This review focuses on the development of microbial biofuel cells to demonstrate how similar principles apply to the development of bioelectronic devices. The low specificity of microorganism-based amperometric biosensors can be exploited in designing microbial biofuel cells, enabling them to consume a broader range of chemical fuels. Charge transfer efficiency is among the most challenging and critical issues while developing biofuel cells. Nanomaterials and particular redox mediators are exploited to facilitate charge transfer between biomaterials and biofuel cell electrodes. The application of conductive polymers (CPs) can improve the efficiency of biofuel cells while CPs are well-suitable for the immobilization of enzymes, and in some specific circumstances, CPs can facilitate charge transfer. Moreover, biocompatibility is an important issue during the development of implantable biofuel cells. Therefore, biocompatibility-related aspects of conducting polymers with microorganisms are discussed in this review. Ways to modify cell-wall/membrane and to improve charge transfer efficiency and suitability for biofuel cell design are outlined.

Microbial fuel cells (MFCs) are a candidate for green energy sources due to microbes’ ability to generate charge in their metabolic processes. The main problem in MFCs is slow charge transfer between microorganisms and electrodes. Several methods to improve charge transfer have been used until now: modification of microorganisms by conductive polymers, use of lipophilic mediators, and conductive nanomaterials. We created an MFC with a graphite anode, covering it with 9,10-phenatrenequinone and polypyrrole-modified Saccharomyces cerevisiae with and without 10 nm sphere gold nanoparticles. The MFC was evaluated using cyclic voltammetry and power density measurements. The peak current from cyclic voltammetry measurements increased from 3.76 mA/cm² to 5.01 mA/cm² with bare and polypyrrole-modified yeast, respectively. The MFC with polypyrrole- and nanoparticle-modified yeast reached a maximum power density of 150 mW/m² in PBS with 20 mM Fe(III) and 20 mM glucose, using a load of 10 kΩ. The same MFC with the same load in wastewater reached 179.2 mW/m². These results suggest that this MFC configuration can be used to improve charge transfer.

Microbial fuel cells (MFCs) are one of the contributors to the novel sustainable energy generation from organic waste. However, the application of MFCs is limited due to the slow charge transfer between cells and electrodes. This problem can be solved by modifying cells with conductive polymers, such as polypyrrole (PPy). We investigated the viability and electroactivity of modified cells at five different pyrrole concentrations, namely 8, 25, 50, 100, and 200 mM. The 100 mM concentration of PPy solution had the highest impact on yeast cells’ proliferation and growth, with the CFU/mL of PPy-treated yeast cells being 0.6 × 10⁷ ± 5 × 10⁻². The power density of the constructed MFC was evaluated by using an external load. The MFCs were analyzed using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Although CV results with different pyrrole concentrations were similar, DPV indicated that yeast modification with 50 mM pyrrole resulted in the most significant current density, which may be attributed to an increase in charge transfer due to the conductive properties of polypyrrole. The power density achieved with modified yeast in wastewater, 12 mW/m², reached levels similar to those in laboratory solutions, 45 mW/m².