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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Murtomäki, Lasse
Aalto University
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (4/4 displayed)
- 2018Time-Dependent Behavior of Cation Transport through Cellulose Acetate-Cationic Polyelectrolyte Membranescitations
- 2017Determination of physical emulsion stabilization mechanisms of wood hemicelluloses via rheological and interfacial characterizationcitations
- 2017Simulation of electrochemical processes during oxygen evolution on Pb-MnO2 composite electrodescitations
- 2016Determination of physical emulsion stabilization mechanisms of wood hemicellulosescitations
Places of action
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article
Simulation of electrochemical processes during oxygen evolution on Pb-MnO2 composite electrodes
Abstract
<p>The geometric properties of Pb-MnO<sub>2</sub> composite electrodes are studied, and a general formula is presented for the length of the triple phase boundary (TPB) on two dimensional (2D) composite electrodes using sphere packing and cutting simulations. The difference in the geometrical properties of 2D (or compact) and 3D (or porous) electrodes is discussed. It is found that the length of the TPB is the only reasonable property of a 2D electrode that follows a 1/r particle radius relationship. Subsequently, sphere packing cuts are used to derive a statistical electrode surface that is the basis for the earlier proposed simulations of different electrochemical mechanisms. It is shown that two of the proposed mechanisms (conductivity and a two-step-two-material kinetic mechanism) can explain the current increase at Pb-MnO<sub>2</sub> anodes compared to standard lead anodes. The results show that although MnO<sub>2</sub> has low conductivity, when combined with Pb as the metal matrix, the behaviour of the composite is not purely ohmic but is also affected by activation overpotentials, increasing the current density close to the TPB. Current density is inversely proportional to the radius of the catalyst particles, matching with earlier experimental results. Contrary to earlier SECM experiments, mass transport of sulphuric acid is not likely to have any influence, as confirmed with simulations. A hypothetical two-step-two-material mechanism with intermediate H<sub>2</sub>O<sub>2</sub> that reacts on both the Pb matrix and MnO<sub>2</sub> catalyst is studied. It was found that assuming quasi-reversible generation of H<sub>2</sub>O<sub>2</sub> followed by its chemical decomposition on MnO<sub>2</sub>, results are obtained that agree with the experiments. If the quasi-reversible formation of H<sub>2</sub>O<sub>2</sub> occurs near the peroxide decomposition catalyst, current increases, leading to an active TPB and to the current density that scales with 1/r. It is further emphasised that both the Pb matrix and MnO<sub>2</sub> catalyst are necessary and their optimum ratio depends on the used current density. Yet, additional experimental evidence is needed to support the postulated mechanism.</p>