Expanding the Repertoire of Molecular Linkages to Silicon: Si–S, Si–Se, and Si–Te Bonds

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• 作者：Minjia Hu ; Fenglin Liu ; Jillian M. Buriak
• 刊名：ACS Applied Materials & Interfaces
• 出版年：2016
• 出版时间：May 4, 2016
• 年：2016
• 卷：8
• 期：17
• 页码：11091-11099
• 全文大小：614K
• 年卷期：0
• ISSN：1944-8252

文摘

Silicon is the foundation of the electronics industry and is now the basis for a myriad of new hybrid electronics applications, including sensing, silicon nanoparticle-based imaging and light emission, photonics, and applications in solar fuels, among others. From interfacing of biological materials to molecular electronics, the nature of the chemical bond plays important roles in electrical transport and can have profound effects on the electronics of the underlying silicon itself, affecting its work function, among other things. This work describes the chemistry to produce ≡Si–E bonds (E = S, Se, and Te) through very fast microwave heating (10–15 s) and direct thermal heating (hot plate, 2 min) through the reaction of hydrogen-terminated silicon surfaces with dialkyl or diaryl dichalcogenides. The chemistry produces surface-bound ≡Si–SR, ≡Si–SeR, and ≡Si–TeR groups. Although the interfacing of molecules through ≡Si–SR and ≡Si–SeR bonds is known, to the best of our knowledge, the heavier chalcogenide variant, ≡Si–TeR, has not been described previously. The identity of the surface groups was determined by Fourier transform infrared (FTIR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and depth profiling with time-of-flight-secondary ionization mass spectrometry (ToF-SIMS). Possible mechanisms are outlined, and the most likely, based upon parallels with well-established molecular literature, involve surface silyl radicals or dangling bonds that react with either the alkyl or aryl dichalcogenide directly, REER, or its homolysis product, the alkyl or aryl chalcogenyl radical, RE· (where E = S, Se, and Te).