Bulk crystalline copper electrodeposited on polycrystalline gold surfaces observed by in-situ scanning tunnelling microscopy
Bulk copper electrodeposition onto technical gold surfaces in electrolytes of 0.05 M H 2SO 4 and 1 mM CuSO 4 was investigated by in-situ scanning tunnelling microscopy at fixed overpotentials. At potentials between -60 and -30 mV the growth of bulk copper proceeds in cycles of nucleation, agglomerat...
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Veröffentlicht in: | Surface & coatings technology 1994-11, Vol.70 (1), p.87-95 |
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creator | Andersen, Jens E.T. Bech-Nielsen, G. Møller, Per |
description | Bulk copper electrodeposition onto technical gold surfaces in electrolytes of 0.05 M H
2SO
4 and 1 mM CuSO
4 was investigated by
in-situ scanning tunnelling microscopy at fixed overpotentials. At potentials between -60 and -30 mV the growth of bulk copper proceeds in cycles of nucleation, agglomeration and crystallization. Crystalline copper is seen as involving an intermediate stage in the progress of growth. The final stage in the growth involves an equilibrium of copper electrochemically dissolving and precipitating.
The drift velocity was measured for a gold surface subjected to flame annealing and subsequently installed in the cell compartment. It was found that the drift velocity decays with time in an exponential-like manner, and a 70 min waiting time before experiments with atomic resolution is recommended. Atomic resolution on Au(111) has been obtained, and an apparent surface reconstruction was observed. It is suggested that in reality no reconstruction took place, and that the observation was due to a distortion of the image caused by a constant drift velocity. A mathematical expression which relates the observed surface structure to the drift velocity is presented. |
doi_str_mv | 10.1016/0257-8972(94)90079-5 |
format | Article |
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2SO
4 and 1 mM CuSO
4 was investigated by
in-situ scanning tunnelling microscopy at fixed overpotentials. At potentials between -60 and -30 mV the growth of bulk copper proceeds in cycles of nucleation, agglomeration and crystallization. Crystalline copper is seen as involving an intermediate stage in the progress of growth. The final stage in the growth involves an equilibrium of copper electrochemically dissolving and precipitating.
The drift velocity was measured for a gold surface subjected to flame annealing and subsequently installed in the cell compartment. It was found that the drift velocity decays with time in an exponential-like manner, and a 70 min waiting time before experiments with atomic resolution is recommended. Atomic resolution on Au(111) has been obtained, and an apparent surface reconstruction was observed. It is suggested that in reality no reconstruction took place, and that the observation was due to a distortion of the image caused by a constant drift velocity. A mathematical expression which relates the observed surface structure to the drift velocity is presented.</description><identifier>ISSN: 0257-8972</identifier><identifier>EISSN: 1879-3347</identifier><identifier>DOI: 10.1016/0257-8972(94)90079-5</identifier><identifier>CODEN: SCTEEJ</identifier><language>eng</language><publisher>Lausanne: Elsevier B.V</publisher><subject>Cross-disciplinary physics: materials science; rheology ; Electrodeposition, electroplating ; Exact sciences and technology ; Materials science ; Methods of deposition of films and coatings; film growth and epitaxy ; Physics</subject><ispartof>Surface & coatings technology, 1994-11, Vol.70 (1), p.87-95</ispartof><rights>1994</rights><rights>1995 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c364t-9fe6259cbbd83fa4b2add580b71859a96a8e2d1a1fdaeea0d74fa295bb6427913</citedby><cites>FETCH-LOGICAL-c364t-9fe6259cbbd83fa4b2add580b71859a96a8e2d1a1fdaeea0d74fa295bb6427913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0257-8972(94)90079-5$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3455189$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Andersen, Jens E.T.</creatorcontrib><creatorcontrib>Bech-Nielsen, G.</creatorcontrib><creatorcontrib>Møller, Per</creatorcontrib><title>Bulk crystalline copper electrodeposited on polycrystalline gold surfaces observed by in-situ scanning tunnelling microscopy</title><title>Surface & coatings technology</title><description>Bulk copper electrodeposition onto technical gold surfaces in electrolytes of 0.05 M H
2SO
4 and 1 mM CuSO
4 was investigated by
in-situ scanning tunnelling microscopy at fixed overpotentials. At potentials between -60 and -30 mV the growth of bulk copper proceeds in cycles of nucleation, agglomeration and crystallization. Crystalline copper is seen as involving an intermediate stage in the progress of growth. The final stage in the growth involves an equilibrium of copper electrochemically dissolving and precipitating.
The drift velocity was measured for a gold surface subjected to flame annealing and subsequently installed in the cell compartment. It was found that the drift velocity decays with time in an exponential-like manner, and a 70 min waiting time before experiments with atomic resolution is recommended. Atomic resolution on Au(111) has been obtained, and an apparent surface reconstruction was observed. It is suggested that in reality no reconstruction took place, and that the observation was due to a distortion of the image caused by a constant drift velocity. A mathematical expression which relates the observed surface structure to the drift velocity is presented.</description><subject>Cross-disciplinary physics: materials science; rheology</subject><subject>Electrodeposition, electroplating</subject><subject>Exact sciences and technology</subject><subject>Materials science</subject><subject>Methods of deposition of films and coatings; film growth and epitaxy</subject><subject>Physics</subject><issn>0257-8972</issn><issn>1879-3347</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNp9kE1L5TAUhsOgMNfr_INZZDEMuqgmadI2mwEVv0Bwo-uQJqeXaG_SSVqh4I839Yq4cnXO4nnPx4PQb0pOKKHVKWGiLhpZsyPJjyUhtSzED7SiTW7Kktd7aPWJ_EQHKT0RQmgt-Qq9nk_9MzZxTqPue-cBmzAMEDH0YMYYLAwhuREsDh4PoZ-_opvQW5ym2GkDCYc2QXzJZDtj54ucmnAy2nvnN3icvIcltcFbZ2JIec18iPY73Sf49VHX6PHq8uHipri7v769OLsrTFnxsZAdVExI07a2KTvNW6atFQ1pa9oIqWWlG2CWatpZDaCJrXmnmRRtW3FWS1qu0d_d3CGG_xOkUW1dMvkc7SFMSbGqFIxRkkG-A5cLU4RODdFtdZwVJWpRrRaPavGoJFfvqpXIsT8f83V-uO-i9salz2zJhaCNzNi_HQb51xcHUSXjwBuwLmbZygb3_Z43hj-XFQ</recordid><startdate>19941101</startdate><enddate>19941101</enddate><creator>Andersen, Jens E.T.</creator><creator>Bech-Nielsen, G.</creator><creator>Møller, Per</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>19941101</creationdate><title>Bulk crystalline copper electrodeposited on polycrystalline gold surfaces observed by in-situ scanning tunnelling microscopy</title><author>Andersen, Jens E.T. ; Bech-Nielsen, G. ; Møller, Per</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c364t-9fe6259cbbd83fa4b2add580b71859a96a8e2d1a1fdaeea0d74fa295bb6427913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Cross-disciplinary physics: materials science; rheology</topic><topic>Electrodeposition, electroplating</topic><topic>Exact sciences and technology</topic><topic>Materials science</topic><topic>Methods of deposition of films and coatings; film growth and epitaxy</topic><topic>Physics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andersen, Jens E.T.</creatorcontrib><creatorcontrib>Bech-Nielsen, G.</creatorcontrib><creatorcontrib>Møller, Per</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Surface & coatings technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andersen, Jens E.T.</au><au>Bech-Nielsen, G.</au><au>Møller, Per</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Bulk crystalline copper electrodeposited on polycrystalline gold surfaces observed by in-situ scanning tunnelling microscopy</atitle><jtitle>Surface & coatings technology</jtitle><date>1994-11-01</date><risdate>1994</risdate><volume>70</volume><issue>1</issue><spage>87</spage><epage>95</epage><pages>87-95</pages><issn>0257-8972</issn><eissn>1879-3347</eissn><coden>SCTEEJ</coden><abstract>Bulk copper electrodeposition onto technical gold surfaces in electrolytes of 0.05 M H
2SO
4 and 1 mM CuSO
4 was investigated by
in-situ scanning tunnelling microscopy at fixed overpotentials. At potentials between -60 and -30 mV the growth of bulk copper proceeds in cycles of nucleation, agglomeration and crystallization. Crystalline copper is seen as involving an intermediate stage in the progress of growth. The final stage in the growth involves an equilibrium of copper electrochemically dissolving and precipitating.
The drift velocity was measured for a gold surface subjected to flame annealing and subsequently installed in the cell compartment. It was found that the drift velocity decays with time in an exponential-like manner, and a 70 min waiting time before experiments with atomic resolution is recommended. Atomic resolution on Au(111) has been obtained, and an apparent surface reconstruction was observed. It is suggested that in reality no reconstruction took place, and that the observation was due to a distortion of the image caused by a constant drift velocity. A mathematical expression which relates the observed surface structure to the drift velocity is presented.</abstract><cop>Lausanne</cop><pub>Elsevier B.V</pub><doi>10.1016/0257-8972(94)90079-5</doi><tpages>9</tpages></addata></record> |
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source | Access via ScienceDirect (Elsevier) |
subjects | Cross-disciplinary physics: materials science rheology Electrodeposition, electroplating Exact sciences and technology Materials science Methods of deposition of films and coatings film growth and epitaxy Physics |
title | Bulk crystalline copper electrodeposited on polycrystalline gold surfaces observed by in-situ scanning tunnelling microscopy |
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