A selective fluorescent chemodosimeter for mercury ion based on the mercury-promoted intramolecular cyclic guanylation of thiourea connected on 1, 8-naphthalimide is described.

Solar-blind ultraviolet (UV) photodetectors (PDs) have attracted tremendous attention in the environmental, industrial, military, and biological fields. As a representative III-nitride material, AlGaN alloys have broad development prospects in the field of solar-blind detection due to their superior properties, such as tunable wide bandgaps for intrinsic UV detection. In recent decades, a variety of AlGaN-based PDs have been developed to achieve high-precision solar-blind UV detection. As integrated optoelectronic technology advances, AlGaN-based focal plane arrays (FPAs) are manufactured and exhibit outstanding solar-blind imaging capability. Considering the rapid development of AlGaN detection techniques, this paper comprehensively reviews the progress on AlGaN-based solar-blind UV PDs and FPAs. First, the basic physical properties of AlGaN are presented. The epitaxy and p-type doping problems of AlGaN alloys are then discussed. Diverse PDs, including photoconductors and Schottky, metal–semiconductor–metal (MSM), p-i-n, and avalanche photodiodes (APDs), are demonstrated, and the physical mechanisms are analyzed to improve device performance. Additionally, this paper summarizes imaging technologies used with AlGaN FPAs in recent years. Benefiting from the development of AlGaN materials and optoelectronic devices, solar-blind UV detection technology is greeted with significant revolutions.

Polyester synthesis from the alternating copolymerization of epoxides with cyclic anhydrides via a metal-free route remains a key challenge. This work reports the development of a highly active organocatalytic route for the copolymerization of a spectrum of epoxides and cyclic anhydrides. Fully alternating polyesters were synthesized by a variety of organic Lewis acid–base pairs including organoboranes and quaternary onium salts. The effect of the acidity, type, and size of Lewis pairs on the catalytic activity and selectivity of the copolymerization is presented. The undesirable transesterification and etherification were effectively suppressed even in the case of complete conversion of the cyclic anhydride. This could be ascribed to the formation of a unique tetracoordinate bond-carboxylate (or alkoxide) anion. The Lewis pairs are highly active, with a turnover frequency of 102 and 303 h–1 for the copolymerization of propylene oxide with maleic anhydride and phthalic anhydride, respectively, at 80 °C. Block polyester with narrow polydispersity of 1.05 was achieved via a sequential addition strategy. This work provides robust organocatalysts for the selective copolymerization of epoxides with cyclic anhydrides.

Organic crystals are easily cracked into pieces or powders under applied stress because of their intrinsic brittle nature. This undesired mechanical property directly limits their application in flexible optical and optoelectronic devices. Herein, we developed a compact single-benzene molecule dimethyl 2,5-bis((2-hydroxyethyl)amino)terephthalate, which was easily crystallized to form two polymorphs, A and B. Featuring a single-benzene π-system, both polymorphs A and B display red fluorescence in crystals. More importantly, crystals of polymorph A are flexible and can be elastically bent under mechanical force. Given these advantages, a flexible optical waveguide has been realized in the crystal of polymorph A with a bent shape, highlighting its potential application in flexible devices. In addition, the thermal transformation of crystals from polymorph A to polymorph B, which was accompanied by the change of optical property as well as mechanical elasticity, has been observed.

Hierarchical Cr-doped WO3 microspheres have been successfully synthesized for efficient sensing of H2S gas at low temperatures. The hierarchical structures provide an effective gas diffusion path via well-aligned micro-, meso-, and macroporous architectures, resulting in significant enhancement in sensing response to H2S. The temperature and gas concentration dependence on the sensing properties elucidate that Cr dopants remarkably improve the response and lower the sensor' operating temperature down to 80 °C. Under 0.1 vol % H2S, the response of Cr-doped WO3 sensor is 6 times larger than pristine WO3 sensor at 80 °C. We suggest the increasing number of oxygen vacancies created by Cr dopants to be the underlying reason for enhancement of charge carrier density and accelerated reactions with H2S.