We demonstrate a versatile and easily fabricated paper-based CO2 sensor. The sensor consists of a specially designed fluorescent color-shift chromophore infused into standard filter paper. The emission color of the resulting fluorescent paper changes upon exposure to CO2 due to the formation of carbonic acid, which underlies the sensing mechanism. By using a ratiometric method, the undesirable effects of photobleaching can be eliminated, leading to a stable and repeatable sensor performance. These multiuse sensors have a response time on the order of 1 min and feature low detection limits for a paper-based CO2 gas sensor, suggesting possible low-cost applications in smart buildings or other facilities in which CO2 levels are required to be continuously monitored.

The development of wideband lasing media has deep implications for imaging, sensing, and display technologies. We show that a single chromophore can be engineered to feature wide-gamut fluorescence and lasing throughout the entire visible spectrum and beyond. This exceptional color tuning demonstrates a chemically controlled paradigm for light emission applications with precise color management. Achieving such extensive color control requires a molecular blueprint that yields a high quantum efficiency and a high solubility in a wide variety of liquids and solids while featuring a heterocyclic structure with good steric access to the lone pair electrons. With these requirements in mind, we designed a lasing chromophore that encloses a lasing color space twice as large as the sRGB benchmark. This record degree of color tuning can in principle be adapted to the solid state by incorporating the chromophore into polymer films. By appropriately engineering the base molecular structure, the widest range of lasing wavelengths observed for a conventional gain medium can be achieved, in turn establishing a possible route toward high-efficiency light emitters and lasers with near-perfect chromaticity.

Hybrid fluorescent metal−organic frameworks (MOFs) use long-range intermolecular structural motifs in which the properties of the scaffold molecular system can be designed for specific applications. In this work, we constructed a MOF−chromophore system with a strongly polarized fluorescence and a large emission wavelength shift. To achieve this, we first devised a fluorophore with a linear conjugated backbone, bulky and noninteracting side chains, and easily accessible nitrogen atoms on its pyridine end groups. The linear nature of the conjugated backbone can lead to a strongly polarized luminescence, the side groups assist structural stability and minimize intermolecular interactions, and the sterically accessible pyridines provide a large fluorescence colorchanging ability. These features were demonstrated by synthesizing a planar Zn-based MOF in which the linear backbone of the chromophore molecules was highly aligned. The MOFs demonstrated a strong polarization effect and a color-shifting ability from green-yellow to orange. The results show that hybrid metal−organic materials can be designed to generate a strong command of the material luminescence, in terms of both emission color and polarization.