Stable and metastable phases of water adsorbed on Cu(111)
Metastable and stable phases of water adsorbed at low coverages on Cu(111) were studied using vibrational spectroscopy (both time-resolved and high-resolution electron energy-loss spectroscopies) and temperature programmed desorption. The two water species have distinct spectroscopic signatures and...
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Veröffentlicht in: | The Journal of chemical physics 1992-02, Vol.96 (4), p.3262-3268 |
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description | Metastable and stable phases of water adsorbed at low coverages on Cu(111) were studied using vibrational spectroscopy (both time-resolved and high-resolution electron energy-loss spectroscopies) and temperature programmed desorption. The two water species have distinct spectroscopic signatures and different desorption kinetics. The more stable species appears to be three-dimensional clusters of bulklike, polycrystalline ice while the metastable species was observed to have a higher desorption rate despite a larger activation enthalpy for desorption. A simple model is proposed to explain this intriguing result. The conversion from the metastable to the stable species, as well as the affects of preadsorbed carbon monoxide on the adsorption/desorption kinetics, are also discussed. |
doi_str_mv | 10.1063/1.461971 |
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H</creatorcontrib><title>Stable and metastable phases of water adsorbed on Cu(111)</title><title>The Journal of chemical physics</title><description>Metastable and stable phases of water adsorbed at low coverages on Cu(111) were studied using vibrational spectroscopy (both time-resolved and high-resolution electron energy-loss spectroscopies) and temperature programmed desorption. The two water species have distinct spectroscopic signatures and different desorption kinetics. The more stable species appears to be three-dimensional clusters of bulklike, polycrystalline ice while the metastable species was observed to have a higher desorption rate despite a larger activation enthalpy for desorption. A simple model is proposed to explain this intriguing result. The conversion from the metastable to the stable species, as well as the affects of preadsorbed carbon monoxide on the adsorption/desorption kinetics, are also discussed.</description><subject>Applied sciences</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Metals. 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H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c322t-10e254fe305dbcab2355b7f2151b2f61af4e927263f2a3a74d32b9ee0303a24e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Applied sciences</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Metals. Metallurgy</topic><topic>Solid-gas interface</topic><topic>Surface physical chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>HICH, B. J</creatorcontrib><creatorcontrib>DUBOIS, L. H</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><jtitle>The Journal of chemical physics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HICH, B. J</au><au>DUBOIS, L. H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stable and metastable phases of water adsorbed on Cu(111)</atitle><jtitle>The Journal of chemical physics</jtitle><date>1992-02-15</date><risdate>1992</risdate><volume>96</volume><issue>4</issue><spage>3262</spage><epage>3268</epage><pages>3262-3268</pages><issn>0021-9606</issn><eissn>1089-7690</eissn><coden>JCPSA6</coden><abstract>Metastable and stable phases of water adsorbed at low coverages on Cu(111) were studied using vibrational spectroscopy (both time-resolved and high-resolution electron energy-loss spectroscopies) and temperature programmed desorption. The two water species have distinct spectroscopic signatures and different desorption kinetics. The more stable species appears to be three-dimensional clusters of bulklike, polycrystalline ice while the metastable species was observed to have a higher desorption rate despite a larger activation enthalpy for desorption. A simple model is proposed to explain this intriguing result. The conversion from the metastable to the stable species, as well as the affects of preadsorbed carbon monoxide on the adsorption/desorption kinetics, are also discussed.</abstract><cop>Woodbury, NY</cop><pub>American Institute of Physics</pub><doi>10.1063/1.461971</doi><tpages>7</tpages></addata></record> |
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subjects | Applied sciences Chemistry Exact sciences and technology General and physical chemistry Metals. Metallurgy Solid-gas interface Surface physical chemistry |
title | Stable and metastable phases of water adsorbed on Cu(111) |
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