scholarly journals Electrochemical oxidation of Pt(111) beyond the place-exchange model

2022 ◽  
pp. 139881
Author(s):  
Leon Jacobse ◽  
Vedran Vonk ◽  
Ian T. McCrum ◽  
Christoph Seitz ◽  
Marc T.M. Koper ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Exchange Model ◽  
Place Exchange

scholarly journals Kinetic Monte Carlo Simulations of Electrochemical Oxidation and Reduction of Pt(111)

2019 ◽  
Vol 166 (16) ◽  
pp. H888-H896
Author(s):  
J. Erlebacher ◽  
J. Kubal ◽  
Z. Zeng ◽  
J. Greeley ◽  
K. Struk ◽  
...  
Keyword(s):  
Monte Carlo ◽  
Monte Carlo Simulations ◽  
Electrochemical Oxidation ◽  
Kinetic Monte Carlo ◽  
Complex Surface ◽  
Surface Roughening ◽  
Morphological Response ◽  
Kinetic Monte Carlo Simulations ◽  
Place Exchange ◽  
The Stability

Kinetic Monte Carlo simulations of electrochemical oxidation and reduction are presented that match many features of the experimentally observed electrochemical and morphological response of Pt(111). Included in the simulation are all relevant microscopic transitions, including the formation of Pt-OH and Pt-O from Pt, surface diffusion of all three species, as well as an effective place exchange diffusion at high potential. A detailed description of this approach to modeling such a complex surface is also presented. Overall, it is found that many features of the Pt(111) CV, including hydroxylation, hysteresis, and surface roughening, can be correlated to events associated with n-coordinated surface species, such as the hydroxylation wave corresponding to a one-electron oxidation of 9-coordinated terrace sites. Oxidation to Pt-O species at potentials above 1.0 V are shown to correlate to the presence of growing surface roughness, and the simulations suggest the onset of Pt-O formation in steady-state cyclic voltammetry is dominated by the oxidation of 8-coordinated step edges rather than terrace sites. Implications for the stability of Pt(111) catalysts after thousands of voltammetric cycles are discussed.

Double exchange model and the unique properties of the manganites

2001 ◽  
Vol 171 (2) ◽  
pp. 121 ◽  
Author(s):  
Yurii A. Izyumov ◽  
Yu.N. Skryabin
Keyword(s):  
Double Exchange ◽  
Exchange Model

ELECTROCHEMICAL OXIDATION OF NITROGEN (II) OXIDE IN THE NEUTRAL MEDIUM

THE BULLETIN ◽  
2019 ◽  
Vol 2 (378) ◽  
Author(s):  
Abduali Baeshov ◽  
Gulnar Aibolova ◽  
Elmira Tuleshova ◽  
M. A. Ozler
Keyword(s):  
Electrochemical Oxidation ◽  
Neutral Medium

Electrochemical Oxidation of Hydrazine in Membraneless Fuel Cells

2014 ◽  
Vol 5 (3) ◽  
pp. 73-81 ◽  
Author(s):  
S. Durga ◽  
K. Ponmani ◽  
S. Kiruthika ◽  
B. Muthukumaran
Keyword(s):  
Fuel Cells ◽  
Electrochemical Oxidation ◽  
Membraneless Fuel Cells

Electrochemical Oxidation of Perfluorooctanesulfonate by Magnéli Phase Ti4O7 Electrode in the Presence of Trichloroethylene

2020 ◽  
Vol 1 (4) ◽  
Author(s):  
Peizeng Yang ◽  
Yaye Wang ◽  
Junhe Lu ◽  
Viktor Tishchenko ◽  
Qingguo Huang ◽  
...  
Keyword(s):  
Electrochemical Oxidation ◽  
Current Density ◽  
First Order ◽  
Degradation Rates ◽  
Oxidation Technology ◽  
Magnéli Phase ◽  
Polyfluoroalkyl Substances ◽  
Titanium Suboxide ◽  
Gas Tight ◽  
Magneli Phase

This study examined the degradation of perfluorooctanesulfonate (PFOS) in electrochemical oxidation (EO) processes in the presence of trichloroethylene (TCE). The EO experiment was performed in a gas-tight reactor using Magnéli phase titanium suboxide (Ti4O7) as the anode. The experimental data demonstrated that 75% of PFOS (2 μM) was degraded at 10 mA/cm2 current density in 30 min without TCE present in the solution, while the presence of 76 μM TCE apparently inhibited the degradation of PFOS, reducing its removal down to 53%. Defluorination ratio suggested that PFOS was significantly mineralized upon EO treatment, and it appeared to be not influenced by the presence of TCE. The respective pseudo-first order rate constants (kobs) of PFOS removal were 0.0471 and 0.0254 min-1 in the absence and presence of TCE. The degradation rates of both PFOS and TCE increased with current density rising from 2.5 to 20 mA/cm2. In the presence of TCE, chloride, chlorate, and perchlorate were formed that accounted for 79.7 %, 5.53%, and 1.51% of the total chlorine at 60 min. This work illustrates the promise of the Magnéli phase Ti4O7 electrode based electrochemical oxidation technology for degrading per- and polyfluoroalkyl substances (PFASs) and co-contaminants in groundwaters.

Electrochemical oxidation of benzothiophenes

1978 ◽  
Vol 43 (8) ◽  
pp. 2015-2023 ◽  
Author(s):  
Jan Šrogl ◽  
Miroslav Janda ◽  
Ivan Stibor ◽  
Jan Kos ◽  
Vlastimil Vyskočil
Keyword(s):  
Electrochemical Oxidation

Properties of electrochemically generated primary cationradicals of phenyl- and 2-(4-tolyl)-1,3,4,7-tetramethylisoindoles

1980 ◽  
Vol 45 (6) ◽  
pp. 1669-1676 ◽  
Author(s):  
Pavel Kubáček
Keyword(s):  
Electrochemical Oxidation ◽  
Spin Polarization ◽  
High Spin ◽  
Epr Spectroscopy ◽  
Half Life ◽  
Electrochemical Behaviour ◽  
Epr Spectra ◽  
Electrochemical Generation ◽  
Splitting Constant ◽  
Reduced Temperature

The first step of electrochemical oxidation of 2-phenyl- and 2-(4-tolyl)-1,3,4,7-tetramethylisoindoles in anhydrous acetonitrile produces relatively stable cationradicals which have been studied by means of EPR spectroscopy using the method of internal electrochemical generation of radicals under reduced temperature. The same electrochemical behaviour of the both studied derivatives and identical EPR spectra of their cationradicals can be explained within the Huckel MO method. The largest contribution to the magnitude of splitting constant of nitrogen nucleus is due to π-σ-spin polarization of C-N bonds caused by high spin abundance of pz-AO of carbon atoms. Half-life of decomposition of the studied cationradicals is 4 min at -30°C.

Anodic voltammetry of pyrazolone derivatives with the help of the self-cleaning rotating electrode

1987 ◽  
Vol 52 (1) ◽  
pp. 66-71 ◽  
Author(s):  
Vesselin C. Noninski ◽  
Emanuel B. Sobowale
Keyword(s):  
Electrochemical Oxidation ◽  
The Self ◽  
Good Reproducibility ◽  
Rotating Electrode ◽  
Pyrazolone Derivatives ◽  
Self Cleaning ◽  
Anodic Voltammetry

Nine pyrazolone derivatives have been studied by anodic voltammetry using gold self-cleaning rotating electrode (SRE). Voltamograms of good reproducibility are presented. On the basis of voltammetric data a mechanism is proposed for the electrochemical oxidation of sodium 1-phenyl-2,3-dimethyl-4-(N-methylamino)pyrazol-5-one-N-methansulphonate and 1-phenyl-2,3-dimethyl-4-(dimethylamino)pyrazol-5-one in protic medium.

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