Effect of Lithium Salt on Lithium-Mediated Ammonia Synthesis
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Recently, the lithium-mediated nitrogen reduction reaction (Li-NRR) has emerged as a promising approach for electrochemical ammonia synthesis, facilitating more localized production. However, the systematic investigation of lithium salts in this process, especially when coupled with a hydrogen oxidation reaction (HOR) at the anode side in a continuous-flow reactor, remains largely underexplored. This study systematically investigates the effects of various lithium salts on Li-NRR selectivity and efficiency in a continuous-flow reactor coupled with the HOR at the anode. Among the evaluated salts, lithium tetrafluoroborate (LiBF 4 ) demonstrated the highest NH 3 selectivity of 61% under ambient conditions. Conversely, lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) showed a significantly lower Faradaic efficiency (FE) of 18%, due to its decomposition and subsequent sulfur poisoning of the HOR catalysts. These findings highlight the importance of selecting appropriate lithium salts and establishing critical design principles for more efficient and stable electrolytes for Li-NRR and advancing sustainable ammonia synthesis.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Caching and Content Delivery · Hydrogen Storage and Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physics, Technical University of Denmark, 2800 Kongens Lyngby, Denmark
Funding
HORIZON EUROPE Marie Sklodowska-Curie Actions · Villum Fonden
References (37)
Show source-provided references
1. 10.1038/ngeo32510.1038/ngeo325 ↗
2. 10.1038/s43586-021-00053-y10.1038/s43586-021-00053-y ↗
3. 10.1126/science.abl430010.1126/science.abl4300 ↗
4. 10.1021/acscatal.6b0303510.1021/acscatal.6b03035 ↗
5. 10.1038/s41586-019-1260-x10.1038/s41586-019-1260-x ↗
6. 10.1038/s41467-020-19130-z10.1038/s41467-020-19130-z ↗
7. 10.1038/s41563-023-01702-110.1038/s41563-023-01702-1 ↗
8. 10.1002/hlca.1930013060410.1002/hlca.19300130604 ↗
9. 10.1246/cl.1993.85110.1246/cl.1993.851 ↗
10. 10.1016/0022-0728(93)03025-K10.1016/0022-0728(93)03025-K ↗
11. 10.1016/j.joule.2019.02.00310.1016/j.joule.2019.02.003 ↗
12. 10.1016/j.isci.2021.10310510.1016/j.isci.2021.103105 ↗
13. 10.1021/acsenergylett.1c0210410.1021/acsenergylett.1c02104 ↗
14. 10.1016/j.joule.2022.07.00910.1016/j.joule.2022.07.009 ↗
15. 10.1038/s41586-022-05108-y10.1038/s41586-022-05108-y ↗
16. 10.1126/science.adf440310.1126/science.adf4403 ↗
17. 10.1038/s41467-024-46803-w10.1038/s41467-024-46803-w ↗
18. 10.1039/D0EE02246B10.1039/D0EE02246B ↗
19. 10.1038/s41586-024-07276-510.1038/s41586-024-07276-5 ↗
20. 10.1039/D3EE04235A10.1039/D3EE04235A ↗
21. 10.1038/s41929-020-0455-810.1038/s41929-020-0455-8 ↗
22. 10.1021/acscatal.2c0053810.1021/acscatal.2c00538 ↗
23. 10.1007/s10692-011-9256-910.1007/s10692-011-9256-9 ↗
24. 10.1016/j.jpowsour.2006.03.05810.1016/j.jpowsour.2006.03.058 ↗
25. 10.1002/(SICI)1097-4628(19980718)69:3<611::AID-APP21>3.0.CO;2-U10.1002/(SICI)1097-4628(19980718)69:3<611::AID-APP21>3.0.CO;2-U ↗
26. 10.1255/ejms.74210.1255/ejms.742 ↗
27. 10.1016/j.mser.2018.07.00110.1016/j.mser.2018.07.001 ↗
28. 10.1039/D2EE03901J10.1039/D2EE03901J ↗
29. 10.1021/acsami.1c1890510.1021/acsami.1c18905 ↗
30. 10.1021/acsaem.2c0228410.1021/acsaem.2c02284 ↗
31. 10.1016/j.electacta.2010.05.00410.1016/j.electacta.2010.05.004 ↗
32. 10.1021/acsenergylett.2c0158710.1021/acsenergylett.2c01587 ↗
33. 10.1149/2.0901802jes10.1149/2.0901802jes ↗
34. 10.1039/C4TA00214H10.1039/C4TA00214H ↗
35. 10.1016/j.jpowsour.2006.12.05210.1016/j.jpowsour.2006.12.052 ↗
36. 10.1016/j.tetlet.2021.15314610.1016/j.tetlet.2021.153146 ↗
37. 10.1002/cssc.20230101110.1002/cssc.202301011 ↗