journal article·2021-09

Generalized synthesis of biomolecule-derived and functionalized fluorescent carbon nanoparticle

Santu Ghosh, Haydar Ali, Suman Pal, Sekhar C Ray, Nikhil R Jana

Bulletin of Materials Science· Volume 44· Issue 3
Publisher page

Abstract

Although wide variety of molecular precursors have been used for carbonization-based synthesis of fluorescent carbon nanoparticle, biomolecule-derived carbon nanoparticle with tunable fluorescence is difficult to synthesize. Here, we report a generalized approach for the preparation of fluorescent carbon nanoparticle from various biomolecules, such as lactose, ascorbic acid, tyrosine and sucrose. The method involves controlled carbonization of molecular precursor in ethylene glycol at 190°C in the presence of Na3PO4. The presented synthetic method can produce 20–30 mg of nanoparticles in one batch with fluorescence quantum yield in the range of 1–10% and nanoparticles can be conjugated with primary amine-terminated chemical/biochemical by simple incubation. These fluorescent carbon nanoparticles can be transformed into different nanobioconjugates for various biomedical applications.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Carbon and Quantum Dots Applications · Nanocluster Synthesis and Applications · Graphene and Nanomaterials Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (23)

Show source-provided references
1. Xu X Y, Ray R, Gu Y L, Ploehn H J, Gearheart L, Raker K et al 2004 J. Am. Chem. Soc. 126 1273610.1021/ja040082h ↗
2. Sun Y-P, Zhou B, Lin Y, Wang W, Fernando K A S, Pathak P et al 2006 J. Am. Chem. Soc. 128 775610.1021/ja062677d ↗
3. Liu H P, Ye T and Mao C D 2007 Angew. Chem. Int. Ed. 46 647310.1002/anie.200701271 ↗
4. Ray S C, Saha A, Jana N R and Sarkar R 2009 J. Phys. Chem. C 113 1854610.1021/jp905912n ↗
5. Baker S N and Baker G A 2010 Angew. Chem. Int. Ed. 49 672610.1002/anie.200906623 ↗
6. Bhunia S K, Saha A, Maity A R, Ray S C and Jana N R 2013 Sci. Rep. 3 147310.1038/srep01473 ↗
7. Jiang K, Sun S, Zhang L, Lu Y, Wu A, Cai C et al 2015 Angew. Chem. Int. Ed. 54 536010.1002/anie.201501193 ↗
8. Fan Y, Guo X Y, Zhang Y Q, Lv Y, Zhao J L and Liu X Y 2016 ACS Appl. Mater. Interfaces 8 3186310.1021/acsami.6b10654 ↗
9. Ali H, Bhunia S K, Dalal C and Jana N R 2016 ACS Appl. Mater. Interfaces 8 930510.1021/acsami.5b11318 ↗
10. Wang C, Jiang K, Wu Q, Wu J and Zhang C 2016 Chem. Eur. J. 22 1447510.1002/chem.201602795 ↗
11. He J L, He Y L, Chen Y H, Lei B F, Zhuang J L, Xiao Y et al 2017 Small 13 170007510.1002/smll.201700075 ↗
12. Wang Z, Yuan F, Li X, Li Y, Zhong H, Fan L et al 2017 Adv. Mater. 29 170291010.1002/adma.201702910 ↗
13. Yuan F L, Yuan T, Sui L Z, Wang Z B, Xi Z F, Li Y C et al 2018 Nat. Commun. 9 224910.1038/s41467-018-04635-5 ↗
14. Ding H, Wei J S, Zhang P, Zhou Z Y, Gao Q Y and Xiong H M 2018 Small 14 180061210.1002/smll.201800612 ↗
15. Chakraborty A, Dalal C and Jana N R 2018 Langmuir 34 1346110.1021/acs.langmuir.8b00376 ↗
16. Maity A R, Palmal S, Basiruddin S K, Karan N S, Sarkar S, Pradhan N et al 2013 Nanoscale 5 550610.1039/c3nr00549f ↗
17. Maity A R, Saha A, Roy A and Jana N R 2013 ChemPlusChem 78 25910.1002/cplu.201200296 ↗
18. Palmal S, Basiruddin S, Maity A R, Ray S C and Jana N R 2013 Chem. Eur. J. 19 94310.1002/chem.201203083 ↗
19. Mandal K and Jana N R 2018 ACS Appl. Nano Mater. 1 353110.1021/acsanm.8b00673 ↗
20. Bhunia S K, Pradhan N and Jana N R 2014 ACS Appl. Mater. Interfaces 6 767210.1021/am500964d ↗
21. Ali H, Ghosh S and Jana N R 2018 MRS Adv. 3 77910.1557/adv.2018.80 ↗
22. Ghosh S, Ali H and Jana N R 2019 ACS Sustain. Chem. Eng. 7 12629
23. Ghosh S, Panja P, Dalal C and Jana N R 2019 ACS Appl. Bio. Mater. 2 33910.1021/acsabm.8b00617 ↗