CoFe Nanoparticle-Decorated Reduced Graphene Oxide for the Highly Efficient Reduction of 4-Nitrophenol
Source abstract
Abstract
High-performance, nonprecious metal catalysts with special morphologies and easy-to-recycle properties are essential for the treatment of environmental pollutants. Herein, CoFe nanoparticle-decorated reduced graphene oxide (RGO) catalysts were designed and successfully fabricated, and the catalyst was then used to reduce 4-nitrophenol into 4-aminophenol. Outstanding catalytic properties with a reduction rate constant of 4.613 min–1 were achieved due to the synergistic properties of the CoFe metal alloy and the high-conductivity RGO components in the catalysts. In addition, the catalyst was conveniently recovered via magnets due to its inherent magnetic properties. The facile preparation, outstanding catalytic performance, structural stability, and low material costs make the CoFe/RGO nanocatalyst a promising candidate for potential applications in catalysis.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Nanomaterials for catalytic reactions · Advanced Photocatalysis Techniques · Graphene research and applications
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Ministry of Education Key Laboratory for Non-equilibrium Synthesis and Modulation of Condensed Matter, Shaanxi Province Key Laboratory of Advanced Functional Materials and Mesoscopic Physics, School of Physics, Xi’an Jiaotong University, Xi’an 710049, China
Beijing Institute of Control Engineering, Beijing 100190, China
Funding
Ministry of Education of the People's Republic of China · National Natural Science Foundation of China · Natural Science Foundation of Shaanxi Province
References (37)
Show source-provided references
1. 10.1016/j.apcatb.2014.07.00910.1016/j.apcatb.2014.07.009 ↗
2. 10.1016/j.cej.2019.12220210.1016/j.cej.2019.122202 ↗
3. 10.31635/ccschem.021.20210095810.31635/ccschem.021.202100958 ↗
4. 10.1021/acs.langmuir.9b0264510.1021/acs.langmuir.9b02645 ↗
5. 10.1039/c4nr02096k10.1039/c4nr02096k ↗
6. 10.1021/acs.langmuir.7b0174210.1021/acs.langmuir.7b01742 ↗
7. 10.1016/j.carbon.2014.05.02810.1016/j.carbon.2014.05.028 ↗
8. 10.1021/acs.inorgchem.9b0211410.1021/acs.inorgchem.9b02114 ↗
9. 10.1038/nmat417010.1038/nmat4170 ↗
10. 10.1021/cr500537t10.1021/cr500537t ↗
11. 10.1016/j.jallcom.2020.15453610.1016/j.jallcom.2020.154536 ↗
12. 10.1021/acscentsci.0c0126210.1021/acscentsci.0c01262 ↗
13. 10.1016/j.scib.2020.05.00510.1016/j.scib.2020.05.005 ↗
14. 10.1021/acsanm.9b0080910.1021/acsanm.9b00809 ↗
15. 10.1016/j.jcis.2019.09.06410.1016/j.jcis.2019.09.064 ↗
16. 10.1016/j.ceramint.2019.04.16510.1016/j.ceramint.2019.04.165 ↗
17. 10.1016/j.surfcoat.2018.04.02510.1016/j.surfcoat.2018.04.025 ↗
18. 10.1016/j.colsurfa.2015.11.01410.1016/j.colsurfa.2015.11.014 ↗
19. 10.1039/c8qi00479j10.1039/c8qi00479j ↗
20. 10.1021/acs.jpcc.6b1172110.1021/acs.jpcc.6b11721 ↗
21. 10.1016/j.apsusc.2016.07.14610.1016/j.apsusc.2016.07.146 ↗
22. 10.1002/adma.20180450410.1002/adma.201804504 ↗
23. 10.1021/acscatal.8b0266610.1021/acscatal.8b02666 ↗
24. 10.1002/aenm.20160242010.1002/aenm.201602420 ↗
25. 10.1016/j.electacta.2019.01.17010.1016/j.electacta.2019.01.170 ↗
26. 10.1021/am404858z10.1021/am404858z ↗
27. 10.1039/c4tc01351d10.1039/c4tc01351d ↗
28. 10.1016/j.matlet.2018.10.17910.1016/j.matlet.2018.10.179 ↗
29. 10.1021/acs.langmuir.9b0223710.1021/acs.langmuir.9b02237 ↗
30. 10.1021/acs.langmuir.0c0321610.1021/acs.langmuir.0c03216 ↗
31. 10.1021/acs.langmuir.0c0052610.1021/acs.langmuir.0c00526 ↗
32. 10.1021/la500811n10.1021/la500811n ↗
33. 10.1021/acs.langmuir.0c0062910.1021/acs.langmuir.0c00629 ↗
34. 10.1016/j.seppur.2019.11570010.1016/j.seppur.2019.115700 ↗
35. 10.1039/c8nr08302a10.1039/c8nr08302a ↗
36. 10.1016/s1872-2067(16)62561-510.1016/s1872-2067(16)62561-5 ↗
37. 10.1016/j.jhazmat.2016.08.01910.1016/j.jhazmat.2016.08.019 ↗