Facile approach to synthesize highly fluorescent multicolor emissive carbon dots via surface functionalization for cellular imaging

[Display omitted] Luminescent nanomaterials are encouraging scaffolds for diverse applications such as chemical sensors and biosensors, imaging, drug delivery, diagnostics, catalysis, energy, photonics, medicine, and so on. Carbon dots (CDs) are a new class of luminescent carbonaceous nanomaterial t...

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Published inJournal of colloid and interface science Vol. 513; pp. 505 - 514
Main Authors Kundu, Aniruddha, Lee, Jungpyo, Park, Byeongho, Ray, Chaiti, Sankar, K. Vijaya, Kim, Wook Sung, Lee, Soo Hyun, Cho, Il-Joo, Jun, Seong Chan
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.03.2018
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Summary:[Display omitted] Luminescent nanomaterials are encouraging scaffolds for diverse applications such as chemical sensors and biosensors, imaging, drug delivery, diagnostics, catalysis, energy, photonics, medicine, and so on. Carbon dots (CDs) are a new class of luminescent carbonaceous nanomaterial that have appeared recently and reaped tremendous scientific interest. Herein, we have exploited a simple approach to prepare tuneable and highly fluorescent CDs via surface functionalization. The successful synthesis of CDs is manifested from several investigations like high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The CDs exhibit excellent water solubility and with increasing nitrogen content fluorescence quantum yield increases whereas cell toxicity decreases. The CD synthesized at high temperature (180 °C) shows very high quantum yield (more than 56%). The tuneable optical properties of CDs are systematically studied using UV-vis and fluorescence spectroscopy. The cell viability evaluation and in vitro imaging study reveals that the synthesized CDs can be employed as a potential fluorescent probe for bio-imaging without further modification.
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ISSN:0021-9797
1095-7103
DOI:10.1016/j.jcis.2017.10.095