Food toxins are regarded as a major source of health risks, serious illnesses susceptible to even death. These dangerous pathogens may lead to significant economic impact worldwide. The food production chain undergoes different stages like harvesting, processing, storage, packaging, distribution, and lastly preparation, and consumption. Therefore, each step is susceptible to risks of environmental contamination. Nowadays, the carbon quantum dots (CDs) are regarded as one of the most widely used hybrid carbon nanomaterials due to their different magical physical and chemical properties. The CDs have a size below 10 nm and show the fluorescent property. The CDs find vast applications in different fields like sensing, food safety, drug delivery, bioimaging, catalyst, energy conversion, etc. Compared to other available methods, the fluorescence detection techniques have low cost, easy handling, and safe operating system. There is a need for a review to compile the fluorescence properties of carbon nanodots used to detect food pathogens. This brief review is addressed in that direction and mostly focused on the synthesis of carbon dots-based fluorescence sensors for detecting pathogens and toxins in foods and beverages. The detailed mechanisms and origin of fluorescence properties of carbon quantum dots are also highlighted herewith.

Nitrogen-doped carbon dots (N-CDs), derived from the biomass (anthocyanin), are the novel additive to the nanocarbon materials, which is expected to bring a wide spectrum of novel applications. Moreover, metallic oxides are emerging for their unique potential for electrocatalysis. Herein, we report the synthesis of N-CDs for the selective detection of Fe3+ with a limit of detection of 2.57 μM in the range of 5–60 μM using ethylenediamine and H2O2 by a hydrothermal method. The obtained N-CDs displayed a spherical morphology with a particle size range of 2–7 nm and emitted blue luminescence at 394 nm under excitation at 319 nm. Meanwhile, we have demonstrated the fabrication of cost-efficient electrocatalysts for oxygen evolution reaction (OER) in an alkaline medium, employing N-CDs. Owing to the successful incorporation of N-CDs into NiO nanospheres, the resulting N-CDs/NiO with large surface areas, fast charge transfer, and increased conductivity vastly improved the catalytic activity. Remarkably, the optimal of N-CDs/NiO composite requires the overpotential of only 380 mV at a current density of 10 mA cm− 2 and a relatively low Tafel slope of 57.96 mV dec− 1 compared with pure NiO. These results open up a facile route for the application of N-CDs and offer prospects for CD-metal hybrids as high OER catalysts in electrochemical energy devices.