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基于等离子体结构的可逆和可调谐光化学开关。

Reversible and tunable photochemical switch based on plasmonic structure.

机构信息

Laser and plasma Research Institute, Shahid Beheshti University, G. C. Tehran, Iran.

Faculty of Sciences 2, LPA, Lebanese University, BP 90656, Jdeidet, Lebanon.

出版信息

Sci Rep. 2020 Mar 20;10(1):5110. doi: 10.1038/s41598-020-62058-z.

Abstract

For the first time, pyranine (8-hydroxypyrene-1,3,6-trisulfonate, HPTS) is studied for realizing active plasmonic control, which is attracted considerable attention owing to its unique photophysical and photochemical properties. We have used this photoacid (HPTS) as an active surrounding medium that can be optically controlled and used for modulating plasmon resonances. In this paper, the fabrication of 2D-plasmonic grating coated by thin film of HPTS exposed to UV irradiation is reported. By switching the UV light on and off, the HPTS thin film maintains an excited-state proton transfer (ESPT) process followed by green fluorescence resulting in a plasmonic redshift caused by the variation of the refractive index. Furthermore, this photochemical active medium has also played another important role in plasmonic sensing, in which the emission-based response of HPTS thin film in 2D-plasmonic grating to water vapor upon photoexcitation is demonstrated, for both s and p polarizations. This tunable, flexible and reversible light-driven system will enhance the development of active plasmonic structures and will have a great influence on many fields such as, biochemical optical sensors and all-optical plasmonic circuits.

摘要

首次研究了荧蒽(8-羟基芘-1,3,6-三磺酸,HPTS)以实现主动等离子体控制,由于其独特的光物理和光化学性质,它引起了相当大的关注。我们已经使用这种光酸(HPTS)作为一种可以进行光学控制的活性周围介质,用于调节等离子体共振。在本文中,报道了涂有 HPTS 薄膜的 2D 等离子体光栅的制备,该薄膜在紫外光照射下暴露。通过打开和关闭紫外光,HPTS 薄膜保持激发态质子转移(ESPT)过程,随后发出绿色荧光,导致折射率变化引起的等离子体红移。此外,这种光化学活性介质在等离子体传感中也发挥了另一个重要作用,其中演示了在光激发下,2D 等离子体光栅中 HPTS 薄膜对水蒸气的基于发射的响应,对于 s 和 p 偏振。这种可调谐、灵活和可逆的光驱动系统将增强对活性等离子体结构的发展,并将对许多领域产生重大影响,如生化光学传感器和全光学等离子体电路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2aa7/7083958/0b98d7442379/41598_2020_62058_Fig1_HTML.jpg

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