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利用甲醇氧化酶生物阳极和空气呼吸漆酶生物阴极从甲醇基质中产生电能的生物燃料电池。

Biofuel cell for generating power from methanol substrate using alcohol oxidase bioanode and air-breathed laccase biocathode.

机构信息

Centre For Energy, Indian Institute of Technology Guwahati, Guwahati 781039, Assam, India.

Department of Biotechnology, Indian Institute of Technology Guwahati, Guwahati 781039, Assam, India.

出版信息

Biosens Bioelectron. 2014 Sep 15;59:184-91. doi: 10.1016/j.bios.2014.03.016. Epub 2014 Mar 25.

Abstract

We report here an alcohol oxidase (AOx) based third generation bioanode for generating power from methanol substrate in a fuel cell setup using air breathed laccase biocathode. A composite three dimensional microporous matrix containing multiwalled carbon nanotubes, carbon paste and nafion was used as electroactive support for immobilization of the enzymes on toray carbon paper as supporting electrode in the fabrication of the bioelectrodes. Polyethylenimine was used to electrostatically stabilize the AOx (pI 4.3) on the anode operating on direct electrochemistry principle. Osmium tetroxide on poly (4-vinylpyridine) was used to wire the laccase for electron transfer in the biocathode. The enzymatic biofuel cell (EFC) generated an open circuit potential of 0.61 (±0.02) V with a maximum power density of 46 (±0.002) µW cm(-2) at an optimum of 1M methanol, 25 °C and an internal resistance of 0.024 µΩ. The operation and storage half life (t1/2) of the EFC were 17.22 h and 52 days, respectively at a fixed load of 1.85 Ω. The findings have demonstrated the feasibility of developing EFC using AOx based bioanode and laccase based biocathode without applying any toxic free mediator and metal electrode supports for generating electricity.

摘要

我们在此报告了一种基于醇氧化酶(AOx)的第三代生物阳极,用于在燃料电池装置中从甲醇基质中产生电力,使用空气呼吸漆酶生物阴极。复合三维微孔基质含有多壁碳纳米管、碳糊和纳滤膜,用作电活性支撑物,用于将酶固定在托雷碳纸上,作为支撑电极在生物电极的制造中。聚乙烯亚胺用于通过直接电化学原理在阳极上静电稳定 AOx(pI 4.3)。聚(4-乙烯基吡啶)上的四氧化锇用于在生物阴极中为电子转移布线漆酶。在最佳条件为 1M 甲醇、25°C 和内阻为 0.024 µΩ 时,酶促燃料电池(EFC)产生 0.61(±0.02)V 的开路电位和 46(±0.002)µW cm(-2) 的最大功率密度。在固定负载为 1.85 Ω 时,EFC 的工作和存储半衰期(t1/2)分别为 17.22 小时和 52 天。这些发现证明了使用基于 AOx 的生物阳极和基于漆酶的生物阴极开发 EFC 的可行性,而无需应用任何有毒的无介体和金属电极支撑物来发电。

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