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Abstract Angle‐resolved photoemission spectroscopy (ARPES) has been a widely adopted technique in the studies of quantum materials. The surface sensitivity of photoelectric effect also makes it a powerful tool to investigate surface and shallow interface phenomena. While an overwhelming majority of its use focuses on extracting the eigenenergy of the electron Bloch states in momentum space, attempts to extract information of the wave function via ARPES has been limited to molecular systems. In this perspective, it is proposed and advocated use ARPES to investigate and unravel wave function properties, as opposed to only the electron energy‐momentum dispersion relation, in crystalline solids and their interfaces. This can help enhance the rapidly growing development of material properties based on the spatial and geometric properties of the electronic wave functions. 

A central problem in modern condensed matter physics is the understanding of materials with strong electron correlations. Despite extensive work, the essential physics of many of these systems is not understood and there is very little ability to make predictions in this class of materials. In this manuscript we share our personal views on the major open problems in the field of correlated electron systems. We discuss some possible routes to make progress in this rich and fascinating field. This manuscript is the result of the vigorous discussions and deliberations that took place at Johns Hopkins University during a three-day workshop January 27, 28, and 29, 2020 that brought together six senior scientists and 46 more junior scientists. Our hope, is that the topics we have presented will provide inspiration for others working in this field and motivation for the idea that significant progress can be made on very hard problems if we focus our collective energies. 

In heavily hole-doped cuprates, superconductivity does not die by simply dissolving into a uniform metal due to the lack of pairing, but rather survives by shattering into nanoscale superconducting puddles. 

Two-dimensional electron gas (2DEG) states at oxide interfaces between two ferroic materials have been fertile ground to realize controllable multiferroicity. Here, we investigate the 2DEG states at the interface of ferroelectric BaTi⁢O3 and a magnetic layer of iron using angle-resolved photoemission spectroscopy. Orbital-selective charge transfer occurs on the surprisingly robust 2DEG. Based on first-principles calculations, we show how the interfacial hybridization can give rise to the unexpected charge transfer in the magnetic 2DEG. Our study reveals a close interplay on a 2DEG between magnetic and ferroelectric interfaces, which sheds light on future design principles of multiferroic 2DEG states. 

Angle-resolved photoemission spectroscopy (ARPES) is a powerful tool for probing the momentum-resolved single-particle spectral function of materials. Historically, in situ magnetic fields have been carefully avoided as they are detrimental to the control of photoelectron trajectory during the photoelectron detection process. However, magnetic field is an important experimental knob for both probing and tuning symmetry-breaking phases and electronic topology in quantum materials. In this paper, we introduce an easily implementable method for realizing an in situ tunable magnetic field at the sample position in an ARPES experiment and analyze magnetic-field-induced artifacts in the ARPES data. Specifically, we identified and quantified three distinct extrinsic effects of a magnetic field: constant energy contour rotation, emission angle contraction, and momentum broadening. We examined these effects in three prototypical quantum materials, i.e., a topological insulator (Bi2Se3), an iron-based superconductor (LiFeAs), and a cuprate superconductor (Pb-Bi2Sr2CuO6+x), and demonstrate the feasibility of ARPES measurements in the presence of a controllable magnetic field. Our studies lay the foundation for the future development of the technique and interpretation of ARPES measurements of field-tunable quantum phases. 

Abstract We examine key aspects of the theory of the Bardeen–Cooper–Schrieffer (BCS) to Bose–Einstein condensation (BEC) crossover, focusing on the temperature dependence of the chemical potential,μ. We identify an accurate method of determining the change ofμin the cuprate high temperature superconductors from angle-resolved-photoemission data (along the ‘nodal’ direction), and show thatμvaries by less than a few percent of the Fermi energy over a range of temperatures from far below to several times above the superconducting transition temperature,T_c. This shows, unambiguously, that not only are these materials always on the BCS side of the crossover (which is a phase transition in thed-wave case), but are nowhere near the point of the crossover (where the chemical potential approaches the band bottom). 

Abstract Non-volatile phase-change memory devices utilize local heating to toggle between crystalline and amorphous states with distinct electrical properties. Expanding on this kind of switching to two topologically distinct phases requires controlled non-volatile switching between two crystalline phases with distinct symmetries. Here, we report the observation of reversible and non-volatile switching between two stable and closely related crystal structures, with remarkably distinct electronic structures, in the near-room-temperature van der Waals ferromagnet Fe_5−δGeTe₂. We show that the switching is enabled by the ordering and disordering of Fe site vacancies that results in distinct crystalline symmetries of the two phases, which can be controlled by a thermal annealing and quenching method. The two phases are distinguished by the presence of topological nodal lines due to the preserved global inversion symmetry in the site-disordered phase, flat bands resulting from quantum destructive interference on a bipartite lattice, and broken inversion symmetry in the site-ordered phase.