| 1. |
- Collaboration, The PANDA, et al.
(författare)
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Feasibility studies of time-like proton electromagnetic form factors at PANDA at FAIR
- 2016
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Ingår i: European Physical Journal A. - : Springer Publishing Company. - 1434-6001 .- 1434-601X. ; 52:10
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Tidskriftsartikel (refereegranskat)abstract
- Simulation results for future measurements of electromagnetic proton form factors at P ¯ ANDA (FAIR) within the PandaRoot software framework are reported. The statistical precision with which the proton form factors can be determined is estimated. The signal channel p¯ p→ e+e- is studied on the basis of two different but consistent procedures. The suppression of the main background channel, i.e.p¯ p→ π+π-, is studied. Furthermore, the background versus signal efficiency, statistical and systematical uncertainties on the extracted proton form factors are evaluated using two different procedures. The results are consistent with those of a previous simulation study using an older, simplified framework. However, a slightly better precision is achieved in the PandaRoot study in a large range of momentum transfer, assuming the nominal beam conditions and detector performance.
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| 2. |
- Singh, B., et al.
(författare)
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Feasibility study for the measurement of pi N transition distribution amplitudes at (P)over-barANDA in (P)over-barp -> J/psi pi(0)
- 2017
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Ingår i: Physical Review D. - : AMER PHYSICAL SOC. - 2470-0010 .- 2470-0029. ; 95:3
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Tidskriftsartikel (refereegranskat)abstract
- The exclusive charmonium production process in (P) over barp annihilation with an associated pi 0 meson (p) over barp -> J/psi pi(0) is studied in the framework of QCD collinear factorization. The feasibility of measuring this reaction through the J/psi -> e(+) e(-) decay channel with the AntiProton ANnihilation at DArmstadt ((P) over bar ANDA) experiment is investigated. Simulations on signal reconstruction efficiency as well as the background rejection from various sources including the (P) over barp -> pi(+)pi(-)pi(0) and (p) over barp -> J/psi pi(0)pi(0) reactions are performed with PANDAROOT, the simulation and analysis software framework of the (P) over bar ANDA experiment. It is shown that the measurement can be done at (P) over bar ANDA with significant constraining power under the assumption of an integrated luminosity attainable in four to five months of data taking at the maximum design luminosity.
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| 3. |
- Singh, B., et al.
(författare)
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Study of doubly strange systems using stored antiprotons
- 2016
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Ingår i: Nuclear Physics A. - : Elsevier. - 0375-9474 .- 1873-1554. ; 954, s. 323-340
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Tidskriftsartikel (refereegranskat)abstract
- Bound nuclear systems with two units of strangeness are still poorly known despite their importance for many strong interaction phenomena. Stored antiprotons beams in the GeV range represent an unparalleled factory for various hyperon-antihyperon pairs. Their outstanding large production probability in antiproton collisions will open the floodgates for a series of new studies of systems which contain two or even more units of strangeness at the PANDA experiment at FAIR. For the first time, high resolution gamma-spectroscopy of doubly strange Lambda Lambda-hypernuclei will be performed, thus complementing measurements of ground state decays of Lambda Lambda-hypernuclei at J-PARC or possible decays of particle unstable hypernuclei in heavy ion reactions. High resolution spectroscopy of multistrange Xi(-) -atoms will be feasible and even the production of Omega(-) -atoms will be within reach. The latter might open the door to the vertical bar S vertical bar = 3 world in strangeness nuclear physics, by the study of the hadronic Omega(-) -nucleus interaction. For the first time it will be possible to study the behavior of Xi(+) in nuclear systems under well controlled conditions.
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| 4. |
- Beutler, A., et al.
(författare)
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Adsorption properties of a mixed surface studied by high resolution core level photoemission : CO/0.5 ML Pd/Rh(111)
- 1998
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Ingår i: Surface Science. - 0039-6028. ; 411:1-2, s. 111-122
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Tidskriftsartikel (refereegranskat)abstract
- The coverage-dependent adsorption properties of a laterally heterogeneous bimetallic surface have been investigated by high resolution core level photoemission and low energy electron diffraction. The specific system under study was CO adsorbed on a Rh(111) surface onto which 2D Pd islands (coverage 0.5 ML) were formed by vapor deposition. The CO adsorption properties of the heterogeneous surface were compared with CO adsorption on a Rh(111) surface covered with a full Pd monolayer and with previous results for the CO/Rh(111) system. For low exposures CO is only found on the Rh(111) patches which can be explained by diffusion of CO from the Pd islands onto Rh parts in the adsorption process. At higher exposures CO diffusion from Rh to Pd is indicated. The origin of the diffusion processes can be found in the different coverage-dependent CO adsorption energies on the two surface parts.
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| 5. |
- Beutler, A., et al.
(författare)
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Identification of a laterally mobile state during CO adsorption
- 2000
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Ingår i: Journal of Physics: Condensed Matter. - : IOP Publishing. - 0953-8984 .- 1361-648X. ; 12:6, s. 765-772
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Tidskriftsartikel (refereegranskat)abstract
- We have investigated CO adsorption at 300 K on ∼ 1.5 atomic layer thick Pd films on a Mo(110) surface by high-resolution core level photoemission. We describe how high-resolution core level spectroscopy may be utilized to study the influence of laterally mobile states on the sticking probability of molecules on such a laterally heterogeneous surface. The present Pd films are laterally heterogeneous in the sense that the additional ∼ 0.5 atomic Pd layer forms mesoscopic one-layer thick islands on top of the first Pd layer. At 300 K, CO chemisorbs on these two-layer thick islands but not on the one-layer parts of the film. The rate at which these two-layer islands are filled by CO molecules as the surface is exposed to CO is found to be consistent with a picture where CO molecules that initially impinge on the one-layer parts of the surface enter a laterally mobile state and diffuse to the two-layer islands and adsorb there. This mobile state is in many respects similar to a classical precursor state.
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| 6. |
- Beutler, A., et al.
(författare)
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The influence of preadsorbed oxygen on the adsorption of CO on two-dimensional Pd islands on a Rh (111) surface
- 1998
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Ingår i: Surface Science. - 0039-6028. ; 418:2, s. 457-465
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Tidskriftsartikel (refereegranskat)abstract
- The influence of preadsorbed oxygen on the CO adsorption properties of a laterally heterogeneous bimetallic surface consisting of Pd islands on Rh(111) at a Pd coverage of 0.5 monolayers has been studied by high resolution core level photoemission. A surface consisting of clean Pd islands surrounded by oxygen-covered Rh(111) patches was prepared by predosing oxygen at room temperature. By applying core level photoemission to the Pd 3d5/2 and the C 1s levels, the adsorption of CO on this surface was studied with particular attention being paid to possible CO diffusion between the two surface parts. The CO molecules are found to diffuse from the oxygen-covered Rh(111) patches onto the Pd islands for low to medium CO exposures. This diffusion direction is opposite of that found previously for the 0.5 ML Pd on Rh(111) system with no oxygen predosing. This reversal of the diffusion direction is argued to be due to a large reduction of the CO adsorption energy on the Rh patches of the surface caused by the preadsorbed oxygen.
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| 7. |
- Jaworowski, A. J., et al.
(författare)
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Adsorption sites in O and CO coadsorption phases on Rh(111) investigated by high-resolution core-level photoemission
- 1999
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Ingår i: Surface Science. - 0039-6028. ; 431:1, s. 33-41
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Tidskriftsartikel (refereegranskat)abstract
- High-resolution core-level spectroscopy is used in combination with low-energy electron diffraction (LEED) and photoelectron diffraction to identify the adsorption sites for three different coadsorbed phases consisting of ordered overlayers of oxygen coadsorbed with CO on the Rh(111) single-crystal surface. The three ordered overlayer structures, which may be denoted as 2O + CO/Rh(111), O + CO/Rh(111) and O+2CO/Rh(111), all show (2 × 2) LEED patterns. In the 2O + CO and O + CO phases the CO molecules are found to occupy only on-top sites while the O + 2CO phase shows CO molecules in both on-top and three-fold hollow sites. In all cases the oxygen atoms are found in three-fold hollow sites. For the O + CO and O + 2CO phases our results confirm previous determinations by LEED, while the 2O + CO phase has not been observed before on Rh(111). The core-level binding energies of the C 1s and O 1s core levels for both adsorbates are characteristics of the adsorption site and are very close to the binding energies found for the pure cases of only oxygen or CO adsorbed on Rh(111). In the coadsorption phases we find that the interaction between the adsorbates has only a minor influence on the core-level binding energies. For the O + 2CO/Rh(111) coadsorption phase we find that a full CO coverage is not obtained; less than 80% of the unit cells contain two CO molecules, in line with previous findings.
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| 8. |
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| 9. |
- Strisland, F., et al.
(författare)
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Adsorption sites in coadsorption systems determined by photoemission spectroscopy : K and CO coadsorbed on Rh(111)
- 1998
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Ingår i: Surface Science. - 0039-6028. ; 410:2-3, s. 330-343
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Tidskriftsartikel (refereegranskat)abstract
- The adsorption sites of coadsorbed K and CO on the Rh(111) surface have been determined using high-resolution core-level spectroscopy, low-energy electron diffraction and site-resolved photoelectron diffraction. For both a (2 × 2)-2CO-1K and a (2√3 × 2√3)-6CO-1K structure, we find that the CO molecules occupy threefold hollow sites and the K atoms on-top sites, contrary to the adsorption sites of K (threefold hollow site) and CO (on-top site below 0.5 monolayers) if adsorbed alone on Rh(111). Deposition of K onto a CO precovered surface is found to induce large shifts towards lower binding energy of the C and O 1s core levels (∼0.7 eV for C 1s and ∼1.5 eV for O 1s). The major part of these shifts is shown to arise from the K-induced site change of the CO molecules. This finding may be of importance in the interpretation of XPS data of related co-adsorption systems. Finally, it is suggested that the C and O 1s binding energies provide useful fingerprints of the CO adsorption site also for co-adsorption systems.
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| 10. |
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