Scanning Tunneling Microscope Study of Etch Pits on Highly Oriented Pyrolytic Graphite Heated in an Atomic Absorption Electrothermal Analyzer

1997 ◽  
Vol 51 (12) ◽  
pp. 1896-1904 ◽  
Author(s):  
Kurt G. Vandervoort ◽  
Kristin N. McLain ◽  
David J. Butcher

Scanning tunneling microscopy (STM) was used to elucidate monolayer etch pits that form on highly oriented pyrolytic graphite (HOPG) heated in an electrothermal analyzer. Pits form at elevated temperatures due to reactions between oxygen and exposed carbon edge atoms (defects) and additionally with intraplanar carbon atoms (through abstraction). Samples of HOPG without analyte or matrix modifier were placed in the depression of a pure pyrolytic graphite platform and heated by using standard analysis furnace programs. Under argon stop-flow conditions, pits form in less than a second at atomization temperatures equal to and above 1200 °C. With low argon flow rates (40 mL/min), pits formed at atomization temperatures equal to and greater than 1750 °C in less than a second. Quantitative pit formation rates were used to indicate oxygen partial pressure, which may be as high as ∼ 10−3 atm at 1200 °C. Reaction rates were used to predict surface degradation due to oxygen attack and determine that 1-μm depth normal to the surface would be removed by 200 successive 5-second-period furnace firings at 1200 °C. Implications for increases in surface reactivity and analyte intercalation are discussed.

2016 ◽  
Vol 18 (2) ◽  
pp. 916-925 ◽  
Author(s):  
C. Müller ◽  
K. Németh ◽  
S. Vesztergom ◽  
T. Pajkossy ◽  
T. Jacob

The interface between highly oriented pyrolytic graphite (HOPG) and 1-butyl-3-metyl-imidazolium hexafluorophosphate (BMIPF6) has been studied using cyclic voltammetry, electrochemical impedance spectroscopy, immersion charge measurements and in situ scanning tunneling microscopy (in situ STM).


2000 ◽  
Vol 654 ◽  
Author(s):  
Ulrike Diebold

AbstractSurface defects are important in oxide surface chemistry, because they change not only the surface geometric structure, but also affect the local electronic structure. Scanning Tunneling Microscopy (STM) images with atomic-scale resolution, in combination with area-averaging surface spectroscopies, is an ideal tool to study local surface defects and their relationship to surface reactivity. We report STM results onTiO2(110) surfaces which show the surprising influence of bulk defects on surface properties. Thereduced crystals used in this and other surface science studies contain Ti interstitials and oxygen vacancies. Re-oxidation at elevated temperatures results in the growth of additional TiO2 layers with Ti coming from the bulk of the crystal and O from the gas phase. This often result in partially incomplete surface structures with many undercoordinated atoms. The esorption behavior of elemental S, dosed at room temperature, depends on the reduction state of the sample. This is explained by a mechanism where desorption froma weaklybound precursor state competes with the availability of new adsorption sites in the form of oxygen vacancies which migrate from the bulk to the surface.


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