Recently, two-dimensional band insulators with a topologically nontrivial (almost) flat band in which integer and fractional quantum Hall effect can be realized without an orbital magnetic field have been studied extensively. Realizing a topological flat band generally requires longer range hoppings in a lattice Hamiltonian. It is natural to ask what is the minimal hopping range required. In this letter, we prove that the mean hopping range of the flat-band Hamiltonian with Chern number C_1 and total number of bands N has a universal lower bound of \sqrt 4\vertC_1 |/\pi N.

The cooling of hot electrons in graphene is the critical process underlying the operation of exciting new graphene-based optoelectronic and plasmonic devices, but the nature of this cooling is controversial. We extract the hot-electron cooling rate near the Fermi level by using graphene as a novel photothermal thermometer that measures the electron temperature (T(t)) as it cools dynamically.

A proposed design for a reconfigurable x-ray Pixel Array Detector (PAD) is described. It operates by integrating a high-end commercial field programmable gate array (FPGA) into a 3-layer device along with a high-resistivity diode detection layer and a custom, application-specific integrated circuit (ASIC) layer. The ASIC layer contains an energy-discriminating photon-counting front end with photon hits streamed directly to the FPGA via a massively parallel, high-speed data connection.

It has recently been realized that a general class of non-Abelian defects can be created in conventional topological states by introducing extrinsic defects, such as lattice dislocations or superconductor-ferromagnet domain walls in conventional quantum Hall states or topological insulators. In this paper, we begin by placing these defects within the broader conceptual scheme of extrinsic twist defects associated with symmetries of the topological state.

The transient optical conductivity of freely suspended graphene was examined by femtosecond time-resolved spectroscopy using pump excitation at 400 nm and probe radiation at 800 nm. The optical conductivity (or, equivalently, absorption) changes abruptly upon excitation and subsequently relaxes to its initial value on the time scale of 1 ps. The form of the induced change in the optical conductivity varies strongly with excitation conditions, exhibiting a crossover from enhanced to decreased optical conductivity with increasing pump fluence.

Topological degeneracy is the degeneracy of the ground states in a many-body system in the large-system-size limit. Topological degeneracy cannot be lifted by any local perturbation of the Hamiltonian. The topological degeneracies on closed manifolds have been used to discover/define topological order in many-body systems, which contain excitations with fractional statistics. In this paper, we study a new type of topological degeneracy induced by condensing anyons along a line in two-dimensional topological ordered states.

When pure water is cooled at ∼106 K/s, it forms an amorphous solid (glass) instead of the more familiar crystalline phase. The presence of solutes can reduce this required (or "critical") cooling rate by orders of magnitude. Here, we present critical cooling rates for a variety of solutes as a function of concentration and a theoretical framework for understanding these rates. For all solutes tested, the critical cooling rate is an exponential function of concentration. The exponential's characteristic concentration for each solute correlates with the solute's Stokes radius.

Small angle x-ray scattering (SAXS) is a versatile and widely used technique for obtaining low-resolution structures of macromolecules and complexes. SAXS experiments measure molecules in solution, without the need for labeling or crystallization. However, radiation damage currently limits the application of SAXS to molecules that can be produced in microgram quantities; for typical proteins, 10-20 μL of solution at 1 mg/mL is required to accumulate adequate signal before irreversible x-ray damage is observed.

A series of studies that provide a consistent and illuminating picture of global radiation damage to protein crystals, especially at temperatures above 200 K, are described. The radiation sensitivity shows a transition near 200 K, above which it appears to be limited by solvent-coupled diffusive processes. Consistent with this interpretation, a component of global damage proceeds on timescales of several minutes at 180 K, decreasing to seconds near room temperature. As a result, data collection times of order 1 s allow up to half of global damage to be outrun at 260 K.