Carbon quantum dots (CQDs) are an emerging research area in the biomedical field due to their biocompatibility and multifunctionality. Herein, we report CQDs synthesized in a green, fast, facile manner in a recyclable mineral oilmediated pyrolysis medium using citric acid as the main carbon source and thiourea as N- and S-doping source. The assynthesized CQDs exhibit excitation-dependent photoemission (Φ = 0.57) with notable energy upconversion behavior at longer wavelengths, suggesting possible utilization in multiphoton microscopy. FT-IR characterization suggest diverse functional groups on the surface which include carboxylic acids, amines, and thiocyanates among others. Photothermal analysis supported the NIR-emissive behavior and showed that CQD solution temperature could potentially increase nearly 20°C higher after 10 min irradiation by 630-nm LED laser source powered at 1 W/cm2. CQDs have been tested in vitro and has been used as multicolor cellular imaging agent.
Carbon quantum dots (CQDs) are an emerging research area in the biomedical field due to their biocompatibility and multifunctionality. Herein, we report CQDs synthesized in a green, fast, facile manner in a recyclable mineral oil-mediated pyrolysis medium using citric acid as the main carbon source and thiourea as N- and S-doping source. The assynthesized CQDs exhibit excitation-dependent photoemission (Φ = 0.57) with notable energy upconversion behavior at longer wavelengths, suggesting possible utilization in multiphoton microscopy. FT-IR characterization suggest diverse functional groups on the surface which include carboxylic acids, amines, and thiocyanates among others. Photothermal analysis supported the NIR-emissive behavior and showed that CQD solution temperature could potentially increase nearly 20°C higher after 10 min irradiation by 630-nm LED laser source powered at 1 W/cm2. CQDs have been tested in vitro and has been used as multicolor cellular imaging agent.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.