Described herein are initial experimental details and properties of a silicon core, silica glass-clad optical fiber fabricated using conventional optical fiber draw methods. Such semiconductor core fibers have potential to greatly influence the fields of nonlinear fiber optics, infrared and THz power delivery. More specifically, x-ray diffraction and Raman spectroscopy showed the core to be highly crystalline silicon. The measured propagation losses were 4.3 dB/m at 2.936 microm, which likely are caused by either microcracks in the core arising from the large thermal expansion mismatch with the cladding or to SiO(2) precipitates formed from oxygen dissolved in the silicon melt. Suggestions for enhancing the performance of these semiconductor core fibers are provided. Here we show that lengths of an optical fiber containing a highly crystalline semiconducting core can be produced using scalable fiber fabrication techniques.

Long lengths (250 meters) of a flexible 150 microm diameter glass-clad optical fiber containing a 15 microm diameter crystalline and phase-pure germanium core was fabricated using conventional optical fiber draw techniques. X-ray diffraction and spontaneous Raman scattering measurements showed the core to be very highly crystalline germanium with no observed secondary phases. Elemental analysis confirmed a very well-defined core-clad interface with a step-profile in composition and nominally 4 weight-percent oxygen having diffused into the germanium core from the glass cladding. For this proof-of-concept fiber, polycrystalline n-type germanium of unknown dopant concentration was used. The measured infrared transparency of the starting material was poor and, as a likely outcome, the attenuation of the resultant fiber was too high to be measured. However, the larger Raman cross-section, infrared and terahertz transparency of germanium over silicon should make these fibers of significant value for fiber-based mid- to long-wave infrared and terahertz waveguides and Raman-shifted infrared light sources once high-purity, high-resistivity germanium is employed.

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The preparation and photophysical properties of two heavier main group element analogues of boron-dipyrromethene (BODIPY) chromophores are described. Specifically, we have prepared dipyrrin complexes of dichlorogallate (GADIPY) or phenylphosphenium (PHODIPY) units. Whereas cationic PHODIPY is labile, decomposing to a phosphine over time, GADIPY is readily prepared in good yield as a crystalline solid having moderate air- and water-stability. Crystallographically characterized GADIPY displays intense green photoluminescence (λem = 505 nm, Φem = 0.91 in toluene). These inaugural heavier main group element analogues of BODIPY offer a glimpse into the potential for elaboration to a panoply of chromophores with diverse photophysical properties.

Nature provides a rich panoply of structural motifs comprised of composites whose mechanical properties exceed those of their individual components. The human endeavor to likewise craft value‐added structural materials from underappreciated, sustainably sourced feedstocks remains a formidable challenge. Herein, efforts are made to achieve durable composites by synergistic combination of sulfur and cellulose. Composites are achieved in which bulk sulfur is reinforced by a network of 1–20% by mass cellulose cross‐linked with polysulfide chains. Composites described herein are remeltable and have flexural strength exceeding that of Portland cement. A thorough analysis of these materials has been undertaken through nuclear magnetic resonance, infrared spectroscopy, Raman spectroscopy, elemental analysis, thermogravimetric analysis, differential scanning calorimetry, and dynamic mechanical analysis. These analyses of both as‐prepared composites and fractionated materials unequivocally validate the formulation of these composites and the separability of the bulk sulfur from the reinforcing polysulfide‐cross‐linked cellulose network. The thermomechanical properties of these recyclable composites portend their tantalizing potential to supplant inherently unsustainable structural elements in numerous commercial applications. Further applications to improve the environmental resistance and flexural strength of Portland cement by treatment with the sulfur–cellulose composites are also discussed.

The highly nonequilibrium conditions under which optical fibers conventionally are drawn afford considerable, yet underappreciated, opportunities to realize fibers comprised of novel materials or materials that themselves cannot be directly fabricated into fiber form using commercial scalable methods. Presented here is an in-depth analysis of the physical, compositional, and selected optical properties of silica-clad erbium-doped yttrium aluminosilicate glass optical fibers derived from undoped, 0.25, and 50 wt % Er3+-doped yttrium aluminum garnet (YAG) crystals. The YAG-derived fibers were found to be noncrystalline as evidenced by x-ray diffraction and corroborated by spectroscopic measurements. Elemental analysis across the core/clad interface strongly suggests that diffusion plays a large role in this amorphization. Despite the noncrystalline nature of the fibers, they do exhibit acceptable low losses (∼0.15–0.2 dB/m) for many applications, broad-band emissions in the near-infrared, and enhanced thermal conductivity along their length while maintaining equivalent mechanical strength with respect to conventional silica optical fibers. Further, considerably higher rare-earth doping levels are realized than can be achieved by conventional solution or vapor-phase doping schemes. A discussion of opportunities for such approaches to nontraditional fiber materials is presented.

For the first time to the best of our knowledge a glass-clad optical fiber comprising a crystalline binary III-V semiconductor core has been fabricated. More specifically, a phosphate glass-clad fiber containing an indium antimonide (InSb) core was drawn using a molten core approach. The core was found to be highly crystalline with some oxygen and phosphorus diffusing in from the cladding glass. While optical transmission measurements were unable to be made, most likely due to free carrier absorption associated with the conductivity of the core, this work constitutes a proof-of-concept that optical fibers comprising semiconductor cores of higher crystallographic complexity than previously realized can be drawn using conventional fiber fabrication techniques. Such binary semiconductors may open the door to future fiber-based nonlinear devices.

We have developed an angle-resolved photoemission spectrometer with tunable vacuum ultraviolet laser as a photon source. The photon source is based on the fourth harmonic generation of a near IR beam from a Ti:sapphire laser pumped by a CW green laser and tunable between 5.3 eV and 7 eV. The most important part of the set-up is a compact, vacuum enclosed fourth harmonic generator based on potassium beryllium fluoroborate crystals, grown hydrothermally in the US. This source can deliver a photon flux of over 10(14) photon/s. We demonstrate that this energy range is sufficient to measure the k(z) dispersion in an iron arsenic high temperature superconductor, which was previously only possible at synchrotron facilities.