Facile green synthesis of fluorescent N-doped carbon dots from Actinidia deliciosa and their catalytic activity and cytotoxicity applications

被引:110
作者
Arul, Velusamy [1 ]
Sethuraman, Mathur Gopalakrishnan [1 ]
机构
[1] Deemed Univ, Gandhigram Rural Inst, Dept Chem, Gandhigram 624302, Tamil Nadu, India
关键词
Actinidia deliciosa; Fluorescent nitrogen doped carbon dots; Rhodamine-B; Catalytic activity; Cytotoxicity; RHODAMINE-B DYE; PHOTOCATALYTIC DEGRADATION; SELECTIVE DETECTION; MOLECULAR-SIEVES; FRUIT EXTRACT; QUANTUM DOTS; PHOTOLUMINESCENCE; GRAPHENE; REMOVAL; SENSOR;
D O I
10.1016/j.optmat.2018.02.029
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Green synthesis of fluorescent nitrogen doped carbon dots (N-CDs) using Actinidia deliciosa (A. deliciosa) fruit extract as a carbon precursor and aqueous ammonia as a nitrogen dopant is reported here. The synthesized N-CDs were characterized by high resolution transmission electron microscopy (HR-TEM), energy dispersive spectroscopy (EDS), selected area electron diffraction (SAED), UV Visible spectroscopy (UV Vis), fluorescence spectroscopy, Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), Raman spectroscopy and X-ray photoelectron spectroscopy (XPS). The average size of the N-CDs was approximately 3.59 nm and the calculated inter layer distance was found to be 0.21 nm. Raman spectroscopy and SAED pattern revealed the graphitic nature of the synthesized N-CDs. The N-CDs were found to emit intense blue color at 405 nm under the excitation of 315 nm. The doping of nitrogen over the surface of the N-CDs was confirmed by EDS, FT-IR and XPS studies. The synthesized N-CDs were found to exhibit excellent catalytic activity in the reduction of Rhodamine-B using sodium borohydrate. The MIT assay was used to evaluate the cytotoxicity and biocompatibility of N-CDs towards L-929 and MCF-7 cells. From the results obtained, it was found that the N-CDs exhibit low cytotoxicity and superior biocompatibility on both L-929 and MCF-7 cells. (C) 2018 Published by Elsevier B.V.
引用
收藏
页码:181 / 190
页数:10
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