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An enchanting yet challenging task is the development of higher productivity in plants to meet the ample food demands for the growing global population while harmonizing the ecosystem using front-line technologies. This has kindled the practice of green microalgae cultivation as a driver of key biostimulant products, targeting agronomic needs. To this end, a prodigious and economical strategy for producing bioactive compounds (sources of secondary metabolites) from microalgae using carbon-based nanomaterials (CNMs) as a platform can circumvent these hurdles. Recently, the nanobionics approach of incorporating CNMs with living systems has emerged as a promising technique to develop organelles with new and augmented functions. Herein, we discuss the importance of 2D carbon nanosheets (CNS) as an alternative carbon source for the phototrophic cultivation of microalgae. CNS not only aids in cost reduction for algal cultivation but also confers combinatorial innate or exogenous functions that enhance its programmed biosynthetic metabolism, proliferation, or tolerance to stress. Moreover, the inherent ability of CNS to act as efficient biocatalysts can enhance the rate of photosynthesis. The primary focus of this mini-review is the development of an economic route for enhanced yield of bioactive compounds while simultaneously serving as a heterogeneous platform for enhancing the sustainable production of biostimulants including bioactive compounds from algal biomass for pharmaceutical and nutraceutical applications.

Engineered well-ordered hybrid nanomaterials are symbolically at a pivotal point, just ahead of the long-anticipated transformation of the human race. Incorporating newer carbon nanomaterials like graphene quantum dots (GQDs) with tetrapyrrolic porphyrins (Pp) and phthalocyanines (Pc) is crucial for achieving exquisite molecular nanoarchitectures that are superior to their individual components. The outcomes of this, particularly in the case of graphene quantum dot-porphyrin/phthalocyanine (GQD-Pp/Pc) hybrids, remain comprehensively unexplored to date. Interestingly, GQD-Pp/Pc hybrids provide a modern strategy to regulate matter by utilising intramolecular and organisational properties to create well-defined nanocomposites

The ongoing race of biomedical applications has given momentum to the development of graphene quantum dots (GQDs). GQDs are zero-dimensional fluorescent carbon-nanomaterials, with a pronounced quantum confinement effect, and abundant edge states and functional groups. Despite their potential applications, mass-scale synthesis of single crystalline graphene quantum dots (GQDs) with high quantum yields derived via a direct green synthesis approach from bio-wastes is a major challenge. Hitherto, green extract (i.e. sugarcane molasses) driven single crystalline sulphur-doped GQDs (S-GQDs) with a longer decay time, high quantum yield, and excellent biocompatibility have remained unexplored in the bioimaging arena. At the same time, this agro-industrial waste has value in terms of both products and byproducts i.e. zero waste generation resulting in reduced human footprint on the environment. For the first time, we present a facile, large-scale, one-step, economical, template- and catalyst-free synthesis of sustainable, highly crystalline S-GQDs via a hydrothermal route from second generation (2G) bio-wastes. Mechanistic insight into the formation of S-GQDs from their precursor was obtained using powder X-ray diffraction patterns (PXRD). S-GQDs directly obtained from bio-wastes without surface passivation showed the highest quantum yield (QY) ∼ 47% obtained to date. The wide and symmetric emission spectrum of these S-GQDs is instrumental for sensitive detection as labelling nanoprobes. Moreover, their non-toxic behavior, in vitro and in vivo, has a future in quick point-of-care screening and real-time bioimaging. Thus, the as-synthesized bio-waste derived S-GQDs accomplished the purpose of an advanced environmentally friendly and sustainable material which is non-toxic, viable, safe, and cheap. This unprecedented work advances the synthesis of high-quality S-GQDs from bio-waste, which provides a breakthrough in the bioimaging field.

The advent of novel carbonaceous nanomaterials (CMs) associated with microalgae paved an alternate way for the bioeconomic production of biofuels as well as high value added compounds. Herein, we for the first time, present a holistic approach for sustainable biomass and lipid production from Chlorella pyrenoidosa, wherein CMs, namely N-doped carbon nanosheets (CNS) and N-doped graphene nanosheets (NGS) were used as one of the algal growth supporting factors. Doping carbon nanomaterials with nitrogen can effectively tune its electronic structure and other intrinsic properties for efficient photocatalysis. The utilization of CNS and NGS in this process lead to rapid, environment friendly, and facile assimilation of biomass and lipids for the development of nutraceuticals, pharmaceuticals, and other bioenergy associated applications. Employing a suite of characterization methods, the intrinsic structural and morphological properties of CMs were revealed. Compared with control, the lipid content obtained in ...

Graphene quantum dots (GQDs) are the harbingers of a paradigm shift that revitalize self-assembly of the colloidal puzzle by adding shape and size to the material-design palette. Although self-assembly is ubiquitous in nature, the extent to which these molecular legos can be engineered reminds us that we are still apprenticing polymer carpenters. In this quest to unlock exotic nanostructures ascending from eventual anisotropy, we have utilized different concentrations of GQDs as a filler in free-radical-mediated aqueous copolymerization. Extensive polymer grafting over the geometrically confined landscape of GQDs (0.05%) bolsters crystallization instilling a loom which steers interaction of polymeric cilia into interlaced equilateral triangles with high sophistication. Such two-dimensional (2D) assemblies epitomizing the planar tiling of "Star of David" forming a molecular kagome lattice (KL) without metal templation evoke petrichor. Interestingly, a higher percentage (0.3%) of GQDs allow selective tuning of the interfacial property of copolymers breaking symmetry due to surface energy incongruity, producing exotic Janus nanomicelles (JNMs). Herein, with the help of a suite of characterizations, we delineate the mechanism behind the formation of the KL and JNMs which forms a depot of heightened drug accretion with targeted delivery of 5-fluorouracil in the colon as validated by gamma scintigraphy studies.

Graphical abstract, Highlights • CQDs can act as a multi-site inhibitor by blocking the viral entry, RNA strand synthesis, and replication step. • Triazole functionalized heteroatom co-doped carbon quantum dots (TFH-CQDs) can synergistically exert an intensified antiviral response. • TFH-CQDs may block the viral entry by perturbing various interactions with the host cells. • TFH-CQDs may block the viral enzymes such as helicase and 3CLpro, important for viral replication. • Understanding the receptor recognition mechanism of human coronaviruses with host cells is imperative to elucidate the inhibitory mechanism of TFH-CQDs., 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.