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通过无机晶态纳米复合材料控制碳纳米点的荧光和室温磷光行为。

Controlling the fluorescence and room-temperature phosphorescence behaviour of carbon nanodots with inorganic crystalline nanocomposites.

机构信息

School of Chemistry, University of Leeds, Woodhouse Lane, Leeds, LS2 9JT, UK.

School of Physics and Astronomy, University of Leeds, Leeds, LS2 9JT, UK.

出版信息

Nat Commun. 2019 Jan 14;10(1):206. doi: 10.1038/s41467-018-08214-6.

Abstract

There is a significant drive to identify alternative materials that exhibit room temperature phosphorescence for technologies including bio-imaging, photodynamic therapy and organic light-emitting diodes. Ideally, these materials should be non-toxic and cheap, and it will be possible to control their photoluminescent properties. This was achieved here by embedding carbon nanodots within crystalline particles of alkaline earth carbonates, sulphates and oxalates. The resultant nanocomposites are luminescent and exhibit a bright, sub-second lifetime afterglow. Importantly, the excited state lifetimes, and steady-state and afterglow colours can all be systematically controlled by varying the cations and anions in the host inorganic phase, due to the influence of the cation size and material density on emissive and non-emissive electronic transitions. This simple strategy provides a flexible route for generating materials with specific, phosphorescent properties and is an exciting alternative to approaches relying on the synthesis of custom-made luminescent organic molecules.

摘要

人们迫切希望找到在室温下能发出磷光的替代材料,这些材料可应用于生物成像、光动力疗法和有机发光二极管等技术领域。理想情况下,这些材料应该是无毒且廉价的,并且能够控制其光致发光性能。本工作通过将碳纳米点嵌入碱土金属碳酸盐、硫酸盐和草酸盐的结晶颗粒中,实现了这一目标。得到的纳米复合材料具有发光性,并在激发后呈现出明亮的、持续时间小于 1 秒的余辉。重要的是,通过改变主体无机相中阳离子和阴离子,可以系统地控制激发态寿命以及稳态和余辉颜色,这是由于阳离子尺寸和材料密度对发光和非发光电子跃迁的影响所致。这种简单的策略为生成具有特定磷光特性的材料提供了一种灵活的途径,是一种有前途的替代方法,可替代依赖于定制发光有机分子合成的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a57/6331607/1911376d0cc1/41467_2018_8214_Fig1_HTML.jpg

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