Synergistic In-Layer Cobalt Doping and Interlayer Iron Intercalation into Layered MnO2 Produces an Efficient Water Oxidation Electrocatalyst AITranslate
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Described is a synthetic method to enhance the electrocatalytic activity of the layered manganese oxide, birnessite, for the oxygen evolution reaction (OER) through the development of a Mn/Co/Fe ternary phase. The ternary phase was synthesized by the simultaneous doping of Co3+ into the manganese oxide lattice and intercalation of Fe2+ within the interlayer region of birnessite (KxFe[Co0.16Mn0.84O2]). The material was characterized by X-ray diffractometry, electron microscopy, X-ray photoelectron, energy dispersive, and Raman spectroscopies and electrochemical analysis. The KxFe[Co0.16Mn0.84O2] material demonstrated efficient OER electrocatalysis with an overpotential (η) of 375 mV (at 10 mA/cm2) and Tafel slope (b) of 56 mV/dec, surpassing the catalytic activity of both standard potassium birnessite (η ≈ 800 mV, b = 240 mV/dec) and cobalt-doped birnessite with a Co:Mn ratio of 1:5 (η ≈ 750 mV, b = 230 mV/dec) and with a catalytic lifetime 150-fold greater than that of standard birnessite and 100-fold greater than that of the iron-free cobalt-doped birnessite at 5 mA/cm2.
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DOI:https://doi.org/10.1021/acsenergylett.8b01217
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Described is a synthetic method to enhance the electrocatalytic activity of the layered manganese oxide, birnessite, for the oxygen evolution reaction (OER) through the development of a Mn/Co/Fe ternary phase. The ternary phase was synthesized by the simultaneous doping of Co3+ into the manganese oxide lattice and intercalation of Fe2+ within the interlayer region of birnessite (KxFe[Co0.16Mn0.84O2]). The material was characterized by X-ray diffractometry, electron microscopy, X-ray photoelectron, energy dispersive, and Raman spectroscopies and electrochemical analysis. The KxFe[Co0.16Mn0.84O2] material demonstrated efficient OER electrocatalysis with an overpotential (η) of 375 mV (at 10 mA/cm2) and Tafel slope (b) of 56 mV/dec, surpassing the catalytic activity of both standard potassium birnessite (η ≈ 800 mV, b = 240 mV/dec) and cobalt-doped birnessite with a Co:Mn ratio of 1:5 (η ≈ 750 mV, b = 230 mV/dec) and with a catalytic lifetime 150-fold greater than that of standard birnessite and 100-fold greater than that of the iron-free cobalt-doped birnessite at 5 mA/cm2.
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| GB/T 7714-2015 | [1] Ian G. McKendry, Loveyy J. Mohamad, Akila C. Thenuwara, et al. ACS Energy Letters, 2018(3). DOI:10.1021/acsenergylett.8b01217. |
| MLA | [1] Ian G. McKendry, et al., ACS Energy Letters, no. 3, 2018, https://doi.org/10.1021/acsenergylett.8b01217. |
| APA | [1] Ian G. McKendry, Loveyy J. Mohamad, Akila C. Thenuwara, Tim Marshall, Eric Borguet, Daniel R. Strongin, & Michael J. Zdilla. (2018). ACS Energy Letters(3). https://doi.org/10.1021/acsenergylett.8b01217 |
| IEEE | [1] Ian G. McKendry, Loveyy J. Mohamad, Akila C. Thenuwara, Tim Marshall, Eric Borguet, Daniel R. Strongin, and Michael J. Zdilla, ACS Energy Letters, no. 3, 2018, doi: 10.1021/acsenergylett.8b01217. |
