首页> 外文期刊>Analytical chemistry >Enhanced Performance of a Glucose/O_2 Biofuel Cell Assembled with Laccase-Covalently Immobilized Three-Dimensional Macroporous Gold Film-Based Biocathode and Bacterial Surface Displayed Glucose Dehydrogenase-Based Bioanode
【24h】

Enhanced Performance of a Glucose/O_2 Biofuel Cell Assembled with Laccase-Covalently Immobilized Three-Dimensional Macroporous Gold Film-Based Biocathode and Bacterial Surface Displayed Glucose Dehydrogenase-Based Bioanode

机译:葡萄糖/ O_2生物燃料电池与漆酶共价固定的三维大孔金膜基生物阴极和细菌表面展示的葡萄糖脱氢酶基生物阳极组装的增强的性能。

获取原文
获取原文并翻译 | 示例
           

摘要

The power output and stability of enzyme-based biofuel cells (BFCs) is greatly dependent on the properties of both the biocathode and bioanode, which may be adapted for portable power production. In this paper, a novel highly uniform three-dimensional (3D) macroporous gold (MP-Au) film was prepared by heating the gold "supraspheres", which were synthesized by a bottom-up protein templating approach, and followed by modification of laccase on the MP-Au film by covalent immobilization. The as-prepared laccase/MP-Au biocathode exihibited an onset potential of 0.62 V versus saturated calomel electrode (SCE, or 0.86 V vs NHE, normal hydrogen electrode) toward O_2 reduction and a high catalytic current of 0.61 mAcm~(-2). On the other hand, mutated glucose dehydrogenase (GDH) surface displayed bacteria (GDH-bacteria) were used to improve the stability of the glucose oxidation at the bioanode. The as-assembled membraneless glucose/O_2 fuel cell showed a high power output of 55.8 ± 2.0 μW cm~(-2) and open circuit potential of 0.80 V, contributing to the improved electrocatalysis toward O_2 reduction at the laccase/MP-Au biocathode. Moreover, the BFC retained 84% of its maximal power density even after continuous operation for 55 h because of the high stability of the bacterial surface displayed GDH mutant toward glucose oxidation. Our findings may be promising for the development of more efficient glucose BFC for portable battery or self-powered device applications.
机译:酶基生物燃料电池(BFC)的功率输出和稳定性在很大程度上取决于生物阴极和生物阳极的特性,它们可适用于便携式发电。本文通过加热金“超球”制备了一种新颖的高度均匀的三维(3D)大孔金(MP-Au)膜,该金通过自下而上的蛋白质模板方法合成,然后修饰漆酶通过共价固定在MP-Au膜上。所制备的漆酶/ MP-Au生物阴极相对于饱和甘汞电极(SCE,或相对于NHE,普通氢电极,0.86 V)对O_2还原具有0.62 V的起始电势,且催化电流为0.61 mAcm〜(-2)。 。另一方面,使用突变的葡萄糖脱氢酶(GDH)表面展示细菌(GDH-细菌)来提高生物阳极处葡萄糖氧化的稳定性。组装后的无膜葡萄糖/ O_2燃料电池显示出55.8±2.0μWcm〜(-2)的高功率输出和0.80 V的开路电势,有助于改善漆酶/ MP-Au生物阴极对O_2还原的电催化作用。 。此外,由于细菌表面表现出对葡萄糖氧化的GDH突变体的高稳定性,即使连续操作55小时后,BFC仍保留其最大功率密度的84%。我们的发现对于为便携式电池或自供电设备应用开发更高效的葡萄糖BFC可能具有希望。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号