Carbon dots as a sustainable nanoplatform

被引:3
作者
Korah, Binila K. [1 ]
Murali, Aiswarya [2 ]
John, Bony K. [1 ]
John, Neenamol [1 ]
Mathew, Beena [1 ]
机构
[1] Mahatma Gandhi Univ, Sch Chem Sci, Piyadarsini Hills PO, Kottayam 686560, Kerala, India
[2] Christ Coll, Trichur 680125, Kerala, India
关键词
Carbon dots; Metal nanosynthesis; Sustainability; Applications; Fluorescence sensing; Electrochemical sensing; pH sensor; Fluorescent ink; GRAPHENE QUANTUM DOTS; MICROWAVE-ASSISTED PREPARATION; HUMAN SERUM-ALBUMIN; GREEN SYNTHESIS; SELECTIVE DETECTION; INTRACELLULAR PH; ONE-STEP; INDUCED CHEMILUMINESCENCE; ELECTROCHEMICAL SYNTHESIS; DEPENDENT FLUORESCENCE;
D O I
10.1007/s13399-023-04650-7
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Carbon dots (CDs), a new member of the nanocarbon family, are revolutionizing a wide range of fields. This new member has been the subject of extensive international research. Its synthesis methods, characteristics, and applications are active research areas. Carbon dots are nanoparticles composed of carbon with a diameter of less than 10 nm. The distinctive structure and size of CDs suggest that their physical, chemical, electrical, and optical properties are modifiable. In addition, they possess properties such as low toxicity, high water solubility, chemical stability, photoluminescence, photostability, electroluminescence, high quantum yield, high surface area, heteroatom doping capability, abundance of surface functional groups, good conductivity, and environmental friendliness. This review attempts to provide an introductory story of carbon dots. From the early beginning of CDs through the myriad of synthesis techniques used to date, the review advances to the properties and applications that have not yet been fully explored. The principal applications covered include fluorescence detection, electrochemical sensing, pH monitoring, fluorescent ink, and metal nanoparticle synthesis. Recent developments, gaps, and obstacles for each of these applications have been discussed.
引用
收藏
页码:24889 / 24910
页数:22
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