Growth mechanisms of CuSCN films electrodeposited on ITO in EDTA-chelated copper(II) and KSCN aqueous solution
Electrodeposition of β-CuSCN films was investigated on transparent conducting ITO substrates in an aqueous electrolyte containing EDTA-chelated Cu(II) and KSCN. It has been observed that the instability of CuSO 4 and KSCN aqueous solution without EDTA is due to the formation of Cu(SCN) 2 precipitati...
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Veröffentlicht in: | Electrochimica acta 2005-04, Vol.50 (11), p.2343-2349 |
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creator | Wu, Weibing Jin, Zhengguo Hua, Zhen Fu, Yanan Qiu, Jijun |
description | Electrodeposition of β-CuSCN films was investigated on transparent conducting ITO substrates in an aqueous electrolyte containing EDTA-chelated Cu(II) and KSCN. It has been observed that the instability of CuSO
4 and KSCN aqueous solution without EDTA is due to the formation of Cu(SCN)
2 precipitation, which can transform into CuSCN and (SCN)
x
at room temperature. Research results illuminate that the deposited film at −0.5
V versus Ag/AgCl
sat at 298
K is uniform and dense and composed of nanocrystals. The film is p-type with stoichiometric excess of SCN and a direct transition gap of 3.7
eV. Deposition mechanisms of CuSCN films at varied temperatures are studied based on the proposed energetic model. At or below room temperature, the electron quantum tunnel through deposition layer is predominant at the very beginning. However, the growth is limited when the thickness of CuSCN film reaches the size comparable to the diffusion length of electrons. Above room temperature, the thermal activation of surface states plays an important role in the continuous growth of large crystals through holes transport in the valence band. The calculated activation energy for crystal growth is 0.5
eV. |
doi_str_mv | 10.1016/j.electacta.2004.10.048 |
format | Article |
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4 and KSCN aqueous solution without EDTA is due to the formation of Cu(SCN)
2 precipitation, which can transform into CuSCN and (SCN)
x
at room temperature. Research results illuminate that the deposited film at −0.5
V versus Ag/AgCl
sat at 298
K is uniform and dense and composed of nanocrystals. The film is p-type with stoichiometric excess of SCN and a direct transition gap of 3.7
eV. Deposition mechanisms of CuSCN films at varied temperatures are studied based on the proposed energetic model. At or below room temperature, the electron quantum tunnel through deposition layer is predominant at the very beginning. However, the growth is limited when the thickness of CuSCN film reaches the size comparable to the diffusion length of electrons. Above room temperature, the thermal activation of surface states plays an important role in the continuous growth of large crystals through holes transport in the valence band. The calculated activation energy for crystal growth is 0.5
eV.</description><identifier>ISSN: 0013-4686</identifier><identifier>EISSN: 1873-3859</identifier><identifier>DOI: 10.1016/j.electacta.2004.10.048</identifier><identifier>CODEN: ELCAAV</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Activation energy ; Applied sciences ; Chemistry ; CuSCN ; Deposition mechanism ; Electrochemistry ; Electrodeposition ; Energy ; Exact sciences and technology ; General and physical chemistry ; Natural energy ; Photovoltaic conversion ; Solar cell ; Solar cells. Photoelectrochemical cells ; Solar energy ; Study of interfaces ; Surface state</subject><ispartof>Electrochimica acta, 2005-04, Vol.50 (11), p.2343-2349</ispartof><rights>2004 Elsevier Ltd</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-71440c8b0c10d49744337240ba6161e21be2c898b3f3b3edb6b9089d2fc87e523</citedby><cites>FETCH-LOGICAL-c442t-71440c8b0c10d49744337240ba6161e21be2c898b3f3b3edb6b9089d2fc87e523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.electacta.2004.10.048$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16603439$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Weibing</creatorcontrib><creatorcontrib>Jin, Zhengguo</creatorcontrib><creatorcontrib>Hua, Zhen</creatorcontrib><creatorcontrib>Fu, Yanan</creatorcontrib><creatorcontrib>Qiu, Jijun</creatorcontrib><title>Growth mechanisms of CuSCN films electrodeposited on ITO in EDTA-chelated copper(II) and KSCN aqueous solution</title><title>Electrochimica acta</title><description>Electrodeposition of β-CuSCN films was investigated on transparent conducting ITO substrates in an aqueous electrolyte containing EDTA-chelated Cu(II) and KSCN. It has been observed that the instability of CuSO
4 and KSCN aqueous solution without EDTA is due to the formation of Cu(SCN)
2 precipitation, which can transform into CuSCN and (SCN)
x
at room temperature. Research results illuminate that the deposited film at −0.5
V versus Ag/AgCl
sat at 298
K is uniform and dense and composed of nanocrystals. The film is p-type with stoichiometric excess of SCN and a direct transition gap of 3.7
eV. Deposition mechanisms of CuSCN films at varied temperatures are studied based on the proposed energetic model. At or below room temperature, the electron quantum tunnel through deposition layer is predominant at the very beginning. However, the growth is limited when the thickness of CuSCN film reaches the size comparable to the diffusion length of electrons. Above room temperature, the thermal activation of surface states plays an important role in the continuous growth of large crystals through holes transport in the valence band. The calculated activation energy for crystal growth is 0.5
eV.</description><subject>Activation energy</subject><subject>Applied sciences</subject><subject>Chemistry</subject><subject>CuSCN</subject><subject>Deposition mechanism</subject><subject>Electrochemistry</subject><subject>Electrodeposition</subject><subject>Energy</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Natural energy</subject><subject>Photovoltaic conversion</subject><subject>Solar cell</subject><subject>Solar cells. Photoelectrochemical cells</subject><subject>Solar energy</subject><subject>Study of interfaces</subject><subject>Surface state</subject><issn>0013-4686</issn><issn>1873-3859</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNqFUE1vEzEQtRBIhMJvwBcQHDYdf8TrPUZpKVGr9tBwtrzeWcXRxl7sTRH_Hm9TwRFppNHMvHlv5hHykcGSAVOXhyUO6CZbYskBZOkuQepXZMF0LSqhV81rsgBgopJKq7fkXc4HAKhVDQsSblL8Ne3pEd3eBp-Pmcaebk6Pm3va-6GUz-wpdjjG7CfsaAx0u3ugPtDrq926cnsc7Nx3cRwxfdluv1IbOno7U9ifJ4ynTHMcTpOP4T1509sh44eXfEF-fLvebb5Xdw832836rnJS8qmqmZTgdAuOQSebWkohai6htYophpy1yJ1udCt60QrsWtU2oJuO907XuOLignw-844plhPyZI4-OxwGG-Z7DNcrEIzPwPoMdCnmnLA3Y_JHm34bBmb21xzMX3_N7O88KP6WzU8vEjY7O_TJBufzv3WlQEjRFNz6jMPy75PHZLLzGBx2PhVe00X_X60_qEuUDw</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>Wu, Weibing</creator><creator>Jin, Zhengguo</creator><creator>Hua, Zhen</creator><creator>Fu, Yanan</creator><creator>Qiu, Jijun</creator><general>Elsevier Ltd</general><general>Elsevier</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QQ</scope><scope>7SP</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8FD</scope><scope>FR3</scope><scope>H8G</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20050401</creationdate><title>Growth mechanisms of CuSCN films electrodeposited on ITO in EDTA-chelated copper(II) and KSCN aqueous solution</title><author>Wu, Weibing ; Jin, Zhengguo ; Hua, Zhen ; Fu, Yanan ; Qiu, Jijun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-71440c8b0c10d49744337240ba6161e21be2c898b3f3b3edb6b9089d2fc87e523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Activation energy</topic><topic>Applied sciences</topic><topic>Chemistry</topic><topic>CuSCN</topic><topic>Deposition mechanism</topic><topic>Electrochemistry</topic><topic>Electrodeposition</topic><topic>Energy</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Natural energy</topic><topic>Photovoltaic conversion</topic><topic>Solar cell</topic><topic>Solar cells. Photoelectrochemical cells</topic><topic>Solar energy</topic><topic>Study of interfaces</topic><topic>Surface state</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Weibing</creatorcontrib><creatorcontrib>Jin, Zhengguo</creatorcontrib><creatorcontrib>Hua, Zhen</creatorcontrib><creatorcontrib>Fu, Yanan</creatorcontrib><creatorcontrib>Qiu, Jijun</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Ceramic Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Copper Technical Reference Library</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>Wu, Weibing</au><au>Jin, Zhengguo</au><au>Hua, Zhen</au><au>Fu, Yanan</au><au>Qiu, Jijun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Growth mechanisms of CuSCN films electrodeposited on ITO in EDTA-chelated copper(II) and KSCN aqueous solution</atitle><jtitle>Electrochimica acta</jtitle><date>2005-04-01</date><risdate>2005</risdate><volume>50</volume><issue>11</issue><spage>2343</spage><epage>2349</epage><pages>2343-2349</pages><issn>0013-4686</issn><eissn>1873-3859</eissn><coden>ELCAAV</coden><abstract>Electrodeposition of β-CuSCN films was investigated on transparent conducting ITO substrates in an aqueous electrolyte containing EDTA-chelated Cu(II) and KSCN. It has been observed that the instability of CuSO
4 and KSCN aqueous solution without EDTA is due to the formation of Cu(SCN)
2 precipitation, which can transform into CuSCN and (SCN)
x
at room temperature. Research results illuminate that the deposited film at −0.5
V versus Ag/AgCl
sat at 298
K is uniform and dense and composed of nanocrystals. The film is p-type with stoichiometric excess of SCN and a direct transition gap of 3.7
eV. Deposition mechanisms of CuSCN films at varied temperatures are studied based on the proposed energetic model. At or below room temperature, the electron quantum tunnel through deposition layer is predominant at the very beginning. However, the growth is limited when the thickness of CuSCN film reaches the size comparable to the diffusion length of electrons. Above room temperature, the thermal activation of surface states plays an important role in the continuous growth of large crystals through holes transport in the valence band. The calculated activation energy for crystal growth is 0.5
eV.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.electacta.2004.10.048</doi><tpages>7</tpages></addata></record> |
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source | ScienceDirect Journals (5 years ago - present) |
subjects | Activation energy Applied sciences Chemistry CuSCN Deposition mechanism Electrochemistry Electrodeposition Energy Exact sciences and technology General and physical chemistry Natural energy Photovoltaic conversion Solar cell Solar cells. Photoelectrochemical cells Solar energy Study of interfaces Surface state |
title | Growth mechanisms of CuSCN films electrodeposited on ITO in EDTA-chelated copper(II) and KSCN aqueous solution |
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