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Change of 7Be decay rate in exohedral and endohedral C60 fullerene compounds and its implications

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 Added by Amlan Ray
 Publication date 2005
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and research's language is English




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The half-life of 7Be implanted in a C60 pellet and gold foil has been measured to be about the same within about 0.2%. Using a radiochemical technique, we also measured that the probability of formation of endohedral 7Be@C60 by nuclear implantation technique was (5.6+-0.45)%. It is known from earlier works that the half-life of endohedral 7Be@C60 is about 1.2% shorter than that of 7Be implanted in gold. An analysis of these results using linear muffin-tin orbital method calculations indicates that most of the implanted 7Be ions in fullerene C60 stay at a distance of about 5.3 Angstrom from the centers of nearest C60 molecules forming exohedral compounds and those who enter the fullerene cages go to the centers of the cages forming endohedral 7Be@C60 compounds.

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The 12B excitation energy spectrum has been obtained from coincidence measurements of the 9Be+7Li -> 2alpha+8Li reaction at E{0}=52 MeV. The decay of the states at excitations between 10 and 16 Mev into alpha$+8Li has been observed for the first time. Observed alpha-decay indicates possible cluster structure of the 12B excited states. The influence of these states on the cross section of the astrophysically important 8Li(alpha,n)11B and 9Be+t reactions is discussed and the results are compared with existing results.
It is demonstrated that in fullerene C70 which can be considered as a deformed fullerene C60 in some sense there is a withdrawal of an electrodynamical forbiddance of a strong quadrupole light-molecule interaction which is realized in the fullerene C60. This situation occurs because of the reduction of symmetry of C60 from the icosahedral symmetry group Yh to the group D5h. The withdrawal results in appearance of the lines in the SERS spectra of C70 which are forbidden in usual Raman scattering and are allowed in infrared absorption while such lines are forbidden in the SERS spectrum of the fullerene C60 due to the electrodynamical forbiddance. The measured SERS spectra of C70 demonstrates existence of such lines that strongly confirms our ideas about the dipole quadrupole SERS mechanism.
159 - V. Kumar , M. Hass , Y. Nir-El 2008
The electron-capture (EC) decay rate of 7Be in metallic Cu host and the beta-decay rate of 198Au in the host alloy Al-Au have been measured simultaneously at several temperatures, ranging from 0.350 K to 293 K. No difference of the half-life of 198Au between 12.5 K and 293 K is observed to a precision of 0.1%. By utilizing the special characteristics of our double-source assembly, possible geometrical effects that influence the individual rates could be eliminated. The ratio of 7Be to 198Au activity thus obtained also remains constant for this temperatures range to the experimental precision of 0.15(0.16)%. The resulting null temperature dependence is discussed in terms of the inadequacy of the often-used Debye-Huckel model for such measurements.
It is demonstrated that the forbidden lines, which must be present in the SERS, TERS and SEIRA spectra of molecules with sufficiently high symmetry, associated with a strong quadrupole light-molecule interaction, are absent in the fullerene C60. This result is an experimental manifestation of an electrodynamical forbiddance of the strong quadrupole light-molecule interaction, which must be not only in molecules with cubic symmetry groups, but in the fullerene C60 also.
We analyze using Poisson equation the spatial distributions of the positive charge of carbon atomic nuclei shell and negative charge of electron clouds forming the electrostatic potential of the C60 fullerene shell as a whole. We consider also the case when an extra positive charge appears inside C60 in course of e.g. photoionization of an endohedral A@C. We demonstrate that frequently used radial square-well potential U(r) simulating the C60 shell leads to nonphysical charge densities of the shell in both cases - without and with an extra positive charge inside. We conclude that the square well U(r) modified by adding a Coulomb-potential-like term does not describe the interior polarization of the shell by the electric charge located in the center of the C60 shell. We suggest another model potential, namely that of hyperbolic cosine shape with properly adjusted parameters that is able to describe the monopole polarization of C60 shell. As a concrete illustration, we have calculated the photoionization cross-sections of H@C60 taking into account the monopole polarization of the shell in the frame of suggested model. We demonstrate that proper account of this polarization does not change the photoionization cross-section.
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