Snapshots into carbon dots formation through a combined spectroscopic approach.
Ontology highlight
ABSTRACT:
SUBMITTER: Rigodanza F
PROVIDER: S-EPMC8113590 | biostudies-literature |
REPOSITORIES: biostudies-literature
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2024-11-23 | GSE189428 | GEO
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Project description:Biofilms are deleterious in many biomedical and industrial applications and prevention of their formation has been a pressing challenge. Here, carbon dots, CDs-LP that were easily synthesized from the biomass of Lactobacillus plantarum by one-step hydrothermal carbonization, were demonstrated to prevent biofilm formation of E. coli. CDs-LP did not thwart the growth of E. coli, indicating the anti-biofilm effect was not due to the bactericidal effect. Moreover, CDs-LP did not affect the growth of the animal cell AT II, showing low cytotoxicity, good safety and excellent biocompatibility. Therefore, CDs-LP could overcome the cytotoxicity issue found in many current antibiofilm agents. CDs-LP represent a new type of anti-biofilm materials, opening up a novel avenue to the development of biofilm treatment.
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Project description:Reported in 2004, carbon dots (CDs) have been widely used in various fields due to their excellent optical properties. However, the mechanism of their fluorescence modulation is still a controversial issue, which also seriously affects the further development of carbon dots. In this paper, m-hydroxybenzaldehyde is used as a raw material to obtain multicolor luminescent CDs by pyrolysis under different reaction conditions, thereby revealing the forbidden band tuning and formation mechanism of CDs. Different acid-base conditions lead to different reaction paths of the precursors, forming molecular fluorophores with different conjugated structures, which aggregate to eventually form CDs and further enhance the photoluminescence of the system by inhibiting the movement of the fluorescent centers.
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Project description:Carbon dots (CDs), defined by their size of less than 10 nm, are a class of photoluminescent (PL) and electrochemiluminescent (ECL) nanomaterials that include a variety of carbon-based nanoparticles. However, the control of their properties, especially ECL, remains elusive and afflicted by a series of problems. Here, the authors report CDs that display ECL in water via coreactant ECL, which is the dominant mechanism in biosensing applications. They take advantage of a multicomponent bottom-up approach for preparing and studying the luminescence properties of CDs doped with a dye acting as PL and ECL probe. The dependence of luminescence properties on the surface chemistry is further reported, by investigating the PL and ECL response of CDs with surfaces rich in primary, methylated, or propylated amino groups. While precursors that contribute to the core characterize the PL emission, the surface states influence the efficiency of the excitation-dependent PL emission. The ECL emission is influenced by surface states from the organic shell, but states of the core strongly interact with the surface, influencing the ECL efficiency. These findings offer a framework of pre- and post-synthetic design strategies to improve ECL emission properties, opening new opportunities for exploring biosensing applications of CDs.
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Project description:Room temperature magnetic ordering is reported for very small carbon dots (CDs), mat-like polyaniline nanofibers (Mat-PANI) and a composite of CDs@Mat-PANI containing 0.315?wt% CDs. We have found saturation magnetization (M S ) of CDs, Mat-PANI and CDs@Mat-PANI at 5 (20/300) K equals to 0.0079 (0.0048/0.0019), 0.0116 (0.0065/0.0055) and 0.0349 (0.0085/0.0077) emu/g, respectively. The M S enhancement in CDs@Mat-PANI (200% and 40% at 5?K and 300?K, respectively) is attributed to electron transfer from Mat-PANI imine N-atoms to the encapsulated CDs. Changes in M S values reveal that 0.81 (0.08) electron/CD is transferred at 5 (300) K, which is supported by observation of CDs photoluminescence (PL) redshift while in CDs@Mat-PANI. Band-bending and bandgap-renormalization calculations are used to predict a redshift of 117?meV at 300?K as a result of the electron transfer, in excellent agreement with the PL data (110?meV). Raman, X-ray diffraction and X-ray photoelectron spectroscopy data are used to confirm the electron transfer process as well as the strong interaction of CDs with PANI within CDs@Mat-PANI, which increases the crystalline domain size of Mat-PANI from about 4.8?nm to 9.2?nm while reducing the tensile strain from about 6.2% to 1.8%.
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