2017
DOI: 10.1103/physrevlett.118.136401
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Band-Resolved Double Photoemission Spectroscopy on Correlated Valence Electron Pairs in Metals

Abstract: Correlated valence electrons in Ag and Cu are investigated using double photoemission spectroscopy driven by a high-order harmonic light source. Electron pairs consisting of two d electrons as well as pairs with one sp and one d electron are resolved in the two-dimensional energy spectrum. Surprisingly, the intensity ratio of sp-d to d-d pairs from Ag is 3 times higher than in the self-convoluted density of states. Our results directly show the band-resolved configurations of electron pairs in solids and empha… Show more

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Cited by 21 publications
(12 citation statements)
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“…Although not as clear as in the 2e DOS these spectra display changes in the slope. We have marked energy positions by arrows which roughly agree with the kink position of the 2e DOS and are also in agreement with a recent report on DPE from a Ag(100) surface obtained with a much better energy resolution [9]. The arrow at 5.3 eV in Fig.…”
Section: Photon Energy Dependence Ag(100)supporting
confidence: 91%
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“…Although not as clear as in the 2e DOS these spectra display changes in the slope. We have marked energy positions by arrows which roughly agree with the kink position of the 2e DOS and are also in agreement with a recent report on DPE from a Ag(100) surface obtained with a much better energy resolution [9]. The arrow at 5.3 eV in Fig.…”
Section: Photon Energy Dependence Ag(100)supporting
confidence: 91%
“…It turns out that the self-convolution of the electronic density of states becomes a better approximation for increasing photon energy. We find some fine structure in the sum energy spectrum similar to our previous reports with lower photon energies [9]. Near the high-energy cutoff we record a finite coincidence intensity.…”
Section: Introductionsupporting
confidence: 89%
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“…Two-particle correlations in photoemission have been used previously to study electronic interactions in equilibrium [24][25][26]. The process discussed here is an emission of two electrons by two photons from the same ultrashort pulse (different from a double photo-emission where one photon leads to the emission of two electrons due to secondary processes), and thus allows a theoretical interpretation along the same lines as the conventional theory for time-resolved photoemission spectroscopy [27][28][29].…”
mentioning
confidence: 95%