Ir-Surface Enriched Porous Ir–Co Oxide Hierarchical Architecture for High Performance Water Oxidation in Acidic Media
Source abstract
Abstract
The large-scale application of acidic water electrolysis as a viable energy storage technology has been hindered by the high demand of precious metal oxides at anode to catalyze the oxygen evolution reaction (OER). We report an Ir-Co binary oxide electrocatalyst for OER fabricated by a multistep process of selective leaching of Co from Co-rich composite oxides prepared through thermal decomposition. The stepwise leaching of the Co component from the composites leads to the formation of macro- and mesoscale voids walled by a cross-linked nanoporous network of rod- and wedge-like building units of Ir-Co binary oxide with a rutile phase structure and an Ir-enriched surface. In comparison, Ir-Co binary oxide with similar composition prepared by direct thermal decomposition method exhibits a loose nanoparticle aggregation morphology with a Co-enriched surface. The cross-linked porous Ir-Co binary oxide from selective leaching is about 3-fold more active for the OER than that from direct thermal decomposition. Compared with pure IrO2 from thermal decomposition, the Co-leached binary oxide is ca. two times more active and is much more durable during continuous oxygen evolution under a constant potential of 1.6 V, thus showing a possibility of reducing the demand of the expensive and scarce Ir in OER electrocatalyst for acidic water splitting.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Advanced battery technologies research · Nanomaterials for catalytic reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Hubei Key Laboratory of Electrochemical Power Sources, Department of Chemistry, Wuhan University, Wuhan 430072, China
Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Applications of Organic Functional Molecules, Hubei University, Wuhan 430062, China
Funding
Ministry of Science and technology of china
References (51)
Show source-provided references
1. Edwards P. P. · Energy Policy · 2008 · 36 · 435610.1016/j.enpol.2008.09.036 ↗
2. deKrafft K. E. · ACS Appl. Mater. Interfaces · 2012 · 4 · 60810.1021/am2018095 ↗
3. Liu X. · Chem. Mater. · 2014 · 26 · 188910.1021/cm4040903 ↗
4. Jin S. · Science · 2011 · 334 · 138310.1126/science.1212858 ↗
5. Tang D. · ACS Appl. Mater. Interfaces · 2014 · 6 · 791810.1021/am501256x ↗
6. Gao M. R. · J. Am. Chem. Soc. · 2012 · 134 · 293010.1021/ja211526y ↗
7. Singh A. · Chem. Mater. · 2013 · 25 · 109810.1021/cm3041345 ↗
8. Kanan M. W. · Science · 2008 · 321 · 107210.1126/science.1162018 ↗
9. Reece S. Y. · Science · 2011 · 334 · 64510.1126/science.1209816 ↗
10. Smith R. D. L. · Science · 2013 · 340 · 6010.1126/science.1233638 ↗
11. Smith R. D. L. · J. Am. Chem. Soc. · 2013 · 135 · 1158010.1021/ja403102j ↗
12. Parrondoa J. · RSC Adv. · 2014 · 4 · 987510.1039/c3ra46630b ↗
13. Millet P. · Int. J. Hydrogen Energy · 2009 · 34 · 497410.1016/j.ijhydene.2008.11.114 ↗
14. Han J. H. · Chem. Mater. · 2012 · 24 · 140710.1021/cm200989t ↗
15. Lee E. · Ultrason. Sonochem. · 2014 · 21 · 31710.1016/j.ultsonch.2013.05.006 ↗
16. Cheng S. · ACS Appl. Mater. Interfaces · 2011 · 3 · 394810.1021/am200831b ↗
17. Dai Y. · J. Phys. Chem. C · 2011 · 115 · 216210.1021/jp109975s ↗
18. Stamenkovic V. R. · Science · 2007 · 315 · 49310.1126/science.1135941 ↗
19. Hu W. · J. Mater. Chem. · 2012 · 22 · 601010.1039/c2jm16506f ↗
20. Ortel E. · Chem. Mater. · 2011 · 23 · 320110.1021/cm200761f ↗
21. Nakagawa T. · J. Phys. Chem. C · 2009 · 113 · 1295810.1021/jp9060076 ↗
22. Nakagawa T. · J. Am. Chem. Soc. · 2009 · 131 · 1557810.1021/ja9063298 ↗
23. Michaux K. E. · Langmuir · 2013 · 29 · 1225410.1021/la4025876 ↗
24. Smith R. D. L. · Chem. Mater. · 2014 · 26 · 165410.1021/cm4041715 ↗
25. Marshall A. · Int. J. Hydrogen Energy · 2007 · 32 · 232010.1016/j.ijhydene.2007.02.013 ↗
26. Panic V. V. · Phys. Chem. Chem. Phys. · 2010 · 12 · 752110.1039/b921582d ↗
27. Marshall A. · Electrochim. Acta · 2006 · 51 · 316110.1016/j.electacta.2005.09.004 ↗
28. Li G. · Phys. Chem. Chem. Phys. · 2013 · 15 · 285810.1039/c2cp44496h ↗
29. Li G. · J. Power Sources · 2014 · 249 · 17510.1016/j.jpowsour.2013.10.088 ↗
30. Xu C. · Nanoscale · 2010 · 2 · 90610.1039/b9nr00351g ↗
31. Wang R. Y. · Adv. Mater. · 2010 · 22 · 184510.1002/adma.200903548 ↗
32. Déronzier T. · Chem. Mater. · 2011 · 23 · 528710.1021/cm202105k ↗
33. Wang R. · Environ. Sci. · 2012 · 5 · 5281
34. Oezaslan M. · J. Am. Chem. Soc. · 2012 · 134 · 51410.1021/ja2088162 ↗
35. Baer D. R. · J. Electron Spectrosc. Relat. Phenom. · 2010 · 178 · 41510.1016/j.elspec.2009.09.003 ↗
36. Skriver H. L. · Phys. Rev. B: Condens. Matter Mater. Phys. · 1992 · 46 · 715710.1103/PhysRevB.46.7157 ↗
37. Schmidt T. J. · 2003 · 316
38. Sun Y. · Phys. Chem. Chem. Phys. · 2012 · 14 · 227810.1039/c2cp22761d ↗
39. Mayrhofer K. · Electrochim. Acta · 2008 · 53 · 318110.1016/j.electacta.2007.11.057 ↗
40. Gerken J. B. · J. Am. Chem. Soc. · 2011 · 133 · 1443110.1021/ja205647m ↗
41. Yeo B. S. · J. Am. Chem. Soc. · 2011 · 133 · 558710.1021/ja200559j ↗
42. Da Silva L. M. · Electrochim. Acta · 2004 · 49 · 397710.1016/j.electacta.2003.11.039 ↗
43. Reier T. · ACS Catal. · 2012 · 2 · 176510.1021/cs3003098 ↗
44. Rasten E. · Electrochim. Acta · 2003 · 48 · 394510.1016/j.electacta.2003.04.001 ↗
45. Hu J. M. · Int. J. Hydrogen Energy · 2004 · 29 · 79110.1016/j.ijhydene.2003.09.007 ↗
46. Siracusano S. · Int. J. Hydrogen Energy · 2010 · 35 · 555810.1016/j.ijhydene.2010.03.102 ↗
47. De Faria L. A. · J. Appl. Electrochem. · 1996 · 26 · 119510.1007/BF00243745 ↗
48. Cheng J. B. · Electrochim. Acta · 2009 · 54 · 625010.1016/j.electacta.2009.05.090 ↗
49. Hou Y. Y. · Electrochim. Acta · 2006 · 51 · 625810.1016/j.electacta.2006.04.008 ↗
50. Ye F. · Electrolysis · 2010 · 35 · 8049
51. Panić V. V. · J. Serb. Chem. Soc. · 2008 · 73 · 108310.2298/JSC0811083P ↗