Efficient three-wave mixing devices have numerous applications, including wavelength conversion, dispersion compensation, and all-optical switching. Second-harmonic generation (SHG) is a useful diagnostic for near-degenerate operation of these devices. With buried waveguides formed in periodically poled lithium niobate by annealed and reverse proton exchange, we demonstrate what is believed to be the highest normalized conversion efficiency (150%/W cm(2)) for SHG in the 1550-nm communications band reported to date.

We present a device to facilitate single-photon detection at communication wavelengths based on continuous-wave sum-frequency generation with an upconversion efficiency exceeding 90%. Sum-frequency generation in a periodically poled lithium niobate waveguide is used to upconvert signal photons to the near infrared, where detection can be performed efficiently by use of silicon avalanche photodiodes.

We report 99% pump depletion in single-pass second-harmonic generation. Quasi-cw pulses at 1550 nm were frequency doubled in an annealed proton-exchanged waveguide formed in periodically poled lithium niobate. Measurements of pump depletion and second-harmonic generation agree with results from numerical integration of the coupled-mode equations that describe the process.

Conventional gate oxide layers (e.g., SiO(2), Al(2)O(3), or HfO(2)) in silicon field-effect transistors (FETs) provide highly active surfaces, which can be exploited for electronic pH sensing. Recently, great progress has been achieved in pH sensing using compact integrateable nanowire FETs. However, it has turned out to be much harder to realize a true reference electrode, which--while sensing the electrostatic potential--does not respond to the proton concentration. In this work, we demonstrate a highly effective reference sensor, a so-called reference FET, whose proton sensitivity is suppressed by as much as 2 orders of magnitude. To do so, the Al(2)O(3) surface of a nanowire FET was passivated with a self-assembled monolayer of silanes with a long alkyl chain. We have found that a full passivation can be achieved only after an extended period of self-assembling lasting several days at 80 °C. We use this slow process to measure the number of active proton binding sites as a function of time by a quantitative comparison of the measured nonlinear pH-sensitivities to a theoretical model (site-binding model). Furthermore, we have found that a partially passivated surface can sense small changes in the number of active binding sites reaching a detection limit of δN(s) ≈ 170 μm(-2) Hz(-1/2) at 10 Hz and pH 3.

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