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CeO2-Assisted Biocatalytic Nanostructures for Laccase-Based Biocathodes and Biofuel Cells
A hybrid CeO2-based biocatalytic nanostructure carrying catalytically active oxygen-rich nanoparticles is described as a general platform for laccase (Lac)-based biocathodes and biofuel cells. To design the bioelectrodes, the particles and the enzyme were deposited on reduced graphene or carbon nano...
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Published in: | Journal of the Electrochemical Society 2017-01, Vol.164 (9), p.G92-G98 |
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container_end_page | G98 |
container_issue | 9 |
container_start_page | G92 |
container_title | Journal of the Electrochemical Society |
container_volume | 164 |
creator | Karimi, Anahita Andreescu, Silvana |
description | A hybrid CeO2-based biocatalytic nanostructure carrying catalytically active oxygen-rich nanoparticles is described as a general platform for laccase (Lac)-based biocathodes and biofuel cells. To design the bioelectrodes, the particles and the enzyme were deposited on reduced graphene or carbon nanotube-based buckypaper using conducting poly(3,4-ethylenedioxythiophene):poly-styrene-sulfonic acid (PEDOT:PSS). The use of CeO2 into the biocatalytic layer enhanced the bioelectrocatalytic reduction current and enabled functionality of the bioelectrode and biofuel cell in oxygen-limited conditions. These results open up new avenues for designing biointerfaces for protecting activity of immobilized enzymes and providing functionality in oxygen-limited environments. The hybrid nanostructure described in this work may be used as a general platform for the immobilization of other enzymes for a variety of biosensing, biofuel cells and bioelectronics applications. |
doi_str_mv | 10.1149/2.0931709jes |
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To design the bioelectrodes, the particles and the enzyme were deposited on reduced graphene or carbon nanotube-based buckypaper using conducting poly(3,4-ethylenedioxythiophene):poly-styrene-sulfonic acid (PEDOT:PSS). The use of CeO2 into the biocatalytic layer enhanced the bioelectrocatalytic reduction current and enabled functionality of the bioelectrode and biofuel cell in oxygen-limited conditions. These results open up new avenues for designing biointerfaces for protecting activity of immobilized enzymes and providing functionality in oxygen-limited environments. The hybrid nanostructure described in this work may be used as a general platform for the immobilization of other enzymes for a variety of biosensing, biofuel cells and bioelectronics applications.</description><identifier>EISSN: 1945-7111</identifier><identifier>DOI: 10.1149/2.0931709jes</identifier><language>eng</language><publisher>The Electrochemical Society</publisher><ispartof>Journal of the Electrochemical Society, 2017-01, Vol.164 (9), p.G92-G98</ispartof><rights>2017 The Electrochemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Karimi, Anahita</creatorcontrib><creatorcontrib>Andreescu, Silvana</creatorcontrib><title>CeO2-Assisted Biocatalytic Nanostructures for Laccase-Based Biocathodes and Biofuel Cells</title><title>Journal of the Electrochemical Society</title><addtitle>J. Electrochem. Soc</addtitle><description>A hybrid CeO2-based biocatalytic nanostructure carrying catalytically active oxygen-rich nanoparticles is described as a general platform for laccase (Lac)-based biocathodes and biofuel cells. To design the bioelectrodes, the particles and the enzyme were deposited on reduced graphene or carbon nanotube-based buckypaper using conducting poly(3,4-ethylenedioxythiophene):poly-styrene-sulfonic acid (PEDOT:PSS). The use of CeO2 into the biocatalytic layer enhanced the bioelectrocatalytic reduction current and enabled functionality of the bioelectrode and biofuel cell in oxygen-limited conditions. These results open up new avenues for designing biointerfaces for protecting activity of immobilized enzymes and providing functionality in oxygen-limited environments. 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Electrochem. Soc</addtitle><date>2017-01</date><risdate>2017</risdate><volume>164</volume><issue>9</issue><spage>G92</spage><epage>G98</epage><pages>G92-G98</pages><eissn>1945-7111</eissn><abstract>A hybrid CeO2-based biocatalytic nanostructure carrying catalytically active oxygen-rich nanoparticles is described as a general platform for laccase (Lac)-based biocathodes and biofuel cells. To design the bioelectrodes, the particles and the enzyme were deposited on reduced graphene or carbon nanotube-based buckypaper using conducting poly(3,4-ethylenedioxythiophene):poly-styrene-sulfonic acid (PEDOT:PSS). The use of CeO2 into the biocatalytic layer enhanced the bioelectrocatalytic reduction current and enabled functionality of the bioelectrode and biofuel cell in oxygen-limited conditions. These results open up new avenues for designing biointerfaces for protecting activity of immobilized enzymes and providing functionality in oxygen-limited environments. The hybrid nanostructure described in this work may be used as a general platform for the immobilization of other enzymes for a variety of biosensing, biofuel cells and bioelectronics applications.</abstract><pub>The Electrochemical Society</pub><doi>10.1149/2.0931709jes</doi><tpages>7</tpages></addata></record> |
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title | CeO2-Assisted Biocatalytic Nanostructures for Laccase-Based Biocathodes and Biofuel Cells |
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