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The isomeric first excited state of the isotope 229Th exhibits the lowest nuclear excitation energy in the whole landscape of known atomic nuclei. For a long time this energy was reported in the literature as 3.5(5) eV, however, a new experiment corr ected this energy to 7.6(5) eV, corresponding to a UV transition wavelength of 163(11) nm. The expected isomeric lifetime is $tau=$ 3-5 hours, leading to an extremely sharp relative linewidth of Delta E/E ~ 10^-20, 5-6 orders of magnitude smaller than typical atomic relative linewidths. For an adequately chosen electronic state the frequency of the nuclear ground-state transition will be independent from influences of external fields in the framework of the linear Zeeman and quadratic Stark effect, rendering 229mTh a candidate for a reference of an optical clock with very high accuracy. Moreover, in the literature speculations about a potentially enhanced sensitivity of the ground-state transition of $^{229m}$Th for eventual time-dependent variations of fundamental constants (e.g. fine structure constant alpha) can be found. We report on our experimental activities that aim at a direct identification of the UV fluorescence of the ground-state transition energy of 229mTh. A further goal is to improve the accuracy of the ground-state transition energy as a prerequisite for a laser-based optical control of this nuclear excited state, allowing to build a bridge between atomic and nuclear physics and open new perspectives for metrological as well as fundamental studies.
45 - D. Habs , P. G. Thirolf , C. Lang 2012
We study the production of radioisotopes for nuclear medicine in (gamma,gamma) photoexcitation reactions or (gamma,xn + yp) photonuclear reactions for the examples of ^195mPt, ^117mSn and ^44Ti with high flux [(10^13 - 10^15) gamma/s], small beam dia meter and small energy band width (Delta E/E ~ 10^-3 -10^-4) gamma beams. In order to realize an optimum gamma-focal spot, a refractive gamma-lens consisting of a stack of many concave micro-lenses will be used. It allows for the production of a high specific activity and the use of enriched isotopes. For photonuclear reactions with a narrow gamma beam, the energy deposition in the target can be reduced by using a stack of thin target wires, hence avoiding direct stopping of the Compton electrons and e^+e^- pairs. The well-defined initial excitation energy of the compound nucleus leads to a small number of reaction channels and enables new combinations of target isotope and final radioisotope. The narrow-bandwidth gamma excitation may make use of collective resonances in gamma-width, leading to increased cross sections. (gamma,gamma) isomer production via specially selected gamma cascades allows to produce high specific activity in multiple excitations, where no back-pumping of the isomer to the ground state occurs. The produced isotopes will open the way for completely new clinical applications of radioisotopes. For example ^195mPt could be used to verify the patients response to chemotherapy with platinum compounds before a complete treatment is performed. In targeted radionuclide therapy the short-range Auger and conversion electrons of ^195mPt and ^117mSn enable a very local treatment. The generator ^44Ti allows for a PET with an additional gamma-quantum (gamma-PET), resulting in a reduced dose or better spatial resolution.
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