AI Video Guide  
Wanxue Wei 1,2†Muyang Zhang 3†Zhuoqun Yuan 3Weike Wang 3[ ... ]Kebin Shi 1,2,4,5,7,*
Author Affiliations
Abstract
1 State Key Laboratory of Mesoscopic Physics and Frontiers Science Center for Nano-optoelectronics, School of Physics, Peking University, Beijing 100871, China
2 National Biomedical Imaging Center, Peking University, Beijing 100871, China
3 Institute of Modern Optics, Nankai University, Tianjin Key Laboratory of Micro-Scale Optical Information Science and Technology, Tianjin 300350, China
4 Collaborative Innovation Center of Extreme Optics, Shanxi University, Taiyuan 030006, China
5 Peking University Yangtze Delta Institute of Optoelectronics, Nantong 226010, China
6 e-mail: ymliang@nankai.edu.cn
7 e-mail: kebinshi@pku.edu.cn
Multi-angle illumination is a widely adopted strategy in various super-resolution imaging systems, where improving computational efficiency and signal-to-noise ratio (SNR) remains a critical challenge. In this study, we propose the integration of the iterative kernel correction (IKC) algorithm with a multi-angle (MA) illumination scheme to enhance imaging reconstruction efficiency and SNR. The proposed IKC-MA scheme demonstrates the capability to significantly reduce image acquisition time while achieving high-quality reconstruction within 1 s, without relying on extensive experimental datasets. This ensures broad applicability across diverse imaging scenarios. Experimental results indicate substantial improvements in imaging speed and quality compared to conventional methods, with the IKC-MA model achieving a remarkable reduction in data acquisition time. This approach offers a faster and more generalizable solution for super-resolution microscopic imaging, paving the way for advancements in real-time imaging applications.
Photonics Research
2025, 13(7): 1973
AI超清视频导读  
张宏飞 1,2施可彬 1,2,3,*
作者单位
摘要
1 北京大学物理学院人工微结构和介观物理国家重点实验室,北京 100871
2 北京大学物理学院纳光电子前沿科学中心,北京 100871
3 山西大学极端光学协同创新中心,山西 太原 030006
讨论了超快生物光子学在生物体系中的应用及发展。重点介绍了超快光学技术如何被应用于探测生物体系中发生在皮秒至飞秒时间尺度上的重要过程,通过结合先进的显微成像技术,超快测量方法不仅实现了高时间分辨率,还可以实现高空间分辨率,这使得实时观察生物分子在超快时间尺度上的动态行为成为可能,对深入理解生物分子的功能和机制至关重要。从超快时间分辨率、超高时空分辨率和超快非线性光谱技术三个方面介绍了超快探测方法与生物光子学的交叉应用。
超快探测 生物超快过程 超分辨成像 超快非线性光谱技术 
光学学报
2024, 44(17): 1732008
AI Video Guide  
Ziheng Ji 1,2Wentao Yu 2,3Dashan Dong 2,4Hong Yang 2,4,5[ ... ]Kebin Shi 2,4,5,*
Author Affiliations
Abstract
1 Harbin Institute of Technology (Shenzhen), School of Science, Ministry of Industry and Information Technology Key Lab of Micro-Nano Optoelectronic Information System, Shenzhen, China
2 Peking University, School of Physics, State Key Laboratory for Mesoscopic Physics and Frontiers Science Center for Nano-Optoelectronics, Beijing, China
3 Nanjing University of Science and Technology, Institute of Interdisciplinary Physical Sciences, School of Science, Nanjing, China
4 Shanxi University, Collaborative Innovation Center of Extreme Optics, Taiyuan, China
5 Peking University Yangtze Delta Institute of Optoelectronics, Nantong, China
Chiral sum-frequency generation (SFG) has proven to be a versatile spectroscopic and imaging tool for probing chirality. However, due to polarization restriction, the conventional chiral SFG microscopes have mostly adopted noncollinear beam configurations, which only partially cover the aperture of microscope and strongly spoil the spatial resolution. In this study, we report the first experimental demonstration of collinear chiral SFG microscopy, which fundamentally supports diffraction-limited resolution. This advancement is attributed to the collinear focus of a radially polarized vectorial beam and a linearly polarized (LP) beam. The tightly focused vectorial beam has a very strong longitudinal component, which interacts with the LP beam and produces the chiral SFG. The collinear configuration can utilize the full aperture and thus push the spatial resolution close to the diffraction limit. This technique can potentially boost the understanding of chiral systems.
chiral sum-frequency generation radially polarized beam nonlinear optical microscopy 
Advanced Photonics Nexus
2024, 3(2): 026006
AI Video Guide  
Author Affiliations
Abstract
1 State Key Laboratory for Mesoscopic Physics, Department of Physics, Peking University, Beijing 100871, China
2 State Key Laboratory of Membrane Biology, School of Life Sciences, and Biomedical Pioneering Innovation Center (BIOPIC), Peking University, Beijing 100871, China
3 School of Physics, Xi’an Jiaotong University, Xi’an 710049, China
4 Collaborative Innovation Center of Extreme Optics, Shanxi University, Taiyuan 030006, China
5 Peking University Yangtze Delta Institute of Optoelectronics, Nantong 226010, China
Light-sheet fluorescence microscopy (LSFM) has played an important role in bio-imaging due to its advantages of high photon efficiency, fast speed, and long-term imaging capabilities. The perpendicular layout between LSFM excitation and detection often limits the 3D resolutions as well as their isotropy. Here, we report on a reflective type light-sheet microscope with a mini-prism used as an optical path reflector. The conventional high NA objectives can be used both in excitation and detection with this design. Isotropic resolutions in 3D down to 300 nm could be achieved without deconvolution. The proposed method also enables easy transform of a conventional fluorescence microscope to high performance light-sheet microscopy.
Photonics Research
2024, 12(2): 271
 
作者单位
摘要
1 南通市口腔医院,江苏 南通 226000
2 南通市中西医结合医院,江苏 南通 226000
3 北京大学长三角光电科学研究院,江苏 南通 226000
4 人工微结构和介观物理国家重点实验室,北京大学物理学院,北京 100871
与可见光区(400~700 nm)和近红外一区(NIR-I,700~900 nm)荧光成像(FL)相比,近红外二区(NIR-II,1000~1700 nm)荧光成像具有更深的穿透深度、更高的信噪比。开发亮度高、吸收/发射波长长、生物相容性好的NIR-II荧光探针一直是NIR-II荧光成像领域的一个重要研究方向。有机NIR-II荧光探针以其优异的生物相容性和良好的药代动力学特性而备受关注。本文从红移吸收/发射波长、提高荧光量子产率/摩尔吸光系数、改善生物相容性等角度系统总结了近年来花菁类染料、D-A-D小分子、聚合物点等有机NIR-II荧光探针的研究进展,重点介绍了具有代表性的荧光探针在活体NIR-II荧光成像中的应用,最后讨论了有机NIR-II荧光探针迈向临床应用面临的潜在挑战。
医用光学 近红外二区 荧光探针 花菁类染料 有机小分子 聚集诱导发光 共轭聚合物 
中国激光
2023, 50(21): 2107101
Yu He 1†Yunhua Yao 1Yilin He 1Zhengqi Huang 1[ ... ]Shian Zhang 1,5,6,*
Author Affiliations
Abstract
1 East China Normal University, School of Physics and Electronic Science, State Key Laboratory of Precision Spectroscopy, Shanghai, China
2 Shenzhen University, Institute of Microscale Optoelectronics, Nanophotonics Research Center, Shenzhen Key Laboratory of Micro-Scale Optical Information Technology, Shenzhen, China
3 Peking University, Biomedical Engineering Department, Beijing, China
4 Peking University, School of Physics, State Key Laboratory for Mesoscopic Physics and Frontiers Science Center for Nano-optoelectronics, Beijing, China
5 East China Normal University, Joint Research Center of Light Manipulation Science and Photonic Integrated Chip of East China Normal University and Shandong Normal University, Shanghai, China
6 Shanxi University, Collaborative Innovation Center of Extreme Optics, Taiyuan, China
Structured illumination microscopy (SIM) has been widely applied in the superresolution imaging of subcellular dynamics in live cells. Higher spatial resolution is expected for the observation of finer structures. However, further increasing spatial resolution in SIM under the condition of strong background and noise levels remains challenging. Here, we report a method to achieve deep resolution enhancement of SIM by combining an untrained neural network with an alternating direction method of multipliers (ADMM) framework, i.e., ADMM-DRE-SIM. By exploiting the implicit image priors in the neural network and the Hessian prior in the ADMM framework associated with the optical transfer model of SIM, ADMM-DRE-SIM can further realize the spatial frequency extension without the requirement of training datasets. Moreover, an image degradation model containing the convolution with equivalent point spread function of SIM and additional background map is utilized to suppress the strong background while keeping the structure fidelity. Experimental results by imaging tubulins and actins show that ADMM-DRE-SIM can obtain the resolution enhancement by a factor of ∼1.6 compared to conventional SIM, evidencing the promising applications of ADMM-DRE-SIM in superresolution biomedical imaging.
structured illumination microscopy superresolution imaging resolution enhancement untrained neural network 
Advanced Photonics Nexus
2023, 2(4): 046005
Yilin He 1†Yunhua Yao 1Dalong Qi 1Yu He 1[ ... ]Shian Zhang 1,4,*
Author Affiliations
Abstract
1 East China Normal University, School of Physics and Electronic Science, State Key Laboratory of Precision Spectroscopy, Shanghai, China
2 Shenzhen University, Institute of Microscale Optoelectronics, Nanophotonics Research Center, Shenzhen Key Laboratory of Micro-Scale Optical Information Technology, Shenzhen, China
3 Peking University, School of Physics, Frontiers Science Center for Nanooptoelectronics, State Key Laboratory for Mesoscopic Physics, Beijing, China
4 Shanxi University, Collaborative Innovation Center of Extreme Optics, Taiyuan, China
Various super-resolution microscopy techniques have been presented to explore fine structures of biological specimens. However, the super-resolution capability is often achieved at the expense of reducing imaging speed by either point scanning or multiframe computation. The contradiction between spatial resolution and imaging speed seriously hampers the observation of high-speed dynamics of fine structures. To overcome this contradiction, here we propose and demonstrate a temporal compressive super-resolution microscopy (TCSRM) technique. This technique is to merge an enhanced temporal compressive microscopy and a deep-learning-based super-resolution image reconstruction, where the enhanced temporal compressive microscopy is utilized to improve the imaging speed, and the deep-learning-based super-resolution image reconstruction is used to realize the resolution enhancement. The high-speed super-resolution imaging ability of TCSRM with a frame rate of 1200 frames per second (fps) and spatial resolution of 100 nm is experimentally demonstrated by capturing the flowing fluorescent beads in microfluidic chip. Given the outstanding imaging performance with high-speed super-resolution, TCSRM provides a desired tool for the studies of high-speed dynamical behaviors in fine structures, especially in the biomedical field.
super-resolution microscopy high-speed imaging compressive sensing deep learning image reconstruction 
Advanced Photonics
2023, 5(2): 026003
Wenkai Yang 1,2†Lige Liu 1,2†Dashan Dong 1,2Xin Zhang 3[ ... ]Kebin Shi 1,2,5,*
Author Affiliations
Abstract
1 State Key Laboratory for Mesoscopic Physics and Frontiers Science Center for Nano-optoelectronics, School of Physics, Peking University, Beijing 100871, China
2 Collaborative Innovation Center of Extreme Optics, Shanxi University, Taiyuan 030006, China
3 MIIT Key Laboratory for Low-Dimensional Quantum Structure and Devices, School of Materials Sciences and Engineering, Beijing Institute of Technology, Beijing 100081, China
4 School of Science, RMIT University, Melbourne 3000, VIC, Australia
5 Peking University Yangtze Delta Institute of Optoelectronics, Nantong 226010, China
Perovskite-enabled optical devices have drawn intensive interest and have been considered promising candidates for integrated optoelectronic systems. As one of the important photonic functions, optical phase modulation previously was demonstrated with perovskite substrate and complex refractive index engineering with laser scribing. Here we report on the new scheme of achieving efficient phase modulation by combining detour phase design with 40 nm ultrathin perovskite films composed of nanosized crystalline particles. Phase modulation was realized by binary amplitude patterning, which significantly simplifies the fabrication process. Perovskite nanocrystal films exhibit significantly weak ion migration effects under femtosecond laser writing, resulting in smooth edges along the laser ablated area and high diffractive optical quality. Fabrication of a detour-phased perovskite ultrathin planar lens with a diameter of 150 μm using femtosecond laser scribing was experimentally demonstrated. A high-performance 3D focus was observed, and the fabrication showed a high tolerance with different laser writing powers. Furthermore, the high-quality imaging capability of perovskite ultrathin planar lenses with a suppressed background was also demonstrated.
Photonics Research
2022, 10(12): 2768
 
穆书奇 1,2董大山 1,2施可彬 1,2,*
作者单位
摘要
1 北京大学物理学院人工微结构和介观物理国家重点实验室,北京 100871
2 山西大学极端光学协同创新中心,山西 太原 030006
无标记光学成像以非侵入性的特点,能够对生物活体细胞进行长时程、无损伤的高分辨观测,在生物医学和临床诊断上有着巨大的前景。无标记成像技术可以分为特异性成像和非特异性成像两类,主要概述目前常用的无标记成像技术。详细介绍了各种无标记成像技术的成像原理、优缺点和最新研究进展。最后,对无标记光学成像未来的发展进行展望。
无标记显微成像 特异性成像 非特异性成像 生物光子学 
激光与光电子学进展
2022, 59(12): 1200001
作者单位
摘要
1 北京大学 物理学院 人工微结构和介观物理国家重点实验室,北京 100871
2 山西大学 极端光学协同创新中心,太原 030006
相干拉曼散射以其无标记、高灵敏、化学特异性等优势,被广泛应用于生物、医学、物理和化学的光谱与成像应用。通过对光场各项参数的调控,从时域、频域、相位、偏振等特性入手,可以解决光谱与成像应用中的实际问题。本文以光场调控原理为主线,综述了相干拉曼散射光谱与成像应用的研究进展。
相干拉曼散射 相干反斯托克斯拉曼散射 受激拉曼散射 光场调控 Coherent Raman scattering Coherent anti-Stokes Raman scattering Stimulated Raman scattering Engineering of optical fields 
光子学报
2022, 51(1): 0151108

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