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We describe the first investigations on the influence of an imposed network on the photonic band gap (PBG) structure of the liquid crystal (LC) phase through the polymer template technique. The technique consists of using a cholesteric (Ch) phase as a base for photopolymerizing a difunctional monomer, which is then removed after polymerization, leaving only the polymer scaffold template. The templated structure obtained is utilized to adjust the PBG structure of the filled LC material, exhibiting both a one-dimensional PBG (Ch phase) and a three-dimensional PBG structure (TGBC* phase with smectic C* blocks). Selective reflection measurements indicate that the imprint polymer network of the template impacts the pitch of the Ch and TGBC* phases. The absorption peaks are visible because of two distinct twisted arrangements, one originating from the template and the other from the refilled chiral substance. In the templated cell, the central wavelength (λ min ) of PBG of the refilled sample red-shifts, as well as the width of the PBG gets enhanced compared to that for the sample in the regular (nontemplated) cell. For example, in the TGBC* phase, the λ min value red-shifts by 369 nm, and the width of the PBG enlarges by 50%. Additionally, the lattice spacing arising due to the periodicity of the SmC* helix in 2-dimension in the TGBC* phase gets enhanced. These findings demonstrate the polymer template method's effectiveness in tuning the mesophase's PBG in all three dimensions.

Recently, there has been a great deal of interest in devices which effectively shield near-infrared light with an additional feature of external field tunability, particularly for energy-saving applications. This article demonstrates an approach for fabricating a highly efficient near-infrared regulating device based on a polymer network liquid crystal reinforced with nanosheets of hexagonal-boron nitride (BN). The device achieves ∼84% IR scattering capability over a wavelength range of 800-2300 nm, and can also be regulated by an electric field. Interestingly, the observed high IR regulation is despite individual components of the composite being IR transparent, in stark contrast to earlier attempted incorporation of IR-absorbing/scattering particles. Detailed experimental characterization methods including FESEM corroborated with EDS and Raman spectroscopy suggest that the preferential positioning of the BN nanosheets, a consequence of the photo-polymerization process, is responsible for the observed feature. The IR reflectivity/back scattering that is doubled upon incorporation of the nanosheets results in an enhanced convective/radiative heat barrier capability, as evidenced by thermal imaging and significant (2 °C) reduction in ambient temperature upon one-Sun illumination. Numerical simulation results are also found to be in good agreement with the observed enhanced reflectance values for the BN-incorporated case. The presence of BN augments the mechanical rigidity of the system by a factor of 6.8 without compromising on the device operating voltage. The protocol employed is quite general and thus advantageous with far-reaching applications in passive cooling of buildings and structures, in thermal camouflaging, and in overall energy management.