Construction of a Synergistic Ag/Co(OH) 2 Composite for Efficient Nitrate Electroreduction to Ammonia
Source abstract
Abstract
Developing efficient electrocatalysts for the nitrate reduction reaction (NO 3 RR) to produce ammonia is of great significance. In this work, a Ag nanoparticle-modified Co(OH) 2 catalyst was prepared by electrodeposition and liquid-phase deposition. The Ag/Co(OH) 2 composite exhibits significantly enhanced NO 3 RR performance in comparison with Co(OH) 2, achieving a high NH 3 FE and a yield rate of 95.6% and 97.1 μmol h –1 cm –2 at −0.6 V in a neutral medium. Comprehensive characterizations confirm the strong interfacial coupling between Ag and Co(OH) 2, while electrochemical studies reveal synergistic effects that simultaneously enhance nitrate adsorption and moderate hydrogen adsorption. Such a probable NO 3 RR tandem mechanism is proposed in which Ag dominates the initial 2e – pathway (*NO 3 →*NO 2 ) and Co(OH) 2 was prior in the subsequent *NO hydrogenation into *NH 3 . This work provides both a novel catalyst and fundamental insights into the composite material design for electrochemical NO 3 RR.
Source: openalex_inverted_index · 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
College of Chemical and Biological Engineering
Shandong University of Science and Technology
College of Materials Science and Engineering
Funding
Natural Science Foundation of Qingdao Municipality · National Natural Science Foundation of China · Natural Science Foundation of Shandong Province
References (40)
Show source-provided references
1. 10.1002/aenm.20180036910.1002/aenm.201800369 ↗
2. 10.1038/s41929-019-0252-410.1038/s41929-019-0252-4 ↗
3. 10.1039/D1CS00857A10.1039/D1CS00857A ↗
4. 10.1039/D3TA05300H10.1039/D3TA05300H ↗
5. 10.1039/D4SC07619B10.1039/D4SC07619B ↗
6. 10.1002/adma.20230402110.1002/adma.202304021 ↗
7. 10.1016/j.jmst.2020.10.05610.1016/j.jmst.2020.10.056 ↗
8. 10.1039/D4GC04640D10.1039/D4GC04640D ↗
9. 10.1021/acsaem.3c0289210.1021/acsaem.3c02892 ↗
10. 10.1002/adsu.20240093410.1002/adsu.202400934 ↗
11. 10.1021/acssuschemeng.2c0711410.1021/acssuschemeng.2c07114 ↗
12. 10.1002/adma.20230469510.1002/adma.202304695 ↗
13. 10.1016/j.cej.2023.14196010.1016/j.cej.2023.141960 ↗
14. 10.1016/j.jcis.2022.09.01210.1016/j.jcis.2022.09.012 ↗
15. 10.1016/j.jcis.2022.09.04910.1016/j.jcis.2022.09.049 ↗
16. 10.1007/s40843-024-2798-510.1007/s40843-024-2798-5 ↗
17. 10.1002/adfm.20240691710.1002/adfm.202406917 ↗
18. 10.1021/acscatal.3c0274710.1021/acscatal.3c02747 ↗
19. 10.1002/anie.20240020610.1002/anie.202400206 ↗
20. 10.1021/acsnano.3c0679810.1021/acsnano.3c06798 ↗
21. 10.1002/anie.20241035610.1002/anie.202410356 ↗
22. 10.1021/acs.inorgchem.3c0081410.1021/acs.inorgchem.3c00814 ↗
23. 10.1021/acscatal.2c0103810.1021/acscatal.2c01038 ↗
24. 10.1002/smll.20240351710.1002/smll.202403517 ↗
25. 10.1016/j.scib.2024.06.01510.1016/j.scib.2024.06.015 ↗
26. 10.1038/s41467-022-35533-610.1038/s41467-022-35533-6 ↗
27. 10.1002/anie.20231691010.1002/anie.202316910 ↗
28. 10.1002/anie.20241025110.1002/anie.202410251 ↗
29. 10.1002/adma.20240868010.1002/adma.202408680 ↗
30. 10.1002/adfm.20240971410.1002/adfm.202409714 ↗
31. 10.1039/D4TA00091A10.1039/D4TA00091A ↗
32. 10.1021/acscatal.3c0108810.1021/acscatal.3c01088 ↗
33. 10.1021/jacs.4c0498510.1021/jacs.4c04985 ↗
34. 10.1021/jacs.4c0042910.1021/jacs.4c00429 ↗
35. 10.1021/jacs.3c1232110.1021/jacs.3c12321 ↗
36. 10.1021/jacs.4c0081810.1021/jacs.4c00818 ↗
37. 10.1002/anie.20240941910.1002/anie.202409419 ↗
38. 10.1016/j.desal.2021.11534010.1016/j.desal.2021.115340 ↗
39. 10.1016/j.jece.2024.11455410.1016/j.jece.2024.114554 ↗
40. 10.1016/j.cej.2025.15987410.1016/j.cej.2025.159874 ↗