journal article·2015-06-25

Tracking Site-Specific C–C Coupling of Formaldehyde Molecules on Rutile TiO2(110)

Ke Zhu, Yaobiao Xia, Miru Tang, Zhi-Tao Wang, Bryan Jan, Igor Lyubinetsky, Qingfeng Ge, Zdenek Dohnálek, Kenneth T. Park, Zhenrong Zhang

The Journal of Physical Chemistry C· Volume 119· Issue 25
Publisher page

Abstract

Direct imaging of site-specific reactions of individual molecules as a function of temperature has been a long-sought goal in molecular science. Here, we report the direct visualization of molecular coupling of formaldehyde on reduced rutile TiO 2 (110) surfaces as we track the same set of molecules using scanning tunneling microscopy (STM) when the temperature is increased from 75 to 170 K. Our previous study showed that formaldehyde preferably adsorbs at bridging-bonded oxygen (O b ) vacancy (V O ) defect site. Herein, images from the same area as the temperature is increased show that V O -bound formaldehyde couples with Ti-bound formaldehyde forming a diolate intermediate. Consequently, exposure of formaldehyde at room temperature leads to diolate as the majority species on the surface, and no V O -bound formaldehyde is observed. The diolate species are the key reaction intermediates in the formation of ethylene reported in previous ensemble-averaged studies.
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Research context

OpenAlex topics: Electronic and Structural Properties of Oxides · Catalysis and Oxidation Reactions · Catalytic Processes in Materials Science

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

Affiliations

Department of Physics, Baylor University, Waco, Texas 76798, United States

Department of Chemistry and Biochemistry, Southern Illinois University, Carbondale, Illinois 62901, United States

Funding

American Chemical Society Petroleum Research Fund · U.S. Department of Energy (DOE) Basic Energy Science (BES) · U.S. DOE BES, Division of Chemical Sciences, Biosciences and Geosciences

References (31)

Show source-provided references
1. Chheda J. N. · Angew. Chem., Int. Ed. · 2007 · 46 · 716410.1002/anie.200604274 ↗
2. Hirao T. · Top. Curr. Chem. · 2007 · 279 · 5310.1007/128_2007_120 ↗
3. Wikipedia Formaldehyde.http://en.wikipedia.org/wiki/Formaldehyde.
4. Pelaez M. · Appl. Catal., B · 2012 · 125 · 33110.1016/j.apcatb.2012.05.036 ↗
5. Shen M. · J. Am. Chem. Soc. · 2009 · 131 · 870810.1021/ja9023379 ↗
6. Queeney K. T. · Surf. Sci. · 1998 · 418 · L3110.1016/S0039-6028(98)00754-7 ↗
7. Wang H. · J. Phys. Chem. C · 2012 · 116 · 1063910.1021/jp301364w ↗
8. Qiu H. · J. Phys. Chem. C · 2008 · 112 · 982810.1021/jp801327b ↗
9. Haubrich J. · Chem.—Eur. J. · 2011 · 17 · 449610.1002/chem.201002588 ↗
10. Senanayake S. D. · Catal. Today · 2003 · 85 · 31110.1016/S0920-5861(03)00397-3 ↗
11. Kim J. · J. Phys. Chem. C · 2010 · 114 · 1701710.1021/jp102710m ↗
12. Truong C. M. · J. Am. Chem. Soc. · 1993 · 115 · 364710.1021/ja00062a032 ↗
13. Yuan Q. · J. Phys. Chem. C · 2014 · 118 · 2042010.1021/jp5061733 ↗
14. Benz L. · ACS Nano · 2011 · 5 · 83410.1021/nn103144u ↗
15. Salciccioli M. · J. Am. Chem. Soc. · 2011 · 133 · 799610.1021/ja201801t ↗
16. Brown N. F. · J. Phys. Chem. · 1994 · 98 · 1273710.1021/j100099a043 ↗
17. Queeney K. · J. Am. Chem. Soc. · 1996 · 118 · 389610.1021/ja953987r ↗
18. Capote A. J. · J. Am. Chem. Soc. · 1989 · 111 · 357010.1021/ja00192a013 ↗
19. Acharya D. P. · ACS Nano · 2013 · 7 · 1041410.1021/nn404934q ↗
20. Muir J. M. R. · Chem. Phys. Lett. · 2013 · 572 · 12510.1016/j.cplett.2013.03.070 ↗
21. Liu H. · J. Phys. Chem. C · 2012 · 116 · 804410.1021/jp210465u ↗
22. Xu C. · J. Phys. Chem. Lett. · 2013 · 4 · 266810.1021/jz401349q ↗
23. Zehr R. T. · Surf. Sci. · 2008 · 602 · 223810.1016/j.susc.2008.04.045 ↗
24. Idriss H. · Catal. Lett. · 1996 · 40 · 14710.1007/BF00815275 ↗
25. Clawin P. M. · Chem.—Eur. J. · 2014 · 20 · 766510.1002/chem.201402102 ↗
26. Zhang Z. · Top. Catal. · 2015 · 58 · 10310.1007/s11244-014-0349-6 ↗
27. Diebold U. · Surf. Sci. Rep. · 2003 · 48 · 5310.1016/S0167-5729(02)00100-0 ↗
28. Horcas I. · Rev. Sci. Instrum. · 2007 · 78 · 01370510.1063/1.2432410 ↗
29. Li Z. · Phys. Chem. Chem. Phys. · 2013 · 15 · 1218010.1039/c3cp50687h ↗
30. Zhang Z. · J. Phys. Chem. B · 2006 · 110 · 2184010.1021/jp063619h ↗
31. Zhu, K.; Xia, Y.; Tang, M.; Wang, Z.; Jan, B.; Lyubinetsky, I.; Dohnálek, Z.; Ge, Q.; Park, K. T.; Zhang, Z.Manuscript in preparation.