Chemosensors

A novel acridine-based fluorescent sensor (Sensor ANT) for the highly selective and sensitive detection of cyanide ions (CN⁻) was rationally designed and synthesized via the conjugation reaction of acridine-9-amine with 3-nitrophenyl isothiocyanate. The sensing mechanism is triggered by the specific interaction between exogenous CN⁻ and the hydrogen-bonding moieties within the sensor’s molecular framework, which induces a distinct fluorescence quenching response. Systematic titration experiments confirmed that Sensor ANT exhibits rapid response kinetics, excellent selectivity, and reliable qualitative/quantitative detection capabilities toward CN⁻. Complementary biocompatibility assays, including in vitro cellular imaging and in vivo zebrafish experiments, further verified the promising application potential of this sensor in practical and biological detection scenarios. The detection limit (DL) of Sensor ANT for CN⁻ was calculated to be 2.89 × 10⁻⁷ M, with a 1:1 binding stoichiometry and a binding constant of 1.95 × 10⁴ M⁻¹. These findings demonstrate that Sensor ANT represents a robust candidate for CN⁻ detection in environmental and biological systems.

The growing demand for sustainable, biocompatible, and multifunctional sensing materials has intensified interest in melanin and its derivatives, including melanin-inspired polymers and composites. Melanin is a naturally occurring biopolymer whose intricate structure and diverse chemical composition give rise to a remarkable combination of optical, electrical, and chemical properties. Key physicochemical characteristics, such as broadband optical absorption, hydration-dependent conductivity, redox activity, and metal ion coordination, are closely linked to melanin’s signal transduction capabilities and underpin its relevance in sensing applications. Recent advances in melanin-based sensing technologies encompass pH, humidity, chemical, biological, and optical platforms, with particular emphasis on hybrid systems incorporating graphene, silicon, or nanomaterials, and printable or wearable device architectures. These developments have enabled enhanced performance and broadened potential application fields. However, persistent challenges, including intrinsic heterogeneity, limited selectivity, relatively low electrical conductivity, and poor long-term operational stability, still limit practical implementation. Emerging molecular engineering and advanced fabrication strategies are being developed to address these limitations. Together, these findings position melanin as a versatile, eco-compatible, and functionally rich material, with a significant potential to underpin the next generation of sustainable sensing technologies.

This study presents a unified first-principles investigation of CO₂, NO₂, SO₂, and H₂O adsorption on Al₂O₃ (001), TiO₂ (001), and SiO₂ (001) surfaces, establishing the first cross-material, chemically consistent benchmark for oxide–gas interactions. Calculated adsorption energies reveal strong chemisorption of SO₂ and NO₂ on Al₂O₃ and TiO₂, moderate H₂O binding—particularly on TiO₂ where hydroxylation is favored—and generally weak CO₂ interactions across all surfaces. Bader charge analysis provides atom-resolved insight into these trends, showing substantial electron transfer and pronounced oxygen-site polarization for strongly adsorbing gases, in contrast to the minimal charge redistribution characteristic of physisorbed CO₂. These charge-transfer signatures distinguish binding mechanisms, clarify the origins of material-specific selectivity, and link adsorption to expected variations in surface conductivity and sensor response. The combined energetic and electronic analysis also reveals competitive effects between humidity and CO₂ on surface hydroxylation and local electronic structure, a phenomenon critical for realistic sensing environments but previously unaddressed. Overall, this work delivers a rigorous comparative framework for understanding gas interactions with technologically relevant oxides and provides a solid foundation for future studies involving defects, dopants, surface reconstructions, and advanced functionalization strategies for environmental monitoring and energy-conversion devices.