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用于氨合成的锂介导氮还原中的局部高浓度电解质

Localized High-Concentration Electrolyte in Li-Mediated Nitrogen Reduction for Ammonia Synthesis.

作者信息

Yun Hyeju, Lim Chaeeun, Kwon Minjun, Lee Dongmin, Yun Yongju, Seo Dong-Hwa, Yong Kijung

机构信息

Surface Chemistry Laboratory of Electronic Materials (SCHEMA), Department of Chemical Engineering, Pohang University of Science and Technology (POSTECH), Pohang, 37673, South Korea.

Research Center for Carbon-zero Green Ammonia Cycling, Pohang University of Science and Technology (POSTECH), Pohang, 37673, Republic of Korea.

出版信息

Adv Mater. 2024 Dec;36(49):e2408280. doi: 10.1002/adma.202408280. Epub 2024 Oct 21.

Abstract

The lithium-mediated nitrogen reduction reaction (Li-NRR) is a promising green alternative to the Haber-Bosch process for ammonia synthesis. The solid electrolyte interphase (SEI) is crucial for high efficiency and stability, as it regulates reactant diffusion and suppresses side reactions. The SEI properties are greatly influenced by the Li ion solvation structure, which is controllable through electrolyte engineering. Although anion-derived SEI enhances selectivity and stability, it has typically been engineered using high-concentration electrolytes (HCEs), which face mass transfer, viscosity, and cost issues. In this study, a localized high-concentration electrolyte (LHCE) in the Li-NRR is first introduced, enabling the formation of anion-derived SEI in a low-concentration electrolyte (LCE) by enhancing the Li-anion coordination using an antisolvent. Among various antisolvents, 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (TTE) achieves the highest ammonia Faradaic efficiency (73.6 ± 2.5%), more than double that of the LCE (34.3 ± 2.8%) and exceeding the HCE (56.0 ± 2.8%). Systematic calculations and experimental analyses show that the LHCE exhibits anion-rich solvation structures and forms thin, inorganic SEI. Moreover, the LHCE has advantages of low viscosity and high N solubility, which facilitate mass transport. This study suggests the application of LHCE as an effective electrolyte engineering strategy to enhance the Li-NRR efficiency.

摘要

锂介导的氮还原反应(Li-NRR)是一种有前景的绿色替代哈伯-博施法合成氨的方法。固体电解质界面(SEI)对于高效率和稳定性至关重要,因为它调节反应物扩散并抑制副反应。SEI的性质受锂离子溶剂化结构的极大影响,而锂离子溶剂化结构可通过电解质工程来控制。尽管阴离子衍生的SEI提高了选择性和稳定性,但通常是使用高浓度电解质(HCEs)来设计的,而高浓度电解质面临传质、粘度和成本问题。在本研究中,首次在Li-NRR中引入了局部高浓度电解质(LHCE),通过使用抗溶剂增强锂-阴离子配位,从而在低浓度电解质(LCE)中形成阴离子衍生的SEI。在各种抗溶剂中,1,1,2,2-四氟乙基-2,2,3,3-四氟丙醚(TTE)实现了最高的氨法拉第效率(73.6±2.5%),是LCE(34.3±2.8%)的两倍多,且超过了HCE(56.0±2.8%)。系统的计算和实验分析表明,LHCE呈现出富阴离子的溶剂化结构并形成薄的无机SEI。此外,LHCE具有低粘度和高氮溶解度的优点,有利于传质。本研究表明,LHCE作为一种有效的电解质工程策略可用于提高Li-NRR效率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/71af/11619219/c45949781370/ADMA-36-2408280-g005.jpg

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