journal article·2024-02Open access

Carbon Monoxide Reduction Reaction to Produce Multicarbon Products in Acidic Electrolytes Using Gas Diffusion Electrode Loaded with Copper Nanoparticles

Ryo Kurihara, Kaito Nagita, Keitaro Ohashi, Yoshiharu Mukouyama, Takashi Harada, Shuji Nakanishi, Kazuhide Kamiya

Advanced Materials Interfaces· Volume 11· Issue 6

Abstract

Abstract The synthesis of multi‐carbon products (C2+) by electrochemical CO2 reduction reaction (CO2RR) is a promising technology that will contribute to the realization of a carbon‐neutral society. In particular, efficient CO2RR to produce C2+ in acidic electrolytes is desirable because the conversion of CO2 to inert (bi)carbonate can be suppressed under acidic conditions, thereby increasing the efficiency of substrate CO2 utilization. Herein, since C2+ products are produced via the dimerization of carbon monoxide, an intermediate in CO2RR, the focus is on the carbon monoxide reduction reaction (CORR). A gas diffusion electrode loaded with copper nanoparticles is used in acidic electrolytes to investigate the conditions necessary for efficient C2+ production. The faradaic efficiency and partial current density for C2+ production attained 75% and 280 mA cm−2 in a pH 2.0 solution, and they reached up to 66% and 260 mA cm−2 even in a pH 1.0 solution. Numerical simulations showed that increasing the alkalinity of the electrode surface to greater than pH 7 by consuming protons is necessary to facilitate the production of C2+ during the CORR. When the desired level of alkalinity is achieved, the concentration and type of alkali cations present at the electrode surface have an impact on the selectivity for C2+ production.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Advanced battery technologies research · Electrocatalysts for Energy Conversion

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

Affiliations

Research Center for Solar Energy Chemistry Graduate School of Engineering Science Osaka University 1–3 Machikaneyama Toyonaka Osaka 560‐8531 Japan

Division of Science College of Science and Engineering Tokyo Denki University Hatoyama Saitama 350–0394 Japan

Innovative Catalysis Science Division Institute for Open and Transdisciplinary Research Initiatives (ICS‐OTRI) Osaka University Suita Osaka 565‐0871 Japan

Funding

New Energy and Industrial Technology Development Organization · Core Research for Evolutional Science and Technology

References (48)

Show source-provided references
1. 10.1246/cl.20069110.1246/cl.200691 ↗
2. 10.1002/advs.20170027510.1002/advs.201700275 ↗
3. 10.1021/acs.chemrev.8b0070510.1021/acs.chemrev.8b00705 ↗
4. 10.1126/science.aad499810.1126/science.aad4998 ↗
5. 10.1126/science.aav350610.1126/science.aav3506 ↗
6. 10.1039/C8EE00097B10.1039/C8EE00097B ↗
7. 10.1002/adma.20180716610.1002/adma.201807166 ↗
8. 10.1038/s41929-022-00803-510.1038/s41929-022-00803-5 ↗
9. 10.1002/aenm.20220058610.1002/aenm.202200586 ↗
10. 10.1246/cl.1985.169510.1246/cl.1985.1695 ↗
11. 10.1246/cl.1986.89710.1246/cl.1986.897 ↗
12. 10.1002/cphc.20170073610.1002/cphc.201700736 ↗
13. 10.1016/0013-4686(94)85172-710.1016/0013-4686(94)85172-7 ↗
14. 10.1021/jacs.9b0212410.1021/jacs.9b02124 ↗
15. 10.1126/science.aay421710.1126/science.aay4217 ↗
16. 10.1039/D1EE01696B10.1039/D1EE01696B ↗
17. 10.1039/D0EE00047G10.1039/D0EE00047G ↗
18. 10.1038/s41929-022-00761-y10.1038/s41929-022-00761-y ↗
19. 10.1038/s41467-020-19135-810.1038/s41467-020-19135-8 ↗
20. 10.1039/D2EY00035K10.1039/D2EY00035K ↗
21. 10.1039/C8EE03134G10.1039/C8EE03134G ↗
22. 10.1038/s41467-020-20397-510.1038/s41467-020-20397-5 ↗
23. 10.1126/science.abg658210.1126/science.abg6582 ↗
24. 10.1038/s41467-022-35415-x10.1038/s41467-022-35415-x ↗
25. 10.5796/electrochemistry.20-6403610.5796/electrochemistry.20-64036 ↗
26. 10.1021/acs.langmuir.7b0069610.1021/acs.langmuir.7b00696 ↗
27. 10.1021/acssuschemeng.8b0627810.1021/acssuschemeng.8b06278 ↗
28. 10.1021/jacs.0c1039710.1021/jacs.0c10397 ↗
29. 10.1038/s41467-021-24936-610.1038/s41467-021-24936-6 ↗
30. 10.1021/acscatal.1c0513510.1021/acscatal.1c05135 ↗
31. 10.1038/s41929-022-00788-110.1038/s41929-022-00788-1 ↗
32. 10.1002/cctc.20220005210.1002/cctc.202200052 ↗
33. 10.1002/adma.20220129510.1002/adma.202201295 ↗
34. 10.1002/anie.20221610210.1002/anie.202216102 ↗
35. 10.1021/acsanm.1c0051410.1021/acsanm.1c00514 ↗
36. 10.1021/acsami.0c1605910.1021/acsami.0c16059 ↗
37. 10.1007/s10800-005-9058-y10.1007/s10800-005-9058-y ↗
38. 10.1149/1945-7111/ab987a10.1149/1945-7111/ab987a ↗
39. 10.1039/D0EE01760D10.1039/D0EE01760D ↗
40. 10.1002/celc.20210114110.1002/celc.202101141 ↗
41. 10.1021/acscatal.1c0107210.1021/acscatal.1c01072 ↗
42. 10.1021/jacs.7b0676510.1021/jacs.7b06765 ↗
43. 10.1039/C9EE01341E10.1039/C9EE01341E ↗
44. 10.1021/acscatal.8b0120010.1021/acscatal.8b01200 ↗
45. 10.1021/acscatal.1c0552010.1021/acscatal.1c05520 ↗
46. 10.1126/science.aas910010.1126/science.aas9100 ↗
47. 10.1038/s41467-022-35772-710.1038/s41467-022-35772-7 ↗
48. 10.1021/acscatal.2c0365010.1021/acscatal.2c03650 ↗