Nitrogen-doped graphene approach to enhance the performance of a membraneless enzymatic biofuel cell

被引:10
|
作者
Yazdi, Alireza Ahmadian [1 ]
Xu, Jie [1 ]
机构
[1] Univ Illinois, Dept Mech & Ind Engn, Chicago, IL 60607 USA
关键词
enzymatic fuel cell; nitrogen-doped graphene; reduced graphene oxide; catalyst-free synthesis; MODIFIED LINEAR POLY(ETHYLENIMINE); DEPENDENT GLUCOSE-DEHYDROGENASE; PRUSSIAN BLUE; HYDROGEN-PEROXIDE; OXYGEN REDUCTION; FUEL-CELLS; CATHODES; CATALYST; OXIDASE; ANTHRACENE;
D O I
10.1007/s11708-018-0529-3
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Heteroatom-doping of pristine graphene is an effective route for tailoring new characteristics in terms of catalytic performance which opens up potentials for new applications in energy conversion and storage devices. Nitrogen-doped graphene (N-graphene), for instance, has shown excellent performance in many electrochemical systems involving oxygen reduction reaction (ORR), and more recently glucose oxidation. Owing to the excellent H2O2 sensitivity of N-graphene, the development of highly sensitive and fast-response enzymatic biosensors is made possible. However, a question that needs to be addressed is whether or not improving the anodic response to glucose detection leads to a higher overall performance of enzymatic biofuel cell (eBFC). Thus, here we first synthesized N-graphene via a catalyst-free single-step thermal process, and made use of it as the biocatalyst support in a membraneless eBFC to identify its role in altering the performance characteristics. Our findings demonstrate that the electron accepting nitrogen sites in the graphene structure enhances the electron transfer efficiency between the mediator (redox polymer), redox active site of the enzymes, and electrode surface. Moreover, the best performance in terms of power output and current density of eBFCs was observed when the bioanode was modified with highly doped N-graphene.
引用
收藏
页码:233 / 238
页数:6
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