Evolution of the giant dipole resonance properties with excitation energy

The studies of the evolution of the hot Giant Dipole Resonance (GDR) properties as a function of excitation energy are reviewed. The discussion will mainly focus on the A ∼ 100-120 mass region where a large amount of data concerning the width and the strength evolution with excitation energy are available. Models proposed to interpret the main features and trends of the experimental results will be presented and compared to the available data in order to extract a coherent scenario on the limits of the development of the collective motion in nuclei at high excitation energy. Experimental results on the GDR built in hot nuclei in the mass region A ∼ 60-70 will be also shown, allowing to investigate the mass dependence of the main GDR features. The comparison between limiting excitation energies for the collective motion and critical excitation energies extracted from caloric curve studies will suggest a possible link between the disappearance of collective motion and the liquid-gas phase transition.     

Pre-equilibrium dipole strength in charge asymmetric peripheral heavy-ion reactions

We report on the results obtained from the study of the ³²S + ⁶⁴Ni and ³²S + ⁵⁸Ni peripheral reactions at incident energies E _lab = 288 MeV and E _lab = 320 MeV, respectively. High-energy γ-rays were detected in an array of 8 seven-pack BaF₂ clusters. Coincidence with complex fragments detected in 12 three-stage telescopes ensured the selection of peripheral reaction events. All of the relevant reaction parameters were kept constant with the exception of the different initial dipole moment caused by the different entrance channel charge asymmetry. While for quasi-elastic events no N/Z effect was observed in the differential γ-ray multiplicities of the two reactions, for deep-inelastic events a larger dipole γ-ray emission occurs during the more N/Z asymmetric reaction. A theoretical interpretation based on a collective Bremsstrahlung analysis of the reaction dynamics is presented. Received: 26 September 2002 / Accepted: 13 November 2002 / Published online: 6 March 2003 RID="a" ID="a"e-mail: pierroutsakou@na.infn.it RID="b" ID="b"Present address: INFN, Laboratori Nazionali di Legnaro, Padova, Italy. Communicated by C. Signorini     

System dependence of the correlation function of IMFs in Ar + Sn at 35 MeV/u

The inclusive reduced velocity correlation functions of the intermediate mass fragments were measured in the reactions of ³⁶Ar + ^112,124Sn at 35 MeV/u. The anti-correlation is observed to be stronger in ³⁶Ar + ¹²⁴Sn system than that in ³⁶Ar + ¹¹²Sn. The difference of the correlation functions between the two reactions is mainly contributed by the particle pairs with high momenta. A three body Coulomb repulsive trajectory model is employed to calculate the emission time scale of the IMFs for the two systems. The time scale is 150 fm/c in ³⁶Ar + ¹¹²Sn and 120 fm/c in the ³⁶Ar + ¹²⁴Sn, respectively.     

Inclusive and exclusive measurements of high energy γ-rays in the 101 MeV <Superscript>19</Superscript>F +<Superscript>181</Superscript>Ta fusion reaction

The high energy γ-rays from the fusion-evaporation reaction 101 MeV ¹⁹F +¹⁸¹Ta have been measured in coincidence with different γ-ray fold windows or discrete γ-rays in final residual nuclei. The line-shape analysis of the high energy γ-ray spectra confirms the large deformation of the ²⁰⁰Pb nuclei at high angular momenta. Coincidences with discrete γ-transitions evidence a strong correlation between γ-rays in the Giant Dipole Resonance region (E_γ≥ 8 MeV) and final evaporation residues. Received: 14 September 1999 / Revised version: 17 December 1999     

Prompt dipole γ-ray emission in fusionlike heavy-ion reactions

The ³²S + ¹⁰⁰Mo and ³⁶S + ⁹⁶Mo fusionlike reactions were studied at incident energy of E _lab = 298 MeV and 320 MeV, respectively, with the aim of probing the influence of the entrance channel charge asymmetry on the dipole γ-ray emission. The excitation energy and spin distribution of the compound nucleus created in these reactions were identical, the only difference being associated with the unequal charge asymmetry of the two entrance channels. High-energy γ-rays were detected in an array of 9 seven-pack BaF₂ clusters. Coincidence with fusionlike residues detected in four PPAC ensured the selection of central reaction events. By studying the differential γ-ray multiplicity associated with the two reactions it was shown that the dipole strength excited in the compound nucleus increases with the entrance channel charge asymmetry. From the linearized spectra, the increase of the GDR γ-ray intensity was found to be ∼ 25% for the more charge asymmetric system. The results are discussed and compared with those of previous data obtained at different incident energies. Received: 21 October 2002 / Accepted: 23 December 2002 / Published online: 1 April 2003     

Giant monopole resonances in the statistical model

The strength functions fore ⁺ e ^– pair decay of the isoscalar and isovector giant monopole resonances in highly excited nuclei are derived and used in a statistical model calculation of thee ⁺ e ^– pair energy spectrum from compound nuclear decay in¹¹⁰Sn following a fusion evaporation reaction. This result is then compared to thee ⁺ e ^– spectrum derived from internal pair decay of the giant dipole and giant quadrupole resonances. The computation shows that the pair decay from the excited-state GDR dominates the pair spectrum over the region of all giant resonances, exceedingL=0 transitions by at least a factor of ten. We also compute the angular correlations betweene ⁺ ande ^– for theL=0, L=1 andL=2 transitions and estimate their power to discriminate between the various multipolarities.Dedicated to Prof. Dr. P. Kienle on the occasion of his 60th birthday     

Analysis of alpha-cluster transfer in O + C and C + O at energies near Coulomb barrier

The aim of this work is to track the phenomenon of α-cluster transfer mechanism at low energies 1.25, 1.5 and 1.75 MeV/n, close to the Coulomb barrier energy for ¹²C(¹⁶O, ¹²C)¹⁶O and ¹⁶O(¹²C, ¹⁶O)¹²C nuclear systems. The measurements of the angular distribution show a significant increase in the differential cross section at large angles due to alpha-transfer mechanism. The optical model code SPI-GENOA could be used effectively for fitting the experimental data with the theoretical predictions nearly up to angle 90°, where the differential cross section decreases steadily with increasing the scattering angle. For the second hemisphere, at angles greater than 100°, there is a large increase in cross section due to the contribution of α-transfer mechanism, and the Distorted Wave Born Approximation (DWBA) method could be used effectively for fitting the experimental data with the theoretical predictions at this region using (DWUCK5) code.     

Quasifission and difference in formation of evaporation residues in the O + W and F + Ta reactions

The role of the entrance channel has been studied to ascertain a cause of the observed difference between the evaporation residue cross sections normalized to the fusion cross sections in the ¹⁹F + ¹⁸¹Ta and ¹⁶O + ¹⁸⁴W reactions at high excitation energies. The theoretical analysis performed in the framework of the dinuclear system and advanced statistical models showed that the more intense yield of evaporation residues in the ¹⁶O + ¹⁸⁴W reaction in comparison with that in the ¹⁹F + ¹⁸¹Ta reaction was explained by the large capture and fusion cross sections in the former reaction, which is in agreement with the experimental data. The observed decrease in the evaporation residue cross section normalized to the fusion cross section in the ¹⁹F + ¹⁸¹Ta reaction, in comparison with one in the ¹⁶O + ¹⁸⁴W reaction at large excitation energies, is caused by the unintentional inclusion of the quasifission and fast fission contributions in the fissionlike fragment yields that were used in reconstructing the experimental fusion cross section in the normalizing procedure. The range of the angular momentum distribution for both systems was similar, but the partial cross sections are different, showing the presence of a difference in the hindrance to complete fusion in both reactions.     

Low-energy monopole and dipole response in nuclei at finite temperature

The multipole response of nuclei at temperatures T=0–2 MeV$T=0\text{–}2\text{MeV}$ is studied using a self-consistent finite-temperature RPA (random phase approximation) based on relativistic energy density functionals. Illustrative calculations are performed for the isoscalar monopole and isovector dipole modes and, in particular, the evolution of low-energy excitations with temperature is analyzed, including the modification of pygmy structures. Both for the monopole and dipole modes, in the temperature range T=1–2 MeV$T=1\text{–}2\text{MeV}$ additional transition strength appears at low energies due to thermal unblocking of single-particle orbitals close to the Fermi level. A concentration of dipole strength around 10 MeV excitation energy is predicted in ^60,62Ni. The principal effect of finite temperature on low-energy strength that is already present at zero temperature, e.g. in ⁶⁸Ni and ¹³²Sn, is the spreading of this structure to even lower energy and the appearance of states that correspond to thermally unblocked transitions.     

Coulomb corrections to Delbrück scattering

The emission of high-energy-rays in the deexcitation of hot⁴⁰Ca and³⁹K nuclei formed in heavy-ion fusion reactions at excitation energyE _x 90 MeV has been studied. The high energy-rays were measured in coincidence with evaporation residues or light charged particles. The spectrum from the self-conjugated compound nucleus⁴⁰Ca shows an appreciable yield suppression in the Giant Dipole Resonance (GDR) energy region with respect to the³⁹K, due to isospin selection rules in the dipole-decay. The spectral line shapes of the spectra are well reproduced by using a statistical code which treats explicitly the isospin quantum number in evaluating level densities and transmission coefficients. The GDR parameters determined from the present coincidence measurements are in good agreement with the systematic in theA 40 mass region at lower bombarding energy based on the analysis of inclusive spectra.We thank M. Caldogno for technical support in the development of evaporation residues detectors. We acknowledge the participation of M. Anghinolfi, P. Corvisiero, M. Taiuti and A. Zucchiatti in the early stages of this work. Thanks are due to M. Kicinska-Habior for providing the isospin-dependent code. Discussions with B. Fornal are also gratefully acknowledged.     

Adsorption and decomposition of triethylsilane on Si(1 0 0)

The adsorption and decomposition of triethylsilane (TES) on Si(1 0 0) were studied using temperature programmed desorption (TPD), high resolution electron energy loss spectroscopy (HREELS), electron stimulated desorption (ESD), and X-ray photoelectron spectroscopy (XPS). TPD and HREELS data indicate that carbon is thermally removed from the TES-dosed Si(1 0 0) surface via a β-hydride elimination process. At high exposures, TPD data shows the presence of physisorbed TES on the surface. These species are characterized by desorption of TES fragments at 160 K. Non-thermal decomposition of TES was studied at 100 K by irradiating the surface with 600 eV electrons. ESD of mass 27 strongly suggests that a β-hydride elimination process is a channel for non-thermal desorption of ethylene. TPD data indicated that electron irradiation of physisorbed TES species resulted in decomposition of the parent molecule and deposition of methyl groups on the surface that desorbed thermally at about 900 K. Without electron irradiation, mass 15 was not detected in the TPD spectra, indicating that the production of methyl groups in the TPD spectra was a direct result of electron irradiation. XPS data also showed that following electron irradiation of TES adsorbed on Si(1 0 0), carbon was deposited on the surface and could not be removed thermally.     

Density functional theory study of hydrogenation mechanism in Fe-doped Mg(0 0 0 1) surface

Using density functional theory (DFT) in combination with nudged elastic band (NEB) method, the dissociative chemisorptions and diffusion processes of hydrogen on both pure and Fe-doped Mg(0 0 0 1) surfaces are studied. Firstly, the dissociation pathway of H₂ and the relative barrier were investigated. The calculated dissociation barrier (1.08 eV) of hydrogen molecule on a pure Mg(0 0 0 1) surface is in good agreement with comparable experimental and theoretical studies. For the Fe-doped Mg(0 0 0 1) surface, the activated barrier decreases to 0.101 eV due to the strong interaction between the s orbital of H and the d orbital of Fe. Then, the diffusion processes of atomic hydrogen on pure and Fe-doped Mg(0 0 0 1) are presented. The obtained diffusion barrier to the first subsurface is 0.45 eV and 0.98 eV, respectively. Finally, Chou method was used to investigate the hydrogen sorption kinetic mechanism of pure MgH₂ and Mg mixed with 5 at.% Fe atoms composites. The obtained activation energies are 0.87 ± 0.02 and 0.31 ± 0.01 eV for H₂ dissociation on the pure surface and H atom diffusion in Fe-doped Mg surfaces, respectively. It suggests that the rate-controlling step is dissociation of H₂ on the pure Mg surface while it is diffusion of H atom in the Fe-doped Mg surface. And both of fitting data are matching well with our calculation results.     

Adsorption, reaction and desorption of hydrogen on modified Pd(1 1 1) surfaces

The interaction of hydrogen (deuterium) with different modified Pd(1 1 1) surfaces has been investigated. The focus was put on the energy and angel dependence of the desorbing molecules from oxygen covered, potassium covered and vanadium oxide covered surfaces. Conventional adsorption/desorption as well as permeation/desorption experiments were performed. For the oxygen covered surface optimum reaction rates for water production and the energy distribution of the reaction products were determined, both for the reaction of oxygen with molecular hydrogen as well as with atomic hydrogen. Potassium on the surface enhances the activation barrier for hydrogen adsorption resulting in a hyper-thermal desorption flux and a forward focused angular distribution of desorption. Permeation/desorption of deuterium from ultra-thin vanadium oxide films yield mainly thermalized desorbing molecules or slightly hyper-thermal, depending on the oxidation state of the surface oxide.     

The gold and oxygen (3 × 1) structures on W(1 1 2)

The adsorption of two very different adsorbates, gold and oxygen, induce the formation of a (3 × 1) surface structure on both W(1 1 2) and Mo(1 1 2). In spite of similar adsorbate unit cells, the surface electronic structure, derived from photoemission, exhibits pronounced differences for the two adsorbates. Indeed, both experiment and simulations indicate substantial changes in electronic structures of (1 × 1) and (3 × 1) gold overlayers supported by highly anisotropic (1 1 2) plane. We speculate that (3 × 1) is a favored periodicity in the atomic rearrangement of the (1 1 2) surfaces of molybdenum and tungsten due in part as a result of the initial state band structure of these surfaces.     

Excitation functions of evaporation residues in the interaction of 16O with 103Rh at incident energies up to 400 MeV

The excitation functions for production of 48 residues in the interaction of ¹⁶O with ¹⁰³Rh have been measured at incident energies varying from about 40 to 400MeV. Their analysis shows that many competing reaction mechanism contribute to the formation of these residues including complete fusion, break-up-fusion reactions and ¹⁶O inelastic scattering. The cross-sections of most of these mechanisms are obtained by independent measurements of the spectra of intermediate-mass fragments observed in the interaction of ¹⁶O on ⁹³Nb. The agreement between measured and calculated excitation functions is satisfactory in most of the cases.     

Growth of Ag thin films on ZnO(0 0 0 −1) investigated by AES and STM

The growth of Ag films on ZnO(0 0 0 −1) has been investigated by Auger electron spectroscopy (AES) and scanning tunneling microscopy (STM). A high density of islands is nucleated at the earliest stages of the growth. An upstepping mechanism causes these islands to coalesce while the uncovered fraction of the ZnO surface remains constant (30%).     

Self-assembled monolayers of radical molecules physisorbed on HOPG(0 0 0 1) substrate studied by scanning tunnelling microscopy and electron paramagnetic resonance techniques

In this paper, we present a combined STM and EPR study on the adsorption and self-organization of monolayers formed from 2-(14-Carboxytetradecyl)-2-ethyl-4,4-dimethyl-3-oxazolidinyloxy (16DS) and 4′,4′-Dimethylspiro(5α-cholestane-3,2′-oxazolidin)-3′-yloxy (CSL) adsorbed on a highly oriented pyrolitic graphite HOPG(0 0 0 1) substrate. Both 16DS and CSL molecules are persistent free radicals containing a paramagnetic doxyl group. The STM measurements of 16DS on HOPG(0 0 0 1) were performed at the liquid-solid interface while the studies of CSL on HOPG(0 0 0 1) were carried out under ultrahigh vacuum conditions. It was found that the 16DS molecules on the HOPG(0 0 0 1) surface form a highly-ordered monolayer with a domain structure. The high-resolution STM images show structural details of 16DS molecules on HOPG(0 0 0 1) revealing the paramagnetic doxyl group. In contrast, CSL molecules on HOPG(0 0 0 1) form a well-ordered monolayer without domain structure. The EPR results indicate that both compounds deposited on HOPG(0 0 0 1) substrate are not reduced and retain their paramagnetic character. We believe that the molecular systems described can be used in single spin detection experiments using an electron spin noise-scanning tunnelling microscopy (ESN-STM) technique. In particular, the possibility of obtaining contrast spin signals from the paramagnetic and diamagnetic parts of molecules increases the significance of our results.     

Kinetics of the H + NCO reaction

Ab initio transition state theory (TST) based master equation simulations are used to predict the temperature and pressure dependence of the H + NCO reaction rate and product branching. The barrierless entrance channels to form singlet HNCO and NCOH are studied with variable reaction coordinate TST employing a potential energy surface obtained from multi-reference configuration interaction ab initio calculations. The remaining channels, including reactions on the triplet surface, are studied with standard TST methods employing high level electronic structure results. The energy transfer parameters for the master equation simulations arise from a fit to the experimentally observed HNCO dissociation rate. The lowest energy threshold to formation of bimolecular products, ³NH + CO, lies well below the reactants. The bottleneck for intersystem crossing, which precedes the formation of ³NH + CO from the singlet adducts, becomes the dominant bottleneck for that channel at quite low energies relative to reactants. The effect of this bottleneck is studied with model calculations designed to reproduce detailed experimental observations of photolysis branching ratios. This bottleneck greatly reduces the flux from H + NCO to ³NH + CO via the singlet adducts. As a result, stabilization and reaction on solely the triplet surface are significant components of the overall rate. The present predictions for the high pressure and collisionless limit rate coefficients are accurately reproduced over the 200-2500 K range by the expressions, 1.53 × 10⁻⁵T^−1.86exp(−399/T) + 1.07 × 10³T^−3.15exp(−15219/T) and 5.62 × 10⁻¹²T^0.493exp(148/T) cm³ molecule⁻¹ s⁻¹, respectively, where T is in K. These predictions are in reasonably satisfactory agreement with the somewhat discordant experimental rate measurements.     

Behavior of N atoms in atomic-order nitrided Si0.5Ge0.5(1 0 0)

Behavior of N atoms in atomic-order nitrided Si_0.5Ge_0.5(1 0 0) by heat treatment in Ar at 600 °C was investigated by X-ray photoelectron spectroscopy (XPS). For thermal nitridation by NH₃ at 400 °C, nitridation of surface Si atoms tends to proceed preferentially over nitridation of surface Ge atoms. It is also clear that, with the heat treatment, nitridation of Si atoms proceeds by transfer of N atoms from Ge atoms. Angle-resolved XPS results show that Ge fraction beneath the surface nitrided layer increases significantly at 600 °C compared to the initial surface. These results indicate that preferential nitridation of Si atoms at surface over Ge atoms induces Ge segregation beneath the surface nitrided layer at higher temperatures above 400 °C.     

Origin of Unexpected Isotopic Trends in Synthesis of Superheavy Nuclei

We investigate the dependence of the yield of superheavy nuclei with Z = 110, 112, 114 on the neutron excess of the projectile nucleus with a two-parameter Smoluchowski equation. It is confirmed that in some cases, the cold fusion reactions with less neutron excess are more favourable than those with more neutron excess. In order to probe the origin of these unexpected isotopic trends, we also investigate the probabilities of capture, fusion and survival in the cold fusion reactions in detail It is found that the maximal ER cross sections of the superheavy nuclei exponentially increase as a function of Bf - Sn with Bf being the fission barrier and Sn being the neutron separation energy. Although the probabilities of capture and fusion have some influences, the unexpected isotopic trends mainly due to the dependence of the ER cross sections on the Bf - Sn value. Therefore, the reactions with larger Bf - Sn values should be more favourable for synthesis of superheavy nuclei.