Wang Ping, Meziani Mohammed J, Fu Yingqiang, Bunker Christopher E, Hou Xiaofang, Yang Liju, Msellek Hind, Zaharias Melina, Darby Jasmine P, Sun Ya-Ping
Department of Chemistry and Laboratory for Emerging Materials and Technology, Clemson University Clemson South Carolina 29634 USA
Department of Natural Sciences, Northwest Missouri State University Maryville Missouri 64468 USA
Nanoscale Adv. 2021 Feb 26;3(8):2316-2324. doi: 10.1039/d1na00002k. eCollection 2021 Apr 20.
Carbon dots (CDots) are defined as surface-passivated small carbon nanoparticles, with the effective passivation generally achieved by organic functionalization. Photoexcited CDots are both potent electron donors and acceptors, and their characteristic bright and colorful fluorescence emissions make them excellent fluorescence sensors for organic analytes and metal ions. For the latter extraordinarily low detection limits based on extremely efficient quenching of fluorescence intensities by the targeted metal cations have been observed and reported in the literature. However, all of the dot samples in those reported studies were made from "one-pot" carbonization of organic precursors mostly under rather mild processing conditions, unlikely to be sufficient for the required level of carbonization. Those dot samples should therefore be more appropriately considered as "nano-carbon/organic hybrids", characterized structurally as being highly porous and spongy, which must be playing a dominating role in the reported sensing results. In this study, we compared the dot samples from carbonization syntheses under similarly mild and also more aggressive processing conditions with the classically defined and structured CDots for the fluorescence sensing of copper(ii) cations in aqueous solutions. The observed dramatic decoupling between quenching results for fluorescence intensities and lifetimes of the carbonization samples, with the former being extraordinary and the latter within the diffusion controlled limit, suggested that the quenching of fluorescence intensities was greatly affected by the higher local quencher concentrations than the bulk associated with the porous and spongy sample structures, especially for the sample from carbonization under too mild processing conditions. The major differences between the classical CDots and the nano-carbon/organic hybrids are highlighted, and the tradeoffs between sensitivity and accuracy or reproducibility in the use of the latter for fluorescence sensing are discussed.
碳点(CDots)被定义为表面钝化的小碳纳米颗粒,其有效的钝化通常通过有机功能化来实现。光激发的碳点既是有效的电子供体又是受体,并且它们独特的明亮且多彩的荧光发射使其成为用于有机分析物和金属离子的出色荧光传感器。对于后者,基于目标金属阳离子对荧光强度的极其有效的猝灭,文献中已观察到并报道了极低的检测限。然而,那些报道研究中的所有点样品大多是在相当温和的加工条件下通过有机前体的“一锅法”碳化制成的,不太可能达到所需的碳化水平。因此,那些点样品更应被视为“纳米碳/有机杂化物”,其结构特征是高度多孔且呈海绵状,这必定在报道的传感结果中起主导作用。在本研究中,我们将在类似温和以及更苛刻加工条件下碳化合成得到的点样品与经典定义和结构的碳点进行比较,用于水溶液中铜(II)阳离子的荧光传感。观察到碳化样品的荧光强度猝灭结果与寿命之间存在显著解耦,前者非常显著而后者处于扩散控制极限内,这表明荧光强度的猝灭受比与多孔海绵状样品结构相关的本体更高的局部猝灭剂浓度的极大影响,特别是对于在过于温和加工条件下碳化得到的样品。突出了经典碳点与纳米碳/有机杂化物之间的主要差异,并讨论了在使用后者进行荧光传感时灵敏度与准确性或重现性之间的权衡。