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Page 1: Introduction to optical spectroscopy Chemistry 243.

Introduction to optical spectroscopy

Chemistry 243

Page 2: Introduction to optical spectroscopy Chemistry 243.

Fundamentals of electromagnetic radiation

34Planck's constant 6.626 10 J s

=frequency in Hz

E h

h

8 mspeed of light 3.00 10 s=wavelength

c

c

(s-1)Eswavenumbercm

11

hE c

Page 3: Introduction to optical spectroscopy Chemistry 243.

Electromagnetic spectrum

http://www.yorku.ca/eye/spectrum.gif

HighEnergy

LowEnergy

Page 4: Introduction to optical spectroscopy Chemistry 243.

Terminology Spectroscopy is the study of the interaction of

light and matter NMR or X-Ray spectroscopy; spectroscopist

Spectrometry is the establishment of the pattern of interaction (as a function of energy) of light with particular forms of matter Mass spectrometry (MS); spectrometrist

Spectrophotometry is the quantitative study of the interaction of light with matter UV-Visible spectrophotometry (I’ve never heard anyone called a spectrophotometrist)

Page 5: Introduction to optical spectroscopy Chemistry 243.

What chemical and/or material properties can we measure using spectral methods? Broad and powerful applications Elemental composition (often metals; CHNO) Identity of a pure substance (what is it?) Components of a mixture (purity?) Amount of a substance in a mixture (how much?) Bulk/major component, minor component,

trace component, ultra-trace component Surface composition Material property (stress/strain, polymer cross-

linking, change of state, temperature) Reaction rate, mechanism, products

Page 6: Introduction to optical spectroscopy Chemistry 243.

What properties of incident or generated light can we measure?

Absorption Fluorescence (fast) & Phosphorescence (slow) Thermal Emission Chemiluminescence Scattering Refraction or Refractive Index Polarization, Phase Interference/Diffraction Coherence Chemistry consequent to the above

Page 7: Introduction to optical spectroscopy Chemistry 243.

What atomic/molecular properties affect or are affected by light?

Rotation (typically refers to a molecule) Vibration (typically refers to a molecule) Electronic Excitation (atomic or molecular) Ionization (loss of electron to yield a cation) Combinations of the above:

Rotation-vibration (infrared/Raman) Rotational, vibrational, electron excitation (UV-Vis) Ionization with UV absorbance (strong excitation)

Page 8: Introduction to optical spectroscopy Chemistry 243.

The properties you want to studyhelp to select a suitable wavelength

High Energy

Low Energy

Page 9: Introduction to optical spectroscopy Chemistry 243.

Why wavenumber?

The energy difference between two wavenumbers is the same regardless of spectral region or λ

Wavelength is not proportional to energy; it has a reciprocal relation to energy, so:

The energy difference between two wavelengths (in nm or angstroms) varies as a function of spectral region.

11 cmunit

)(

hcE

hc

hc

hE

c

E1

Page 10: Introduction to optical spectroscopy Chemistry 243.

Selecting the right optical method

Page 11: Introduction to optical spectroscopy Chemistry 243.

Emission

Plasma, flame, or chemical

Focus

Sorting of Energy,

Space, and Time

Detection

Computer control enhances and optimizes the info extracted from each

instrument component.

Excitation Source

Chemiluminescence is emissioncaused by a chemical reaction.

Fluorescence is emissioncaused by excitation

Page 12: Introduction to optical spectroscopy Chemistry 243.

Absorption

Light Source Focus Specimen Focus

Energy, Space, and

Time SortingDetection

Transmissionand/or

Reflection canalso occur

Nearly linear light path geometryfor multi-wavelength,

simultaneous light detection

Relaxation is non-radiative;sample warms up a bit via vibration and rotation

Ab

so

rba

nc

eWavelength (λ)

Page 13: Introduction to optical spectroscopy Chemistry 243.

Fluorescence (fast) & Phosphorescence (slow)

Light Source

(Laser)

Focus

Focus Detection

Specimen

Energy, Space, and

Time Sorting

May include energy sorting

Typical geometry 90°, but angle variable

Em

issi

on

Po

wer

Radiative

Page 14: Introduction to optical spectroscopy Chemistry 243.

Raman Scattering

Light Source

Laser

Focus

Focus Detection

Specimen

Energy, Space, and

Time Sorting

Typical geometry 90°, but angle variable

Same geometrical layout as fluorescence and phosphorescence,… But what happens is not the same as absorption or emission

Page 15: Introduction to optical spectroscopy Chemistry 243.

Raman Scattering

Elastic scattering: Eex = Eout

Inelastic scattering: Ein < Eout and Ein > Eout Eexcitation

Eex +E-E

virtual statevirtual state

Page 16: Introduction to optical spectroscopy Chemistry 243.

Emission

Flame, plasma, chemistry

Absorbance(UV/Vis or IR)Lamps, LEDs

Fluorescence/Phosphoresence

Lamps, LEDs, lasers

lasers

Raman scattering

Different classes of optical spectroscopy

Page 17: Introduction to optical spectroscopy Chemistry 243.

Classes of light sources

Page 18: Introduction to optical spectroscopy Chemistry 243.

Light sources:Common examples

Blackbody radiation Light emitting diode (LEDs) Arc lamp/hollow cathode lamp Lasers

Solid-state Gas/excimer Dye laser

Thermal excitation Combinations (laser to vaporize

sample leading to thermal emission)

Page 19: Introduction to optical spectroscopy Chemistry 243.

Continuum spectra and blackbody radiation

6

6

6

2.898 10 K nm

2.898 10 K nm9.82 m

295 K

2.898 10 K nm9.35 m

310 K

peak

roomtemp

human

T

A solid is heated to incandescence It emits thermal blackbody radiation in a continuum

of wavelengths

Skoog, Fig. 6-22

High E = Low λ = High T

T

bblackbodypeak Wien’s

Law

b is Wein’s displacement constant

Page 20: Introduction to optical spectroscopy Chemistry 243.

Continuum spectra and blackbody radiation

http://en.wikipedia.org/wiki/Image:Blackbody-lg.pnghttp://en.wikipedia.org/wiki/Black_body

T ≈ 1200° CT ≈ 1473 K

Page 21: Introduction to optical spectroscopy Chemistry 243.

Continuum sources Common sources

Deuterium lamp (common Ultraviolet source) Ar, Xe, or Hg lamps (UV-vis)

Not always continuous; spectral structure possible

http://www1.union.edu/newmanj/lasers/Light%20Production/LampSpectra.gifhttp://creativelightingllc.info/450px-Deuterium_lamp_1.png

Page 22: Introduction to optical spectroscopy Chemistry 243.

Light emitting diodes (LEDs) First practical visible region LED

invented by Nick Holonyak in 1962 (GE; UIUC since 1963) “Father of the light-emitting-diode”

http://en.wikipedia.org/wiki/Nick_Holonyakhttp://upload.wikimedia.org/wikipedia/commons/7/7c/PnJunction-LED-E.PNG

http://www.pti-nj.com/images/TimeMasterLED/LED-spectra_remade.gif

An LED is a semiconductorwhich emits electroluminescence

Page 23: Introduction to optical spectroscopy Chemistry 243.

Light emitting diodes (LEDs) Cheap, low energy, long-lasting, small, fast Commonly used in display screens, stoplights,

circuit boards as state indicators Lots of colors Infrared LEDs used in remote controls

http://en.wikipedia.org/wiki/File:Verschiedene_LEDs.jpg

Page 24: Introduction to optical spectroscopy Chemistry 243.

Line (emission) sources

Continuous wave Hollow cathode discharge lamp Microwave discharge Flames and argon plasmas

Pulsed Pulsed hollow cathode Spark discharge

All these are non-laser

A line source is a light sourcethat emits at a narrow wavelength

called an emission “line”

Page 25: Introduction to optical spectroscopy Chemistry 243.

Lasers

Light Amplification byStimulated Emission

of Radiation

• Intense light source• Narrow bandwidth (small range λ < 0.01 nm)• Coherent light (in phase)

Page 26: Introduction to optical spectroscopy Chemistry 243.

Lasers

Light Amplification byStimulated Emission

of Radiation

• Pumping• Spontaneous Emission• Stimulated Emission• Population Inversion

Page 27: Introduction to optical spectroscopy Chemistry 243.

Laser design

Lasing medium is often: • a crystal, like ruby• a dye solution• a gas or plasma

A photoncascade!

Skoog, Fig. 7-4

Page 28: Introduction to optical spectroscopy Chemistry 243.

Pumping

Generation of excited electronic states by thermal, optical, or chemical means.

Skoog, Fig. 7-5

Page 29: Introduction to optical spectroscopy Chemistry 243.

Spontaneous emission or relaxation Random in time No directionality Monochromatic (same λ), but incoherent (not in phase) Solid vs. dashed line – 2 different photons

Skoog, Fig. 7-5

Page 30: Introduction to optical spectroscopy Chemistry 243.

Stimulated emission

The excited state is struck by photons of precisely the same energy causing immediate relaxation

Emission is COHERENT Emitted photons travel in same direction Emitted photons are precisely in phase

Skoog, Fig. 7-5

Page 31: Introduction to optical spectroscopy Chemistry 243.

Population inversion

When the population of excited state species is greater than ground state, an incoming photon will lead to more stimulated emission instead of absorption. Inverted population

Normal population distribution

Pexcited > Pground

Pexcited < Pground

Skoog, Fig. 7-6

Page 32: Introduction to optical spectroscopy Chemistry 243.

3- and 4-state lasers

Population inversion easier in 4-state system

Skoog, Fig. 7-7

Things stackup here.

Populationinversion easily

achieved.

Populationrelatively low

down here

Page 33: Introduction to optical spectroscopy Chemistry 243.

Laser design

Lasing medium is often: • a crystal, like ruby• a dye solution• a gas or plasma

A photoncascade!

Skoog, Fig. 7-4

Page 34: Introduction to optical spectroscopy Chemistry 243.

Continuous wavelaser sources Nd3+:Yttrium aluminum garnet (YAG: Y3Al5O12)

Solid state 1064 nm, 532 nm, 355 nm, 266 nm

The GTE Sylvania Model 605, uses a Nd-YAG laser rod set in a "double elliptical“ reflector, is pumped by two 500-W incandescent lamps, and is limited to a low order mode by an aperture in the laser cavity.

Page 35: Introduction to optical spectroscopy Chemistry 243.

Continuous wavelaser sources Helium-Neon (HeNe)

Gas, but emission comes from generated plasma (very excited state atoms)

632.8 nm, 612 nm, 603 nm, and 543.5 nm; 1.15 & 3.39 μm Emission lines all the way out to 100 μm

99.9% reflective

99% reflective

Page 36: Introduction to optical spectroscopy Chemistry 243.

Continuous wavelaser sources Ar+

Gas laser, but emission comes from ions Uses lots of electrical power to generate ions

351.1 nm, 363.8 nm, 454.6 nm, 457.9 nm, 465.8 nm, 476.5 nm, 488.0 nm, 496.5 nm, 501.7 nm, 514.5 nm, 528.7 nm, 1092.3 n

Coherent Innova 90Up to 5 W of output!~100x my laser pointer

Page 37: Introduction to optical spectroscopy Chemistry 243.

Other continuous wavelaser sources Cu vapor

520 nm HeCd

440 nm, 325 nm Dye lasers

Page 38: Introduction to optical spectroscopy Chemistry 243.

Pulsed lasers sources Nd:YAG

Solid state Often nanosecond pulses 1064 nm, 532 nm, 355 nm

Ti:sapphire Solid state—often pumped by Nd:YAG Tunable output aroudn 800-1200 nm Produces femtosecond pulses

Nitrogen Gas 337 nm

Excimer lasers (gas mixtures; excited state is stable) Tunable dye lasers (λ is selective within limits)

Page 39: Introduction to optical spectroscopy Chemistry 243.

Laser diodes

Used in CD and DVD players (not very strong)

Wavelengths now available from IR to near UV regions

Band gapenergy, Eg

Skoog, Figs. 7-8 & 7-9.

ResonantCavity emitsAt 975 nm

Page 40: Introduction to optical spectroscopy Chemistry 243.

Tip going forward

Keep your variables straight v for velocity or for frequency

Microsoft equation editor gives:

I will use m for integer, textbook uses n Easy to get mixed up with refractive index, n

(m/s) vee

(1/s)nu

v

Page 41: Introduction to optical spectroscopy Chemistry 243.

Properties of electromagnetic radiation

Transmission Refraction Reflection Scattering Optical Components Interference Diffraction

Page 42: Introduction to optical spectroscopy Chemistry 243.

Properties of electromagnetic radiation

tAy

tAy

2sin

2

sin

y = magnitude of the electric field at time tA = ymax – also called the amplitude of yν = frequency in s -1 (cycles per second)φ = phase angle (an offset relative to a reference sine wave)ω = angular velocity in radians/sec (a handy definition)

Recall: π radians = 180 degrees

Page 43: Introduction to optical spectroscopy Chemistry 243.

Constructive Interference - In Phase

-7

-6

-5

-4

-3

-2

-1

0

1

2

0 2 4 6 8 10 12

Time

Am

plit

ud

e

A

B

A+B

B is in phase with A

Interference – magnitudes add or subtract

Page 44: Introduction to optical spectroscopy Chemistry 243.

Destructive Interference - Half Wave Shift

-7

-6

-5

-4

-3

-2

-1

0

1

2

0 2 4 6 8 10 12

Time

Am

plit

ud

e

A

B

A+B

B is 180 degrees (π radians) shifted from A

Interference – magnitudes add or subtract

Page 45: Introduction to optical spectroscopy Chemistry 243.

Interference -- Quarter Wave Shift

-7

-6

-5

-4

-3

-2

-1

0

1

2

0 2 4 6 8 10 12

Time

Am

plit

ud

e

AB

A+B

B is 90 degrees (π / 2 radians) shifted from A

Interference – magnitudes add or subtract

Page 46: Introduction to optical spectroscopy Chemistry 243.

Interference between waves of different frequency

Wave 1 + 2

21

Skoog, Fig. 6-5

Page 47: Introduction to optical spectroscopy Chemistry 243.

Transmission through materials Compared to vacuum, the velocity of light is reduced

when propagating through materials that have polarizable electrons. Wavelength also decreases All electrons are polarizable to some extent

ii

cn

v

Skoog, Fig 6-2.

mediumc

constant

hE

cvacuum = 2.99792 x 108 m ● s-1

Page 48: Introduction to optical spectroscopy Chemistry 243.

Index of Refraction

Refractive index is measure of how much light is slowed:

Refractive index is wavelength- and temperature-dependent for many materials:

1.46Quartz

1.49Toluene

1.43Hexadecane

1.58Glass(light flint)

1.33Water

1.00Vacuum (air)

n @ 589.3 nmMaterial Wavelength-dependence of nSiO2

http://www.rp-photonics.com/refractive_index.html

nwater vs Temperature

1.316

1.318

1.32

1.322

1.324

1.326

1.328

1.33

1.332

1.334

1.336

0 20 40 60 80 100

temperature (oC)

refr

ac

tiv

e in

de

x

lengthgiven wave aat velocity

1)(lengthgiven wave aat index refractive

i

i

vacuumi

v

v

cn

Page 49: Introduction to optical spectroscopy Chemistry 243.

Refraction Snell’s law:

Oil immersion lenses for high magnification microscopy

2

1

1

2

2

1

sin

sin

v

v

n

n

Velocities, not frequencies

Medium 1Medium 2

Here, n2 > n1

Skoog, Fig. 6-10

Page 50: Introduction to optical spectroscopy Chemistry 243.

For your information …

Book Error on page 141, equation 6-12:

2 medium invelocity

1 medium invelocity

sin

sin

2

1

1

2

2

1 v

v

n

n

This is correct: Snell’s Law of Refraction

Page 51: Introduction to optical spectroscopy Chemistry 243.

Reflection Amount of loss at a reflection increases with refractive

index mismatch. For right angle light entrance into a medium:

Reflective loss is angle-dependent Fresnel equations (which we will skip) Most important case is: total internal reflection

22 1

20 2 1

r n nI

I n n

1

intensityincident

intensity reflected

Page 52: Introduction to optical spectroscopy Chemistry 243.

Total internal reflection Light incident upon a material

of lesser refractive index is bent away from the normal so that the exit angle is greater than then incident angle. At the critical incident angle,

the exit angle is 90° - beam does not exit

Angles larger than the critical incident angle lead to total internal refection (TIR)

exitcriticalentry

exitcriticalentry

exitentry

nn

nn

nn

nn

sin

)90sin(sin

sinsin

sinsin

21

2211

Medium1

Medium2

nentry

nexit

1

2

Modified from Skoog

nentry > nexit

θ2 > θ1

When this is true, θ1 = critical entry angle for TIR

Page 53: Introduction to optical spectroscopy Chemistry 243.

Total internal reflection

TIR fluorescence microscopy:

http://hyperphysics.phy-astr.gsu.edu/Hbase/phyopt/totint.htmlhttp://www.olympusmicro.com/primer/techniques/fluorescence/tirf/tirfintro.html

exitcriticalentry nn sin

When this is true,θ1 = critical entry angle for TIR.

If θ1 > θcritical result is TIR.

Evanescent wave samples a very narrow slice of the sample very near

to the dielectric interfaceTypically ~200 nm

Page 54: Introduction to optical spectroscopy Chemistry 243.

Total internal reflection

TIR fluorescence microscopy:

exitcriticalentry nn sin

When this is true,θ1 = critical entry angle for TIR.

If θ1 > θcritical result is TIR.

http://hyperphysics.phy-astr.gsu.edu/Hbase/phyopt/totint.htmlhttp://www.olympusmicro.com/primer/techniques/fluorescence/tirf/tirfintro.html

Good for studying adhered cells; low background

Page 55: Introduction to optical spectroscopy Chemistry 243.

Fiber optics Extruded strands of glass

or plastic that guide light via total internal reflection. Core has higher refractive

index than cladding. Flexible Material choice allows

transmission in UV, visible, or IR

Skoog, Fig 7-39.

Follows all the rules ofSnell’s Law

Page 56: Introduction to optical spectroscopy Chemistry 243.

Scattering

Raman scattering Inelastic scattering

offset from by frequency of molecular vibrations Rayleigh scattering

Molecules or aggregates smaller than l Intensity ~ 1/l4

Mie scattering Particles large (or comparable) to l Used for particle sizing

Page 57: Introduction to optical spectroscopy Chemistry 243.

Essential optical elements

Lenses Mirrors Prisms Filters Gratings

Page 58: Introduction to optical spectroscopy Chemistry 243.

Basic optical components Mirrors

Reflection

Concave mirror is converging

Convex mirror is diverging

Prisms Refraction

Snell’s Law

1 1 2 2sin sinn n

Page 59: Introduction to optical spectroscopy Chemistry 243.

Filters Absorption filters

Cheap, visible region; colored glass

Cutoff filters – long-passshort-pass

Interference filters2

cos

2

cosinterger

air

air

dm

n

dn

mm

Skoog, Fig. 7-12

θ is usually zeroso, cos θ = 1.

Also, m is usually 1

d = thickness of dielectric layern = refractive index of dielectric medium

m = integerʹ = wavelength in the dielectric material

Page 60: Introduction to optical spectroscopy Chemistry 243.

Interference filters Almost

monochromatic

Skoog, Fig. 7-13

Bandwidth of a filter is width at half-height

(aka full-width @ half-max)

Page 61: Introduction to optical spectroscopy Chemistry 243.

Diffraction of coherent radiation: Interference at work

Consequence of interference

Skoog, Figs. 6-7, 6-8

integer

sin

m

dm constructive

destructive

constructive

constructive

destructive

d = distance from slit B to C

Distance x to y is one λ

(m is the order of interference)

m is: • 0 for E• 1 for D

m used here, text uses n

Page 62: Introduction to optical spectroscopy Chemistry 243.

Diffraction of coherent radiation: Interference at work

Consequence of interference

integer

sin

m

dm

(m is the order of interference)

OD

DEBC

dm

sin

m used here, text uses n

You can now determine thewavelength of light

based on things thatare easy to measure!

Skoog, Fig. 6-8

Page 63: Introduction to optical spectroscopy Chemistry 243.

Monochromators

Used to spatially separate different wavelengths of light: prisms, gratings

Czerny-Turner grating monochromatorBunsen prism monochromator

Skoog, Fig. 7-18

Page 64: Introduction to optical spectroscopy Chemistry 243.

Gratings and monochromatorsReflection + diffraction: echellette-type grating

sin

sin

sin sin

m CB BD

CB d i

BD d r

m d i r

Skoog, Fig. 7-21

The condition forconstructive interference.

The m = 1 line is most intense.

The surface contains “grooves” or “blazes”.

Take a look atExample 7-1,

Page 184.

Page 65: Introduction to optical spectroscopy Chemistry 243.

Monochromators

Used to spatially separate different wavelengths of light: prisms, gratings

Czerny-Turner grating monochromator

Skoog, Fig. 7-18

Page 66: Introduction to optical spectroscopy Chemistry 243.

Useful metrics for monochromators Dispersion (page 185); high dispersion is good

Integration of at constant i gives the angular dispersion:

Linear dispersion, D, is the variation of λ along the focal plane position, y:

Reciprocal linear dispersion, D-1:

sin sinm d i r

cos

dr m

d d r

focal length

dy f drD

d df

1 cos for small r

d d r dD

dy mf mf

r = angle of reflectiond = distance between blazes

More useful, results inD-1 in nm per mm

or similar

A measure ofthe ability to

separate wavelengths

Page 67: Introduction to optical spectroscopy Chemistry 243.

Useful metrics for monochromators—continued Resolving power (R; unitless)

Limit of monochromator’s ability to distinguish between adjacent wavelengths.

Light gathering power (f-number, F; unitless) Collection efficiency—improve for maximizing S/N Efficiency scales as the inverse square of F

focal length of collimating mirror or lens

diameter of collimating optic

F f d

f

d

dilluminate blazes grating ofNumber

(unitless)

N

mNR

2

f

dE

Page 68: Introduction to optical spectroscopy Chemistry 243.

Complications with monochromators

Overlap of orders m = 1, l= 600 nm and m = 2, l = 300 nm spatially overlap

You can get ’s mixed up if light source contains many wavelengths

Additional wavelength selection often needed Filter, prism, detector λ selection device, digital

analysis after data collection, background subtraction

Might need to use a different light source if your wavelength of interest is not “clean”

Page 69: Introduction to optical spectroscopy Chemistry 243.

Slit width and spectral resolution of a spectrometer Tradeoff exists between sensitivity and resolution

High intensity = high sensitivity (low noise) Two basic concepts:

If you make the entrance slit width too big, you let in a lot of light (that’s good – high intensity), but it can be multi-wavelength; a large section of light dispersed in l is let in Good light intensity, poor spectral resolution

If you make the entrance slit width too small, you let in less light (less intensity), but its l range is smaller Poor light intensity, good spectral resolution

Entrance slit (creates image) and exit slit (output filter) Usually the same width

Optimal slit width based upon grating dispersion

Page 70: Introduction to optical spectroscopy Chemistry 243.

Slit width

Skoog, Fig. 7-24

For just passing l2

Page 71: Introduction to optical spectroscopy Chemistry 243.

Skoog, Fig. 7-25

Ptotal

If spectral bandwidth is Dl/2, good spectral

resolution

Both entrance and exit slits

narrowed from top to bottom

Slit width

w is slit width

Page 72: Introduction to optical spectroscopy Chemistry 243.

Skoog, Fig. 7-26

Slit width

Watch the effect of adjusting the slit width and the resultant spectral bandwidth on the following data sets of benzene vapor.

w is slit width

Page 73: Introduction to optical spectroscopy Chemistry 243.

Optical Photodetectors

A. Photomultiplier tube (PMT)

B. CdS photoconductivity

C. GaAs photovoltaic cell

D. CdSe photoconductivity cell

E. Se/SeO photovoltaic cell

F. Si photodiode

G. PbS photoconducitivity

H. Thermocouple

I. Golay cell

These generally make currentor voltage when light hits them.

More sensitive

Less sensitive

Page 74: Introduction to optical spectroscopy Chemistry 243.

Ideal photodetector(photon transducer)

High sensitivity High S/N Fast response time Signal directly

proportional to # of photons detected

Zero dark current The blank is zero

counted PhotonsN

S

kPS Or, equivalently,

Page 75: Introduction to optical spectroscopy Chemistry 243.

High sensitivity High S/N Fast response time Signal directly

proportional to # of photons detected

Zero dark current The blank is zero

Ideal photodetector (photon transducer)

High sensitivity High S/N Fast response time Signal directly

proportional to # of photons

Zero dark current

S kP

darkS kP k Reality

Intrudes

Here’s what really happens:

Signal isFunction of λ

Constant darkcurrent term (non-zero)

Page 76: Introduction to optical spectroscopy Chemistry 243.

Three mainphotodetector types

Photon transducers (directly “count” photons) Photomultiplier tubes (PMTs)

Charge transfer devices Charge injection devices (CID) Charge coupled devices (CCD)

Thermal transducers Photons strike the transducer

Temp increases Temp increase increases conductivity

Current or voltage are measured

Page 77: Introduction to optical spectroscopy Chemistry 243.

Vacuum phototube

Cathode is coated with photo-emissive material

Emitted electrons are collected anode.

# of electrons is directly proportional to # of photons.

Current is easy to amplify. Usually have small dark

current. Operate at ~ 90V bias Not so portable

Skoog, Fig. 7-29.

Page 78: Introduction to optical spectroscopy Chemistry 243.

Photomultiplier tube (PMT) # of electrons is amplified

by photoelectric effect upon acceleration towards dynodes Each dynode biased ~ 90V

more positive than previous dynode (or cathode)

Voltage drop accelerates electrons to dynode cascade

Amplification: 106-107 electrons per incident photon; electron cascade

http://www.nt.ntnu.no/users/floban/KJ%20%203055/PMT.jpg

Page 79: Introduction to optical spectroscopy Chemistry 243.

Photomultiplier tube (PMT) Advantages:

Very sensitive in UV-Vis region, single photon sensitivity

Cooled PMT has very low background (kdark approaches zero)

Linear response Fast response

Disadvantages Easily damaged by intense (ambient)

light Noise is power dependent Single channel: can’t use for imaging

Page 80: Introduction to optical spectroscopy Chemistry 243.

Photovoltaic cell Light strikes a

semiconductor (Se) and generates electrons and holes

Magnitude of current is proportional to # of photons

Requires no external power supply!

Disadvantages: hard to amplify signal and fatigue (wears out)

Useful for portable analyses, field work, outdoor setting

Skoog, Fig. 7-28

Page 81: Introduction to optical spectroscopy Chemistry 243.

Photodiodes(Silicon 190-1100 nm, InGaAs 900 – 1600 nm)

Reverse-biased p-n junction Conductance goes to near

zero Photons create electron hole

pairs that migrate to opposite contacts and generate current

Battery powered Portable applications Are not as prone to some

electronic noise sources 60 Hz line noise

Skoog, Fig. 7-32

Page 82: Introduction to optical spectroscopy Chemistry 243.

Multichannel transducers

Allow simultaneous interrogation of multiple wavelengths

Imaging Photodiode arrays (1-D array) Charge-transfer devices (2-D array)

Charge-injection devices Charge-coupled device (CCD) CMOS

Page 83: Introduction to optical spectroscopy Chemistry 243.

Photodiode arrays Each diode has defined

spatial address Advantages

Multichannel (used for imaging)

More robust than PMT Disadvantages

Not as sensitive as PMT Slower response time

Common in cheaper UV-Vis instruments Often perfectly adequate

Skoog, Fig. 7-33

Page 84: Introduction to optical spectroscopy Chemistry 243.

Charge transfer devices Converts light into charge Negative-biasing leads to

increased capture of holes under pixel electrodes Potential well

Photon ejects electron and the device collects and stores charges 105-106 charges per pixel

Configured as CID or CCD

Skoog, Fig. 7-35

Schematic is for CID

Page 85: Introduction to optical spectroscopy Chemistry 243.

Charge transfer devices (continued) Charge-injection device (CID)-measures

accumulated voltage change (nondestructive read; persistent after read) Measurements can be made while integrating

Charge-coupled device (CCD)-moves accumulated charges to amplifier and readout (destructive read; gone after read) Very high sensitivity; 104-105 pixels High resolution spectral imaging

Complementary metal oxide semiconductor (CMOS) Webcam technology: CHEAP! OK sensitivity, large pixel density

Page 86: Introduction to optical spectroscopy Chemistry 243.

CCD (charge coupled device) Pixels read one at a time by sequential

transfer of accumulated charge

From: “CCD vs. CMOS: Facts and Fiction” by Dave Litwiller, in Photonics Spectra, January 2001

Page 87: Introduction to optical spectroscopy Chemistry 243.

CMOS detectors

Digital camera and webcam technology Each pixel can be read individually

From: “CCD vs. CMOS: Facts and Fiction” by Dave Litwiller, in Photonics Spectra, January 2001 Image from Wikipedia

Page 88: Introduction to optical spectroscopy Chemistry 243.

CCD CMOS Essentially serial Each pixel read one at a

time by common external circuitry Voltage conversion and

buffering Outputs an analog signal Historically gave higher-

resolution images Relatively expensive

High power consumption Up to 100x more than

CMOS

Essentially parallel Each pixel has its own red

out circuitry “on-chip” Allows amplification and

noise correction More susceptible to noise

Outputs a digital signal Reduced area for light

absorption Relatively inexpensive

Highly commercialized fab Runs on less power

Requires less “off-chip” circuitry

Both approaches exist today

Page 89: Introduction to optical spectroscopy Chemistry 243.

Photoconductivity transducers

Semiconductors whose resistance decreases when they absorb light

Absorption promotes electron to conduction band.

Useful in near IR( = 0.75 to 3 m) Cooling allows extension to longer

wavelengths by reducing thermal noise

Page 90: Introduction to optical spectroscopy Chemistry 243.

Thermal transducers

Solution for IR region (low energy photons) Thermocouples

Light absorbed heats the junction (two pieces of dissimilar metal) which leads to a change in voltage relative to a reference thermocouple.

Bolometer (thermistor) Material changes resistance as a function of temp

Pyroelectric devices Temperature-dependent capacitor Change in temperature leads to change in circuit current