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Intercalation of Magnesium into a Layered Vanadium Oxide with High Capacity AITranslate

Pusan National University; University of Illinois at Chicago;Advanced Light Source, Lawrence Berkeley National Lab; University of Illinois at Chicago; University of Illinois at Chicago; Argonne National Laboratory; Argonne National Laboratory; University of Illinois at Chicago; Argonne National Laboratory; University of Illinois at Chicago; Argonne National Laboratory; University of Illinois at Chicago; Argonne National Laboratory; University of Illinois at Chicago; Argonne National Laboratory; Argonne National Laboratory; University of Illinois at Chicago
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Publisher: ACS
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Abstract AITranslate

While α-V2O5 has traditionally been considered as a promising oxide to reversibly intercalate high levels of Mg2+ at high potential, recent reports indicate that previously observed electrochemical activity is dominated by intercalation of H+ rather than Mg2+, even in moderately dry nonaqueous electrolytes. Consequently, the inherent functionality of oxides to intercalate Mg2+ remains in question. By conducting electrochemistry in a chemically and anodically stable ionic liquid electrolyte, we report that, at 110 °C, layered α-V2O5 is indeed capable of reversibly intercalating 1 mol Mg2+ per unit formula, to accumulate capacities above 280 mAh g–1. Multimodal characterization confirmed intercalation of Mg2+ by probing the elemental, redox, and morphological changes undergone by the oxide. After cycling at 110 °C, the electrochemical activity at room temperature was significantly enhanced. The results renew prospects for functional Mg rechargeable batteries surpassing the levels of energy density of current Li-ion batteries.

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DOI:https://doi.org/10.1021/acsenergylett.9b00788

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Citation Information:

While α-V2O5 has traditionally been considered as a promising oxide to reversibly intercalate high levels of Mg2+ at high potential, recent reports indicate that previously observed electrochemical activity is dominated by intercalation of H+ rather than Mg2+, even in moderately dry nonaqueous electrolytes. Consequently, the inherent functionality of oxides to intercalate Mg2+ remains in question. By conducting electrochemistry in a chemically and anodically stable ionic liquid electrolyte, we report that, at 110 °C, layered α-V2O5 is indeed capable of reversibly intercalating 1 mol Mg2+ per unit formula, to accumulate capacities above 280 mAh g–1. Multimodal characterization confirmed intercalation of Mg2+ by probing the elemental, redox, and morphological changes undergone by the oxide. After cycling at 110 °C, the electrochemical activity at room temperature was significantly enhanced. The results renew prospects for functional Mg rechargeable batteries surpassing the levels of energy density of current Li-ion batteries.

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GB/T 7714-2015 [1] Hyun Deog Yoo, Jacob R. Jokisaari, YoungSang Yu, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.9b00788.
MLA [1] Hyun Deog Yoo, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.9b00788.
APA [1] Hyun Deog Yoo, Jacob R. Jokisaari, YoungSang Yu, Bob Jin Kwon, Linhua Hu, Soojeong Kim, SangDon Han, Mario Lopez, Saul H. Lapidus, Gene M. Nolis, Brian J. Ingram, Igor Bolotin, Shabbir Ahmed, Robert F. Klie, John T. Vaughey, Timothy T. Fister, & Jordi Cabana. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.9b00788
IEEE [1] Hyun Deog Yoo, Jacob R. Jokisaari, YoungSang Yu, Bob Jin Kwon, Linhua Hu, Soojeong Kim, SangDon Han, Mario Lopez, Saul H. Lapidus, Gene M. Nolis, Brian J. Ingram, Igor Bolotin, Shabbir Ahmed, Robert F. Klie, John T. Vaughey, Timothy T. Fister, and Jordi Cabana, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.9b00788.