Carbonyl oxides, or Criegee intermediates, are formed from the gas phase ozonolysis of alkenes and play a pivotal role in night-time and urban area atmospheric chemistry. Significant discrepancies exist among measurements of the strong B ̃(1)A'-X ̃(1)A' electronic transition of the simplest Criegee intermediate, CH2OO in the visible/near-UV. We report room temperature spectra of the B ̃(1)A'-X ̃(1)A' electronic absorption band of CH2OO acquired at higher resolution using both single-pass broadband absorption and cavity ring-down spectroscopy. The new absorption spectra confirm the vibrational structure on the red edge of the band that is absent from ionization depletion measurements. The absolute absorption cross sections over the 362-470 nm range are in good agreement with those reported by Ting et al. Broadband absorption spectra recorded over the temperature range of 276-357 K were identical within their mutual uncertainties, confirming that the vibrational structure is not due to hot bands.

We show that it is possible to obtain 2 x 2 waveguide couplers with new power splitting ratios for cross coupling of 7%, 64%, 80% and 93% by cascading two short MMI sections. These couplers have simple geometry and low loss. They offer valuable new possibilities for designing waveguide power taps, high-Q ring resonators, ladder-structure optical filters, and loop-mirror partial reflectors.

We show that it is possible to obtain 2 x 2 waveguide couplers with arbitrary power splitting ratios by interconnecting a pair of unequal width waveguides as the phase-tuning section into the middle of two short MMI sections. These couplers have simple geometry and low loss. They offer valuable new possibilities for designing waveguide-based photonic integrated circuits.

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