Engineering Stable CO 2 -to-Formic Acid Electrocatalysis: Individual Ultrathin Bismuth-Assembled Nanosheets for Long-Term Operation in Solid-Electrolyte Electrolyzers
Source abstract
Abstract
Developing electrocatalysts that combine high efficiency with long-term stability for CO 2 reduction to formic acid remains a significant challenge, especially at industrial-scale current densities. Here, we report individual ultrathin bismuth-assembled nanosheets (Bi-INS) synthesized via a triethanolamine (TEA)-directed solvothermal method. The coordinating role of TEA guides the two-dimensional assembly of a basic bismuth carbonate precursor, effectively suppressing nanosheet stacking. This unique architecture provides abundant accessible active sites and accelerates interfacial charge transfer and intermediates adsorption. Consequently, Bi-INS achieves a peak formate Faradaic efficiency (FE) of 90% and maintains an FE above 80% over a broad potential range. In a solid-electrolyte membrane electrode assembly electrolyzer, the catalyst demonstrates exceptional durability for producing formic acid solution, operating stably for 300 h at 100 mA·cm −2 with an average FE of 82.6%. This work demonstrates that surfactant-assisted structural regulation is a robust strategy for designing scalable and durable catalysts for industrial CO 2 electrolysis.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Carbon dioxide utilization in catalysis · Catalysts for Methane Reforming
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Institute of New Energy Materials, School of Materials Science and Engineering
Tianjin University
School of Architectural Engineering
Tianjin Renai College
Purification Equipment Research Institute
References (39)
Show source-provided references
1. 10.1016/j.cherd.2024.07.01410.1016/j.cherd.2024.07.014 ↗
2. 10.1016/j.jcou.2019.09.00710.1016/j.jcou.2019.09.007 ↗
3. 10.1039/D1TA01516H10.1039/D1TA01516H ↗
4. 10.1016/j.jechem.2024.01.06210.1016/j.jechem.2024.01.062 ↗
5. 10.1038/s41467-020-17403-110.1038/s41467-020-17403-1 ↗
6. 10.1016/j.ces.2021.11673110.1016/j.ces.2021.116731 ↗
7. 10.1038/s41560-019-0451-x10.1038/s41560-019-0451-x ↗
8. 10.1016/j.nanoen.2021.10574510.1016/j.nanoen.2021.105745 ↗
9. 10.1002/anie.20210474710.1002/anie.202104747 ↗
10. 10.1126/science.aas910010.1126/science.aas9100 ↗
11. 10.1002/aenm.20220097010.1002/aenm.202200970 ↗
12. 10.1021/acsami.3c1828510.1021/acsami.3c18285 ↗
13. 10.1002/adfm.20230198410.1002/adfm.202301984 ↗
14. 10.1021/acsami.1c2521710.1021/acsami.1c25217 ↗
15. 10.1039/d4ta06898j10.1039/d4ta06898j ↗
16. 10.1149/1945-7111/abf06310.1149/1945-7111/abf063 ↗
17. 10.1002/adsc.7027110.1002/adsc.70271 ↗
18. 10.1038/s41467-018-03712-z10.1038/s41467-018-03712-z ↗
19. Fu X. · Adv. Funct. Mater. · 2022 · 32 · 2107182.10.1002/adfm.202107182 ↗
20. 10.1039/d0se00445f10.1039/d0se00445f ↗
21. 10.1016/j.apcatb.2020.11862510.1016/j.apcatb.2020.118625 ↗
22. 10.1002/anie.20200557710.1002/anie.202005577 ↗
23. 10.1038/s41467-020-14914-910.1038/s41467-020-14914-9 ↗
24. 10.1039/c9nr07863k10.1039/c9nr07863k ↗
25. 10.1039/d4ta00091a10.1039/d4ta00091a ↗
26. 10.1021/ja992541y10.1021/ja992541y ↗
27. 10.1139/v84-48410.1139/v84-484 ↗
28. 10.1016/S0020-1693(02)01381-610.1016/S0020-1693(02)01381-6 ↗
29. 10.1002/smll.20241014510.1002/smll.202410145 ↗
30. 10.1002/anie.20201434110.1002/anie.202014341 ↗
31. 10.1038/s41467-023-36263-z10.1038/s41467-023-36263-z ↗
32. 10.1021/acscatal.0c0531710.1021/acscatal.0c05317 ↗
33. 10.3390/coatings1202023310.3390/coatings12020233 ↗
34. 10.1002/adma.20241563910.1002/adma.202415639 ↗
35. 10.1021/jacs.2c0317210.1021/jacs.2c03172 ↗
36. 10.31635/ccschem.022.20220206810.31635/ccschem.022.202202068 ↗
37. 10.1039/D3EE02029K10.1039/D3EE02029K ↗
38. 10.1007/s12274-021-3903-010.1007/s12274-021-3903-0 ↗
39. 10.1002/anie.20221495910.1002/anie.202214959 ↗