Prospect of making XPS a high-throughput analytical method illustrated for a CuxNi1-xOy combinatorial material library

被引:6
作者
Bodenstein-Dresler, Lucas C. W. [1 ]
Kama, Adi [2 ,3 ]
Frisch, Johannes [1 ]
Hartmann, Claudia [1 ]
Itzhak, Anat [2 ,3 ]
Wilks, Regan G. [1 ,4 ]
Cahen, David [2 ,3 ,5 ]
Baer, Marcus [1 ,4 ,6 ,7 ]
机构
[1] Helmholtz Zentrum Berlin Mat & Energie GmbH, Dept Interface Design, Berlin, Germany
[2] Bar Ilan Univ, Bar Ilan Inst Nanotechn & Adv Mat, BINA, IL-5290002 Ramat Gan, Israel
[3] Bar Ilan Univ, Dept Chem, IL-5290002 Ramat Gan, Israel
[4] Helmholtz Zentrum Berlin Mat & Energie GmbH, Energy Mat In Situ Lab Berlin EMIL, Berlin, Germany
[5] Weizmann Inst Sci, Dept Mol Chem & Mat Sci, IL-7610001 Rehovot, Israel
[6] Friedrich Alexander Univ Erlangen Nurnberg, Dept Chem & Pharm, Erlangen, Germany
[7] Helmholtz Inst Erlangen Nurnberg Renewable Energy, Berlin, Germany
关键词
HIGH-PERFORMANCE; FILMS; CU;
D O I
10.1039/d1ra09208a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Combinatorial material science crucially depends on robust, high-throughput characterization methods. While X-ray photoelectron spectroscopy (XPS) may provide detailed information about chemical and electronic properties, it is a time-consuming technique and, therefore, is not viewed as a high-throughput method. Here we present preliminary XPS data of 169 measurement spots on a combinatorial 72 x 72 cm(2) CuxNi1-xOy compositional library to explore how characterization and evaluation routines can be optimized to improve throughput in XPS for combinatorial studies. In particular, two quantification approaches are compared. We find that a simple integration (of XPS peak regions) approach is suited for fast evaluation of, in the example system, the [Cu]/([Cu] + [Ni]) ratio. Complementary to that, the time-consuming (XPS peak-) fit approach provides additional insights into chemical speciation and oxidation state changes, without a large deviation of the [Cu]/([Cu] + [Ni]) ratio. This insight suggests exploiting the fast integration approach for 'real time' analysis during XPS data collection, paving the way for an 'on-the-fly' selection of points of interest (i.e., areas on the sample where sudden composition changes have been identified) for detailed XPS characterization. Together with the envisioned improvements when going from laboratory to synchrotron-based excitation sources, this will shorten the analysis time sufficiently for XPS to become a realistic characterization option for combinatorial material science.
引用
收藏
页码:7996 / 8002
页数:7
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