Abstract:We demonstrate mode-division multiplexed WDM transmission over 50-km of few-mode fiber using the fiber's LP 01 and two degenerate LP 11 modes. A few-mode EDFA is used to boost the power of the output signal before a few-mode coherent receiver. A 6×6 time-domain MIMO equalizer is used to recover the transmitted data. We also experimentally characterize the 50-km few-mode fiber and the few-mode EDFA.

Poly(N‐isopropylacrylamide)‐block‐poly{6‐[4‐(4‐methylphenyl‐azo) phenoxy] hexylacrylate} (PNIPAM‐b‐PAzoM) was synthesized by successive reversible addition‐fragmentation chain transfer (RAFT) polymerization. In H2O/THF mixture, amphiphilic PNIPAM‐b‐PAzoM self‐assembles into giant micro‐vesicles. Upon irradiation of light at 365 nm, fusion of the vesicles was observed directly under an optical microscope. The real‐time fusion process is presented and the derivation is preliminarily due to the perturbation by the photoinduced trans‐to‐cis isomerization of azobenzene units in the vesicles.magnified image

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We report writing polymer optical fiber (POF) gratings in photosensitive POFs doped with benzildimethylketal (BDK) (BPOF in short) using a 355 nm laser for what we believe to be the first time. Both multimode and single-mode FBGs were fabricated with relatively low writing intensity. The enhanced photosensitivity of the doped POFs is also evident by the observation of obvious change in the UV-visible absorption.

Poly(N‐isopropylacrylamide)‐block‐poly{6‐[4‐(4‐pyridyazo)phenoxy] hexylmethacrylate} (PNIPAM‐b‐PAzPy) was synthesized by successive reversible addition‐fragmentation chain transfer (RAFT) polymerization. In a water/tetrahydrofuran (H2O/THF) mixture, amphiphilic PNIPAM‐b‐PAzPy self‐assembles into giant micro‐vesicles. Upon alternate ultraviolet (UV) and visible light irradiation, obvious reversible swelling‐shrinking of the vesicles was observed directly under an optical microscope. The maximum percentage increase in volume, caused by the UV light, reached 17%. Moreover, the swelling could be adjusted using the UV light power density. The derivation of this effect is due to photoinduced reversible isomerization of azopyridine units in the vesicles.

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Optofluidic lasers (OFLs) are an emerging technological platform for biochemical sensing, and their good performance especially high sensitivity has been demonstrated. However, high-throughput detection with an OFL remains a major challenge due to the lack of reproducible optical microcavities. Here, we introduce the concept of a distributed fibre optofluidic laser (DFOFL) and demonstrate its potential for high-throughput sensing applications. Due to the precise fibre geometry control via fibre drawing, a series of identical optical microcavities uniformly distributed along a hollow optical fibre (HOF) can be achieved to obtain a one-dimensional (1D) DFOFL. An enzymatic reaction catalysed by horseradish peroxidase (HRP) can be monitored over time, and the HRP concentration is detected by DFOFL-based arrayed colorimetric detection. Experimentally, five-channel detection in parallel with imaging has been demonstrated. Theoretically, spatial multiplexing of hundreds of channels is achievable with DFOFL-based detection. The DFOFL wavelength is tuned over hundreds of nanometers by optimizing the dye concentration or reconfiguring the liquid gain materials. Extending this concept to a two-dimensional (2D) chip through wavelength multiplexing can further enhance its multi-functionality, including multi-sample detection and spectral analysis. This work opens the door to high-throughput biochemical sensing.