Applications of FTIR to Advanced Packaging Final

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Applications of FTIR Spectroscopy to Advanced Applications of FTIR Spectroscopy to Advanced Packaging Packaging John JH Reche 945 E. Verde Lane, Tempe, AZ 85284  [email protected] 11th Symposium on Polymers for Microelectronics May 6, 20 04 Wintherthur Museum and Gar dens, DE

Transcript of Applications of FTIR to Advanced Packaging Final

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Applications of FTIR Spectroscopy to AdvancedApplications of FTIR Spectroscopy to AdvancedPackagingPackaging

John JH Reche945 E. Verde Lane, Tempe, AZ 85284

 [email protected]

11th Symposium on Polymers for Microelectronics

May 6, 2004 Wintherthur Museum and Gardens, DE

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OutlineOutline Brief review of FTIR (Fourier Transform Infrared) spectroscopy

 – How does it work?

 – Data acquisition techniques

 – What information do we get?

 – Interpretation of the data

Applications to semiconductor 

 – Polymer processing – Identification of polymers

 – Plasma processing

 – Sputtering

  – Failure analysis

 – Quality control

• Incoming inspection

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Harmonic oscillator modelHarmonic oscillator model

IR radiation interacts with molecules

Bonds between atoms vibrate when absorbing specific wavelength

 – Bonds absorb energy at some characteristic frequency of their 

functional groups

 – To absorb IR energy, the vibration of a bond must induce a net change

in dipole moment as a result of vibrational or rotational motion – Simple harmonic oscillator model

 – Vibrations can be subdivided into two classes, depending on whether 

the bond length or angle is changing

• Stretching (symmetric and asymmetric)

• Bending (scissoring, rocking, wagging and twisting)

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Examples of IR induced vibrational modesExamples of IR induced vibrational modes

Energies associated with the vibrational found between 4000 cm-1

and 650 cm-1

Rotational energies are generally much smaller (below 300 cm-1)

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Preferred FTIR equipment for packagingPreferred FTIR equipment for packaging

Covers IR spectra from 4500 cm-1 to 650 cm-1

ATR (Attenuated Total Reflectance) – Sample spatial resolution < 150 µm

Micro ATR microscope Objective

 – Sample spatial resolution ~ 25 µm Reflectance microscope objective

 – Diffraction limited by microscope objective

FTIR mapping – Can spatially map absorbance over a sample

 – Invaluable to map contamination boundaries of materials

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Attenuated Total ReflectanceAttenuated Total Reflectance (ATR) set(ATR) set--upup

Most versatile instrumentation for fab

Micro diamond ATR objective to handle micro-areas – The red area indicates the IR beam path

 – Penetration depth:

where λ  is the wavelength of light,

λ c, = λ /nc and ns is the refractive index of the sample

nc is the refractive index of the internal reflection element

θ is the internal reflection element

ý is the half-angle acceptance of the microscopeobjective.

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IR Microscope Reflectance ObjectiveIR Microscope Reflectance Objective

Modified Schwarzschild all

reflective elements objective

A refractive optical element

is mounted in the center to

allow inspection of a large

field in the visible

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Removing atmospheric background absorptionRemoving atmospheric background absorption

Absorption from the atmosphere (H2O, CO2 etc.) must be

removed from the raw spectrum data

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Wavenumber vsWavenumber vs WavelengthWavelength

Why use wavenumbers? direct relationship to energy

 – The energy of light can be expressed as:

E= hc /λ = hn

• where h is Plank’s constant (6.63 × 10-34 J·s)

• c is the speed of light in vacuum (3.0 × 10 8 m·s-1)

• λ is the wavelength of the light.

In practice the IR radiant energy units are wavenumbers n

Wavenumbers are the reciprocal of the wavelength, λ

 – i.e. the number of waves per unit length

The SI unit is m –1, but a commonly used unit is cm –1.

 – Reference:• IUPAC Compendium of Chemical Terminology 2nd Edition (1997)

Conversion between wavelength and wavenumber 

ν in cm-1λ in µm4

10

1

×= λ ν 

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LambertLambert

--BeerBeer

´´s laws law

FTIR spectra can provide quantitative information

Lambert-Beer´s law correlates physical properties and chemicalcomposition :

 – The concentration of a sample can be estimated by:

 –  A = -log T ε.c.d 

 – Where:• T is the intensity of the light transmited through the sample

• ε is the molar absorption coefficient

• c is the sample concentration

• d is the sample thickness

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Practical FTIR applications in packagingPractical FTIR applications in packaging Polymer processing

 – Curing

 – Photolitho, metallization etc.

Plasma etching

 – Descuming, patterning

Identification of materials:

 – Polymer dielectrics

 – Inorganic thin films

 – Contamination

 – Unknown compounds

Analysis of formulations

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An example of polyimide spectrumAn example of polyimide spectrum

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PeaksPeaks deconvolutiondeconvolution Uncovering hidden peaks

Unmasking peak height

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Drying and Curing polymersDrying and Curing polymers

Drying of photo-sensitive materials is critical

 – Impacts photo response

Optimizing curing:

 – Determine optimum intermediate curing in multi-layer applications

• Curing level kept low for layer to promote inter-layer bonding

• Curing level high enough to withstand sputtering thermal load

 – Trade-off curing time vs temperature

 – Checking on consistency of curing level

 – Determining curing level and completion

 – Checking on the effects of novel curing methods

• Microwave

• e-beam

Optimizing curing profile

 – Ramping speed, dwell time

 – Monitoring effects of background curing atmosphere

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Evaluation of BEvaluation of B--staging a polymerstaging a polymer

Photo polymers are very sensitive to drying conditions

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Distinguishing dried and cured wafersDistinguishing dried and cured wafers

Stray wafer lot orphaned after exposure and development

 – No partial curing

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Drying photoresistDrying photoresist Optimization of positive photoresist drying

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Drying polyimideDrying polyimide Identification of material condensing on walls of a poorly

ventilated drying oven

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Monitoring product after curingMonitoring product after curing

Curing atmosphere:

 – Evaluation of thermo-oxidative and thermal stability

 – Stability check of cured polymers to environment

• Post curing oxidation in air 

 – Troubleshooting curing oven problems

Moisture absorption

Evaluation of oxygen or moisture barrier capabilities

Detection of molecular impurities or additives present in

amounts of 1% and in some cases as low as 0.01%

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Final cure temperatureFinal cure temperature Optimizing and monitoring final curing

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Monitoring effects of curing levelMonitoring effects of curing level A common bumping job-shop issue:

 – wafers from different sources may react differently

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Plasma etchingPlasma etching Detection of etching endpoint

 – contact via holes

 – polymer  – oxide

Detection of etching problems

 – Residual Fluorine on polymer surface

 – Polymer or metal oxidation

 – Polymer degradation: Identification of bonds damaged by plasma

chemistry

Cleaning of via holes

 – Very thin films are not detectable in an optical microscope

 – Over-etching and under-etching control

 – Detection and identification of residues (e.g. ash)

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Plasma etchingPlasma etching

Effect of introducing H2 in etching gas

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Plasma etching process developmentPlasma etching process development

Spectra before and after plasma etching

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Monitoring effects of processing stepsMonitoring effects of processing steps Sputtering

 – Many systems have poor thermal control (no wafer cooling)

 – Monitor effects of thermal load on polymer 

 – Cassette to cassette consistency

 – Variation of thermal load imposed within cassette

Etching (Wet and Plasma)

 – Identification of damage caused by etching chemistry

 – Optimize plasma etching gas

Photoresist removal – Wet

• Damage to underlying polymer 

• Check in conjunction with curing level

 – Plasma

• Optimizing gas mixture and timing

• Check on descuming

Cleaning materials

 – Damage caused by strong solvents used to remove solder flux

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Identification of contaminationIdentification of contamination

Flux residues:

 – Present on solder balls – Contamination of the passivation layer 

Chemical contamination of parts in processing

 – e.g. Permeation or absorption of chemicals in a polymer  Contamination of parts induced by handling, processing,

shipping etc.

Aging of vacuum roughing lubricants – Deterioration of plasma pump oil

• Acidification, oxidation or fluorination

Vacuum chamber contamination

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Identifying contaminationIdentifying contamination Degassing from improperly dryed photoresist contaminating a

stepper optical system

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Identification of Materials and ChemicalsIdentification of Materials and Chemicals

Identification of compounds

 – Matching spectrum of unknown compound with reference spectrum

(fingerprinting)

Identification of functional groups in unknown substances

Identification of reaction components and kinetic studies of 

reactions Identification of molecular orientation in polymer films

 – Need polarized IR set-up

Identification of polymers, plastics, and resins

Analysis of formulations

 – Wet etchants

 – Cleaning solutions

 – Solvents

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Monitoring SOG (SpinMonitoring SOG (Spin

--on glass)on glass)

Same SOG material on different wafers

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Plasma treatment of SiPlasma treatment of Si

33NN

44 Oxidation of the surface after O2 plasma  Electrochemical and Solid-State Letters, 5 (9) page G89-G92 (2002)

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From L. Brandner “Ozone Oxidation of Ti and Al on a Flexible Substrate for Thin Film Transistors “ U. Illinois, July 31, 2003

on a Flexible Substrate for 

Thin Film Transistors

Monitoring of oxidation of an Aluminum filmSpectra of Thin Inorganic FilmsSpectra of Thin Inorganic Films

10 A

65 A

40 A

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FTIR limitationsFTIR limitations

Molecule must be active in the IR region. (When exposed to IR

radiation, a minimum of one vibrational motion must alter the netdipole moment of the molecule in order for absorption to be

observed.)

Minimal elemental information is given for most samples.

Material under test must have some transparency in the spectral

region of interest.

Accuracy greater than 1% obtainable when analysis is done

under favorable conditions Expect accuracy of ± 5% for routine analyses

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ConclusionConclusion

FTIR is a simple and sensitive analytical tool

 – Provide fast data acquisition tool

 – Simple to operate

 – Most useful analytical tool

• to determine the composition of organic materials

• to identify IR transparent or semi-transparent inorganic films

• provides quantitative determination of compounds in mixtures

Con:

 – Interpretation of the data requires some experience

 – No useful detailed database available for the semiconductor 

processes