Iron-Doped Zinc Selenide: Spectroscopy and Laser Development
Spectroscopy of Rare Earth Doped...
Transcript of Spectroscopy of Rare Earth Doped...
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Spectroscopy of Rare Earth Doped Glasses
Anderson S. L. [email protected]
Department of PhysicsUniversidade Federal de Pernambuco
Recife, PE, Brazil
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Rare Earth
Doped Glasses
OPTICALAMPLIFIERS
OPTICALSWITCHES
LASERS
SENSORS
PHOSPHORSID DEVICES
NANODEVICES
BASIC SCIENCE
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Recife, PE, Brazil
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UFPE
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Spectroscopy of Rare Earth Doped Glasses
Lessons Plan
Part I - Basics
I.1 Rare Earth ElementsI.2 Glass MatricesI.3 Rare Earth Doped Glasses (REDG)I.4 Theoretical AspectsI.5 Spectroscopic Techniques for Optical
Assessment
Literature
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Spectroscopy of Rare Earth Doped Glasses
Lessons Plan
Part II – Upconversion spectroscopyand Applications of REDG
II.1 Up-conversion Spectroscopy II.2 REDG Ceramics
Applications of REDGII.3 REDG for LasersII.4 REDG for Fiber Lasers and AmplifiersII.5 REDG Planar and Channel WaveguidesII.6 REDG Microbarcodes
Literature
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Spectroscopy of Rare Earth Doped Glasses
Lessons Plan
Part III – More Applications and OtherRecent Advances in RED Materials
III.1 REDG containing nanoparticlesIII.2 REDG for SensorsIII.3 Rare Earth Doped Photonic Materials
( An overview from Optical Materialsspecial issue vol 28, 575-893 (2006))
Literature
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Spectroscopy of Rare Earth Doped Lecture I
Part I - Basics
I.1 Rare Earth ElementsI.2 Glass MatricesI.3 Rare Earth Doped Glasses (REDG)I.4 Theoretical Aspects I.5 Spectroscopic Techniques for Optical
Assessment
Literature
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I.1 RARE EARTHELEMENTS
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A little bit of history …the NOT SO RARERARE EARTH ELEMENTS
....found all over (earth, moon, some stars.....);
....more abundant than Hg and I;
....first one was found in 1794 (Yttrium);
....last one was found in 1945 (Promethium);
....applications: from jewellery to nuclear industry,naturally including PHOTONICS APPLICATIONS.
I.1 RARE EARTHELEMENTS
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http://osoon.ut.ee/~hahha/re/index.html
Rare Earth Elements On The Net
General InformationHistory
PropertiesUsesLinks
I.1 RARE EARTHELEMENTS
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IN OPTICS, REE were first exploited in 1906, byBecquerel, who identified line narrowing at lowtemperatures (~85K);
Subsequent years flourished with theoretical work, driven by the development of quantum mechanics,culminating with the work by Dieke and Crosswhite(Appl. Opt. 2, 602(1963)), which is the basis forspectroscopy of REE.
G. H. Dieke
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At the end of the 1960’s, energy transfer andanti-Stokes emission became one of the importantways to study REE in crystals and glasses;
Frequency up-conversion is the experimentalmethod to study emission from frequencies higherthan the excitation frequency.I.1 RARE EARTH
ELEMENTS
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I.1 RARE EARTHELEMENTS
REE can be found as divalent, trivalent or tetravalent.
For optics, the trivalent lanthanides are therevelant ions, whose electronics distributionis as follows:
•La and Lu – closed outer shell (N= 0 and 14)
•All the others – outer shell 4f partially filled
(Those REE are the focus of our attention!)
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4f electrons are screened by the other outer-shellconfigurations (5s2 ,5p6), because the wavefunctionradius is smaller for 4f than for 5s and 5p.
I.1 RARE EARTHELEMENTS
The word lanthanide has a Greek origin(‘‘λανθανειν’’) which means ‘‘to lie hidden’’.
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Important consequences and implications:
1. Electronic states of 4f weakly affected by the host;
2. Energy spectrum is practically independent of host(which means they are determined by 4f);
3. In crystals, absorption and emission spectra verynarrow ( ~0.1nm); much broader in glasses;
4. The hamiltonian, which will be used to calculatethe energy levels, can be written as the sum ofthe free ion + a perturbative term arising from thehost:
Free ion host
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The free ion hamiltonian can be given by:
Kinetic energy
Effective Coulombian potential
Coulombian repulsion
Spin-orbit interaction
ξ(r) is the spin-orbit coupling parameter
Nt total number of eletrons ; N = 1 to 13
H0 > Hc > Hso
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Last two terms are responsible to rise the degeneracy
Spin-orbit interaction:
Arises from atom magnetic field + spin magnetic dipole
Generates a total angular momentum J = L+S
increases with atomic number
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On the other hand, the Coulombian interactiondecreases as Z increases (since the atomic radiusincreases, thus increasing the distance betweenelectrons).
http://olla.ichf.edu.pl/lect/SS2005/Buenzli_lecture1.pdf
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I.1 RARE EARTHELEMENTS
The characteristic of a quantum state is specified by the notation,
2S+1LetterJ
S = Spin angular momentumJ = Total angular momentum
Prescription for the “Letter” symbol
etc.IHGFDPSLetter
etc.6543210L
Energy levels follows spectroscopic notation:
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I.1 RARE EARTHELEMENTS
E.g.: Ground State of Neodymium
Spectroscopic Notation = 4 I 9/2
Degeneracy = 2J+1 = 10
There are 10 different wave functions describing this state.
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Element Symbol Atomic no.
Atomic wt.
Electronic state
Fundamental State
Ionic radius
Cerium Ce 58 140,12 [Xe]4f15s25p6 2F5/2 1.11
Praseodymium Pr 59 140,98 [Xe]4f25s25p6 3H4 1.09
Neodymium Nd 60 144,24 [Xe]4f35s25p6 4I9/2 1.08
Promethium Pm 61 145 [Xe]4f45s25p6 5I4 1.06
Samarium Sm 62 150,4 [Xe]4f55s25p6 6H5/2 1.04
Europium Eu 63 151,96 [Xe]4f65s25p6 7F0 1.03
Gadolinium Gd 64 157,25 [Xe]4f75s25p6 8S7/2 1.02
Terbium Tb 65 158,93 [Xe]4f85s25p6 7F6 1.00
Dysprosium Dy 66 162,5 [Xe]4f95s25p6 6H15/2 0.99
Holmium Ho 67 164,93 [Xe]4f105s25p6 5I8 0.97
Erbium Er 68 167,26 [Xe]4f115s25p6 4I15/2 0.96
Thulium Tm 69 168,93 [Xe]4f125s25p6 3H6 0.95
Ytterbium Yb 70 173,04 [Xe]4f135s25p6 2F7/2 0.94
The optically interesting REE
I.1 RARE EARTHELEMENTS
(Å)
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Energy levels for the REE in aLaCl3 crystal
G. H. Dieke andH. M. CrosswhiteAppl. Opt. 2, 675 (1963)
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I.2 GLASS MATRICES
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I.2 GLASS MATRICES
Glasses
• Amorphous solids• No crystal structure• No long-range order• Resemble “frozen liquids”
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Forming a Glass
• Requirements– Material must have high viscosity at melting point– Material must have difficulty nucleating crystal
• Procedure– Melt material to eliminate crystal structure– Cool material quickly through melting
temperature– Form supercooled liquid– Cool until solid
I.2 GLASS MATRICES
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I.2 GLASS MATRICES
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I.2 GLASS MATRICES
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I.2 GLASS MATRICES
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Some classes of Some classes of glassesglasses
OXIDESSiO2GeO2BeO3P2O5
METTALICFe - NiP - BCu - Zn
CHALCOGENIDESGa2S3 - La2S3As2S3, As2Se3Ge - Se
HALIDESZnCl2BeF2ZrF4AlF3InF3GaF3
I.2 GLASS MATRICES
ORGANICSpolymers
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I.2 GLASS MATRICES
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I.2 GLASS MATRICES
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Quartz• Quartz is silicon dioxide (silica)• Is an excellent network former
– Slow cooling forms regular network– Fast cooling forms irregular network
• High viscosity at melting point• However, nucleates crystals easily• Melting point of Quartz is very high
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I.2 GLASS MATRICES
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I.2 GLASS MATRICES
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Soda-Lime-Silica Glass• Adding sodium oxide (soda) lowers melting point• Adding calcium oxide (lime) makes it insoluble• Sodium and calcium ions terminate the network and
soften the glass• Soda-lime-silica glass is common glass
I.2 GLASS MATRICES
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Borosilicate Glass
• Soda-lime-silica glass expands much when heated– Breaks easily during heating or cooling
• Boron-oxide-silica glass expands less– Tolerates heating or cooling reasonably well
• Pyrex and Kimax are borosilicate glasses
I.2 GLASS MATRICES
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Vapour or Plasma Liquid Solid
•Evaporation•Plasma•Aerosol
•Cooling•Dissolution•Sol-gel
•Decomposition•Amorphization byirradiation
•Amorphization bygrinding• Amorphizationby wave
Methods of preparation
I.2 GLASS MATRICES
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Reagent mixing
Thermal treatment
At T< Tg.
Sample preparation:
cutting and polishing
Fusion in platinum/alumina
crucible
Fast solidification
in pre-heated brass
molde
Slow cooling untilRoom temperature
Typical glass preparation
I.2 GLASS MATRICES
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GLASS PREPARATION
I.2 GLASS MATRICES
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Several Important glass hosts
SilicatesPhosphatesBoratesGermanatesTelluritesFluorozirconateSulfidesChalcogenidesFluoroindatesAntimonyTungstates
Main differences:
Physicochemical characteristicsPreparation methodsTransmission windowPhonon Energy
I.2 GLASS MATRICES
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Phonons are a quantum mechanical version of a special type of vibrational motion, known as normal modes in classical mechanics, in which each part of a lattice oscillates with the same frequency.
A phonon is the quanta of energy of such vibrations.I.2 GLASS MATRICES http://dept.kent.edu/projects/ksuviz/leeviz/phonon/phonon.html
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REE incorporation methods
I.3 REDG-Can start from doped mixture (with REE)
Ex. Fluoroindate glass with Nd3+ and/or Pr3+
-Can incorporate element (like in fibers fabrication)
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Rare Earth Doped Glasses (REDG)
Free ion host
Let us remind that, once incorporated in the host, the REDG hamiltonian is given by:
The aperiodic glass structureintroduces variationsin the Hh term, leadingto an inhomogeneousbroadening in the linewidth
SiO2
I.3 REDG
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I.3 REDG
Inhomogeneous broadening
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Theoretical Aspects
I.4 THEORETICALASPECTS
Objective: calculate the radiative and nonradiativeREE transitions
J.H.Van Vleck J. Phys. Chem. 41 (1937) 67.Studied Absorption and Emission, atributted to 4fand mechanisms: electric dipole, electric quadrupolemagnetic dipole
Broer, Gorter, Hoogschagen; Physica 11 (1945) 231Showed that electric quadrupole and magnetic dipole could notExplain the intense emission of the REE, and forced electricDipole model would suffice.
B.R. Judd; Phys. Rev. 127 (1962) 750.G.S. Ofelt; J. Chem. Phys. 37 (1962) 511.Independently, introduced definitive formalism basedon forced electric dipole
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Possible physical process followingabsorption of a photon by a molecule
I.4 THEORETICALASPECTS
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Possible physical process followingabsorption of a photon by a molecule
I.4 THEORETICALASPECTS
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Luminescence
I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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A taste of Judd-Offelt Theory
The oscillator strength of a spectral line due to a electric dipole fundamental to excited statetransition is given by:
χ- Lorentz field correctionm – mass of electronh – Planck constantν- transition frequencyq – related to input polarizationD – atomic displacement operator
spherical harmonics
I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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I.4 THEORETICALASPECTS
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After some more manipulation, one can show that:
Judd-Ofelt parameter
I.4 THEORETICALASPECTS
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About nonradiative transitions:
where:
· AT (αJ ) is the total radiative relaxation rate;
· WT (αJ ) is the total nonradiative relaxation rate;
· τR is the excited state radiative lifetime;
· τNR is the excited state nonradiative lifetime, given by WT (αJ) -1.
I.4 THEORETICALASPECTS
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Regarding WT (αJ) the following empiricalrelation has been demonstrated
Where:
· WAB (0) is the multiphonon emission rate at lowtemperature;
· ħω is the maximum phonons energy;
· ∆E is the energy diference between the levelsinvolved in the phonon transition
•KB is the Boltzmann constant and T is thetemperature.
I.4 THEORETICALASPECTS
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Gap Law -
I.4 THEORETICALASPECTS
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Spectroscopic Techniques for Optical Assessment
I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
AbsorptionLuminescenceRaman spectroscopyBrillouin spectroscopyUp-conversion spectroscopy
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AbsorptionSample
Normally uses commercially available equipments
In the linear behaviour, the absorption coefficient αfor a sample of thickness L is given by theLambert-Beers law:
L in cm, α in cm-1
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I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
L. E. E. de Araújo, A. S. L. Gomes, C. B. de Araújo, Y. Messaddeq, A. Florez, and M. A. Aegerter, Phys. Rev. B 50, 16219 (1994).
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The absorption coefficient is related to theImaginary part of the refractive index through
Other related quantity to the absorption spectra are:
Transmission
OpticalDensity
Extinctioncoefficient(C is the concentration in mol l -1), ε in mol-1 l cm-1)
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The absorption cross section
where N is the absorption centers density in cm-3
The amount of power absorbed by an ion:
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Luminescence
133
LASER Ar+
LASER Ti:Sapphire
LENS LENS
SAMPLE
DIGITAL OSCILLOSCOPE
PC
SPEX + PMT
MECHANICAL CHOPPER
MIRROR
CCD
•cw or pulsedexcitation
•Varyingλexc whilelooking at one emissionleads toexcitationspectrum
Typical experimental setup
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I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
L. E. E. de Araújo, A. S. L. Gomes, C. B. de Araújo, Y. Messaddeq, A. Florez, and M. A. Aegerter, Phys. Rev. B 50, 16219 (1994).
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Fluorescence decay time (lifetime)
Luminescenceintensity Excitation
intensity
Decay function
Two kinds of decay times can be considered:
1) Mean durationof the fluorescence
2)
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For a purely exponential decay
Integration of the I(t) equation gives:
I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
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The quantum yield Φ of an absorbing system is given by
Where
Nem is the number of spontaneous emitted photonsper unit time
Nabs is the total number of absorbed photonsper unit time
(difficult to measure)
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We can write:
Considering negligible the T dependence of σ:
Therefore:
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In general, the fluorescence decay function isnot exponential, due to local inhomogeneities.
For most cases, it can be described by a stretchedexponential:I.5 SPECTROSCOPIC
TECHNIQUESFOR OPTICALASSESSMENT
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If two different components of the fluorescenceDecay function can be observed, then:
Where A and B described the relative amountOf the chemical species.
In particular cases when the decay curves exhibittwo well separated components, it is possibleto determine the amount of the two kinds of ionsinvolved in the process:
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I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
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Raman and Brillouin scattering for opticalglasses characterization
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I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
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GexS1-x glasses compositions with 11<x<45
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Absorption and emissioncross-section measurement
The McCumber Theory
Based on general assumptions:
1 -there is a thermal distribution of population among theindividual Stark level components of each Stark manifold.
2. the energy width of each individual Stark level is smallcompared with kBT, where kB is the Boltzmann constantand T is the absolute temperature.
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I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
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The McCumber relation states that the absorptioncross-section σa(ν) and the emission cross-sectionσe(ν) between these manifolds are related by
ε is as the net free energy required to excite one Er3+
ion from the 4I15/2 to the 4I13/2 state at temperature T:
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I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
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The effective bandwidth Δλ, related to the emissioncross-section, is defined by
Δλ = ∫σe(λ)dλ/σP(λ),
where σP(λ) is the peak value of theemission cross-section
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I.5 SPECTROSCOPICTECHNIQUESFOR OPTICALASSESSMENT
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let us have lunch!!!
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Literature
G.H. Diecke and H.M. Crosswhite Appl. Optics 2 (1963), p. 675.
G. C. Righini and M FerrariPhotoluminescence of rare-earth-doped-glassesLa Rivista del Nuovo Cimento 28, 1-53 (2006)
Oscar L. Malta and Luís D. CarlosIntensities of 4f-4f transitions in glass materialsQuim. Nova, Vol. 26, No. 6, 889-895, 2003
L. E. E. de Araújo, A. S. L. Gomes, C. B. de Araújo, Y. Messaddeq, A. Florez, and M. A. AegerterFrequency upconversion of orange light into blue light in Pr3+-doped Fluoroindate glassesPhys. Rev. B 50, 16219 (1004)