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Richard F. Haglund Jr

Publications and source records attributed to Richard F. Haglund Jr.

4 recordsLinked to original sources

Mapping nanoscale charge states and phase domains with quantitative hyperspectral coherent diffractive imaging spectroscopy

The critical properties of functional materials and nanoscale devices often originate from the coexistence of different thermodynamic phases and / or oxidization states, but sample makeup is seldom completely known a priori. Coherent diffractive imaging (CDI) provides the spatial resolution needed to observe nanoscale coexistence while returning the full amplitude and phase information of an object, but to date lacks the spectral information necessary for composition identification. Here we demonstrate CDI spectroscopy (CDIS), acquiring images of the prototypical quantum material vanadium oxide across the vanadium L2,3 and oxygen K X-ray absorption edges with nanometer scale resolution. Using the hyperspectral X-ray image we show coexistence of multiple oxidization states and phases in a single sample and extract the full complex refractive index of V2O5 and the monoclinic insulating and rutile conducting phases of VO2. These results constrain the role of hidden phases in the insulator-to-metal transition in VO2.

physics.optics

Nanoscale spectroscopic imaging of phase separation in a correlated material by resonant X-ray holography

Nanoscale phase coexistence and inhomogeneity are ubiquitous in correlated electron materials, existing in doped Mott insulators, manganites, and high-temperature superconductors. The small length scales and lack of contrast mechanisms make it extremely challenging to measure real-space images of the phase coexistence with high resolution. Yet, images aid our understanding of how phase coexistence and domain boundaries dictate the exotic material properties. Here we show that resonant soft-X-ray holography, previously employed to image magnetic domains, can be used to image phase separation on the nanoscale. We observe nucleation and growth of nanometre-sized metallic domains out of the insulating phase of the prototypical correlated material VO2, using linearly polarized coherent synchrotron radiation. By spectrally resolving the holograms, we extract differential soft X-ray absorption spectra with 50 nm spatial resolution. Furthermore, when combined with ultra-bright and ultra-short X-ray sources, X-ray holography could capture both nanoscale spatial variations and temporal fluctuations that occur close to the transition temperatures or are induced by femtosecond light pulses that cannot be observed with alternative imaging methods.

cond-mat.mes-hall

Ultrafast Plasmonic Control of Second Harmonic Generation

Efficient frequency conversion techniques are crucial to the development of plasmonic metasurfaces for information processing and signal modulation. In principle, nanoscale electric-field confinement in nonlinear materials enables higher harmonic conversion efficiencies per unit volume than those attainable in bulk materials. Here we demonstrate efficient second-harmonic generation (SHG) in a serrated nanogap plasmonic geometry that generates steep electric field gradients on a dielectric metasurface. An ultrafast pump is used to control plasmon-induced electric fields in a thin-film material with inversion symmetry that, without plasmonic enhancement, does not exhibit an an even-order nonlinear optical response. The temporal evolution of the plasmonic near-field is characterized with ~100as resolution using a novel nonlinear interferometric technique. The ability to manipulate nonlinear signals in a metamaterial geometry as demonstrated here is indispensable both to understanding the ultrafast nonlinear response of nanoscale materials, and to producing active, optically reconfigurable plasmonic devices

physics.optics

Efficient Forward Second-Harmonic Generation from Planar Archimedean Nanospirals

The enhanced electric field at plasmonic resonances in nanoscale antennas can lead to efficient harmonic generation, especially when the plasmonic geometry is asymmetric on either inter-particle or intra-particle levels. The planar Archimedean nanospiral offers a unique geometrical asymmetry for second-harmonic generation (SHG) because the SHG results neither from arranging centrosymmetric nanoparticles in asymmetric groupings, nor from non-centrosymmetric nanoparticles that retain a local axis of symmetry. Here we report forward SHG from planar arrays of Archimedean nanospirals using 15 fs pulse from a Ti:sapphire oscillator tuned to 800 nm wavelength. The measured harmonic-generation efficiencies are 2.6*10-9, 8*10-9 and 1.3*10-8 for left-handed circular, linear, and right-handed circular polarizations, respectively. The uncoated nanospirals are stable under average power loading of as much as 300 uW per nanoparticle. The nanospirals also exhibit a selective conversion between polarization states. These experiments show that the intrinsic asymmetry of the nanospirals results in a highly efficient, two-dimensional harmonic generator that can be incorporated into metasurface optics.

physics.optics