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Jennifer Rigden

Publications and source records attributed to Jennifer Rigden.

3 recordsLinked to original sources

Bulk and surface electronic structure of MoAlB(010)

The bulk and surface electronic structure of MoAlB(010) is studied by a combination of angle-resolved photoemission spectroscopy and density functional calculations. The observed bulk Fermi-level crossings agree with the previously reported bulk Fermi surface of the material. Additionally, we find several surface states in the wide projected bulk band gaps around the Fermi energy. The surface states differ in their stability under residual-gas exposure in the vacuum system and in the magnitude of their Rashba-type spin-orbit splitting. We explain this in terms of their elemental and orbital character. A surface state arising from Al dangling bonds is sensitive to surface contamination, whereas a mainly Mo-derived surface state exhibits the stronger spin-orbit splitting. The surface states show symmetry-enforced crossings near the $\bar{\mathrm{S}}$ point of the surface Brillouin zone. These are protected by the mirror-symmetry elements of the p2mm wallpaper group.

cond-mat.mtrl-sci

Clustering-Enhanced Time- and Angle-Resolved Photoemission Study of LaTe$_3$: Absence of a Photoinduced Secondary CDW in the Electronic Structure

Optical control offers a compelling route for tailoring material properties on an ultrafast time scale. Ordered states such as charge density waves (CDWs) can be transiently melted by an ultrafast light excitation. This is also the case for the rare-earth tritelluride LaTe$_3$, a prototypical CDW compound. For this material it has recently been reported that the suppression of the primary CDW allows the transient formation of a second CDW, whose wave vector is orthogonal to the primary one. This creates the intriguing scenario where light enables switching between two distinct ordered phases of the material. While the second CDW has so far been observed by structural techniques, it remains an open question how the interplay of the two CDW phases is reflected in the material's electronic structure. We investigate this via time- and angle-resolved photoemission measurements of LaTe$_3$. The complex Fermi contour is probed using a FeSuMa analyzer, which records the photoemission intensity of the entire Fermi contour at once. The dynamics revealed by the FeSuMa analyzer are complemented by measurements using a conventional hemispherical electron analyzer. We combine conventional data analysis with $k$-means clustering, an unsupervised machine learning technique, demonstrating its strong potential for disentangling large datasets. While we do not find any features that cannot be explained by the melting and re-establishment of the primary CDW, distinct dynamics and coherent oscillations are observed in the different branches of the Fermi contour.

cond-mat.str-el

Line shapes in time- and angle-resolved photoemission spectroscopy explored by machine learning

Time- and angle-resolved photoemission spectroscopy is a powerful technique for investigating the dynamics of excited carriers in quantum materials. Typically, data analysis proceeds via the inspection of time distribution curves (TDCs), which represent the time-dependent photoemission intensity in a region of interest -- often chosen somewhat arbitrarily -- in energy-momentum space. Here, we employ $k$-means, an unsupervised machine learning technique, to systematically investigate trends in TDC line shape for quasi-free-standing monolayer graphene and for a simple analytical model. Our analysis reveals how finite energy and time resolution can affect the TDC line shape. We discuss how this can be taken into account in a quantitative analysis, and under what conditions the time-dependent photoemission intensity after laser excitation can be approximated by a simple exponential decay.

cond-mat.str-el