2 If a fluid of bosons is cooled to sufficiently low temperature, a significant fraction will condense into the lowest quantum state, forming a Bose condensate. Bose condensation is a consequence of the even symmetry of the many-body wave function of bosons under particle interchange, and allows for the manifestation of macroscopic quantum phenomena, the most striking being superfluidity.Traditionally, Bose condensates are said to come in two types. Bose-Einstein condensates (BECs) occur in systems of stable bosons, such as dilute atomic gases or liquid Excitons are bosons that are bound states between an electron and hole in a solid, and were predicted long ago to Bose condense (2,3,4). Because of their light mass and high binding energy, exciton condensates should be stable at higher temperature than traditional BEC or BCS phases (5,6).Different theories predict that a Bose condensate of excitons could be a superfluid (5) or innately insulating (7), so there is tremendous need for experimental input. Identifying an exciton condensate in nature could have a profound impact on future understanding of macroscopic quantum phenomena, as well the classic problem of the metal-insulator transition in band solids, in which exciton condensation has long been believed to play a fundamental role (2,3,4).Condensed phases of photogenerated excitons have been realized in semiconductor quantum wells in resonance with a Fabry-Perot cavity which, although not fully thermally equilibrated, have exhibited evidence for transient superfluidity (8). Excitonic phases have also been realized in quantumHall bilayers in a perpendicular magnetic field (9). Although the order in these two-dimensional structures is not strictly long-ranged, and the order parameter cannot be measured directly, compelling evidence for excitonic correlations has been observed in Coulomb drag experiments (9). Despite these 3 achievements, there is a great need to identify an exciton condensate in a fully thermalized, threedimensional system in which the order is long-ranged.An ideal approach would be to identify a material in which an exciton condensate forms "naturally." Long ago, a BCS condensate of excitons was predicted to arise spontaneously in semimetals in which an indirect band gap is tuned close to zero ( Fig. 1) (2,3,4). This condensate is expected to break a spatial symmetry, rather than the U(1) symmetry broken by a superconductor, and in the absence of pinning should exhibit perfect conductivity without a Meissner effect (10). This phase can be thought of as a solid crystal of excitons, which early authors dubbed "excitonium" (4), and is the two-band analogue of the Wigner crystal instability of an interacting electron gas (10). This condensate is closely related to that in bilayer quantum wells (9), the coherence developing between electrons and holes in different bands ( Fig. 1) rather than in different layers. If found, this exciton condensate would be threedimensional, guaranteed to reside in thermodynamic equilibrium, and could potentially...

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When electrons in a solid are excited with light, they can alter the free energy landscape and access phases of matter that are beyond reach in thermal equilibrium. This accessibility becomes of vast importance in the presence of phase competition, when one state of matter is preferred over another by only a small energy scale that, in principle, is surmountable by light. Here, we study a layered compound, LaTe3, where a small in-plane (a-c plane) lattice anisotropy results in a unidirectional charge density wave (CDW) along the c-axis. Using ultrafast electron diffraction, we find that after photoexcitation, the CDW along the c-axis is weakened and subsequently, a different competing CDW along the a-axis emerges. The timescales characterizing the relaxation of this new CDW and the reestablishment of the original CDW are nearly identical, which points towards a strong competition between the two orders. The new density wave represents a transient non-equilibrium phase of matter with no equilibrium counterpart, and this study thus provides a framework for unleashing similar states of matter that are "trapped" under equilibrium conditions.

A central mystery in high-temperature superconductivity is the origin of the so-called strange metal (i.e., the anomalous conductor from which superconductivity emerges at low temperature). Measuring the dynamic charge response of the copper oxides, [Formula: see text], would directly reveal the collective properties of the strange metal, but it has never been possible to measure this quantity with millielectronvolt resolution. Here, we present a measurement of [Formula: see text] for a cuprate, optimally doped BiSrCaCuO ( = 91 K), using momentum-resolved inelastic electron scattering. In the medium energy range 0.1-2 eV relevant to the strange metal, the spectra are dominated by a featureless, temperature- and momentum-independent continuum persisting to the electronvolt energy scale. This continuum displays a simple power-law form, exhibiting behavior at low energy and/ behavior at high energy. Measurements of an overdoped crystal ( = 50 K) showed the emergence of a gap-like feature at low temperature, indicating deviation from power law form outside the strange-metal regime. Our study suggests the strange metal exhibits a new type of charge dynamics in which excitations are local to such a degree that space and time axes are decoupled.

Topological defects, potential information carriers, were written into and erased from a solid with femtosecond light pulses.

One of the most fundamental properties of an interacting electron system is its frequency-and wave-vector-dependent density response function, χ(q, ω). The imaginary part, χ (q, ω), defines the fundamental bosonic charge excitations of the system, exhibiting peaks wherever collective modes are present. χ quantifies the electronic compressibility of a material, its response to external fields, its ability to screen charge, and its tendency to form charge density waves. Unfortunately, there has never been a fully momentum-resolved means to measure χ(q, ω) at the meV energy scale relevant to modern electronic materials. Here, we demonstrate a way to measure χ with quantitative momentum resolution by applying alignment techniques from x-ray and neutron scattering to surface high-resolution electron energy-loss spectroscopy (HR-EELS). This approach, which we refer to here as "M-EELS", allows direct measurement of χ (q, ω) with meV resolution while controlling the momentum with an accuracy better than a percent of a typical Brillouin zone. We apply this technique to finite-q excitations in the optimally-doped high temperature superconductor, Bi 2 Sr 2 CaCu 2 O 8+x (Bi2212), which exhibits several phonons potentially relevant to dispersion anomalies observed in ARPES and STM experiments. Our study defines a path to studying the long-sought collective charge modes in quantum materials at the meV scale and with full momentum control.

X-ray diffraction was employed to study the evolution of the charge density wave (CDW) in Cu_{x}TiSe_{2} as a function of copper intercalation in order to clarify the relationship between the CDW and superconductivity. The results show a CDW incommensuration arising at an intercalation value coincident with the onset of superconductivity at around x=0.055(5). Additionally, it was found that the charge density wave persists to higher intercalant concentrations than previously assumed, demonstrating that the CDW does not terminate inside the superconducting dome. A charge density wave peak was observed in samples up to x=0.091(6), the highest copper concentration examined in this study. The phase diagram established in this work suggests that charge density wave incommensuration may play a role in the formation of the superconducting state.

2The observation of chirality is ubiquitous in nature. Contrary to intuition, the population of opposite chiralities is surprisingly asymmetric at fundamental levels [1,2]. Examples range from parity violation in the subatomic weak force [1] to the homochirality in essential biomolecules [2]. The ability to achieve chiralityselective synthesis (chiral induction) is of great importance in stereochemistry, molecular biology and pharmacology [2]. In condensed matter physics, a crystalline electronic system is geometrically chiral when it lacks any mirror plane, space inversion center or roto-inversion axis [3]. Typically, the geometrical chirality is predefined by a material's chiral lattice structure, which is fixed upon the formation of the crystal. By contrast, a particularly unconventional scenario is the gyrotropic order [4][5][6][7][8], where chirality spontaneously emerges across a phase transition as the electron system breaks the relevant symmetries of an originally achiral lattice. Such a gyrotropic order, proposed as the quantum analogue of the cholesteric liquid crystals, has attracted significant interest [4][5][6][7][8][9][10][11][12][13][14][15][16][17]. However, to date, a clear observation and manipulation of the gyrotropic order remain challenging. We report the realization of optical chiral induction and the observation of a gyrotropically ordered phase in the transition-metal dichalcogenide semimetal 1T -TiSe 2 . We show that shining mid-infrared circularly polarized light near the critical temperature leads to the preferential formation of one chiral domain. As a result, we are able to observe an out-of-plane circular photogalvanic current, whose direction depends on the optical induction. Our study provides compelling evidence for the spontaneous emergence of chirality in the correlated semimetal TiSe 2 [18]. Such chiral induction provides a new way of optical control over novel orders in quantum materials.In the presence of strong correlations, the behavior of electrons in a metal can signficantly deviate from a weakly-interacting Fermi gas, forming a wide range of complex, broken symmetry phases [19]. Recent theoretical works have highlighted their analogy with classical liquids [19], where a rich set of liquid crystalline phases that exhibit varying degrees of symmetry breaking and transport properties have been observed. A well-studied case is the nematic order [19][20][21], i.e., the spontaneous emergence of rotational anisotropy. In classical liquids, this is known as the nematic liquid crystal, whereas in quantum materials, it has recently been observed in quantum Hall systems, ruthenates, high temperature supercon-3 ductors [19], heavy-fermion superconductors [20], and correlated metallic pyrochlores [21].Another fascinating case is the gyrotropic order, i.e., the spontaneous emergence of geometrical chirality. In classical liquids, this is known as the cholesteric liquid crystal. In quantum materials, despite fundamental interest [4][5][6][7][8][9][10][11][12][13][14][15][16], a clear ...