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Quantitative MCs_n~+ - SIMS for Direct Compositional Analysis of Interfaces of Low-Dimensional Structures

机译:定量MCS_N〜+ - 用于直接组成分析的低维结构的直接组成分析

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Excellent detection sensitivity, high dynamic range and good depth resolution make the Secondary ion Mass spectrometry (SIMS) technique extremely powerful for the chemical analysis of surfaces and interfaces of condensed matter systems. However, a serious problem in SIMS analysis is its "matrix effect" that hinders the quantification of a certain species in a sample and consequently, probing the composition of surfaces or interfaces by SIMS is greatly hindered. Appropriate corrective measures are therefore, needed to calibrate the secondary ion currents into respective concentrations for accurate compositional analysis. Working in the MCs~+-SIMS mode (M - element to be analyzed, Cs~+ - bombarding ions) can circumvent the matrix effect. The emission process for the species M~0 is decoupled from the MCs~+ ion formation process, in analogy with the ion formation in secondary neutral mass spectrometry (SNMS), resulting in a drastic decrease in matrix effect in the MCs~+- SIMS mode. Although this technique has found its applicability in direct quantification, it generally suffers from a low useful yield. In such cases, detection of MCs_n~+ (n = 2, 3,...) molecular ions offers a better sensitivity (even by several orders of magnitude), as the yields of such molecular ion complexes have often been found to be higher than that of MCs~+ ions. Several works have been reported on the emission of MCs_n~+ molecular ions, but a complete understanding on the formation mechanisms of these ion complexes is still lacking. However, irrespective of the formation mechanisms, MCs_n~+-SIMS technique in all its complexities has great relevance in the elemental analysis of materials. The talk will address on the possible formation mechanisms and potential applications of MCs_n~+ molecular ion complexes in the interfacial analysis of ultrathin films, metallic multilayers, semiconductor superlattices, quantum structures and also in the compositional analysis of MBE grown Si_(1-x)Ge_x alloys.
机译:优异的检测灵敏度,高动态范围和良好的深度分辨率使二次离子质谱(SIMS)技术非常强大,用于凝聚物系统的表面和界面的化学分析。然而,SIMS分析中的严重问题是其“矩阵效应”,其阻碍了样品中某些物种的定量,因此,通过SIMS探测表面或界面的组成受到了极大的阻碍。因此,需要适当的校正措施,以校准二次离子电流以精确组成分析的相应浓度。在MCS〜+ -SIMS模式下工作(要分析的M - 元素,CS〜+ - 轰击离子)可以规避基质效应。对于M〜0从MCS〜+离子形成过程去耦的物种的发射过程中,与二次中性质谱(SNMS)的离子形成类比,导致在MCS〜+中基体效应的急剧下降 - SIMS模式。虽然这种技术已在直接定量方面发现其适用性,但它通常存在低的有用产率。在这种情况下,检测MCS_N〜+(n = 2,3,...)分子离子提供更好的敏感性(即使甚至几个数量级),因为这种分子离子配合物的产量通常被发现更高比MCS〜+离子的。已经报告了几种作品对MCS_N〜+分子离子的发射,但仍然缺乏对这些离子复合物的形成机制的完全理解。然而,无论形成机制如何,所有复杂性的MCS_N〜+ -SIMS技术在材料的元素分析中都具有很大的相关性。讲座将在可能的形成机制和超薄薄膜,金属多层薄膜,半导体超晶格,量子结构以及在生长SI_ MBE的组成分析的界面分析MCs_n〜+分子离子复合物的潜在应用涉及(1-x)的Ge_x合金。

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