TY - JOUR
T1 - Femtosecond-Laser-Induced Nanoscale Blisters in Polyimide Thin Films through Nonlinear Absorption
AU - Godfrey, Alan T.K.
AU - Kallepalli, Deepak L.N.
AU - Ratté, Jesse
AU - Zhang, Chunmei
AU - Corkum, P. B.
N1 - Publisher Copyright:
© 2020 American Physical Society.
PY - 2020/10/29
Y1 - 2020/10/29
N2 - Nonlinear absorption of femtosecond laser pulses provides a unique opportunity to confine energy deposition in any medium to a region that is below the focal diameter of a pulse. Illumination of a polymer film through a transparent high-band-gap material such as glass, followed by nonlinear absorption of 800-nm light in polymers, allows us to further restrict absorption to a very thin layer along the propagation direction. We demonstrate this confinement by simulating femtosecond-laser-induced polymer modification by linear, two-photon, and three-photon absorption, and discuss the control over energy absorption in polymers that multiphoton processes offer. Energy deposited in a thin polymer film induces a protruding blister. We present experimental results for blister diameter and height scaling with variation of pulse energy. Using pulse energies of 20-200 nJ and 0.4-NA focusing, we fabricate blisters with diameters of 1-5.5μm and heights of 75nm to 2μm. Using 0.95-NA focusing, we obtain laser-induced blisters with diameters as small as 700 nm, suggesting blister-based laser-induced forward transfer is possible on and below the 1-μm scale. Submicrometer blister formation with use of femtosecond lasers also offers a method of direct, precise laser writing of microstructures on films with single laser pulses. This method is a possible alternative to lithography, laser milling, and laser-based additive machining.
AB - Nonlinear absorption of femtosecond laser pulses provides a unique opportunity to confine energy deposition in any medium to a region that is below the focal diameter of a pulse. Illumination of a polymer film through a transparent high-band-gap material such as glass, followed by nonlinear absorption of 800-nm light in polymers, allows us to further restrict absorption to a very thin layer along the propagation direction. We demonstrate this confinement by simulating femtosecond-laser-induced polymer modification by linear, two-photon, and three-photon absorption, and discuss the control over energy absorption in polymers that multiphoton processes offer. Energy deposited in a thin polymer film induces a protruding blister. We present experimental results for blister diameter and height scaling with variation of pulse energy. Using pulse energies of 20-200 nJ and 0.4-NA focusing, we fabricate blisters with diameters of 1-5.5μm and heights of 75nm to 2μm. Using 0.95-NA focusing, we obtain laser-induced blisters with diameters as small as 700 nm, suggesting blister-based laser-induced forward transfer is possible on and below the 1-μm scale. Submicrometer blister formation with use of femtosecond lasers also offers a method of direct, precise laser writing of microstructures on films with single laser pulses. This method is a possible alternative to lithography, laser milling, and laser-based additive machining.
UR - http://www.scopus.com/inward/record.url?scp=85095564828&partnerID=8YFLogxK
U2 - 10.1103/PhysRevApplied.14.044057
DO - 10.1103/PhysRevApplied.14.044057
M3 - Article
AN - SCOPUS:85095564828
SN - 2331-7019
VL - 14
JO - Physical Review Applied
JF - Physical Review Applied
IS - 4
M1 - 044057
ER -