Vibrational and Electronic Characterization of Ethynyl Derivatives Granted onto Hydrogenated Si(111) Surfaces

被引:20
作者
Yang, F. [1 ]
Hunger, R. [2 ]
Roodenko, K. [3 ,4 ]
Hinrichs, K. [3 ]
Rademann, K. [5 ]
Rappich, J. [1 ]
机构
[1] Helmholtz Zentrum Berlin Mat & Energie GmbH, Inst Si Photovolta, D-12489 Berlin, Germany
[2] Tech Univ Darmstadt, Inst Mat Sci, D-64287 Darmstadt, Germany
[3] ISAS Inst Analyt Sci, Dept Berlin, D-12489 Berlin, Germany
[4] Univ Texas Dallas, Dept Mat Sci & Engn, Richardson, TX 75080 USA
[5] Humboldt Univ, Dept Chem, D-12489 Berlin, Germany
关键词
SILICON; 111; SURFACES; ALKYL MONOLAYERS; X-RAY; ORGANIC MONOLAYERS; CLICK CHEMISTRY; SI SURFACES; HIGH-RESOLUTION; POROUS SILICON; PHOTOELECTRON-SPECTROSCOPY; ORGANOMETALLIC CHEMISTRY;
D O I
10.1021/la900871g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Covalent grafting of ethynyl derivatives(-C C-H, -C C-CH3, -C C-aryl) onto H-terminated Si(111) surfaces was performed by a one-step anodic treatment in Grignard electrolytes. The electrochemical grafting Of Such ethynyl derivatives, which tends to form ultrathin polymeric layers, can be controlled by the current and charge flow passing through the Si electrode. The prepared ultrathin layers cover the Si surface and had a thickness up to 20 rim, as investigated by the scanning electron microscopy (SEM) technique. Exchanging Cl for Br in the ethynyl Grignard reagent leads to very thin layers, even under the same electrochemical conditions. However, for all ethynyl derivatives, high-resolution synchrotron X-ray photoelectron spectroscopy (SXPS) investigations reveal the incorporation of halogen atoms in the organic layers obtained. Moreover, it was observed that the larger the end group of the ethynyl derivative, the thinner the thickness of the ultrathin polymeric layers as measured by both SXPS and SEM techniques after low and high current flow respectively. For the first time, these new types of ultrathin organic layers on Si surfaces were investigated using infrared spectroscopic ellipsometry (IRSE). The different possible reaction pathways are discussed.
引用
收藏
页码:9313 / 9318
页数:6
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