电化学
电解质
锂(药物)
电极
氧化还原
化学
电流密度
参比电极
氨
离子
能量密度
电流(流体)
无机化学
化学物理
热力学
工程物理
物理化学
内分泌学
工程类
有机化学
物理
医学
量子力学
作者
Romain Tort,Olivia Westhead,Matthew Spry,Bethan J. V. Davies,Mary P. Ryan,Maria‐Magdalena Titirici,Ifan E. L. Stephens
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-01-18
卷期号:8 (2): 1003-1009
被引量:28
标识
DOI:10.1021/acsenergylett.2c02697
摘要
The performance of the Li-mediated ammonia synthesis has progressed dramatically since its recent reintroduction. However, fundamental understanding of this reaction is slower paced, due to the many uncontrolled variables influencing it. To address this, we developed a true nonaqueous LiFePO4 reference electrode, providing both a redox anchor from which to measure potentials against and estimates of sources of energy efficiency loss. We demonstrate its stable electrochemical potential in operation using different N2- and H2-saturated electrolytes. Using this reference, we uncover the relation between partial current density and potentials. While the counter electrode potential increases linearly with current, the working electrode remains stable at lithium plating, suggesting it to be the only electrochemical step involved in this process. We also use the LiFePO4/Li+ equilibrium as a tool to probe Li-ion activity changes in situ. We hope to drive the field toward more defined systems to allow a holistic understanding of this reaction.
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