Boron-Induced Cationic Vacancy on Copper Cobalt Oxide toward Formate Selectivity: New Insights into Methanol Oxidation Reaction
Source abstract
Abstract
In noble metal-based fuel cells, adsorbed carbon monoxide plays a vital role in hindering their efficiency. To alleviate this problem, constructing non-noble metals, particularly selective toward formate formation, will be an ideal solution. Further, to improve the electrochemical properties, we deliberately introduced point defects, namely, cationic vacancies. Herein, we have chosen boron as a dopant that introduces the cationic vacancy in copper cobalt oxide (B/CuCo2O4) and improves the methanol absorption capability. Our synthesized B/CuCo2O4 electrocatalyst showed 91 mA cm–2 (∼4-fold) higher current density than the pristine electrocatalyst. Most importantly, unlike noble metals, our synthesized electrocatalyst was selective toward formate formation and obtained a faradic efficiency of 43% as demonstrated by NMR, and the reaction pathway was predicted by density calculation theory.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Electrochemical Analysis and Applications · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Physics and Nanotechnology, SRM Institute of Science and Technology, Kattankulathur 603203, Tamil Nadu, India
Department of Chemistry, SRM Institute of Science and Technology, Kattankulathur 603203, Tamil Nadu, India
National Centre for Catalysis Research (NCCR), Department of Chemistry, Indian Institute of Technology Madras, Chennai 600036, India
Funding
SRM Institute of Science and Technology · Council for Scientific and Industrial Research
References (40)
Show source-provided references
1. 10.1039/D0NR02950E10.1039/D0NR02950E ↗
2. 10.1039/D0DT02567D10.1039/D0DT02567D ↗
3. 10.1039/C7NR02264F10.1039/C7NR02264F ↗
4. 10.1038/s41467-020-18459-910.1038/s41467-020-18459-9 ↗
5. 10.1039/D0NR04822D10.1039/D0NR04822D ↗
6. 10.1021/acsami.7b0387610.1021/acsami.7b03876 ↗
7. 10.1038/s41467-019-11766-w10.1038/s41467-019-11766-w ↗
8. 10.1002/anie.20200431410.1002/anie.202004314 ↗
9. 10.1002/adma.20150440110.1002/adma.201504401 ↗
10. 10.1021/acsaem.0c0146110.1021/acsaem.0c01461 ↗
11. 10.1021/acsami.1c0625810.1021/acsami.1c06258 ↗
12. 10.1002/ange.20200430110.1002/ange.202004301 ↗
13. 10.1016/j.apcatb.2020.11951010.1016/j.apcatb.2020.119510 ↗
14. 10.1002/cssc.20190292110.1002/cssc.201902921 ↗
15. 10.1002/aenm.20200139710.1002/aenm.202001397 ↗
16. 10.1016/j.ijhydene.2009.12.14510.1016/j.ijhydene.2009.12.145 ↗
17. 10.1016/j.electacta.2015.03.00810.1016/j.electacta.2015.03.008 ↗
18. 10.1039/C8TA08242A10.1039/C8TA08242A ↗
19. 10.1002/chem.20190106410.1002/chem.201901064 ↗
20. 10.1016/j.apcatb.2018.12.01710.1016/j.apcatb.2018.12.017 ↗
21. 10.1021/acsanm.0c0241110.1021/acsanm.0c02411 ↗
22. 10.1021/acsenergylett.9b0034810.1021/acsenergylett.9b00348 ↗
23. 10.1016/j.apcatb.2021.12051510.1016/j.apcatb.2021.120515 ↗
24. 10.1002/ange.20190918210.1002/ange.201909182 ↗
25. 10.1007/s00339-020-04198-710.1007/s00339-020-04198-7 ↗
26. 10.1021/jp202396r10.1021/jp202396r ↗
27. 10.1038/srep3112010.1038/srep31120 ↗
28. 10.1021/acssuschemeng.9b0377610.1021/acssuschemeng.9b03776 ↗
29. 10.1016/j.apsusc.2020.14562110.1016/j.apsusc.2020.145621 ↗
30. 10.1021/acsnano.9b0996310.1021/acsnano.9b09963 ↗
31. 10.1007/s11581-017-2081-210.1007/s11581-017-2081-2 ↗
32. 10.1002/cctc.20190149610.1002/cctc.201901496 ↗
33. 10.1021/jp070951010.1021/jp0709510 ↗
34. 10.1016/j.jechem.2018.08.00910.1016/j.jechem.2018.08.009 ↗
35. 10.1016/j.matlet.2021.13041610.1016/j.matlet.2021.130416 ↗
36. 10.1016/j.solener.2020.03.07710.1016/j.solener.2020.03.077 ↗
37. 10.1016/j.apcatb.2016.10.01210.1016/j.apcatb.2016.10.012 ↗
38. 10.1002/adma.20210081210.1002/adma.202100812 ↗
39. 10.1039/C6CP08522A10.1039/C6CP08522A ↗
40. 10.1039/D0CC03177A10.1039/D0CC03177A ↗