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Gamma spectroscopy

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877:. Electrons in the conduction band can respond to the electric field in the detector, and therefore move to the positive contact that is creating the electrical field. The gap created by the moving electron is called a "hole", and is filled by an adjacent electron. This shuffling of holes effectively moves a positive charge to the negative contact. The arrival of the electron at the positive contact and the hole at the negative contact produces the electrical signal that is sent to the preamplifier, the MCA, and on through the system for analysis. The movement of electrons and holes in a solid-state detector is very similar to the movement of ions within the sensitive volume of gas-filled detectors such as 270: 25: 856: 361: 82: 2056: 971: 325:
interaction or pair production, a portion of the energy may escape from the detector volume, without being absorbed. The absorbed energy thus gives rise to a signal that behaves like a signal from a ray of lower energy. This leads to a spectral feature overlapping the regions of lower energy. Using larger detector volumes reduces this effect. More sophisticated methods of reducing this effect include using
944:(Figure 1, the first peak left of the Compton edge), the so-called backscatter peak. The detailed shape of backscatter peak structure is influenced by many factors, such as the geometry of the experiment (source geometry, relative position of source, shielding and detector) or the type of the surrounding material (giving rise to different ratios of the cross sections of Photo- and Compton-effect). 770: 2068: 584: 477:
the energy of the gamma ray and usually shown as percentage. Using the preceding example, the resolution of the detector is 7.5% at 122 keV, and 12.5% at 662 keV. A typical resolution of a coaxial germanium detector is about 2 keV at 1332 keV, yielding a relative resolution of 0.15%.
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or MeV) or relative terms. For example, a sodium iodide (NaI) detector may have a FWHM of 9.15 keV at 122 keV, and 82.75 keV at 662 keV. These resolution values are expressed in absolute terms. To express the energy resolution in relative terms, the FWHM in eV or MeV is divided by
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If a gamma spectrometer is used for identifying samples of unknown composition, its energy scale must be calibrated first. Calibration is performed by using the peaks of a known source, such as caesium-137 or cobalt-60. Because the channel number is proportional to energy, the channel scale can then
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of the detector. High-efficiency detectors produce spectra in less time than low-efficiency detectors. In general, larger detectors have higher efficiency than smaller detectors, although the shielding properties of the detector material are also important factors. Detector efficiency is measured by
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To accurately determine the energy of the gamma ray, it is advantageous if the photoelectric effect occurs, as it absorbs all of the energy of the incident ray. Absorbing all the energy is also possible when a series of these interaction mechanisms take place within the detector volume. With Compton
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The energy of the gamma rays being detected is an important factor in the efficiency of the detector. An efficiency curve can be obtained by plotting the efficiency at various energies. This curve can then be used to determine the efficiency of the detector at energies different from those used to
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gamma ray of a specified energy passing through the detector will interact and be detected. Relative efficiency values are often used for germanium detectors, and compare the efficiency of the detector at 1332 keV to that of a 3 in Ă— 3 in NaI detector (i.e., 1.2×10  cp
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Efficiency, like resolution, can be expressed in absolute or relative terms. The same units are used (i.e., percentages); therefore, the spectroscopist must take care to determine which kind of efficiency is being given for the detector. Absolute efficiency values represent the probability that a
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by analogy to optical spectroscopy. The width of the peaks is determined by the resolution of the detector, a very important characteristic of gamma spectroscopic detectors, and high resolution enables the spectroscopist to separate two gamma lines that are close to each other. Gamma spectroscopy
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ADC, a technique pioneered by Marek Dolleiser. Specialized computer software performs pulse-height analysis on the digitized waveform, forming a complete MCA. Sound cards have high-speed but low-resolution (up to 192 kHz) ADC chips, allowing for reasonable quality for a low-to-medium count
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The MCA can send its data to a computer, which stores, displays, and further analyzes the data. A variety of software packages are available from several manufacturers, and generally include spectrum analysis tools such as energy calibration (converting bins to energies), peak area and net area
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use crystals that emit light when gamma rays interact with the atoms in the crystals. The intensity of the light produced is usually proportional to the energy deposited in the crystal by the gamma ray; a well known situation where this relationship fails is the absorption of < 200 keV
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Electron hole recombination will emit light that can re-excite pure scintillation crystals; however, the thallium dopant in NaI(Tl) provides energy states within the band gap between the conduction and valence bands. Following excitation in doped scintillation crystals, some electrons in the
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Germanium detectors provide significantly improved energy resolution in comparison to sodium iodide detectors, as explained in the preceding discussion of resolution. Germanium detectors produce the highest resolution commonly available today. However, a disadvantage is the requirement of
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The spectrum in Figure 1 was measured using a NaI-crystal on a photomultiplier, an amplifier, and a multichannel analyzer. The figure shows the number of counts within the measuring period versus channel number. The spectrum indicates the following peaks (from left to right):
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be converted to an energy scale. If the size of the detector crystal is known, one can also perform an intensity calibration, so that not only the energies but also the intensities of an unknown source—or the amount of a certain isotope in the source—can be determined.
416:. Each channel represents a specific range of energy in the spectrum, the number of detected signals for each channel represents the spectral intensity of the radiation in this energy range. By changing the number of channels, it is possible to fine-tune the spectral 925:
processes (e.g. in the housing material of the radioactive source, in shielding material or material otherwise surrounding the experiment) before entering the detector material. This leads to a peak structure that can be seen in the above shown energy spectrum of
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A detailed analysis of this spectrum is typically used to determine the identity and quantity of gamma emitters present in a gamma source, and is a vital tool in radiometric assay. The gamma spectrum is characteristic of the gamma-emitting
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Because of the poor resolution of NaI-based detectors, they are not suitable for the identification of complicated mixtures of gamma ray-producing materials. Scenarios requiring such analyses require detectors with higher resolution.
472:(FWHM). This is the width of the gamma ray peak at half of the highest point on the peak distribution. Energy resolution figures are given with reference to specified gamma ray energies. Resolution can be expressed in absolute (i.e., 866:, also called solid-state detectors, are fundamentally different from scintillation detectors: They rely on detection of the charge carriers (electrons and holes) generated in semiconductors by energy deposited by gamma ray photons. 982:
can occur. The resulting positron annihilates with one of the surrounding electrons, typically producing two photons with 511 keV. In a real detector (i.e. a detector of finite size) it is possible that after the annihilation:
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Some photons will undergo a Compton scattering process in e.g. the shielding material or the housing of the source with a scattering angle close to 180° and some of these photons will subsequently be detected by the
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Most radioactive sources produce gamma rays, which are of various energies and intensities. When these emissions are detected and analyzed with a spectroscopy system, a gamma-ray energy spectrum can be produced.
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Not all gamma rays emitted by the source that pass through the detector will produce a count in the system. The probability that an emitted gamma ray will interact with the detector and produce a count is the
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Laboratory equipment for determination of Îł-radiation spectrum with a scintillation counter. The output from the scintillation counter goes to a Multichannel Analyzer which processes and formats the data.
253:) may occur in the continuum spectra observed in astrophysics and elementary particle physics. The difference between gamma rays and X-rays is somewhat blurred. Gamma rays arise from transitions between 839:
caused by changes in environmental temperature will shift the spectrum on the horizontal axis. Peak shifts of tens of channels or more are commonly observed. Such shifts can be prevented by using
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conduction band will migrate to the activator states; the downward transitions from the activator states will not re-excite the doped crystal, so the crystal is transparent to this radiation.
527:; a photocathode converts the light into electrons; and then by using dynodes to generate electron cascades through delta ray production, the signal is amplified. Common scintillators include 1887: 305:. Through these processes, the energy of the gamma ray is absorbed and converted into a voltage signal by detecting the energy difference before and after the interaction (or, in a 448:
Gamma spectroscopy systems are selected to take advantage of several performance characteristics. Two of the most important include detector resolution and detector efficiency.
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The Compton distribution is a continuous distribution that is present up to channel 150 in Figure 1. The distribution arises because of primary gamma rays undergoing
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If many gamma rays are present in a spectrum, Compton distributions can present analysis challenges. To reduce gamma rays, an anticoincidence shield can be used—
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Scintillation gamma spectrum of a radioactive Am-Be-source. Visible are the main photopeak of C neutron excitation and the two escape peaks associated with it.
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comparing a spectrum from a source of known activity to the count rates in each peak to the count rates expected from the known intensities of each gamma ray.
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within the crystal: Depending on the scattering angle, the Compton electrons have different energies and hence produce pulses in different energy channels.
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at 25 cm). Relative efficiency values greater than one hundred percent can therefore be encountered when working with very large germanium detectors.
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NaI(Tl) is also convenient to use, making it popular for field applications such as the identification of unknown materials for law enforcement purposes.
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Gamma spectroscopy detectors are passive materials that are able to interact with incoming gamma rays. The most important interaction mechanisms are the
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are the energy-sensitive radiation detector and the electronic devices that analyse the detector output signals, such as a pulse sorter (i.e.,
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Kasani, H.; Ashrafi, S.; Ghal-Eh, N. (July 2021). "High count-rate digital gamma-ray spectroscopy using a low-cost COTS digitizer system".
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One of the two photons escapes the detector and only one of the photons deposits its energy in the detector, resulting in a peak with
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Marek works at The University of Sydney, with third year physics students, and developed PRA as an educational tool for his students.
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In semiconductor detectors, an electric field is applied to the detector volume. An electron in the semiconductor is fixed in its
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Amateur gamma spectrometry of a chunk of a black mold picked in Minamisoma, close to the Fukushima Dai-ichi nuclear plant. Japan.
313:). The voltage of the signal produced is proportional to the energy of the detected gamma ray. Common detector materials include 241:, corresponding to the typical energy levels in nuclei with reasonably long lifetimes. Such sources typically produce gamma-ray 1998: 1968: 1899: 1833: 1521: 357:(ADC). In new systems with a very high-sampling-rate ADC, the analog-to-digital conversion can be performed without reshaping. 832:
source that has not been subtracted. A backscatter peak can be seen near channel 150, similar to the second peak in Figure 1.
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energy due to their shorter wavelength. Because of this, the energy of gamma-ray photons can be resolved individually, and a
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systems are designed and adjusted to produce symmetrical peaks of the best possible resolution. The peak shape is usually a
285:). Additional components may include signal amplifiers, rate meters, peak position stabilizers, and data handling devices. 261:, which are monoenergetic), or are electrically generated (X-ray tube, linear accelerator) and have a broad energy range. 1725: 1630: 1083: 1073: 1058: 958:
The result is a peak structure with approximately the energy of the incident photon minus the energy of the Compton edge.
546:(BGO). Because photomultipliers are also sensitive to ambient light, scintillators are encased in light-tight coverings. 1859: 1706: 1595: 1332: 2015: 1854: 1823: 1756: 1038: 520: 354: 242: 828:) The two gamma lines can be seen well-separated; the peak to the left of channel 200 most likely indicates a strong 39: 33: 257:
energy levels and are monoenergetic, whereas X-rays are either related to transitions between atomic energy levels (
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Sodium iodide systems, as with all scintillator systems, are sensitive to changes in temperature. Changes in the
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The voltage pulses produced for every gamma ray that interacts within the detector volume are then analyzed by a
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Gamma rays detected in a spectroscopic system produce peaks in the spectrum. These peaks can also be called
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Ibrahim, Maslina Mohd; Yussup, Nolida; Lombigit, Lojius; Rahman, Nur Aira Abdul; Jaafar, Zainudin (2014).
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The above Am-Be-source spectrum shows an example of single and double escape peak in a real measurement.
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For incident photon energies E larger than two times the rest mass of the electron (1.022 MeV),
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rate. The "sound card spectrometer" has been further refined in amateur and professional circles.
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in the crystal until a gamma ray interaction provides the electron enough energy to move to the
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radiation by intrinsic and doped sodium iodide detectors. The mechanism is similar to that of a
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obtain the curve. High-purity germanium (HPGe) detectors typically have higher sensitivity.
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Development of multichannel analyzer using sound card ADC for nuclear spectroscopy system
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absorbers can be placed around the measurement apparatus to reduce background radiation.
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shape. From this shape, the signal is then converted into a digital form, using a fast
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emits a single gamma line of 662 keV. The 662 keV line shown is actually produced by
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In a real detector setup, some photons can and will undergo one or potentially more
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it produces intense bursts of light compared to other spectroscopic scintillators.
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temperatures for the operation of germanium detectors, typically by cooling with
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Germanium gamma spectrum of Co (Cobalt-60); compare with the NaI spectrum above.
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Both photons deposit their energy in the detector. This results in a peak with
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The backscatter peak usually appears wide and occurs at lower than 250 keV.
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can measure and display the energies of the gamma-ray photons detected.
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Thallium-doped sodium iodide (NaI(Tl)) has two principal advantages:
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It can be produced in large crystals, yielding good efficiency, and
1341:– Cited for early mention of Marek Dolleiser's PRA software. 854: 768: 582: 268: 762:. Gamma ray reduction techniques are especially useful for small 222:, visible light, infrared, radio) but having (in general) higher 1026: 820:, with two gamma rays with 1.17 MeV and 1.33 MeV respectively. ( 1542: 1538: 1333:"NaI Scintillation Probe and Gamma Spectroscopy – PocketMagic" 468:
The most common figure used to express detector resolution is
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Quantitative study of the energy spectra of gamma-ray sources
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Both photons escape the detector, resulting in a peak with
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Kim, Sangrok; Kim, Taeyoon; Yang, Hyungjin (1 June 2022).
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An example of a NaI spectrum is the gamma spectrum of the
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Because some radioactivity is present everywhere (i.e.,
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Figure 1: Sodium iodide gamma spectrum of caesium-137 (
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a photopeak (full energy peak) at an energy of 662 keV
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and employing segmented detectors with add-back (see:
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Figure 2: Sodium iodide gamma spectrum of cobalt-60 (
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On-line gamma-ray energy spectrum conversion utility
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Lee, I Y; Deleplanque, M A; Vetter, K (2003-07-01).
2024: 1961: 1920: 1913: 1875: 1847: 1789: 1739: 1639: 1576: 549:Scintillation detectors can also be used to detect 249:), whereas much higher energies (upwards of 1  1221:"Developments in large gamma-ray detector arrays" 991:, identical to the energy of the incident photon. 1452:Fundamentals of Nuclear Science and Engineering 798:The gamma spectrum shown in Figure 2 is of the 364:Pulse-Height Analyzer Principle: Three pulses, 1554: 947:The basic principle, however, is as follows: 884:Common semiconductor-based detectors include 8: 1626:Vibrational spectroscopy of linear molecules 951:Gamma-ray sources emit photons isotropically 1005:− 2 × 511 keV, the double escape peak. 1917: 1621:Nuclear resonance vibrational spectroscopy 1561: 1547: 1539: 1450:Shultis, John K.; Faw, Richard E. (2007). 826:article for the decay scheme of cobalt-60. 408:Additional logic in the MCA then performs 210:Gamma rays are the highest-energy form of 1994:Inelastic electron tunneling spectroscopy 1674:Resonance-enhanced multiphoton ionization 1434: 1275:"THE MULTICHANNEL ANALYZER, PHYSICS 359E" 1109:John Wiley & Sons, Chichester: 1995, 428:calculation, and resolution calculation. 198:contained in the source, just like in an 69:Learn how and when to remove this message 1762:Extended X-ray absorption fine structure 1454:(2nd ed.). CRC Press. p. 175. 1182:"Gamma Spectroscopy | nuclear-power.com" 969: 359: 245:(i.e., many photons emitted at discrete 80: 32:This article includes a list of general 1149: 998:− 511 keV, the single escape peak. 317:scintillation counters and high-purity 1124:John Wiley & Sons, Inc. NY:2000, 966:Single escape and double escape peaks 766:-doped germanium (Ge(Li)) detectors. 7: 2067: 1122:Radiation Detection and Measurement. 1013:Calibration and background radiation 1331:Motisan, Radu (November 29, 2010). 265:Components of a gamma spectrometer 85:The gamma-ray spectrum of natural 38:it lacks sufficient corresponding 14: 1979:Deep-level transient spectroscopy 1731:Saturated absorption spectroscopy 1396:10.1016/j.radphyschem.2021.109438 1107:Practical Gamma-Ray Spectrometry. 2066: 2055: 2054: 1984:Dual-polarization interferometry 376:are detected at different times 23: 1999:Scanning tunneling spectroscopy 1974:Circular dichroism spectroscopy 1969:Acoustic resonance spectroscopy 1376:Radiation Physics and Chemistry 727:low energy x radiation (due to 214:, being physically the same as 1928:Fourier-transform spectroscopy 1616:Vibrational circular dichroism 1225:Reports on Progress in Physics 912:Interpretation of measurements 538:(NaI(Tl))—often simplified to 523:. The detectors are joined to 309:, the emitted photons using a 1: 1726:Cavity ring-down spectroscopy 1631:Thermal infrared spectroscopy 1084:Total absorption spectroscopy 1074:Perturbed angular correlation 1059:Liquid scintillation counting 851:Semiconductor-based detectors 737:at the low energy end of the 561:Sodium iodide-based detectors 1860:Inelastic neutron scattering 1921:Data collection, processing 1797:Photoelectron/photoemission 1494:"Compton effect (spectrum)" 1039:Alpha-particle spectroscopy 521:thermoluminescent dosimeter 355:analog-to-digital converter 327:Compton-suppression shields 2131: 2006:Photoacoustic spectroscopy 1948:Time-resolved spectroscopy 1245:10.1088/0034-4885/66/7/201 1139:. Accessed 8 October 2008. 470:full width at half maximum 452:Detector energy resolution 2050: 2032:Astronomical spectroscopy 2011:Photothermal spectroscopy 277:The main components of a 212:electromagnetic radiation 206:Gamma ray characteristics 1322:www.gammaspectacular.com 1137:Gamma Spectrum Generator 1105:Gilmore G, Hemingway J. 2016:Pump–probe spectroscopy 1905:Ferromagnetic resonance 1697:Laser-induced breakdown 864:Semiconductor detectors 793:a different measurement 516:Scintillation detectors 511:Scintillation detectors 53:more precise citations. 1712:Glow-discharge optical 1692:Raman optical activity 1606:Rotational–vibrational 1069:Mössbauer spectroscopy 1049:Gamma ray spectrometer 975: 894:cadmium zinc telluride 860: 795: 606: 437:consumer off-the-shelf 435:can serve as a cheap, 405: 274: 228:gamma-ray spectrometer 186:spectrum measurement. 180:Gamma-ray spectrometry 164:Gamma-ray spectroscopy 160: 1933:Hyperspectral imaging 1476:"Backscattered peaks" 1186:www.nuclear-power.com 1162:www.sciencedirect.com 1089:Scintillation counter 973: 858: 837:operating temperature 772: 586: 463:Gaussian distribution 410:pulse-height analysis 363: 343:multichannel analyzer 307:scintillation counter 283:multichannel analyzer 272: 259:characteristic X rays 84: 1685:Coherent anti-Stokes 1640:UV–Vis–NIR "Optical" 1318:"Software Downloads" 1280:. Western University 1023:background radiation 841:spectrum stabilizers 830:background radiation 739:Compton distribution 444:Detector performance 295:photoelectric effect 233:Radioactive nuclei ( 200:optical spectrometer 1989:Hadron spectroscopy 1779:Conversion electron 1740:X-ray and Gamma ray 1647:Ultraviolet–visible 1436:10.3390/app12115613 1388:2021RaPC..18409438K 1337:www.pocketmagic.net 1237:2003RPPh...66.1095L 879:ionization chambers 759:Compton suppression 729:internal conversion 699:secular equilibrium 540:sodium iodide (NaI) 481:Detector efficiency 315:sodium iodide (NaI) 2037:Force spectroscopy 1962:Measured phenomena 1953:Video spectroscopy 1657:Cold vapour atomic 1527:2013-05-10 at the 1300:"MCA box settings" 1094:X-ray spectroscopy 1079:Pandemonium effect 976: 923:Compton scattering 861: 796: 750:Compton scattering 731:of the gamma ray), 607: 406: 279:gamma spectrometer 275: 161: 2082: 2081: 2046: 2045: 1938:Spectrophotometry 1865:Neutron spin echo 1839:Beta spectroscopy 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111: 109: 108: 101: 100: 74: 67: 63: 60: 54: 49:this article by 40:inline citations 27: 26: 19: 2130: 2129: 2125: 2124: 2123: 2121: 2120: 2119: 2105:Nuclear physics 2085: 2084: 2083: 2078: 2042: 2020: 1957: 1909: 1871: 1843: 1785: 1735: 1635: 1596:Resonance Raman 1572: 1567: 1529:Wayback Machine 1518: 1513: 1512: 1502: 1500: 1492: 1491: 1487: 1480:ns.ph.liv.ac.uk 1474: 1473: 1469: 1462: 1449: 1448: 1444: 1416: 1415: 1411: 1373: 1372: 1368: 1350: 1349: 1345: 1330: 1329: 1316: 1315: 1311: 1298: 1297: 1293: 1283: 1281: 1277: 1273: 1272: 1268: 1218: 1217: 1213: 1204: 1203: 1199: 1190: 1188: 1180: 1179: 1175: 1166: 1164: 1156: 1155: 1151: 1146: 1102: 1035: 1015: 980:pair production 968: 940: 938: 937: 936: 932: 930: 929: 928: 927: 919: 914: 906:liquid nitrogen 875:conduction band 853: 816: 814: 813: 812: 808: 806: 805: 804: 803: 787: 785: 784: 783: 779: 777: 776: 775: 774: 715: 713: 712: 711: 707: 705: 704: 703: 702: 693: 691: 690: 689: 685: 683: 682: 681: 680: 670: 668: 667: 666: 662: 660: 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1809: 1804: 1793: 1791: 1787: 1786: 1784: 1783: 1782: 1781: 1771: 1766: 1765: 1764: 1759: 1754: 1743: 1741: 1737: 1736: 1734: 1733: 1728: 1723: 1722: 1721: 1716: 1715: 1714: 1699: 1694: 1689: 1688: 1687: 1677: 1671: 1666: 1661: 1660: 1659: 1649: 1643: 1641: 1637: 1636: 1634: 1633: 1628: 1623: 1618: 1613: 1608: 1603: 1598: 1593: 1588: 1582: 1580: 1574: 1573: 1568: 1566: 1565: 1558: 1551: 1543: 1537: 1536: 1531: 1517: 1516:External links 1514: 1511: 1510: 1485: 1467: 1460: 1442: 1409: 1366: 1343: 1309: 1291: 1266: 1211: 1197: 1173: 1148: 1147: 1145: 1142: 1141: 1140: 1133: 1118: 1101: 1098: 1097: 1096: 1091: 1086: 1081: 1076: 1071: 1066: 1061: 1056: 1054:Isomeric shift 1051: 1046: 1041: 1034: 1031: 1014: 1011: 1007: 1006: 999: 992: 967: 964: 960: 959: 956: 952: 939: 931: 918: 915: 913: 910: 852: 849: 815: 807: 786: 778: 746: 745: 742: 732: 714: 706: 697:, which is in 692: 684: 669: 661: 650: 642: 627: 619: 600: 592: 574: 573: 570: 562: 559: 542:detectors—and 512: 509: 482: 479: 453: 450: 445: 442: 397: 389: 338: 335: 299:Compton effect 290: 287: 266: 263: 243:"line spectra" 207: 204: 172:energy spectra 146: 138: 126: 118: 106: 98: 77: 76: 31: 29: 22: 15: 13: 10: 9: 6: 4: 3: 2: 2127: 2116: 2113: 2111: 2110:Radioactivity 2108: 2106: 2103: 2101: 2098: 2096: 2095:Spectrometers 2093: 2092: 2090: 2075: 2074: 2065: 2063: 2062: 2053: 2052: 2049: 2038: 2035: 2033: 2030: 2029: 2027: 2023: 2017: 2014: 2012: 2009: 2007: 2004: 2000: 1997: 1996: 1995: 1992: 1990: 1987: 1985: 1982: 1980: 1977: 1975: 1972: 1970: 1967: 1966: 1964: 1960: 1954: 1951: 1949: 1946: 1944: 1941: 1939: 1936: 1934: 1931: 1929: 1926: 1925: 1923: 1919: 1916: 1912: 1906: 1903: 1901: 1898: 1896: 1893: 1889: 1886: 1885: 1884: 1881: 1880: 1878: 1874: 1866: 1863: 1862: 1861: 1858: 1856: 1853: 1852: 1850: 1846: 1840: 1837: 1835: 1832: 1830: 1827: 1825: 1822: 1818: 1815: 1813: 1810: 1808: 1805: 1803: 1800: 1799: 1798: 1795: 1794: 1792: 1788: 1780: 1777: 1776: 1775: 1772: 1770: 1767: 1763: 1760: 1758: 1755: 1753: 1750: 1749: 1748: 1745: 1744: 1742: 1738: 1732: 1729: 1727: 1724: 1720: 1717: 1713: 1710: 1709: 1708: 1705: 1704: 1703: 1700: 1698: 1695: 1693: 1690: 1686: 1683: 1682: 1681: 1678: 1675: 1672: 1670: 1669:Near-infrared 1667: 1665: 1662: 1658: 1655: 1654: 1653: 1650: 1648: 1645: 1644: 1642: 1638: 1632: 1629: 1627: 1624: 1622: 1619: 1617: 1614: 1612: 1609: 1607: 1604: 1602: 1599: 1597: 1594: 1592: 1589: 1587: 1584: 1583: 1581: 1579: 1575: 1571: 1564: 1559: 1557: 1552: 1550: 1545: 1544: 1541: 1535: 1532: 1530: 1526: 1523: 1520: 1519: 1515: 1499: 1495: 1489: 1486: 1481: 1477: 1471: 1468: 1463: 1457: 1453: 1446: 1443: 1437: 1432: 1428: 1424: 1420: 1413: 1410: 1405: 1401: 1397: 1393: 1389: 1385: 1381: 1377: 1370: 1367: 1362: 1358: 1354: 1347: 1344: 1338: 1334: 1327: 1323: 1319: 1313: 1310: 1305: 1301: 1295: 1292: 1276: 1270: 1267: 1262: 1258: 1254: 1250: 1246: 1242: 1238: 1234: 1230: 1226: 1222: 1215: 1212: 1207: 1201: 1198: 1187: 1183: 1177: 1174: 1163: 1159: 1153: 1150: 1143: 1138: 1134: 1131: 1130:0-471-07338-5 1127: 1123: 1119: 1116: 1115:0-471-95150-1 1112: 1108: 1104: 1103: 1099: 1095: 1092: 1090: 1087: 1085: 1082: 1080: 1077: 1075: 1072: 1070: 1067: 1065: 1062: 1060: 1057: 1055: 1052: 1050: 1047: 1045: 1042: 1040: 1037: 1036: 1032: 1030: 1028: 1024: 1019: 1012: 1010: 1004: 1000: 997: 993: 990: 986: 985: 984: 981: 972: 965: 963: 957: 953: 950: 949: 948: 945: 924: 916: 911: 909: 907: 903: 897: 895: 891: 887: 882: 880: 876: 872: 867: 865: 857: 850: 848: 844: 842: 838: 833: 831: 827: 825: 801: 794: 771: 767: 765: 761: 760: 753: 751: 743: 740: 736: 733: 730: 726: 725: 724: 720: 700: 678: 677:decay product 673: 636: 631: 612: 585: 581: 577: 571: 568: 567: 566: 560: 558: 556: 552: 547: 545: 541: 537: 536:sodium iodide 534: 530: 526: 522: 517: 510: 508: 504: 502: 498: 492: 489: 480: 478: 475: 471: 466: 464: 459: 451: 449: 443: 441: 438: 434: 429: 425: 423: 419: 415: 411: 403: 395: 387: 384:triggers the 383: 379: 375: 371: 367: 362: 358: 356: 352: 348: 344: 336: 334: 332: 328: 322: 320: 316: 312: 308: 304: 300: 296: 288: 286: 284: 280: 271: 264: 262: 260: 256: 252: 248: 244: 240: 236: 235:radionuclides 231: 229: 225: 221: 217: 213: 205: 203: 201: 197: 191: 187: 185: 181: 177: 173: 170:study of the 169: 165: 159: 155: 150: 130: 110: 92: 88: 83: 73: 70: 62: 59:December 2013 52: 48: 42: 41: 35: 30: 21: 20: 2100:Spectroscopy 2071: 2059: 2039:(a misnomer) 2025:Applications 1943:Time-stretch 1834:paramagnetic 1768: 1652:Fluorescence 1570:Spectroscopy 1501:. Retrieved 1497: 1488: 1479: 1470: 1451: 1445: 1429:(11): 5613. 1426: 1422: 1412: 1379: 1375: 1369: 1352: 1346: 1336: 1325: 1321: 1312: 1303: 1294: 1282:. Retrieved 1269: 1228: 1224: 1214: 1200: 1189:. Retrieved 1185: 1176: 1165:. Retrieved 1161: 1152: 1121: 1106: 1020: 1016: 1008: 1002: 995: 988: 977: 961: 946: 920: 898: 883: 871:valence band 868: 862: 845: 834: 824:decay scheme 821: 797: 791:); see also 756: 754: 747: 721: 635:see Figure 1 634: 608: 578: 575: 564: 557:-radiation. 548: 539: 514: 505: 493: 487: 484: 467: 457: 455: 447: 430: 426: 413: 409: 407: 401: 393: 392:but not the 385: 381: 377: 373: 369: 365: 340: 323: 321:detectors. 292: 276: 232: 209: 192: 188: 184:quantitative 183: 179: 167: 163: 162: 65: 56: 37: 1611:Vibrational 1498:CASSY Lab 2 1304:CASSY Lab 2 1100:Works cited 1044:Gamma probe 735:backscatter 422:sensitivity 394:Upper Level 386:Lower Level 351:trapezoidal 168:qualitative 154:decay chain 51:introducing 2115:Gamma rays 2089:Categories 1817:Two-photon 1719:absorption 1601:Rotational 1382:: 109438. 1191:2023-07-29 1167:2022-11-01 1144:References 488:efficiency 433:sound card 418:resolution 158:Moab, Utah 34:references 1895:Terahertz 1876:Radiowave 1774:Mössbauer 1503:9 January 1404:233696398 1261:121957980 1253:0034-4885 1120:Knoll G, 955:detector. 902:cryogenic 886:germanium 319:germanium 2061:Category 1790:Electron 1757:Emission 1707:emission 1664:Vibronic 1525:Archived 1284:27 March 1206:"X-rays" 1033:See also 822:See the 802:isotope 613:isotope 529:thallium 414:channels 347:Gaussian 289:Detector 247:energies 196:nuclides 91:nuclides 2073:Commons 1900:ESR/EPR 1848:Nucleon 1676:(REMPI) 1384:Bibcode 1233:Bibcode 764:lithium 611:caesium 255:nuclear 218:(e.g., 166:is the 87:uranium 47:improve 1914:Others 1702:Atomic 1458:  1402:  1259:  1251:  1128:  1113:  892:, and 800:cobalt 675:, the 553:- and 431:A USB 372:, and 301:, and 297:, the 224:photon 220:X-rays 132:, and 36:, but 1855:Alpha 1824:Auger 1802:X-ray 1769:Gamma 1747:X-ray 1680:Raman 1591:Raman 1586:FT-IR 1400:S2CID 1278:(PDF) 1257:S2CID 741:, and 701:with 551:alpha 533:doped 458:lines 1505:2024 1456:ISBN 1286:2016 1249:ISSN 1126:ISBN 1111:ISBN 1027:Lead 757:see 555:beta 420:and 1883:NMR 1431:doi 1392:doi 1380:184 1357:doi 1241:doi 679:of 349:or 333:). 251:TeV 239:MeV 174:of 2091:: 1888:2D 1807:UV 1496:. 1478:. 1427:12 1425:. 1421:. 1398:. 1390:. 1378:. 1335:. 1324:. 1320:. 1302:. 1255:. 1247:. 1239:. 1229:66 1227:. 1223:. 1184:. 1160:. 935:Cs 908:. 896:. 888:, 881:. 843:. 811:Co 782:Co 719:. 710:Cs 688:Cs 665:Ba 646:Cs 637:. 623:Cs 596:Cs 501:Bq 474:eV 424:. 368:, 142:Bi 122:Pb 112:, 102:Ra 1562:e 1555:t 1548:v 1507:. 1482:. 1464:. 1439:. 1433:: 1406:. 1394:: 1386:: 1363:. 1359:: 1339:. 1306:. 1288:. 1263:. 1243:: 1235:: 1208:. 1194:. 1170:. 1132:. 1117:. 1003:E 996:E 989:E 633:— 605:) 531:- 499:/ 497:s 402:P 398:U 396:E 390:L 388:E 382:2 378:t 374:3 370:2 366:1 72:) 66:( 61:) 57:( 43:.

Index

references
inline citations
improve
introducing
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uranium
nuclides

Ra


Pb


Bi

decay chain
Moab, Utah
energy spectra
gamma-ray sources
nuclides
optical spectrometer
electromagnetic radiation
all other forms
X-rays
photon
gamma-ray spectrometer
radionuclides
MeV
"line spectra"
energies
TeV
nuclear
characteristic X rays

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