (.ANG./min) were calculated by
the difference in the film thickness before and after the treatment
divided by the 10 min. Film thickness was measured by an optical
measurement tool. The results are shown in table 1.
[0035] The abbreviation used in table 1 are follows;
[0036] TMAF: Tetramethylammoniumfluoride, DMAC: Dimethylacetamide,
DIW: de-ionized water, EG: Ethyleneglycol, PG: Propyleneglycol,
EtOH: Ethanol
1 TABLE 1 Componets of remover Co- Addtional Etch Additive and
inhibitor solvent solvents rate -- CO.sub.2 TMAF EG PG EtOH DMAC
DIW .ANG./min 1 95 0.013 0 0 4.9 0.063 0.024 240 2 95 0.013 0.012 0
4.9 0.051 0.024 230 3 95 0.013 0 0.012 4.9 0.063 0.024 155 4 95
0.013 0 0.024 4.9 0.051 0.024 148 5 95 0.005 0 0 5.1 0.066 0 53 6
95 0.005 0 0.012 4.9 0.054 0 19 7 95 0.013 0 0 4.8 0.165 0 91 8 95
0.013 0 0.03 4.8 0.135 0 67
Example 2
[0037] In the same manner described in the example 1, wafers coated
by the low-k film were prepared. After line and space patterns (180
nm width) were processed by the lithography on the surface,
ordinary etching by fluorocarbon gases and ashing by oxygen plasma.
After one minute cleaning with cleaning reagents listed in the
table 2 under the same condition as the example 1, five minute or
ten minute of the first rinse step using components listed in table
2, followed by ten minutes of the second rinse step with a pure
carbon dioxide. The first rinse reagents used were 0.5 wt % of
listed components, 4.5 wt % of ethanol and 95 wt % of carbon
dioxide. After the release of the pressure by opening the pressure
control valve 11, the imated wafer was taken and provided for the
evaluation. The cleaning performance was evaluated by the
observation of a scanning electron microscope (SEM) with amplitude
of 50000. The performance was checked both residues on the surface
of the line and the liquid-like residues. The criteria used for
investigation was as follows;
[0038] Excellent: No residues remained
[0039] Good: Amount of residues was less than 1 area % on the
patterned side of the wafer.
[0040] NG (Not good: Amount of residues was more than 1 area %.
[0041] The abbreviation used in table 2 are follows;
[0042] TMAF: Tetramethylammoniumfluoride, DMAC: Dimethylacetamide,
H.sub.2O: water (.epsilon.=78), DIW: de-ionized water, EG:
Ethyleneglycol, PG: Propyleneglycol, EtOH: Ethanol, FA: Formamide
(.epsilon.=111), MF: Methylformamide (.epsilon.=182), DMF:
Dimethylformamide (.epsilon.=36.7), MeOH: Methanol (.epsilon.=42),
AC: Acetone (.epsilon.=21)
[0043] According to the cleaning process described in the present
invention, low-k materials that are easily damaged by the cleaning
reagents could be protected by the use of the cleaning reagents
including inhibitors such as polyhydric alcohols added into carbon
dioxide. Besides, residues produced because of the damages of low-k
materials by the cleaning reagents could be removed by a suitable
selection of the rinse reagents. Therefore, the cleaning process
described in the present invention provide one of the optimized
cleaning processes applicable to the microstructure such as
semiconductor wafers.
2 TABLE 2 Components of remover Co- Additional 1 min cleaning + 1
min cleaning + Run Additive and inhibitor solvent solvents 5 min
1st rinse 10 min 1st rinse -- CO.sub.2 TMAF EG PG EtOH DMAC DIW
Rinse liquid-like polymer liquid-like polymer 1 95 0.013 0 0 4.9
0.063 0.024 DMF NG Excellent NG Excellent 2 95 0.013 0 0 4.9 0.063
0.024 MeOH NG Excellent NG Excellent 3 95 0.013 0 0 4.9 0.063 0.024
AC NG Excellent NG Excdllenl 4 95 0.013 0 0 4.9 0.063 0.024
H.sub.2O NC Excellent Excellent Excellent 5 95 0.013 0 0 4.9 0.063
0.024 FA Excellent Excellent Excellent Excellent 6 95 0.013 0 0 4.9
0.063 0.024 MF Excellent Excellent Excellent Excellent 7 95 0.013
0.012 0 4.9 0.051 0.024 H.sub.2O NG Excellent Excellent Excellent 8
95 0.013 0 0.012 4.9 0.063 0.024 H.sub.2O Good Excellent Excellent
Excellent 9 95 0.013 0 0.012 4.9 0.063 0.024 FA Excellent Excellent
Excellent Exccllent 10 95 0.013 0 0.024 4.9 0.051 0.024 H.sub.2O
Excellent Excellent Excellent Excellent 11 95 0.005 0 0 5.1 0.066 0
H.sub.2O Good Good Excellent Good 12 95 0.005 0 0.012 4.9 0.054 0
H.sub.2O Excellent Good Excellent Good 13 95 0.013 0 0 4.8 0.165 0
H.sub.2O Good Excellent Excellent Exccllent 14 95 0.013 0 0 4.8
0.165 0 FA Excellent Excellent Excellent Excellent 15 95 0.013 0
0.03 4.8 0.135 0 H.sub.2O Excellent Excellent Excellent
Excellent
* * * * *