journal article·2020-07-15

Carbon Monoxide Oxidation over rGO-Mediated Gold/Cobalt Oxide Catalysts with Strong Metal–Support Interaction

Shaohua Xie, Yuxi Liu, Jiguang Deng, Jun Yang, Xingtian Zhao, Zhuo Han, Kunfeng Zhang, Yue Lu, Fudong Liu, Hongxing Dai

ACS Applied Materials & Interfaces· Volume 12· Issue 28
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Abstract

The strong interaction between Au nanoparticles and support (Au–metal oxide interface) usually governs the performance of a supported Au catalyst in heterogeneous catalysis. In this study, a series of Au/reduced graphene oxide (rGO)/three-dimensionally ordered macroporous (3DOM) Co3O4 catalysts with similar textural properties were prepared using the poly(methyl methacrylate)-templating and poly(vinyl alcohol)-protected reduction strategies. It was found that introducing reduced graphene oxide (rGO) as an electron-transfer bridge between Au and 3DOM Co3O4 could significantly strengthen the strong metal–support interaction (SMSI), thus enhancing the catalytic activity for CO oxidation. Among all of the catalysts, 1.86 wt % Au/2 wt % rGO/3DOM Co3O4 (1.86Au/2rGO/3DOM Co3O4) showed the highest catalytic activity: the CO reaction rate at 40 °C (432.8 μmol/(gAu s)) was 2 times higher than that (208.2 μmol/(gAu s)) over 1.87Au/3DOM Co3O4. The introduction of rGO could improve the activation of oxygen molecules and hence increase the low-temperature catalytic activity. The strategy for strengthening the SMSI via rGO mediation would guide the designing of highly efficient supported metal catalysts for low-temperature oxidation of CO.
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Research context

OpenAlex topics: Catalytic Processes in Materials Science · Nanomaterials for catalytic reactions · Electrocatalysts for Energy Conversion

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

Affiliations

Beijing Key Laboratory for Green Catalysis and Separation, Key Laboratory of Beijing on Regional Air Pollution Control, and Laboratory of Catalysis Chemistry and Nanoscience, Department of Chemistry and Chemical Engineering, College of Environmental and Energy Engineering, Beijing University of Technology, Beijing 100124, China

Department of Civil, Environmental, and Construction Engineering (CECE), Catalysis Cluster for Renewable Energy and Chemical Transformations (REACT), NanoScience Technology Center (NSTC), University of Central Florida, Orlando, Florida 32816, United States

Funding

National Natural Science Foundation of China · National Natural Science Committee of China-Liaoning Provincial People's Government Joint Fund · Foundation on the Creative Research Team Construction Promotion Project of Beijing Municipal Institutions · Startup Fund from the University of Central Florida

References (56)

Show source-provided references
1. 10.1246/cl.1987.40510.1246/cl.1987.405 ↗
2. 10.1039/c3988000007110.1039/c39880000071 ↗
3. 10.1021/jp960593t10.1021/jp960593t ↗
4. 10.1021/ar400203e10.1021/ar400203e ↗
5. 10.1126/science.281.5383.164710.1126/science.281.5383.1647 ↗
6. 10.1126/science.120727210.1126/science.1207272 ↗
7. 10.1023/A:101908172717310.1023/A:1019081727173 ↗
8. 10.1006/jcat.1999.253110.1006/jcat.1999.2531 ↗
9. 10.1016/j.jcat.2004.01.00110.1016/j.jcat.2004.01.001 ↗
10. 10.1016/j.jcat.2009.08.00310.1016/j.jcat.2009.08.003 ↗
11. 10.1007/BF0081630510.1007/BF00816305 ↗
12. 10.1021/jacs.5b0633610.1021/jacs.5b06336 ↗
13. 10.1038/nature0787710.1038/nature07877 ↗
14. 10.1002/adfm.20190204110.1002/adfm.201902041 ↗
15. 10.1016/j.cattod.2019.02.03910.1016/j.cattod.2019.02.039 ↗
16. 10.1016/j.jhazmat.2011.01.07310.1016/j.jhazmat.2011.01.073 ↗
17. 10.1039/b808815b10.1039/b808815b ↗
18. 10.1039/c3nr04126c10.1039/c3nr04126c ↗
19. 10.1016/j.jcat.2014.09.02410.1016/j.jcat.2014.09.024 ↗
20. 10.1016/j.jcat.2013.10.01910.1016/j.jcat.2013.10.019 ↗
21. 10.1021/acscatal.9b0199510.1021/acscatal.9b01995 ↗
22. 10.1016/j.jcat.2015.09.00810.1016/j.jcat.2015.09.008 ↗
23. 10.1039/C7CY02007D10.1039/C7CY02007D ↗
24. 10.1002/adma.20100106810.1002/adma.201001068 ↗
25. 10.1021/nl072090c10.1021/nl072090c ↗
26. 10.1021/ie301642g10.1021/ie301642g ↗
27. 10.1016/j.apcatb.2012.05.02310.1016/j.apcatb.2012.05.023 ↗
28. 10.1016/j.carbon.2009.11.03410.1016/j.carbon.2009.11.034 ↗
29. 10.1021/cm990776310.1021/cm9907763 ↗
30. 10.1021/cm048759n10.1021/cm048759n ↗
31. 10.1039/b513833g10.1039/b513833g ↗
32. 10.1038/ncomms1290510.1038/ncomms12905 ↗
33. 10.1126/science.115963910.1126/science.1159639 ↗
34. 10.1002/anie.20100045210.1002/anie.201000452 ↗
35. 10.1021/cr010350j10.1021/cr010350j ↗
36. 10.1002/smll.20070129510.1002/smll.200701295 ↗
37. 10.1039/C5NR02216A10.1039/C5NR02216A ↗
38. 10.1021/cs500666310.1021/cs5006663 ↗
39. 10.1088/0022-3719/21/7/00710.1088/0022-3719/21/7/007 ↗
40. 10.1016/j.jcat.2006.04.01810.1016/j.jcat.2006.04.018 ↗
41. 10.1016/j.apcata.2012.12.04910.1016/j.apcata.2012.12.049 ↗
42. 10.1002/cssc.20140005010.1002/cssc.201400050 ↗
43. 10.1016/0926-3373(96)90129-010.1016/0926-3373(96)90129-0 ↗
44. 10.1021/ja906274t10.1021/ja906274t ↗
45. 10.1016/j.jcat.2017.05.01610.1016/j.jcat.2017.05.016 ↗
46. 10.1039/B512799H10.1039/B512799H ↗
47. 10.1016/j.jpowsour.2012.10.06410.1016/j.jpowsour.2012.10.064 ↗
48. 10.1016/j.apcatb.2014.01.06210.1016/j.apcatb.2014.01.062 ↗
49. 10.1021/ja043752s10.1021/ja043752s ↗
50. 10.1006/jcat.1999.251710.1006/jcat.1999.2517 ↗
51. 10.1002/(SICI)1097-4555(199701)28:1<29::AID-JRS59>3.0.CO;2-G10.1002/(SICI)1097-4555(199701)28:1<29::AID-JRS59>3.0.CO;2-G ↗
52. 10.1016/j.cattod.2005.11.05110.1016/j.cattod.2005.11.051 ↗
53. 10.1006/jcat.2000.306910.1006/jcat.2000.3069 ↗
54. 10.1126/science.119177810.1126/science.1191778 ↗
55. 10.1016/j.jcat.2003.09.02010.1016/j.jcat.2003.09.020 ↗
56. 10.1016/j.apcatb.2016.10.03310.1016/j.apcatb.2016.10.033 ↗