Long Report

15
MPhys Long Report Gamma-Ray Spectroscopy Using a High-Purirty Germanium Detector University of Sussex Candidate Number: 107695 May 7 th 2015

description

Example

Transcript of Long Report

  • MPhys Long Report

    Gamma-Ray Spectroscopy Using a High-Purirty

    Germanium Detector

    University of Sussex

    Candidate Number: 107695

    May 7th 2015

  • i

    Gamma-Ray Spectroscopy Using a High-Purirty Germanium

    Detector

    Candidate no.: 107695

    University of Sussex

    Abstract. High-Purity Germanium detectors are used for gamma

    spectroscopy. Three reference radionuclides were used to perform an

    energy calibration. The radio-background was measured these in

    conjunction were used to find a low radioactivity mystery source

    radionuclide make up which was determined to be Radium-226

  • ii

    Preface

    The data collected for this long report was done by both me and my lab partner under the guidance of

    Simon Peeters and Phil Meek

  • Contents

    Abstract i

    Preface ii

    1 Introduction 1

    2 Background 1-6

    2.1 Gamma-ray Interactions 2

    2.1.1 Photoelectric Effect 2

    2.1.2 Compton Effect 2-3

    2.1.3 Pair Production 3

    2.2 Full Spectrum Effects 4

    2.2.1 Secondary Electron Escape 4

    2.2.2 Bremsstrahlung Escape 4

    2.2.3 Characteristic X-Ray Escape 4

    2.2.4 Secondary Radiations 4

    2.2.5 Housing Effects 4-5

    2.2.6 Summation peaks 5

  • 2.2.7 Background Radiations 5

    2.3 Semiconductors 5-6

    2.3.1 HGPe Geometry 6

    3 Experimental Apparatus 6

    4 Results 6-7

    4.1 Data Acquisition 6

    4.2 Energy Calibration 6

    4.3 Background 7

    4.4 Mystery Source 7

    5 Discussion 7-8

    6 Conclusion 8

    References 9

    Appendix A 10

  • 1 Introduction

    Gamma-ray spectroscopy enables the ability to

    determine the energy and photon count-rate of

    gamma radiation. This is useful as different

    radionuclides emit gamma photons at discrete

    energies, thereby allowing the ability to infer the

    sources of the gamma radiation [1]. In more detail if

    a radionuclidal make-up of a source needed to be

    investigated a calibrated gamma spectrometer can

    create a spectrum of energies and the count-rate of

    each of these energies; eliminating any background

    noise then referring back to theoretical or measured

    values of radionuclides spectra will identify the

    source.

    Natural radioactivity was discovered

    accidentally by Becquerel in 1896 including: alpha,

    beta and gamma radiation. In 1900 Villard noticed

    that one of the types of natural radioactivity which

    path did not bend under the influence of magnetic

    fields and was far more penetrative then the other

    types of natural radioactivity, distinguishing it and the

    name gamma-rays being coined as a label. Both of

    these were done with photographic plates, which was

    a slow process, (as they had to get developed) and

    distinguishing the different types of radiation was

    difficult. The process was improved by the creation

    of various types of gas-filled counters greatly

    improving on many of the pitfalls of the photographic

    plate. The first being created by Rutherford and

    Geiger in 1908. Generally these detectors could not

    directly determine the energy of the photons that

    were detected. The next large step in detectors was

    made by Hfstadter in 1948, the NaI(Tl) detectors

    were chemically and physically stable, boasted a

    relatively high resolution and efficiency, and could

    detect photons of energies ~1Mev. Other types of

    detectors were made including magnetic electron

    spectrometers and the diffraction spectrometers each

    with their own techniques, advantages and

    disadvantages in measuring gamma-ray transitions.

    But the next significant jump was the successful

    creation of the Ge(Li) semiconductor based detector

    in 1962 by Freck and Wakefield. These boasted

    resolutions ten-times that of the Na(Tl) detectors!

    Working effectively as a diode with its current being

    the creation of electron-hole pairs acting as charge

    carriers by the absorption and emission of incident

    gamma photons. These detectors had one main

    disadvantage however they had to be kept very cold

    at all times, (Generally liquid nitrogen temperature,

    approximately 77 K), due to the creation of electron-

    hole pairs which happens at appreciably high

    temperatures. This requires a relatively sizable

    upkeep. This has been alleviated somewhat in later

    years with the development of the high-purity

    germanium detector (HPGe) which can be

    transported and stored at room temperature [2]

    2 Background

    Gamma spectrums created by HPGe have certain

    distinct characteristics which broadly are due to one

    or more of the following categories:

    Interaction or lack thereof of gamma

    photons with matter inside the HPGe

    crystal

    Interaction of gamma photons with matter

    inside the housing

  • 2

    Near simultaneous interactions

    2.1 Gamma-Ray Interactions

    Photons interact with matter in three

    different ways:

    The Photoelectric Effect, Compton Effect or by pair

    production. The probability that any particular

    interaction will take place is a function of both the

    energy of the incident gamma photon, E, and the

    atomic number of the material the photon is

    interacting with, Z, (Fig. 2.1)

    .

    Fig. 2.1- Dominance of different interactions of

    matter [3].

    From Fig. 2.1 it is seen that at low incident

    gamma photon energies and high atomic number the

    photoelectric effect is dominant. At high energy

    incident gamma photons and high atomic number

    pair production is dominant. For intermediate photon

    energies the Compton effect is dominant.

    2.1.1 Photoelectric Effect

    In the photoelectric effect an incident

    photon approaches a material then is wholly absorbed

    by an atoms bounded electron of the material

    unbounding the electron, now called a photoelectron.

    The kinetic energy of this photoelectron, Ee-, is

    Ee-=hv - Eb where hv is the energy of the incident

    gamma photon and Eb is the workfunction to liberate

    the electron from its initial energy level. This is

    depicted in Fig. 2.2

    Fig 2.2- Pictorial representation of photoelectric

    effect [3].

    This results in a photopeak (full-energy peak)

    in the spectrum which is seen in Fig 2.3

    Fig. 2.3- Characteristic signature of photopeak with

    E being energy and

    being the count-rate.

    2.1.2 Compton Effect

    Compton scattering is the scattering of photons off a

    quasi-free electron of mass me, decreasing the energy

    of the incident photon, hv, at an angle and

    producing a recoil electron at an angle . Depicted in

    Fig. 2.4.

  • 3

    Fig. 2.4- Pictorial representation of Compton Effect

    [4]

    By energy conservation it can be shown that

    the energy of the recoil electron is

    = =

    2

    1cos()

    1+(

    2)(1cos())

    . (1)

    As any between -180 to 180 degrees is

    realised this leads to the Compton continuum and

    Compton edge in the spectrum. Fig 2.5

    Fig 2.5- Compton effect with E being energy and

    being the count-rate. [3]

    The two extremes of (1) are when =0 and

    =. When =0 the scattered photon retains all of

    its energy and the recoil electron receives zero. When

    = the photon is backscattered; this is the case of

    maximum energy transfer.

    2.1.3 Pair Production

    Pair production is the creation of an electron

    of energy Ee_ and a positron of energy Ee+. This

    happens when an incident photon of energy, hv, is in

    the strong electric field near the nucleus of a materials

    atom. There is a minimum energy contingent for this

    interaction to take place the minimum energy is

    simply the mass-energy of two electrons 2mec2 this

    leads to the following equation,

    Ee_+ Ee+= hv -2mec2. (2)

    This would lead to a peak at the point at hv -2mec2

    called the Double-escape peak In an ideal detector

    these all the gamma interactions would be absorbed

    by the detector however it is not always the case.

    Upon pair production a positron is created. In an

    electron rich environment this would almost

    instantaneously annihilate creating two 0.511 MeV

    photons. Sometimes one of the photons escapes and

    this leads to the single escape peak. Fig. 2.6

    Fig. 2.6- Real life detector showing all the different

    ways gamma photons can interact with the HPGe

    crystal [3]

    Due to the fact that pair production only happens

    above a certain threshold energy theres a splitting in

    the spectrums as depicted below. Fig 2.7

  • 4

    Fig. 2.7- two possible spectrums from the

    interactions stated above [3]

    2.2 Full Spectrum Effects

    There are more subtle effects to also look out for:

    2.2.1 Secondary Electron Escape

    For high energy gamma photons, unbound electrons

    created by the gamma-ray interaction (secondary

    electrons) will also have a high energy. Therefore a

    higher chance of escaping the detector. This will

    change the spectrum by shrinking the photopeak and

    creating a bias in the Compton continuum and other

    sources of low-energy counts such that they will be

    more highly counted relative to the higher energy

    features.

    2.2.2 Bremsstrahlung Escape

    Bremsstrahlung photons are emitted by an electron

    scattering off other nuclei. This is problematic when

    Bremsstrahlung photons are not reabsorbed by the

    detector. This changes the spectrum the same way

    secondary electrons do however can be minimised by

    using materials with a small atomic number.

    2.2.3 Characteristic X-ray Escape

    After the photoelectric effect takes place electrons in

    the atom reconfigure causing the binding energy to

    also be liberated as a characteristic X-ray. If this X-ray

    does not get detected an extra peak forms on the

    spectrum of the photopeaks energy minus the

    characteristic X-rays. Fig 2.8.

    Fig 2.8- pictorial representation and resulting

    spectrum due to X-ray escape peak [3]

    2.2.4 Secondary Radiations

    Secondary radiation are beta minus and beta plus that

    are emitted by the source instead of the intended

    gamma ray. With beta minus Bremsstrahlung

    radiation is created that can penetrate the detector.

    Beta plus will annihilate creating gamma Rays.

    2.2.5 Housing Effects

    Often gamma-rays do not interact with the detector

    however do interact with the detectors housing.

    These in turn may interact with the detector and get

    absorbed. There include:

    Housing photoelectrically absorbs photon

    emitting a characteristic X-ray which is then

    absorbed

    Photon backscatters of housing at an angle

    such that it goes into the detector and is

    absorbed

    Pair production creates a positron which

    annihilates creating a 0.511 MeV photon

    which is absorbed. Fig. 2.9

  • 5

    Fig. 2.9- Pictorial demonstration of housing effects

    and adding effects of housing on spectrum [3]

    2.2.6 Summation Peaks

    Summations peaks occur when the source emits two

    gamma photons in a very small period of time such

    that they are detected as being the one signal.

    2.2.7 Background Radiations

    Other peaks can come from background radiation.

    Contributions from the background include:

    Natural radioactivity from materials in the

    detector

    Natural radioactivity of objects near the

    detector

    Radiation from the Earths surface

    Radiation from the air

    Cosmic Radiation

    2.3 Semiconductors

    The periodic lattice of crystalline materials creates a

    continuum of energies that electrons can exist in

    comparison to discrete energy levels. These

    continuums are called bands. Forbidden energies

    exist between bands. These are aptly called band gaps.

    Two bands that are of particular interest are the

    valences band, corresponding to the outer shell

    electrons in the crystal. The other band of interest is

    the conduction band which is the band after the

    valence band. Electrons in the conduction band and

    holes (lack of electrons where one could exist)

    contribute to the materials electrical conductivity. Let

    us name the gap between the valence band and

    conduction band Eg. For semiconductors the valence

    band is full and has a small Eg this distinguishes it

    from insulators which have a big Eg .Fig 2.10. This has

    the effect that small excitations can liberate electrons

    in the valence band to the conduction band and in

    turn a hole be created in the valence band in

    semiconductors.

    Fig. 2.10- Band structures for insulators (left) and

    semiconductors (right)

  • 6

    Unfortunately thermal excitations can also have this

    effect so the apparatus needs to be immersed in liquid

    nitrogen (77 K) temperatures.

    2.3.1 HPGe Geometry

    In an ideal detection no gamma photons escape. This

    would require a large detector which would be

    expensive to run and cumbersome. To compromise

    in order to maximise the detection of gamma photons

    the HPGe has a coaxial geometry

    3 Experimental Apparatus

    To see block diagram see Appendix A

    The settings for the DPP-PHA were:

    General Energy filter

    DC offset 36 Decay time 50 s

    In range 0.6vpp Rise time 1 s

    Self trig Enabled Flat top 3 s

    Polarity positive Baseline mean 1024

    Digital gain 1 Trapezoid gain 1

    Decimation 1

    TTF

    Threshold 150 LSB

    4 Results

    4.1 Data Acquisition

    The Spectrums of three reference materials: Co-60,

    Ba-133 and Na-22 were found. (860,000 counts each)

    Fig. 4.1- Gamma spectrum for Co-60

    Fig. 4.2- Gamma spectrum for Ba-133

    Fig. 4.3- Gamma spectrum for Na-22

  • 7

    4.2 Energy calibration

    The energy calibration was found using three

    reference known radionuclides: Co-60, Ba-133 and

    Na-22.

    Fig. 4.4- Energy calibration, Bin no. vs reference

    energies of Co-60, Ba-133 and Na-22

    4.3 Background

    The radioactive background was measured (200,000

    counts) as to not measure fake peaks on the

    identification of the mystery source which is relatively

    a weak radioactive source.

    Fig. 4.5- Background spectrum

    The Compton continuum was taken away so a step

    function could be fitted to easily find all the peaks at

    once.

    Fig. 4.6- Peaks found and energies assigned to each

    on background

    4.4 Mystery Source

    The mystery sources spectrum was measured and

    identified the mystery source as Radium-226

    Fig. 4.7- Mystery source spectrum

  • 8

    Fig. 4.8- Uranium-238/Radium-226 decay chain

    (shaded regions show corresponding gamma

    spectrum found)

    5 Discussion

    With all three reference the Compton continuum and

    edge was identified; some showing shifting suggestive

    if one of the full spectrum effects. we fitted Gaussians

    to the peaks and obtained we obtained all the spectral

    lines in the NAI catalogue later cross referencing with

    a more accurate catalogue which covers the most

    abundant peaks. With all of them you could also

    identify an annihilation peak. They were all checked

    beforehand by the oscilloscope for pile-up

    When making the energy calibration we did a

    goodness of fit () and after identifying an over

    estimation of the errors due to using the standard

    deviation of the Gaussian. The error technique was

    changed as the centre of the peak was always very easy

    to distinguish, so the bin error went down from ~7.5

    bins to 1 bin obtaining a reasonable of 0.65.

    The background showed what was expected with 21

    radionuclides ranging from the Th-232, U-238 and K-

    40 families. With the biggest peak not being able to

    be identified as only 7 counts above the baseline after

    a full days detecting and only a few above the noise.

    The first single-escape and double-escape peaks were

    also seen.

    The mystery source showed very clear peaks against

    the noise however finding out what the mystery

    source was proved difficult as the NAI Catalogue

    does not show gamma emission values of

    radionuclides of certain half-life ranges. However

    after this revelation finding out the mystery source

    was quick using the other catalogue.

    6 Conclusion and Suggestions

    The mystery source was demystified as radium-226.

    Going further in this experiment could include seeing

    how the Gaussian changes as a function of energy the

    bias voltage could also be changed to see whether it

    has an effect.

    In retrospect I feel a longer detection time of both the

    background and the mystery source with that the

    smaller peaks could have been discerned.

  • 9

    References

    [1]- Knoll, G. F. (1979). Radiation Detection and

    Meaurement. 4th ed. United States of America: Wiley &

    Sons. Page 321

    [2]- Debertin, K. and Helmer, R. G. (1988). Gamma-

    and X-Ray Spectrometry with Semiconductor Detectors.

    Amsterdam: Elsevier Science. Pages 8-12

    [3]- Rittersdorf, I (2007). Gamma Ray Spectroscopy. Michagan: University of Michigan. Pages 5-44.

    [4]-

    http://hyperphysics.phyastr.gsu.edu/hbase/quantu

    m/comptint.html

  • 10

    Appendix A

    Fig A.1- Block diagram of setup

    Fig A.2- Diagram of HPGe

    and Dewar

    Computer MCA (CLEN 075730)

    HPGe Detector

    Oscilloscope

    MCA Counts

    MCA Data

    Detector Signal

    Low voltage power

    High voltage power