A holistic detection system, in principle sensitive to any molecular species in the vapor phase is proposed. The sensor consists of a polymeric multilayered distributed Bragg reflector made of a perfluorinated polar polymer, Aquivion, and a nonpolar polymer, poly(N‐vinylcarbazole). Alternated layers of the two polymers provide a characteristic optical response that depends on the chemical species intercalating within the structure. Such differences arise from Flory–Huggins polymer–solvent interactions. Then, the presence of polar, nonpolar, and perfluorinated moieties in the structures, potentially, allows sensitivity to any molecular species, providing a detection system with no need for any additional chemical receptors. As a proof of concept, the study demonstrates the sensitivity of the sensor to very diverse classes of molecules in the vapor phase including perfluorinated, nonpolar hydrophobic, and hydrophilic species and the capability to distinguish them, even in binary mixtures. Additionally, a connection between the dynamic temporal response of the sensors and the chemical–physical properties of the analytes, their concentration, and effective diffusion coefficient within the polymer structure is revealed.

Preventing solar heating is nowadays of paramount interest in energy savings and health preservation. For instance, in building thermalization solar heating consumes an excess of energy leading to harmful CO 2 emissions, while in food and beverage packaging it may lead to variation of organoleptic properties or even health issues. The phenomenon is attributed to the large presence of moieties with highly absorbing vibrational overtones and combination bands in the near-infrared spectral region that induces heating in water, moisture, and in polymers used in packaging. Thus, reducing and controlling the light absorbed by these materials with effective low-cost passive systems can play a major role in energy saving and health preservation. In this work, different polymer dielectric mirrors are reported, made of poly(N-vinylcarbazole) and either cellulose acetate or poly(acrylic acid), and able to selectively reflect near-infrared radiation while maintaining high transparency in the visible range. To this end, simple, tandem, and superperiodic mirrors are used to shield radiation impinging on samples of water and paraffin, demonstrating shielding efficiencies up to 52% with respect to unshielded references, promising a new paradigm to solve thermal management issues.

Controlling the radiative rate of emitters with macromolecular photonic structures promises flexible devices with enhanced performances that are easy to scale up. For instance, radiative rate enhancement empowers low-threshold lasers, while rate suppression affects recombination in photovoltaic and photochemical processes. However, claims of the Purcell effect with polymer structures are controversial, as the low dielectric contrast typical of suitable polymers is commonly not enough to provide the necessary confinement. Here we show all-polymer planar microcavities with photonic band gaps tuned to the photoluminescence of a diketopyrrolopyrrole derivative, which allows a change in the fluorescence lifetime. Radiative and nonradiative rates were disentangled systematically by measuring the external quantum efficiencies and comparing the planar microcavities with a series of references designed to exclude any extrinsic effects. For the first time, this analysis shows unambiguously the dye radiative emission rate variations obtained with macromolecular dielectric mirrors. When different waveguides, chemical environments, and effective refractive index effects in the structure were accounted for, the change in the radiative lifetime was assigned to the Purcell effect. This was possible through the exploitation of photonic structures made of polyvinylcarbazole as a high-index material and the perfluorinated Aquivion as a low-index one, which produced the largest dielectric contrast ever obtained in planar polymer cavities. This characteristic induces the high confinement of the radiation electric field within the cavity layer, causing a record intensity enhancement and steering the radiative rate. Current limits and requirements to achieve the full control of radiative rates with polymer planar microcavities are also addressed.

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The control of radiative decay rate is a crucial issue both for fundamental studies in quantum electrodynamics and for the development of efficient lasers, light emitting devices and photovoltaic cells....

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