Ameliorated 3 × 3 coupler-based demodulation algorithm using iteratively reweighted ellipse specific fitting.

Passive demodulation scheme using 3 × 3 coupler has been widely used in phase-sensitive optical time-domain reflectometry (φ-OTDR), interrogation of fiber Bragg gratings or fiber optic interferometric sensors, and sensor multiplexing. However, the asymmetry of the 3 × 3 coupler in real applications affects the demodulation performance seriously. We proposed an ameliorated 3 × 3 coupler-based demodulation algorithm using iteratively reweighted ellipse specific fitting (IRESF) to overcome the drawback. IRESF combines iterative reweight technology with ellipse specific fitting, which decreases the weights of high noise points and always outputs ellipse solutions. Any two output signals from the 3 × 3 coupler-based interferometer are fitted by the IRESF and then corrected as a pair of quadrature signals. The stability of the fitting parameters is utilized to resolve the failures of IRESF under small signals. A real-time 1/4 ellipse arc judging module is designed, if the Lissajous figure is larger than 1/4 ellipse arc, IRESF is executed to offer ellipse correction parameters. Otherwise, the fixed parameters preset in the algorithm are used. The fixed parameters are mean values of the fitting parameters of IRESF under a large stimulus. The desired phase signal is finally extracted from the corrected quadrature signals. Experimental results show that the ameliorated algorithm does not require strict symmetry of the 3 × 3 coupler and can work under small signals. The noise floor of the proposed algorithm is -112 dB re rad/√Hz and the demodulated amplitude is 23.15 dB (14.37 rad) at 1 kHz when THD is 0.0488%. Moreover, the response linearity is as high as 99.999%. Compared to the algorithm using direct least squares, the proposed demodulation algorithm is more robust and precise, which has broad application prospects.

Thermal stress-assisted formation of submicron pillars from a thin film of CoCrCuFeNi high entropy alloy: experiments and simulations.

In this work, for the first time, the thermal stress-assisted formation of submicron pillars (SPs) from a high entropy alloy (HEA) thin film is made possible, and novel molecular dynamics (MD) simulations are proposed to assess the underlying mechanisms. In a series of experiments, the growth of quasi-equiatomic HEA SPs from CoCrCuFeNi HEA thin films was demonstrated under different heating and cooling conditions. Atomistic simulations are performed to probe possible formation mechanisms in two ways. One is to first obtain surface elastic constants and then conduct surface stability analysis with the consideration of size-dependent surface stress. The other is to effectively apply large compressive stress while simplifying the molecular dynamics (MD) model by using the Stoney equation to perform long-term MD simulations. From the former, it is suggested that surface diffusion is likely not the dominant cause for the observed pillar formation. From the latter, it is revealed that the level of compressive stress plays a much greater role than the crystalline structure of the film sample. Light has been shed on the stress-assisted formation of submicron pillars from CoCrCuFeNi HEA films by both experimental and simulation approaches.

A new phenylspirodrimane dimer from the fungus Stachybotrys chartarum.

A new phenylspirodrimane dimer, named stachartarin A (1), was isolated from cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Its structures were elucidated by means of spectroscopic methods. At the same time, the compound was tested for its cytotoxicity against HL-60, SMMC-7721, A-549, MCF-7, and SW480 cells.

A novel phenylspirodrimane dimer from cultures of the fungus Stachybotrys chartarum.

Stachartone A (1), a novel phenylspirodrimane dimer, was isolated from cultures of the tin mine tailings-associated fungus Stachybotrys chartarum. Its structure was elucidated by means of spectroscopic methods. At the same time, compound (1) was tested for its cytotoxicity against five human cancer cell lines.