Until now, the green and facile synthesis of multicolor fluorescent silicon nanoparticles (SiNPs) with favorable biocompatibility for cellular imaging and biosensors is still a challenge. Herein, a facile one-step room temperature method for preparing fluorescent SiNPs displayed different emission wavelengths was reported. Green and red fluorescent SiNPs (G-SiNPs and R-SiNPs) were synthesized by adjusting the concentration of the reducing agent 2,4-diaminophenol hydrochloride when the amount of N-[3-(trimethoxysilyl)-propyl]-ethylenediamine was consistent. Characterized by Fourier transform infrared spectroscopy, transmission electron microscopy, and X-ray photoelectron spectroscopy, the results revealed that the G-SiNPs and R-SiNPs were assembled by polymerization of different building blocks, and the emission characteristics of these SiNPs were attributed to the difference in their structural composition and particle size. Interestingly, these fluorescent SiNPs exhibited excellent water solubility, salt tolerance, pH stability, photobleaching resistance, and low cytotoxicity, which facilitated multicolor cell imaging, and further led to these SiNPs were highly attractive in a variety of applications, such as multi-channel sensing and biological imaging. Furthermore, the R-SiNPs have shown the potential to detect acid phosphatase, which is a biomarker of prostate cancer.
Keywords: acid phosphatase; cell imaging; fluorescent mechanism; silicon nanoparticles; tunable emission features.