光学均匀蓝色石墨烯量子点的原子团调制三重态发射

IF 3.2 3区 化学 Q2 CHEMISTRY, PHYSICAL
Anwesha Banerjee, , , Shreyasi Chakraborty, , , Anwesha Biswas, , and , Ujjal Bhattacharjee*, 
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引用次数: 0

摘要

氧化石墨烯和石墨烯量子点(GOQDs)由于其可调的带隙和水溶性而引起了相当大的兴趣,这是由它们的氧含量、表面官能团和尺寸属性决定的。在这项研究中,我们报道了由氧化碳含量为58%的高氧化氧化石墨烯(hoGO)在水介质中通过温和的过氧化氧化获得的蓝色发射石墨烯量子点(b-GOQDs)的合成。在温和的条件下,高氧含量有利于石墨烯晶格内的可控解理,产生的b-GOQDs具有与激发无关的发射光谱,表明发射器的高度均匀性。它们的光致发光类似于分子发射,主要来源于均匀的表面缺陷(与石墨核中sp2碳中心的损失有关),量子产率为0.17。我们进一步研究了这些b-GOQDs在微秒到毫秒范围内的长寿命光物理行为,因为已知这种缺陷态支持三重态激子。在低温下,长寿命激发态与短寿命激发态的比例接近6:1,突出了这些材料在需要延长发射寿命的应用中的潜力。此外,我们证明了2,2,6,6-四甲基哌啶- n -氧(TEMPO)介导的多通道三重态收获通过p型延迟荧光和磷光。值得注意的是,观察到长达25秒的余辉,表现出双分子特征和在TEMPO存在下的显著猝灭,已知TEMPO通过系统间交叉增强磷光。这项工作强调了合成方法对b-GOQDs光物理性质的关键影响,并介绍了一种调整其发射特性的新方法,从而提高了它们在无毒、长寿命光电子应用中的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Radical-Modulated Triplet Emission in Optically Homogeneous Blue Graphene Quantum Dots

Radical-Modulated Triplet Emission in Optically Homogeneous Blue Graphene Quantum Dots

Radical-Modulated Triplet Emission in Optically Homogeneous Blue Graphene Quantum Dots

Graphene oxide and graphene quantum dots (GOQDs) have attracted considerable interest due to their tunable bandgap and aqueous solubility, which are governed by their oxygen content, surface functional groups, and dimensional attributes. In this study, we report the synthesis of blue-emitting graphene quantum dots (b-GOQDs) derived from highly oxidized graphene oxide (hoGO) possessing an oxidized carbon content of 58%, achieved via mild peroxide oxidation in an aqueous medium. The elevated oxygen content facilitates controlled cleavage within the graphene lattice under mild conditions, yielding b-GOQDs that exhibit excitation-independent emission spectra indicative of a high degree of emitter homogeneity. Their photoluminescence, which resembles molecular-like emission, originates primarily from uniform surface defects (associated with the loss of sp2 carbon centers in the graphitic core), with a quantum yield of 0.17. We further investigate the long-lived photophysical behavior of these b-GOQDs in the microsecond to millisecond regime, as such defect states are known to support triplet excitons. At cryogenic temperatures, the ratio of long-lived to short-lived excited states approaches 6:1, highlighting the potential of these materials for applications requiring extended emission lifetimes. Additionally, we demonstrate 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO)-mediated multichannel triplet harvesting via P-type delayed fluorescence and phosphorescence. Notably, an afterglow lasting up to 25 s was observed, exhibiting bimolecular characteristics and significant quenching in the presence of TEMPO, which is known to enhance phosphorescence through intersystem crossing. This work emphasizes the critical influence of synthetic methodology on the photophysical properties of b-GOQDs and introduces a novel approach for tuning their emission characteristics, thereby advancing their potential for incorporation into nontoxic, long-lifetime optoelectronic applications.

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来源期刊
The Journal of Physical Chemistry C
The Journal of Physical Chemistry C 化学-材料科学:综合
CiteScore
6.50
自引率
8.10%
发文量
2047
审稿时长
1.8 months
期刊介绍: The Journal of Physical Chemistry A/B/C is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.
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