Development of a 3D Ni-Mn binary oxide anode for energy-efficient electro-oxidation of organic pollutants
At a Glance
Section titled āAt a Glanceā| Metadata | Details |
|---|---|
| Publication Date | 2024-03-20 |
| Journal | Journal of environmental chemical engineering |
| Authors | Keyvan Mirehbar, Jaime S. SƔnchez, Sergio Pinilla, F. Palacio, Ignasi SirƩs |
| Institutions | IMDEA Energy Institute, Universitat de Barcelona |
| Citations | 4 |
Abstract
Section titled āAbstractāThe depletion of clean water resources and the consequent accumulation of contaminants in aquatic systems must be urgently addressed by means of innovative solutions. Electro-oxidation (EO) is considered a promising technology, prized for its versatility and eco-friendliness. However, the excessively high prices and the toxicity associated with some of the materials currently employed for EO impede its broader application. This study introduces cost-effective Ni-Mn binary oxide anodes prepared on Ni foam (NF) substrate. A scalable synthesis route that enables a 35-fold increase in the production of active material through a single optimization step has been devised. The synthesized binary oxide material underwent electrochemical characterization, and its effectiveness was assessed in an electrochemical flow-through cell, benchmarked against single Ni or Mn oxides and more conventional alternatives like boron-doped diamond (BDD) and dimensionally-stable anode (DSA). The novel binary oxide anode demonstrated exceptional performance, achieving complete removal of phenol at very low current density of 5 mA cm-2, along with an 80% of chemical oxygen demand (COD) decay within only 60 min. The NF/NiMnO3 anode outperformed the BDD and DSA when using comparable projected surface areas, owing to its high porosity and ability to produce hydroxyl radicals, as confirmed from the degradation profiles in the presence of radical scavengers. Furthermore, GC/MS analysis served to elucidate the degradation pathways of phenol.
Tech Support
Section titled āTech SupportāOriginal Source
Section titled āOriginal SourceāReferences
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