Publications

Ensembles of particles rotating in a two-dimensional fluid can exhibit chaotic dynamics yet develop signatures of hidden order. Such "rotors" are found in the natural world spanning vastly disparate length scales - from the rotor proteins in cellular membranes to models of atmospheric dynamics. Here we show that an initially random distribution of either ideal vortices in an inviscid fluid, or driven rotors in a viscous membrane, spontaneously self assembles. Despite arising from drastically different physics, these systems share a Hamiltonian structure that sets geometrical conservation laws resulting in distinct structural states. We find that the rotationally invariant interactions isotropically suppress long wavelength fluctuations - a hallmark of a disordered hyperuniform material. With increasing area fraction, the system orders into a hexagonal lattice. In mixtures of two co-rotating populations, the stronger population will gain order from the other and both will become phase enriched. Finally, we show that classical 2D point vortex systems arise as exact limits of the experimentally accessible microscopic membrane rotors, yielding a new system through which to study topological defects.

We introduce a simple entropy-based formalism to characterize the role of mixing in pressure-balanced multiphase clouds, and demonstrate example applications using Enzo-E (magneto)hydrodynamic simulations. Under this formalism, the high-dimensional description of the system's state at a given time is simplified to the joint distribution of mass over pressure (P) and entropy (K=P/ργ). As a result, this approach provides a way for (empirically and analytically) quantifying the impact of different initial conditions and sets of physics on the system evolution. We find that mixing predominantly alters the distribution along the K direction and illustrate how the formalism can be used to model mixing and cooling for fluid elements originating in the cloud. We further confirm and generalize a previously suggested criterion for cloud growth in the presence of radiative cooling, and demonstrate that the shape of the cooling curve, particularly at the low temperature end, can play an important role in controlling condensation. Moreover, we discuss the capacity of our approach to generalize such a criterion to apply to additional sets of physics, and to build intuition for the impact of subtle higher order effects not directly addressed by the criterion.

We introduce a toy model for the time-frequency structure of fast radio bursts (FRB), in which the observed emission is produced as a narrowly-peaked intrinsic spectral energy distribution sweeps down in frequency across the instrumental bandpass as a power-law in time. Though originally motivated by emission models which invoke a relativistic shock, the model could in principle apply to a wider range of emission scenarios. We quantify the burst's detectability using the frequency bandwidth over which most of its signal-to-noise ratio (SNR) is accumulated. We demonstrate that by varying just a single parameter of the toy model-the power-law index \beta of the frequency drift rate-one can transform a long (and hence preferentially time-resolved) burst with a narrow time-integrated spectrum into a shorter burst with a broad power-law time-integrated spectrum. We suggest that burst-to-burst diversity in the value of \beta could generate the dichotomy between burst duration and frequency-width recently found by CHIME. In shock models, the value of \beta is related to the radial density profile of external medium, which in light of the preferentially longer duration of bursts from repeating sources may point to diversity in the external environments surrounding repeating versus one-off FRB sources.

A new algorithmic framework is developed for holographic coherent diffraction imaging (HCDI) based on maximum likelihood estimation (MLE). This method provides superior image reconstruction results for various practical HCDI settings, such as when data is highly corrupted by Poisson shot noise and when low-frequency data is missing due to occlusion from a beamstop apparatus. This method is also highly robust in that it can be implemented using a variety of standard numerical optimization algorithms, and requires fewer constraints on the physical HCDI setup compared to current algorithms. The mathematical framework developed using MLE is also applicable beyond HCDI to any holographic imaging setup where data is corrupted by Poisson shot noise.

The flow of water in carbon nanochannels has defied understanding thus far1, with accumulating experimental evidence for ultra-low friction, exceptionally high water flow rates and curvature-dependent hydrodynamic slippage2–5. In particular, the mechanism of water–carbon friction remains unknown6, with neither current theories7 nor classical8,9 or ab initio molecular dynamics simulations10 providing satisfactory rationalization for its singular behaviour. Here we develop a quantum theory of the solid–liquid interface, which reveals a new contribution to friction, due to the coupling of charge fluctuations in the liquid to electronic excitations in the solid. We expect that this quantum friction, which is absent in Born–Oppenheimer molecular dynamics, is the dominant friction mechanism for water on carbon-based materials. As a key result, we demonstrate a marked difference in quantum friction between the water–graphene and water–graphite interface, due to the coupling of water Debye collective modes with a thermally excited plasmon specific to graphite. This suggests an explanation for the radius-dependent slippage of water in carbon nanotubes4, in terms of the electronic excitations of the nanotubes. Our findings open the way for quantum engineering of hydrodynamic flows through the electronic properties of the confining wall.

We analyze the stability of spin spiral states in the two-dimensional Heisenberg model. Our analysis reveals that the SU(2) symmetric point hosts a dynamic instability that is enabled by the existence of energetically favorable transverse deformations---both in real and spin space---of the spiral order. The instability is universal in the sense that it applies to systems with any spin number, spiral wavevector, and spiral amplitude. Unlike the Landau or modulational instabilities which require impurities or periodic potential modulation of an optical lattice, quantum fluctuations alone are sufficient to trigger the transverse instability. We analytically find the most unstable mode and its growth rate, and compare our analysis with phase space methods. By adding an easy plane exchange coupling that reduces the Hamiltonian symmetry from SU(2) to U(1), the stability boundary is shown to continuously interpolate between the modulational instability and the transverse instability. This suggests that the transverse instability is an important mechanism that hinders the formation of a spin superfluid, even in the presence of strong exchange anisotropy.

In insulators, Born effective charges describe the electrical polarization induced by the displacement of individual atomic sublattices. Such a physical property is at first sight irrelevant for metals and doped semiconductors, where the macroscopic polarization is ill-defined. Here we show that, in clean conductors, going beyond the adiabatic approximation results in nonadiabatic Born effective charges that are well defined in the low-frequency limit. In addition, we find that the sublattice sum of the nonadiabatic Born effective charges does not vanish as it does in the insulating case, but instead is proportional to the Drude weight. We demonstrate these formal results with density functional perturbation theory calculations of Al, and electron-doped SnS

First-principles calculations and analysis of the thermodynamic, structural, and electronic properties of liquid SiO

Can non-invasive imaging with fluorescence lifetime imaging microscopy (FLIM) detect metabolic differences in euploid versus aneuploid human blastocysts? FLIM has identified significant metabolic differences between euploid and aneuploid blastocysts. Prior studies have demonstrated that FLIM can detect metabolic differences in mouse oocytes and embryos and in discarded human blastocysts.

Angle-resolved photoelectron spectroscopy is an extremely powerful probe of materials to access the occupied electronic structure with energy and momentum resolution. However, it remains blind to those dynamic states above the Fermi level that determine technologically relevant transport properties. In this work, we extend band structure mapping into the unoccupied states and across the entire Brillouin zone by using a state-of-the-art high repetition rate, extreme ultraviolet fem- tosecond light source to probe optically excited samples. The wide-ranging applicability and power of this approach are demonstrated by measurements on the 2D semiconductor WSe2, where the energy-momentum dispersion of valence and conduction bands are observed in a single experiment. This provides a direct momentum-resolved view not only on the complete out-of-equilibrium band gap but also on its renormalization induced by electron-hole interaction and screening. Our work establishes a new benchmark for measuring the band structure of materials, with direct access to the energy-momentum dispersion of the excited-state spectral function.