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Scanning electrochemical microscopy imaging with laser-pulled probes
The fabrication of Pt nanoelectrodes (NEs) and ultramicroelectrodes (UMEs) were explored through the use of a precision laser electrode puller. As a result of the heated pull, the Pt tips of the NEs were exposed immediately during the fabrication process. Newly fabricated NEs were immediately used t...
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Published in: | Journal of electroanalytical chemistry (Lausanne, Switzerland) Switzerland), 2016-11, Vol.781, p.126-135 |
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description | The fabrication of Pt nanoelectrodes (NEs) and ultramicroelectrodes (UMEs) were explored through the use of a precision laser electrode puller. As a result of the heated pull, the Pt tips of the NEs were exposed immediately during the fabrication process. Newly fabricated NEs were immediately used to observe the topographical and electrochemical characteristics of a TEM grid by scanning electrochemical microscopy (SECM) horizontal line scans. While higher spatial resolution would be offered by NEs, their use in imaging can be restricted due to sample size and instrumental limitations. To accurately characterize an independently addressable microband electrode (IAME) by SECM, a Pt UME of a known size and geometry was used. SECM depth scan and constant height images were obtained of an unbiased IAME. By utilizing a SECM probe that is similar in size to the Pt and glass microbands of the IAME (4.4 vs. 5μm, respectively), redox cycling phenomenon was detected. From these electrochemical images, the Pt microbands appeared to be larger than their physical dimensions, while the glass microbands appeared much smaller. Since redox cycling can be affected by sample tilt, the tilt angle of the IAME was quantified through 3 different methods. The first approach was to use the traditional PAC comparison method over different locations on the sample, while the second and third approaches relied heavily on 3D finite elemental analysis simulations representative of the SECM experiments. The first of these two methods required the fitting of a tilted experimental horizontal sweep against a fixed IAME, while the second approach relied on the direct fitting of the experimental data onto tilted depth scan simulations. Each methodology delivered approximately the same tilt angle, confirming the viability of all the methodologies.
[Display omitted]
•Scanning electrochemical microscopy (SECM) imaging was conducted.•Nanoscale and microscale Pt electrodes were fabricated by a laser puller.•3D simulations allowed for sample characterization.•Unbiased independently addressable microband electrodes confirmed redox cycling.•Simulated SECM depth scan maps investigated tilt angle of sample |
doi_str_mv | 10.1016/j.jelechem.2016.06.043 |
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[Display omitted]
•Scanning electrochemical microscopy (SECM) imaging was conducted.•Nanoscale and microscale Pt electrodes were fabricated by a laser puller.•3D simulations allowed for sample characterization.•Unbiased independently addressable microband electrodes confirmed redox cycling.•Simulated SECM depth scan maps investigated tilt angle of sample</description><identifier>ISSN: 1572-6657</identifier><identifier>EISSN: 1873-2569</identifier><identifier>DOI: 10.1016/j.jelechem.2016.06.043</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>COMSOL simulations ; Cycles ; Electrodes ; Experiments ; Image detection ; Independently addressable microband electrodes (IAMEs) ; Laser beam heating ; Lasers ; Microscopy ; Nanoelectrode fabrication ; Redox cycling ; Research methodology ; Scanning electrochemical microscopy (SECM) ; SECM imaging ; Simulation ; Spatial resolution ; Tips ; Viability</subject><ispartof>Journal of electroanalytical chemistry (Lausanne, Switzerland), 2016-11, Vol.781, p.126-135</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright Elsevier Science Ltd. Nov 15, 2016</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-b42b15c7a64162b3ad379f15db8b525c7181423152cf2ae12f5abef9533949c3</citedby><cites>FETCH-LOGICAL-c340t-b42b15c7a64162b3ad379f15db8b525c7181423152cf2ae12f5abef9533949c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Li, Michelle S.M.</creatorcontrib><creatorcontrib>Filice, Fraser P.</creatorcontrib><creatorcontrib>Ding, Zhifeng</creatorcontrib><title>Scanning electrochemical microscopy imaging with laser-pulled probes</title><title>Journal of electroanalytical chemistry (Lausanne, Switzerland)</title><description>The fabrication of Pt nanoelectrodes (NEs) and ultramicroelectrodes (UMEs) were explored through the use of a precision laser electrode puller. As a result of the heated pull, the Pt tips of the NEs were exposed immediately during the fabrication process. Newly fabricated NEs were immediately used to observe the topographical and electrochemical characteristics of a TEM grid by scanning electrochemical microscopy (SECM) horizontal line scans. While higher spatial resolution would be offered by NEs, their use in imaging can be restricted due to sample size and instrumental limitations. To accurately characterize an independently addressable microband electrode (IAME) by SECM, a Pt UME of a known size and geometry was used. SECM depth scan and constant height images were obtained of an unbiased IAME. By utilizing a SECM probe that is similar in size to the Pt and glass microbands of the IAME (4.4 vs. 5μm, respectively), redox cycling phenomenon was detected. From these electrochemical images, the Pt microbands appeared to be larger than their physical dimensions, while the glass microbands appeared much smaller. Since redox cycling can be affected by sample tilt, the tilt angle of the IAME was quantified through 3 different methods. The first approach was to use the traditional PAC comparison method over different locations on the sample, while the second and third approaches relied heavily on 3D finite elemental analysis simulations representative of the SECM experiments. The first of these two methods required the fitting of a tilted experimental horizontal sweep against a fixed IAME, while the second approach relied on the direct fitting of the experimental data onto tilted depth scan simulations. Each methodology delivered approximately the same tilt angle, confirming the viability of all the methodologies.
[Display omitted]
•Scanning electrochemical microscopy (SECM) imaging was conducted.•Nanoscale and microscale Pt electrodes were fabricated by a laser puller.•3D simulations allowed for sample characterization.•Unbiased independently addressable microband electrodes confirmed redox cycling.•Simulated SECM depth scan maps investigated tilt angle of sample</description><subject>COMSOL simulations</subject><subject>Cycles</subject><subject>Electrodes</subject><subject>Experiments</subject><subject>Image detection</subject><subject>Independently addressable microband electrodes (IAMEs)</subject><subject>Laser beam heating</subject><subject>Lasers</subject><subject>Microscopy</subject><subject>Nanoelectrode fabrication</subject><subject>Redox cycling</subject><subject>Research methodology</subject><subject>Scanning electrochemical microscopy (SECM)</subject><subject>SECM imaging</subject><subject>Simulation</subject><subject>Spatial resolution</subject><subject>Tips</subject><subject>Viability</subject><issn>1572-6657</issn><issn>1873-2569</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqFUNtKxDAQDaLguvoLUvC5Nfemb8p6hQUf3PeQpNPdlG5bk67i35uy-iwMc2HOnJk5CF0TXBBM5G1btNCB28G-oKkucDLOTtCCqJLlVMjqNOWipLmUojxHFzG2GFOlCF2gh3dn-t7322zmmMIw83hnuiz5MEQ3jN-Z35vtDPny0y7rTISQj4eugzobw2AhXqKzxnQRrn7jEm2eHjerl3z99vy6ul_njnE85ZZTS4QrjeREUstMzcqqIaK2ygqaGkQRThkR1DXUAKGNMBaaSjBW8cqxJbo50qatHweIk26HQ-jTRk2xqkomqKoSSh5R8_kxQKPHkB4I35pgPQumW_0nmJ4F0zgZZ2nw7jgI6YVPD0FH56F3UPuQpNH14P-j-AHh03ej</recordid><startdate>20161115</startdate><enddate>20161115</enddate><creator>Li, Michelle S.M.</creator><creator>Filice, Fraser P.</creator><creator>Ding, Zhifeng</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20161115</creationdate><title>Scanning electrochemical microscopy imaging with laser-pulled probes</title><author>Li, Michelle S.M. ; Filice, Fraser P. ; Ding, Zhifeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-b42b15c7a64162b3ad379f15db8b525c7181423152cf2ae12f5abef9533949c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>COMSOL simulations</topic><topic>Cycles</topic><topic>Electrodes</topic><topic>Experiments</topic><topic>Image detection</topic><topic>Independently addressable microband electrodes (IAMEs)</topic><topic>Laser beam heating</topic><topic>Lasers</topic><topic>Microscopy</topic><topic>Nanoelectrode fabrication</topic><topic>Redox cycling</topic><topic>Research methodology</topic><topic>Scanning electrochemical microscopy (SECM)</topic><topic>SECM imaging</topic><topic>Simulation</topic><topic>Spatial resolution</topic><topic>Tips</topic><topic>Viability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Michelle S.M.</creatorcontrib><creatorcontrib>Filice, Fraser P.</creatorcontrib><creatorcontrib>Ding, Zhifeng</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of electroanalytical chemistry (Lausanne, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Michelle S.M.</au><au>Filice, Fraser P.</au><au>Ding, Zhifeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Scanning electrochemical microscopy imaging with laser-pulled probes</atitle><jtitle>Journal of electroanalytical chemistry (Lausanne, Switzerland)</jtitle><date>2016-11-15</date><risdate>2016</risdate><volume>781</volume><spage>126</spage><epage>135</epage><pages>126-135</pages><issn>1572-6657</issn><eissn>1873-2569</eissn><abstract>The fabrication of Pt nanoelectrodes (NEs) and ultramicroelectrodes (UMEs) were explored through the use of a precision laser electrode puller. As a result of the heated pull, the Pt tips of the NEs were exposed immediately during the fabrication process. Newly fabricated NEs were immediately used to observe the topographical and electrochemical characteristics of a TEM grid by scanning electrochemical microscopy (SECM) horizontal line scans. While higher spatial resolution would be offered by NEs, their use in imaging can be restricted due to sample size and instrumental limitations. To accurately characterize an independently addressable microband electrode (IAME) by SECM, a Pt UME of a known size and geometry was used. SECM depth scan and constant height images were obtained of an unbiased IAME. By utilizing a SECM probe that is similar in size to the Pt and glass microbands of the IAME (4.4 vs. 5μm, respectively), redox cycling phenomenon was detected. From these electrochemical images, the Pt microbands appeared to be larger than their physical dimensions, while the glass microbands appeared much smaller. Since redox cycling can be affected by sample tilt, the tilt angle of the IAME was quantified through 3 different methods. The first approach was to use the traditional PAC comparison method over different locations on the sample, while the second and third approaches relied heavily on 3D finite elemental analysis simulations representative of the SECM experiments. The first of these two methods required the fitting of a tilted experimental horizontal sweep against a fixed IAME, while the second approach relied on the direct fitting of the experimental data onto tilted depth scan simulations. Each methodology delivered approximately the same tilt angle, confirming the viability of all the methodologies.
[Display omitted]
•Scanning electrochemical microscopy (SECM) imaging was conducted.•Nanoscale and microscale Pt electrodes were fabricated by a laser puller.•3D simulations allowed for sample characterization.•Unbiased independently addressable microband electrodes confirmed redox cycling.•Simulated SECM depth scan maps investigated tilt angle of sample</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.jelechem.2016.06.043</doi><tpages>10</tpages></addata></record> |
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subjects | COMSOL simulations Cycles Electrodes Experiments Image detection Independently addressable microband electrodes (IAMEs) Laser beam heating Lasers Microscopy Nanoelectrode fabrication Redox cycling Research methodology Scanning electrochemical microscopy (SECM) SECM imaging Simulation Spatial resolution Tips Viability |
title | Scanning electrochemical microscopy imaging with laser-pulled probes |
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