Characterization and Oxidation of Fe Nanoparticles Deposited onto Highly Oriented Pyrolytic Graphite, Using X-ray Photoelectron Spectroscopy

2009 ◽  
Vol 113 (16) ◽  
pp. 6418-6425 ◽  
Author(s):  
D.-Q. Yang ◽  
E. Sacher
2021 ◽  
Vol 13 (8) ◽  
pp. 4158
Author(s):  
Marcos A. Bento ◽  
Sara Realista ◽  
Ana S. Viana ◽  
Ana M. Ferraria ◽  
Paulo N. Martinho

Reproducible materials that have detection properties towards a certain molecule are very important for applications in the fabrication of devices. Among all the substrates that are used, highly oriented pyrolytic graphite allows to clearly image a monolayer. On the other hand, cryptand molecules are versatile because they can sense certain analytes with high selectivity. The highly oriented pyrolytic graphite electrode was first functionalized with an aryl bearing a bromine or an alkyne group to further attach cryptand molecules to its surface. The functionalization was performed through the electroreduction of aryl diazonium salts. While functionalization with an aryl-bromine produced a 20 nm-thick dendritic layer, functionalization of the surface with an aryl bearing a terminal alkyne produced a 9.7 nm-thick multilayer. However, if the diazonium salt is prepared in situ, a 0.9 nm monolayer with aryl–alkyne groups is formed. The alkyne functionalized electrode reacted with a bromo-cryptand through a Sonogashira C–C coupling reaction yielding electrodes functionalized with cryptands. These were immersed in a solution of a Co(II) salt resulting in Co(II)-cryptate modified electrodes, highlighting the ability of the cryptands’ modified electrode to sense metal ions. The electrode surface was analyzed by X-ray photoelectron spectroscopy after each modification step, which confirmed the successful functionalization of the substrate with both the cryptand and the cryptate. Cyclic voltammetry studies showed stable current response after approximately six cycles. Different reduction processes were detected for both cryptand (−1.40 V vs. SCE) and cryptate (−1.22 V vs. SCE) modified highly oriented pyrolytic graphite.


2008 ◽  
Vol 63 (12) ◽  
pp. 1443-1446 ◽  
Author(s):  
Mohammad Sahabul Alam ◽  
Andreas Scheurer ◽  
Rolf W. Saalfrank ◽  
Paul Müller

C2-symmetric nickel(II) salen complexes [NiL] 1 were deposited on a highly oriented pyrolytic graphite (HOPG) surface from their acetone solutions. They aggregate easily to single, segregated, homochiral polymeric chains of (M)-1D- 1n [NiL] (2) on the substrate as also found in single crystals. In STM topography, the single helical 1D structures 2 found on the surface were in excellent agreement with the dimension of aligned dimeric aggregates of 1 obtained from X-ray crystallography. Weak intermolecular NiII...OMe coordinations (dMeO−Ni = 0.35 nm) were found to be responsible for the formation of the chiral, helical and 1D assemblies on the substrate.


2016 ◽  
Vol 49 (3) ◽  
pp. 835-844 ◽  
Author(s):  
Yoshinori Ohmasa ◽  
Susumu Shimomura ◽  
Ayano Chiba

In small-angle X-ray scattering from highly oriented pyrolytic graphite, radial streak patterns are observed. The streaks change their direction with sample rotation and appear and disappear in pairs. This streak pattern can be explained by double Bragg scattering. The directions of the streaks calculated as functions of the rotation angle are in good agreement with experiment. In addition, asymmetry in the intensity of the streaks and a small deviation from the radial pattern are observed, and they can be explained by the finite sample-size effect. The necessity of taking double Bragg scattering into account in small-angle X-ray scattering studies of crystalline materials is emphasized.


2007 ◽  
Vol 62 (6-7) ◽  
pp. 577-585 ◽  
Author(s):  
V.A. Arkadiev ◽  
A.A. Bjeoumikhov ◽  
M. Haschke ◽  
N. Langhoff ◽  
H. Legall ◽  
...  

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