RESUMO
An induced-transmission filter (ITF) uses an ultrathin metallic layer positioned at an electric-field node within a dielectric thin-film bandpass filter to select one transmission band while suppressing other bands that would have been present without the metal layer. We introduce a switchable mid-infrared ITF where the metal can be "switched on and off", enabling the modulation of the filter response from a single band to multiband. The switching is enabled by the reversible insulator-to-metal phase transition of a subwavelength film of vanadium dioxide (VO2). Our work generalizes the ITFâa niche type of bandpass filterâinto a new class of tunable devices. Furthermore, our fabrication processâwhich begins with thin-film VO2 on a suspended membraneâenables the integration of VO2 into any thin-film assembly that is compatible with physical vapor deposition processes and is thus a new platform for realizing tunable thin-film filters.
RESUMO
We demonstrate a novel differential phase-shift-keying (DPSK) demodulator based on coherent perfect absorption (CPA). Our DPSK demodulator chip device, which incorporates a silicon ring resonator, two bus waveguide inputs, and monolithically integrated detectors, operates passively at a bit rate of 10 Gbps at telecommunication wavelengths, and fits within a mm-scale footprint. Critical coupling is used to achieve efficient CPA by tuning the gap between the ring and bus waveguides. The device has a vertical eye opening of 12.47 mV and a quality factor exceeding 3×104. The fundamental principle behind this photonic circuit can be extended to other formats of integrated demodulators.
RESUMO
Towards a future lab-on-a-chip spectrometer, we demonstrate a compact chip-scale air-clad silicon pedestal waveguide as a Mid-Infrared (Mid-IR) sensor capable of in situ monitoring of organic solvents. The sensor is a planar crystalline silicon waveguide, which is highly transparent, between λ = 1.3 and 6.5 µm, so that its operational spectral range covers most characteristic chemical absorption bands due to bonds such as C-H, N-H, O-H, C-C, N-O, C=O, and C≡N, as opposed to conventional UV, Vis, Near-IR sensors, which use weaker overtones of these fundamental bands. To extend light transmission beyond λ = 3.7 µm, a spectral region where a typical silicon dioxide under-clad is absorbing, we fabricate a unique air-clad silicon pedestal waveguide. The sensing mechanism of our Mid-IR waveguide sensor is based on evanescent wave absorption by functional groups of the surrounding chemical molecules, which selectively absorb specific wavelengths in the mid-IR, depending on the nature of their chemical bonds. From a measurement of the waveguide mode intensities, we demonstrate in situ identification of chemical compositions and concentrations of organic solvents. For instance, we show that when testing at λ = 3.55 µm, the Mid-IR sensor can distinguish hexane from the rest of the tested analytes (methanol, toluene, carbon tetrachloride, ethanol and acetone), since hexane has a strong absorption from the aliphatic C-H stretch at λ = 3.55 µm. Analogously, applying the same technique at λ = 3.3 µm, the Mid-IR sensor is able to determine the concentration of toluene dissolved in carbon tetrachloride, because toluene has a strong absorption at λ = 3.3 µm from the aromatic C-H stretch. With our demonstration of an air-clad silicon pedestal waveguide sensor, we move closer towards the ultimate goal of an ultra-compact portable spectrometer-on-a-chip.
Assuntos
Tetracloreto de Carbono/análise , Hexanos/análise , Dispositivos Lab-On-A-Chip , Silício/química , Tolueno/análise , Ar , Espectrofotometria Infravermelho/instrumentaçãoRESUMO
We have demonstrated a high-sensitivity, room-temperature quantum-cascade (QC) laser sensor for detection of SO2 and SO3 under conditions relevant to aircraft test combustor exhaust. Two QC lasers probe infrared absorption features at 7.50 and 7.16 microm for SO2 and SO3, respectively, with a common dual-beam detection system. We inferred a noise-equivalent absorbance of approximately 1 x 10(-4) Hz(-1/2). We have demonstrated detection limits for both SO2 and SO3 of 1-2 ppmv m/Hz(1/2) (where ppmv is parts in 10(6) by volume) for 300 torr, elevated temperature, and path lengths near 1 m. This level of sensitivity permits measurement of < 1 ppmv of SO2 and SO3 at these conditions with modest signal averaging.