journal article·2018-04-19

Enhanced Oxygen Evolution Reaction Activity of Co Ions Isolated in the Interlayer Space of Buserite MnO2

Kotaro Fujimoto, Takuya Okada, Masaharu Nakayama

The Journal of Physical Chemistry C· Volume 122· Issue 15
Publisher page

Abstract

We have fabricated a thin film of layered manganese dioxide (MnO 2 ) that accommodates cobalt ions in its interlayer space, constructing the so-called buserite structure, via electrodeposition and the subsequent ion-exchange. The MnO 2 layers could isolate Co 2+ ions to provide an environment beneficial for oxygen evolution reactions (OERs) in alkaline electrolyte, where fast electron transfer and high utilization efficiency were achieved. The catalyst with isolated Co 2+ ions exhibited a mass activity as high as 63.5 A/g Co at an overpotential (η) of 0.4 V, which was much larger than those of Co ions bound in the oxide network. Moreover, it also exhibited excellent stability for long-term OER operation. Namely, the potential needed to generate a current density of 10 mA/cm 2 increased only 0.073 V during 100 h operation, and no significant change was seen after 100 consecutive potential cycles between +1.0 and +2.0 V versus the reversible hydrogen electrode.
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Research context

OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Electrochemical Analysis and Applications

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Affiliations

Department of Applied Chemistry, Graduate School of Sciences and Technology for Innovation, Yamaguchi University, 2-16-1 Tokiwadai, Ube 755-8611, Japan

Funding

Electric Technology Research Foundation of Chugoku · Japan Society for the Promotion of Science · Sasakura Enviro-Science Foundation

References (41)

Show source-provided references
1. 10.1016/0013-4686(84)85004-510.1016/0013-4686(84)85004-5 ↗
2. 10.1016/j.ijhydene.2006.06.04710.1016/j.ijhydene.2006.06.047 ↗
3. 10.1021/jz201650710.1021/jz2016507 ↗
4. 10.1021/ja509673310.1021/ja5096733 ↗
5. 10.1039/c3ee42696c10.1039/c3ee42696c ↗
6. 10.1002/anie.20150161610.1002/anie.201501616 ↗
7. 10.1002/anie.20160437210.1002/anie.201604372 ↗
8. 10.1021/ja901006x10.1021/ja901006x ↗
9. 10.1021/nl300973b10.1021/nl300973b ↗
10. 10.1021/acscatal.6b0055310.1021/acscatal.6b00553 ↗
11. 10.1038/ncomms1080110.1038/ncomms10801 ↗
12. 10.1007/s12274-016-0986-010.1007/s12274-016-0986-0 ↗
13. 10.1016/j.jssc.2012.10.03010.1016/j.jssc.2012.10.030 ↗
14. 10.1016/j.jhazmat.2011.09.02710.1016/j.jhazmat.2011.09.027 ↗
15. 10.1039/c5ta08106h10.1039/c5ta08106h ↗
16. 10.1021/ja402771510.1021/ja4027715 ↗
17. 10.1039/c6qi00009f10.1039/c6qi00009f ↗
18. 10.1039/c3tc32578d10.1039/c3tc32578d ↗
19. 10.1246/cl.2004.67010.1246/cl.2004.670 ↗
20. 10.1021/ic048691d10.1021/ic048691d ↗
21. 10.1016/j.elecom.2017.09.01210.1016/j.elecom.2017.09.012 ↗
22. 10.1149/1.346786510.1149/1.3467865 ↗
23. 10.1007/s10008-010-1125-610.1007/s10008-010-1125-6 ↗
24. 10.1021/la048173f10.1021/la048173f ↗
25. 10.1016/0003-2670(92)80064-e10.1016/0003-2670(92)80064-e ↗
26. 10.1073/pnas.96.7.344710.1073/pnas.96.7.3447 ↗
27. 10.1016/j.electacta.2015.08.05710.1016/j.electacta.2015.08.057 ↗
28. 10.1021/acscatal.6b0198010.1021/acscatal.6b01980 ↗
29. 10.1021/acs.langmuir.7b0041910.1021/acs.langmuir.7b00419 ↗
30. 10.1149/1.139351510.1149/1.1393515 ↗
31. 10.1021/cm020408q10.1021/cm020408q ↗
32. 10.1021/jp044511+10.1021/jp044511+ ↗
33. 10.1021/jp908548f10.1021/jp908548f ↗
34. 10.1016/j.apcatb.2016.03.00510.1016/j.apcatb.2016.03.005 ↗
35. 10.1021/ja505186m10.1021/ja505186m ↗
36. 10.1021/jacs.6b0918410.1021/jacs.6b09184 ↗
37. 10.1016/j.electacta.2016.06.08510.1016/j.electacta.2016.06.085 ↗
38. Bard A. J. · 2001
39. 10.1038/s41467-017-01949-810.1038/s41467-017-01949-8 ↗
40. 10.1021/jp952985q10.1021/jp952985q ↗
41. 10.1039/c6ta04078k10.1039/c6ta04078k ↗