Facile synthesis of iron-ruthenium bimetallic oxide nanoparticles on carbon nanotube composites by liquid phase plasma method for supercapacitor
Iron-ruthenium bimetallic oxide nanoparticles were precipitated on carbon nanotubes by liquid-phase plasma method. We also evaluated the physicochemical and electrochemical properties of prepared composite for supercapacitor electrode. Polycrystalline about 10 to 25 nm-sized bimetallic nanoparticles...
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| Published in | The Korean journal of chemical engineering Vol. 34; no. 11; pp. 2993 - 2998 |
|---|---|
| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
New York
Springer US
01.11.2017
Springer Nature B.V 한국화학공학회 |
| Subjects | |
| Online Access | Get full text |
| ISSN | 0256-1115 1975-7220 |
| DOI | 10.1007/s11814-017-0205-z |
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| Abstract | Iron-ruthenium bimetallic oxide nanoparticles were precipitated on carbon nanotubes by liquid-phase plasma method. We also evaluated the physicochemical and electrochemical properties of prepared composite for supercapacitor electrode. Polycrystalline about 10 to 25 nm-sized bimetallic nanoparticles were evenly precipitated on the carbon nanotube (CNT) and consisted of Fe
3+
and Ru
4+
. Bimetallic oxide nanoparticles’ composition depended on the ratio of the metal precursor concentration and standard reduction potential. The C-V area and specific capacitance of iron-ruthenium oxide nanoparticle/carbon nanotube (IRCNT) composite electrodes was higher than that of untreated CNT electrode, and increased with increasing ruthenium content. The cycling stability of IRCNT composite electrode was higher than untreated CNT electrode, especially iron element was more stable. |
|---|---|
| AbstractList | Iron-ruthenium bimetallic oxide nanoparticles were precipitated on carbon nanotubes by liquid-phase plasma method. We also evaluated the physicochemical and electrochemical properties of prepared composite for supercapacitor electrode. Polycrystalline about 10 to 25 nm-sized bimetallic nanoparticles were evenly precipitated on the carbon nanotube (CNT) and consisted of Fe
3+
and Ru
4+
. Bimetallic oxide nanoparticles’ composition depended on the ratio of the metal precursor concentration and standard reduction potential. The C-V area and specific capacitance of iron-ruthenium oxide nanoparticle/carbon nanotube (IRCNT) composite electrodes was higher than that of untreated CNT electrode, and increased with increasing ruthenium content. The cycling stability of IRCNT composite electrode was higher than untreated CNT electrode, especially iron element was more stable. Iron-ruthenium bimetallic oxide nanoparticles were precipitated on carbon nanotubes by liquid-phase plasma method. We also evaluated the physicochemical and electrochemical properties of prepared composite for supercapacitor electrode. Polycrystalline about 10 to 25 nm-sized bimetallic nanoparticles were evenly precipitated on the carbon nanotube (CNT) and consisted of Fe3+ and Ru4+. Bimetallic oxide nanoparticles’ composition depended on the ratio of the metal precursor concentration and standard reduction potential. The C-V area and specific capacitance of iron-ruthenium oxide nanoparticle/carbon nanotube (IRCNT) composite electrodes was higher than that of untreated CNT electrode, and increased with increasing ruthenium content. The cycling stability of IRCNT composite electrode was higher than untreated CNT electrode, especially iron element was more stable. Iron-ruthenium bimetallic oxide nanoparticles were precipitated on carbon nanotubes by liquid-phase plasma method. We also evaluated the physicochemical and electrochemical properties of prepared composite for supercapacitor electrode. Polycrystalline about 10 to 25 nm-sized bimetallic nanoparticles were evenly precipitated on the carbon nanotube (CNT) and consisted of Fe3+ and Ru4+. Bimetallic oxide nanoparticles’ composition depended on the ratio of the metal precursor concentration and standard reduction potential. The C-V area and specific capacitance of iron-ruthenium oxide nanoparticle/carbon nanotube (IRCNT) composite electrodes was higher than that of untreated CNT electrode, and increased with increasing ruthenium content. The cycling stability of IRCNT composite electrode was higher than untreated CNT electrode, especially iron element was more stable. KCI Citation Count: 45 |
| Author | Jeong, Sangmin Jung, Sang-Chul An, Kay-Hyeok Park, Young-Kwon Lee, Won-June Lee, Heon Kim, Byung-Joo |
| Author_xml | – sequence: 1 givenname: Won-June surname: Lee fullname: Lee, Won-June organization: Department of Environmental Engineering, Sunchon National University – sequence: 2 givenname: Sangmin surname: Jeong fullname: Jeong, Sangmin organization: Department of Environmental Engineering, Sunchon National University – sequence: 3 givenname: Heon surname: Lee fullname: Lee, Heon organization: Department of Environmental Engineering, Sunchon National University – sequence: 4 givenname: Byung-Joo surname: Kim fullname: Kim, Byung-Joo organization: R&D Division, Korea Institute of Carbon Convergence Technology – sequence: 5 givenname: Kay-Hyeok surname: An fullname: An, Kay-Hyeok organization: Department of Nano & Advanced Materials Engineering, Jeonju University – sequence: 6 givenname: Young-Kwon surname: Park fullname: Park, Young-Kwon organization: School of Environmental Engineering, University of Seoul – sequence: 7 givenname: Sang-Chul surname: Jung fullname: Jung, Sang-Chul email: jsc@sunchon.ac.kr organization: Department of Environmental Engineering, Sunchon National University |
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| Cites_doi | 10.1166/sam.2014.1815 10.1039/b923153f 10.1002/1616-3028(200110)11:5<387::AID-ADFM387>3.0.CO;2-G 10.1063/1.1800011 10.1016/S0013-4686(97)81190-5 10.1016/j.ijhydene.2014.08.085 10.1016/j.matchemphys.2007.02.038 10.1016/j.nanoen.2012.07.016 10.1007/s11814-015-0262-0 10.1186/s11671-016-1557-8 10.1039/C4TA04996A 10.1166/sam.2016.2887 10.1016/S0378-7753(00)00485-7 10.1016/j.mee.2014.07.014 10.5185/amlett.2016.6110 10.1007/s11051-005-9058-1 10.1002/adfm.200900971 10.1016/j.electacta.2006.09.039 10.1016/S0378-7753(03)00600-1 10.1039/c1ee01094h 10.1007/s11814-014-0392-9 10.1016/j.ijhydene.2016.02.011 |
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| Keywords | Specific Capacitance Liquid Phase Plasma Iron Ruthenium Bimetallic Oxide Nanoparticle |
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| References | WanC.AzumiK.KonnoH.Electrochim. Acta20075230611:CAS:528:DC%2BD2sXht1Gmt78%3D10.1016/j.electacta.2006.09.039 BurkeA.J. Power Sources200091371:CAS:528:DC%2BD3cXlvVWlsL4%3D10.1016/S0378-7753(00)00485-7 ZhangY.LiL.SuH.HuangW.DongX.J. Mater. Chem. A20153431:CAS:528:DC%2BC2cXhslGnsrfK10.1039/C4TA04996A ParkK.C.JangI.Y.WongwiriyapanW.MorimotoS.KimY. J.JungY.C.ToyaT.EndoM.J. Mater. Chem.20102053451:CAS:528:DC%2BC3cXntlGisbo%3D10.1039/b923153f VenugopalN.KimW. S.Korean J. Chem. Eng.20153219181:CAS:528:DC%2BC2MXnvFegtrw%3D10.1007/s11814-014-0392-9 LeeH.ParkS. H.KimS. J.ParkY. K.KimB. H.JungS.C.Microelectron. Eng.20141261531:CAS:528:DC%2BC2cXht1CkurjO10.1016/j.mee.2014.07.014 LeeH.ParkS. H.KimS. J.ParkY. K.KimB. J.AnK. H.KiS. J.JungS. C.Int. J.^Hydrogen Energy2015407541:CAS:528:DC%2BC2cXhsFWgtrzM10.1016/j.ijhydene.2014.08.085 LeeH.ParkS. H.KimS. J.ParkY. K.AnK. H.KimB. J.JungS.C.J. Nanomater.2014 ShanY.GaoL.Mater. Chem. Phys.20071032061:CAS:528:DC%2BD2sXlslOnsLs%3D10.1016/j.matchemphys.2007.02.038 SansonettiJ. E.MartinW. C.J. Phys. Chem. Ref. Data20053415591:CAS:528:DC%2BD2MXht1GjsbjO10.1063/1.1800011 KimB. H.ParkY. K.AnK. H.LeeH.JungS. C.Sci. Adv. Mater.2016817691:CAS:528:DC%2BC2sXptVygsrY%3D10.1166/sam.2016.2887 AnK. H.KimW. S.ParkY. S.MoonJ. M.BaeD. J.LimS. C.LeeY. S.LeeY.H.Adv. Funct. Mater.2001113871:CAS:528:DC%2BD3MXnsVCgtrw%3D10.1002/1616-3028(200110)11:5<387::AID-ADFM387>3.0.CO;2-G LiuT.C.PellW.G.ConwayB.E.Electrochim. Acta19974235411:CAS:528:DyaK2sXnsFGksbY%3D10.1016/S0013-4686(97)81190-5 ReddyR. N.ReddyR. G.J. Power Sources20031243301:CAS:528:DC%2BD3sXmvF2ksrw%3D10.1016/S0378-7753(03)00600-1 SunS.H.JungS. C.Korean J. Chem. Eng.20163310751:CAS:528:DC%2BC28XitFalu7c%3D10.1007/s11814-015-0262-0 XieJ.F.SunX.ZhangN.XuK.ZhouM.XieY.Nano Energy20132651:CAS:528:DC%2BC3sXhsVyntbk%3D10.1016/j.nanoen.2012.07.016 LeeH.KimB. H.ParkY. K.AnK. H.ChoiY. J.JungS. C.Int. J. Hydrogen Energy20164175821:CAS:528:DC%2BC28Xjt1eks74%3D10.1016/j.ijhydene.2016.02.011 LeeH.KimS. J.AnK. H.KimJ. S.KimB. H.JungS. C.Adv. Mater. Lett.20167981:CAS:528:DC%2BC28XotlShtrs%3D10.5185/amlett.2016.6110 SalomonssonA.PetoralR.M.JrUvdalK.AulinC.KallP.O.OjamaeL.StrandM.SanatiM.SpetzA. L.J. Nanoparticle Res.200688991:CAS:528:DC%2BD28Xht1elt7rP10.1007/s11051-005-9058-1 LeiZ.B.ChristovN.ZhaoX. S.Energy Environ. Sci.2011418661:CAS:528:DC%2BC3MXmslOju7o%3D10.1039/c1ee01094h ChenZ.QinY. C.WengD.XiaoQ. F.PengY.T.WangX. L.LiH. X.WeiF.LuY. F.Adv. Funct. Mater.20091934201:CAS:528:DC%2BD1MXhtlKhtLjF10.1002/adfm.200900971 LeeS. J.LeeH.JeonK. J.ParkH.ParkY. K.JungS. C.Nanoscale Res. Lett.20161134410.1186/s11671-016-1557-8 LeeD. J.KimS. J.LeeJ.LeeH.KimH. G.JungS. C.Sci. Adv. Mater.2014615991:CAS:528:DC%2BC2cXht1ems7nK10.1166/sam.2014.1815 R. N. Reddy (205_CR4) 2003; 124 T.C. Liu (205_CR12) 1997; 42 H. Lee (205_CR6) 2015; 40 S. J. Lee (205_CR17) 2016; 11 Z.B. Lei (205_CR2) 2011; 4 J.F. Xie (205_CR13) 2013; 2 K. H. An (205_CR7) 2001; 11 Y. Zhang (205_CR9) 2015; 3 S.H. Sun (205_CR16) 2016; 33 D. J. Lee (205_CR18) 2014; 6 C. Wan (205_CR5) 2007; 52 Z. Chen (205_CR3) 2009; 19 H. Lee (205_CR15) 2014; 126 Y. Shan (205_CR10) 2007; 103 H. Lee (205_CR11) 2016; 41 H. Lee (205_CR14) 2014 H. Lee (205_CR19) 2016; 7 B. H. Kim (205_CR20) 2016; 8 N. Venugopal (205_CR8) 2015; 32 J. E. Sansonetti (205_CR21) 2005; 34 K.C. Park (205_CR22) 2010; 20 A. Burke (205_CR1) 2000; 91 A. Salomonsson (205_CR23) 2006; 8 |
| References_xml | – reference: LiuT.C.PellW.G.ConwayB.E.Electrochim. Acta19974235411:CAS:528:DyaK2sXnsFGksbY%3D10.1016/S0013-4686(97)81190-5 – reference: ChenZ.QinY. C.WengD.XiaoQ. F.PengY.T.WangX. L.LiH. X.WeiF.LuY. F.Adv. Funct. Mater.20091934201:CAS:528:DC%2BD1MXhtlKhtLjF10.1002/adfm.200900971 – reference: ParkK.C.JangI.Y.WongwiriyapanW.MorimotoS.KimY. J.JungY.C.ToyaT.EndoM.J. Mater. Chem.20102053451:CAS:528:DC%2BC3cXntlGisbo%3D10.1039/b923153f – reference: LeiZ.B.ChristovN.ZhaoX. S.Energy Environ. Sci.2011418661:CAS:528:DC%2BC3MXmslOju7o%3D10.1039/c1ee01094h – reference: AnK. H.KimW. S.ParkY. S.MoonJ. M.BaeD. J.LimS. C.LeeY. S.LeeY.H.Adv. Funct. Mater.2001113871:CAS:528:DC%2BD3MXnsVCgtrw%3D10.1002/1616-3028(200110)11:5<387::AID-ADFM387>3.0.CO;2-G – reference: VenugopalN.KimW. S.Korean J. Chem. Eng.20153219181:CAS:528:DC%2BC2MXnvFegtrw%3D10.1007/s11814-014-0392-9 – reference: WanC.AzumiK.KonnoH.Electrochim. 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| Snippet | Iron-ruthenium bimetallic oxide nanoparticles were precipitated on carbon nanotubes by liquid-phase plasma method. We also evaluated the physicochemical and... |
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| SubjectTerms | Bimetals Biotechnology Carbon Carbon nanotubes Catalysis Chemistry Chemistry and Materials Science Electrochemical analysis Electrodes Electronic Industrial Chemistry/Chemical Engineering Inorganic Iron Materials (Organic Materials Science Nanoparticles Nanotubes Ruthenium Ruthenium oxide Supercapacitors Thin Films 화학공학 |
| Title | Facile synthesis of iron-ruthenium bimetallic oxide nanoparticles on carbon nanotube composites by liquid phase plasma method for supercapacitor |
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