Chirality has attracted extensive attention in many fields ranging from chemistry to life sciences. Carbon dots (CDs) with good biocompatibility and unique photochemical properties have become a new star in the nanocarbon family. Endowed with chirality, CDs will exhibit more marvellous properties and bridge the fields of material chemistry and life sciences tightly. Herein, we report a facile one-step alkali-assisted electrochemical method to fabricate chiral CDs from cysteine (cys). We showed the chiral evolution of CDs with highly symmetrical circular dichroism (CD) signals in the range from 205 to 350 nm. These chiral CDs have been further demonstrated to be capable of tuning the activity of laccase: the l-CDs can improve the activity of the enzyme up to 20.2%, whereas the d-CDs decrease the activity to 10.4%. A series of experiments confirm that it is the synergistic effect of nanosize and chirality of CDs that induces the change in the structure of laccase and thus leads to the tuning of the laccase activity.

Carbon dots (CDs) have attracted increasing attention in disease therapy owing to their low toxicity and good biocompatibility. Their therapeutic effect strongly depends on the CDs structure (e.g., size or functional groups). However, the impact of CDs chirality on maltase and blood glucose level has not yet been fully emphasized and studied. Moreover, in previous reports, chiral CDs with targeted optical activity have to be synthesized from precursors of corresponding optical rotation, severely limiting chiral CDs design. Here, chiral CDs with optical rotation opposite to that of the precursor are facilely prepared through electrochemical polymerization. Interestingly, their chirality can be regulated by simply adjusting reaction time. At last, the resultant (+)‐DCDs (700 µg mL−1) are employed to modify maltase in an effort to regulate the hydrolytic rate of maltose, showing an excellent inhibition ratio to maltase of 54.7%, significantly higher than that of (−)‐LCDs (15.5%) in the same reaction conditions. The superior performance may be attributed to the preferable combination of DCDs with maltase. This study provides an electrochemical method to facilely regulate CDs chirality, and explore new applications of chiral CDs as antihyperglycemic therapy for controlling blood glucose levels.

N,S-CDs display an unambiguous bioimaging ability in the detection of intracellular temperature and tetracycline with satisfactory results.