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Electrochemical behaviour of tris(1,10-phenanthroline)ruthenium(II) at a surface modified electrode. Electrocatalytic reduction of dioxygen
A gold electrode modified by thiocyanate anion used as cathode for the reduction of dioxygen via Ru(phen)32+. [Display omitted] •Cyclic voltammetry of [Ru(phen)3]2+ at a gold electrode modified by thiocyanate is studied.•Five one-electron ligand reductions are identified on the negative side of NHE....
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Published in: | Inorganica Chimica Acta 2017-09, Vol.466, p.349-357 |
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description | A gold electrode modified by thiocyanate anion used as cathode for the reduction of dioxygen via Ru(phen)32+.
[Display omitted]
•Cyclic voltammetry of [Ru(phen)3]2+ at a gold electrode modified by thiocyanate is studied.•Five one-electron ligand reductions are identified on the negative side of NHE.•[Ru(phen)3]2+ gets absorbed on the SCN− modified gold electrode.•Au-SCN-Ru(phen)32+ electrode shows electrocatalytic reductions of dioxygen.•The heterogeneous rate constant ks,h for O2+e→O2− is found to be 2.99×10−3cms−1.•This ks,h at an unmodified Au electrode is 1.21×10−3cms−1.
Cyclic voltammetry (CV) of [Ru(phen)3]2+ (phen=1,10-phenanthroline) is studied in CH3CN under N2 at a gold electrode whose surface is modified by thiocyanate. Five one-electron ligand reductions are observed on the negative side of normal hydrogen electrode (NHE), which is unprecedented. Using Randles-Sevcik equation, the electrochemical radius of the electrode has been estimated as 0.86mm (cf. physical radius: 1mm). When the Au-SCN electrode is dipped in an CH3CN solution of [Ru(phen)3]2+ for 2h, the cation gets adsorbed on the electrode surface. The resulting Au-SCN-Ru(phen)32+ electrode shows two reductions in plain CH3CN under N2. The number of electrons in each step is found to be 2 when Laviron’s equation is applied with a transfer coefficient α of 0.5. Ferrocene at the Au-SCN-Ru(phen)32+ electrode in CH3CN shows a one-electron oxidation at 0.681V vs NHE. The radius of the electrode comes out as 1.02mm. The heterogeneous rate constant ks,h for the oxidation of ferrocene is found to be 2.77×10−2cms−1 and that at an unmodified Au electrode in CH3CN 1.03×10−2cms−1. When CV is performed in CH3CN in air, the Au-SCN-Ru(phen)32+ electrode shows electro-catalytic reductions of dioxygen (O2+e→O2− and O2−+e→O22−). The ks,h of the first step is found to be 2.99×10−3cms−1 by Nicholson’s method (with α=0.306). This ks,h at an unmodified Au electrode is 1.21×10−3cms−1. In course of the studies, it has been necessary to determine the X-ray crystal structures of [Ru(phen)3](NCS)2 and [Ru(phen)3]2[Fe(CN)6]Cl·18.5H2O. |
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[Display omitted]
•Cyclic voltammetry of [Ru(phen)3]2+ at a gold electrode modified by thiocyanate is studied.•Five one-electron ligand reductions are identified on the negative side of NHE.•[Ru(phen)3]2+ gets absorbed on the SCN− modified gold electrode.•Au-SCN-Ru(phen)32+ electrode shows electrocatalytic reductions of dioxygen.•The heterogeneous rate constant ks,h for O2+e→O2− is found to be 2.99×10−3cms−1.•This ks,h at an unmodified Au electrode is 1.21×10−3cms−1.
Cyclic voltammetry (CV) of [Ru(phen)3]2+ (phen=1,10-phenanthroline) is studied in CH3CN under N2 at a gold electrode whose surface is modified by thiocyanate. Five one-electron ligand reductions are observed on the negative side of normal hydrogen electrode (NHE), which is unprecedented. Using Randles-Sevcik equation, the electrochemical radius of the electrode has been estimated as 0.86mm (cf. physical radius: 1mm). When the Au-SCN electrode is dipped in an CH3CN solution of [Ru(phen)3]2+ for 2h, the cation gets adsorbed on the electrode surface. The resulting Au-SCN-Ru(phen)32+ electrode shows two reductions in plain CH3CN under N2. The number of electrons in each step is found to be 2 when Laviron’s equation is applied with a transfer coefficient α of 0.5. Ferrocene at the Au-SCN-Ru(phen)32+ electrode in CH3CN shows a one-electron oxidation at 0.681V vs NHE. The radius of the electrode comes out as 1.02mm. The heterogeneous rate constant ks,h for the oxidation of ferrocene is found to be 2.77×10−2cms−1 and that at an unmodified Au electrode in CH3CN 1.03×10−2cms−1. When CV is performed in CH3CN in air, the Au-SCN-Ru(phen)32+ electrode shows electro-catalytic reductions of dioxygen (O2+e→O2− and O2−+e→O22−). The ks,h of the first step is found to be 2.99×10−3cms−1 by Nicholson’s method (with α=0.306). This ks,h at an unmodified Au electrode is 1.21×10−3cms−1. In course of the studies, it has been necessary to determine the X-ray crystal structures of [Ru(phen)3](NCS)2 and [Ru(phen)3]2[Fe(CN)6]Cl·18.5H2O.</description><identifier>ISSN: 0020-1693</identifier><identifier>EISSN: 1873-3255</identifier><identifier>DOI: 10.1016/j.ica.2017.05.074</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Catalysis ; Crystal structure ; Dioxygen reduction ; Electrocatalysis ; Electrochemical analysis ; Electrochemistry ; Electrodes ; Gold ; Ligands ; Oxidation ; Ru(II) complex ; Ruthenium ; Ruthenium compounds ; Studies ; Surface modified electrode ; Voltammetry</subject><ispartof>Inorganica Chimica Acta, 2017-09, Vol.466, p.349-357</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright Elsevier Science Ltd. Sep 1, 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c325t-cd6dbe33bc586fa239a0e08fee1c3a896a8c739bc2e2d157be97f0704a0ca0cc3</citedby><cites>FETCH-LOGICAL-c325t-cd6dbe33bc586fa239a0e08fee1c3a896a8c739bc2e2d157be97f0704a0ca0cc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Shee, Nirmal K.</creatorcontrib><creatorcontrib>Patra, Shanti G.</creatorcontrib><creatorcontrib>Drew, Michael G.B.</creatorcontrib><creatorcontrib>Lu, Liping</creatorcontrib><creatorcontrib>Zangrando, Ennio</creatorcontrib><creatorcontrib>Datta, Dipankar</creatorcontrib><title>Electrochemical behaviour of tris(1,10-phenanthroline)ruthenium(II) at a surface modified electrode. Electrocatalytic reduction of dioxygen</title><title>Inorganica Chimica Acta</title><description>A gold electrode modified by thiocyanate anion used as cathode for the reduction of dioxygen via Ru(phen)32+.
[Display omitted]
•Cyclic voltammetry of [Ru(phen)3]2+ at a gold electrode modified by thiocyanate is studied.•Five one-electron ligand reductions are identified on the negative side of NHE.•[Ru(phen)3]2+ gets absorbed on the SCN− modified gold electrode.•Au-SCN-Ru(phen)32+ electrode shows electrocatalytic reductions of dioxygen.•The heterogeneous rate constant ks,h for O2+e→O2− is found to be 2.99×10−3cms−1.•This ks,h at an unmodified Au electrode is 1.21×10−3cms−1.
Cyclic voltammetry (CV) of [Ru(phen)3]2+ (phen=1,10-phenanthroline) is studied in CH3CN under N2 at a gold electrode whose surface is modified by thiocyanate. Five one-electron ligand reductions are observed on the negative side of normal hydrogen electrode (NHE), which is unprecedented. Using Randles-Sevcik equation, the electrochemical radius of the electrode has been estimated as 0.86mm (cf. physical radius: 1mm). When the Au-SCN electrode is dipped in an CH3CN solution of [Ru(phen)3]2+ for 2h, the cation gets adsorbed on the electrode surface. The resulting Au-SCN-Ru(phen)32+ electrode shows two reductions in plain CH3CN under N2. The number of electrons in each step is found to be 2 when Laviron’s equation is applied with a transfer coefficient α of 0.5. Ferrocene at the Au-SCN-Ru(phen)32+ electrode in CH3CN shows a one-electron oxidation at 0.681V vs NHE. The radius of the electrode comes out as 1.02mm. The heterogeneous rate constant ks,h for the oxidation of ferrocene is found to be 2.77×10−2cms−1 and that at an unmodified Au electrode in CH3CN 1.03×10−2cms−1. When CV is performed in CH3CN in air, the Au-SCN-Ru(phen)32+ electrode shows electro-catalytic reductions of dioxygen (O2+e→O2− and O2−+e→O22−). The ks,h of the first step is found to be 2.99×10−3cms−1 by Nicholson’s method (with α=0.306). This ks,h at an unmodified Au electrode is 1.21×10−3cms−1. In course of the studies, it has been necessary to determine the X-ray crystal structures of [Ru(phen)3](NCS)2 and [Ru(phen)3]2[Fe(CN)6]Cl·18.5H2O.</description><subject>Catalysis</subject><subject>Crystal structure</subject><subject>Dioxygen reduction</subject><subject>Electrocatalysis</subject><subject>Electrochemical analysis</subject><subject>Electrochemistry</subject><subject>Electrodes</subject><subject>Gold</subject><subject>Ligands</subject><subject>Oxidation</subject><subject>Ru(II) complex</subject><subject>Ruthenium</subject><subject>Ruthenium compounds</subject><subject>Studies</subject><subject>Surface modified electrode</subject><subject>Voltammetry</subject><issn>0020-1693</issn><issn>1873-3255</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNp9kM9q3DAQxkVpods0D5CboJcEYndkrS2bnErIn4VALslZyKNxV4vX2khyyD5DXzpaNr0GBgaG-b5v5sfYmYBSgGh-b0qHpqxAqBLqEtTyC1uIVslCVnX9lS0AKihE08nv7EeMGwAJjawX7N_NSJiCxzVts8PIe1qbV-fnwP3AU3DxXFwKKHZrmsyU1sGPbqKLMKc8cPP2fLW64CZxw-McBoPEt966wZHldHS2VPL_ISaZcZ8c8kB2xuT8dEixzr_t_9L0k30bzBjp9KOfsOfbm6fr--Lh8W51_eehwPxMKtA2ticpe6zbZjCV7AwQtAORQGnarjEtKtn1WFFlRa166tQACpYGMBfKE_br6LsL_mWmmPQm_zvlSF3BsoGqVqDyljhuYfAxBhr0LritCXstQB-Y643OxPSBuYZaZ-ZZc3XUUD7_1VHQER1NSNaFTEBb7z5RvwPr3IyQ</recordid><startdate>20170901</startdate><enddate>20170901</enddate><creator>Shee, Nirmal K.</creator><creator>Patra, Shanti G.</creator><creator>Drew, Michael G.B.</creator><creator>Lu, Liping</creator><creator>Zangrando, Ennio</creator><creator>Datta, Dipankar</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>20170901</creationdate><title>Electrochemical behaviour of tris(1,10-phenanthroline)ruthenium(II) at a surface modified electrode. Electrocatalytic reduction of dioxygen</title><author>Shee, Nirmal K. ; Patra, Shanti G. ; Drew, Michael G.B. ; Lu, Liping ; Zangrando, Ennio ; Datta, Dipankar</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c325t-cd6dbe33bc586fa239a0e08fee1c3a896a8c739bc2e2d157be97f0704a0ca0cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Catalysis</topic><topic>Crystal structure</topic><topic>Dioxygen reduction</topic><topic>Electrocatalysis</topic><topic>Electrochemical analysis</topic><topic>Electrochemistry</topic><topic>Electrodes</topic><topic>Gold</topic><topic>Ligands</topic><topic>Oxidation</topic><topic>Ru(II) complex</topic><topic>Ruthenium</topic><topic>Ruthenium compounds</topic><topic>Studies</topic><topic>Surface modified electrode</topic><topic>Voltammetry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shee, Nirmal K.</creatorcontrib><creatorcontrib>Patra, Shanti G.</creatorcontrib><creatorcontrib>Drew, Michael G.B.</creatorcontrib><creatorcontrib>Lu, Liping</creatorcontrib><creatorcontrib>Zangrando, Ennio</creatorcontrib><creatorcontrib>Datta, Dipankar</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Inorganica Chimica Acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shee, Nirmal K.</au><au>Patra, Shanti G.</au><au>Drew, Michael G.B.</au><au>Lu, Liping</au><au>Zangrando, Ennio</au><au>Datta, Dipankar</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrochemical behaviour of tris(1,10-phenanthroline)ruthenium(II) at a surface modified electrode. Electrocatalytic reduction of dioxygen</atitle><jtitle>Inorganica Chimica Acta</jtitle><date>2017-09-01</date><risdate>2017</risdate><volume>466</volume><spage>349</spage><epage>357</epage><pages>349-357</pages><issn>0020-1693</issn><eissn>1873-3255</eissn><abstract>A gold electrode modified by thiocyanate anion used as cathode for the reduction of dioxygen via Ru(phen)32+.
[Display omitted]
•Cyclic voltammetry of [Ru(phen)3]2+ at a gold electrode modified by thiocyanate is studied.•Five one-electron ligand reductions are identified on the negative side of NHE.•[Ru(phen)3]2+ gets absorbed on the SCN− modified gold electrode.•Au-SCN-Ru(phen)32+ electrode shows electrocatalytic reductions of dioxygen.•The heterogeneous rate constant ks,h for O2+e→O2− is found to be 2.99×10−3cms−1.•This ks,h at an unmodified Au electrode is 1.21×10−3cms−1.
Cyclic voltammetry (CV) of [Ru(phen)3]2+ (phen=1,10-phenanthroline) is studied in CH3CN under N2 at a gold electrode whose surface is modified by thiocyanate. Five one-electron ligand reductions are observed on the negative side of normal hydrogen electrode (NHE), which is unprecedented. Using Randles-Sevcik equation, the electrochemical radius of the electrode has been estimated as 0.86mm (cf. physical radius: 1mm). When the Au-SCN electrode is dipped in an CH3CN solution of [Ru(phen)3]2+ for 2h, the cation gets adsorbed on the electrode surface. The resulting Au-SCN-Ru(phen)32+ electrode shows two reductions in plain CH3CN under N2. The number of electrons in each step is found to be 2 when Laviron’s equation is applied with a transfer coefficient α of 0.5. Ferrocene at the Au-SCN-Ru(phen)32+ electrode in CH3CN shows a one-electron oxidation at 0.681V vs NHE. The radius of the electrode comes out as 1.02mm. The heterogeneous rate constant ks,h for the oxidation of ferrocene is found to be 2.77×10−2cms−1 and that at an unmodified Au electrode in CH3CN 1.03×10−2cms−1. When CV is performed in CH3CN in air, the Au-SCN-Ru(phen)32+ electrode shows electro-catalytic reductions of dioxygen (O2+e→O2− and O2−+e→O22−). The ks,h of the first step is found to be 2.99×10−3cms−1 by Nicholson’s method (with α=0.306). This ks,h at an unmodified Au electrode is 1.21×10−3cms−1. In course of the studies, it has been necessary to determine the X-ray crystal structures of [Ru(phen)3](NCS)2 and [Ru(phen)3]2[Fe(CN)6]Cl·18.5H2O.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.ica.2017.05.074</doi><tpages>9</tpages></addata></record> |
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subjects | Catalysis Crystal structure Dioxygen reduction Electrocatalysis Electrochemical analysis Electrochemistry Electrodes Gold Ligands Oxidation Ru(II) complex Ruthenium Ruthenium compounds Studies Surface modified electrode Voltammetry |
title | Electrochemical behaviour of tris(1,10-phenanthroline)ruthenium(II) at a surface modified electrode. Electrocatalytic reduction of dioxygen |
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