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Electrodeposition of antimony telluride thin films from acidic nitrate-tartrate baths
Sb x Te 1− x thin films were electrodeposited from acidic nitrate baths where the film composition and crystal structure were tailored by controlling electrolytic composition, deposition rate, and applied potential. Various electroanaltyical techniques were also utilized to understand the deposition...
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Published in: | Electrochimica acta 2011-06, Vol.56 (16), p.5611-5615 |
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container_title | Electrochimica acta |
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creator | Jung, Hyunsung Myung, Nosang V. |
description | Sb
x
Te
1−
x
thin films were electrodeposited from acidic nitrate baths where the film composition and crystal structure were tailored by controlling electrolytic composition, deposition rate, and applied potential. Various electroanaltyical techniques were also utilized to understand the deposition mechanism.
Electrochemical quartz crystal microbalance (EQCM) and rotating disk electrode (RDE) techniques were utilized to systematically investigate the electrodeposition of Sb
x
Te
1−
x
(0.1
<
x
<
0.8). In addition, the effect of applied potential and agitation were correlated to the film composition, crystal structure, and morphology. Although the film composition was independent of the agitation rate, the deposition rate, current efficiency, crystallinity and phase of Sb
x
Te
1−
x
were all strongly influenced by it. The deposition rate monotonically increased with increases in the rotation rate because of the faster diffusion rate of HTeO
2
+ ions to the cathode. Amorphous thin films were electrodeposited in the absence of agitation, whereas polycrystalline Sb
2Te
3 with elemental Sb and Te were co-deposited at a higher agitation independent of the applied deposition potential. |
doi_str_mv | 10.1016/j.electacta.2011.04.010 |
format | article |
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x
Te
1−
x
thin films were electrodeposited from acidic nitrate baths where the film composition and crystal structure were tailored by controlling electrolytic composition, deposition rate, and applied potential. Various electroanaltyical techniques were also utilized to understand the deposition mechanism.
Electrochemical quartz crystal microbalance (EQCM) and rotating disk electrode (RDE) techniques were utilized to systematically investigate the electrodeposition of Sb
x
Te
1−
x
(0.1
<
x
<
0.8). In addition, the effect of applied potential and agitation were correlated to the film composition, crystal structure, and morphology. Although the film composition was independent of the agitation rate, the deposition rate, current efficiency, crystallinity and phase of Sb
x
Te
1−
x
were all strongly influenced by it. The deposition rate monotonically increased with increases in the rotation rate because of the faster diffusion rate of HTeO
2
+ ions to the cathode. Amorphous thin films were electrodeposited in the absence of agitation, whereas polycrystalline Sb
2Te
3 with elemental Sb and Te were co-deposited at a higher agitation independent of the applied deposition potential.</description><identifier>ISSN: 0013-4686</identifier><identifier>EISSN: 1873-3859</identifier><identifier>DOI: 10.1016/j.electacta.2011.04.010</identifier><identifier>CODEN: ELCAAV</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Agitation ; Antimony ; Antimony telluride ; Chemistry ; Crystal structure ; Deposition ; Electrochemical quartz crystal microbalance ; Electrochemistry ; Electrodeposition ; Electrodes ; Exact sciences and technology ; General and physical chemistry ; Microorganisms ; Rotating disk electrode ; Study of interfaces ; Thermoelectrics ; Thin films ; Under-potential deposition</subject><ispartof>Electrochimica acta, 2011-06, Vol.56 (16), p.5611-5615</ispartof><rights>2011 Elsevier Ltd</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-adeb9722adfe2e1c86fc66999d9096219025595577928b72d203903e7d67a7703</citedby><cites>FETCH-LOGICAL-c443t-adeb9722adfe2e1c86fc66999d9096219025595577928b72d203903e7d67a7703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24272445$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, Hyunsung</creatorcontrib><creatorcontrib>Myung, Nosang V.</creatorcontrib><title>Electrodeposition of antimony telluride thin films from acidic nitrate-tartrate baths</title><title>Electrochimica acta</title><description>Sb
x
Te
1−
x
thin films were electrodeposited from acidic nitrate baths where the film composition and crystal structure were tailored by controlling electrolytic composition, deposition rate, and applied potential. Various electroanaltyical techniques were also utilized to understand the deposition mechanism.
Electrochemical quartz crystal microbalance (EQCM) and rotating disk electrode (RDE) techniques were utilized to systematically investigate the electrodeposition of Sb
x
Te
1−
x
(0.1
<
x
<
0.8). In addition, the effect of applied potential and agitation were correlated to the film composition, crystal structure, and morphology. Although the film composition was independent of the agitation rate, the deposition rate, current efficiency, crystallinity and phase of Sb
x
Te
1−
x
were all strongly influenced by it. The deposition rate monotonically increased with increases in the rotation rate because of the faster diffusion rate of HTeO
2
+ ions to the cathode. Amorphous thin films were electrodeposited in the absence of agitation, whereas polycrystalline Sb
2Te
3 with elemental Sb and Te were co-deposited at a higher agitation independent of the applied deposition potential.</description><subject>Agitation</subject><subject>Antimony</subject><subject>Antimony telluride</subject><subject>Chemistry</subject><subject>Crystal structure</subject><subject>Deposition</subject><subject>Electrochemical quartz crystal microbalance</subject><subject>Electrochemistry</subject><subject>Electrodeposition</subject><subject>Electrodes</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Microorganisms</subject><subject>Rotating disk electrode</subject><subject>Study of interfaces</subject><subject>Thermoelectrics</subject><subject>Thin films</subject><subject>Under-potential deposition</subject><issn>0013-4686</issn><issn>1873-3859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFkE9LxDAQxYMouK5-BnMRT62TNE2ao4j_QPCi55BNppilbdYkK_jt7bqyV2Fg5vDevJkfIZcMagZM3qxrHNAVO1fNgbEaRA0MjsiCdaqpmq7Vx2QBwJpKyE6ekrOc1wCgpIIFeb_fmVP0uIk5lBAnGntqpxLGOH3TgsOwTcEjLR9hon0Yxkz7FEdqXfDB0SmUZAtWxabfga5s-cjn5KS3Q8aLv74k7w_3b3dP1cvr4_Pd7UvlhGhKZT2utOLc-h45MtfJ3kmptfYatORMA29b3bZKad6tFPccGg0NKi-VVQqaJbne792k-LnFXMwYsptvthPGbTZdpwXodg5bErVXuhRzTtibTQqjTd-GgdlxNGtz4Gh2HA0IM3OcnVd_GTY7O_TJTi7kg50LrrgQ7ay73etwfvgrYDLZBZwc-pDmvcbH8G_WD57PjWo</recordid><startdate>20110630</startdate><enddate>20110630</enddate><creator>Jung, Hyunsung</creator><creator>Myung, Nosang V.</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QQ</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20110630</creationdate><title>Electrodeposition of antimony telluride thin films from acidic nitrate-tartrate baths</title><author>Jung, Hyunsung ; Myung, Nosang V.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-adeb9722adfe2e1c86fc66999d9096219025595577928b72d203903e7d67a7703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Agitation</topic><topic>Antimony</topic><topic>Antimony telluride</topic><topic>Chemistry</topic><topic>Crystal structure</topic><topic>Deposition</topic><topic>Electrochemical quartz crystal microbalance</topic><topic>Electrochemistry</topic><topic>Electrodeposition</topic><topic>Electrodes</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Microorganisms</topic><topic>Rotating disk electrode</topic><topic>Study of interfaces</topic><topic>Thermoelectrics</topic><topic>Thin films</topic><topic>Under-potential deposition</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, Hyunsung</creatorcontrib><creatorcontrib>Myung, Nosang V.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Ceramic Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Electrochimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, Hyunsung</au><au>Myung, Nosang V.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrodeposition of antimony telluride thin films from acidic nitrate-tartrate baths</atitle><jtitle>Electrochimica acta</jtitle><date>2011-06-30</date><risdate>2011</risdate><volume>56</volume><issue>16</issue><spage>5611</spage><epage>5615</epage><pages>5611-5615</pages><issn>0013-4686</issn><eissn>1873-3859</eissn><coden>ELCAAV</coden><abstract>Sb
x
Te
1−
x
thin films were electrodeposited from acidic nitrate baths where the film composition and crystal structure were tailored by controlling electrolytic composition, deposition rate, and applied potential. Various electroanaltyical techniques were also utilized to understand the deposition mechanism.
Electrochemical quartz crystal microbalance (EQCM) and rotating disk electrode (RDE) techniques were utilized to systematically investigate the electrodeposition of Sb
x
Te
1−
x
(0.1
<
x
<
0.8). In addition, the effect of applied potential and agitation were correlated to the film composition, crystal structure, and morphology. Although the film composition was independent of the agitation rate, the deposition rate, current efficiency, crystallinity and phase of Sb
x
Te
1−
x
were all strongly influenced by it. The deposition rate monotonically increased with increases in the rotation rate because of the faster diffusion rate of HTeO
2
+ ions to the cathode. Amorphous thin films were electrodeposited in the absence of agitation, whereas polycrystalline Sb
2Te
3 with elemental Sb and Te were co-deposited at a higher agitation independent of the applied deposition potential.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.electacta.2011.04.010</doi><tpages>5</tpages></addata></record> |
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language | eng |
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source | ScienceDirect Freedom Collection 2022-2024 |
subjects | Agitation Antimony Antimony telluride Chemistry Crystal structure Deposition Electrochemical quartz crystal microbalance Electrochemistry Electrodeposition Electrodes Exact sciences and technology General and physical chemistry Microorganisms Rotating disk electrode Study of interfaces Thermoelectrics Thin films Under-potential deposition |
title | Electrodeposition of antimony telluride thin films from acidic nitrate-tartrate baths |
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