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-sp2 hybridization. However, the controlled synthesis of such hybrid sp-sp2 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 (As3+) sensing in groundwater samples (from riverbanks), which depicted superior sensitivity (0.22 mA µM-1) even at extremely lower concentrations (0.0001 µM), corroborating the impedance spectroscopy analysis.

Graphene quantum dots-hybrid hydrogel as an avant-garde biomimetic scaffold for diabetic wound healing.

In the age of fathoming biomedical predicaments, ardently emerged the field of materiobiology to effectively counter the archetypal and outdated therapies. Correspondingly, the subpar activity of the over-the-counter wound dressing pharmaceuticals have been dominated with the implementation of biocompatible, water-retaining exotic hydrogels to facilitate accelerated diabetic wound healing. Considering a strategy to develop a pragmatic biomimetic scaffold having the ability of dynamic wound healing with diminutive inflammation, we investigated the creation of graphene quantum dot (GQD)-polyacrylic acid (PAA) hybrid hydrogel. We observe appropriate percentage of GQD incorporation in PAA to demonstrate lower pro-inflammatory cytokines, interleukin (IL-6), and tumour necrosis factor (TNF-α) along with higher anti-inflammatory (IL-10) expressions in contrast to natural and standard controls. Likewise, histological examinations corresponding to the in-vitro and in-vivo toxicological analysis of GQD-PAA manifested to be a non-toxic, biocompatible saviour of diabetic wounds. This hybrid hydrogel reports the quickest diabetic wound healing of 13 days. Additionally, the hybrid hydrogel also demonstrates salient antibacterial activity against E. coli. We explore a multifaceted mechanistic approach attributed by the hybrid framework as an avant-garde solution in materiobiology and diabetic wound healing nexus. We believe the GQD-hybrid hydrogel reveals an advancement that could portray a new horizon against diabetic wounds.

Exploring the role of triazole functionalized heteroatom co-doped carbon quantum dots against human coronaviruses.

Preventing the trajectory of human coronaviruses including the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic could rely on the sprint to design a rational roadmap using breakneck strategies to counter its prime challenges. Recently, carbon quantum dots (CQDs), zero-dimensional (0D) carbon-based nanomaterials, have emerged as a fresh antiviral agent owing to their unique physicochemical properties. Additionally, doping instils beneficial properties in CQDs, augmenting their antiviral potential. The antiviral properties of CQDs can be reinforced by heteroatom doping. Bestowed with multifaceted features, functionalized CQDs can interact with the spike protein of the human coronaviruses and perturb the virus-host cell recognition. Recently, triazole derivatives have been explored as potent inhibitors of human coronaviruses by blocking the viral enzymes such as 3-chymotrypsin-like protease (3CLpro) and helicase, important for viral replication. Moreover, they offer a better aromatic heterocyclic core for therapeutics owing to their higher thermodynamic stability. To curb the current outbreak, triazole functionalized heteroatom co-doped carbon quantum dots (TFH-CQDs) interacting with viral cells spanning the gamut of complexity can be utilized for deciphering the mystery of its inhibitory mechanism against human coronaviruses. In this quest to unlock the potential of antiviral carbon-based nanomaterials, CQDs and triazole conjugated CQDs template comprising a series of bioisosteres, CQDs-1 to CQDs-9, can extend the arsenal of functional antiviral materials at the forefront of the war against human coronaviruses.