Antonio Jesimiel Glaycon Rodrigues, Franco Jefferson Honorio, Almeida Paula Z, Almeida Thiago S, Teixeira de Morais Polizeli Maria de Lourdes, Minteer Shelley D, Rodrigues de Andrade Adalgisa
Department of Chemistry, Faculty of Philosophy Sciences and Letters at Ribeirão Preto, University of São Paulo, 14040-901 Ribeirão Preto, SP, Brazil.
Department of Biology, Faculty of Philosophy Sciences and Letters at Ribeirão Preto, University of São Paulo, 14040-901 Ribeirão Preto, SP, Brazil.
ACS Mater Au. 2021 Oct 18;2(2):94-102. doi: 10.1021/acsmaterialsau.1c00029. eCollection 2022 Mar 9.
We report a hybrid catalytic system containing metallic PtSn nanoparticles deposited on multiwalled carbon nanotubes (PtSn/MWCNTs), prepared by the microwave-assisted method, coupled to the enzyme oxalate oxidase (OxOx) for complete ethylene glycol (EG) electrooxidation. PtSn/MWCNTs, without OxOx, showed good electrochemical activity toward EG oxidation and all the byproducts. PtSn/MWCNTs cleaved the glyoxilic acid C-C bond, producing CO and formic acid, which was further oxidized at the electrode. Concerning EG oxidation, the catalytic activity of the hybrid system (PtSn/MWCNTs+OxOx) was twice the catalytic activity of PtSn/MWCNTs. Long-term electrolysis revealed that PtSn/MWCNTs+OxOx was much more active for EG oxidation than PtSn/MWCNTs: the charge increased by 65%. The chromatographic results proved that PtSn/MWCNTs+OxOx collected all of the 10 electrons per molecule of the fuel and was able to catalyze EG oxidation to CO due to the associative oxidation between the metallic nanoparticles and the enzymatic pathway. Overall, PtSn/MWCNTs+OxOx proved to be a promising system to enhance the development of enzymatic biofuel cells for further application in the bioelectrochemistry field.
我们报道了一种混合催化体系,该体系包含通过微波辅助法制备的负载在多壁碳纳米管上的金属PtSn纳米颗粒(PtSn/MWCNTs),并与草酸氧化酶(OxOx)耦合用于乙二醇(EG)的完全电氧化。不含OxOx的PtSn/MWCNTs对EG氧化及其所有副产物表现出良好的电化学活性。PtSn/MWCNTs裂解乙醛酸的C-C键,生成CO和甲酸,甲酸在电极上进一步氧化。关于EG氧化,混合体系(PtSn/MWCNTs+OxOx)的催化活性是PtSn/MWCNTs的两倍。长期电解表明,PtSn/MWCNTs+OxOx对EG氧化的活性比PtSn/MWCNTs高得多:电荷量增加了65%。色谱结果证明,PtSn/MWCNTs+OxOx每分子燃料收集了全部10个电子,并且由于金属纳米颗粒与酶促途径之间的缔合氧化,能够催化EG氧化为CO。总体而言,PtSn/MWCNTs+OxOx被证明是一个有前景的体系,可促进酶生物燃料电池的发展,以便在生物电化学领域进一步应用。