journal article·2022-04

Interfacial Microextraction Boosting Nitrogen Feed for Efficient Ambient Ammonia Synthesis in Aqueous Electrolyte

Xiaowei Shen, Sisi Liu, Xinyao Xia, Mengfan Wang, Haoqing Ji, Zhenkang Wang, Jie Liu, Xinsong Zhang, Chenglin Yan, Tao Qian

Advanced Functional Materials· Volume 32· Issue 17
Publisher page

Abstract

Abstract The extremely low nitrogen (N2) solubility in aqueous solution greatly limits the gas reactant supply to catalysts resulting in a bottleneck in establishing efficient electrocatalytic N2 reduction reaction (NRR). Here, aiming at fairly few N2 dissolving in aqueous electrolyte, an N2‐microextractor (NME) that can extract the N2 from water, then feed it to catalysts on electrodes, is reported. The NME consists of polymer framework and extractant that possess high solubility for N2, which serves as an ultra‐thin interfacial system wrapping around electrodes. As expected, the enhancement of N2 supply in NRR leads to a record‐high Faradaic efficiency (80.1%) with an ammonia yield rate of 58.3 µg h−1 mg−1 under ambient conditions. This is of great significance to a sustainable “Ammonia Economy.”
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Ammonia Synthesis and Nitrogen Reduction · Advanced Photocatalysis Techniques · Caching and Content Delivery

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Electrical Engineering Nantong University Nantong 226019 China

College of Energy Key Laboratory of Core Technology of High Specific Energy Battery and Key Materials for Petroleum and Chemical Industry Soochow University Suzhou 215006 China

School of Chemistry and Chemical Engineering Nantong University Nantong 226019 China

Funding

National Natural Science Foundation of China · Natural Science Foundation of Jiangsu Province

References (31)

Show source-provided references
1. 10.1038/nature1524610.1038/nature15246 ↗
2. 10.1021/acscatal.8b0380210.1021/acscatal.8b03802 ↗
3. 10.1002/adfm.20200124410.1002/adfm.202001244 ↗
4. 10.1016/j.joule.2018.04.01410.1016/j.joule.2018.04.014 ↗
5. 10.1038/s41929-019-0252-410.1038/s41929-019-0252-4 ↗
6. 10.1038/s41929-018-0092-710.1038/s41929-018-0092-7 ↗
7. 10.1093/nsr/nwaa13610.1093/nsr/nwaa136 ↗
8. 10.1021/acs.chemrev.9b0022010.1021/acs.chemrev.9b00220 ↗
9. 10.1021/j100783a02810.1021/j100783a028 ↗
10. 10.1038/s41929-021-00599-w10.1038/s41929-021-00599-w ↗
11. 10.1002/cssc.20150032210.1002/cssc.201500322 ↗
12. 10.1021/acscatal.9b0036610.1021/acscatal.9b00366 ↗
13. 10.1021/acsenergylett.8b0048710.1021/acsenergylett.8b00487 ↗
14. 10.1038/s41467-021-23360-010.1038/s41467-021-23360-0 ↗
15. 10.1039/C1CP22271F10.1039/C1CP22271F ↗
16. 10.1038/s41467-018-08120-x10.1038/s41467-018-08120-x ↗
17. 10.1002/adma.20190270910.1002/adma.201902709 ↗
18. 10.1002/anie.20181333110.1002/anie.201813331 ↗
19. 10.1063/1.55583910.1063/1.555839 ↗
20. 10.1038/s41467-018-05758-510.1038/s41467-018-05758-5 ↗
21. 10.1149/2.0231607jes10.1149/2.0231607jes ↗
22. 10.1038/s41929-019-0241-710.1038/s41929-019-0241-7 ↗
23. 10.1038/s41929-019-0354-z10.1038/s41929-019-0354-z ↗
24. 10.1007/BF0064924410.1007/BF00649244 ↗
25. 10.1021/je500613y10.1021/je500613y ↗
26. 10.1016/j.cej.2018.01.11610.1016/j.cej.2018.01.116 ↗
27. 10.1002/aenm.20180036910.1002/aenm.201800369 ↗
28. 10.1038/s41467-019-11846-x10.1038/s41467-019-11846-x ↗
29. 10.1038/s41586-019-1260-x10.1038/s41586-019-1260-x ↗
30. 10.1002/anie.20210978510.1002/anie.202109785 ↗
31. 10.1073/pnas.170637111410.1073/pnas.1706371114 ↗