A universal green synthesis approach of several quantum dots (QDs), including iron oxide (Fe 3 O 4 ) QDs, gold (Au) QDs, zirconium oxide (ZrO 2 ) QDs, and graphene (Gr) QDs, was demonstrated in this study. Nanozyme-based signal amplification strategy of those QDs was also examined, which may have significant advantages for the development of biosensors with visual read-outs. A synergetic peroxidase-like activity of Fe 3 O 4 QDs was observed for the facile, visual, fieldportable, and sensitive detection of H 2 O 2 . The fluorescence emission, UV−vis spectrum, and circular dichroism spectra of the Fe 3 O 4 QDs were located at 419, 395, and 335 nm, respectively. The band gap energy of synthesized Fe 3 O 4 QDs was estimated to be 2.0 eV based on the Tauc plot. The X-ray photoelectron spectroscopic analysis revealed that the Fe(II) to Fe(III) ratio was increased when the Fe 3 O 4 NPs were converted to the Fe 3 O 4 QDs. The nonenzymatic activity of those QDs was further investigated using a mixture of 3,3′,5,5′-tetramethylbenzidine (TMB) and H 2 O 2 . The Fe 3 O 4 QDs possessed high peroxidaselike activity and exhibited Michaelis−Menten kinetics behavior. Kinetic studies revealed that the Fe 3 O 4 QDs demonstrated a higher affinity toward TMB than the standard enzyme horseradish peroxidase. This prolonged peroxidase-like Fe 3 O 4 QD catalytic activity was successfully applied for the detection of H 2 O 2 with a limit of detection (LOD) of 3.87 nM, which was calculated based on the standard deviation method. While similar approach was examined with Au QDs, ZrO 2 QDs, and Gr QDs in this study, no characteristic enzymatic activity was observed, which confirmed the unique properties of the Fe 3 O 4 QDs. The facile synthesis approach and the unique nanozymatic activity of the Fe 3 O 4 QDs described in the present study open a new horizon in materials chemistry and the development of colorimetric biosensors for environmental, energy, and medical applications.