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Springer eBooks

Electron-doping Evolution of the Quasiparticle Band of the Cuprates

Christopher Dahnken, Michael Potthoff, Enrico Arrigoni, Werner R. Hanke

Published Mar 2, 2006• 0 citations
Publisher
DOI
10.1007/3-540-29064-8_3

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Abstract How a Mott insulator develops into a weakly coupled metal upon doping is a central question to understanding various emergent correlated phenomena. To analyze this evolution and its connection to the high-Tc cuprates, we study the single-particle spectrum for the doped Hubbard model using cluster perturbation theory on superclusters. Starting from extremely low doping, we identify a heavily renormalized quasiparticle dispersion that immediately develops across the Fermi level, and a weakening polaronic side band at higher binding energy. The quasiparticle spectral weight roughly grows at twice the rate of doping in the low doping regime, but this rate is halved at optimal doping. In the heavily doped regime, we find both strong electron-hole asymmetry and a persistent presence of Mott spectral features. Finally, we discuss the applicability of the single-band Hubbard model to describe the evolution of nodal spectra measured by angle-resolved photoemission spectroscopy (ARPES) on the single-layer cuprate La2−xSrxCuO4 (0 ≤ x ≤ 0.15). This work benchmarks the predictive power of the Hubbard model for electronic properties of high-Tc cuprates.
We study the evolution of the single-particle spectrum with electron doping in a scheme which adds multiple exchange of transverse spin excitations to the mean-field antiferromagnetic insulator. Away from half-filling small Fermi surface pockets appear first around the X points, and simultaneously new spectral weight grows in the insulating gap. With further doping the in-gap states develop the character of a renormalized quasiparticle band near the chemical potential. The essential features in momentum-energy space agree well with recent studies using angle-resolved photoemission spectroscopy on electron-doped cuprates. We interpret the origins and the nature of the in-gap states using a simple variational wave function.