In this review, we introduce photonic crystal fibre as a novel optofluidic microdevice that can be employed as both a versatile chemical sensor and a highly efficient microreactor. We demonstrate that it provides an excellent platform in which light and chemical samples can strongly interact for quantitative spectroscopic analysis or photoactivation purposes. The use of photonic crystal fibre in photochemistry and sensing is discussed and recent results on gas and liquid sensing as well as on photochemical and catalytic reactions are reviewed. These developments demonstrate that the tight light confinement, enhanced light-matter interaction and reduced sample volume offered by photonic crystal fibre make it useful in a wide range of chemical applications.
Liquid-filled hollow-core photonic crystal fibers (HC-PCFs) are perfect optofluidic channels, uniquely providing low-loss optical guidance in a liquid medium. As a result, the overlap of the dissolved specimen and the intense light field in the micronsized core is increased manyfold compared to conventional bioanalytical techniques, facilitating highly-efficient photoactivation processes. Here we introduce a novel integrated analytical technology for photochemistry by microfluidic coupling of a HC-PCF nanoflow reactor to supplementary detection devices. Applying a continuous flow through the fiber, we deliver photochemical reaction products to a mass spectrometer in an online and hence rapid fashion, which is highly advantageous over conventional cuvette-based approaches.
Laser Doppler velocimetry is used to measure very accurately the velocity and position of a microparticle propelled and guided by laser light in liquid-filled photonic crystal fiber. Periodic variations in particle velocity are observed that correlate closely with modal beating between the two lowest order guided fiber modes.
We investigate fluorescence blinking of individual RC-LH1 (reaction-centre-light-harvesting 1) complexes from the photosynthetic purple bacterium Rhodopseudomonas palustris. For both the on- and off-periods the telegraph-like intermittency of the fluorescence intensity follows power-law statistics with exponents between 1 and 2. Yet, this behaviour was only observed for a small fraction of the complexes studied. We argue that the majority of the complexes reside in a prolonged on-state, due to a mechanism that is similar to the Coulomb blockade in semiconductor quantum dots, and which results here from the photoinduced charges located within the RC upon photoexcitation of the LH1 antenna.
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