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不同溶剂中氢键形成过程中N掺杂聚合物碳点供体-受体性质的表现

Manifestation of Donor-Acceptor Properties of N-Doped Polymer Carbon Dots During Hydrogen Bonds Formation in Different Solvents.

作者信息

Korepanova Anisiya, Laptinskiy Kirill, Dolenko Tatiana

机构信息

Department of Physics, Moscow State University, 119991 Moscow, Russia.

Skobeltsyn Institute of Nuclear Physics, Moscow State University, 119991 Moscow, Russia.

出版信息

Polymers (Basel). 2024 Dec 21;16(24):3585. doi: 10.3390/polym16243585.


DOI:10.3390/polym16243585
PMID:39771437
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11679973/
Abstract

The effective use of polymer carbon dots (PCD) in various fields of science and technology requires a more detailed understanding of the mechanisms of their photoluminescence formation and change as a result of their interaction with the environment. In this study, PCD synthesized via a hydrothermal method from citric acid and ethylenediamine are studied in various solvents using FTIR spectroscopy, optical absorption spectroscopy, and photoluminescence spectroscopy. As a result of the analysis of the obtained dependencies of such PCD spectral characteristics as the photoluminescence FWHM, the photoluminescence quantum yield, the photoluminescence lifetime on the acidity and basicity of the solvent, a hypothesis was formulated on the formation mechanism of hydrogen bonds between the PCD surface groups and the molecules of the environment, and conclusions were made about the donor-acceptor nature of the synthesized PCD.

摘要

要在各种科学技术领域有效利用聚合物碳点(PCD),需要更详细地了解其光致发光形成机制以及与环境相互作用导致的变化机制。在本研究中,使用傅里叶变换红外光谱(FTIR)、光吸收光谱和光致发光光谱,对通过水热法由柠檬酸和乙二胺合成的PCD在各种溶剂中进行了研究。通过分析PCD光谱特性(如光致发光半高宽、光致发光量子产率、光致发光寿命)与溶剂酸碱度之间的依赖关系,提出了关于PCD表面基团与环境分子之间氢键形成机制的假设,并对合成的PCD的供体 - 受体性质得出了结论。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/4ba4b00a701b/polymers-16-03585-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/c800fd93e756/polymers-16-03585-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/040363f81e61/polymers-16-03585-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/8f35e5c0b016/polymers-16-03585-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/08bfb66f89fc/polymers-16-03585-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/96ad3d284508/polymers-16-03585-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/9c9d2f292d03/polymers-16-03585-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/cea152510a79/polymers-16-03585-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/57ca41a66206/polymers-16-03585-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/4ba4b00a701b/polymers-16-03585-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/c800fd93e756/polymers-16-03585-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/040363f81e61/polymers-16-03585-g002a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/8f35e5c0b016/polymers-16-03585-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/08bfb66f89fc/polymers-16-03585-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/96ad3d284508/polymers-16-03585-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/9c9d2f292d03/polymers-16-03585-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/cea152510a79/polymers-16-03585-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/57ca41a66206/polymers-16-03585-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/143d/11679973/4ba4b00a701b/polymers-16-03585-g009.jpg

相似文献

[1]
Manifestation of Donor-Acceptor Properties of N-Doped Polymer Carbon Dots During Hydrogen Bonds Formation in Different Solvents.

Polymers (Basel). 2024-12-21

[2]
Polymerization-Driven Photoluminescence in Alkanolamine-Based C-Dots.

Chemistry. 2021-2-1

[3]
Surface States Induced Photoluminescence Enhancement of Nitrogen-Doped Carbon Dots Via Post-Treatments.

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[4]
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[5]
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Spectrochim Acta A Mol Biomol Spectrosc. 2017-10-21

[6]
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Chemphyschem. 2019-4-16

[7]
Solvent effect on the absorption and emission spectra of carbon dots: evaluation of ground and excited state dipole moment.

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[8]
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Light Sci Appl. 2022-4-11

[9]
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Nanoscale. 2019-1-23

[10]
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Molecules. 2024-3-18

本文引用的文献

[1]
The effect of polarity and hydrogen bonding on the electronic and vibrational structure of the salicylate anion in acetonitrile and water: implicit and explicit solvation approaches.

RSC Adv. 2024-9-18

[2]
Fluorescent carbon dots for sensing applications: a review.

Anal Sci. 2024-8

[3]
Dye-Derived Red-Emitting Carbon Dots for Lasing and Solid-State Lighting.

ACS Nano. 2023-11-14

[4]
Carbon Dots: From Synthesis to Unraveling the Fluorescence Mechanism.

Small. 2024-1

[5]
Pure and doped carbon quantum dots as fluorescent probes for the detection of phenol compounds and antibiotics in aquariums.

Sci Rep. 2023-8-8

[6]
Nitrogen and Chlorine Co-doped Carbon Dots as a Highly Selective and Sensitive Fluorescent Probe for Sensing of PH, Tetracycline Detection and Cell Imaging.

J Fluoresc. 2024-5

[7]
The Shift in the Behavior of Methylene Blue Toward the Sensitivity of Medium: Solvatochromism, Solvent Parameters, Regression Analysis and Investigation of Cosolvent on the Acidity Constants.

J Fluoresc. 2023-11

[8]
Water-soluble graphene quantum dot-based polymer nanoparticles with internal donor/acceptor heterojunctions for efficient and selective detection of cancer cells.

J Colloid Interface Sci. 2023-5

[9]
Implementing neural network approach to create carbon-based optical nanosensor of heavy metal ions in liquid media.

Spectrochim Acta A Mol Biomol Spectrosc. 2023-2-5

[10]
Multicolor Nitrogen-Doped Carbon Quantum Dots for Environment-Dependent Emission Tuning.

ACS Omega. 2022-8-1

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