Citation: WANG Chen, WEI Zi-Zhang, LÜ Yong-Kang, XING Bin, WANG Gui-Chang. Theoretical Investigation of Structure-Sensitivity of Styrene Epoxidation on Ag(111) and Ag(110) Surfaces[J]. Acta Physico-Chimica Sinica doi: 10.3866/PKU.WHXB201302043 shu

Theoretical Investigation of Structure-Sensitivity of Styrene Epoxidation on Ag(111) and Ag(110) Surfaces

1.
1 Key Laboratory of Coal Science and Technology, Ministry of Education and Shanxi Province, Taiyuan University of Technology, Taiyuan 030024, P. R. China;
2 Tianjin Enviromental Engineering Assessment Center, Tianjin 300191, P. R. China;
3 Department of Chemistry and the Tianjin Key Laboratory of Metal and Molecule-based Material Chemistry, Nankai University, Tianjin 300071, P. R. China

Received Date: 7 November 2012
Available Online: 4 February 2013
Fund Project: 国家自然科学基金(21078252)资助项目 (21078252)

The selective oxidation of styrene on oxygen-covered Ag(110) and Ag(111) surfaces is studied by density functional theory (DFT) calculations with the periodic slab model. On the Ag(110) surface, a pre-adsorbed oxygen atom prefers the 3-fold hollow site (3h) with an adsorption energy of -3.59 eV. On the Ag(111) surface, the most stable adsorption site for a pre-adsorbed oxygen atom is the fcc site, and the adsorption energy is -3.69 eV. The reaction process of the selective oxidation of styrene includes two steps: the formation of surface intermediates (branched oxametallacycle and linear oxametallacycle) and the subsequent formation of different products. The calculated results show that the formation of styrene oxide via the linear oxametallacycle (i.e., the pre-adsorbed atomic oxygen bound to the methylene group in styrene) is the favorable reaction mechanism on both Ag(110) and Ag(111) surfaces. The reaction barriers for the different reaction steps of styrene epoxidation on the Ag(110) surface are generally higher than those on the Ag(111) surface. Moreover, the micro-kinetic simulation results indicate that the relative selectivity towards the formation of styrene oxide on the Ag(111) surface is much higher than that on the Ag(110) surface (0.38 vs 0.003) because the energy barrier for the styrene epoxidation is smaller than that for the formation of phenyl acetaldehyde and its combustion intermediate on Ag(111) surface. The reverse trends occurred on the Ag(110) surface.
- Styrene,
- Selective oxidation,
- Structure sensitivity,
- Ag catalyst,
- Density functional theory calculation
1. [1]
  
  (1) Barteau, M. A. Surf. Sci. 2006, 600, 5021. doi: 10.1016/j.susc.2006.09.024
2. [2]
  (2) Klust, A.; Madix, R. J. Surf. Sci. 2006, 600, 5025. doi: 10.1016/j.susc.2006.08.049
3. [3]
  (3) Serafin, J. G.; Liu, A. C.; Seyedmonir, S. R. J. Mol. Catal. A:Chem. 1998, 131, 157. doi: 10.1016/S1381-1169(97)00263-X
4. [4]
  (4) Bocquet, M. L.; Sautet, P.; Cerda, J.; Carlisle, C. I.;Webb, M. J.;King, D. A. J. Am. Chem. Soc. 2003, 125, 3119. doi: 10.1021/ja027634l
5. [5]
  (5) Linic, S.; Barteau, M. A. J. Am. Chem. Soc. 2002, 124, 310. doi: 10.1021/ja0118136
6. [6]
  (6) Linic, S.; Barteau, M. A. J. Am. Chem. Soc. 2003, 125, 4034.doi: 10.1021/ja029076g
7. [7]
  (7) Park, D. M.; Ghazali, S.; Gau, G. Appl. Catal. 1983, 6 (2), 175.doi: 10.1016/0166-9834(83)80263-2
8. [8]
  (8) Zhou, L.; Madix, R. J. Surf. Sci. 2009, 603, 1751. doi: 10.1016/j.susc.2008.08.032
9. [9]
  (9) Bocquet, M. L.; Loffreda, D. J. Am. Chem. Soc. 2005, 127,17207. doi: 10.1021/ja051397f
10. [10]
  (10) Linic, S.; Piao, H.; Adib, K.; Barteau, M. A. Angew. Chem. Int.Edit. 2004, 43, 2918.
11. [11]
  (11) Christopher, P.; Linic, S. J. Am. Chem. Soc. 2008, 130, 11264.doi: 10.1021/ja803818k
12. [12]
  (12) Chen, H. T.; Chang, J. G.; Ju, S. P.; Chen, H. L. J. Phys. Chem.Lett. 2010, 1, 739. doi: 10.1021/jz900469f
13. [13]
  (13) Barteau, M. A.; Madix, R. J. Surf. Sci. 1981, 103 (2-3), L171.
14. [14]
  (14) Roberts, J. T.; Madix, R. J. J. Am. Chem. Soc. 1988, 110, 8540.doi: 10.1021/ja00233a038
15. [15]
  (15) Lambert, R. M.;Williams, F. J.; Cropley, R. L.; Palermo, A.J. Mol. Catal. A: Chem. 2005, 228 (1-2), 27. doi: 10.1016/j.molcata.2004.09.077
16. [16]
  (16) Hawker, S.; Mukoid, C.; Badyal, J. P. S.; Lambert, R. M. Surf.Sci. Lett. 1989, 219 (3), L615.
17. [17]
  (17) Williams, F. J.; Bird, D. P. C.; Palermo, A.; Santra, A. K.;Lambert, R. M. J. Am. Chem. Soc. 2004, 126, 8509. doi: 10.1021/ja039378y
18. [18]
  (18) Klust, A.; Madix, R. J. J. Am. Chem. Soc. 2006, 128, 1034. doi: 10.1021/ja054845s
19. [19]
  (19) Liu, X. Y.; Klust, A.; Madix, R. J.; Friend, C. M. J. Phys. Chem.C 2007, 111, 3675. doi: 10.1021/jp066560n
20. [20]
  (20) Zhou, L.; Madix, R. J. J. Phys. Chem. C 2008, 112, 4725. doi: 10.1021/jp7119558
21. [21]
  (21) Mukoid, C.; Hawker, S.; Badyal, J. P. S.; Lambert, R. M. Catal.Lett. 1990, 4 (1), 57. doi: 10.1007/BF00764871
22. [22]
  (22) Deng, X. Y.; Friend, C. M. J. Am. Chem. Soc. 2005, 127, 17178.doi: 10.1021/ja0557031
23. [23]
  (23) Quiller, R. G.; Liu, X. Y.; Friend, C. M. Chemistry-An AsianJournal 2010, 5 (1), 78. doi: 10.1002/asia.v5:1
24. [24]
  (24) Kresse, G.; Furthmüller, J. Comp. Mater. Sci. 1996, 6, 15. doi: 10.1016/0927-0256(96)00008-0
25. [25]
  (25) Kresse, G.; Hafner, J. Phys. Rev. B 1994, 49, 14251. doi: 10.1103/PhysRevB.49.14251
26. [26]
  (26) Perdew, J. P.; Chevary, J. A.; Vosko, S. H.; Jackson, K. A.;Pederson, M. R.; Singh, D. J.; Fiolhais, C. Phys. Rev. B 1992,46, 6671. doi: 10.1103/PhysRevB.46.6671
27. [27]
  (27) Kresse, G.; Joubert, D. Phys. Rev. B 1999, 59, 1758. doi: 10.1103/PhysRevB.59.1758
28. [28]
  (28) Blouml, P. E. Phys. Rev. B 1994, 50, 17953. doi: 10.1103/PhysRevB.50.17953
29. [29]
  (29) Henkelman, G.; Uberuaga, B. P.; Jónsson, H. J. Chem. Phys.2000, 113, 9901. doi: 10.1063/1.1329672
30. [30]
  (30) Monkhorst, H. J.; Pack, J. D. Phys. Rev. B 1976, 13, 5188. doi: 10.1103/PhysRevB.13.5188
31. [31]
  (31) Li,W. X.; Stampfl, C.; Scheffler, M. Phys. Rev. B 2002, 65,075407. doi: 10.1103/PhysRevB.65.075407
32. [32]
  (32) Shi, H. Q.; Stampfl, C. Phys. Rev. B 2007, 76, 075327. doi: 10.1103/PhysRevB.76.075327
33. [33]
  (33) Bocquet, M. L.; Michaelides, A.; Loffreda, D.; Sautet, P.; Alavi,A.; King, D. A. J. Am. Chem. Soc. 2003, 125, 5620. doi: 10.1021/ja0297741
34. [34]
  (34) Pang, X. Y.; Xing, B.; Xue, L. Q.;Wang, G. C. J. Comput.Chem. 2010, 31, 1618.
35. [35]
  (35) Xue, L. Q.; Pang, X. Y.;Wang, G. C. J. Comput. Chem. 2009,30, 438. doi: 10.1002/jcc.v30:3
36. [36]
  (36) Torres, D.; Lopez, N.; Illas, F.; Lambert, R. M. J. Am. Chem.Soc. 2005, 127, 10774. doi: 10.1021/ja043227t
37. [37]
  (37) Torres, D.; Lopez, N.; Illas, F. J. Catal. 2006, 243 (2), 404. doi: 10.1016/j.jcat.2006.08.011
38. [38]
  (38) Lukaski, A. C.; Enever, M. C. N.; Barteau, M. A. Surf. Sci.2007, 601, 3372. doi: 10.1016/j.susc.2007.06.015
39. [39]
  (39) Toni ld, K.; Gross, A. J. Chem. Phys. 2010, 132, 224701. doi: 10.1063/1.3439691
40. [40]
  (40) Grimme, S. J. Comput. Chem. 2006, 27, 1787.
41. [41]
  (41) Grimme, S.; Antony, J.; Ehrlich, S.; Krieg, H. J. Chem. Phys.2010, 132, 154104. doi: 10.1063/1.3382344
42. [42]
  (42) Benco, L.; Bucko, T.; Hafner, J. J. Catal. 2011, 277, 104.
43. [43]
  (43) Torres, D.; Lopez, N.; Illas, F.; Lambert, R. M. Angew. Chem.Int. Edit. 2007, 46, 2055.
44. [44]
  (44) Wang, H. F.; Liu, Z. P. J. Am. Chem. Soc. 2008, 130, 10996.
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