Tin‐doped bismuth dendrites for highly efficient electrocatalytic reduction of CO2 by using bipolar membrane in ultrathin liquid reactor
Source abstract
Abstract
Abstract Electrochemical CO2 reduction reaction is a promising protocol to achieve a carbon‐neutral cycle. Herein, we report a general strategy to regulate the growth of Sn‐doped Bi dendritic electrode with numerous labyrinthine and porous channels to provide abundant tips, edges, terraces, and low coordination sites for efficient conversion of CO2 into formate. As a result, the dendritic Sn‐doped Bi achieves a high partial current density (30 mA/cm2), a high Faradic efficiency of formate (95.5%), and a long‐term durability (>60 h). Most remarkably, the self‐made bipolar membrane can effectually prohibit the cross‐over of formate from cathode to anode and the oxidization of small organic molecules in anode can promote the production of formate on both anode and cathode sides. This work provides helpful insights to the design of electrocatalysts, bipolar membrane, and ultrathin liquid reactor. image
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Research context
OpenAlex topics: CO2 Reduction Techniques and Catalysts · Ionic liquids properties and applications · Advanced Thermoelectric Materials and Devices
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory for Modification of Chemical Fibers and Polymer Materials College of Materials Science and Engineering, Donghua University Shanghai China
Shanghai Institute of Pollution Control and Ecological Security Shanghai China
Department of Applied Physics and Research Institute for Smart Energy Hong Kong Polytechnic University Kowloon Hong Kong, China
Funding
Donghua University · Hong Kong Polytechnic University · Science and Technology Commission of Shanghai Municipality
References (40)
Show source-provided references
1. 10.1039/C3CS60323G10.1039/C3CS60323G ↗
2. 10.1016/j.nanoen.2017.05.06510.1016/j.nanoen.2017.05.065 ↗
3. 10.1002/cssc.20200209910.1002/cssc.202002099 ↗
4. 10.1016/j.scib.2020.01.02010.1016/j.scib.2020.01.020 ↗
5. 10.1016/j.apcatb.2019.11844710.1016/j.apcatb.2019.118447 ↗
6. 10.1038/s41467-019-08805-x10.1038/s41467-019-08805-x ↗
7. 10.1039/C8TA10752A10.1039/C8TA10752A ↗
8. 10.1002/anie.20191653810.1002/anie.201916538 ↗
9. 10.1016/j.jallcom.2020.15578910.1016/j.jallcom.2020.155789 ↗
10. 10.1021/jacs.8b0826710.1021/jacs.8b08267 ↗
11. 10.1002/advs.20190298910.1002/advs.201902989 ↗
12. 10.1002/ange.20210283210.1002/ange.202102832 ↗
13. 10.1016/j.electacta.2019.13492310.1016/j.electacta.2019.134923 ↗
14. 10.1038/s41467-019-10819-410.1038/s41467-019-10819-4 ↗
15. 10.1002/aenm.20187013810.1002/aenm.201870138 ↗
16. 10.1016/j.electacta.2020.13747810.1016/j.electacta.2020.137478 ↗
17. 10.1039/C9TA11363K10.1039/C9TA11363K ↗
18. 10.1021/acscatal.7b0070710.1021/acscatal.7b00707 ↗
19. 10.1038/nature1906010.1038/nature19060 ↗
20. 10.1039/D0TA03645E10.1039/D0TA03645E ↗
21. 10.1038/s41557-020-00602-010.1038/s41557-020-00602-0 ↗
22. 10.1016/j.cej.2021.13045410.1016/j.cej.2021.130454 ↗
23. 10.1002/er.581010.1002/er.5810 ↗
24. 10.1021/acsenergylett.7b0101710.1021/acsenergylett.7b01017 ↗
25. 10.1002/adma.20180716610.1002/adma.201807166 ↗
26. 10.1016/j.joule.2017.09.00310.1016/j.joule.2017.09.003 ↗
27. 10.1038/s41467-018-03712-z10.1038/s41467-018-03712-z ↗
28. 10.1038/s41586-019-1782-210.1038/s41586-019-1782-2 ↗
29. 10.1039/C9EE00909D10.1039/C9EE00909D ↗
30. 10.1039/D0EE00047G10.1039/D0EE00047G ↗
31. 10.1016/j.cej.2020.12696510.1016/j.cej.2020.126965 ↗
32. 10.1021/acs.iecr.8b0494410.1021/acs.iecr.8b04944 ↗
33. 10.1038/s41560-019-0451-x10.1038/s41560-019-0451-x ↗
34. 10.1038/s41467-020-17403-110.1038/s41467-020-17403-1 ↗
35. 10.1039/D1TA06101A10.1039/D1TA06101A ↗
36. 10.1016/j.jcou.2019.09.00710.1016/j.jcou.2019.09.007 ↗
37. 10.1039/C6TA05508G10.1039/C6TA05508G ↗
38. 10.1002/ange.20200061710.1002/ange.202000617 ↗
39. 10.1016/j.apcatb.2021.12000310.1016/j.apcatb.2021.120003 ↗
40. 10.1016/j.jcis.2020.06.03310.1016/j.jcis.2020.06.033 ↗