femtosecond laser irradiation
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2022 ◽  
Vol 34 (1) ◽  
pp. 012019
Author(s):  
Shuang Liu ◽  
Haiying Song ◽  
Shengnan Wang ◽  
Bairui Du ◽  
Bing Wang ◽  
...  

2022 ◽  
Vol 12 (2) ◽  
pp. 886
Author(s):  
Hun-Kook Choi ◽  
Young-Jun Jung ◽  
Bong-Ahn Yu ◽  
Jae-Hee Sung ◽  
Ik-Bu Sohn ◽  
...  

This paper demonstrates the fabrication of radiation-resistant fiber Bragg grating (FBG) sensors using infrared femtosecond laser irradiation. FBG sensors were written inside acrylate-coated fluorine-doped single-mode specialty optical fibers. We detected the Bragg resonance at 1542 nm. By controlling the irradiation conditions, we improved the signal strength coming out from the FBG sensors. A significant reduction in the Bragg wavelength shift was detected in the fabricated FBG sensors for a radiation dose up to 105 gray, indicating excellent radiation resistance capabilities. We also characterized the temperature sensitivity of the radiation-resistant FBG sensors and detected outstanding performance.


Nanophotonics ◽  
2022 ◽  
Vol 0 (0) ◽  
Author(s):  
Pavel N. Terekhin ◽  
Jens Oltmanns ◽  
Andreas Blumenstein ◽  
Dmitry S. Ivanov ◽  
Frederick Kleinwort ◽  
...  

Abstract Understanding the mechanisms and controlling the possibilities of surface nanostructuring is of crucial interest for both fundamental science and application perspectives. Here, we report a direct experimental observation of laser-induced periodic surface structures (LIPSS) formed near a predesigned gold step edge following single-pulse femtosecond laser irradiation. Simulation results based on a hybrid atomistic-continuum model fully support the experimental observations. We experimentally detect nanosized surface features with a periodicity of ∼300 nm and heights of a few tens of nanometers. We identify two key components of single-pulse LIPSS formation: excitation of surface plasmon polaritons and material reorganization. Our results lay a solid foundation toward simple and efficient usage of light for innovative material processing technologies.


Author(s):  
Ye Ding ◽  
Qiang Li ◽  
Jingyi Li ◽  
Lianfu Wang ◽  
Lijun Yang

Abstract Graphene oxide (GO) has emerged as unique and multifaceted novel material with a wide range of applications in electrochemistry and optoelectronic engineering. In these applications, GO surface is characterized with different functional structures in the micro-nano scale, while the femtosecond laser is a promising and versatile tool for manufacturing these structures comparing with conventional approaches. However, the comprehensive surface responses and corresponding regimes of GO surface under femtosecond laser irradiation are not yet identified, which creates obstacles to the further application of femtosecond laser in programming GO surface with specific nanopatterns. Herein, theoretical models characterizing the electrical response, i.e., the transient spatial and temporal distribution of infrared femtosecond laser-excited free electron density at the GO surface layers are established. The numerical simulations are carried out using the discontinuous Galerkin finite element algorithm with a 5 fs time step. The relationship between the laser polarized electric field and free electron density is revealed. On this basis, the surface plasma distribution is characterized, the accuracy of which is verified through the comparison of experimental ablation morphology. Thermal, morphological and chemical responses of the GO surface using different parameters are analyzed correspondingly, from which the formation and evolution mechanisms of surface nanopatterns with different features are explained. This work offers a new insight into the fundamental regimes and feasibility of ultrafast patterning of GO for the application of multifunctional device engineering.


ACS Omega ◽  
2021 ◽  
Author(s):  
Yan Lin ◽  
Qijun Zhang ◽  
Yongjun Deng ◽  
Qiang Wu ◽  
Xiaofei P. Ye ◽  
...  

2021 ◽  
Vol 119 (23) ◽  
pp. 231603
Author(s):  
Keisuke Takenaka ◽  
Naoki Shinohara ◽  
Masaki Hashida ◽  
Mitsuhiro Kusaba ◽  
Hitoshi Sakagami ◽  
...  

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