Scanning electrochemical microscopy study of ion transfer process across water/2-nitrophenyloctylether interface supported by hydrophobic carbon ceramic electrode
“…Such possibility was investigated earlier by scanning electrochemical microscopy experiments [28]. For this process E DMFc þ =DMFc can be described by following equation [25]:…”
Section: Electrochemistry Of Dmfc Dissolved In 12-dichlorobenzene LImentioning
“…Such possibility was investigated earlier by scanning electrochemical microscopy experiments [28]. For this process E DMFc þ =DMFc can be described by following equation [25]:…”
Section: Electrochemistry Of Dmfc Dissolved In 12-dichlorobenzene LImentioning
“…takes place . Because the NPOE phase does not initially contain the supporting electrolyte, Reaction (4) is likely to occur at a three‐phase junction between the carbon particle, NPOE, and the aqueous phase .…”
Section: Resultsmentioning
confidence: 99%
“…(4) takes place. [35,37,40] Because the NPOE phase does not initially contain the supporting electrolyte, Reaction (4) is likely to occur at at hree-phase junctionb etween the carbonp article, NPOE,a nd the aqueous phase. [35] Otherwise, if the carbonp article facing the aqueous electrolyte is covered by at hin NPOE film, the electron transfer step should occur at the carbonp article-NPOE interface with simultaneous ion transfer across the NPOE-water interface.…”
Here, we report hydrogen peroxide generation at the 2‐nitrophenyloctyl ether (NPOE)/water interface with decamethylferrocene as an electron donor. The progress of this reaction was detected by the observation of a color change in the organic and aqueous phases in a series of shake‐flask experiments. The shape change in cyclic voltammograms recorded at a carbon‐paste electrode with decamethylferrocene in NPOE also indicates a (electro)catalytic reaction. Hydrogen peroxide was electrochemically detected at a Pt microelectrode tip positioned next to the carbon‐paste electrode. For this purpose, scanning electrochemical microscopy (SECM) approach curves were recorded. Analogous experiments demonstrated the possibility of electrochemical regeneration of the electron donor. The (electro)catalytic effect of MoS2 on hydrogen peroxide generation was found by using both shake‐flask and SECM experiments.
“…Cyclic voltammogram of electrode shielded with DMFc solution recorded after incubation in solution of trypsin (MW 23.3 kDa) displays just one set of current peaks corresponding to single electron redox process. This peculiar shape of voltammogramm corresponding to expulsion of DMFc + cathion from organic phase [34][35][36] appeared at second cycle and was unstable.…”
Section: Electrochemistry Of Protein Extracting Electrodesmentioning
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