Electroactive microbial biofilms constitute a still-new research area of bioelectrochemistry, which proposes experimental systems that are original relative to those that have been studied for decades. In bioelectrochemistry, the interface is generally designed by the experimentalist, sometimes by using sophisticated surface modification protocols, in order to immobilize the biological component on the electrode surface in the best possible way. In contrast, in the case of electroactive biofilms, microorganisms do the work. The microbial cells produce slime that glues them to the electrode surface and forms complex biofilm/electrode interfaces, on which the experimentalist has very few action levers. In this context, chemical engineering methods can be very helpful to decipher the numerous interacting steps that control electron transfer and also to scale up the interfaces to actual applications.Electron transfer (ET) inside biofilms can occur through several direct and indirect pathways, which have been detailed elsewhere [1]. Electroactive biofilms can ensure fast electrochemical kinetics, close to reversible (Nernstian) ET. When biofilms display less efficient global kinetics, it is generally assumed that ET between the electrode and the redox biological compounds is not Nernstian. In contrast, it has recently been demonstrated that non-Nernstian global kinetics can be due to the presence of different ET pathways, each following a Nernstian type but around a different redox potential [2]. When this hypothesis is valid, the way to improve the biofilm electroactivity is no longer to try to enhance the ET rate between the electrode and the different redox compounds, but to drive the biofilm towards the production of the most efficient redox compounds. For example, growing an electroactive biofilm around ultra-microelectrodes has been shown to be an excellent way to improve the ET capability of the biofilm matrix, raising current density from 7 to 65 A/m2 on fully flat electrode surfaces [3].The nagging problem of scaling-up microbial electrochemical technologies is addressed in the second part of the presentation, starting with microbial fuel cells (MFC). Ideally, a microbial anode works at close-to-neutral pH, while an abiotic O2-reducing cathode should work at acidic pH. The pH a Corresponding