Department of Chemical & Nuclear Engineering, Center for Emerging Energy Technologies, University of New Mexico, Albuquerque, NM 87131, USA.
Biosens Bioelectron. 2011 Sep 15;27(1):132-6. doi: 10.1016/j.bios.2011.06.029. Epub 2011 Jul 2.
One of the key goals of enzymatic biofuel cells research has been the development of a fully enzymatic biofuel cell that operates under a continuous flow-through regime. Here, we present our work on achieving this task. Two NAD(+)-dependent dehydrogenase enzymes; malate dehydrogenase (MDH) and alcohol dehydrogenase (ADH) were independently coupled with poly-methylene green (poly-MG) catalyst for biofuel cell anode fabrication. A fungal laccase that catalyzes oxygen reduction via direct electron transfer (DET) was used as an air-breathing cathode. This completes a fully enzymatic biofuel cell that operates in a flow-through mode of fuel supply polarized against an air-breathing bio-cathode. The combined, enzymatic, MDH-laccase biofuel cell operated with an open circuit voltage (OCV) of 0.584 V, whereas the ADH-laccase biofuel cell sustained an OCV of 0.618 V. Maximum volumetric power densities approaching 20 μW cm(-3) are reported, and characterization criteria that will aid in future optimization are discussed.
酶生物燃料电池研究的一个关键目标是开发能够在连续流动体系下运行的全酶生物燃料电池。在这里,我们介绍了实现这一任务的工作。两种 NAD(+)依赖的脱氢酶,苹果酸脱氢酶(MDH)和醇脱氢酶(ADH),分别与聚亚甲绿(poly-MG)催化剂偶联,用于生物燃料电池阳极的制备。真菌漆酶通过直接电子转移(DET)催化氧气还原,用作呼吸式阴极。这就完成了一个全酶生物燃料电池,它以流动燃料供应模式运行,相对于呼吸式生物阴极施加偏压。组合酶 MDH-漆酶生物燃料电池的开路电压(OCV)为 0.584V,而 ADH-漆酶生物燃料电池的 OCV 为 0.618V。报道了接近 20μW cm(-3)的最大体积功率密度,并讨论了有助于未来优化的特征化标准。