激光阈值
拓扑(电路)
激光器
光子学
生物传感器
光子晶体
极化(电化学)
材料科学
脂质双层
光电子学
光学
纳米技术
膜
物理
化学
物理化学
组合数学
生物化学
数学
作者
Chaoyang Gong,真 高橋,Zhiyi Yuan,Shih‐Hsiu Huang,Wenjie Wang,Pin Chieh Wu,Yu‐Cheng Chen
标识
DOI:10.1002/advs.202100096
摘要
Lasers are the pillars of modern photonics and sensing. Recent advances in microlasers have demonstrated its extraordinary lasing characteristics suitable for biosensing. However, most lasers utilized lasing spectrum as a detection signal, which can hardly detect or characterize nanoscale structural changes in microcavity. Here the concept of amplified structured light-molecule interactions is introduced to monitor tiny bio-structural changes in a microcavity. Biomimetic liquid crystal droplets with self-assembled lipid monolayers are sandwiched in a Fabry-Pérot cavity, where subtle protein-lipid membrane interactions trigger the topological transformation of output vector beams. By exploiting Amyloid β (Aβ)-lipid membrane interactions as a proof-of-concept, it is demonstrated that vector laser beams can be viewed as a topology of complex laser modes and polarization states. The concept of topological-encoded laser barcodes is therefore developed to reveal dynamic changes of laser modes and Aβ-lipid interactions with different Aβ assembly structures. The findings demonstrate that the topology of vector beams represents significant features of intracavity nano-structural dynamics resulted from structured light-molecule interactions.
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