A. V. Yeremin

Synthesis of nuclei of the superheavy element 114 in reactions induced by 48Ca

The stability of heavy nuclides, which tend to decay by α-emission and spontaneous fission, is determined by the structural properties of nuclear matter. Nuclear binding energies and lifetimes increase markedly in the vicinity of closed shells of neutrons or protons (nucleons), corresponding to ‘magic’ numbers of nucleons; these give rise to the most stable (spherical) nuclear shapes in the ground state. For example, with a proton number of Z = 82 and a neutron number of N = 126, the nucleus 208Pb is ‘doubly-magic’ and also exceptionally stable. The next closed neutron shell is expected at N = 184, leading to the prediction of an ‘island of stability’ of superheavy nuclei, for a broad range of isotopes with Z = 104 to 120 (refs 1, 2). The heaviest known nuclei have lifetimes of less than a millisecond, but nuclei near the top of the island of stability are predicted to exist for many years. (In contrast, nuclear matter consisting of about 300 nucleons with no shell structure would undergo fission within about 10−20 seconds.) Calculations indicate that nuclei with N > 168 should already benefit from the stabilizing influence of the closed shell at N = 184. Here we report the synthesis of an isotope containing 114 protons and 173 neutrons, through fusion of intense beams of 48Ca ions with 242Pu targets. The isotope decays by α-emission with a half-life of about five seconds, providing experimental confirmation of the island of stability.

Chemical characterization of element 112

The heaviest elements to have been chemically characterized are seaborgium (element 106), bohrium (element 107) and hassium (element 108). All three behave according to their respective positions in groups 6, 7 and 8 of the periodic table, which arranges elements according to their outermost electrons and hence their chemical properties. However, the chemical characterization results are not trivial: relativistic effects on the electronic structure of the heaviest elements can strongly influence chemical properties. The next heavy element targeted for chemical characterization is element 112; its closed-shell electronic structure with a filled outer s orbital suggests that it may be particularly susceptible to strong deviations from the chemical property trends expected within group 12. Indeed, first experiments concluded that element 112 does not behave like its lighter homologue mercury. However, the production and identification methods used cast doubt on the validity of this result. Here we report a more reliable chemical characterization of element 112, involving the production of two atoms of 283112 through the alpha decay of the short-lived 287114 (which itself forms in the nuclear fusion reaction of 48Ca with 242Pu) and the adsorption of the two atoms on a gold surface. By directly comparing the adsorption characteristics of 283112 to that of mercury and the noble gas radon, we find that element 112 is very volatile and, unlike radon, reveals a metallic interaction with the gold surface. These adsorption characteristics establish element 112 as a typical element of group 12, and its successful production unambiguously establishes the approach to the island of stability of superheavy elements through 48Ca-induced nuclear fusion reactions with actinides.

Production and decay of269110

In an experiment carried out to identify element 110, we have observed anα-decay chain, that can be unambiguously assigned to269110. In a scries of preexperiments the excitation functions of the fusion reactions50Ti +208Pb→258104* and58Fe +208Pb→266108* were measured with high precision in order to get the optimum projectile energies for the production of these heavy elements. The cross-section maxima of the 1n evaporation channels were observed at excitation energies of 15.6 MeV and 13.4 MeV, respectively. These data result in an optimum excitation energy of 12.3 MeV of the compound nucleus for the production of269110 in the reaction62Ni +208Pb→269110 + 1n. In irradiations at the corresponding beam energy of 311 MeV we have observed a decay chain of 4 subsequent a decays. This can be assigned to the isotope with the mass number 269 of the element 110 on the basis of delayed α-α coincidences. The accurately measured decay data of the daughter isotopes of the elements 108 to 102, obtained in the previous experiments, were used. The isotope269110 decays with a hair-life of (270-120+1300) μs by emission of (11.132±0.020) MeV alpha particles. The production cross-section is (3.3-2.7+6.2) pb.

The new element 111

The new element 111 was produced and unambiguously identified in an experiment at SHIP, GSI Darmstadt. Three nuclei of the isotope272111 were observed in irradiations of209Bi targets with64Ni projectiles of 318 MeV and 320 MeV energy. The cross-sections are (1.7−1.4+3.3) pb and (3.5−2.3+4.6) pb, respectively. The nuclei decay by a emission into the new and so far the heaviest isotopes of the elements 109 and 107 with mass numbers A=268 and A=264. Theα-decay chains were followed down to the known nuclei260105 and256Lr.

The new element 112

The new element 112 was produced and identified unambiguously in an experiment at SHIP, GSI Darmstadt. Two decay chains of the isotope277112 were observed in irradiations of208Pb targets with70Zn projectiles of 344 MeV kinetic energy. The isotope decays by emission of α particles with a half-life of (240−90+430)µs. Two different α energies of (11,649±20) keV and (11,454±20) keV were measured for the two observed decays. The cross-section measured in three weeks of irradiations is (1.0−0.4+1.8) pb.

Indication for a volatile element 114

Abstract Recently, the chemical investigation of element 112 revealed a highly volatile, noble metallic behaviour, as expected for the last group 12 member of the periodic table. The observed volatility and chemical inertness were ascribed to the growing influence of relativistic effects on the chemical properties of the heaviest elements with increasing nuclear charge. Here, we report for the first time on gas phase chemical experiments aiming at a determination of element 114 properties. This element was investigated using its isotopes 287114 and 288114 produced in the nuclear fusion reactions of 48Ca with 242Pu and 244Pu, respectively. Identification of three atoms of element 114 in thermochromatography experiments and their deposition pattern on a gold surface indicates that this element is at least as volatile as simultaneously investigated elements Hg, At, and element 112. This behaviour is rather unexpected for a typical metal of group 14.

Review of even element super-heavy nuclei and search for element 120

Abstract.The reaction 54Cr

Large size foil-microchannel plate timing detectors

+

The Vassilissa facility for electrostatic separation and study of complete fusion reaction products

248Cm was investigated at the velocity filter SHIP at GSI, Darmstadt, with the intention to study production and decay properties of isotopes of element 120. Three correlated signals were measured, which occurred within a period of 279ms. The heights of the signals correspond with the expectations for a decay sequence starting with an isotope of element 120. However, a complete decay chain cannot be established, since a signal from the implantation of the evaporation residue cannot be identified unambiguously. Measured properties of the event chain are discussed in detail. The result is compared with theoretical predictions. Previously measured decay properties of even element super-heavy nuclei were compiled in order to find arguments for an assignment from the systematics of experimental data. In the course of this review, a few tentatively assigned data could be corrected. New interpretations are given for results which could not be assigned definitely in previous studies. The discussion revealed that the cross-section for production of element 120 could be high enough so that a successful experiment seems possible with presently available techniques. However, a continuation of the experiment at SHIP for a necessary confirmation of the results obtained in a relatively short irradiation of five weeks is not possible at GSI presently. Therefore, we decided to publish the results of the measurement and of the review as they exist now. In the summary and outlook section we also present concepts for the continuation of research in the field of super-heavy nuclei.

GABRIELA: A new detector array for γ-ray and conversion electron spectroscopy of transfermium elements

Abstract A large area foil-microchannel plate time-of-flight (TOF) system is presented. The parameters of the system are as follows: 55 cm 2 active area, 99.8% detection efficiency, 100% transparency and 700 ps time resolution. The TOF system, unique in size and conditions of exploitation, consists of two (or three) detectors used also as anticoincidence units for the analysing multistrip Si-detector array.