Unravelling the formation of carbyne nanocrystals from graphene nanoconstrictions through the hydrothermal treatment of agro-industrial waste molasses.

The delicate synthesis of one-dimensional (1D) carbon nanostructures from two-dimensional (2D) graphene moiré layers holds tremendous interest in materials science owing to its unique physiochemical properties exhibited during the formation of hybrid configurations with sp-sp hybridization. However, the controlled synthesis of such hybrid sp-sp configurations remains highly challenging. Therefore, we employed a simple hydrothermal technique using agro-industrial waste as the carbon source to synthesize 1D carbyne nanocrystals from the nanoconstricted zones of 2D graphene moiré layers. By employing suite of characterization techniques, we delineated the mechanism of carbyne nanocrystal formation, wherein the origin of carbyne nanochains was deciphered from graphene intermediates due to the presence of a hydrothermally cut nanoconstriction regime engendered over well-oriented graphene moiré patterns. The autogenous hydrothermal pressurization of agro-industrial waste under controlled conditions led to the generation of epoxy-rich graphene intermediates, which concomitantly gave rise to carbyne nanocrystal formation in oriented moiré layers with nanogaps. The unique growth of carbyne nanocrystals over a few layers of holey graphene exhibits excellent paramagnetic properties, the predominant localization of electrons and interfacial polarization effects. Further, we extended the application of the as-synthesized carbyne product (Cp) for real-time electrochemical-based toxic metal (As) sensing in groundwater samples (from riverbanks), which depicted superior sensitivity (0.22 mA μM) even at extremely lower concentrations (0.0001 μM), corroborating the impedance spectroscopy analysis.