Laser ablation of a triazene polymer studied by ns-interferometry and shadowgraphy

被引:9
作者
Hauer, M [1 ]
Funk, DJ [1 ]
Lippert, T [1 ]
Wokaun, A [1 ]
机构
[1] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
来源
HIGH-POWER LASER ABLATION IV, PTS 1 AND 2 | 2002年 / 4760卷
关键词
laser ablation; shadowgraphy; interference surface profiling; interferometry; triazene polymer; photopolymer;
D O I
10.1117/12.482093
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Nanosecond-interferometry and shadowgraphy is used to observe the dynamic behavior of the etching process during and after the irradiation pulse. Commercially available polymers exhibit quite often poor laser ablation properties for irradiation wavelengths greater than or equal to 248 nm. At these wavelengths the absorption is due to the quite photostable aromatic groups. A photolabile triazene polymer was selected to compare the influence of a photolabile group on the laser ablation process. The photochemical active triazene reveals a strong absorption band at 332 nm and is responsible for the observed high etch rates and the low threshold for 308 nm irradiation. The absorption coefficients at 193 nm and at 308 nm are comparable, allowing to study the influence of the different absorption sites by ns-interferometry and shadowgraphy measurements. The etching of the triazene polymer starts and ends with the laser beam. No surface swelling, which is assigned to photothermal ablation, is detected for fluences above the threshold of the ablation. The expansion of the laser ablation induced shockwave was measured for the photolabile triazene polymer and the photostable polyimide. The speed of the shockwave increases with fluence and is higher for irradiation with 193 nm than for 308 nm. A shockwave with equal or higher velocity is observed for the triazene polymer than for the polyimide.
引用
收藏
页码:259 / 268
页数:10
相关论文
共 23 条
[1]   Laser induced microexplosions of a photosensitive polymer [J].
Bennett, LS ;
Lippert, T ;
Furutani, H ;
Fukumura, H ;
Masuhara, H .
APPLIED PHYSICS A-MATERIALS SCIENCE & PROCESSING, 1996, 63 (04) :327-332
[2]   Dynamics of excited and ionic states of N,N,N′,N′-tetramethyl-p-phenylenediamine in poly(methyl methacrylate) under ablation condition [J].
Fujiwara, H ;
Fukumoto, H ;
Fukumura, H ;
Masuhara, H .
RESEARCH ON CHEMICAL INTERMEDIATES, 1998, 24 (08) :879-892
[3]   TIME-RESOLVED SPECTROSCOPIC AND PHOTOGRAPHIC STUDIES ON LASER-ABLATION OF POLY(METHYL METHACRYLATE) FILM DOPED WITH BIPHENYL [J].
FUKUMURA, H ;
TAKAHASHI, E ;
MASUHARA, H .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (02) :750-757
[4]   NANOSECOND TIME-RESOLVED INTERFEROMETRIC STUDY ON MORPHOLOGICAL DYNAMICS OF DOPED POLY(METHYL METHACRYLATE) FILM UPON LASER-ABLATION [J].
FURUTANI, H ;
FUKUMURA, H ;
MASUHARA, H .
APPLIED PHYSICS LETTERS, 1994, 65 (26) :3413-3415
[5]   Laser-induced decomposition and ablation dynamics studied by nanosecond interferometry .1. A triazenopolymer film [J].
Furutani, H ;
Fukumura, H ;
Masuhara, H ;
Lippert, T ;
Yabe, A .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (32) :5742-5747
[6]   Laser-induced decomposition and ablation dynamics studied by nanosecond interferometry. 2. A reactive nitrocellulose film [J].
Furutani, H ;
Fukumura, H ;
Masuhara, H ;
Kambara, S ;
Kitaguchi, T ;
Tsukada, H ;
Ozawa, T .
JOURNAL OF PHYSICAL CHEMISTRY B, 1998, 102 (18) :3395-3401
[7]  
GAHAGAN KT, 2002, UNPUB J APPL PHYS
[8]   COHERENT RAMAN MEASUREMENTS OF POLYMER THIN-FILM PRESSURE AND TEMPERATURE DURING PICOSECOND LASER-ABLATION [J].
HARE, DE ;
FRANKEN, J ;
DLOTT, DD .
JOURNAL OF APPLIED PHYSICS, 1995, 77 (11) :5950-5960
[9]   PICOSECOND COHERENT RAMAN-STUDY OF SOLID-STATE CHEMICAL-REACTIONS DURING LASER POLYMER ABLATION [J].
HARE, DE ;
DLOTT, DD .
APPLIED PHYSICS LETTERS, 1994, 64 (06) :715-717
[10]  
HAUER M, IN PRESS APPL SURF S