Imaging Chemical Kinetics of Radical Polymerization with an Ultrafast Coherent Raman Microscope

被引:35
|
作者
Li, Haozheng [1 ,2 ]
Cheng, Yong [1 ,2 ]
Tang, Huajun [1 ,2 ]
Bi, Yali [1 ,2 ]
Chen, Yage [1 ,2 ]
Yang, Guang [1 ,2 ]
Guo, Shoujing [1 ,2 ]
Tian, Sidan [1 ,2 ]
Liao, Jiangshan [1 ,2 ]
Lv, Xiaohua [1 ,2 ]
Zeng, Shaoqun [1 ,2 ]
Zhu, Mingqiang [1 ,2 ]
Xu, Chenjie [3 ]
Cheng, Ji-Xin [4 ]
Wang, Ping [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Britton Chance Ctr Biomed Photon, Wuhan Natl Lab Optoelect, Wuhan 430074, Hubei, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Engn Sci, Collaborat Innovat Ctr Biomed Engn, MoE Key Lab Biomed Photon, Wuhan 430074, Hubei, Peoples R China
[3] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637457, Singapore
[4] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
基金
中国国家自然科学基金;
关键词
chemical kinetics; polymer synthesis; radical polymerization; stimulated Raman scattering; ultrafast chemical imaging; vibrational spectroscopy; LABEL-FREE; SCATTERING MICROSCOPY; MASS-SPECTROMETRY; IN-VIVO; SENSITIVITY; SPECTROSCOPY; ACRYLAMIDE; TISSUE; LIGHT; UV;
D O I
10.1002/advs.201903644
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Numerous mechanisms have been proposed for polymerization to provide qualitative and quantitative prediction of how monomers spatially and temporally arrange into the polymeric chains. However, less is known about this process at the molecular level because the ultrafast chemical reaction is inaccessible for any form of microscope so far. Here, to address this unmet challenge, a stimulated Raman scattering microscope based on collinear multiple beams (COMB-SRS) is demonstrated, which allows label-free molecular imaging of polymer synthesis in action at speed of 2000 frames per second. The field of view of the developed 2 kHz SRS microscope is 30 x 28 mu m(2) with 50 x 46 pixels and 7 mu s dwell time. By catching up the speed of chemical reaction, COMB-SRS is able to quantitatively visualize the ultrafast dynamics of molecular vibrations with submicron spatial resolution and sub-millisecond temporal resolution. The propagating polymer waves driven by reaction rate and persistent UV initiation are observed in situ. This methodology is expected to permit the development of novel functional polymers, controllable photoresists, 3D printing, and other new polymerization technologies.
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页数:9
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