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Yau Chuen Yam

Publications and source records attributed to Yau Chuen Yam.

2 recordsLinked to original sources

Probing the Penetration Depth of Topological Surface States by Magnetic Impurity Scattering in V-doped Sb$_2$Te$_3$

Topological insulators host Dirac surface states (SS) protected by time-reversal symmetry. Inter-surface hybridization can gap the SS and give rise to the quantum spin Hall effect in films that are sufficiently thin compared to the SS penetration depth. However, quantifying the SS penetration depth typically requires painstaking synthesis of multiple films with varying thickness. Here we introduce a direct method to probe the SS penetration depth in bulk crystals, by studying the interplay between SS and magnetic impurities in \SVT. Using scanning tunneling microscopy and spectroscopy, we find that even sparse magnetic impurities ($\lesssim0.25\%$ vanadium) can gap the Dirac SS. However, a single V impurity induces only localized states, and does not form an impurity band, so the gapped Dirac dispersion is preserved away from the impurity. In high magnetic fields, we observe an energy shift of the $0^\text{th}$ Landau level and a suppression of quasiparticle lifetime at the Dirac point, indicating \newtext{magnetic} scattering of the SS. Crucially, by employing V impurities at different depths as precise scattering probes, we reveal the SS penetration depth on the sub-nanometer scale in a bulk crystal.

cond-mat.mes-hall↗

Angle-resolved photoemission intensity for multi-orbital bands: Complex interplay between the self-energy matrix and the optical matrix elements

We use a simple one-dimensional two-band model with electron-phonon coupling to illustrate some of the complications that arise in multi-band systems when trying to extract a self-energy using the typical approach used for single-band systems when analyzing angle-resolved photoemission spectroscopy (ARPES) data. The underlying reason is that in multi-band models the self-energy is a matrix, not a scalar, and the result obtained from the ARPES analysis is a complicated function of all these self-energy matrix elements, weighted by different dipole matrix elements of the relevant Wannier orbitals. We contrast the results for Holstein and Peierls electron-phonon couplings to further illustrate differences between models with a local versus non-local self-energy matrix.

cond-mat.str-el↗