钝化
电解质
锂(药物)
氨
电化学
透射电子显微镜
材料科学
反应性(心理学)
无机化学
化学
化学工程
纳米技术
图层(电子)
电极
有机化学
医学
替代医学
物理化学
病理
内分泌学
工程类
作者
Katherine Steinberg,Xintong Yuan,Nikifar Lazouski,Channing K. Klein,Karthish Manthiram,Yuzhang Li
标识
DOI:10.26434/chemrxiv-2022-9v3nw
摘要
Electrifying ammonia synthesis will be vital to the decarbonization of the chemical industry, as the Haber-Bosch process contributes significantly to global carbon emissions. A lithium-mediated pathway is among the most promising ambient-condition electrochemical ammonia synthesis methods. However, the role of metallic lithium and its passivation layer, the solid electrolyte interphase (SEI), remains unresolved. Here, we apply a multiscale approach that leverages the powerful cryogenic transmission electron microscopy (cryo-TEM) technique to reveal new insights that were previously inaccessible with conventional methods. We discover that the proton donor (e.g. ethanol) governs lithium reactivity toward nitrogen fixation. Without ethanol, the SEI passivates lithium metal, rendering it inactive for ammonia production. Ethanol disrupts this passivation layer, enabling continuous reactivity at the lithium surface. As a result, metallic lithium is consumed via reactions with nitrogen, proton donor, and other electrolyte components. This reactivity across the SEI is vital to device-level performance of lithium-mediated ammonia synthesis.
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