Friction force microscopy : a simple technique for identifying graphene on rough substrates and mapping the orientation of graphene grains on copper

At a single atom thick, it is challenging to distinguish graphene from its substrate using conventional techniques. In this paper we show that friction force microscopy (FFM) is a simple and quick technique for identifying graphene on a range of samples, from growth substrates to rough insulators. We show that FFM is particularly effective for characterizing graphene grown on copper where it can correlate the graphene growth to the three-dimensional surface topography. Atomic lattice stick–slip friction is readily resolved and enables the crystallographic orientation of the graphene to be mapped nondestructively, reproducibly and at high resolution. We expect FFM to be similarly effective for studying graphene growth on other metal/locally crystalline substrates, including SiC, and for studying growth of other two-dimensional materials such as molybdenum disulfide and hexagonal boron nitride

Depressed clad hollow optical fiber with fundamental LP01 mode cut-off

We propose a depressed clad hollow optical fiber with fundamental (LP01) mode cut-off suitable for high power short-wavelength, especially three-level, fiber laser operation by introducing highly wavelength dependent losses at longer wavelengths. The cut-off characteristic of such fiber structure was investigated. A Yb-doped depressed clad hollow optical fiber laser generating 59.1W of output power at 1046nm with 86% of slope efficiency with respect to the absorbed pump power was realised by placing the LP01 mode cut-off at ~1100nm

Anisotropic strains and magnetoresistance of La_{0.7}Ca_{0.3}MnO_{3}

Thin films of perovskite manganite La_{0.7}Ca_{0.3}MnO_{3} were grown epitaxially on SrTiO_3(100), MgO(100) and LaAlO_3(100) substrates by the pulsed laser deposition method. Microscopic structures of these thin film samples as well as a bulk sample were fully determined by x-ray diffraction measurements. The unit cells of the three films have different shapes, i.e., contracted tetragonal, cubic, and elongated tetragonal for SrTiO_3, MgO, and LaAlO_3 cases, respectively, while the unit cell of the bulk is cubic. It is found that the samples with cubic unit cell show smaller peak magnetoresistance than the noncubic ones do. The present result demonstrates that the magnetoresistance of La_{0.7}Ca_{0.3}MnO_{3} can be controlled by lattice distortion via externally imposed strains.Comment: Revtex, 10 pages, 2 figure

20 K superconductivity in heavily electron doped surface layer of FeSe bulk crystal

A superconducting transition temperature Tc as high as 100 K was recently discovered in 1 monolayer (1ML) FeSe grown on SrTiO3 (STO). The discovery immediately ignited efforts to identify the mechanism for the dramatically enhanced Tc from its bulk value of 7 K. Currently, there are two main views on the origin of the enhanced Tc; in the first view, the enhancement comes from an interfacial effect while in the other it is from excess electrons with strong correlation strength. The issue is controversial and there are evidences that support each view. Finding the origin of the Tc enhancement could be the key to achieving even higher Tc and to identifying the microscopic mechanism for the superconductivity in iron-based materials. Here, we report the observation of 20 K superconductivity in the electron doped surface layer of FeSe. The electronic state of the surface layer possesses all the key spectroscopic aspects of the 1ML FeSe on STO. Without any interface effect, the surface layer state is found to have a moderate Tc of 20 K with a smaller gap opening of 4 meV. Our results clearly show that excess electrons with strong correlation strength alone cannot induce the maximum Tc, which in turn strongly suggests need for an interfacial effect to reach the enhanced Tc found in 1ML FeSe/STO.Comment: 5 pages, 4 figure

RGB generation by four-wave mixing in small-core holey fibers

We report the generation of white light comprising red, green, and blue spectral bands from a frequency-doubled fiber laser by an efficient four-wave mixing process in submicron-sized cores of microstructured holey fibers. A master-oscillator power amplifier (MOPA) source based on Yb-doped fiber is employed to generate 80 ps pulses at 1060 nm wavelength with 32 MHz repetition rate, which are then frequency-doubled in an LBO crystal to generate up to 2 W average power of green light. The green pump is then carefully launched into secondary cores of the cladding of photonic bandgap fibers. These secondary cores with diameters of about 400 to 800 nm act as highly nonlinear waveguides. At the output, we observe strong red and blue sidebands which, together with the remaining green pump light, form a visible white light source of about 360 mW. The generating process is identified as four-wave mixing where phase matching is achieved by birefringence in the secondary cores which arises from non-symmetric deformation during the fiber fabrication. Numerical models of the fiber structure and of the nonlinear processes confirm our interpretation. Finally, we discuss power scaling and limitations of the white light source due to the damage threshold of silica fibers