Scattering-controlled femtosecond-laser induced nanostructuring of TiO2 thin films

被引:3
|
作者
Das, S. K. [1 ]
Rosenfeld, A. [1 ]
Bock, M. [1 ]
Pfuch, A. [2 ,3 ]
Seeber, W. [2 ]
Grunwald, R. [1 ]
机构
[1] Max Born Inst Nichtlineare Opt & Kurzzeitspektros, Max Born Str 2A, D-12489 Berlin, Germany
[2] Friedrich Schiller Univ, Otto Schott Inst, D-07743 Jena, Germany
[3] INNOVENT eV Technologieentwicklung Jena, D-07743 Jena, Germany
关键词
Laser induced periodic surface structures; TiO2 thin films; scattering centers; sub-wavelength ripples; nanoripples; femtosecond lasers; ultrashort pulses; nonlinear excitation; BIOCOMPATIBILITY; ABLATION; SCALE;
D O I
10.1117/12.874519
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The formation of laser induced periodic surface structures (LIPSS) is to a large extent of self-organizing nature and in its early stages essentially influenced by optical scattering. The evolution of related mechanisms, however, has still to be studied in detail and strongly depends on materials and laser parameters. Excitation with highly intense ultrashort pulses leads to the creation of nanoripple structures with periods far below the fundamental wavelength because of opening multiphoton excitation channels. Because of the drastically reduced spatial scale of such laser induced periodic nanostructures (LIPNS), a particular influence of scattering is expected in this special case. Here we report on first investigations of femtosecond-laser induced nanostructuring of sputtered titanium dioxide (TiO2) layers in comparison to bulk material. The crucial role of the optical film quality for the morphology of the resulting LIPNS was worked out. Typical periods of nanoripples were found to be within the range of 80-180 nm for an excitation wavelength of 800 nm. Unlike our previously reported results on bulk TiO2, LIPNS in thin films appeared preferentially at low pulse numbers (N=5-20). This observation was explained by a higher number of scattering centers caused by the thin film structure and interfaces. The basic assumptions are further supported by supplementary experiments with polished and unpolished surfaces of bulk TiO2 single crystals.
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页数:9
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