Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-26T14:57:32.002Z Has data issue: false hasContentIssue false

A Mathematical Model for Determining Carbon Coating Thickness and Its Application in Electron Probe Microanalysis

Published online by Cambridge University Press:  04 November 2016

Ruo-Xi Zhang
Affiliation:
State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Wuhan 430074, PR China
Shui-Yuan Yang*
Affiliation:
State Key Laboratory of Geological Processes and Mineral Resources, China University of Geosciences, Wuhan 430074, PR China
*
*Corresponding author.[email protected]
Get access

Abstract

In electron probe microanalysis where materials are coated with a thin conductive carbon coat before analysis, the X-ray intensity detected from a specimen may be affected to various degrees by the thickness of the carbon coating. Differences in the carbon film thickness between specimens and standards may lead to errors in analytical results, particular for lower energy X-rays. In this study, we demonstrate that the location and the distance of the specimen relative to the carbon tip in the coating chamber can affect the thickness of the carbon film produced on the specimen surface during carbon coating. The closer the specimen is to the carbon tip contacting point, the thicker is the carbon film deposited. A mathematical model to calculate the carbon film thickness at different locations on the coater plate is established, based on the assumption that carbon atoms evaporate from the carbon tip equally in all directions during the coating process. In order to reduce the differences in the carbon coating thickness, we suggest moving the carbon rod to a higher position, moving the thinner samples to the center and thicker samples to the edge of the coater plate, and using a rotating circular coater plate during coating.

Type
Instrumentation and Software Techniques
Copyright
© Microscopy Society of America 2016 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Alexander, M.R., Thompson, G.E., Zhou, X., Beamson, G. & Fairley, N. (2002). Quantification of oxide film thickness at the surface of aluminium using XPS. Surf Interface Anal 34, 485489.Google Scholar
Buse, B. & Kearns, S. (2015). Importance of carbon contamination in high-resolution (FEG) EPMA of silicate minerals. Microsc Microanal 21, 594605.Google Scholar
Hofmann, S. (1998). Sputter depth profile analysis of interfaces. Rep Prog Phys 61, 827888.Google Scholar
Kato, T. (2007). Monte Carlo study of quantitative electron probe microanalysis of monazite with a coating film: Comparison of 25 nm carbon and 10 nm gold at E0=15 and 25 keV. Geostand Geoanal Res 31, 8994.Google Scholar
Kerrick, D.M., Eminhizer, L.B. & Villaume, J.F. (1973). The role of carbon film thickness in electron microprobe analysis. Am Miner 58, 920925.Google Scholar
Kolbe, M., Beckhoff, B., Krumrey, M. & ULM, G. (2005). Thickness determination for Cu and Ni nanolayers: Comparison of completely reference-free fundamental parameter-based X-ray fluorescence analysis and X-ray reflectometry. Spectrochim Acta Part B At Spectrosc 60, 505510.Google Scholar
Limandri, S.P., Carreras, A.C. & Trincavelli, J.C. (2010). Effects of the carbon coating and the surface oxide layer in electron probe microanalysis. Microsc Microanal 16, 583593.Google Scholar
McGee, J.J. & Keil, K. (2001). Application of electron probe microanalysis to the study of geological and planetary materials. Microsc Microanal 7, 200210.Google Scholar
Reed, S.J.B. (1972). Electron microprobe analysis at low operating voltage: Discussion. Am Miner 57, 15501551.Google Scholar
Reed, S.J.B. (1975). Electron Microprobe Analysis. Cambridge: Cambridge University Press.Google Scholar
Sweatman, T.R. & Long, J.V.P. (1969). Quantitative electron-probe microanalysis of rock-forming minerals. J Petrol 10, 332379.Google Scholar
Thomsen-Schmidt, P., Hasche, K., Ulm, G., Herrmann, K., Krumrey, M., Ade, G., Stümpel, J., Busch, I., Schädlich, S., Schindler, A., Frank, W., Hirsch, D., Proco, P.M. & Beck, U. (2004). Realisation and metrological characterisation of thickness standards below 100 nm. Appl Phys A 78, 645649.Google Scholar
Waldo, R.A. (1988). An iteration procedure to calculate film compositions and thickness in electron probe microanalysis. In Microbeam Analysis, Newbury, D.E. (Ed.), pp. 310–314. San Francisco: San Francisco Press.Google Scholar
Zhao, D., Zhang, Y. & Essene, E.J. (2015). Electron probe microanalysis and microscopy: Principles and applications in characterization of mineral inclusions in chromite from diamond deposit. Ore Geol Rev 65, 733748.Google Scholar