Surface Contamination and Cleaning
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about chemical bonding and molecular structure. This information can be used to detect th e types of organic materials present on the surface. 4.3.2.2. Raman spectroscopy (RS) [7, 8] It is used to examine the energy levels of molecules that cannot be well character-ized via infrared spectroscopy. Th e two techniques, however, are complimentary. In the RS, a sample is irradiated with a strong monochromatic light source (usu-ally a laser). Most of the radiation will scatter or "reflect off' the sample at the same energy as the incoming laser radiation. However, a small amount will scat-ter from the sample at a wavelength slightly shifted from the original wavelength. It is possible to study the molecular structure or determine the chemical identity of the sample. It is quite straightforward to identify compounds by spectral library search. Due to extensive library spectral information, the unique spectral finger-print of every compound, and the ease with which such analyses can be per-formed, the RS is a very useful technique for various applications. An important application of the RS is the rapid, nondestructive characterization of diamond, diamond-like, and amorphous-carbon films. 4.3.2.3. Scanning electron microscopy (SEM) / energy dispersive X-ra y analysis (EDX) [7, 8] The SEM produce s detailed photographs that provide important information about the surface structure and morphology of almost any kind of sample. Image analy-sis is often the first and most important step in problem solving and failure analy-sis. With SEM, a focused beam of high-energy electrons is scanned over the sur-face of a material, causing a variety of signals, secondary electrons, X-rays, photons, etc. - each of which may be used to characterize the material with re-spect to specific properties . The signals are used to modulate the brightness on a CRT display, thereb y providing a high-resolution map of the selected material property. It is a surface imaging technique, but with Energy Dispersive X-ray (EDX) it can identify elements in the near-surface region. This technique is most useful for imaging particles. 4.3.2.4. X-ray fluorescence (XRF) [7, 8] Incident X-rays are used to excite surface atoms. The atoms relax through the emission of an X-ray with energy characteristic of the parent atoms and the inten-sity proportional to the amount of the element present. It is a bulk or "total mate-rials" characterization technique for rapid, simultaneous, and nondestructive analysis of elements having an atomic number higher than that of boron. Tradi-tional bulk analysis applications include identifying metals and alloys, detecting trace elements in liquids, and identifying residues and deposits. 4.3.2.5. Total-reflection X-ray fluorescence (TXRF) [7, 8] It is a special XRF technique that provides extremely sensitive measures of the elements present in a material's outer surface. Applications include searching for metal contamination in thin films on silicon wafers and detecting picogram-levels o f arsenic, lead, mercury and cadmium on hazardous, chemical fume hoods.

2003 ◽  
pp. 43-45

electromagnetic field at the particl e has to be computed numerically. An example of such a computation using a program based on [49] is given in Fig. 4. But not only doe s the Mie theory describe an enhancement of the laser intensity in the particles' near field, it also predicts that for certain values of the size parameter nd/X (d denoting the particle diameter, À the laser wavelength) the enhancement should be particularly efficient, resulting in a resonant intensity enhancement, the so-called "Mie-resonances". 3.2.2. Near-field induced substrate damage When inspecting contaminated samples by scanning electron microscopy (SEM) or atomic force microscopy (AFM ) after DLC using ns laser pulses, the consequences of the field enhancement process became obvious: all over the cleaned areas w e found substrate damages localized exactly at the former particle positions [35, 37-39]. These damages manifested as melting pools or even holes in the surface, typical examples can be seen in Fig. 5. The consequences for the laser cleaning process are obvious. The intensity enhancement reduces the maximum laser fluence that can be applied in the process. Usually in laser cleaning studies [19, 31 ] the laser fluence corresponding to the melting threshold of a bare surface is taken as the damage threshold fluence. Our experiments show clearly that this is an inadequate definition. Instead one must take into account the enhanced laser fluence underneath the particles, as it will be discussed in Section 4. Fro m the obtained AFM images we were able to analyse in detail the surface profile at the damaged sites. Here we found that for high field enhancement factors the silicon substrate was not only molten , but that some material was even ablated (see Sec. 4). The momentum transfer to the particles during the ablation process significantly contributes to the cleanin g process and hence local substrate ablation

2003 ◽  
pp. 327-330

CONCLUSION While cleaned silica-based glass surfaces have similar surface compositions, their susceptibility to strongly adsorbing organic contaminant s depends strongly on the glass composition and the cleaning procedure. For the three glass species exam-ined: silica, aluminoborosilicate, and sodalime glass , the glass surfaces behave similarly after chromic acid cleaning. They show significant differences in their properties followin g a dry cleaning procedure, such as pyrolysis or UV/ozone cleaning. The cleaned silica surfaces show a high susceptibility to adsorbing or-ganic contamination following pyrolysis cleaning, while the pyrolyzed sodalime glass appears to be virtually immune to strongly adsorbing organic molecules. Py-rolyzed aluminoborosilicate glass shows an intermediate susceptibility to adsorb-ing organic contaminants. The chromic acid cleaned glass surfaces all show an in-termediate susceptibility to contamination by adsorbed organic molecules. Thus, it may be an oversimplification to consider a clean glass surface as a high energy substrate that is bound to attract ambient organic contamination. The wettability behavior of the cleaned glass surfaces showed features associ-ated with their exposed chemical functions. The non-dispersive interaction energy between glass and water as a function of pH showed evidence of charging of the surface silanol groups. The point of zero charge for these surface chemical func-tions was observed at pH 3. An estimate of the non-dispersive interaction energy between glass and water at the point of zero charge enables a reasonable estima-tion of the density of surface silanol groups on the cleaned glass. The trends ob-served for the surface charge as a function of pH correlate with the observed sus-ceptibility for adsorbing organic contamination to the cleaned glass surfaces. Charge-adsorbed surfactant monolayers indicated a negative surface charge on the cleaned glass, as expected for silica-based glass surfaces at neutral pH. The wettability of grafted self-assembled octadecylsilane monolayers indicated high quality coatings on the cleaned glass surfaces. The coating quality was identical for all three glass species following chromic acid cleaning. The UV/ozone cleaned glass surfaces showed the highest coating quality on the silica surface, followed by the aluminoborosilicate surface and the sodalime glass surface. The trends in coating quality for all chromic acid cleaned surfaces and UV/ozone cleaned surfaces correlate with those seen for susceptibility to organic contamina-tion of the cleaned glass surfaces exposed to unpurified liquid octane. REFERENCES

2003 ◽  
pp. 114-116

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