Department of Chemistry, University of Kurdistan, 66177-15175 Sanandaj, Iran.
Biosens Bioelectron. 2013 Dec 15;50:186-93. doi: 10.1016/j.bios.2013.05.047. Epub 2013 Jun 24.
In this study, the preparation of an integrated modified electrode based on the covalent attachment of glucose dehydrogenase (GDH) enzyme and safranin O to amine-derivative multiwalled carbon nanotubes (MWCNTs-NH2) modified glassy carbon (GC) electrode using G2.5-carboxylated PAMAM dendrimer (Den) as linking agent is reported. The obtained results indicated that the proposed system has effective bioelectrocatalytic activity toward glucose oxidation at 100 mV with onset potential of -130 mV (vs. Ag/AgCl). The performance of the prepared hybrid system of GC/MWCNTs-NH2/Den/GDH/Safranin as anode in a membraneless enzyme-based glucose/O2 biofuel cell is further evaluated. The biocathode in this system was composed of bilirubin oxidase (BOX) enzyme immobilized onto a bilirubin modified carbon nanotube GC electrode. Immobilized BOX onto CNTs/bilirubin not only show direct electron transfer but also it has excellent electrocatalytic activity toward oxygen reduction at a positive potential of 610 mV. The open circuit voltage of the cell was 590 mV. The maximum current density was 0.5 mA cm(-2), while maximum power density of 108 μW cm(-2) was achieved at voltage of 330 mV. The immobilized enzymes in anode and cathode are very stable and output power of the BFC is approximately constant after 12 h continues operation.
本研究报告了一种基于共价附着葡萄糖脱氢酶(GDH)酶和藏红 O 到胺衍生的多壁碳纳米管(MWCNTs-NH2)修饰玻碳(GC)电极的集成修饰电极的制备,使用 G2.5-羧基化 PAMAM 树状大分子(Den)作为连接剂。所得结果表明,该体系在 100 mV 下对葡萄糖氧化具有有效的生物电催化活性,起始电位为-130 mV(相对于 Ag/AgCl)。进一步评估了无膜酶葡萄糖/O2 生物燃料电池中 GC/MWCNTs-NH2/Den/GDH/Safranin 制备的混合体系作为阳极的性能。该系统的生物阴极由固定在胆红素修饰的碳纳米管 GC 电极上的胆红素氧化酶(BOX)酶组成。固定在 CNTs/胆红素上的 BOX 不仅显示出直接电子转移,而且在 610 mV 的正电势下对氧还原具有出色的电催化活性。电池的开路电压为 590 mV。最大电流密度为 0.5 mA cm(-2),而在 330 mV 的电压下可实现 108 μW cm(-2)的最大功率密度。阳极和阴极中的固定酶非常稳定,BFC 的输出功率在 12 小时连续运行后基本保持不变。