4.6 Article

Expanding the Scope of Diamond Surface Chemistry: Stille and Sonogashira Cross-Coupling Reactions

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 121, 期 42, 页码 23446-23454

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.7b06426

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资金

  1. UHasselt
  2. Research Foundation Flanders (FWO Vlaanderen)
  3. Czech Science Foundation [15-01809S]
  4. European Regional Development Fund [CZ.02.1.01/0.0/0.0/15 003/0000464]
  5. FWO

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Well-defined covalent surface functionalization of diamond is a crucial, yet nontrivial, matter because of diamond's intrinsic chemical inertness and stability. Herein, we demonstrate a two-step functionalization approach for H-terminated boron doped diamond thin films, which can lead to significant advances in the field of diamond hybrid photovoltaics. Primary diamond surface functionalization is performed via electrochemical diazonium grafting of in situ diazotized 4-iodoaniline. The freshly grafted iodophenyl functional moieties are then employed to couple a layer of thiophene molecules to the diamond surface via two well-established Pd-catalyzed cross-coupling reactions, i.e., Stile and Sonogashira. X-ray photoelectron spectroscopy analysis indicates a dense coverage and successful cross-coupling in both cases. However, we find that the Stille reaction is generally accompanied by severe surface contamination, in spite of process optimization and thorough rinsing. Sonogashira cross-coupling on the other hand provides a clean, high quality functionalization over a broad range of reaction conditions. The protocols employing Sonogashira reactions thus appear to be the method of choice toward future fabrication of high-performance dye-functionalized diamond electrodes for photovoltaic applications.

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