The majority of efforts on microbial and photosynthetic microbial fuel cells are both curiosity driven and made to possibly meet the future growing demand for sustainable energy. The most metabolically versatile purple bacteria Rhodobacter capsulatus is a potential candidate for this purpose. However, utilizing bacteria in such systems requires efficient electronic transfer communication between the microbial cells and the electrodes, which is one of the greatest challenges. Previous studies demonstrated that osmium redox polymers (ORPs) could be used for extracellular electron transfer between the cells and electrodes. Recently, heterotrophically grown R. capsulatus has been wired with ORP modified electrodes. Here in this communication, we report electron transfer from R. capsulatus grown under heterotrophic as well as under photoheterotrophic conditions to electrodes. The cells, immobilized on bare graphite and ORP modified graphite electrodes, were excited with visible light and subsequent photosynthetic electron transfer was recorded using cyclic voltammetric and chronoamperometric measurements. Photoheterotrophically grown R. capsulatus cells on bare graphite generate a significant photocurrent density of 3.46 µA cm−2, whereas on an ORP modified electrode the current density increases to 8.46 µA cm−2. Furthermore, when 1 mM p‐benzoquinone is added to the electrolyte the photocurrent density reaches 12.25 µA cm−2. Our results could have significant implications in photosynthetic energy conversion and in development of photobioelectrochemical devices.

As surface‐enhanced Raman scattering (SERS) crucially depends on the morphology of nanostructured metal surfaces, we developed a convenient approach to produce a size gradient of truncated spherical Au nanovoids on a single bipolar electrode. The continuous potential drop in solution implies a linearly changing interfacial potential difference at the wireless electrode, leading to a linearly changing rate of Au electrodeposition. Such a structural gradient enables fast and reproducible screening for those structures, evoking high SERS intensity in a particular experiment. The optimal Au deposition potential with respect to the highest SERS amplification was determined and applied for the fabrication of highly active SERS substrates.

Bipolar electrochemistry has been shown to enable and control various kinds of propulsion of nonwired conducting objects: translation, rotation, and levitation. There is a very rapid development in the field of controlled motion combined with other functionalities. Here we integrate two different concepts in one system to generate wireless electrochemical motion of a specifically designed rotor and track its polarization simultaneously by electrochemical light emission. Locally produced hydrogen bubbles at the cathodic pole of the bipolar rotor are the driving force of the motion, whereas [Ru(bpy)]Cl and tripropylamine react at the anodic extremity, thus generating an electrochemiluminescence signal with an intensity directly correlated with the orientation of the rotor arms. This allows in a straightforward way the qualitative visualization of the changing interfacial potential differences during rotation and shows for the first time that light emission can be coupled to autonomously rotating bipolar electrodes.

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Electrochemical techniques offer high temporal resolution for studying the dynamics of electroactive species at samples of interest. To monitor fastest concentration changes, a micro- or nanoelectrode is accurately positioned in the vicinity of a sample surface. Using a microelectrode array, it is even possible to investigate several sites simultaneously and to obtain an instantaneous image of local dynamics. However, the spatial resolution is limited by the minimal electrode size required in order to contact the electrodes. To provide a remedy, we introduce the concept of scanning bipolar electrochemical microscopy and the corresponding experimental system. This technique allows precise positioning of a wireless scanning bipolar electrode to convert spatially heterogeneous concentrations of the analyte of interest into an electrochemiluminescence map of the sample reactivity. After elucidating the working principle by recording bipolar line and array scans, a bipolar electrode array is positioned at the site of interest to record an electrochemical image of the localized release of analyte molecules.