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有机深度剖析中的成分测量:VAMAS实验室间研究的结果

Measuring Compositions in Organic Depth Profiling: Results from a VAMAS Interlaboratory Study.

作者信息

Shard Alexander G, Havelund Rasmus, Spencer Steve J, Gilmore Ian S, Alexander Morgan R, Angerer Tina B, Aoyagi Satoka, Barnes Jean-Paul, Benayad Anass, Bernasik Andrzej, Ceccone Giacomo, Counsell Jonathan D P, Deeks Christopher, Fletcher John S, Graham Daniel J, Heuser Christian, Lee Tae Geol, Marie Camille, Marzec Mateusz M, Mishra Gautam, Rading Derk, Renault Olivier, Scurr David J, Shon Hyun Kyong, Spampinato Valentina, Tian Hua, Wang Fuyi, Winograd Nicholas, Wu Kui, Wucher Andreas, Zhou Yufan, Zhu Zihua, Cristaudo Vanina, Poleunis Claude

机构信息

†National Physical Laboratory, Teddington, Middlesex TW11 0LW, United Kingdom.

‡Laboratory of Biophysics and Surface Analysis, University of Nottingham, Nottingham NG7 2RD, United Kingdom.

出版信息

J Phys Chem B. 2015 Aug 20;119(33):10784-97. doi: 10.1021/acs.jpcb.5b05625. Epub 2015 Aug 6.

Abstract

We report the results of a VAMAS (Versailles Project on Advanced Materials and Standards) interlaboratory study on the measurement of composition in organic depth profiling. Layered samples with known binary compositions of Irganox 1010 and either Irganox 1098 or Fmoc-pentafluoro-l-phenylalanine in each layer were manufactured in a single batch and distributed to more than 20 participating laboratories. The samples were analyzed using argon cluster ion sputtering and either X-ray photoelectron spectroscopy (XPS) or time-of-flight secondary ion mass spectrometry (ToF-SIMS) to generate depth profiles. Participants were asked to estimate the volume fractions in two of the layers and were provided with the compositions of all other layers. Participants using XPS provided volume fractions within 0.03 of the nominal values. Participants using ToF-SIMS either made no attempt, or used various methods that gave results ranging in error from 0.02 to over 0.10 in volume fraction, the latter representing a 50% relative error for a nominal volume fraction of 0.2. Error was predominantly caused by inadequacy in the ability to compensate for primary ion intensity variations and the matrix effect in SIMS. Matrix effects in these materials appear to be more pronounced as the number of atoms in both the primary analytical ion and the secondary ion increase. Using the participants' data we show that organic SIMS matrix effects can be measured and are remarkably consistent between instruments. We provide recommendations for identifying and compensating for matrix effects. Finally, we demonstrate, using a simple normalization method, that virtually all ToF-SIMS participants could have obtained estimates of volume fraction that were at least as accurate and consistent as XPS.

摘要

我们报告了一项关于有机深度剖析中成分测量的VAMAS(凡尔赛先进材料与标准项目)实验室间研究的结果。在一批中制备了每层具有已知的Irganox 1010与Irganox 1098或芴甲氧羰基 - 五氟 - L - 苯丙氨酸二元组成的分层样品,并分发给20多个参与实验室。使用氩簇离子溅射和X射线光电子能谱(XPS)或飞行时间二次离子质谱(ToF - SIMS)对样品进行分析以生成深度剖析图。要求参与者估计其中两层的体积分数,并向他们提供所有其他层的组成。使用XPS的参与者提供的体积分数在标称值的0.03范围内。使用ToF - SIMS的参与者要么没有尝试,要么使用了各种方法,其结果的体积分数误差范围从0.02到超过0.10,后者对于标称体积分数0.2代表50%的相对误差。误差主要是由于补偿初级离子强度变化的能力不足以及SIMS中的基体效应。随着初级分析离子和二次离子中原子数的增加,这些材料中的基体效应似乎更加明显。利用参与者的数据,我们表明有机SIMS基体效应可以被测量,并且在仪器之间非常一致。我们提供了识别和补偿基体效应的建议。最后,我们使用一种简单的归一化方法证明,几乎所有ToF - SIMS参与者都可以获得至少与XPS一样准确和一致的体积分数估计值。

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