MnCo2O4 Nanostructure Anchored on Functionalized Carbon Black for the Enhanced Bifunctional Electrocatalytic Performance of OER and HER
ABSTRACT The electrocatalytic oxygen and hydrogen evolution reactions (OER and HER) are key processes used in energy storage and conversion. We have developed a highly efficient MnCo2O4 nanostructure anchored with functionalized carbon black (MnCo2O4/f‐CB), which has been characterized by XRD, FT‐IR...
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Veröffentlicht in: | Luminescence (Chichester, England) England), 2024-12, Vol.39 (12), p.e70052-n/a |
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The electrocatalytic oxygen and hydrogen evolution reactions (OER and HER) are key processes used in energy storage and conversion. We have developed a highly efficient MnCo2O4 nanostructure anchored with functionalized carbon black (MnCo2O4/f‐CB), which has been characterized by XRD, FT‐IR, Raman spectra, FE‐SEM, and HR‐TEM analyses as robust bifunctional electrocatalysts for both HER and OER. At a characteristic 10 mA cm−2 current density, the MnCo2O4/f‐CB composite ECs exhibit low overpotentials of 330 mV for OER and 360 mV for HER, respectively. Furthermore, the MnCo2O4/f‐CB composite ECs exhibit superior current density, the shortest Tafel slope, and admirable durable stability in OER and HER together. Due to the supported f‐CB, the MnCo2O4 composite catalyst has more active sites, effective charge transfer, and longer durability. A high‐efficiency dual electrocatalyst can be developed from these highly efficient and dual ECs, which are comparable to standard noble metal–based catalysts. The synergetic coupling effects of high‐activity f‐CB and MnCo2O4 composites with appropriate morphologies are critical factors for the enhanced catalytic performances of the MnCo2O4/f‐CB composite.
The MnCo2O4/f‐CB composite ECs exhibit superior current density, the shortest Tafel slope, and admirable durable stability in OER and HER together. Due to the supported f‐CB, the MnCo2O4 composite catalyst has more active sites, effective charge transfer, and a longer durability. |
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ISSN: | 1522-7235 1522-7243 1522-7243 |
DOI: | 10.1002/bio.70052 |