A Fermi arc is a disconnected segment of a Fermi surface observed in the pseudogap phase of cuprate superconductors. This simple description belies the fundamental inconsistency in the physics of Fermi arcs, specifically that such segments violate th
e topological integrity of the band. Efforts to resolve this contradiction of experiment and theory have focused on connecting the ends of the Fermi arc back on itself to form a pocket, with limited and controversial success. Here we show the Fermi arc, while composed of real spectral weight, lacks the quasiparticles to be a true Fermi surface. To reach this conclusion we developed a new photoemission-based technique that directly probes the interplay of pair-forming and pair-breaking processes with unprecedented precision. We find the spectral weight composing the Fermi arc is shifted from the gap edge to the Fermi energy by pair-breaking processes. While real, this weight does not form a true Fermi surface, because the quasiparticles, though significantly broadened, remain at the gap edge. This non-quasiparticle weight may account for much of the unexplained behavior of the pseudogap phase of the cuprates.
Using angle-resolved photoemission spectroscopy (ARPES), we investigate the electronic band structure and Fermi surface of ferromagnetic La$_{2-2x}$Sr$_{1+2x}$Mn$_2$O$_7$ ($x=0.38$). Besides the expected two hole pockets and one electron pocket of ma
jority-spin $e_g$ electrons, we show an extra electron pocket around the $Gamma$ point. A comparison with first-principles spin-polarized band-structure calculations shows that the extra electron pocket arises from $t_{2g}$ electrons of minority-spin character, indicating this compound is not a complete half-metallic ferromagnet, with similar expectations for lightly-doped cubic manganites. However, our data suggest that a complete half-metallic state is likely to be reached as long as the bandwidth is mildly reduced. Moreover, the band-resolved capability of ARPES enables us to investigate the band structure effects on spin polarization for different experimental conditions.
We report a 2mu m ultrafast solid-state Tm:Lu2O3 laser, mode-locked by single-layer graphene, generating transform-limited~410fs pulses, with a spectral width~11.1nm at 2067nm. The maximum average output power is 270mW, at a pulse repetition frequenc
y of 110MHz. This is a convenient high-power transform-limited laser at 2mu m for various applications, such as laser surgery and material processing.
The effect of thermal fluctuations on spin-transfer switching has been studied for a broad range of time scales (sub-ns to seconds) in a model system, a uniaxial thin film nanomagnet. The nanomagnet is incorporated into a spin-valve nanopillar, which
is subject to spin-polarized current pulses of variable amplitude and duration. Two physical regimes are clearly distinguished: a long pulse duration regime, in which reversal occurs by spin-transfer assisted thermal activation over an energy barrier, and a short time large pulse amplitude regime, in which the switching probability is determined by the spin angular momentum in the current pulse.
In correlated electron systems such as cuprate superconductors and colossal magnetoresistive (CMR) oxides there is often a tendency for a nanoscale self-organization of electrons that can give rise to exotic properties and to extreme non-linear respo
nses. The driving mechanisms for this self-organization are highly debated, especially in the CMR oxides in which two types of self-organized stripes of charge and orbital order coexist with each other. By utilizing angle-resolved photoemission spectroscopy measurements over a wide doping range, we show that one type of stripe is exclusively linked to long flat portions of nested Fermi surface, while the other type prefers to be commensurate with the real space lattice but also may be driven away from this by the Fermi surface. Complementarily, the Fermi surface also appears to be driven away from its non-interacting value at certain doping levels, giving rise to a host of unusual electronic properties.
Graphene is at the center of a significant research effort. Near-ballistic transport at room temperature and high mobility make it a potential material for nanoelectronics. Its electronic and mechanical properties are also ideal for micro and nanomec
hanical systems, thin-film transistors and transparent and conductive composites and electrodes. Here we exploit the optoelectronic properties of graphene to realize an ultrafast laser. A graphene-polymer composite is fabricated using wet-chemistry techniques. Pauli blocking following intense illumination results in saturable absorption, independent of wavelength. This is used to passively mode-lock an Erbium-doped fibre laser working at 1559nm, with a 5.24nm spectral bandwidth and ~460fs pulse duration, paving the way to graphene-based photonics.
