Antiresonant fiber-enhanced Raman spectroscopy gas sensing with 1†ppm sensitivity.

Antiresonant hollow-core fiber (AR-HCF) exhibits unprecedented optical performance in low transmission attenuation, broad transmission bandwidth, and single spatial mode quality. However, due to its lower numerical aperture, when utilizing the Fiber-Enhanced Raman Spectroscopy (FERS) principle for gas detection, the efficiency of AR-HCF in collecting Raman signals per unit length is significantly lower than that of hollow-core photonic crystal fiber. Nonetheless, AR-HCF effectively suppresses higher-order modes and offers bandwidth in hundreds of nanometers. By increasing the length of AR-HCF, its advantages can be effectively harnessed, leading to a considerable enhancement in the system's ability for low-concentration gas detection. We combine the nodeless antiresonant hollow-core fiber and Raman spectroscopy for enhanced Raman gas sensing in a forward scattering measurement configuration to investigate the attenuation behavior of the silica background signals. The silica background attenuation behavior enables the low baseline of the gas Raman spectroscopy and extends the integration time of the system. In addition, a convenient spatial filtering method is investigated. A multimode fiber with a suitable core diameter was employed to transmit the signal so that the fiber end face plays the role of pinhole, thus filtering the silica signal and reducing the baseline. The natural isotopes 12C16O2, 13C16O2, and 12C18O16O in ambient air can be observed using a 5-meter-long AR-HCF at 1 bar with a laser output power of 1.8 W and an integration time of 300 seconds. Limits of detection have been determined to be 0.5 ppm for 13C16O2 and 1.2 ppm for 12C16O2, which shows that the FERS with AR-HCF has remarkable potential for isotopes and multigas sensing.

Tapered multicore fiber interferometer for ultra-sensitive temperature sensing with thermo-optical materials.

An in-line interferometer based on tapered multicore embedded into a flexible thermo-optical material is proposed and investigated, theoretically and experimentally. The device consists of a tapered multicore fiber spliced between two single-mode fibers covered with PDMS, with high thermo-optic coefficient. The temperature sensitivity improvement obtained from PDMS applied on a tapered multicore fiber (TMCF) interferometer has been fundamentally and experimentally verified. The experimental results show the temperature sensitivity can be improved by reducing the tapered waist diameter of TMCF. The sensor exhibits the high sensitivity of 5-25 nm/°C within the decreasing temperature range from 50 °C down to 10 °C. A sequence of simulations and corresponding experiments are performed to clarify the evolution of the interference fading and consequently build the criteria for sensor design and reachable lower limit of temperature sensing. The proposed sensor can be employed as photonic thermometer with ultra-high sensitivity for biological and deep-sea applications, particularly based on the claimed quantitative criteria.

Tapered multicore fiber interferometer for refractive index sensing with graphene enhancement.

An in-line, highly sensitive refractive index (RI) sensor based on a tapered multicore fiber (MCF) structure sandwiched between two single-mode fibers is proposed and demonstrated. The fiber tapering technique was employed to fabricate in-line interferometers based on the multicore fiber. The waist diameter is one of the dominant factors of the intercore coupling. The tapered MCF interferometer is highly sensitive to the surrounding refractive index with a maximum sensitivity of 9194.6 nm/RIU in the RI range of 1.4264 to 1.4278 when the waist diameter is 9 µm. The enhancement of the evanescent field by graphene coating is proved to be able to improve the RI sensitivity further. A graphene-coated MCF interferometer with waist diameter of 9 µm offers the maximum sensitivity of 12617.6 nm/RIU in the RI range of 1.4144 to 1.4159. The experimental data have good agreement with the simulated results.

CrSi(2) hexagonal nanowebs.

Single-crystalline CrSi(2) nanostructures with a unique hexagonal nanoweb morphology have been successfully synthesized for the first time. These nanowebs span 150-200 nm and are composed of <112̅0> nanowire segments with a thickness of 10-30 nm. It is proposed that surface charges on the {101̅0} sidewalls and the minimization of electrostatic energy induce the nanoweb formation. Calculations of the electrostatic energies were used to predict the transitions between different modes of bending, which agreed well with the experimental observations.

Shape-controlled fabrication of micro/nanoscale triangle, square, wire-like, and hexagon pits on silicon substrates induced by anisotropic diffusion and silicide sublimation.

We report the fabrication of micro/nanoscale pits with facile shape, orientation, and size controls on an Si surface via an Au-nanoparticles-assisted vapor transport method. The pit dimensions can be continuously tuned from 70 nm to several mum, and the shapes of triangles, squares, and wire/hexagons are prepared on Si (111), (100), and (110) substrates, respectively. This reliable shape control hinges on the anisotropic diffusivity of Co in Si and the sublimation of cobalt silicide nanoislands. The experimental conditions, in particular the substrate orientation and the growth temperature, dictate the pit morphology. On the basis of this understanding of the mechanism and the morphological evolution of the pits, we manage to estimate the diffusion coefficients of Co in bulk Si along the 100 and 111 directions, that is D(100) and D(111). These diffusion coefficients show strong temperature dependence, for example, D(100) is ca. 3 times larger than D(111) at 860 degrees C, while they approach almost the same value at 1000 degrees C. This simple bottom-up route may help to develop new technologies for Si-based nanofabrication and to find potential applications in constructing nanodevices.

Highly efficient avalanche multiphoton luminescence from coupled Au nanowires in the visible region.

We demonstrate highly efficient avalanche multiphoton luminescence (MPL) from ordered-arrayed gold nanowires (NWs) with low time-average excitation intensity, Iexc (5.0-9.1 kW/cm2). The intensity of avalanche MPL, IMPL, is about 10(4) times larger than that of three-photon luminescence, the slope partial differential log IMPL/ partial differential log Iexc of avalanche MPL reaches as high as 18.3, and the corresponding polarization dependence of IMPL has a form of cos50 phip. The emission dynamics of avalanche MPL and three-photon luminescence are also studied comparatively. These observations indicate that the highly efficient avalanche MPL is attributed to the giant enhancement and coupling of longitudinal surface plasmon resonance of ordered-arrayed gold NWs.