One-Minute Synthesis via Electroless Reduction of Amorphous Phosphorus-Doped Graphene for Oxygen Reduction Reaction
Source abstract
Abstract
This study reports a simple one-step electroless reduction synthesis of amorphous phosphorus-doped graphene (RGO-P). In just 1 min, RGO-P was synthesized under ambient conditions via a one-step simultaneous reduction and doping of graphene oxide (GO). RGO-P was found to be amorphous with P being essential for the formation of the amorphous structure. RGO-P exhibited enhanced electrocatalytic performance for the oxygen reduction reaction (ORR). The amorphous RGO-P demonstrated superior specific activity and durability compared to crystalline reduced graphene oxide (RGO). Annealing results showed that the amorphous nature of RGO-P was the key factor in its high catalytic activity.
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
School of Mechanical & Aerospace Engineering, Nanyang Technological University, 50 Nanyang Avenue, 639798, Singapore
Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, 999077 Hong Kong, China
Funding
Singapore Ministry of Education
References (30)
Show source-provided references
1. 10.1021/ja500432h10.1021/ja500432h ↗
2. 10.1021/jacs.5b0379910.1021/jacs.5b03799 ↗
3. 10.1016/j.cej.2020.12515410.1016/j.cej.2020.125154 ↗
4. 10.1021/acs.nanolett.1c0024210.1021/acs.nanolett.1c00242 ↗
5. 10.1021/jz300702910.1021/jz3007029 ↗
6. 10.1002/adfm.20110103710.1002/adfm.201101037 ↗
7. 10.1002/adma.20130187010.1002/adma.201301870 ↗
8. 10.1038/ncomms1036410.1038/ncomms10364 ↗
9. 10.1126/sciadv.160182110.1126/sciadv.1601821 ↗
10. 10.1039/C8CP02545B10.1039/C8CP02545B ↗
11. 10.1016/j.physb.2014.08.02010.1016/j.physb.2014.08.020 ↗
12. 10.1002/cctc.20200016410.1002/cctc.202000164 ↗
13. 10.1039/c2jm33209d10.1039/c2jm33209d ↗
14. 10.1016/j.carbon.2013.12.08210.1016/j.carbon.2013.12.082 ↗
15. 10.1016/j.synthmet.2013.04.02010.1016/j.synthmet.2013.04.020 ↗
16. 10.1063/1.514462610.1063/1.5144626 ↗
17. 10.1039/C6RA21329D10.1039/C6RA21329D ↗
18. 10.1039/c3ra41079j10.1039/c3ra41079j ↗
19. 10.1038/nnano.2013.4610.1038/nnano.2013.46 ↗
20. 10.1016/j.physrep.2009.02.00310.1016/j.physrep.2009.02.003 ↗
21. 10.1002/chem.20150217010.1002/chem.201502170 ↗
22. 10.1088/2053-1583/ab185d10.1088/2053-1583/ab185d ↗
23. 10.1021/jz100533t10.1021/jz100533t ↗
24. 10.1126/science.116804910.1126/science.1168049 ↗
25. 10.1021/acscatal.9b0391910.1021/acscatal.9b03919 ↗
26. 10.1002/slct.20160116910.1002/slct.201601169 ↗
27. 10.1021/ja500275r10.1021/ja500275r ↗
28. 10.1016/j.ijhydene.2016.11.10810.1016/j.ijhydene.2016.11.108 ↗
29. 10.1039/C3CC47519K10.1039/C3CC47519K ↗
30. 10.1039/C5CC08669H10.1039/C5CC08669H ↗