journal article·2017-09-20

A Rational Solid-State Synthesis of Supported Au–Ni Bimetallic Nanoparticles with Enhanced Activity for Gas-Phase Selective Oxidation of Alcohols

Wuzhong Yi, Wentao Yuan, Ye Meng, Shihui Zou, Yuheng Zhou, Wei Hong, Jianwei Che, Mengjia Hao, Bin Ye, Liping Xiao, Yong Wang, Hisayoshi Kobayashi, Jie Fan

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Abstract

A facile confined solid-state seed-mediated alloying strategy is applied for the rational synthesis of supported Au–Ni bimetallic nanoparticles (BMNPs). The method sequentially deposits nickel salts and AuNP seeds into the ordered array of extra-large mesopores (EP-FDU-12 support) followed by a high-temperature annealing process. The size, structure, and composition of the AuNi BMNPs can be well tuned by varying the AuNP seeds, annealing temperature, and feeding ratio of metal precursors. Kinetic studies and DFT calculations suggest that the introduction of the Ni component can significantly prompt the O 2 activation on AuNPs, which is critical for the selective alcohol oxidation using molecular O 2 as the oxidant. The optimal Au–Ni BMNP catalyst showed the highest turnover frequency (TOF) (59 000 h –1, 240 °C) and highest space-time yield (STY) of benzyl aldehyde (BAD) productivity (9.23 kg·g Au –1 ·h –1 ) in the gas-phase oxidation of benzyl alcohol (BA), which is at least about 5-fold higher than that of other supported Au catalysts.
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Research context

OpenAlex topics: Catalytic Processes in Materials Science · Catalysis and Oxidation Reactions · Oxidative Organic Chemistry Reactions

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

Affiliations

Department of Chemistry and Materials Technology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan

Funding

Ministry of Education of the People's Republic of China · Fok Ying Tong Education Foundation · National Natural Science Foundation of China · Shell

References (37)

Show source-provided references
1. 10.1021/cr020011610.1021/cr0200116 ↗
2. 10.1039/b707319b10.1039/b707319b ↗
3. 10.1002/asia.20070035910.1002/asia.200700359 ↗
4. 10.1038/376238a010.1038/376238a0 ↗
5. 10.1126/science.118359110.1126/science.1183591 ↗
6. 10.1021/ja067316c10.1021/ja067316c ↗
7. 10.1021/ar400203e10.1021/ar400203e ↗
8. Enache D. I. · Science · 2006 · 311 · 36210.1126/science.1120560 ↗
9. 10.1021/jp101845d10.1021/jp101845d ↗
10. 10.1021/jp503758t10.1021/jp503758t ↗
11. 10.1002/adma.20100369510.1002/adma.201003695 ↗
12. 10.1016/j.jcat.2007.02.00810.1016/j.jcat.2007.02.008 ↗
13. 10.1021/ja102752410.1021/ja1027524 ↗
14. 10.1002/smll.20100168510.1002/smll.201001685 ↗
15. 10.1103/RevModPhys.64.104510.1103/RevModPhys.64.1045 ↗
16. 10.1002/(SICI)1097-461X(2000)77:5<895::AID-QUA10>3.0.CO;2-C10.1002/(SICI)1097-461X(2000)77:5<895::AID-QUA10>3.0.CO;2-C ↗
17. 10.1103/PhysRevLett.77.386510.1103/PhysRevLett.77.3865 ↗
18. 10.1103/PhysRevB.41.789210.1103/PhysRevB.41.7892 ↗
19. 10.1021/ja100845v10.1021/ja100845v ↗
20. 10.1021/cs400197t10.1021/cs400197t ↗
21. 10.1016/j.jallcom.2009.11.11110.1016/j.jallcom.2009.11.111 ↗
22. 10.1016/j.jpowsour.2014.06.15110.1016/j.jpowsour.2014.06.151 ↗
23. 10.1021/acs.jpcc.6b1299510.1021/acs.jpcc.6b12995 ↗
24. Baker H. · 1992 · 3
25. 10.1021/cm303816g10.1021/cm303816g ↗
26. 10.1039/C2CY20579C10.1039/C2CY20579C ↗
27. 10.1007/s00269005026510.1007/s002690050265 ↗
28. 10.1007/s11426-014-5266-910.1007/s11426-014-5266-9 ↗
29. 10.1126/science.125255310.1126/science.1252553 ↗
30. Hagen J. · 201510.1002/9783527684625 ↗
31. 10.1039/C4TA01503G10.1039/C4TA01503G ↗
32. 10.1016/j.catcom.2008.05.00810.1016/j.catcom.2008.05.008 ↗
33. 10.1002/cctc.20110028610.1002/cctc.201100286 ↗
34. 10.1002/anie.20070437010.1002/anie.200704370 ↗
35. 10.1016/j.apcata.2010.03.02610.1016/j.apcata.2010.03.026 ↗
36. 10.1002/cphc.20080058710.1002/cphc.200800587 ↗
37. 10.1021/cs300551r10.1021/cs300551r ↗