TY - GEN
T1 - Enzymatic biofuel cell with self-regulating enzyme-nanotube ensemble films
AU - Miyake, Takeo
AU - Yoshino, Syuhei
AU - Yamada, Takeo
AU - Hata, Kenji
AU - Nishizawa, Matsuhiko
N1 - Funding Information:
This work was supported by a Core Research for Evolutional Science and Technology grant from the Japan Science and Technology Agency and by a Grant-in-Aid for Creative Scientific Research (Creation of Nano Energetic Systems) from the Ministry of Education, Science and Culture, Japan.
PY - 2012
Y1 - 2012
N2 - Nanostructured carbons have been widely used for fabricating enzyme-modified electrodes due to their large specific surface area. However, because they are random aggregates of particular or tubular nanocarbons, the post-modification of enzymes to their intra-nanospace is generally hard to control. Here, we describe a free-standing film of carbon nanotube forest (CNTF) that can form a hybrid ensemble with enzymes through liquid-induced shrinkage. This provides in-situ regulation of its intra-nanospace (inter CNT pitch) to the size of enzymes, and eventually serves as a highly active electrode. The CNTF ensemble with fructose dehydrogenase (FDH) showed the oxidation current density of 16 mA cm -2 in stirred 200 mM fructose solution. The power density of a biofuel cell using the FDH-CNTF anode and the Laccase-CNTF cathode reached 1.8 mW cm -2 (at 0.45 V) in the stirred oxygenic fructose solution, more than 80 % of which could be maintained after continuous operation for 24 h. Application of the free-standing, flexible character of the enzyme-CNTF ensemble electrodes is demonstrated via their use in the patch or wound form.
AB - Nanostructured carbons have been widely used for fabricating enzyme-modified electrodes due to their large specific surface area. However, because they are random aggregates of particular or tubular nanocarbons, the post-modification of enzymes to their intra-nanospace is generally hard to control. Here, we describe a free-standing film of carbon nanotube forest (CNTF) that can form a hybrid ensemble with enzymes through liquid-induced shrinkage. This provides in-situ regulation of its intra-nanospace (inter CNT pitch) to the size of enzymes, and eventually serves as a highly active electrode. The CNTF ensemble with fructose dehydrogenase (FDH) showed the oxidation current density of 16 mA cm -2 in stirred 200 mM fructose solution. The power density of a biofuel cell using the FDH-CNTF anode and the Laccase-CNTF cathode reached 1.8 mW cm -2 (at 0.45 V) in the stirred oxygenic fructose solution, more than 80 % of which could be maintained after continuous operation for 24 h. Application of the free-standing, flexible character of the enzyme-CNTF ensemble electrodes is demonstrated via their use in the patch or wound form.
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U2 - 10.1557/opl.2012.208
DO - 10.1557/opl.2012.208
M3 - Conference contribution
AN - SCOPUS:84865007685
SN - 9781605113920
T3 - Materials Research Society Symposium Proceedings
SP - 87
EP - 92
BT - MEMS, BioMEMS and Bioelectronics - Materials and Devices
T2 - 2011 MRS Fall Meeting
Y2 - 28 November 2011 through 2 December 2012
ER -