The breakthrough enables low‑temperature, energy‑efficient carbon‑based gas sensors, opening new markets for portable and industrial monitoring applications.
Graphdiyne (GDY) has long been hailed for its unique sp‑sp2 hybridized network, offering high surface area and tunable electronic properties. However, translating these theoretical benefits into functional devices has been hampered by poor crystallinity and limited charge‑transfer pathways. By confining single‑atom silver within nitrogen‑substituted GDY pores, researchers not only achieve unprecedented metal loading but also trigger a lattice rearrangement that yields a defect‑free hexagonal crystal, effectively turning the carbon scaffold into a high‑mobility conduit for electrons.
The AgSAs/GDY sensor leverages this engineered structure to create a direct Ag‑to‑adsorbate charge‑transfer channel. The reoriented 4d orbitals of the silver atoms strengthen d‑p interactions with ethanol molecules, accelerating adsorption kinetics and producing a pronounced conductance change at temperatures under 100 °C. Compared with conventional metal‑oxide sensors, the device exhibits faster response times, lower power consumption, and robust repeatability, addressing key performance gaps that have limited carbon‑based sensors in commercial settings.
Beyond ethanol monitoring, the monatomic‑metal embedding strategy offers a versatile platform for a broad range of chemical detection and catalytic applications. The ability to fine‑tune charge‑transfer pathways at the atomic level could accelerate the development of next‑generation environmental sensors, wearable health monitors, and low‑temperature catalytic reactors. As industries seek greener, more energy‑efficient technologies, the AgSAs/GDY approach positions carbon nanomaterials as a competitive alternative to traditional semiconductor and metal‑oxide systems, potentially reshaping market dynamics in the sensor and catalysis sectors.
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