Mechanism of Oxygen Reduction Reaction on Transition Metal–Nitrogen–Carbon Catalysts: Establishing the Role of Nitrogen-containing Active Sites
Source abstract
Abstract
Using molecular probes that have unique spectral signatures and have strong selective binding to the potential active sites allows elucidating the mechanism of different reactions. The mechanism of oxygen reduction reaction in metal–nitrogen–carbon (MNC) catalysts has been studied by using a bisphosphonate complexing agent, which improves the selectivity of ORR by blocking the protonated and hydrogenated nitrogen that are catalyzing the partial reduction of oxygen to hydrogen peroxide. A combination of theoretical, electrochemical and spectroscopic with focus on near-ambient pressure X-ray photoelectron spectroscopy is used to directly probe the competition between binding of oxygen and molecular probe to the surface of MNC catalyst and to identify the role of different types of nitrogen in the mechanism of ORR.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Molecular Junctions and Nanostructures · Fuel Cells and Related Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Biological Engineering, Center for Micro-Engineered Materials (CMEM), University of New Mexico, Albuquerque, New Mexico 87131, United States
Theoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, United States
Funding
Office of Integrative Activities
References (28)
Show source-provided references
1. 10.1039/C7TA05222G10.1039/C7TA05222G ↗
2. 10.1021/acscatal.7b0399110.1021/acscatal.7b03991 ↗
3. 10.1021/acsenergylett.8b0025810.1021/acsenergylett.8b00258 ↗
4. 10.1021/nn501506p10.1021/nn501506p ↗
5. 10.1021/ja502646c10.1021/ja502646c ↗
6. 10.1039/C0EE00011F10.1039/C0EE00011F ↗
7. 10.1021/acsenergylett.8b0014410.1021/acsenergylett.8b00144 ↗
8. 10.1021/jp204680p10.1021/jp204680p ↗
9. 10.1038/nmat436710.1038/nmat4367 ↗
10. 10.1021/nn203393d10.1021/nn203393d ↗
11. 10.1021/acs.jpcc.5b0765310.1021/acs.jpcc.5b07653 ↗
12. 10.1016/j.nanoen.2016.03.02510.1016/j.nanoen.2016.03.025 ↗
13. 10.1021/acsaem.8b0002010.1021/acsaem.8b00020 ↗
14. 10.1126/science.aan225510.1126/science.aan2255 ↗
15. 10.1002/celc.20180006710.1002/celc.201800067 ↗
16. 10.1021/acs.jpcc.7b0377910.1021/acs.jpcc.7b03779 ↗
17. 10.1021/acscatal.7b0289710.1021/acscatal.7b02897 ↗
18. 10.1038/ncomms1328510.1038/ncomms13285 ↗
19. 10.1021/acscatal.6b0178610.1021/acscatal.6b01786 ↗
20. 10.1021/jz101628410.1021/jz1016284 ↗
21. 10.1021/acs.jpcc.6b1172110.1021/acs.jpcc.6b11721 ↗
22. 10.1021/acsaem.7b0000210.1021/acsaem.7b00002 ↗
23. 10.1021/acs.jpcc.6b0977810.1021/acs.jpcc.6b09778 ↗
24. 10.1016/j.nanoen.2017.02.03910.1016/j.nanoen.2017.02.039 ↗
25. 10.1021/acs.jpcc.5b0765310.1021/acs.jpcc.5b07653 ↗
26. 10.1021/acsenergylett.7b0039110.1021/acsenergylett.7b00391 ↗
27. 10.1016/j.coelec.2018.03.00910.1016/j.coelec.2018.03.009 ↗
28. 10.1021/jp500781v10.1021/jp500781v ↗