Yi Zhu , JiQiu Yang , Wei Shi , Jianxin Xie , Bingshan Zhou , Jiuguang Wang , Shihao Zheng , Shuguang Li , Wenjing Chen
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引用次数: 0
Abstract
In this study, in order to achieve high quantum yield (QY) and tunable multicolor carbon dots, the influence of quantum size effects and surface state changes were considered comprehensively. Blue-emitting seed carbon dots (S-CDs) were synthesized using 1,2,4-benzenetricarboxylic acid and urea as precursors. Green-emitting carbon dots (G-CDs) were then prepared by oxidizing S-CDs with 3 % H2O2, followed by treatment with 0.1 M NaOH to produce strong blue-emitting carbon dots (B-CDs). Compared with S-CDs, the QY of G-CDs and B-CDs increased by 35 times and 75 times, respectively. The improvement in quantum yield (QY) and the adjustment in emission wavelength were attributed to the disruption of hydrogen bonds and modifications in surface groups caused by treatments with hydrogen peroxide and sodium hydroxide. By combining B-CDs and G-CDs with commercial red phosphors, warm W-LEDs with a color rendering index as high as 91.4 and a correlated color temperature of 5437 K was successfully prepared, which was suitable for indoor lighting. In addition, B-CDs and G-CDs were used as fluorescent markers for latent fingerprints identification on different substrates, the results showed that B-CDs and G-CDs significantly enhanced the resolution of fingerprint imaging. The synthesized G-CDs and B-CDs offer several advantages, including high quantum yield, excellent photostability, low cost and a straightforward synthesis method. These properties provide a solid material foundation for enhancing the performance of white LEDs and detecting latent fingerprints.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.