The holographic polymer network formed in liquid crystal (LC) phase modulators via a He-Ne laser in this study demonstrates ultra-fast optically response and low light scattering. These advantages are mainly caused by the small LC domains and uniform polymer network when processing LC cells via holographic exposure to a He-Ne laser. The use of this method to fabricate LC cells as phase modulators results in a decay time of 49 μs under 2π phase modulation at room temperature. The predicted fast optical response can be achieved when operating devices at high temperatures.

A hole-patterned electrode liquid crystal (LC) lens with electrically switching coaxial bi-focus and single focus modes of tuning is demonstrated. The proposed LC lens mainly consists of a two LC layer (TLCL) structure with different thicknesses to achieve higher focusing power than the conventional hole-patterned electrode LC lens with the same aperture size. In the TLCL structure, one LC layer, doped with 3 wt % RM257, was photopolymerized to achieve a fixed focusing power of 18.5 Diopter. Due to polarization dependence in TLCL lenses, an additional 90 • twisted nematic (TN) cell was used to change the incident polarization in order to switch lens functions on or off. As a result, a fixed focusing power of 18.5 Diopter was achieved when voltages of 10 V rms were applied to the 90 • TN cell. In addition, the switching capabilities of the bi-focus and single focus modes were achieved when operating individually with applied voltages from 20 V rms to 90 V rms , and higher voltages of over 90 V rms , respectively. The maximum focusing power in the fabricated TLCL lens is 30.9 Diopter.

Photocurable monomer-doped liquid crystal (LC) cells were processed via holographic exposure using a low-power He-Ne laser to generate holographic polymer networks. The polymer network LC (PNLC) cells are used to fabricate infrared phase modulators at 1550 nm wavelength possessing favorable electro-optical performance. Compared with our previous work, the percentages of ingredients in the LC mixture filled in PNLC cells underwent a slight change. The 2 wt% concentration of anisotropic monomer RM257 were in place of isotropic monomer N-vinyl-2-pyrrolidinone (NVP). As a result, the fabricated phase modulators also maintained well homogeneous LC alignments and optical-scattering-free characteristics. Furthermore, NVP dopant successfully reduced the operating voltages from 95 V rms to 79 V rms to prevent polymer network deformation when electrically operating with higher voltages. The fabricated infrared phase modulators had a good average response time (i.e., rising time of 0.88 ms and falling time of 0.40 ms).

Typically, a diffuse reflectance spectroscopy (DRS) system employing a continuous wave light source would need to acquire diffuse reflectances measured at multiple source-detector separations for determining the absorption and reduced scattering coefficients of turbid samples. This results in a multi-fiber probe structure and an indefinite probing depth. Here we present a novel DRS method that can utilize a few diffuse reflectances measured at one source-detector separation for recovering the optical properties of samples. The core of innovation is a liquid crystal (LC) cell whose scattering property can be modulated by the bias voltage. By placing the LC cell between the light source and the sample, the spatial distribution of light in the sample can be varied as the scattering property of the LC cell modulated by the bias voltage, and this would induce intensity variation of the collected diffuse reflectance. From a series of Monte Carlo simulations and phantom measurements, we found that this new light distribution modulated DRS (LDM DRS) system was capable of accurately recover the absorption and scattering coefficients of turbid samples and its probing depth only varied by less than 3% over the full bias voltage variation range. Our results suggest that this LDM DRS platform could be developed to various low-cost, efficient, and compact systems for in-vivo superficial tissue investigation.

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