Novel CdFe Bimetallic Complex-Derived Ultrasmall Fe- and N-Codoped Carbon as a Highly Efficient Oxygen Reduction Catalyst
Source abstract
Abstract
During the development of oxygen reduction reaction electrocatalysts, transition-metal nanoparticles embedded in N-doped graphene have attracted increasing attention owing to their low-priced, minimal environmental impact, and satisfying performance. In this study, a new organic-cadmium (Cd) complex formed through Cd2+ coordination with p-phenylenediamine (PPD) was used to synthesize highly active Fe-embedded N-doped carbon catalysts for the first time. It is significant that with the decreasing molar ratio of Cd/Fe, an obvious microstructure evolution was observed in Cd–Fe–PPD from diamond-like blocks to thick flakes, and further bloomed into flowerlike shapes with ultrathin petals and then eventually exhibited large block starfish-like shapes. After carbonization, Cd was removed, slack and porous N-doped carbon was formed, and Fe was assembled in the N-doped carbon. Similar phenomenon was also observed in Co–PPD. The optimized Fe/NPC-2 material featuring uniform and well-dispersed 3–5 nm Fe nanoparticles embedded in two-dimensional ultrathin carbon nanosheets delivered excellent electrocatalytic performance (Eonset: 0.96 V vs reversible hydrogen electrode (RHE), E1/2: 0.84 V vs RHE), which is very close to those of commercial platinum on carbon (Pt/C) (Eonset: 0.95 V vs RHE, E1/2: 0.84 V vs RHE), and its methanol tolerance and durability also surpass those of Pt/C.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Electrocatalysts for Energy Conversion · Fuel Cells and Related Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Luminescent and Real-Time Analytical Chemistry, Ministry of Education, Institute for Clean Energy and Advanced Materials, Faculty of Materials and Energy, Southwest University, Chongqing 400715, P. R. China
Funding
Natural Science Foundation of Chongqing · National Natural Science Foundation of China · Chongqing Key Laboratory for Advanced Materials and Technologies · Chongqing Engineering Research Center for Micro-Nano Biomedical Materials and Devices
References (47)
Show source-provided references
1. 10.1021/acs.chemrev.5b0046210.1021/acs.chemrev.5b00462 ↗
2. 10.1002/adma.20170252610.1002/adma.201702526 ↗
3. 10.1039/C8NR02492H10.1039/C8NR02492H ↗
4. 10.1002/adma.20160307510.1002/adma.201603075 ↗
5. 10.1002/aenm.20170054410.1002/aenm.201700544 ↗
6. 10.1021/jacs.7b1066310.1021/jacs.7b10663 ↗
7. 10.1021/jacs.7b0813310.1021/jacs.7b08133 ↗
8. 10.1021/acsami.5b1049310.1021/acsami.5b10493 ↗
9. 10.1002/adma.20160680010.1002/adma.201606800 ↗
10. 10.1002/anie.20140035810.1002/anie.201400358 ↗
11. 10.1021/ja512913210.1021/ja5129132 ↗
12. 10.1002/adfm.20160360710.1002/adfm.201603607 ↗
13. 10.1039/c4cc02781g10.1039/c4cc02781g ↗
14. 10.1002/anie.20160188710.1002/anie.201601887 ↗
15. 10.1039/C5NR00013K10.1039/C5NR00013K ↗
16. 10.1016/j.jpowsour.2018.11.02410.1016/j.jpowsour.2018.11.024 ↗
17. 10.1039/C8TA06743K10.1039/C8TA06743K ↗
18. 10.1021/jacs.6b0947010.1021/jacs.6b09470 ↗
19. 10.1002/adfm.20170755110.1002/adfm.201707551 ↗
20. 10.1021/ja303056510.1021/ja3030565 ↗
21. 10.1002/adfm.20160063610.1002/adfm.201600636 ↗
22. 10.1039/C7CY01721A10.1039/C7CY01721A ↗
23. 10.1021/acsami.7b1964510.1021/acsami.7b19645 ↗
24. 10.1039/C4CC09062D10.1039/C4CC09062D ↗
25. 10.1021/acsami.7b1693610.1021/acsami.7b16936 ↗
26. 10.1039/C6TA03820D10.1039/C6TA03820D ↗
27. 10.1002/adma.20150504510.1002/adma.201505045 ↗
28. 10.1038/ncomms142710.1038/ncomms1427 ↗
29. 10.1016/j.nanoen.2016.04.04210.1016/j.nanoen.2016.04.042 ↗
30. 10.1002/adma.20150231510.1002/adma.201502315 ↗
31. 10.1002/adfm.20180259610.1002/adfm.201802596 ↗
32. 10.1002/adfm.20150231110.1002/adfm.201502311 ↗
33. 10.1039/C8NR07463A10.1039/C8NR07463A ↗
34. 10.1002/adfm.20170079510.1002/adfm.201700795 ↗
35. 10.1016/j.apcatb.2017.10.01510.1016/j.apcatb.2017.10.015 ↗
36. 10.1021/acsami.7b0878610.1021/acsami.7b08786 ↗
37. 10.1016/j.electacta.2016.04.03710.1016/j.electacta.2016.04.037 ↗
38. 10.1002/adfm.20170453710.1002/adfm.201704537 ↗
39. 10.1002/adfm.20160619010.1002/adfm.201606190 ↗
40. 10.1039/C7NR09373J10.1039/C7NR09373J ↗
41. 10.1021/acsnano.7b0583210.1021/acsnano.7b05832 ↗
42. 10.1016/j.jpowsour.2018.12.04710.1016/j.jpowsour.2018.12.047 ↗
43. 10.1039/C4DT03726J10.1039/C4DT03726J ↗
44. 10.1002/anie.20161011910.1002/anie.201610119 ↗
45. 10.1039/c1cp21665a10.1039/c1cp21665a ↗
46. 10.1021/cs500673k10.1021/cs500673k ↗
47. 10.1007/s12274-016-1374-510.1007/s12274-016-1374-5 ↗