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Tunable Photoluminescence Across the Entire Visible Spectrum from Carbon Dots Excited by White Light
Author(s) -
Hu Shengliang,
Trinchi Adrian,
Atkin Paul,
Cole Ivan
Publication year - 2015
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201411004
Subject(s) - photoluminescence , carbon fibers , excited state , fluorescence , materials science , wavelength , optoelectronics , excitation , photochemistry , analytical chemistry (journal) , chemistry , optics , atomic physics , organic chemistry , physics , quantum mechanics , composite number , composite material
Although reports have shown shifts in carbon dot emission wavelengths resulting from varying the excitation wavelength, this excitation‐dependent emission does not constitute true tuning, as the shifted peaks have much weaker intensity than their dominant emission, and this is often undesired in real world applications. We report for the first time the synthesis and photoluminescence properties of carbon dots whose peak fluorescence emission wavelengths are tunable across the entire visible spectrum by simple adjustment of the reagents and synthesis conditions, and these carbon dots are excited by white light. Detailed material characterization has revealed that this tunable emission results from changes in the carbon dots’ chemical composition, dictated by dehydrogenation reactions occurring during carbonization. These significantly alter the nucleation and growth process, resulting in dots with either more oxygen‐containing or nitrogen‐containing groups that ultimately determine their photoluminescence properties, which is in stark contrast to previous observations of carbon dot excitation‐dependent fluorescence. This new ability to synthesize broadband excitable carbon dots with tunable peak emissions opens up many new possibilities, particularly in multimodal sensing, in which multiple analytes and processes could be monitored simultaneously by associating a particular carbon dot emission wavelength to a specific chemical process without the need for tuning the excitation source.

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