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Investigation of MnO(2) and Ordered Mesoporous Carbon Composites as Electrocatalysts for Li-O(2) Battery Applications
The electrocatalytic activities of the MnO(2)/C composites are examined in Li-O(2) cells as the cathode catalysts. Hierarchically mesoporous carbon-supported manganese oxide (MnO(2)/C) composites are prepared using a combination of soft template and hydrothermal methods. The composites are character...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5302531/ https://www.ncbi.nlm.nih.gov/pubmed/28344278 http://dx.doi.org/10.3390/nano6010021 |
Sumario: | The electrocatalytic activities of the MnO(2)/C composites are examined in Li-O(2) cells as the cathode catalysts. Hierarchically mesoporous carbon-supported manganese oxide (MnO(2)/C) composites are prepared using a combination of soft template and hydrothermal methods. The composites are characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy, small angle X-ray scattering, The Brunauer–Emmett–Teller (BET) measurements, galvanostatic charge-discharge methods, and rotating ring-disk electrode (RRDE) measurements. The electrochemical tests indicate that the MnO(2)/C composites have excellent catalytic activity towards oxygen reduction reactions (ORRs) due to the larger surface area of ordered mesoporous carbon and higher catalytic activity of MnO(2). The O(2) solubility, diffusion rates of O(2) and O(2)(•−) coefficients ([Formula: see text] and [Formula: see text]), the rate constant (k(f)) for producing O(2)(•−), and the propylene carbonate (PC)-electrolyte decomposition rate constant (k) of the MnO(2)/C material were measured by RRDE experiments in the 0.1 M TBAPF(6)/PC electrolyte. The values of k(f) and k for MnO(2)/C are 4.29 × 10(−2) cm·s(−1) and 2.6 s(−1), respectively. The results indicate that the MnO(2)/C cathode catalyst has higher electrocatalytic activity for the first step of ORR to produce O(2)(•−) and achieves a faster PC-electrolyte decomposition rate. |
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