Old Versions

Abstract:

Fuel cells, also known as flow batteries, hold great promise for generation of electricity in previously unimaginable ways, but rely upon platinum catalysts to do so.  Biological fuel cells (BFCs) use organic catalysts and fuels and are able to derive electricity from nearly any biological process.  Power density and longevity limitations of BFCs have prevented their widespread adoption.  A novel BFC design incorporating bioregenerative microorganism(s) is currently undergoing testing.  Applications include a suite of self-powered implantable medical devices, wastewater treatment plants, and biosensors as well as low-cost remote power generation from waste materials.  

Intro:

Fuel cells are much like traditional batteries in that the energy in chemical bonds is liberated to produce electricity, but differ significantly in that they are open flow systems, facilitating extended run times on the order of decades.  Traditional fuel cells use precious metals, most commonly platinum, to catalyze reduction and oxidation (REDOX) reactions at the electron generating anode and the electron receiving cathode.  Traditional fuel cells are very promising for their abilities to convert previously unusable feedstocks into electricity at high efficiencies in remote and biological applications, but suffer from two major draw backs intrinsic to their basic design: the first is a high cost due to the precious metal catalysts, and the second is the reliance on pure fuels, which can be impossible to obtain in the envisioned applications. 

To address these issues, researchers have turned to biological fuel cells (BFCs) which utilize biological components to catalyze the REDOX reactions; BFCs are significantly more cost effective and can utilize a wider array of impure feed stocks including waste water and solid agricultural wastes. Biofuel cells have been limited by the selection of cathode catalysts, and their low power output; recently however, Sane et al. have reported that crude laccase from Trametes versicolor can be used to construct a BFC cathode with a higher open circuit potential (OCP), and longer run time than comparable platinum cathodes. 

The present research focuses on creating a practical laccase-based cathode that can outperform a platinum-based cathode in both OCP and longevity.  Two strategies were adopted to this end: producing the laccase in different fermentation styles and incorporating a laccase producing organism into a BFC cathode chamber.  These designs serve respectively as a practical cathode design for the four electron reduction of oxygen to water, as well as a model for a new class of

Results:

Po

6-Feb

10-Feb

14-Feb

 

12.664

12.461

12.218

 

13.216

12.704

13.338

 

13.149

12.771

12.286

AVG

13.00966667

12.64533333

12.614

SD

0.301224722

0.163114479

0.627923562

BLNK

12.48833333

12.01166667

11.76466667

AVG - BLNK

0.521333333

0.633666667

0.849333333

 

 

 

 

Tv

6-Feb

10-Feb

14-Feb

 

33.108

23.735

12.151

 

33.863

23.655

12.07

 

34.039

22.508

11.881

AVG

33.67

23.29933333

12.034

SD

0.494597816

0.686481124

0.138553239

BLNK

12.88833333

12.59166667

11.83633333

AVG - BLNK

20.78166667

10.70766667

0.197666667

 

 

 

 

 

 

 

 

Fo

6-Feb

10-Feb

14-Feb

 

41.483

36.695

11.881

 

39.069

38.772

12.421

 

39.312

39.029

13.756

AVG

39.95466667

38.16533333

12.686

SD

1.329140449

1.279813398

0.96518133

BLNK

12.96033333

12.05233333

12.06566667

AVG - BLNK

26.99433333

26.113

0.620333333

Methods:

20X100mm carbon rods were purchased from hBarScientific, yeast extract was purchased from Difco, laccase (13.6U/mg) was purchased from MyBioSource.com (L3030862).  Polyvinylidene fluoride (PVDF), ABTS, catalase, succinic acid, and glucose were purchased from Sigma Aldrich.  Carbon nanotubes (CNTs) were obtained from MER corporation.

Electrodes were prepared by dip-coating acetone cleaned carbon rods into a mixture of 10% PVDF in acetone with a CNT loading of 2mg/mL and allowing them to dry at 4C overnight. 

Laccase was produced by growing fungi directly in GYE media (LSF) or on substrate soaked in GYE media (SSF), for 10 days.  A crude enzyme supernatant was prepared by filtering the growth medium through a sterile 0.45um cellulose filter.  Pre-prepared electrodes were then immersed in filtrate for 12 hours to adsorb laccase to the CNTs to facilitate direct electron transfer (DET).  

Discussion:

Three dimensional electrodes utilizing biocompatible TiO2-based binders are currently being optimized to prevent mycelial interference at the cathode surface and facilitate the implementation of the new cathode into existing fuel cells and biomedical devices including: waste water treatment facilities, stand-alone fuel cell generators, implantable glucose sensors, and lab-on-a-chip diagnostic arrays.  Future work will include vertical integration of electricity production with waste treatment, and production of food and building materials.  

References:

1. Arechederra RL, Minteer SD. Organelle-based biofuel cells: immobilized mitochondria on

carbon paper electrodes. Electrochim Acta 2008;53:6698--6703.

2. Calabrese Barton S, Kim H, Binyamin G, Zhang Y, Heller A. Electroreduction of O2 to

water on the “wired” laccase cathode. J Phys Chem B 2001;105:11917--11921.

3. Atanassov P, Apblett C, Banta S, Brozik S, Calabrese Barton S, Cooney MJ, Liaw BY,

Mukerjee S,Minteer SD. Enzymatic biofuel cells. ElectrochemSoc Interface 2007;16:28--31.

4. Kano K, Ikeda T. Bioelectrocatalysis, powerful means of connecting electrochemistry to biochemistry and biotechnology. Electrochemistry 2003;71:86--99.

5. Vaddiraju S, Tomazos I, Burgess DJ, Jain FC, Papadimitrakopoulos F. Emerging synergy

between nanotechnology and implantable biosensors: a review. Biosens Bioelectron

2010;25:1553--1565.

6. Heller A. Miniature biofuel cells. Phys Chem Chem Phys 2004;6:209--216.

7. Heller A. Potentially implantable miniature batteries. Anal Bioanal Chem 2006;385:

469--473.