scholarly journals Evaluation of Different Bottom-up Routes for the Fabrication of Carbon Dots

Nanomaterials ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 1316
Author(s):  
Diana M. A. Crista ◽  
Joaquim C. G. Esteves da Silva ◽  
Luís Pinto da Silva

Carbon dots (CDs) are carbon-based nanoparticles with very attractive luminescence features. Furthermore, their synthesis by bottom-up strategies is quite flexible, as tuning the reaction precursors and synthesis procedures can lead to an endless number of CDs with distinct properties and applications. However, this complex variability has made the characterization of the structural and optical properties of the nanomaterials difficult. Herein, we performed a systematic evaluation of the effect of three representative bottom-up strategies (hydrothermal, microwave-assisted, and calcination) on the properties of CDs prepared from the same precursors (citric acid and urea). Our results revealed that these synthesis routes led to nanoparticles with similar sizes, identical excitation-dependent blue-to-green emission, and similar surface-functionalization. However, we have also found that microwave and calcination strategies are more efficient towards nitrogen-doping than hydrothermal synthesis, and thus, the former routes are able to generate CDs with significantly higher fluorescence quantum yields than the latter. Furthermore, the different synthesis strategies appear to have a role in the origin of the photoluminescence of the CDs, as hydrothermal-based nanoparticles present an emission more dependent on surface states, while microwave- and calcination-based CDs present an emission with more contributions from core states. Furthermore, calcination and microwave routes are more suitable for high-yield synthesis (~27–29%), while hydrothermal synthesis present almost negligible synthesis yields (~2%). Finally, life cycle assessment (LCA) was performed to investigate the sustainability of these processes and indicated microwave synthesis as the best choice for future studies.

2008 ◽  
Vol 62 (6-7) ◽  
pp. 914-917 ◽  
Author(s):  
Ping Ou ◽  
Gang Xu ◽  
Zhaohui Ren ◽  
Xiaohong Hou ◽  
Gaorong Han

1992 ◽  
Vol 70 (11) ◽  
pp. 2777-2784 ◽  
Author(s):  
Pierre D. Harvey ◽  
Benoit Daoust

The lowest energy singlet state in di-3-(N-ethylcarbazoylidene)acetone (dNECa), a luminescent model compound at room temperature for dibenzylideneacetone (dba), has been assigned to a charge transfer (CT) state using the medium polarity effect on λmax(F) and the fluorescence polarized spectra of dNECa at 77 K. The dNECa fluorescence quantum yields [Formula: see text] and lifetimes (τF) are solvent sensitive where both [Formula: see text] and τF tend to increase with polarity. The very weak and moderately structured phosphorences have been located for the first time for both dba and dNECa in the 550–800 nm range and are also assigned to a CT state. In this case the CT interactions are less pronounced than λ(0–0)P and τP are much less solvent sensitive. Finally, EHMO type calculations confirm that the CT transition is the lowest energy transition in dba and di-3-(N-methylindoylidene)acetone (a model compound for dNECa), but also suggest that the nπ* state must lie near the CT state in dba.


Soft Matter ◽  
2021 ◽  
Author(s):  
Zhenzhen Lu ◽  
Luke W Giles ◽  
Rico Tabor ◽  
Boon M. Teo

Recently, carbon dots (CDs) have attracted wide attention for their potential use as fluorescence probes in biological and analytical chemistry due to their great stability and high fluorescence quantum yields....


2018 ◽  
Vol 22 (01n03) ◽  
pp. 46-55 ◽  
Author(s):  
İlke Gürol ◽  
Gülay Gümüş ◽  
Deniz Kutlu Tarakci ◽  
Ömer Güngör ◽  
Mahmut Durmuş ◽  
...  

The synthesis and characterization of novel zinc(II) (1a–4a) and oxo-titanium(IV) (1b–4b) phthalocyanine derivatives bearing 1H,1H-nona?uoro-3,6-dioxaheptan-1-ol groups are described for the first time. These phthalocyanines (1a–4a and 1b–4b) were characterized by elemental analysis and different spectroscopic techniques such as UV-vis, [Formula: see text]H NMR, FTIR and mass. Furthermore, the photophysical (fluorescence quantum yields and lifetimes) and photochemical (singlet oxygen generation and photodegradation) properties of these phthalocyanines were investigated in tetrahydrofuran (THF) solution. The influence of the number of the substituted groups (tetra or octa), position of the substituents (peripheral or non-peripheral) and central metal atom (zinc or titanium) on the photophysical and photochemical properties of these phthalocyanines were evaluated.


2019 ◽  
Vol 29 (2) ◽  
pp. 495-504 ◽  
Author(s):  
Marco Lamperti ◽  
Arianna Maria Giani ◽  
Angelo Maspero ◽  
Guglielmo Vesco ◽  
Alessandro Cimino ◽  
...  

Nanoscale ◽  
2016 ◽  
Vol 8 (33) ◽  
pp. 15281-15287 ◽  
Author(s):  
Yongqiang Zhang ◽  
Xingyuan Liu ◽  
Yi Fan ◽  
Xiaoyang Guo ◽  
Lei Zhou ◽  
...  

2016 ◽  
Vol 12 ◽  
pp. 2739-2747 ◽  
Author(s):  
Lukas J Patalag ◽  
Daniel B Werz

Herein, we report on the synthesis and characterization of novel fluorescent fatty acids with large Stokes shifts. Three examples consisting of the same number of carbon atoms and thus of similar chain length are presented differing in their degree of unsaturation. As major fluorogenic contributor at the terminus benzo[c][1,2,5]thiadiazole was used. Respective syntheses based on Wittig reactions followed by iodine-mediated isomerization are presented. The absorption properties are modulated by the number of conjugated C=C double bonds of the oligoene chain ranging from one to three. Large Stokes shifts of about 4900–5700 cm−1 and fluorescence quantum yields of up to 0.44 were observed.


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