AVS 62nd International Symposium & Exhibition | |
Plasma Science and Technology | Monday Sessions |
Session PS+SE-MoM |
Session: | Atmospheric Pressure Plasma Processing I |
Presenter: | Andrew Knoll, University of Maryland, College Park |
Authors: | A.J. Knoll, University of Maryland, College Park P. Luan, University of Maryland, College Park E.A.J. Bartis, University of Maryland, College Park G.S. Oehrlein, University of Maryland, College Park |
Correspondent: | Click to Email |
In this study, we investigate the etching mechanism of atmospheric pressure plasma jet (APPJ) treated poly(methyl methacrylate)-based 193 nm photoresist polymer and polystyrene-based 248 nm photoresist polymer using in situ ellipsometry to monitor film thickness and refractive index in real time. The kHz-driven, two-ring electrode APPJ used in this work operated with low admixtures of O2 and N2 to Ar feed gas flowed at 2 slm. Additionally, we used attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and x-ray photoelectron spectroscopy to characterize the surface modifications post treatment. With pure argon feed gas, we observed etching of the photoresist polymers even when the visible plume is not in direct contact with the polymer surface. This etching rate is sensitive to the Ar gas flow rate and local gas environment. APPJ treatments were compared to a surface microdischarge source with a O2/ N2 gas flow added but no etching was seen for that source. Furthermore, the etching was shown to be directional by placing a grounded mesh directly over the sample during treatment. No etching was seen without direct line of sight from source to sample. Optical filters were used to investigate the effect of high energy photons on polymer etching and modification. When a MgF2 filter with a 114 nm cutoff wavelegth is placed directly over the sample, etching still occurs. When a sapphire filter with cutoff wavelength of 142 nm is used, no etching is seen. Ar2* excimer species are known to be created in atmospheric pressure plasma and emit photons at 128 nm. Vacuum-ultraviolet (VUV)-induced etching is further supported by experiments that show that etching increases in nitrogen environments compared to oxygen environments as oxygen more effectively absorbs VUV radiation. ATR-FTIR of treated samples shows comparable bulk modifications with or without MgF2 filter over the sample. These results are consistent with photoresists treated with VUV from low pressure plasma. APPJs are sources of a variety of reactive chemical species which can be used for numerous industrial and medical applications. While the VUV effect of APPJ sources on biodeactivation has been investgiated1,2, polymer etching has not been seen prior to this work. The authors gratefully acknowledge financial support by US Department of Energy (DE-SC0001939) and National Science Foundation (PHY-1415353).
1 Lackmann, J. W., et al. (2013). Journal of the Royal Society Interface 10(89).
2 Schneider, S., et al. (2011). Journal of Physics D-Applied Physics 44(29).