Polar engineering regulates photoluminescence-tunable carbon dots for microalgal lipid imaging. Issue 21 (22nd August 2022)
- Record Type:
- Journal Article
- Title:
- Polar engineering regulates photoluminescence-tunable carbon dots for microalgal lipid imaging. Issue 21 (22nd August 2022)
- Main Title:
- Polar engineering regulates photoluminescence-tunable carbon dots for microalgal lipid imaging
- Authors:
- Fu, Fangmei
Huang, Sirui
Pan, Xiaoqin
Lin, Junjie
Huang, Xiaoman
Liang, Zishan
Zeng, Guiling
Li, Wei
Zhang, Haoran
Zhang, Xuejie
Zheng, Mingtao
Zheng, Yinjian
Li, Qingming
Lei, Bingfu - Abstract:
- Abstract : Synthesis and purification of three carbon dots and the application of R-CDs in microalgae lipid imaging. Abstract : At present, research on the regulation strategy and mechanism of carbon dots (CDs) fluorescence emission from short wavelength to long wavelength is a hot topic. Herein, o -phenylenediamine (O-PDA) was used as the sole precursor and the polarity of the reaction solvent was adjusted by changing the volume ratio of N, N -dimethylformamide (DMF) to H2 O to synthesize green (G-CDs), orange (O-CDs), and red CDs (R-CDs). All three types of CDs exhibited uniform particle sizes and excitation-independent photoluminescence (PL) emissions. The fluorescence lifetime decay curves revealed that the emission centers of G-CDs to O-CDs or R-CDs changed from double-emission centers to pure surface emission, which led to their different solvatochromic effects. X-Ray photoelectron spectroscopy (XPS), nuclear magnetic resonance spectroscopy (NMR), and mass spectroscopy (MS) techniques proved that the appropriate polarity of the reaction solvent could extend the π-conjugation of the fluorescent molecular structure on the surface of the CDs and induce a red-shift of the CDs emission. In addition, R-CDs had a relatively large nonpolar aromatic structure that showed low polarity and lipophilicity. The R-CDs dispersed in glycerol trioleate showed bright yellow fluorescence with a quantum yield (QY) of 43.52% but almost no fluorescence in water. At the same time, R-CDs hadAbstract : Synthesis and purification of three carbon dots and the application of R-CDs in microalgae lipid imaging. Abstract : At present, research on the regulation strategy and mechanism of carbon dots (CDs) fluorescence emission from short wavelength to long wavelength is a hot topic. Herein, o -phenylenediamine (O-PDA) was used as the sole precursor and the polarity of the reaction solvent was adjusted by changing the volume ratio of N, N -dimethylformamide (DMF) to H2 O to synthesize green (G-CDs), orange (O-CDs), and red CDs (R-CDs). All three types of CDs exhibited uniform particle sizes and excitation-independent photoluminescence (PL) emissions. The fluorescence lifetime decay curves revealed that the emission centers of G-CDs to O-CDs or R-CDs changed from double-emission centers to pure surface emission, which led to their different solvatochromic effects. X-Ray photoelectron spectroscopy (XPS), nuclear magnetic resonance spectroscopy (NMR), and mass spectroscopy (MS) techniques proved that the appropriate polarity of the reaction solvent could extend the π-conjugation of the fluorescent molecular structure on the surface of the CDs and induce a red-shift of the CDs emission. In addition, R-CDs had a relatively large nonpolar aromatic structure that showed low polarity and lipophilicity. The R-CDs dispersed in glycerol trioleate showed bright yellow fluorescence with a quantum yield (QY) of 43.52% but almost no fluorescence in water. At the same time, R-CDs had the advantages of good biocompatibility, a large Stokes shift (113 nm), and excellent photostability. Finally, as a targeted probe of microalgae lipids, R-CDs could screen the microalgae lipid-rich varieties and monitor changes in microalgae lipid content under N-free culture conditions. … (more)
- Is Part Of:
- Materials advances. Volume 3:Issue 21(2022)
- Journal:
- Materials advances
- Issue:
- Volume 3:Issue 21(2022)
- Issue Display:
- Volume 3, Issue 21 (2022)
- Year:
- 2022
- Volume:
- 3
- Issue:
- 21
- Issue Sort Value:
- 2022-0003-0021-0000
- Page Start:
- 7854
- Page End:
- 7864
- Publication Date:
- 2022-08-22
- Subjects:
- 620.11
- Journal URLs:
- https://pubs.rsc.org/en/journals/journalissues/ma#!issueid=ma001002&type=current&issnonline=2633-5409 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/d2ma00747a ↗
- Languages:
- English
- ISSNs:
- 2633-5409
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
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- 24360.xml