Polymerization Photoinitiators with Near-Resonance Enhanced Two-Photon Absorption Cross-Section: Toward High-Resolution Photoresist with Improved Sensitivity

被引:35
作者
Arnoux, Caroline [1 ]
Konishi, Tatsuki [2 ,3 ]
Van Elslande, Emma [1 ]
Poutougnigni, Eric-Aime [1 ]
Mulatier, Jean-Christophe [1 ]
Khrouz, Lhoussain [1 ]
Bucher, Christophe [1 ]
Dumont, Elise [1 ]
Kamada, Kenji [2 ,3 ]
Andraud, Chantal [1 ]
Baldeck, Patrice [1 ]
Banyasz, Akos [1 ]
Monnereau, Cyrille [1 ]
机构
[1] Univ Lyon, CNRS, ENS Lyon, Lab Chim,UMR 5182,Univ Lyon 1, F-69364 Lyon, France
[2] Natl Inst Adv Ind Sci & Technol, Nanomat Res Inst NMRI, Ikeda, Osaka 5638577, Japan
[3] Kwansei Gakuin Univ, Sch Sci & Technol, Dept Chem, Sanda 6691337, Japan
基金
欧盟地平线“2020”;
关键词
BROMINE SUBSTITUTION PATTERN; MICHLERS KETONE; 3D; STEREOLITHOGRAPHY; MICROFABRICATION; LITHOGRAPHY; DERIVATIVES; INITIATORS; CHALLENGES; POLYMERS;
D O I
10.1021/acs.macromol.0c01518
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We take advantage of the near-resonant enhancement of the third-order nonlinear response to engineer a two-photon polymerization photoinitiator with optimized efficiency in regard to literature benchmarks. We study in detail its linear and resonant third-order nonlinear optical properties, with particular focus on photoinduced radical generation. Careful choice of peripheral substituents enables its direct solubilization into a mixture of commercial multifunctional acrylic monomers, resulting in a homogeneous photoresist with good optical transparency upon simple mixing. When submitted to sub-nanosecond pulsed laser irradiation at 532 nm, the resulting photoresist displays a polymerization threshold up to eight times lower than that obtained with the classically used two-photon initiators, giving rise to sub-100 nm line width at 250 nm interline separation and resulting in highly defined three-dimensional structures.
引用
收藏
页码:9264 / 9278
页数:15
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