首页 | 本学科首页   官方微博 | 高级检索  
     检索      


Calibration of reference materials for total-reflection X-ray fluorescence analysis by heavy ion backscattering spectrometry
Institution:1. Université François Rabelais, Tours, GREMAN, CNRS-UMR7347, INSA-CVL, 16 rue Pierre et Marie Curie, BP 7155, 37071 Tours Cedex 2, France;2. STMicroelectronics, 10 rue Thalès de Milet CS 97155, 37071 Tours Cedex 2, France;1. Electronics and Telecommunications Research Institute (ETRI), 218 Gajeong-ro, Yuseong-gu, Daejeon 34129, Republic of Korea;2. School of Electronics Engineering, Kyungpook National University, Daegu 41566, Republic of Korea;3. Agency for Defense Development, Daejeon 34186, Republic of Korea;1. Department of Materials Science, Fudan University, Shanghai 200433, China;2. National Center for Advanced Packaging, Building D1, 200 Linghu boulevard, Wuxi, Jiangsu 214135, China;3. Institute of Microelectronics of Chinese Academy of Sciences, Beijing 100029, China;1. Texas A & M University at Galveston, Galveston, TX, United States;2. University of Oklahoma, Norman, OK, United States
Abstract:Total-reflection X-ray fluorescence (TXRF) is widely used for the control of metallic contamination caused by surface preparation processes and silicon materials. At least three companies supply a variety of TXRF systems to the silicon integrated circuit (IC) community, and local calibration of these systems is required for their day to day operation. Differences in local calibration methods have become an issue in the exchange of information between IC manufacturers' different FABs (Fabrication Facility) and also between silicon suppliers and IC FABs. The question arises whether a universal set of fluorescence yield curves can be used by these different systems to scale system sensitivity from a single element calibration for calculation of elemental concentrations. This is emphasized by the variety of experimental conditions that are reported for TXRF data (e.g. different angles of incidence for the same X-ray source, different X-ray sources, etc.). It appears that an instrumental factor is required. We believe that heavy ion backscattering spectrometry (HIBS) provides a fundamental method of calibrating TXRF reference materials, and can be used in calculating this instrumental factor. In this paper we briefly describe the HIBS system at the Sandia National Laboratories HIBS User Facility and its application to the calibration of TXRF reference materials. We will compare HIBS and TXRF mapping capabilities and discuss the issues associated with the restrictions of some older TXRF sample stages. We will also discuss Motorola's cross-calibration of several TXRF systems using different elements as references.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号