White carbon: Fluorescent carbon nanoparticles with tunable quantum yield in a reproducible green synthesis

被引:50
作者
Meiling, Till T. [1 ]
Cywinski, Piotr J. [2 ,3 ]
Bald, Ilko [1 ,4 ]
机构
[1] Univ Potsdam, Inst Chem, Phys Chem, D-14476 Potsdam, Germany
[2] Fraunhofer Inst Appl Polymer Res, Funct Mat & Devices, D-14476 Potsdam, Germany
[3] Polish Acad Sci, Inst Phys Chem, Coordinat Complexes & Funct Mat, PL-01224 Warsaw, Poland
[4] Fed Inst Mat Res & Testing, BAM, D-12489 Berlin, Germany
关键词
ELECTROCHEMICAL AVENUE; DOTS; PHOTOLUMINESCENCE; FACILE; FABRICATION; CYTOTOXICITY; NANOCRYSTALS; PERFORMANCE; NANODOTS; PROBES;
D O I
10.1038/srep28557
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this study, a new reliable, economic, and environmentally-friendly one-step synthesis is established to obtain carbon nanodots (CNDs) with well-defined and reproducible photoluminescence (PL) properties via the microwave-assisted hydrothermal treatment of starch and Tris-acetate-EDTA (TAE) buffer as carbon sources. Three kinds of CNDs are prepared using different sets of above mentioned starting materials. The as-synthesized CNDs: C-CND (starch only), N-CND 1 (starch in TAE) and N-CND 2 (TAE only) exhibit highly homogenous PL and are ready to use without need for further purification. The CNDs are stable over a long period of time (> 1 year) either in solution or as freeze-dried powder. Depending on starting material, CNDs with PL quantum yield (PLQY) ranging from less than 1% up to 28% are obtained. The influence of the precursor concentration, reaction time and type of additives on the optical properties (UV-Vis absorption, PL emission spectrum and PLQY) is carefully investigated, providing insight into the chemical processes that occur during CND formation. Remarkably, upon freeze-drying the initially brown CND-solution turns into a non-fluorescent white/slightly brown powder which recovers PL in aqueous solution and can potentially be applied as fluorescent marker in bio-imaging, as a reduction agent or as a photocatalyst.
引用
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页数:9
相关论文
共 44 条
[1]  
Anastas P.T., 1998, Green chemistry: theory and practice
[2]   Photoluminescence-Tunable Carbon Nanodots: Surface-State Energy-Gap Tuning [J].
Bao, Lei ;
Liu, Cui ;
Zhang, Zhi-Ling ;
Pang, Dai-Wen .
ADVANCED MATERIALS, 2015, 27 (10) :1663-+
[3]  
Brunner G, 2014, SUPERCRIT FLUID SCI, V5, P1
[4]   Carbon dots for multiphoton bioimaging [J].
Cao, Li ;
Wang, Xin ;
Meziani, Mohammed J. ;
Lu, Fushen ;
Wang, Haifang ;
Luo, Pengju G. ;
Lin, Yi ;
Harruff, Barbara A. ;
Veca, L. Monica ;
Murray, Davoy ;
Xie, Su-Yuan ;
Sun, Ya-Ping .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (37) :11318-+
[5]   Competitive Performance of Carbon "Quantum" Dots in Optical Bioimaging [J].
Cao, Li ;
Yang, Sheng-Tao ;
Wang, Xin ;
Luo, Pengju G. ;
Liu, Jia-Hui ;
Sahu, Sushant ;
Liu, Yamin ;
Sun, Ya-Ping .
THERANOSTICS, 2012, 2 (03) :295-301
[6]   Interface-Controlled Synthesis of Heterodimeric Silver-Carbon Nanoparticles Derived from Polysaccharides [J].
Choi, Yuri ;
Ryu, Gyeong Hee ;
Min, Sa Hoon ;
Lee, Bo Ram ;
Song, Myoung Hoon ;
Lee, Zonghoon ;
Kim, Byeong-Su .
ACS NANO, 2014, 8 (11) :11377-11385
[7]  
Derfus AM, 2004, NANO LETT, V4, P11, DOI 10.1021/nl0347334
[8]   Controllable synthesis of biosourced blue-green fluorescent carbon dots from camphor for the detection of heavy metal ions in water [J].
Gaddam, Rohit Ranganathan ;
Vasudevan, D. ;
Narayan, Ramanuj ;
Raju, K. V. S. N. .
RSC ADVANCES, 2014, 4 (100) :57137-57143
[9]   Bioimaging of Hyaluronic Acid Derivatives Using Nanosized Carbon Dots [J].
Goh, Eun Ji ;
Kim, Ki Su ;
Kim, Yi Rang ;
Jung, Ho Sang ;
Beack, Songeun ;
Kong, Won Ho ;
Scarcelli, Giuliano ;
Yun, Seok Hyun ;
Hahn, Sei Kwang .
BIOMACROMOLECULES, 2012, 13 (08) :2554-2561
[10]   Fabrication, gradient extraction and surface polarity-dependent photoluminescence of cow milk-derived carbon dots [J].
Han, Shuai ;
Zhang, He ;
Zhang, Jian ;
Xie, Yujie ;
Liu, Liangliang ;
Wang, Hangxing ;
Li, Xiangkai ;
Liu, Weisheng ;
Tang, Yu .
RSC ADVANCES, 2014, 4 (101) :58084-58089