The impact mechanism of Mn2+ ions on oxygen evolution reaction in zinc sulfate electrolyte
The impact mechanism of Mn2+ on the oxygen evolution reaction (OER) on the fresh lead-based anode in zinc sulfate electrolyte has been studied in detail by several electrochemical methods, XRD, SEM and EDX. The kinetics analysis suggested that the Mn2+ could significantly enhance OER, which was cont...
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Published in | Journal of electroanalytical chemistry (Lausanne, Switzerland) Vol. 811; pp. 53 - 61 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
15.02.2018
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Online Access | Get full text |
ISSN | 1572-6657 1873-2569 |
DOI | 10.1016/j.jelechem.2018.01.040 |
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Abstract | The impact mechanism of Mn2+ on the oxygen evolution reaction (OER) on the fresh lead-based anode in zinc sulfate electrolyte has been studied in detail by several electrochemical methods, XRD, SEM and EDX. The kinetics analysis suggested that the Mn2+ could significantly enhance OER, which was controlled by the electron transfer process between the active site S and H2O (step (2)). This positive effect of Mn2+ on OER was limited with the increase of Mn2+ because of the approaching saturation of active sites. Results obtained from the Arrhenius equation disclosed the larger bond strength of MnO2-OH in decreasing the activation energy of OER (from 55.08 to 47.04 kJ/mol), meanwhile, it also further supported the fact that the OER was electrochemical-controlled and it would not be changed in essence with the addition of Mn2+, which is subject to the activation energy barrier of electron transfer induced by the active site S (step (2)). EIS data revealed adsorption resistance of the intermediate (S-OHads), Ra played a major role among the whole reaction resistance, whereas, the impact contribution of charge transfer resistance, Rt became larger as the Mn2+ increases, which revealed that the inhibition of electron transfer process due to the changes of the anode surface microstructure. Electron microscope technology suggested the key role Mn2+ played in the modification of the active interface structure, and its influence process on OER was revealed by the microstructure analysis of anode surface. Considering the potential of Mn2+ concentration optimization in reducing heavy metal pollutants and energy consumption, enhancing the understanding of impact mechanism of Mn2+ on OER provides a feasible proposal in zinc electrolysis industry. |
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AbstractList | The impact mechanism of Mn2+ on the oxygen evolution reaction (OER) on the fresh lead-based anode in zinc sulfate electrolyte has been studied in detail by several electrochemical methods, XRD, SEM and EDX. The kinetics analysis suggested that the Mn2+ could significantly enhance OER, which was controlled by the electron transfer process between the active site S and H2O (step (2)). This positive effect of Mn2+ on OER was limited with the increase of Mn2+ because of the approaching saturation of active sites. Results obtained from the Arrhenius equation disclosed the larger bond strength of MnO2-OH in decreasing the activation energy of OER (from 55.08 to 47.04 kJ/mol), meanwhile, it also further supported the fact that the OER was electrochemical-controlled and it would not be changed in essence with the addition of Mn2+, which is subject to the activation energy barrier of electron transfer induced by the active site S (step (2)). EIS data revealed adsorption resistance of the intermediate (S-OHads), Ra played a major role among the whole reaction resistance, whereas, the impact contribution of charge transfer resistance, Rt became larger as the Mn2+ increases, which revealed that the inhibition of electron transfer process due to the changes of the anode surface microstructure. Electron microscope technology suggested the key role Mn2+ played in the modification of the active interface structure, and its influence process on OER was revealed by the microstructure analysis of anode surface. Considering the potential of Mn2+ concentration optimization in reducing heavy metal pollutants and energy consumption, enhancing the understanding of impact mechanism of Mn2+ on OER provides a feasible proposal in zinc electrolysis industry. |
Author | Jiang, Linhua Duan, Ning Xu, Fuyuan Zhang, Chenmu |
Author_xml | – sequence: 1 givenname: Chenmu surname: Zhang fullname: Zhang, Chenmu organization: School of Materials Science and Engineering, Beijing Institute of Technology, Beijing 100081, China – sequence: 2 givenname: Ning surname: Duan fullname: Duan, Ning organization: Technology Center for Heavy Metal Cleaner Production Engineering, Chinese Research Academy of Environmental Sciences, Beijing 100012, China – sequence: 3 givenname: Linhua surname: Jiang fullname: Jiang, Linhua email: jlhcraes@163.com organization: Technology Center for Heavy Metal Cleaner Production Engineering, Chinese Research Academy of Environmental Sciences, Beijing 100012, China – sequence: 4 givenname: Fuyuan surname: Xu fullname: Xu, Fuyuan email: fuyuanxu@hotmail.com organization: Technology Center for Heavy Metal Cleaner Production Engineering, Chinese Research Academy of Environmental Sciences, Beijing 100012, China |
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Keywords | Energy consumption Heavy metal pollutants Mn2+ ions Oxygen evolution reaction Activation energy |
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Snippet | The impact mechanism of Mn2+ on the oxygen evolution reaction (OER) on the fresh lead-based anode in zinc sulfate electrolyte has been studied in detail by... |
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SubjectTerms | Activation energy Energy consumption Heavy metal pollutants Mn2+ ions Oxygen evolution reaction |
Title | The impact mechanism of Mn2+ ions on oxygen evolution reaction in zinc sulfate electrolyte |
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