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Adsorption and Thermal Reaction of Short-Chain Alcohols on Ge(100)
The adsorption and thermal decomposition of alcohols (CH3OH, C2H5OH, and C4H9OH) on Ge(100) were investigated with temperature-programmed desorption and X-ray photoelectron spectra. At 105 K, CH3OH adsorbs both molecularly and dissociatively on Ge(100). Chemisorbed CH3OH molecules dissociate to form...
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Published in: | Journal of physical chemistry. C 2013-02, Vol.117 (6), p.2760-2768 |
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container_title | Journal of physical chemistry. C |
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creator | Lin, Tsung-Hsiang Lin, Bo-Yu Hao, Ting Chien, Hsiu-Yun Wang, Jeng-Han Hung, Wei-Hsiu |
description | The adsorption and thermal decomposition of alcohols (CH3OH, C2H5OH, and C4H9OH) on Ge(100) were investigated with temperature-programmed desorption and X-ray photoelectron spectra. At 105 K, CH3OH adsorbs both molecularly and dissociatively on Ge(100). Chemisorbed CH3OH molecules dissociate to form surface CH3O and hydrogen in a temperature range 150–300 K. Surface CH3O can dehydrogenate to yield CH2O as two desorption features, which depend on coverage. At small coverage, surface CH3O undergoes mainly α-hydrogen elimination to desorb CH2O at 490 K. At large coverage, another desorption of CH2O occurs predominantly at 525 K, which is initiated by a recombinative desorption of CH3OH. A calculation with density functional theory at the B3LYP/6-311+G** level shows that the dissociation of the O–H bond has a much smaller barrier (150 kJ/mol). Desorption of CH2O results from the moderate barriers (∼110 kJ/mol) for cleavage of the C–H bond of surface CH3O and weak adsorption energy of CH2O (−56 kJ/mol). The recombination of surface CH3O with H occurs at large coverage with an energy barrier 127–140 kJ/mol. Similarly to CH3OH, C2H5OH and C4H9OH undergo the mechanism of thermal reactions through formation of alkoxyl intermediates. The longer-chain alkoxyl decomposes to desorb aldehyde at lower temperature because the interaction of its alkoxyl chain with the surface is stronger. On annealing to ∼570 K, all alkoxyl groups are completely removed from the surface via dehydrogenation and recombination to desorb aldehyde and alcohol, respectively. At a large coverage, the longer-chain alkoxyl undergoes dehydrogenation to a larger extent than recombinative desorption. |
doi_str_mv | 10.1021/jp308990x |
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At 105 K, CH3OH adsorbs both molecularly and dissociatively on Ge(100). Chemisorbed CH3OH molecules dissociate to form surface CH3O and hydrogen in a temperature range 150–300 K. Surface CH3O can dehydrogenate to yield CH2O as two desorption features, which depend on coverage. At small coverage, surface CH3O undergoes mainly α-hydrogen elimination to desorb CH2O at 490 K. At large coverage, another desorption of CH2O occurs predominantly at 525 K, which is initiated by a recombinative desorption of CH3OH. A calculation with density functional theory at the B3LYP/6-311+G** level shows that the dissociation of the O–H bond has a much smaller barrier (<40 kJ/mol) than those for C–O bond cleavage (>150 kJ/mol). Desorption of CH2O results from the moderate barriers (∼110 kJ/mol) for cleavage of the C–H bond of surface CH3O and weak adsorption energy of CH2O (−56 kJ/mol). The recombination of surface CH3O with H occurs at large coverage with an energy barrier 127–140 kJ/mol. Similarly to CH3OH, C2H5OH and C4H9OH undergo the mechanism of thermal reactions through formation of alkoxyl intermediates. The longer-chain alkoxyl decomposes to desorb aldehyde at lower temperature because the interaction of its alkoxyl chain with the surface is stronger. On annealing to ∼570 K, all alkoxyl groups are completely removed from the surface via dehydrogenation and recombination to desorb aldehyde and alcohol, respectively. At a large coverage, the longer-chain alkoxyl undergoes dehydrogenation to a larger extent than recombinative desorption.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp308990x</identifier><language>eng</language><publisher>Columbus, OH: American Chemical Society</publisher><subject>Chemistry ; Exact sciences and technology ; General and physical chemistry ; Solid-gas interface ; Surface physical chemistry</subject><ispartof>Journal of physical chemistry. C, 2013-02, Vol.117 (6), p.2760-2768</ispartof><rights>Copyright © 2013 American Chemical Society</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a289t-5007017fc65aa183ba6f102bc41663206410c55315d169522d3d0db209e8f1b53</citedby><cites>FETCH-LOGICAL-a289t-5007017fc65aa183ba6f102bc41663206410c55315d169522d3d0db209e8f1b53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27170432$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Lin, Tsung-Hsiang</creatorcontrib><creatorcontrib>Lin, Bo-Yu</creatorcontrib><creatorcontrib>Hao, Ting</creatorcontrib><creatorcontrib>Chien, Hsiu-Yun</creatorcontrib><creatorcontrib>Wang, Jeng-Han</creatorcontrib><creatorcontrib>Hung, Wei-Hsiu</creatorcontrib><title>Adsorption and Thermal Reaction of Short-Chain Alcohols on Ge(100)</title><title>Journal of physical chemistry. C</title><addtitle>J. Phys. Chem. C</addtitle><description>The adsorption and thermal decomposition of alcohols (CH3OH, C2H5OH, and C4H9OH) on Ge(100) were investigated with temperature-programmed desorption and X-ray photoelectron spectra. At 105 K, CH3OH adsorbs both molecularly and dissociatively on Ge(100). Chemisorbed CH3OH molecules dissociate to form surface CH3O and hydrogen in a temperature range 150–300 K. Surface CH3O can dehydrogenate to yield CH2O as two desorption features, which depend on coverage. At small coverage, surface CH3O undergoes mainly α-hydrogen elimination to desorb CH2O at 490 K. At large coverage, another desorption of CH2O occurs predominantly at 525 K, which is initiated by a recombinative desorption of CH3OH. A calculation with density functional theory at the B3LYP/6-311+G** level shows that the dissociation of the O–H bond has a much smaller barrier (<40 kJ/mol) than those for C–O bond cleavage (>150 kJ/mol). Desorption of CH2O results from the moderate barriers (∼110 kJ/mol) for cleavage of the C–H bond of surface CH3O and weak adsorption energy of CH2O (−56 kJ/mol). The recombination of surface CH3O with H occurs at large coverage with an energy barrier 127–140 kJ/mol. Similarly to CH3OH, C2H5OH and C4H9OH undergo the mechanism of thermal reactions through formation of alkoxyl intermediates. The longer-chain alkoxyl decomposes to desorb aldehyde at lower temperature because the interaction of its alkoxyl chain with the surface is stronger. On annealing to ∼570 K, all alkoxyl groups are completely removed from the surface via dehydrogenation and recombination to desorb aldehyde and alcohol, respectively. At a large coverage, the longer-chain alkoxyl undergoes dehydrogenation to a larger extent than recombinative desorption.</description><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Solid-gas interface</subject><subject>Surface physical chemistry</subject><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNptj01LxDAQhoMouK4e_Ae5CO6hOpM0_TjWoquwIOh6LtO0oS3dpiQV9N9bXVkvnmaYeeZlHsYuEW4QBN52o4QkTeHjiC0wlSKIQ6WOD30Yn7Iz7zsAJQHlgt1llbdunFo7cBoqvm1qt6Oev9Skf4bW8NfGuinIG2oHnvXaNrb3fF6t62sEWJ2zE0O9ry9-65K9Pdxv88dg87x-yrNNQCJJp0ABxICx0ZEiwkSWFJn55VKHGEVSQBQiaKUkqgqjVAlRyQqqUkBaJwZLJZdstc_VznrvalOMrt2R-ywQim_54iA_s1d7diSvqTeOBt36w4GIMYZQij-OtC86--6G2eCfvC_xFmJU</recordid><startdate>20130214</startdate><enddate>20130214</enddate><creator>Lin, Tsung-Hsiang</creator><creator>Lin, Bo-Yu</creator><creator>Hao, Ting</creator><creator>Chien, Hsiu-Yun</creator><creator>Wang, Jeng-Han</creator><creator>Hung, Wei-Hsiu</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20130214</creationdate><title>Adsorption and Thermal Reaction of Short-Chain Alcohols on Ge(100)</title><author>Lin, Tsung-Hsiang ; Lin, Bo-Yu ; Hao, Ting ; Chien, Hsiu-Yun ; Wang, Jeng-Han ; Hung, Wei-Hsiu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a289t-5007017fc65aa183ba6f102bc41663206410c55315d169522d3d0db209e8f1b53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Solid-gas interface</topic><topic>Surface physical chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Tsung-Hsiang</creatorcontrib><creatorcontrib>Lin, Bo-Yu</creatorcontrib><creatorcontrib>Hao, Ting</creatorcontrib><creatorcontrib>Chien, Hsiu-Yun</creatorcontrib><creatorcontrib>Wang, Jeng-Han</creatorcontrib><creatorcontrib>Hung, Wei-Hsiu</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Tsung-Hsiang</au><au>Lin, Bo-Yu</au><au>Hao, Ting</au><au>Chien, Hsiu-Yun</au><au>Wang, Jeng-Han</au><au>Hung, Wei-Hsiu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adsorption and Thermal Reaction of Short-Chain Alcohols on Ge(100)</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2013-02-14</date><risdate>2013</risdate><volume>117</volume><issue>6</issue><spage>2760</spage><epage>2768</epage><pages>2760-2768</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>The adsorption and thermal decomposition of alcohols (CH3OH, C2H5OH, and C4H9OH) on Ge(100) were investigated with temperature-programmed desorption and X-ray photoelectron spectra. At 105 K, CH3OH adsorbs both molecularly and dissociatively on Ge(100). Chemisorbed CH3OH molecules dissociate to form surface CH3O and hydrogen in a temperature range 150–300 K. Surface CH3O can dehydrogenate to yield CH2O as two desorption features, which depend on coverage. At small coverage, surface CH3O undergoes mainly α-hydrogen elimination to desorb CH2O at 490 K. At large coverage, another desorption of CH2O occurs predominantly at 525 K, which is initiated by a recombinative desorption of CH3OH. A calculation with density functional theory at the B3LYP/6-311+G** level shows that the dissociation of the O–H bond has a much smaller barrier (<40 kJ/mol) than those for C–O bond cleavage (>150 kJ/mol). Desorption of CH2O results from the moderate barriers (∼110 kJ/mol) for cleavage of the C–H bond of surface CH3O and weak adsorption energy of CH2O (−56 kJ/mol). The recombination of surface CH3O with H occurs at large coverage with an energy barrier 127–140 kJ/mol. Similarly to CH3OH, C2H5OH and C4H9OH undergo the mechanism of thermal reactions through formation of alkoxyl intermediates. The longer-chain alkoxyl decomposes to desorb aldehyde at lower temperature because the interaction of its alkoxyl chain with the surface is stronger. On annealing to ∼570 K, all alkoxyl groups are completely removed from the surface via dehydrogenation and recombination to desorb aldehyde and alcohol, respectively. At a large coverage, the longer-chain alkoxyl undergoes dehydrogenation to a larger extent than recombinative desorption.</abstract><cop>Columbus, OH</cop><pub>American Chemical Society</pub><doi>10.1021/jp308990x</doi><tpages>9</tpages></addata></record> |
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subjects | Chemistry Exact sciences and technology General and physical chemistry Solid-gas interface Surface physical chemistry |
title | Adsorption and Thermal Reaction of Short-Chain Alcohols on Ge(100) |
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