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基于紫苏叶通过pH调节合成多色碳点用于双模式室温荧光和磷光应用

pH-modulated synthesis of multicolor carbon dots from Perilla leaves for dual-mode room-temperature fluorescence and phosphorescence applications.

作者信息

Wang Pengyue, Ren Jiaqi, Wang Xin, Yang Yueqian, Pan Xiao, Ma Yujie, Tan Fenghua, Zeng Jingbin

机构信息

State Key Laboratory of Chemical Safety, College of Chemistry and Chemical Engineering, China University of Petroleum (East China), Qingdao, 266580, China.

出版信息

Mikrochim Acta. 2025 Aug 14;192(9):589. doi: 10.1007/s00604-025-07460-y.

Abstract

Biomass materials represent an ideal carbon source for synthesizing carbon dots (CDs) due to their abundance, elemental diversity, renewability, and low cost. This study presents a straightforward solvothermal method for synthesizing polychromatic carbon dots (MCDs) by systematically adjusting the reaction parameters using biomass-derived precursors (Perilla fruits leaves and tea polyphenols) under pH-modulated conditions (pH 2-13). The MCDs show tunable emission (395-646 nm), overcoming the traditional blue/green limitation of biomass-derived CDs. Mechanistic studies reveal that this spectral tuning arises from the synergistic control of particle size (1-5 nm) and the extent of C = C conjugated domain, facilitating long-wavelength emission. The optimized MCDs exhibit unique room-temperature dual-mode luminescence, including full-color fluorescence and long-life phosphorescence (lifetime ≈ 0.46 s), attributed to a covalent and hydrogen bond network that promotes efficient intersystem crossing. These MCDs exhibit multi-functional applications: (1) as an environmentally friendly means for white light-emitting diodes (WLED) with CIE coordinates of (0.30, 0.34), (2) for high-contrast latent fingerprint visualization, and (3) as advanced anti-counterfeiting ink with time-resolved encryption capability. This work not only establishes a green strategy for multicolor CDs derived from biomass, but also expands their potential in optical security and forensic science.

摘要

生物质材料因其丰富性、元素多样性、可再生性和低成本,是合成碳点(CDs)的理想碳源。本研究提出了一种直接的溶剂热法,通过在pH调节条件(pH 2 - 13)下,使用生物质衍生的前驱体(紫苏果实叶和茶多酚)系统地调整反应参数,来合成多色碳点(MCDs)。MCDs显示出可调谐发射(395 - 646 nm),克服了生物质衍生CDs传统的蓝/绿限制。机理研究表明,这种光谱调谐源于粒径(1 - 5 nm)和C = C共轭域范围的协同控制,有利于长波长发射。优化后的MCDs表现出独特的室温双模发光,包括全色荧光和长寿命磷光(寿命≈0.46 s),这归因于促进有效系间窜越的共价和氢键网络。这些MCDs具有多功能应用:(1)作为一种环境友好的白光发光二极管(WLED)手段,其CIE坐标为(0.30, 0.34);(2)用于高对比度潜指纹可视化;(3)作为具有时间分辨加密能力的先进防伪墨水。这项工作不仅为源自生物质的多色CDs建立了绿色策略,还扩展了它们在光学安全和法医学中的潜力。

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