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Comparing trunk/COonPt/firstTryBibliography.bib (file contents):
Revision 3874 by jmichalk, Wed Mar 13 14:57:09 2013 UTC vs.
Revision 3875 by gezelter, Wed Mar 13 19:18:03 2013 UTC

# Line 2 | Line 2
2   %% http://bibdesk.sourceforge.net/
3  
4  
5 < %% Created for Joseph Michalka at 2013-03-13 10:11:39 -0400
5 > %% Created for Dan Gezelter at 2013-03-13 15:13:24 -0400
6  
7  
8   %% Saved with string encoding Unicode (UTF-8)
# Line 248 | Line 248
248          Volume = {331},
249          Year = {2011}}
250  
251 < @article{TPD_Gold,
252 <        Author = {G. S. Elliot and D. R. Miller},
251 > @inproceedings{TPDGold,
252 >        Author = {G.~S. Elliott and D.~R. Miller},
253 >        Booktitle = {Rarefied gas dynamics:},
254          Date-Added = {2012-12-14 21:32:06 +0000},
255 <        Date-Modified = {2012-12-14 21:33:43 +0000},
256 <        Journal = {Proc. 14th Int. Symp. on Rarefied Gas Dynamics},
255 >        Date-Modified = {2013-03-13 19:13:16 +0000},
256 >        Editor = {H. Oguchi},
257          Pages = {349-58},
258 +        Publisher = {University of Tokyo Press},
259 +        Series = {Proc. 14th Int. Symp. on Rarefied Gas Dynamics},
260 +        Title = {Helium Scattering from \ce{CO} Adsorbed on \ce{Au}(111)},
261 +        Volume = {1},
262          Year = {1984}}
263  
264   @article{Ewald,
# Line 384 | Line 389
389          Title = {A Periodic Density Functional Theory Analysis of CO Chemisorption on Pt(111) in the Presence of Uniform Electric Fields},
390          Volume = {113},
391          Year = {2009},
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393  
394   @article{Ertl:1977,
395          Author = {G. Ertl and M. Neumann and K.M. Streit},
# Line 397 | Line 402
402          Title = {Chemisorption of CO on the Pt(111) Surface},
403          Volume = {64},
404          Year = {1977},
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406  
407   @article{Hopster:1978,
408          Author = {H. Hopster and H. Ibach},
# Line 410 | Line 415
415          Title = {Adsorption of CO on Pt(111) and Pt 6(111) X (111) Studied by High Resolution Electron Energy Loss Spectroscopy and Thermal Desorption Spectroscopy},
416          Volume = {77},
417          Year = {1978},
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419  
420   @article{Pons:1986,
421          Author = {C. Korzeniewski and S. Pons and P. P. Schmidt and M. W. Severson},
# Line 1047 | Line 1052 | and suggest a reaction mechanism which is not observed
1052          Date-Modified = {2012-12-10 16:17:52 +0000},
1053          Journal = jcp,
1054          Pages = {5175-5176},
1055 <        Title = {Transport Coefficients of Liquid Transition Metals: \Uppercase{A} Computer Simulation Study Using the Embedded Atom Model},
1055 >        Title = {Transport Coefficients of Liquid Transition Metals: A Computer Simulation Study Using the Embedded Atom Model},
1056          Volume = 109,
1057          Year = 1998}
1058  
# Line 1087 | Line 1092 | and suggest a reaction mechanism which is not observed
1092          Date-Modified = {2012-12-10 16:17:07 +0000},
1093          Journal = prb,
1094          Pages = {7441-7452},
1095 <        Title = {Model of Metallic Cohesion: \Uppercase{T}He Embedded-Atom Method},
1095 >        Title = {Model of Metallic Cohesion: The Embedded-Atom Method},
1096          Volume = 39,
1097          Year = 1989}
1098  
# Line 1109 | Line 1114 | and suggest a reaction mechanism which is not observed
1114          Journal = prb,
1115          Number = 12,
1116          Pages = {6443-6453},
1117 <        Title = {Embedded-Atom Method: \Uppercase{D}Erivation and Application to Impurities, Surfaces, And Other Defects in Metals},
1117 >        Title = {Embedded-Atom Method: Derivation and Application to Impurities, Surfaces, And Other Defects in Metals},
1118          Volume = 29,
1119          Year = 1984}
1120  
# Line 1269 | Line 1274 | and suggest a reaction mechanism which is not observed
1274          Z8 = {58},
1275          Z9 = {3909},
1276          Zb = {17},
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1278          Bdsk-Url-1 = {http://dx.doi.org/10.1103/PhysRevB.49.14251}}
1279  
1280   @article{doi:10.1126/science.1182122,
# Line 1319 | Line 1324 | and suggest a reaction mechanism which is not observed
1324          Url = {http://link.aps.org/doi/10.1103/PhysRevB.39.7441},
1325          Volume = {39},
1326          Year = {1989},
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1328          Bdsk-Url-1 = {http://link.aps.org/doi/10.1103/PhysRevB.39.7441},
1329          Bdsk-Url-2 = {http://dx.doi.org/10.1103/PhysRevB.39.7441}}
1330  
# Line 1335 | Line 1340 | and suggest a reaction mechanism which is not observed
1340          Title = {Embedded-atom-method functions for the fcc metals Cu, Ag, Au, Ni, Pd, Pt, and their alloys},
1341          Volume = {33},
1342          Year = {1986},
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1344  
1345   @article{doi:10.1021/jp0665729,
1346          Author = {Yim, Wai-Leung and Nowitzki, Tobias and Necke, Mandus and Schnars, Hanno and Nickut, Patricia and Biener, J{\"u}rgen and Biener, Monika M. and Zielasek, Volkmar and Al-Shamery, Katharina and Kl{\"u}ner, Thorsten and B{\"a}umer, Marcus},
# Line 1364 | Line 1369 | and suggest a reaction mechanism which is not observed
1369          Title = {Molecular Dynamics Study of the Photodissociation of Carbon Monoxide from Myoglobin: Ligand Dynamics in the first 10 ps},
1370          Volume = {158},
1371          Year = {1991},
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1373  
1374   @article{Yeo,
1375          Abstract = {Single crystal adsorption calorimetry was applied to investigate the heats of adsorption of CO and oxygen and the reaction heats for the CO oxidation process on Pt􏰊111􏰋 at room temperature. Both sticking probabilities and heats of adsorption for CO and oxygen are presented as a function of coverage. These results are used to interpret the subsequent measurements taken for the CO oxidation process on the same surface. The initial heats of adsorption of CO and oxygen on Pt􏰊111􏰋 are 180􏰛8 and 339􏰛32 kJ/mol, respectively. In addition the pairwise lateral repulsive interaction between CO molecules in a 􏰔􏰜3􏰙􏰜3􏰈R30$\,^{\circ}$ ordered layer at 􏰒􏰚1/3 is found to be 4 kJ/mol. A detailed Monte Carlo modeling of the dissociative adsorption and sticking probability of oxygen on Pt􏰊111􏰋 is performed. The initial rapid fall in heat is attributed to adsorption on defect sites, and subsequent adsorption on the planar 􏰊111􏰋 surface proceeds with a third neighbor interaction energy between the oxygen adatoms 􏰓3􏰌22 kJ/mol. When gaseous CO reacts with preadsorbed oxygen adatoms, the CO2 produced has an excess energy of 16􏰛8 kJ/mol. {\copyright} 1997 American Institute of Physics. 􏰎S0021-9606􏰔97􏰈02601-9􏰉},
# Line 1378 | Line 1383 | and suggest a reaction mechanism which is not observed
1383          Title = {Calorimetric heats for CO and oxygen adsorption and for the catalytic CO oxidation reaction on Pt{111}},
1384          Volume = {106},
1385          Year = {1997},
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1387  
1388   @article{Feibelman:2001,
1389          Abstract = {Notwithstanding half a dozen theoretical publications, well-converged density- functional calculations, whether based on a local-density or generalized-gradient exchange-correlation potential, whether all-electron or employing pseudopotentials, underestimate CO's preference for low-coordination binding sites on Pt(111) and vicinals to it. For example, they imply that CO should prefer hollow- to atop-site adsorption on Pt(111), in apparent contradiction to a host of low-temperature experimental studies.},
# Line 1391 | Line 1396 | and suggest a reaction mechanism which is not observed
1396          Title = {The CO/Pt(111) Puzzle},
1397          Volume = {105},
1398          Year = {2001},
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1400  
1401   @article{Kelemen:1979,
1402          Abstract = {The desorption of CO from clean Pt(lll) and (loo), and from the same surfaces with par- tial overlayers of sulfur, was studied by Thermal Desorption Spectroscopy. The method of desorption rate isotherms was employed for data analysis. The desorption of CO from the (Ill) surface and both surfaces with ordered sulfur overlayers can be described as a first order process with coverage dependent activation energies. The desorption of CO from the clean Pt(100) surface is complicated by the dynamic interaction of the molecule with a thermally activated change of platinum surface structure. On both platinum faces surface sulfur decreases the initial binding energy of CO. As the CO concentration increases, its binding energy decreases very rapidly. This is due to a repulsive interaction which exists between co-adsorbed species.},
# Line 1405 | Line 1410 | and suggest a reaction mechanism which is not observed
1410          Read = {1},
1411          Title = {The Binding Energy of CO on Clean and Sulfur Covered Platinum Surfaces},
1412          Year = {1979},
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