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170309 Low Cure PI Process set-up procedure and margin data

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No. HDM20170309-NS-01
General low temp. curable PI in HDMS
Procedure for process setup
and process margin
Technology Development Center
Hitachi Chemical DuPont MicroSystems
HD MicroSystems Confidential Info.
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Chapter 1: Procedure for process setup
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1. Items for process optimization
At prebake process
- Appearance
- Film thickness
- Uniformity
At exposure/development process
- Film retention* (Determine optimal exposure dose region)
- Pattern appearance ( Check defects such as delamination, residue or crack)
- Pattern CD ( Check mask size vs. patterned size)
* Film retention is ratio of developed thickness / prebaked thickness.
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2. XP-7100-B1 typical flow for process optimization
Step1. Coating and prebake
(1-1) Check appearance & uniformity
NG
Optimize coating recipe
or prebake conditions
(1-2) Check film thickness
NG
Optimize coating speed&time
Step 2. Exposure
Split exposure dose
Step 3. Development
(3-1) Measure film thickness at each exposure dose
(3-2) Check pattern appearance at each exposure dose
(delamination, Residue, Crack etc.)
(3-3) Check pattern CD at optimum exposure dose
NG
1. Create film retention curve
to check exposure dose.
2. Optimize dev. time, prebake
conditions or exposure dose.
NG
Step 4. Cure
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3. Process flow details
Step 1 Prebake
 Coat PI on wafer with tentative spin speed to check uniformity and film thickness.
 Apply 105ºC/120sec + 115ºC/120sec as prebake conditions tentatively.
(1) Check appearance and thickness uniformity
a. Check film appearance and thickness uniformity along with measuring film thickness after prebake.
b. If thickness uniformity is not good, coating recipe or prebake condition is necessary to be tuned.
(2) Check film thickness
File thickness (um)
a. If prebaked thickness does not meet to the target, adjust it by changing coating spin speed.
b. Spin-curve shown in page 12 helps to determine optimal spin speed.
Target thickness
Optimum coating speed
Coating speed (rpm)
Fig. Example of coarting speed vs. film thickness
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Step 2 Exposure
 Split exposure dose on a coated wafer by using stepper.
 In the case of using aligner, expose several wafers with different exposure
dose to check optimal exposure dose.
Exposure dose
X
mJ/cm2
Wafer A
2X
mJ/cm2
Wafer B
3X
mJ/cm2
Wafer C
Exposure dose : split
Focus : 0um
Fig. Exposure method 1(Stepper)
Exposure does and focus can be changed on a wafer.
Fig. Exposure method 2(Aligner)
Several wafers are needed to optimize
exposure dose by aligner.
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Step 3 Development
 Develop exposed wafer(s) by the tentative development time(10 + 10sec, double puddle)
1) Measure film thickness
a. Measure film thickness after development at each exposure dose.
b. Create film retention curve (exposure dose vs film retention) and estimate optimal exposure region
where film retention is constant (See below figure).
2) Check pattern appearance
a. Check whether there are defects such as delamination, residue or crack at each exposure dose or not.
b. If defects are observed, adjust conditions of prebake and development with changing exposure dose
over and over.
3) Check pattern CD
a. Measure and check pattern CD to see whether it is acceptable or not.
* Film retention (FR)
Film retention(%)
- FR(%) = Film thickness after dev. / Film thickness after prebake x 100
- Target exposure dose is region to obtain stable FR after development.
- Too low or too high exposure dose may give defects such as delamination, residue or crack.
Too low
dose
Ideal region
Too high
dose
Exposure dose(mJ/cm2)
Fig. Image of film retention curve
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4. Typical process conditions (Film thickness= 7,10um)
Conditions
Process
unit
Remark
Pre-spin
Coating
@7um target
@10um target
1000/10
1000/10
-
2800/30
2000/30
-
Machine
rpm/sec
Main-spin
Prebake
ºC/sec
Film thickness after prebake
um
Exposure (i-line stepper)
mJ/cm2
PEB (Post Exposure Bake)
105/120+115/120
9.7
ACT8(TEL)
Hot plate
12.9
-
-
400-600
-
FPA-3000iw
(Cannon)
ºC/sec
Not required
(Apply as necessary)
Hot plate
Development (2 step puddle)
sec
10+10
PA-401D 1)
Rinse (Spray/stream)
sec
10
PA-400R 2)
Film thickness after
development
um
Final Cure
ºC/h
7.9
11.1
200/2
1)
2)
ACT8(TEL)
-
-
under N2 gas
u-TF (Koyo)
Developer: Cyclopentanone
Rinse:Propylene glycol monomethyl ether acetate
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5. Typical coating and development recipe
Example of coating recipe
Step
Spin speed Spin time
(rpm)
(sec)
Example of development recipe
Chemical
Function
Step
Spin speed Spin time
(rpm)
(sec)
Chemical
Function
1
0
1
1
200
2
2
30
5
2
50
6
3
0
5
Dispense
3
0
4
1000
10
Pre spin
4
1000
3
5
X
Y
Main spin
5
50
6
6
800
2
6
0
7
800
3
BR-31)
Back rinse
7
1000
8
8
1200
5
BR-3
1)
Back rinse
8
800
10
PA401D+PA400R
Over rap rinse
9
1200
5
9
2000
10
PA400R 3)
Rinse
10
2000
3
10
3000
20
PI
Z
Z
PA401D
2)
4)
1st dispense
1st puddle
PA401D 2)
4)
2nd dispense
2nd puddle
Spin dry
1) Back rinse:BR-3 (Methanol/DMF(Dimethylformamide) =25/75) or
cyclopentanone
2) Developer: Cyclopentanone
3) Rinse: Propylene glycol monomethyl ether acetate
4) Standard is 10sec.
 In the coating recipe, X (main coating speed) or Y (main coating time) is tuned to meet target thickness
after prebake.
 In the development recipe, Z(puddle time) is tuned with checking performance after development.
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6. Film retention
100
Film retention (%)
90
80
70
60
i-line
50
B.B
40
30
0
200
400
600
800
1000
1200
Exposure dose (mJ/cm2)
Prebake conditions: 105ºC/120sec + 115ºC/120sec
Exposure: i-line stepper and broad band aligner
Film retention: Developed thickness / Prebaked thickness X100(%)
(Thickness:12.9um 10um after cure @200ºC/2h)
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7. Example of nozzle moving program at development
 Nozzle moving program can be changed with checking performance
(CD uniformity, residue etc.).
Wafer edge
Wafer center
Wafer edge
Dispense start
Time
Dispense end
Center
P1
Fig. Rough image of nozzle moving during developer dispense
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8. Film thickness curve
Spin time= 30sec
20
20
Film thickness (um)
Prebake
Development
Cure
15
Film thickness (um)
Spin speed= 2000rpm
10
5
Prebake
Development
Cure
15
10
5
0
0
10
1000
1500
2000
2500
3000
20
3500
30
40
50
60
70
Spin time(2000rpm/X sec)
Spin speed (X rpm/30sec)
Coating conditions vs Film thickness
Prebake conditions: 105ºC/120sec + 115ºC/120sec
Exposure: 500mJ/cm2
Cure: 200ºC/2h
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Chapter2: Process margin data
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1. Tips for getting suitable process margin

If cross-linking reaction is not enough after exposure, holding time between exposure and
development is needed (See page 15-17).
[Holding time more than 0.5hr after exposure is needed and 1-3hr is more preferable.]
 Split prebake temperature (e.g. +/- 5C or 10C) and exposure energy at the same time(See
page 20-21).
 General low temp. curable PI in HDMS is designed to be dissolved with developer easily.
10-20sec of puddle time would be enough(See page 24, 25).
[ e.g. (Dispense time 10-15sec +puddle time 10-20sec) x 2 ]
 If delamination and/or residue still emerge due to insufficient cross-linking reaction, PEB (6090C/60sec) is one of the options to promote cross-linking reaction.
 If the rinse is conducted immediately after development, there is a potential of residue by
precipitation of the dissolved film. The rinse by mixture of developer and rinse is highly
recommended to avoid residue formation (See page 9, development recipe: step 8-9) .
[Recommendation: 1.Development  2.Rinse (developer + rinse)  3.Rinse ] *
* Developer: Cyclopentanone, Rinse: Propylene glycol monomethyl ether acetate)
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2. Impact of holding time between exposure and development
100
Film retention(%)
90
80
400mJ/cm2
500mJ/cm2
70
600mJ/cm2
60
0
2
4
6
Holding time (hr)
8
10
12
Holding time vs Film retention
Prebake conditions: 105ºC/120s + 115ºC/120s
Prebaked thickness: 13um, Exposure: i-line stepper
Development:10sec+10sec
Holding time after prebake: 1hr
 Holding time (between exposure and development) more than 0.5 hour is necessary and
1-3 hours are preferable.
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2. Impact of holding time between exposure and development
30
10um via
pattern
20um via
pattern
CD size(um)
25
20
15
10
5
0
0
2
4
6
Holding time (hr)
8
10
12
Holding time vs CD size
Prebake conditions: 105ºC/120s + 115ºC/120s
Prebaked thickness: 13um
Development:10sec+10sec
Holding time after PB: 1hr
Exposure dose : 500mJ/cm2
 Holding time(between exposure and development) more than 0.5 hour is necessary and
longer holding time doesn’t impact on CD size. 1-3 hours holding time is preferable.
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2. Impact of holding time between exposure and development
Holding time
(min)
Exposure dose (mJ/cm2)
500
(HDM standard)
300
Delamination
Residue
700
Delamination
Delamination
5
Delamination and residue
60
Slight delamination
Slight delamination
-
-
Delamination
(HDM
standard)
Slight delamination
Prebake: 105ºC/120sec + 115ºC/120sec, Exposure : i-line stepper,
Development time: 10sec +10sec, Holding time after PB: 1h
 Enough holding time or exposure dose is needed to avoid delamination and/or residue.
 To conduct PEB (60-90ºC/60sec) is one of the options to shorten holding time between
exposure and development.
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2. Impact of holding time between prebake and exposure
100
Film retention(%)
90
80
400mJ/cm2
500mJ/cm2
70
600mJ/cm2
60
0
2
4
6
Holding time (hr)
8
10
12
Holding time vs Film retention
Prebake condition: 105ºC/120s + 115ºC/120s
Prebaked thickness: 13um, Exposure: i-line stepper
Development:10sec+10sec
Holding time after exposure: 1hr
 Holding time between prebake and exposure doesn’t impact on film retention.
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2. Impact of holding time between prebake and exposure
30
10um via
pattern
20um via
pattern
CD size (um)
25
20
15
10
5
0
0
4
8
12
Holding time (hr)
Holding time vs CD size
Prebake conditions: 105ºC/120s + 115ºC/120s
Prebaked thickness: 13um
Development:10sec+10sec
Holding time after exposure: 1h
Exposure dose: 500mJ/cm2(I line)
 Holding time between prebake and exposure doesn’t impact on CD size.
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3. Impact of prebake condition (Film retention)
Exposure dose vs Film retention
PB temp. vs Film retention
100
Film retention(%)
Film retention(%)
100
90
80
X = -5 ℃
X= 0℃
X = +5 ℃
70
60
90
80
70
400mJ/cm2
500mJ/cm2
600mJ/cm2
60
50
50
X = -5
200
300
400
500
600
Exposure dose(mJ/cm2)
X=0
X = +5
700
Prebake temp. (ºC)
Prebake conditions: (105 + X) ºC/120sec +(115 + X) ºC/120sec
Development: 10sec + 10sec
Film retention: (Developed thickness/ Prebaked thickness) x 100
Target thickness: 10um after cure
 Higher prebake temperature tends to lower film retention.
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3. Impact of Pre-bake condition (Resolution and CD size)
Exposure dose vs
resolution(open mask size)
PB temp. vs CD size
20
X = -5 ℃
X= 0℃
X = +5 ℃
15
CD size (um)
Resolution (um)
20
10
5
15
20um via mask
400mJ/cm2
500mJ/cm2
600mJ/cm2
10
5
10um vis mask
0
200
300
400
500
600
Exposure dose(mJ/cm2)
700
0
X= -5C
X= 0
X= +5
Change of PB temp. (℃ )
Prebake conditions: (105 + X) ºC/120sec +(115 + X) ºC/120sec
Development: 10sec + 10sec
Target thickness: 10um after cure
 The change of prebake temperature doesn’t impact on resolution and CD size.
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3. Impact of prebake conditions (Pattern profile)
Prebake condition
(105-5)C/120sec
+ (115-5)C/120sec
105C/120sec
+ 115C/120sec
(105+5)C/120sec
+ (115+5)C/120sec
Prebake conditions: (105 + X) ºC/120sec +(115 + X) ºC/120sec
Development: 10sec + 10sec
Cure: 200C/2h
Exposure dose: 500mJ/cm2
Mask size: 10um, 100um
 No significant change of pattern profile is observed even at different PB temperature.
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4. Impact of development conditions (Film retention)
Development time vs Film retention
Exposure dose vs Film retention
90
90
80
Y= -5 sec
Y= 0 sec
Y= +5 sec
Y +10 sec
70
60
50
Film retention(%)
100
Film retention(%)
100
80
70
400mJ/cm2
500mJ/cm2
60
600mJ/cm2
50
200
300
400
500
600
Exposure dose(mJ/cm2)
700
Y= -5
Y= 0
Y= +5
Y= +10
Change of Development time (sec)
Development: (10 + Y)sec + (10 + Y)sec
Prebake conditions: 105ºC/120sec +115ºC/120sec
Film retention: (thickness after dev./thickness after prebake) x 100
Target thickness: 10um after cure
 There is no big difference for FR by changing development time.
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4. Impact of development conditions (Resolution and CD size)
Development time vs CD size
Exposure dose vs
resolution(open mask size)
20
Y = -5 sec
Y = 0 sec
Y = +5 sec
Y = +10 sec
15
15
CD size(um)
Resolution (um)
20
10
5
0
20um via mask
400mJ/cm2
500mJ/cm2
600mJ/cm2
10
5
10um via mask
0
200
300
400
500
600
Exposure dose(mJ/cm2)
700
Y = -5
Y=0
X = +5
X = +10
Change of development time (sec)
Development: (10 + Y)sec + (10 + Y)sec
Prebake condition: 105ºC/120sec +115ºC/120sec
Target thickness: 10um after cure
 There is no big difference for resolution and CD size by changing development time.
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