journal article·2019-03-27Open access

Boosting the Oxygen Reduction Electrocatalytic Performance of Nonprecious Metal Nanocarbons via Triple Boundary Engineering Using Protic Ionic Liquids

Mo Qiao, Guillermo A. Ferrero, Leticia Fernández Velasco, Wei Vern Hor, Yan Yang, Hui Luo, Peter Lodewyckx, Antonio B. Fuertes, Marta Sevilla, Maria-Magdalena Titirici

ACS Applied Materials & Interfaces· Volume 11· Issue 12

Abstract

The oxygen reduction reaction (ORR) in aqueous media plays a critical role in sustainable and clean energy technologies such as polymer electrolyte membrane and alkaline fuel cells. In this work, we present a new concept to improve the ORR performance by engineering the interface reaction at the electrocatalyst/electrolyte/oxygen triple-phase boundary using a protic and hydrophobic ionic liquid and demonstrate the wide and general applicability of this concept to several Pt-free catalysts. Two catalysts, Fe–N codoped and metal-free N-doped carbon electrocatalysts, are used as a proof of concept. The ionic liquid layer grafted at the nanocarbon surface creates a water-equilibrated secondary reaction medium with a higher O2 affinity toward oxygen adsorption, promoting the diffusion toward the catalytic active site, while its protic character provides sufficient H+/H3O+ conductivity, and the hydrophobic nature prevents the resulting reaction product water from accumulating and blocking the interface. Our strategy brings obvious improvements in the ORR performance in both acid and alkaline electrolytes, while the catalytic activity of FeNC-nanocarbon outperforms commercial Pt–C in alkaline electrolytes. We believe that this research will pave new routes toward the development of high-performance ORR catalysts free of noble metals via careful interface engineering at the triple point.
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 Chemical Engineering, Imperial College London, South Kensington Campus, London SW7 2AZ, U.K.

Instituto Nacional del Carbon (CSIC), P.O. Box 73, Oviedo 33080, Spain

Department of Chemistry, Royal Military Academy, Avenue Renaissance 30, Brussels 1000, Belgium

Funding

Engineering and Physical Sciences Research Council · China Scholarship Council

References (48)

Show source-provided references
1. 10.1002/adma.20160494210.1002/adma.201604942 ↗
2. 10.1021/acsenergylett.8b0024510.1021/acsenergylett.8b00245 ↗
3. 10.1039/c7nr06801h10.1039/c7nr06801h ↗
4. 10.1002/adma.20160645910.1002/adma.201606459 ↗
5. 10.1021/acsnano.7b0583210.1021/acsnano.7b05832 ↗
6. 10.1021/cr500356310.1021/cr5003563 ↗
7. 10.1039/c3ee43463j10.1039/c3ee43463j ↗
8. 10.1002/adma.20120242410.1002/adma.201202424 ↗
9. 10.1002/adma.20170511010.1002/adma.201705110 ↗
10. 10.1002/adma.20160140610.1002/adma.201601406 ↗
11. 10.1002/adma.20160410310.1002/adma.201604103 ↗
12. 10.1016/j.carbon.2017.11.05110.1016/j.carbon.2017.11.051 ↗
13. 10.1039/c6ta04578b10.1039/c6ta04578b ↗
14. 10.1038/nnano.2015.4810.1038/nnano.2015.48 ↗
15. 10.1002/aenm.20150149710.1002/aenm.201501497 ↗
16. 10.1021/cs400192710.1021/cs4001927 ↗
17. 10.1039/c7cc01349c10.1039/c7cc01349c ↗
18. 10.1038/ncomms834310.1038/ncomms8343 ↗
19. 10.1002/adma.20170633010.1002/adma.201706330 ↗
20. 10.1039/c5ta09232a10.1039/c5ta09232a ↗
21. 10.1021/acs.accounts.7b0061610.1021/acs.accounts.7b00616 ↗
22. 10.1021/acs.accounts.6b0031710.1021/acs.accounts.6b00317 ↗
23. 10.1002/adma.20150082110.1002/adma.201500821 ↗
24. 10.1021/acs.accounts.6b0063510.1021/acs.accounts.6b00635 ↗
25. 10.1038/nmat287810.1038/nmat2878 ↗
26. 10.1039/c2ee21411c10.1039/c2ee21411c ↗
27. 10.1021/acscatal.5b0183510.1021/acscatal.5b01835 ↗
28. 10.1002/adfm.20130114410.1002/adfm.201301144 ↗
29. 10.1002/anie.20150833810.1002/anie.201508338 ↗
30. 10.1039/c5cc06256j10.1039/c5cc06256j ↗
31. 10.1039/c6ta10505j10.1039/c6ta10505j ↗
32. 10.1002/adma.20150465210.1002/adma.201504652 ↗
33. 10.1002/adma.20150465210.1002/adma.201504652 ↗
34. 10.1002/chem.20180461010.1002/chem.201804610 ↗
35. 10.1016/j.jcis.2014.10.02410.1016/j.jcis.2014.10.024 ↗
36. 10.1016/j.carbon.2016.05.04210.1016/j.carbon.2016.05.042 ↗
37. 10.1039/c6ra09921a10.1039/c6ra09921a ↗
38. 10.1021/jp500781v10.1021/jp500781v ↗
39. 10.1021/acsnano.6b0124710.1021/acsnano.6b01247 ↗
40. 10.1016/j.carbon.2016.04.08010.1016/j.carbon.2016.04.080 ↗
41. 10.1038/nnano.2012.7210.1038/nnano.2012.72 ↗
42. 10.1149/05901.0137ecst10.1149/05901.0137ecst ↗
43. 10.1016/j.jelechem.2010.05.01610.1016/j.jelechem.2010.05.016 ↗
44. 10.1002/adfm.20170728410.1002/adfm.201707284 ↗
45. Qiao J. · Int. J. Electrochem. Sci. · 2013 · 8 · 118910.1016/S1452-3981(23)14091-0 ↗
46. 10.1016/j.fluid.2014.08.00710.1016/j.fluid.2014.08.007 ↗
47. 10.1016/j.jpowsour.2015.03.04710.1016/j.jpowsour.2015.03.047 ↗
48. 10.1002/(sici)1521-4095(199809)10:13<1036::aid-adma1036>3.0.co;2-z10.1002/(sici)1521-4095(199809)10:13<1036::aid-adma1036>3.0.co;2-z ↗