| 1. |
- Nylén, H., et al.
(författare)
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O KVV Auger emission versus resonant photoemission at the O K edge of high-Tc superconductors
- 1998
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Ingår i: Physica C: Superconductivity and its Applications. - 0921-4534. ; 300:3-4, s. 161-170
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Tidskriftsartikel (refereegranskat)abstract
- Photoelectron spectroscopy results on single crystals of the superconductors Bi2Sr2CaCu2O8,Bi2Sr 2CuO6, Ba0.6K0.4BiO3 and the semiconductor Ba0.9K0.1BiO3 are reported for the photon energy region around the O K absorption threshold. The development of the O-KVV Auger structure has been carefully monitored as a function of photon energy. A non-monotonic behavior displaying a feature at a constant binding energy of about 14 eV was found for Bi2Sr2CaCu2O8 and Bi2Sr2CuO6 in a narrow photon energy region of 1 eV at the main edge of the O K absorption spectrum around 530 eV. The corresponding enhancement, connected with the autoionization of O 2 p states, is absent in Ba1-xKxBiO3 in contrast to Bi2Sr2CaCu2O8 and Bi2Sr2CuO6. The resonant enhancement is more pronounced for Bi2Sr2CuO6 as compared to Bi2Sr2CaCu2O8, which can be explained by a lower charge carrier concentration in the former case, leading to a more localized nature of intermediate O 2 p states. The model parameters Cu d-d and O p-p Coulomb interactions and the charge transfer energy Δ are estimated from the experiments.
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| 2. |
- Qvarford, M, et al.
(författare)
-
Photoemission and x-ray absorption study of superconducting and semiconducting Ba1-xKxBiO3 single crystals
- 1996
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 54:9, s. 6700-6707
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Tidskriftsartikel (refereegranskat)abstract
- Semiconducting Ba0.9K0.1BiO3 and superconducting Ba0.6K0.4BiO3 single crystals cleaved in situ have been studied by core level and valence band photoelectron spectroscopy and O K edge x-ray absorption spectroscopy. It was found that the general shape of the valence band spectrum agrees with the shape predicted by band structure calculations, but the intensity near the Fermi level, was lower in the experimental spectrum as compared to the calculated. The O K edge spectra showed that the metallic phase is not related to the presence of doping inducted O 2p holes. This property of Ba1-xKxBiO3 shows that the semiconductor-metal transition of this system is of a different nature than that of the hole doped cuprate high-T-c superconductors. The core level photoemission spectra of the cations showed a small asymmetry for Ba0.9K0.1BiO3. Corresponding spectra for Ba0.6K0.4BiO3 showed a larger asymmetry resulting in a resolved high binding energy shoulder in the Bi 4f spectrum. The origin of this feature is discussed.
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| 3. |
- Ruus, R., et al.
(författare)
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M4,5N4,5N4,5 Auger decay spectra of the resonantly excited 3d94f configuration of xenonlike ions in solids
- 1994
-
Ingår i: Physical Review B (Condensed Matter). - 0163-1829. ; 49:21, s. 14836-14844
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Tidskriftsartikel (refereegranskat)abstract
- The synchrotron-radiation-induced Auger and photoelectron spectra of the xenonlike ions I- (in CsI), Cs+ (in CsI), Ba2+ (in BaF2), and La3+ (in LaF3) have been measured in the vicinity of the M4,5 absorption edges of these ions. It is shown that the spectra of La and Ba measured at 3d10→3d94f resonances exhibit a very intense 4f-spectator structure which changes its energy and intensity with the energy of the exciting photons. Calculation of the Auger decay of the 3d-14f configuration shows that this structure is due to transitions to the 4d-24f+4p-1 final ionic configuration, the high-energy part of which overlaps the 4d-2 continuum. In the case of Ba this structure coexists with the normal Auger structure which appears as a result of the M4M5N6,7 Coster-Kronig transitions. The spectra of I- contain only the normal M4,5N4,5N4,5 Auger structure related to the 3d-1→4d-2 transitions. The spectra of Cs+ are similar to those of I- with a small admixture of the 4f-spectator-like structure.
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| 4. |
- Zakharov, A. A., et al.
(författare)
-
Metal-dielectric transition in Ba0.6K0.4BiO3-y single crystals studied by scanning photoelectron microscopy
- 1997
-
Ingår i: Physical Review B (Condensed Matter). - 0163-1829. ; 56:10
-
Tidskriftsartikel (refereegranskat)abstract
- The electronic structure of Ba0.6K0.4BiO3-y single crystals has been studied using a scanning photoelectron microscope with a lateral resolution in the one micrometer range. It is possible to change the oxygen content (y) and convert the surface from the metallic to the dielectric state presumably by breaking the Bi-O bonds by using the focused zero-order light to irradiate the sample surface. The electronic states close to the Fermi level after such a treatment show a different doping dependence as compared to the case of potassium doping. By imaging the surface on the micrometer scale we find significant variations in the valence band intensity over the surface and observe a rather large intensity of the density of states close to the Fermi level. This will have a large impact on the discussions of dynamical lattice distortion and pseudogap behavior in the metallic phase.
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| 5. |
- Andersen, J. N., et al.
(författare)
-
Alkali metal adsorption on Al(111)
- 1993
-
Ingår i: Surface Science. - : Elsevier BV. - 0039-6028. ; 289:3, s. 307-334
-
Tidskriftsartikel (refereegranskat)abstract
- The submonolayer adsorption of Na, K, Rb, and Cs on the Al(111) surface at 100 K and at room temperature is investigated by high resolution core level spectroscopy and low energy electron diffraction. It is found that the first alkali atoms on the surface adsorb at surface defects. At higher coverages, up to approximately one third of the maximum submonolayer coverage, alkali atoms adsorbed at defects coexist with a dispersed phase. At higher coverages island formation is found to occur for the majority of the systems. It is argued that all of the ordered structures formed at room temperature involve a disruption of the Al(111) surface in contrast to the situation at 100 K where the alkali atoms adsorb as adatoms.
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| 6. |
- Andersen, J. N., et al.
(författare)
-
Changes in the local surface geometry with conserved adsorbate coverage and long-range order caused by annealing
- 1992
-
Ingår i: Physical Review B (Condensed Matter). - 0163-1829. ; 46:19, s. 12784-12787
-
Tidskriftsartikel (refereegranskat)abstract
- The ordered c(2×2) Na on Al(100) and (3 × 3) R30°K on Al(111) structures formed at either 100 K or at room temperature are studied by high-resolution core-level spectroscopy. For both systems equal alkali coverages are found at these two temperatures. The core-level spectra, however, show strong changes with temperature. This behavior leads to the surprising conclusion that annealing at room temperature causes an irreversible change in the local geometry, i.e., of the adsorption site, of the overlayer even though neither the long-range order nor the adsorbate coverage changes.
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| 7. |
- Andersen, J. N., et al.
(författare)
-
Intermixing in the Na on Al(111) system
- 1992
-
Ingår i: Physical Review Letters. - 0031-9007. ; 68:1, s. 94-97
-
Tidskriftsartikel (refereegranskat)abstract
- Ordered structures formed by Na adsorption on the Al(111) surface are investigated by high-resolution core-level spectroscopy. It is shown that, contrary to the common picture of alkali adsorption, two of the structures formed at room temperature consist of intermixed Na-Al layers. The results for the (3 ×)-rotated-30°structure are also consistent with intermixing although they do not provide any definite proof. For Na layers deposited at 100 K no intermixing is found.
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| 8. |
- Andersen, J. N., et al.
(författare)
-
Surface core-level shifts as a probe of the local overlayer structure : CO on Pd(100)
- 1991
-
Ingår i: Physical Review Letters. - 0031-9007. ; 67:20, s. 2822-2825
-
Tidskriftsartikel (refereegranskat)abstract
- The bonding energies of the Pd 3d and the C 1s core levels have been studied for the p(2 S 2 × 2) R45°, p(3 s2 × S2) R45°, and p(4 S 2 × S 2) R45°structures of CO on Pd(100). Adsorption of CO shifts the Pd 3d surface emission to higher binding energies with the magnitude of the shift depending almost linearly on the number of Pd to CO bonds; the measured shift per bond is close to 0.5 eV. A direct relation is established between the detailed geometry of the CO overlayer and the changes in the Pd 3d spectra.
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| 9. |
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| 10. |
|
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| 11. |
- Lundgren, E., et al.
(författare)
-
Alkali core level binding energy shifts from buried interfaces between alkali films and metallic substrates with different surface index
- 1995
-
Ingår i: Vacuum. - 0042-207X. ; 46:8-10, s. 1159-1163
-
Tidskriftsartikel (refereegranskat)abstract
- Core level binding energy shifts from approximately three layers of different alkali metals deposited on Pd(111), Pd(100), Rh (111), and Rh (110) are presented in order to demonstrate how the packing of the substrate surface affects the layer-resolved alkali core level binding energy shifts. It is found that a more open surface induces a larger alkali core level binding energy shift. It is shown that this behaviour can be explained as a consequence of the higher coordination of the alkali metal atom to the substrate on a more open surface than on a more closed packed surface.
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| 12. |
- Lundgren, E., et al.
(författare)
-
Alkali core-level binding-energy shifts in alkali/4d-metal interface systems
- 1994
-
Ingår i: Physical Review B (Condensed Matter). - 0163-1829. ; 50:7, s. 4711-4717
-
Tidskriftsartikel (refereegranskat)abstract
- Photoemission from different alkali core levels (Na 2p, K 3p, Rb 4p, and Cs 4d) has been studied for thin alkali films deposited on four different 4d metal surfaces: Mo(110), Rh(111), Rh(110), and Pd(100). Alkali atoms at the interface, the bulk, and at the surface of the adsorbed alkali film are found to have different core-level binding energies. It is found that the core-level binding-energy shifts of the alkali metals induced by the 4d-metal substrate increase with increasing atomic number of the alkali metal and with increasing atomic number of the 4d metal. Thermodynamical quantities such as interface segregation energies and adhesion energies are deduced from the layer-resolved shifts. Estimates of the experimental binding-energy shifts are given using semiempirical calculations, and certain complications in doing that are discussed.
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| 13. |
- Lundgren, E., et al.
(författare)
-
Layer dependent core level binding energy shifts : Na, K, Rb and Cs on Al(111)
- 1993
-
Ingår i: Surface Science. - 0039-6028. ; 281:1-2, s. 83-90
-
Tidskriftsartikel (refereegranskat)abstract
- Layer resolved core level spectra are presented for Na, K, Rb and Cs films on Al(111). From the development of the spectra, it is possible to distinguish emission from alkali atoms at the interface, in the bulk, and at the surface of the adsorbed layers. The core level binding energy shifts are discussed in terms of adhesion and interface segregation energies. It is found experimentally that the Al induced core level binding energy shifts of the alkalis are increasing with increasing atomic number of the alkali metal. This trend is qualitatively reproduced by semi-empirical calculations.
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| 14. |
- Lundgren, E., et al.
(författare)
-
Unified behavior of alkali core-level binding-energy shifts induced by sp metals
- 1997
-
Ingår i: Physical Review B (Condensed Matter). - 0163-1829. ; 56:19, s. 12560-12565
-
Tidskriftsartikel (refereegranskat)abstract
- Thin overlayers of Na, K. Rb, and Cs on different sp-metal substrates have been investigated using photo-electron spectroscopy. The alkali core levels show clearly resolved binding-energy shifts between the surface layer, the intermediate layer(s), and the interface layer. The magnitude of these shifts depends on sp metal and on alkali metal. The layer-resolved core-level binding-energy shifts are well reproduced by models based on a thermodynamical description. For three-layer alkali films the core-level binding energy of the intermediate layer is found to exhibit a small but significant shift between different sp-metal substrates. A simple relationship between the core-level binding-energy shift for the interface layer and the difference in rs value between the sp substrate and the adsorbate is shown to exist.
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| 15. |
- Nyholm, R., et al.
(författare)
-
ELECTRONIC AND STRUCTURAL-PROPERTIES OF THE CU-BI2CASR2CU2O8 INTERFACE
- 1991
-
Ingår i: Physica. C, Superconductivity. - 0921-4534 .- 1873-2143. ; 180:1-4, s. 120-123
-
Tidskriftsartikel (refereegranskat)abstract
- The formation of the Cu-Bi2CaSr2Cu2O8 interface has been studied by photoelectron spectroscopy using synchrotron radiation. Photon energies in the range 20-1000 eV were utilized in order to probe both the valence band and to monitor chemical changes upon Cu deposition, as revealed by the core-level shifts. A strong chemical reaction between Bi2CaSr2CuO8 and Cu is manifested by the formation of metallic Bi. From the intensity variations as a function of electron emission angle it is shown that the metallic Bi segregates to the top surface layer.
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| 16. |
- Nyholm, R., et al.
(författare)
-
PHOTOEMISSION-STUDY OF THE BI2CASR2CU2O8 SUPERCONDUCTOR WITH CU, AG AND AU OVERLAYERS
- 1993
-
Ingår i: Physica. C, Superconductivity. - 0921-4534 .- 1873-2143. ; 218:1-2, s. 103-108
-
Tidskriftsartikel (refereegranskat)abstract
- In this paper, we present a photoemission study of the interaction of Cu, Ag and Au with clean single-crystal Bi2CaSr2Cu2O8 superconductor surfaces. Both the valence-band and the Bi 5d, O 1 s and Sr 3d core levels were monitored for all overlayers. Cu, Ag and Au were deposited as consecutively thicker layers starting with a third of a monolayer and progressing in steps up to a deposition in the range of eight monolayers. Comparing the results for the different overlayers reveals the Ag overlayer to be less reactive than Au which causes the formation of metallic Bi on cleaved Bi2CaSr2Cu2O8 surface. Cu is shown to be the most reactive of the three metals. The Au and Ag overlayers display an island-growth mode, while Cu grows in a layer-by-layer fashion.
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| 17. |
- Nyholm, R., et al.
(författare)
-
Surface core-level shifts of the Al(100) and Al(111) surfaces
- 1991
-
Ingår i: Physical Review B (Condensed Matter). - 0163-1829. ; 44:19, s. 10987-10990
-
Tidskriftsartikel (refereegranskat)abstract
- The surface core-level shifts of the Al(100) and Al(111) surfaces have been measured by high-resolution photoelectron spectroscopy. For the Al(100) surface we obtain a value of (-965) meV. This value is in excellent agreement with a recent ab initio calculation by Feibelman. The surface core-level shift of the Al(111) surface is found to be close to zero, and an upper limit of 15 meV is obtained.
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| 18. |
- Nyholm, R., et al.
(författare)
-
SYNCHROTRON-RADIATION SOFT-X-RAY PHOTOEMISSION-STUDY OF LEAD ON BI2CASR2CU2O8
- 1992
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 46:10, s. 6488-6494
-
Tidskriftsartikel (refereegranskat)abstract
- In this paper we present a study of the interaction of Pb with a clean single-crystal Bi2CaSr2Cu2O8 superconductor surface based on photoemission and low-energy electron diffraction (LEED). Deposition of Pb on a Bi2CaSr2Cu2O8 Crystal kept at room temperature gives rise to the formation of metallic Bi and oxidized Pb at the interface. This behavior could not be observed when the crystal was kept at 100 K during Pb deposition. For all investigated Pb overlayers on a cold crystal (100 K), surface-sensitive photoelectron spectroscopy revealed the growth of a covering metallic Pb overlayer film. The growth at 100 K, contrary to the growth at room temperature, preserved the original LEED 5 X 1 pattern even for Pb depositions corresponding to a 24-angstrom thick overlayer indicating epitaxial growth. Furthermore, a rigid 0.4-eV shift of the valence band and the Bi 5d core levels is observed upon initial Pb deposition and is tentatively attributed to electron doping.
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| 19. |
- Nyholm, R., et al.
(författare)
-
The surface core-level shift of the Pd(100) single-crystal surface
- 1992
-
Ingår i: Journal of Physics: Condensed Matter. - : IOP Publishing. - 0953-8984 .- 1361-648X. ; 4:1, s. 277-283
-
Tidskriftsartikel (refereegranskat)abstract
- The surface core-level shift of the Pd(100) single-crystal surface has been measured from high-resolution Pd 3d core-level spectra. The surface atoms are found to have 0.44+or-0.03 eV lower binding energy than the bulk atoms. The result is compared with theoretical estimates.
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| 20. |
- Qvarford, M, et al.
(författare)
-
Doping dependence of the O 1s is core-level photoemission in bi-Sr-Ca-Cu-O superconductors
- 1996
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 53:22, s. 14753-14756
-
Tidskriftsartikel (refereegranskat)abstract
- The O 1s core level of three different Bi-Sr-Ca-Cu-O superconductors has been studied by means of high-resolution x-ray-photoelectron spectroscopy (XPS) and x-ray absorption spectroscopy (XAS). The O 1a XPS spectra could be decomposed into three components that were unambiguously assigned to the emission from the three different oxide layers in the crystal structure. These are, in order of increasing binding energy, Cu-O-2, Sr-O, and Bi-O. Furthermore, the component assigned to the Cu-O-2 layers exhibits a shift which depends on the hole doping as monitored by the XAS spectra.
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| 21. |
- Qvarford, M, et al.
(författare)
-
Doping dependence of the O 1s is core-level photoemission in bi-Sr-Ca-Cu-O superconductors
- 1996
-
Ingår i: PHYSICAL REVIEW B-CONDENSED MATTER. - : AMER INST PHYSICS. - 0163-1829. ; 53:22, s. 14753-14756
-
Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- The O 1s core level of three different Bi-Sr-Ca-Cu-O superconductors has been studied by means of high-resolution x-ray-photoelectron spectroscopy (XPS) and x-ray absorption spectroscopy (XAS). The O 1a XPS spectra could be decomposed into three component
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| 22. |
- Qvarford, M., et al.
(författare)
-
Polarisation-dependent X-ray absorption in high- and low-Tc Bi2Sr2Can-1CunO4+2n superconductors
- 1993
-
Ingår i: Physica C: Superconductivity and its Applications. - : Elsevier BV. - 0921-4534. ; 214:1-2, s. 119-126
-
Tidskriftsartikel (refereegranskat)abstract
- Taking advantage of the linear polarisation of synchrotron radiation, the polarisation dependence of the O K and Cu L3 X-ray absorption edges has been compared for in situ cleaved Bi2Sr2CaCu2O8 and Bi2Sr2CuO6 single crystals. The X-ray absorption spectra were measured by means of total electron yield detection. The spectra show for both crystals that the lowest unoccupied Cu 3d and O 2p orbitals are dominantly oriented parallel to the a-b plane, but also the presence of a small amount of unoccupied orbitals oriented perpendicular to the a-b plane can be deduced from both the O K and Cu L3 absorption spectra. A shift of the order of 0.5 eV between absorption into the in-plane and the out-of-plane Cu 3d orbitals was measured for the Bi2Sr2CaCu2O8 crystal, but no such shift was found for the Bi2Sr2CuO6 crystal.
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| 23. |
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| 24. |
- QVARFORD, M, et al.
(författare)
-
X-RAY-ABSORPTION AND RESONANT-PHOTOEMISSION STUDY OF CA IN THE HIGH-TEMPERATURE SUPERCONDUCTOR BI2SR2CACU2O8
- 1992
-
Ingår i: Physical Review B Condensed Matter. - 0163-1829 .- 1095-3795. ; 46:21, s. 14126-14133
-
Tidskriftsartikel (refereegranskat)abstract
- The electronic structure of Ca in the high-temperature superconductor Bi2Sr2CaCu2O8 has been studied by x-ray-absorption spectroscopy and resonant-photoemission at the Ca L2,3 absorption edge. In the x-ray-absorption spectrum no edge structure is seen at the energy corresponding to the Ca 2p3/2 core-level binding energy, in agreement with the very low Ca density of states at the Fermi level predicted by band-structure calculations. Furthermore, the crystal-field splitting of the Ca 3d level, which is characteristic of ionic Ca compounds, is clearly observed in the x-ray-absorption spectrum. The photoemission spectra display strong resonant enhancements of the Ca 3s and 3p core levels as well as strong changes in the intensity and the line shape of the Ca L2,3M2,3M2,3 Auger structure at the Ca L2,3 threshold, showing the localized nature of the 3d states in core ionized Ca. The 3d induced spectator shift of the Ca L2,3M2,3M2,3 complex is fairly small as compared to what has been reported for CaF2, indicating that the screening of the normal Auger final state by the charge carriers in the surrounding Cu-O2 layers is quite efficient. From the Ca L2,3M2,3M2,3 data it is also suggested that, at the Ca L2 threshold, the excited 3d electron participates in a Coster-Kronig-type decay resulting in a 2p3/2 core hole followed by a normal L3M2,3M2,3 Auger decay.
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| 25. |
- Qvarford, M., et al.
(författare)
-
X-ray absorption study of oxygen in the high-Tc superconductor Bi2Sr2CaCu2O8 near the interfaces to Cu, Ag and Au
- 1996
-
Ingår i: Physica C: Superconductivity and its Applications. - : Elsevier BV. - 0921-4534 .- 1873-2143. ; 265:1-2, s. 113-120
-
Tidskriftsartikel (refereegranskat)abstract
- The influence on O 2p holes in single crystalline Bi2Sr2CaCu2O8 upon the interface formation to Cu, Ag and Au has been studied by O K edge X-ray absorption measurements. It was found that Cu reduces the amount of doping induced O 2p holes significantly in the vicinity of the interface, whereas Ag and Au gave a much smaller reduction of these states. Photoemission spectra confirmed previous findings that Cu causes a strong chemical reaction at the Bi-O surface of Bi2Sr2CaCu2O8, in contrast to Ag and Au which induced only a minimal reaction. The results support the opinion that the Bi-O layers are essential for the doping of the Cu-O2 layers in Bi2Sr2CaCu2O8.
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| 26. |
- ROGELET, T, et al.
(författare)
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ELECTRONIC-STRUCTURE OF NIO(1 0 0) WITH ADSORBED NA
- 1993
-
Ingår i: Solid State Communications. - 0038-1098 .- 1879-2766. ; 85:7, s. 657-660
-
Tidskriftsartikel (refereegranskat)abstract
- Adsorption of Na on single crystals of NiO(1 0 0) at room temperature has been investigated via angle-resolved photoemission spectroscopy and measurements of work-function changes. The drastic changes in the valence band spectra upon Na deposition are assigned to a chemical reaction between Na and O where metallic Ni is left as by-product. At short deposition times, Na mainly acts as an inert electron donor, and at these coverages no dispersion is observed in the angle-resolved photoemission spectra which indicates that the electronic states are localized. The measurements were performed both for a polished and an in-situ cleaved NiO crystal.
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| 27. |
- Soderholm, S, et al.
(författare)
-
A photoelectron spectroscopy and x-ray absorption study of Bi2Sr2CaCu2O8 single crystal with adsorbed Cs : On the origin of the states affected by electron doping and evidence for spatially resolved electron doping
- 1996
-
Ingår i: Journal of Physics. - : IOP Publishing. - 0953-8984 .- 1361-648X. ; 8:9, s. 1307-1320
-
Tidskriftsartikel (refereegranskat)abstract
- The influence of electron doping, via deposition of small amounts of Cs, on the electronic structure of Bi2Sr2CaCu2O8 has been studied by high-resolution photoelectron spectroscopy (PES) and x-ray absorption spectroscopy (XAS), utilizing synchrotron radiation. The changes in the electronic structure were monitored by PES of the valence band and of the O Is, Bi 4f, Bi 5d, Ca 2p and Sr 3d core levels, and by XAS at the O Is, Cu 2p and Ca 2p edges. The experimental data suggest that the loss of the Fermi edge and the loss of spectral intensity down to about 2 eV below the Fermi level, and the substantial loss of spectral intensity of the pre-edge structure in the O 1s XAS spectrum are mainly due to annihilation of states with O 2p character in the Cu-O layer. It is evident from bulk- and surface-sensitive XAS spectra that the electron doping by Cs affects the electronic structure more strongly close to the surface. This implies that the doping occurs locally and that the charge transfer between the different layers in the unit cell is not uniform. Thus it seems possible to alter the electronic properties of Bi2Sr2CaCu2O8 locally through spatially resolved electron doping. When larger amounts of Cs are deposited, a chemical reaction occurs which causes a disruption of the Bi-O layer. This deposition regime is characterized by the presence of caesium oxide and reduced (metallic) Bi.
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| 28. |
- Söderholm, S, et al.
(författare)
-
A photoemission spectroscopy and X-ray absorption study of Bi(2)Sr(2)CaCu(2)O(8) single crystal with adsorbed Cs: On the origin of states affected by electron doping and evidence for spatially resolved electron doping
- 1996
-
Ingår i: Journal of Physics: Condensed Matter. - : IOP Publishing. - 1361-648X .- 0953-8984. ; 8, s. 1307-1320
-
Tidskriftsartikel (refereegranskat)abstract
- The influence of electron doping, via deposition of small amounts of Cs, on the electronic structure of has been studied by high-resolution photoelectron spectroscopy (PES) and x-ray absorption spectroscopy (XAS), utilizing synchrotron radiation. The changes in the electronic structure were monitored by PES of the valence band and of the O 1s, Bi 4f, Bi 5d, Ca 2p and Sr 3d core levels, and by XAS at the O 1s, Cu 2p and Ca 2p edges. The experimental data suggest that the loss of the Fermi edge and the loss of spectral intensity down to about 2 eV below the Fermi level, and the substantial loss of spectral intensity of the pre-edge structure in the O 1s XAS spectrum are mainly due to annihilation of states with O 2p character in the Cu - O layer. It is evident from bulk- and surface-sensitive XAS spectra that the electron doping by Cs affects the electronic structure more strongly close to the surface. This implies that the doping occurs locally and that the charge transfer between the different layers in the unit cell is not uniform. Thus it seems possible to alter the electronic properties of locally through spatially resolved electron doping. When larger amounts of Cs are deposited, a chemical reaction occurs which causes a disruption of the Bi - O layer. This deposition regime is characterized by the presence of caesium oxide and reduced (metallic) Bi.
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| 29. |
- TJERNBERG, O, et al.
(författare)
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ANGLE-RESOLVED PHOTOEMISSION ON NIO - ON THE NATURE OF THE VALENCE-BAND
- 1995
-
Ingår i: Vacuum. - 0042-207X .- 1879-2715. ; 46:8-10, s. 1215-1218
-
Tidskriftsartikel (refereegranskat)abstract
- Angle resolved photoelectron spectroscopy has been performed on the valence band of NiO at the National Swedish Laboratory for Synchrotron Radiation. Normal emission spectra have been recorded for photon energies between 17 and 140 eV in order to study the electronic structure of the valence band. The experimentally determined band structure has been compared with a local density augmented plane wave band structure calculation. Signs of the influence of antiferromagnetic ordering are found and the general agreement between experimental and theoretical oxygen derived bands indicates strong hybridization between Ni 3d and O 2p orbitals.
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| 30. |
- Tjernberg, O, et al.
(författare)
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Evidence of pseudogap related core level shifts in Bi2Sr2Ca1-xYxCu2O8+delta
- 1997
-
Ingår i: Physical Review Letters. - 0031-9007 .- 1079-7114. ; 79:3, s. 499-502
-
Tidskriftsartikel (refereegranskat)abstract
- Photoelectron spectroscopy data from Bi2Sr2Ca1-xYxCu2O8+delta Single crystals, for x = 0, 0.16, and 0.55, are presented. It is shown that there are core level shifts related to the opening of a pseudogap and that similar shifts are observed at the opening of the superconducting gap in optimally doped samples. This result is in agreement with pair formation above T-c as suggested by V.J. Emery and S.A. Kivelson [Nature (London) 374, 434 (1995)].
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| 31. |
- Tjernberg, O, et al.
(författare)
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Evidence of pseudogap related core level shifts in Bi2Sr2Ca1-xYxCu2O8+delta
- 1997
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Ingår i: PHYSICAL REVIEW LETTERS. - : AMER INST PHYSICS. - 0031-9007. ; 79:3, s. 499-502
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Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
- Photoelectron spectroscopy data from Bi2Sr2Ca1-xYxCu2O8+delta Single crystals, for x = 0, 0.16, and 0.55, are presented. It is shown that there are core level shifts related to the opening of a pseudogap and that similar shifts are observed at the opening
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| 32. |
- Tjernberg, O, et al.
(författare)
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Resonant photoelectron spectroscopy on NiO
- 1996
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Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 53:15, s. 10372-10376
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Tidskriftsartikel (refereegranskat)abstract
- Resonant photoelectron spectroscopy studies have been performed on the NiO valence band at photon energies corresponding to the Ni 2p, 3p, and O 1s absorption thresholds. Strong resonances are seen in the vicinity of the Ni 2P threshold, which confirm earlier conclusions from the weaker resonances seen at the Ni 3p threshold. No valence-band resonance is observed at the O 1s threshold. The analysis of this data confirms the picture of NiO as a strongly correlated charge-transfer insulator by identifying the highest-lying states as being of mainly 3d(8)L final-state character. The existence of localized excited Ni states, as well as the delocalized nature of the O states, are confirmed. Comparisons with the configuration-interaction model and quasiparticle calculations are also made.
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