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Dissociation Energy of Iodine by Absorption SpectroscopyFINAL
Dissociation Energy of Iodine by Absorption SpectroscopyFINAL
Dissociation Energy of Iodine by Absorption SpectroscopyFINAL
William Harvey
8446595
School of Physics and Astronomy
The University of Manchester
Third Year Laboratory Report
March 2015
This experiment was performed in collaboration with Alex Fortnam.
Abstract
The dissociation energy of Iodine was calculated using a Birge-Sponer extrapolation on data
obtained from absorption spectra, using a white light bulb and an LED. It was found to be
4283.52 11.371 for the excited state and 13246 22.11 for the ground state.
The excited state equilibrium separation was calculated as 2.9227 0.127. Morse potential
curves were plotted for the ground and excited states.
1. Introduction
When matter is exposed to some form of radiated energy, a spectrum may be produced.
Spectroscopy is the study of this phenomenon. Originally, the interaction between matter and
electromagnetic waves in the optical region was studied, but many different forms of
spectroscopy have since arisen. The radiated energy applied need not be limited to the
optical part of the electromagnetic spectrum, nor even to electromagnetic waves. Nearly any
particle, such as the electron or the muon, may be the source of energy in the form of de
Broglie waves.
In this experiment, the iodine molecule is studied using optical spectroscopy, giving rise to a
diatomic spectrum. Photons with energies equal to the energy of a transition may be absorbed
by the iodine, which will undergo this transition then re-emit the photon and transition back
down to its original state. From this data, the dissociation energy of the Iodine molecule may
be calculated.
2. Experimental Method
2.1. The experimental setup
Our setup consisted of a source emitting light through a collimator lens into a gas tube
containing iodine molecules. Light emitted from the gas tube passed through a focusing lens,
then through the entrance slit of the spectrometer. The light was diffracted, before passing
through an exit slit identical to the entrance slit and entering a photomultiplier tube. This
photomultiplier tube was connected to a computer running data acquisition.
Figure 2
The
apparent
spectral
power
distribution
of
the
LED
was
also
recorded:
Figure 3
Figure 4
A cadmium spectrum was then recorded electronically. Spectra recorded by the software are
produced with values in terms of , necessitating finding the wavelength- relationship.
Using the linear relationship the values of peaks in the calibration spectra were converted to
wavelength values and matched to reference values for cadmium. There is a small quadratic
offset in the relationship between wavelength and , and thus a quadratic fit was applied to
the data (see figure 5), using the lsfr26.m script [2].
Figure 5
3. Theory
3.1. Blazed reflection diffraction grating
The diffraction grating reflected incident light in a direction dependent on wavelength, so
only one wavelength would be able to propagate through the spectrometer (figure 6). A
blazed grating has teeth ruled in its surface, minimising the intensity of any diffraction that is
not first order. The grating equation is:
+ =
(1)
where is the incident angle of the light, is the angle of reflection, is the number of teeth
ruled per millimetre, m is the diffraction order and is the wavelength of the light.
(2)
where is the total internal energy, is the electronic energy, is the vibration
energy and is the rotational energy, where:
103 106
Within each electronic state, there are many vibrational energy levels and within each
vibrational state there are many rotational energy levels, giving coarse vibrational and fine
rotational structure in spectra.
3.3. Vibration
Vibration in the iodine molecule occurs about the equilibrium internuclear separation
distance - the point for which the potential energy is minimised. The vibrational energy is
quantised, with a vibrational quantum number of . Molecular vibration may be
approximated as simple harmonic, but this approximation is poor. Anharmonicity in real
molecules is not negligible, causing higher vibrational levels to crowd together.
Dividing (2) by with in units of 1 gives term-values with units 1:
= + +
(3)
where is the total energy term, is the vibrational energy term and the rotational
energy term [4]. Working in these units allows the energy of a transition to be expressed in
terms of the wavenumber of the transition (the reciprocal of the photon wavelength). All
parameters corresponding to the excited electronic state are primed () and all parameters
corresponding to the lower electronic state will be double primed () from this point onwards.
An electronic-vibrational transition neglecting the rotational energy will therefore be, from
(3):
= ( ) + ( ) + ( )
(4)
where is the wavenumber of the transition. The Boltzmann distribution of our iodine
molecules is:
(5)
where is an energy level with quantum number i, is the probability of finding a particle
in this energy level, is the Boltzmann constant, is the temperature and is the partition
function. Low vibrational levels with less anharmonicity may be approximated as simple
harmonic motion:
1
= ( + 2)
(6)
where is the reduced Plancks constant and is the angular frequency. The partition
function for (6) simplifies to:
1
(7)
(1 )
(8)
where is the probability of finding a molecule in the th vibrational level [5]. From this, it
is found that, at room temperature, almost all iodine molecules are in the = 0 state, and
the electronic transitions are between the ground state (X) and the first excited state (B),
= 0 and = 0. The vibrational energy term for a level is:
1
( ) = ( + 2) ( + 2)2
(9)
1 2
= + ( + 2) ( + 2) .
(10)
Figure 7 1 Morse potential plot calculated using parameters from our data. Diagrammatical representation of molecular
constants.
The Birge-Sponer extrapolation is a plot of the energy level spacings (in 1) between
subsequent vibrational levels against + 1, where values are applied to bands in
absorption spectra using a Deslandres Table [6]. The equation for the energy level spacing,
from equations (4), (9) and (10) is:
= 2 ( + 1)
(11)
thus is the y-intercept and 2 is the gradient of this plot. Integrating to obtain the
area of this plot is identical to summing all of the energy level spacings, giving 0 , the
dissociation energy of the B state:
0 = 0
(12)
= +
(13)
(14)
where ( ) is the energy difference between a ground state atom and an atom in the first
excited state with a value of 75891 [7].
3.4. Rotation, moment of inertia, equilibrium separation and the potential curves
A diatomic molecule may rotate around an axis passing through the centre of and
perpendicular to the bond joining them. , the moment of inertia, is:
= 2
(15)
where is the reduced mass of the molecule and is the equilibrium separation. The Morse
potential energy curve is a good approximation of the molecular potential curve [8]:
( ) = ( () 1)
(16)
(17)
where is Plancks constant. may be obtained [9] using a literature value for :
1
U( )
= + (ln(1 +
(18)
Figure 8.
27
28
29
30
()
0
0
0
0
543.47
541.18
539.89
536.87
Table 1.
A white light spectrum at room temperature, scanned across the wavelength range of interest,
was labelled from bands corresponding to = 28 up to = 40:
Figure 9. Not all of the band heads labelled for the Birge-Sponer extrapolation are labelled on this figure.
Figure 10
Figure 11
18 data points were collected for the Birge-Sponer extrapolation, with peaks matching up
closely to the reference values in Table 1.
Figure 12
From figure 12 (and using a literature value for of 2.66 [10]) we extracted molecular
parameters:
Molecular parameter
Value
127.51 1.25 1
0.935 0.162 1
4283.52 11.371
20835 22.11
13246 22.11
2.9227 0.127
8.995 0.0872
1.894 0.0721
1.143 0.1221
Figure 2
Our results are close to literature values, with the exception of . The spectra produced by
the LED source are obviously superior to the white light spectra. This suggests that laser
spectroscopy would be a logical place to continue, building on the results of this experiment.
Word count: 1980.
5. References
[1]
https://www.teaching.physics.manchester.ac.uk/lab/scripts/year3/pdfs/Iodine_Absorption/201
3_Iodine_Absorption.pdf. Accessed on 17/03/15
[2] Lsfr26.m matlab script available at http://teachweb.ph.man.ac.uk/COURSES/lsq/lsfr26.m.
Accessed on 17/03/15
[3] http://www.shimadzu.com/products/opt/oh80jt0000001uz0.html. Accessed on 17/03/15
[4], [5] http://www.tau.ac.il/~phchlab/experiments_new/LIF/theory.html/ Accessed
on 17/03/15
[6] ROSEN, B., editor, "Tables de Constantes et Donnks Numkriques, 4, Donnkes
Spectroscopiques," Hemann and Co., Paris V, 1951.
[7] Gaydon, A. G., Dissociation Energies, Chapman and Hall, London, 2nd Ed., Rev.,
1953.
[8] Morse, P.M., Phys. Rev., 34, 57 (1929)
[9], [10] I.J.McNaught, J.Chem.Edu., 1980, 57, 2, 101-105.