Nitrogen-Doped PtNi Catalysts on Polybenzimidazole-Functionalized Carbon Support for the Oxygen Reduction Reaction in Polymer Electrolyte Membrane Fuel Cells
Source abstract
Abstract
PtM (M = 3d transition metals) alloys are known as the promising oxygen reduction reaction catalysts and have been considered as the replacement of pure Pt catalysts for the commercialization of proton exchange membrane fuel cells. Although great progress has been made in the past three decades, the performance and durability of PtM catalysts still face stringent challenges from practical applications. Functionalization of a catalyst carbon support with nitrogen-contained groups can add charges onto its surface, which can be utilized to build a more complete ionomer/catalyst interface, to reduce the catalyst particle size, and to improve particle size distribution. Nitriding of PtNi catalysts can effectively improve the catalyst activity and stability by the modification of lattice strain. Hereby, we propose a synergistic approach of combining polybenzimidazole-grafted Vulcan XC72 carbon as the catalyst carbon support and the nitriding of PtNi to develop PtNiN/XC72-polybenzimidazole catalysts. Such PtNiN/XC72-PBI catalysts exhibit the excellent performance of fuel cell membrane electrode assembly (i.e., mass activity, 440 mA mgPt–1; electrochemical surface area, 51 m2 gPt–1; and rated power density, 836 mW cm–2) as well as promising catalyst stability. The developed PtNiN/XC72-PBI meets the US DOE 2020 targets of mass activity for the fuel cell catalysts. This work provides a novel approach and a promising pathway on the development of the catalyst using such a synergistic approach─modification of the catalyst structure by nitrogen doping and functionalization of carbon support by polybenzimidazole for both high performance and high durability.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advanced Memory and Neural Computing
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Mechanical Energy Engineering, Purdue School of Engineering and Technology, Indiana University-Purdue University, Indianapolis, Indiana 46202, United States
School of Mechanical Engineering, Purdue University, West Lafayette, Indiana 47906, United States
Chemistry Division, Brookhaven National Laboratory, Upton, New York 11973, United States
Funding
Fuel Cell Technologies Program
References (29)
Show source-provided references
1. 10.1016/j.matt.2019.07.01510.1016/j.matt.2019.07.015 ↗
2. 10.1021/nl302995z10.1021/nl302995z ↗
3. 10.1021/acscatal.0c0004010.1021/acscatal.0c00040 ↗
4. 10.1149/2.0391815jes10.1149/2.0391815jes ↗
5. 10.1002/anie.20050438610.1002/anie.200504386 ↗
6. 10.1021/acs.jpcc.8b1149410.1021/acs.jpcc.8b11494 ↗
7. 10.1149/2.0341806jes10.1149/2.0341806jes ↗
8. 10.1149/08008.0861ecst10.1149/08008.0861ecst ↗
9. 10.1021/nl303362s10.1021/nl303362s ↗
10. 10.1021/acscatal.0c0303610.1021/acscatal.0c03036 ↗
11. 10.1002/smtd.20180055010.1002/smtd.201800550 ↗
12. 10.1021/acsaem.2c0063110.1021/acsaem.2c00631 ↗
13. 10.1149/2.1621704jes10.1149/2.1621704jes ↗
14. 10.1016/j.electacta.2013.01.09710.1016/j.electacta.2013.01.097 ↗
15. Kinoshita K. · 1988 · 316
16. 10.1149/2.0051707jes10.1149/2.0051707jes ↗
17. 10.1038/s41563-019-0487-010.1038/s41563-019-0487-0 ↗
18. 10.1002/anie.20140899010.1002/anie.201408990 ↗
19. 10.1016/j.nanoen.2015.06.03110.1016/j.nanoen.2015.06.031 ↗
20. Xin L. · ECS Meet. Abstr. · 2016 · 2016 · 258510.1149/MA2016-02/38/2585 ↗
21. 10.1021/acscatal.5b0272210.1021/acscatal.5b02722 ↗
22. 10.1021/ac100306c10.1021/ac100306c ↗
23. Office, U. S. Fuel Cells Technologies Office Corporate. Multi-Year Research, Development, and Demonstration Plan; 2016. (accessed 2022-05-10)
24. 10.1021/acscatal.0c0402110.1021/acscatal.0c04021 ↗
25. 10.1016/j.apcatb.2004.06.02110.1016/j.apcatb.2004.06.021 ↗
26. 10.1149/MA2016-02/38/258410.1149/MA2016-02/38/2584 ↗
27. 10.1126/science.aaw749310.1126/science.aaw7493 ↗
28. 10.1126/science.aau063010.1126/science.aau0630 ↗
29. 10.1039/C4EE02144D10.1039/C4EE02144D ↗