z-logo
Premium
Graphene Quantum Dots from Polycyclic Aromatic Hydrocarbon for Bioimaging and Sensing of Fe 3+ and Hydrogen Peroxide
Author(s) -
Zhou Li,
Geng Junlong,
Liu Bin
Publication year - 2013
Publication title -
particle and particle systems characterization
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.877
H-Index - 56
eISSN - 1521-4117
pISSN - 0934-0866
DOI - 10.1002/ppsc.201300170
Subject(s) - graphene , photoluminescence , quantum dot , quantum yield , photochemistry , fluorescence , quenching (fluorescence) , polycyclic aromatic hydrocarbon , materials science , hydrothermal carbonization , chemistry , carbonization , nanotechnology , organic chemistry , scanning electron microscope , optoelectronics , physics , quantum mechanics , composite material
An easy approach for large‐scale and low‐cost synthesis of photoluminescent (PL) graphene quantum dots (GQDs) based on the carbonization of commercially available polycyclic aromatic hydrocarbon (PAH) precursors with strong acid and followed by hydrothermal reduction with hydrazine hydrate is reported. Transmission electron microscopy (TEM) and atomic force microscopy (AFM) characterizations indicate that the size and height of GQDs are in the range of 5–10 nm and 0.5–2.5 nm, respectively. PAH, which has more benzene rings, generally forms GQDs with relatively larger size. The GQDs show high water solubility, tunable photoluminescence, low cytotoxicity, and good optical stability, which makes them promising fluorescent probes for cellular imaging. In addition, the fluorescence of GQDs shows a sensitive and selective quenching effect to Fe 3+ with a detection limit of 5 × 10 −9 m . By combination with the Fe 2+ /Fe 3+ redox couple, the PL GQDs are able to detect oxidant, using H 2 O 2 as an example. This study opens up new opportunities to make full use of GQDs because of their facile availability, cost‐effective productivity, and robust functionality.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here