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开发一种新型生物阴极用于葡萄糖为燃料的单酶生物燃料电池。

Development of a new biocathode for a single enzyme biofuel cell fuelled by glucose.

机构信息

Nanotechnas - Center of Nanotechnology and Materials Science, Institute of Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Naugarduko st. 24, 03225, Vilnius, Lithuania.

Department of Physical Chemistry, Institute of Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Naugarduko st. 24, 03225, Vilnius, Lithuania.

出版信息

Sci Rep. 2021 Sep 17;11(1):18568. doi: 10.1038/s41598-021-97488-w.

Abstract

In this study, we reported the development of Prussian blue (PB), poly(pyrrole-2-carboxylic acid) (PPCA), and glucose oxidase (GOx) biocomposite modified graphite rod (GR) electrode as a potential biocathode for single enzyme biofuel cell fuelled by glucose. In order to design the biocathode, the GR electrode was coated with a composite of PB particles embedded in the PPCA shell and an additional layer of PPCA by cyclic voltammetry. Meanwhile, GOx molecules were covalently attached to the carboxyl groups of PPCA by an amide bond. The optimal conditions for the biocathode preparation were elaborated experimentally. After optimization, the developed biocathode showed excellent electrocatalytic activity toward the reduction of HO formed during GOx catalyzed glucose oxidation at a low potential of 0.1 V vs Ag/AgCl, as well as good electrochemical performance. An electrocatalytic current density of 31.68 ± 2.70 μA/cm and open-circuit potential (OCP) of 293.34 ± 15.70 mV in O-saturated 10 mM glucose solution at pH 6.0 were recorded. A maximal OCP of 430.15 ± 15.10 mV was recorded at 98.86 mM of glucose. In addition, the biocathode showed good operational stability, maintaining 95.53 ± 0.15% of the initial response after 14 days. These results suggest that this simply designed biocathode can be applied to the construction of a glucose-powered single enzyme biofuel cell.

摘要

在这项研究中,我们报告了普鲁士蓝 (PB)、聚吡咯-2-羧酸 (PPCA) 和葡萄糖氧化酶 (GOx) 生物复合材料修饰石墨棒 (GR) 电极的开发,作为一种潜在的生物阴极,用于由葡萄糖驱动的单酶生物燃料电池。为了设计生物阴极,通过循环伏安法将 PB 颗粒嵌入 PPCA 壳中的复合材料和额外的 PPCA 层涂覆到 GR 电极上。同时,GOx 分子通过酰胺键共价连接到 PPCA 的羧基上。通过实验详细阐述了生物阴极制备的最佳条件。经过优化,所开发的生物阴极在低电位 0.1 V vs Ag/AgCl 下对 GOx 催化葡萄糖氧化过程中形成的 HO 的还原表现出优异的电催化活性,并且具有良好的电化学性能。在 pH 6.0 的 10 mM 葡萄糖溶液中,在 O 饱和条件下记录到 31.68 ± 2.70 μA/cm 的电流密度和 293.34 ± 15.70 mV 的开路电位 (OCP)。在 98.86 mM 的葡萄糖下,记录到最大 OCP 为 430.15 ± 15.10 mV。此外,生物阴极表现出良好的操作稳定性,在 14 天后仍保持初始响应的 95.53 ± 0.15%。这些结果表明,这种简单设计的生物阴极可应用于构建葡萄糖驱动的单酶生物燃料电池。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fac/8448768/53658e9dffb9/41598_2021_97488_Fig1_HTML.jpg

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