Mine Nicolas, Douhard Bastien, Brison Jeremy, Houssiau Laurent
University of Namur (FuNDP), Physics Department, LISE Laboratory; 61, rue de Bruxelles, B-5000 Namur, Belgium.
Rapid Commun Mass Spectrom. 2007;21(16):2680-4. doi: 10.1002/rcm.3135.
In this work, we explored the possibility of performing molecular depth-profiling by using very low-energy (about 200 eV) monoatomic Cs(+) ions. We show, for the first time, that this simple approach is successful on polymer layers of polycarbonate (PC). Under 200 eV Cs(+) irradiation of PC, a fast decrease of all characteristic negatively charged molecular ion signals is first observed but, rather surprisingly, these signals reach a minimum before rising again. A steady state is reached at which time most specific PC fragments are detected, some with even higher signal intensity (e.g. C(6)H(5)O(-)) than before irradiation. It is believed that the implanted Cs plays a major role in enhancing the negative ionisation of molecular fragments, leading to their easy detection for all the profile, although some material degradation obviously occurs. In the positive ion mode, all molecular fragments of the polymer disappear very rapidly, but clusters combining two Cs atoms and one molecular fragment (e.g. Cs(2)C(6)H(5)O(+)) are detected during the profile, proving that some molecular identification remains possible. In conclusion, this work presents a simple approach to molecular depth-profiling, complementary to cluster ion beam sputtering.
在这项工作中,我们探索了使用极低能量(约200电子伏特)的单原子铯离子(Cs(+))进行分子深度剖析的可能性。我们首次表明,这种简单方法在聚碳酸酯(PC)聚合物层上是成功的。在200电子伏特的Cs(+)辐照PC时,首先观察到所有特征性带负电的分子离子信号迅速下降,但令人惊讶的是,这些信号在再次上升之前达到最小值。达到了一个稳定状态,此时检测到了大多数特定的PC碎片,有些碎片的信号强度甚至比辐照前更高(例如C(6)H(5)O(-))。据信,注入的Cs在增强分子碎片的负离子化方面起主要作用,从而导致在整个剖析过程中它们易于被检测到,尽管明显发生了一些材料降解。在正离子模式下,聚合物的所有分子碎片迅速消失,但在剖析过程中检测到了结合两个Cs原子和一个分子碎片的团簇(例如Cs(2)C(6)H(5)O(+)),这证明仍有可能进行一些分子识别。总之,这项工作提出了一种简单的分子深度剖析方法,它是对团簇离子束溅射的补充。