Chemical sputtering of carbon films by simultaneous irradiation with argon ions and molecular oxygen

被引:27
作者
Hopf, C. [1 ]
Schlueter, M. [1 ]
Schwarz-Selinger, T. [1 ]
von Toussaint, U. [1 ]
Jacob, W. [1 ]
机构
[1] EURATOM, Max Planck Inst Plasma Phys, D-85748 Garching, Germany
关键词
D O I
10.1088/1367-2630/10/9/093022
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The erosion of hard amorphous hydrocarbon films by bombardment with argon ions and simultaneous exposure to thermal molecular oxygen is studied as a function of oxygen flux density ( 0 - 11 400 times the ion flux density), ion energy ( 20 - 800 eV), and surface temperature ( 110 - 875 K). While erosion due to Ar+ ions only is dominated by physical sputtering, the additional presence of molecular oxygen leads to a marked increase of erosion, indicating chemical sputtering. The erosion yield increases with both ion energy and oxygen flux density. Starting from about 700K thermal chemical erosion ( combustion) by O-2 is observed even without ion bombardment. Additional ion bombardment in this temperature range causes an increase of the erosion rate over the sum of thermal chemical erosion and the rate observed at room temperature. Below approximate to 300 K, the rate increases with decreasing temperature. We explain the latter behavior by the ion- induced reaction of adsorbed oxygen which constitutes a significant surface coverage only at low temperatures. A rate equation model is presented, which incorporates the mechanisms of physical sputtering, chemical reaction of O2 at reactive sites created by ion bombardment, the ion- induced reaction of adsorbed oxygen and ion- enhanced thermal chemical erosion. The model's nine free parameters are optimized by fitting 68 experimental data points. The model yields good agreement in all investigated dependences.
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页数:27
相关论文
共 68 条
[1]  
[Anonymous], 1991, COMPUTER SIMULATION
[2]   ION-INDUCED ETCHING OF ORGANIC POLYMERS IN ARGON AND OXYGEN RADIOFREQUENCY PLASMAS [J].
BAGGERMAN, JAG ;
VISSER, RJ ;
COLLART, EJH .
JOURNAL OF APPLIED PHYSICS, 1994, 75 (02) :758-769
[3]   Oxidative erosion of graphite in air between 600 and 1000 K [J].
Balden, M ;
Klages, KU ;
Jacob, W ;
Roth, J .
JOURNAL OF NUCLEAR MATERIALS, 2005, 341 (01) :31-44
[4]   Ozone reaction with carbon nanostructures 2: The reaction of ozone with milled graphite and different carbon black grades [J].
Cataldo, Franco .
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2007, 7 (4-5) :1446-1454
[5]   ION-ASSISTED AND ELECTRON-ASSISTED GAS-SURFACE CHEMISTRY - IMPORTANT EFFECT IN PLASMA-ETCHING [J].
COBURN, JW ;
WINTERS, HF .
JOURNAL OF APPLIED PHYSICS, 1979, 50 (05) :3189-3196
[6]   ON THE ROLE OF ATOMIC OXYGEN IN THE ETCHING OF ORGANIC POLYMERS IN A RADIOFREQUENCY OXYGEN DISCHARGE [J].
COLLART, EJH ;
BAGGERMAN, JAG ;
VISSER, RJ .
JOURNAL OF APPLIED PHYSICS, 1995, 78 (01) :47-54
[7]   Tritium retention in next step devices and the requirements for mitigation and removal techniques [J].
Counsell, G. ;
Coad, P. ;
Grisola, C. ;
Hopf, C. ;
Jacob, W. ;
Kirschner, A. ;
Kreter, A. ;
Krieger, K. ;
Likonen, J. ;
Philipps, V. ;
Roth, J. ;
Rubel, M. ;
Salancon, E. ;
Semerok, A. ;
Tabares, F. L. ;
Widdowson, A. .
PLASMA PHYSICS AND CONTROLLED FUSION, 2006, 48 (12B) :B189-B199
[8]   Cleaning of contaminated XUV-optics at BESSY II [J].
Eggenstein, F ;
Senf, F ;
Zeschke, T ;
Gudat, W .
NUCLEAR INSTRUMENTS & METHODS IN PHYSICS RESEARCH SECTION A-ACCELERATORS SPECTROMETERS DETECTORS AND ASSOCIATED EQUIPMENT, 2001, 467 :325-328
[9]   Plasma-material interactions in current tokamaks and their implications for next step fusion reactors [J].
Federici, G ;
Skinner, CH ;
Brooks, JN ;
Coad, JP ;
Grisolia, C ;
Haasz, AA ;
Hassanein, A ;
Philipps, V ;
Pitcher, CS ;
Roth, J ;
Wampler, WR ;
Whyte, DG .
NUCLEAR FUSION, 2001, 41 (12R) :1967-2137
[10]   Removal of carbon deposits in narrow gaps by oxygen plasmas at low pressure [J].
Ferreira, J. A. ;
Tabares, F. L. ;
Tafalla, D. .
JOURNAL OF VACUUM SCIENCE & TECHNOLOGY A, 2007, 25 (04) :746-750