Origin of chronoamperometric responses associated with impacts of single electrolyte droplets at a polarized liquid/liquid interface
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388955%3A_____%2F20%3A00531040" target="_blank" >RIV/61388955:_____/20:00531040 - isvavai.cz</a>
Výsledek na webu
<a href="http://hdl.handle.net/11104/0309797" target="_blank" >http://hdl.handle.net/11104/0309797</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.electacta.2020.136653" target="_blank" >10.1016/j.electacta.2020.136653</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Origin of chronoamperometric responses associated with impacts of single electrolyte droplets at a polarized liquid/liquid interface
Popis výsledku v původním jazyce
Chronoamperometric measurements at a constant potential are used to study the single impacts of the water-in-DCE emulsion droplets containing an electrolyte (tetrapropylammonium chloride, TPrACl) at a polarized water(W)/1,2-dichloroethane (DCE) interface. The impacts give rise to the spike-like current transients, which are characterized by the initial current step (time constant less than 2 ms) followed by a slower exponential current decay with a time constant in tens of milliseconds. It is shown that the theoretical treatment of the current spikes can be based on a modification of the bulk electrolysis model including (1) the droplet collision at the W/DCE interface, (2) a partial coalescence (fusion) of the droplet with the impacted interface, (3) a reorganization of the electric double layer leading to the propagation of the interfacial potential difference from the impacted interface to the surface of the droplet, and (4) stripping (bulk electrolysis) of TPrA+ from the droplet to the DCE phase accompanied by the chloride depletion into the bulk water phase. On assuming that the stripping of TPrA+ is the rate-determining step of the impact event, the theoretical relationships for the current transient are derived, which are confirmed by the experimental data. An analysis of the current transients yields the charge corresponding to the ionic content of the droplets, which is used to evaluate the droplet diameter. Droplet size distribution with the droplet diameter of around 8 μm is verified by an analysis of the microscopic images of the W-in-DCE emulsion, and in part also by the dynamic laser scattering measurements. It is shown that the frequency of the droplet collisions with the W/DCE interface (1–10 Hz) is controlled by migration of the negatively charged droplets towards the interface.
Název v anglickém jazyce
Origin of chronoamperometric responses associated with impacts of single electrolyte droplets at a polarized liquid/liquid interface
Popis výsledku anglicky
Chronoamperometric measurements at a constant potential are used to study the single impacts of the water-in-DCE emulsion droplets containing an electrolyte (tetrapropylammonium chloride, TPrACl) at a polarized water(W)/1,2-dichloroethane (DCE) interface. The impacts give rise to the spike-like current transients, which are characterized by the initial current step (time constant less than 2 ms) followed by a slower exponential current decay with a time constant in tens of milliseconds. It is shown that the theoretical treatment of the current spikes can be based on a modification of the bulk electrolysis model including (1) the droplet collision at the W/DCE interface, (2) a partial coalescence (fusion) of the droplet with the impacted interface, (3) a reorganization of the electric double layer leading to the propagation of the interfacial potential difference from the impacted interface to the surface of the droplet, and (4) stripping (bulk electrolysis) of TPrA+ from the droplet to the DCE phase accompanied by the chloride depletion into the bulk water phase. On assuming that the stripping of TPrA+ is the rate-determining step of the impact event, the theoretical relationships for the current transient are derived, which are confirmed by the experimental data. An analysis of the current transients yields the charge corresponding to the ionic content of the droplets, which is used to evaluate the droplet diameter. Droplet size distribution with the droplet diameter of around 8 μm is verified by an analysis of the microscopic images of the W-in-DCE emulsion, and in part also by the dynamic laser scattering measurements. It is shown that the frequency of the droplet collisions with the W/DCE interface (1–10 Hz) is controlled by migration of the negatively charged droplets towards the interface.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
10405 - Electrochemistry (dry cells, batteries, fuel cells, corrosion metals, electrolysis)
Návaznosti výsledku
Projekt
<a href="/cs/project/GA20-01589S" target="_blank" >GA20-01589S: Nové strategie pro zlepšení senzorových vlastností nových elektrodových materiálů prostřednictvím jejich předúpravy či modifikace povrchu</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2020
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Electrochimica acta
ISSN
0013-4686
e-ISSN
—
Svazek periodika
354
Číslo periodika v rámci svazku
SEP 2020
Stát vydavatele periodika
GB - Spojené království Velké Británie a Severního Irska
Počet stran výsledku
8
Strana od-do
136653
Kód UT WoS článku
000569140400006
EID výsledku v databázi Scopus
2-s2.0-85086891141