化学
质子
电解质
氨
锂(药物)
氨生产
氮气
无机化学
电极
有机化学
物理化学
医学
物理
量子力学
内分泌学
作者
Nikifar Lazouski,Katherine J. Steinberg,Michal L. Gala,Dilip Krishnamurthy,Venkatasubramanian Viswanathan,Karthish Manthiram
出处
期刊:ACS Catalysis
[American Chemical Society]
日期:2022-04-15
卷期号:12 (9): 5197-5208
被引量:119
标识
DOI:10.1021/acscatal.2c00389
摘要
Alternative approaches for producing ammonia are necessary to reduce the environmental impact of its production. The lithium-mediated electrochemical nitrogen reduction reaction (LM-NRR) is one attractive alternative method for producing ammonia at small scales in a distributed process. This process requires a proton donor in the electrolyte to produce ammonia from nitrogen, but the role of the proton donor in selective ammonia production is not well understood. In this work, we experimentally tested several classes of proton donors for the ability to promote LM-NRR. We found that a wide array of alcohols can promote nitrogen reduction and that n -butanol leads to the highest ammonia Faradaic efficiencies. Among the tested proton donors, even slight changes in the proton donor structure can significantly affect the yield of ammonia. In addition, most active proton donors exhibit a thresholding behavior as a function of their concentration, where the selectivity toward ammonia increases dramatically above a certain concentration of the proton donor. We found evidence to imply that these effects could be due to the proton-donor-induced changes in the properties of the solid electrolyte interphase (SEI), which lead to changes in the diffusion of relevant species through the SEI to the reactive electrode. By selectively allowing for diffusion of nitrogen over the proton donor to the electrode, the SEI can promote selective nitrogen reduction to ammonia. A coupled kinetic transport model of the process was proposed to explain the observed trends and to predict ammonia production as a function of operating conditions.
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