Effect of platinum surface oxides on the rate of anodic evolution of oxygen in solutions of sulphuric acid

1973 ◽  
Vol 38 (1) ◽  
pp. 29-41 ◽  
Author(s):  
O. Špalek ◽  
J. Balej
1953 ◽  
Vol 31 (7) ◽  
pp. 665-672
Author(s):  
A. K. Wiebe ◽  
C. A. Winkler

A potential of −0.305 ± 0.005 volt (relative to a saturated calomel electrode) was obtained at a freshly prepared platinum surface within 30 sec. of immersion in oxygen-free N/5 sulphuric acid saturated with hydrogen. In electrolytes saturated with nitrogen or oxygen potentials of +0.05 ± 0.01 volt and +0.745 ± 0.005 volt respectively were more slowly attained. The times required for the electrode to reach maximum potentials, tmax, when it was made a cathode, and corresponding values of tmax when it was rendered anodic, were determined over a range of currents. The values of tmax appear to provide a method of determining the surface areas of platinum electrodes.


2017 ◽  
Vol 8 (4) ◽  
pp. 301-310 ◽  
Author(s):  
Sadaf Tahmasebi ◽  
Ashley A. McMath ◽  
Julia van Drunen ◽  
Gregory Jerkiewicz

2017 ◽  
Vol 19 (34) ◽  
pp. 22915-22925 ◽  
Author(s):  
Mareike Haensch ◽  
Julian Behnken ◽  
Luis Balboa ◽  
Alexander Dyck ◽  
Gunther Wittstock

Cavity-microelectrodes were used to investigate surface oxides on supported platinum nanoparticles and nanoporous gold with the surface interrogation mode of scanning electrochemical microscopy.


1959 ◽  
Vol 12 (2) ◽  
pp. 127 ◽  
Author(s):  
DFA Koch

The overpotential (n)-log current density (log i) curves for the evolution of oxygen at a lead dioxide anode in 2N H2SO4 both in the absence and presence of cobaltous sulphate in solution have been used to determine the electrode kinetic constants α ; i0 for a series of temperatures and also ΔH0*:. At 25 �C in the absence of cobalt α=O.59, i0= 10-11, and ΔH0*= 15 kcal mole-1 When 13 mg/l cobaltous sulphate is added α= 1.0, i0= 10-15, and ΔH0*:=29 kcal mole-1. Possible mechanisms for the reaction are discussed on the basis of these values and the rate determining steps suggested (where M represents the PbO2 surface) are M +H2O =MOH +H+ +e in the absence of cobalt and 2CoOH++ = 2Co++ +H2O + O in its presence.


2019 ◽  
Vol 2 (11) ◽  
pp. 7772-7780 ◽  
Author(s):  
Isaac Martens ◽  
Raphael Chattot ◽  
Miika Rasola ◽  
Maria Valeria Blanco ◽  
Veijo Honkimäki ◽  
...  

2008 ◽  
Vol 396-398 ◽  
pp. 389-392
Author(s):  
Aline Raybolt dos Santos ◽  
Fernando Costa e Silva ◽  
Gloria Dulce de Almeida Soares

In this study, commercially pure titanium (Ti-cp) sheets grade 2 were used as substrates. To investigate the role of composition and characteristics of titanium surface oxides in cellular behavior of osteoblasts, the surface of titanium were modified by anodic oxidation with sulphuric acid. Subsequently were treated part of anodized samples with FN and cultured with osteoblast cells for 30, 120 and 240 minutes. The chemical composition and topography have influenced the interaction between fibronectin and substrate. Cells were found more associated to the surfaces that have been submitted to anodization and FN coating than to the related controls.


Author(s):  
R. L. Lyles ◽  
S. J. Rothman ◽  
W. Jäger

Standard techniques of electropolishing silver and silver alloys for electron microscopy in most instances have relied on various CN recipes. These methods have been characteristically unsatisfactory due to difficulties in obtaining large electron transparent areas, reproducible results, adequate solution lifetimes, and contamination free sample surfaces. In addition, there are the inherent health hazards associated with the use of CN solutions. Various attempts to develop noncyanic methods of electropolishing specimens for electron microscopy have not been successful in that the specimen quality problems encountered with the CN solutions have also existed in the previously proposed non-cyanic methods.The technique we describe allows us to jet polish high quality silver and silver alloy microscope specimens with consistant reproducibility and without the use of CN salts.The solution is similar to that suggested by Myschoyaev et al. It consists, in order of mixing, 115ml glacial actic acid (CH3CO2H, specific wt 1.04 g/ml), 43ml sulphuric acid (H2SO4, specific wt. g/ml), 350 ml anhydrous methyl alcohol, and 77 g thiourea (NH2CSNH2).


Author(s):  
R. L. Hines

The importance of atom layer terraces or steps on platinum surfaces used for catalysis as discussed by Somorjai justifies an extensive investigation of the structure of platinum surfaces through electron microscopy at the atomic resolution level. Experimental and theoretical difficulties complicate the quantitative determination of platinum surface structures but qualitative observation of surface structures on platinum crystals is now possible with good experimental facilities.Ultrathin platinum crystals with nominal 111 orientation are prepared using the procedure reported by Hines without the application of a carbon backing layer. Platinum films with thicknesses of about ten atom layers are strong enough so that they can be mounted on grids to provide ultrathin platinum crystals for examination of surface structure. Crystals as thin as possible are desired to minimize the theoretical difficulties in analyzing image contrast to determine structure. With the current preparation procedures the crystals frequently cover complete openings on a 400 mesh grid.


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