journal article·2025-01-17

Ultrathin Rh Nanosheets as a Catalyst for the Selective Hydrogenation of Phenol to Cyclohexanone

Yuan Fang, Shibin Zhu, Wentao Wang, Yanxi Zhao, Qin Li, Tao Huang, Zhan Zhang

ACS Applied Nano Materials· Volume 8· Issue 2
Publisher page

Abstract

The syntheses and catalytic application of two-dimensional (2D) metallic nanomaterials have attracted much attention due to their extraordinary physical, electronic, chemical, and optical properties. Herein, well-defined large-size ultrathin Rh nanosheets with a thickness of approximately 0.72 nm were successfully prepared by using one step solvothermal method at 180 °C for 4 h with Rh(acac) 3 as a precursor, water as a solvent, EDTA·2Na as a stabilizer, and HCHO as both a reducing agent and a shape-controlling agent. The formation of the large-size ultrathin Rh nanosheets was dependent upon EDTA·2Na as well as the selective adsorption of CO, which was originated from HCHO decomposition during the reaction process, on (111) facets of Rh nucleus. The as-synthesized ultrathin Rh nanosheets exhibited excellent catalytic activity and high selectivity of cyclohexanone in hydrogenation of phenol. 100% conversion of phenol as well as 79.74% selectivity of cyclohexanone was achieved over the ultrathin Rh nanosheets with 0.5 MPa H 2 pressure at room temperature within 1.5 h. These results provide a synthesis strategy for ultrathin precious metal nanosheets with catalytic applications.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanomaterials for catalytic reactions · Copper-based nanomaterials and applications · Nanocluster Synthesis and Applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Key Laboratory of Catalysis and Energy Materials Chemistry of Ministry of Education & Hubei Key Laboratory of Catalysis and Materials Science, College of Chemistry and Materials Science, South-Central Minzu University, Wuhan 430074, China

Funding

National Natural Science Foundation of China

References (50)

Show source-provided references
1. 10.1002/anie.20060396110.1002/anie.200603961 ↗
2. 10.1021/ic102041q10.1021/ic102041q ↗
3. 10.1016/j.cattod.2011.10.01410.1016/j.cattod.2011.10.014 ↗
4. 10.1007/s12274-015-0964-y10.1007/s12274-015-0964-y ↗
5. 10.1007/s40843-017-9073-910.1007/s40843-017-9073-9 ↗
6. 10.1039/C3CE40837J10.1039/C3CE40837J ↗
7. 10.1021/la101213q10.1021/la101213q ↗
8. 10.1002/anie.20080357410.1002/anie.200803574 ↗
9. 10.1021/cr300180310.1021/cr3001803 ↗
10. 10.1016/j.catcom.2012.07.00110.1016/j.catcom.2012.07.001 ↗
11. 10.1021/cs300142u10.1021/cs300142u ↗
12. 10.1007/s12274-014-0501-410.1007/s12274-014-0501-4 ↗
13. 10.1007/s12274-014-0674-x10.1007/s12274-014-0674-x ↗
14. 10.1039/b912833f10.1039/b912833f ↗
15. 10.1002/anie.20120604410.1002/anie.201206044 ↗
16. 10.1039/C4NR06917J10.1039/C4NR06917J ↗
17. 10.1007/s12274-016-1258-810.1007/s12274-016-1258-8 ↗
18. 10.1002/anie.20131059710.1002/anie.201310597 ↗
19. 10.1016/j.electacta.2018.06.12610.1016/j.electacta.2018.06.126 ↗
20. 10.1038/ncomms1558110.1038/ncomms15581 ↗
21. 10.1021/ja801210s10.1021/ja801210s ↗
22. 10.1021/jp302471p10.1021/jp302471p ↗
23. 10.1039/C3CC47567K10.1039/C3CC47567K ↗
24. 10.1039/D2RA07445A10.1039/D2RA07445A ↗
25. 10.1002/cnma.20150012210.1002/cnma.201500122 ↗
26. 10.1021/nl104347j10.1021/nl104347j ↗
27. 10.1021/nl403770g10.1021/nl403770g ↗
28. 10.1002/advs.20150025210.1002/advs.201500252 ↗
29. 10.1021/nl048100g10.1021/nl048100g ↗
30. 10.1002/anie.20050317410.1002/anie.200503174 ↗
31. 10.1021/nl070035y10.1021/nl070035y ↗
32. 10.1039/C4NR05986G10.1039/C4NR05986G ↗
33. 10.1039/c3cc39294e10.1039/c3cc39294e ↗
34. 10.1021/jacs.8b0308010.1021/jacs.8b03080 ↗
35. 10.1002/anie.20100254610.1002/anie.201002546 ↗
36. 10.1021/cm902948v10.1021/cm902948v ↗
37. 10.1021/acsami.6b1121010.1021/acsami.6b11210 ↗
38. 10.1039/C7TA10866D10.1039/C7TA10866D ↗
39. 10.1039/C9NR02153A10.1039/C9NR02153A ↗
40. 10.1002/advs.20150010010.1002/advs.201500100 ↗
41. 10.1038/ncomms409310.1038/ncomms4093 ↗
42. 10.1021/jacs.3c1046510.1021/jacs.3c10465 ↗
43. 10.1021/jacs.0c0021810.1021/jacs.0c00218 ↗
44. 10.1002/adma.20231435110.1002/adma.202314351 ↗
45. 10.1039/D3EE04023B10.1039/D3EE04023B ↗
46. 10.1002/cnma.20200047810.1002/cnma.202000478 ↗
47. 10.1021/acs.chemrev.6b0055810.1021/acs.chemrev.6b00558 ↗
48. 10.1021/acs.chemrev.7b0072710.1021/acs.chemrev.7b00727 ↗
49. 10.1039/C8CS00113H10.1039/C8CS00113H ↗
50. 10.1039/b100237f10.1039/b100237f ↗