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CONTENTS
• OBJECTIVE
• MATERIAL USED
• THEORY
• FABRICATION OF POROUS SILICON
• CHARACTERIZATION
• APPLICATION IN SENSING
• CONCLUSION
• FUTURE PERSPECTIVE
OBJECTIVE
FABRICATION OF POROUS SILICON
EFFECT ON PORE SIZE WITH INCREASING THE CURRENT DENSITY
CHARACTERIZATION OF POROUS SILICON SAMPLES
SENSING APPLICATION OF POROUS SILICON
MATERIAL USED
• SILICON WAFER
• PLATINUM ELECTRODE , ALUMINIUM PLATE
• ETHANOL , ACETONE AND DI WATER
• AMMONIUM HYDROXIDE, HYDROGEN PEROXIDE
• 10% HF SOLUTION, DIMETHYLE FLUORIDE, N-PENTANE
• HYDROCHLORIC ACID, SULPHURIC ACID, SILVER PASTE
• 1 TEFLON TWEEZER, 2 ROUND BOTTLES, 4 BEAKERS, DROPPER, PAINT BRUSH ,HEATER,SENSING SETUP
THEORY
• POROUS SILICON FIRST DEVELOPED IN 1956 BY UHLIR
• SILICON IS THE MOST DOMINANT MATERIAL USED FOR MICROELECTRONIC DEVICE.
• CRYSTALLINE SILICON IN ITS BULK APPEARANCE IS COMMONLY NOT TAKENIN TO CONSIDERATION AS OPTICAL , MECHANICAL OR BIO MEDICAL MATERIAL.
• BUT WHEN THE DIMENSIONS ARE DOWNSCALED THE PROPERTIES ARE CHANGED DRASTICALLY.
• LIGHT EMITTING PROPERTIES OCCUR DUE TO QUANTUM CONFINEMENT.
• POROUS SILICON IS INTERESTING FOR OPTICAL APPLICATIONS DUE TO ITS POROSITY.
FABRICATION OF POROUS SILICON
We have used 5 Silicon
Wafer of
 Diameter: 3” + 0.02”
 Orientation: <100>
 Thickness: 350-406 µm
 Type: P (Boron doped)
PRE-CLEANING
Rinse the sample with DI
water
Boiling(56.3 C)-Silicon
wafer in acetone
Rinse with DI water and
treatment with
ethanol(5min)
Rinse with DI water
Cleaning
Heating in NH4OH: H2O2:
DI water at (1:1:5 at 70c
for 10min)
Rinse with DI water
Dipping for 10min in 3:1
H2SO4 and H202
Rinse with DI water
Dipping in 10% HF
solution
Rinse with DI water
Heating for 10min at 75c
H2O :H2O2 :HCL (6:1:1)
Dip in 10% HF solution
Rinse with DI water
Rinse with DI water
Dry
ETCHING
• Two electrodes are needed to maintain charge neutrality
and to complete the circuit.
• Two reactions are occurring simultaneously , the
anode(oxidation) reaction and cathode(reduction)
reaction.
• Cathode is made up of Platinum wire.
• Anode is of Aluminum Plate mount with Porous sample.
• A constant current is passed between cathode and anode
immersed in HF and DMF(1:3 ratio).
Fig. Etching set-up in our laboratory
SETUP THEORY
Mechanism Of Pore Formation-
SAMPLE NAME SAMPLE IMAGE AFTER ETCHING ETCHING PARAMETERS
A Current Density = 10 mA/cm2
Etching Time = 40 minutes
Electrolyte Conc. (HF:DMF) = 1:3
Current = 0.011304A
B Current Density = 20 mA/cm2
Etching Time = 40 minutes
Electrolyte Conc. (HF:DMF) = 1:3
Current = 0.022608A
C
Current Density = 30 mA/cm2
Etching Time = 40 minutes
Electrolyte Conc. (HF:DMF) = 1:3
Current = 0.033912A
D Current Density = 40 mA/cm2
Etching Time = 40 minutes
Electrolyte Conc. (HF:DMF) = 1:3
Current = 0.044216A
E Current Density = 50 mA/cm2
Etching Time = 40 minutes
Electrolyte Conc. (HF:DMF) = 1:3
Current = 0.05652A
Sample Name E versus T Graphs
A
B
C
D
E
CHARACTERIZATION
SCANNING ELECTRON MICROSCOPY
Sample A-
Current Density = 10 mA/cm2
Sample B-
Current Density = 20mA/cm2
Sample C-
Current Density = 30 mA/cm2
Sample D-
Current Density = 40 mA/cm2
Sample E-
Current Density = 50 mA/cm2
SEM ANALYSIS
Sample No. Current Density,J Etching Time
( Minutes )
Etching Concentration
HF:DMF
Diameterof Pores (µm)
Sample A JA= 10mA/cm2 40 1:3 1.331
Sample B JB= 20mA/cm2 40 1:3 1.427
Sample C JC= 30mA/cm2 40 1:3 1.952
Sample D JD= 40mA/cm2 40 1:3 2.524
Sample E JE= 50mA/cm2 40 1:3 3.217
PL SPECTROSCOPY
Sample
Name
Current
density
(mA/cm2)
PL peak (eV)
A 10 1.72
B 20 1.78
C 30 1.86
D 40 1.93
E 50 1.98
RAMAN SPECTROSCOPY
Sample Name
Current density
(mA/cm2)
Wavenumber
(cm-1)
A 10 519.5
B 20 518.7
C 30 517.9
D 40 517.1
E 50 516.4
FTIR SPECTROSCOPY
Wave number
615
769
1281
Bonding
Si-O-Si
C-Cl
-CH2X
SAMPLE A SAMPLE B
Wave number
509
830
1256
1506
Bonding
C-Br
C-Cl
CH2X
N-O
CONTINUE……..
SAMPLE C Wavenumber
615
840
1275
1506
Bonds
Si-O-Si
C-Cl
C-N
N-O
Wave number
840
1257
1525
1859
2621
Bonds
C-Cl
C-N
N-O
CH2X
O-H
SAMPLE D
CONTINUE…
WaveNumber
632
764
863
1339
1527
Bonds
C-Br
C-Cl
=C-Hbend
N-O symmetric
N-O asymmetric
SAMPLE E
APPLICATION IN SENSING
Sensing setup
Fabricated Sensor of Sample A
Capacitive Sensing Response
Sensitivity Graph
MaximumCapacitance
PPM
CONCLUSION
• SEM IMAGES SHOWS THAT PORE SIZE INCREASE WITH INCREASE IN CURRENT DENSITY.
• PHOTOLUMINESCENCE PEAK SHIFTED TOWARDS RIGHT (BLUE SHIFT).
• RAMAN SPECTRA SHIFTED TOWARDS LEFT (RED SHIFT).
• FTIR SPECTRA SHOWS VARIOUS TYPE OF BONDS ON PS SURFACE AT DIFFERENT CURRENT DENSITY.
• POROUS SILICON SAMPLE PREPARED IS SENSITIVE TO ETHANOL VAPOR.
FUTURE PERSPECTIVE
• WE WILL PREPARE THE POROUSSILICON AT DIFFERENT HF CONCENTRATIONS AND ETCHING TIME.
• WE WILL DO COMPARATIVE STUDY WITH DIFFERENT ORGANIC SOLVENT SUCH AS DIMETHYLFORMAMIDE(DMF), DIMETHYLSULFOXIDE(DMSO) AND ACETONITRILE
(MECN).
• WE WILL DO COMPARATIVE STUDIES OF P-TYPE AND N-TYPE SILICON WAFER.
• WE WILL FIND THE SENSITIVITY, RESPONSE TIME, RECOVERY TIME ETC. FOR DIFFERENT SAMPLES UNDER DIFFERENT CONDITIONS AS MENTIONED ABOVE AND COMPARE
THESE PARAMETERS TO GET THE EFFICIENT SENSOR FROM THEM.
• WE WILL CHARACTERIZE THE DIFFERENT SAMPLES UNDER DIFFERENT CONDITIONS AS MENTIONED ABOVE AND COMPARE THEM ALL IN TERMS OF SURFACE
MORPHOLOGY, STRUCTURE MORPHOLOGY, RAMAN PEAKS AND PL ETC.
Ankit Bhardwaj PPT

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Ankit Bhardwaj PPT

  • 1.
  • 2. CONTENTS • OBJECTIVE • MATERIAL USED • THEORY • FABRICATION OF POROUS SILICON • CHARACTERIZATION • APPLICATION IN SENSING • CONCLUSION • FUTURE PERSPECTIVE
  • 3. OBJECTIVE FABRICATION OF POROUS SILICON EFFECT ON PORE SIZE WITH INCREASING THE CURRENT DENSITY CHARACTERIZATION OF POROUS SILICON SAMPLES SENSING APPLICATION OF POROUS SILICON
  • 4. MATERIAL USED • SILICON WAFER • PLATINUM ELECTRODE , ALUMINIUM PLATE • ETHANOL , ACETONE AND DI WATER • AMMONIUM HYDROXIDE, HYDROGEN PEROXIDE • 10% HF SOLUTION, DIMETHYLE FLUORIDE, N-PENTANE • HYDROCHLORIC ACID, SULPHURIC ACID, SILVER PASTE • 1 TEFLON TWEEZER, 2 ROUND BOTTLES, 4 BEAKERS, DROPPER, PAINT BRUSH ,HEATER,SENSING SETUP
  • 5. THEORY • POROUS SILICON FIRST DEVELOPED IN 1956 BY UHLIR • SILICON IS THE MOST DOMINANT MATERIAL USED FOR MICROELECTRONIC DEVICE. • CRYSTALLINE SILICON IN ITS BULK APPEARANCE IS COMMONLY NOT TAKENIN TO CONSIDERATION AS OPTICAL , MECHANICAL OR BIO MEDICAL MATERIAL. • BUT WHEN THE DIMENSIONS ARE DOWNSCALED THE PROPERTIES ARE CHANGED DRASTICALLY. • LIGHT EMITTING PROPERTIES OCCUR DUE TO QUANTUM CONFINEMENT. • POROUS SILICON IS INTERESTING FOR OPTICAL APPLICATIONS DUE TO ITS POROSITY.
  • 7. We have used 5 Silicon Wafer of  Diameter: 3” + 0.02”  Orientation: <100>  Thickness: 350-406 µm  Type: P (Boron doped)
  • 8. PRE-CLEANING Rinse the sample with DI water Boiling(56.3 C)-Silicon wafer in acetone Rinse with DI water and treatment with ethanol(5min) Rinse with DI water Cleaning Heating in NH4OH: H2O2: DI water at (1:1:5 at 70c for 10min) Rinse with DI water Dipping for 10min in 3:1 H2SO4 and H202 Rinse with DI water Dipping in 10% HF solution Rinse with DI water Heating for 10min at 75c H2O :H2O2 :HCL (6:1:1) Dip in 10% HF solution Rinse with DI water Rinse with DI water Dry
  • 9. ETCHING • Two electrodes are needed to maintain charge neutrality and to complete the circuit. • Two reactions are occurring simultaneously , the anode(oxidation) reaction and cathode(reduction) reaction. • Cathode is made up of Platinum wire. • Anode is of Aluminum Plate mount with Porous sample. • A constant current is passed between cathode and anode immersed in HF and DMF(1:3 ratio). Fig. Etching set-up in our laboratory
  • 11. Mechanism Of Pore Formation-
  • 12. SAMPLE NAME SAMPLE IMAGE AFTER ETCHING ETCHING PARAMETERS A Current Density = 10 mA/cm2 Etching Time = 40 minutes Electrolyte Conc. (HF:DMF) = 1:3 Current = 0.011304A B Current Density = 20 mA/cm2 Etching Time = 40 minutes Electrolyte Conc. (HF:DMF) = 1:3 Current = 0.022608A C Current Density = 30 mA/cm2 Etching Time = 40 minutes Electrolyte Conc. (HF:DMF) = 1:3 Current = 0.033912A D Current Density = 40 mA/cm2 Etching Time = 40 minutes Electrolyte Conc. (HF:DMF) = 1:3 Current = 0.044216A E Current Density = 50 mA/cm2 Etching Time = 40 minutes Electrolyte Conc. (HF:DMF) = 1:3 Current = 0.05652A
  • 13. Sample Name E versus T Graphs A B C D E
  • 15. SCANNING ELECTRON MICROSCOPY Sample A- Current Density = 10 mA/cm2
  • 20. SEM ANALYSIS Sample No. Current Density,J Etching Time ( Minutes ) Etching Concentration HF:DMF Diameterof Pores (µm) Sample A JA= 10mA/cm2 40 1:3 1.331 Sample B JB= 20mA/cm2 40 1:3 1.427 Sample C JC= 30mA/cm2 40 1:3 1.952 Sample D JD= 40mA/cm2 40 1:3 2.524 Sample E JE= 50mA/cm2 40 1:3 3.217
  • 21. PL SPECTROSCOPY Sample Name Current density (mA/cm2) PL peak (eV) A 10 1.72 B 20 1.78 C 30 1.86 D 40 1.93 E 50 1.98
  • 22. RAMAN SPECTROSCOPY Sample Name Current density (mA/cm2) Wavenumber (cm-1) A 10 519.5 B 20 518.7 C 30 517.9 D 40 517.1 E 50 516.4
  • 23. FTIR SPECTROSCOPY Wave number 615 769 1281 Bonding Si-O-Si C-Cl -CH2X SAMPLE A SAMPLE B Wave number 509 830 1256 1506 Bonding C-Br C-Cl CH2X N-O
  • 24. CONTINUE…….. SAMPLE C Wavenumber 615 840 1275 1506 Bonds Si-O-Si C-Cl C-N N-O Wave number 840 1257 1525 1859 2621 Bonds C-Cl C-N N-O CH2X O-H SAMPLE D
  • 26. APPLICATION IN SENSING Sensing setup Fabricated Sensor of Sample A
  • 27. Capacitive Sensing Response Sensitivity Graph MaximumCapacitance PPM
  • 28. CONCLUSION • SEM IMAGES SHOWS THAT PORE SIZE INCREASE WITH INCREASE IN CURRENT DENSITY. • PHOTOLUMINESCENCE PEAK SHIFTED TOWARDS RIGHT (BLUE SHIFT). • RAMAN SPECTRA SHIFTED TOWARDS LEFT (RED SHIFT). • FTIR SPECTRA SHOWS VARIOUS TYPE OF BONDS ON PS SURFACE AT DIFFERENT CURRENT DENSITY. • POROUS SILICON SAMPLE PREPARED IS SENSITIVE TO ETHANOL VAPOR.
  • 29. FUTURE PERSPECTIVE • WE WILL PREPARE THE POROUSSILICON AT DIFFERENT HF CONCENTRATIONS AND ETCHING TIME. • WE WILL DO COMPARATIVE STUDY WITH DIFFERENT ORGANIC SOLVENT SUCH AS DIMETHYLFORMAMIDE(DMF), DIMETHYLSULFOXIDE(DMSO) AND ACETONITRILE (MECN). • WE WILL DO COMPARATIVE STUDIES OF P-TYPE AND N-TYPE SILICON WAFER. • WE WILL FIND THE SENSITIVITY, RESPONSE TIME, RECOVERY TIME ETC. FOR DIFFERENT SAMPLES UNDER DIFFERENT CONDITIONS AS MENTIONED ABOVE AND COMPARE THESE PARAMETERS TO GET THE EFFICIENT SENSOR FROM THEM. • WE WILL CHARACTERIZE THE DIFFERENT SAMPLES UNDER DIFFERENT CONDITIONS AS MENTIONED ABOVE AND COMPARE THEM ALL IN TERMS OF SURFACE MORPHOLOGY, STRUCTURE MORPHOLOGY, RAMAN PEAKS AND PL ETC.