Transforming carbon dioxide (CO₂) into formic acid (HCOOH) and methanol (CH₃OH) as C₁ liquid fuels is central to advancing circular carbon economies and sustainable energy applications. Both CH₃OH and HCOOH possess high energy density and are easily storable and transportable. Beyond their widespread use as solvents and C₁ feedstock chemicals, CH₃OH can be applied in fuel cells or serve as a hydrogen precursor, making it valuable for transportation and grid-level energy storage. HCOOH similarly functions as a safe hydrogen carrier and as a fuel in formic acid fuel cells. Electrochemical CO₂ reduction (eCO₂R) to these C₁ products represents a pivotal step in closing the anthropogenic carbon loop, enabling sustainable energy storage. Recent years have brought notable advances in catalyst development, mechanistic understanding, and system optimization. Although metal-free catalysts and conductive polymers have advanced at a fast pace, transition-metal-containing systems remain the most effective, offering superior activity, selectivity, stability, and Faradaic efficiency (FE). Particularly promising are dual-function systems that integrate CO₂ capture/absorption with electroreduction, offering a promising route toward the direct valorization of industrial CO₂ emissions. This minireview critically evaluates recent advances in molecular and polymer-based electrocatalytic systems, design strategies, and emerging directions for next-generation CO₂-to-C₁ liquid fuel conversion technologies.

Bioelectronics is a rapidly evolving interdisciplinary field that integrates principles of electrical engineering, materials science, and biology to develop electronic interfaces capable of recording and stimulating biological activity of the human body. The conducting polymer poly(3,4- ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) has emerged as a key bioelectronic material due to its unique properties, processing versatility, and biocompatibility. This work provides an overview of PEDOT:PSS-based bioelectronic interfaces and their growing potential in clinical applications. The historical development of PEDOT:PSS is first traced, highlighting its rise as one of the most successful materials in organic bioelectronics. The fundamental properties that make PEDOT:PSS particularly well-suited for bioelectronic interfaces are then examined, with a focus on how these properties can be precisely tuned through advanced processing and fabrication techniques. Both well-established micropatterned interfaces and the latest advancements in multidimensional hydrogel-based structures are discussed. Finally, cutting-edge clinical applications of bioelectronic systems that incorporate PEDOT:PSS are discussed, underscoring their potential in next-generation medical technologies. Overall, this work presents a balanced and forward-looking perspective that connects the evolution of PEDOT:PSS to its emerging role in clinically translatable bioelectronic systems.

In vitro models have now become a realistic alternative to animal models for cardiotoxicity assessment. However, the cost and expertise required to implement in vitro electrophysiology systems to study cardiac cells pose a strong obstacle to their widespread use. This study presents a cost-effective approach forin vitro cardiac electrophysiology using fully printed graphene-based microelectrode arrays (pGMEAs) coupled to an open-source signal acquisition system. We characterized the pGMEAs' electrical properties and biocompatibility, observing low impedance values and cell viability. We demonstrated the platform's capability to record spontaneous electrophysiological activity from HL-1 cell cultures, and we monitored and quantified their responses to chemical stimulation with noradrenaline. This study demonstrates the feasibility of producing fully printed graphene-based devices for in vitro electrophysiology. The accessible and versatile platform we present here represents a step further in the development of alternative methods for cardiac safety screening.

The solid-state field-effect transistor, FET, and its theories were paramount in the discovery and studies of graphene. In the past two decades another transistor based on conducting polymers, called organic electrochemical transistor (ECT), has been developed and largely studied. The main difference between organic ECTs and FETs is the mode and extent of channel doping; while in FETs the channel only has surface doping through dipoles, the mixed ionic-electronic conductivity of the channel material in organic ECTs enables bulk electrochemical doping. As a result, organic ECTs maximize conductance modulation at the expense of speed. To date ECTs have been based on conducting polymers, but here we show that MXenes, a class of 2D materials beyond graphene, enable the realization of electrochemical transistors (ECTs). We show that the formulas for organic ECTs can be applied to these 2D ECTs and used to extract parameters like mobility. These MXene ECTs have high transconductance values but low on-off ratios. We further show that conductance switching data measured using ECT, in combination with other in situ-ex situ electrochemical measurements, is a powerful tool for correlating the change in conductance to that of the redox state, to our knowledge, this is the first report of this important correlation for MXene films. 2D ECTs can draw great inspiration and theoretical tools from the field of organic ECTs and have the potential to considerably extend the capabilities of transistors beyond those of conducting polymer ECTs, with added properties such as extreme heat resistance, tolerance for solvents, and higher conductivity for both electrons and ions than conducting polymers.

Organic electrochemical transistors (OECTs) are promising devices for bioelectronics, such as biosensors. However, current cleanroom-based microfabrication of OECTs hinders fast prototyping and widespread adoption of this technology for low-volume, low-cost applications. To address this limitation, a versatile and scalable approach for ultrafast laser microfabrication of OECTs is herein reported, where a femtosecond laser to pattern insulating polymers (such as parylene C or polyimide) is first used, exposing the underlying metal electrodes serving as transistor terminals (source, drain, or gate). After the first patterning step, conducting polymers, such as poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS), or semiconducting polymers, are spin-coated on the device surface. Another femtosecond laser patterning step subsequently defines the active polymer area contributing to the OECT performance by disconnecting the channel and gate from the surrounding spin-coated film. The effective OECT width can be defined with high resolution (down to 2 µm) in less than a second of exposure. Micropatterning the OECT channel area significantly improved the transistor switching performance in the case of PEDOT:PSS-based transistors, speeding up the devices by two orders of magnitude. The utility of this OECT manufacturing approach is demonstrated by fabricating complementary logic (inverters) and glucose biosensors, thereby showing its potential to accelerate OECT research.

Organic mixed ionic-electronic conductors are promising materials for interfacing and monitoring biological systems, with the aim of overcoming current challenges based on the mismatch between biological materials and convectional inorganic conductors. The conjugated polymer/polyelectrolyte complex poly(3,4-ethylenedioxythiophene):polystyrenesulfonate (PEDOT/PSS) is, up to date, the most widely used polymer for in vitro or in vivo measurements in the field of organic bioelectronics. However, PEDOT/PSS organic electrochemical transistors (OECTs) are limited by depletion mode operation and lack chemical groups that enable synthetic modifications for biointerfacing. Recently introduced thiophene-based polymers with oligoether side chains can operate in accumulation mode, and their chemical structure can be tuned during synthesis, for example, by the introduction of hydroxylated side chains. Here, we introduce a new thiophene-based conjugated polymer, p(g42T-T)-8% OH, where 8% of the glycol side chains are functionalized with a hydroxyl group. We report for the first time the compatibility of conjugated polymers containing ethylene glycol side chains in direct contact with cells. The additional hydroxyl group allows covalent modification of the surface of polymer films, enabling fine-tuning of the surface interaction properties of p(g42T-T)-8% OH with biological materials, either hindering or promoting cell adhesion. We further use p(g42T-T)-8% OH to fabricate the OECTs and demonstrate for the first time the monitoring of epithelial barrier formation of Caco-2 cells in vitro using accumulation mode OECTs. The conjugated polymer p(g42T-T)-8% OH allows organic-electronic-based materials to be easily modified and optimized to interface and monitor biological systems.

Diluting organic semiconductors with a host insulating polymer is used to increase the electronic mobility in organic electronic devices, such as thin film transistors, while considerably reducing material costs. In contrast to organic electronics, bioelectronic devices such as the organic electrochemical transistor (OECT) rely on both electronic and ionic mobility for efficient operation, making it challenging to integrate hydrophobic polymers as the predominant blend component. This work shows that diluting the n-type conjugated polymer p(N-T) with high molecular weight polystyrene (10 KDa) leads to OECTs with over three times better mobility-volumetric capacitance product (µC*) with respect to the pristine p(N-T) (from 4.3 to 13.4 F V−1 cm−1 s−1) while drastically decreasing the amount of conjugated polymer (six times less). This improvement in µC* is due to a dramatic increase in electronic mobility by two orders of magnitude, from 0.059 to 1.3 cm2 V−1 s−1 for p(N-T):Polystyrene 10 KDa 1:6. Moreover, devices made with this polymer blend show better stability, retaining 77% of the initial drain current after 60 minutes operation in contrast to 12% for pristine p(N-T). These results open a new generation of low-cost organic mixed ionic-electronic conductors where the bulk of the film is made by a commodity polymer.

An n-type conjugated polymer based on diazaisoindigo (AIID) and fluorinated thiophene units is introduced. Combining the strong electron-accepting properties of AIID with backbone fluorination produced gAIID-2FT, leading to organic electrochemical transistors (OECTs) with normalized values of 4.09 F cm-1 V-1 s-1 and a normalized transconductance (gm,norm) of 0.94 S cm-1. The resulting OECTs exhibit exceptional operational stability and long shelf-life in ambient conditions, preserving 100% of the original maximum drain current after over 3 h of continuous operation and 28 days of storage in the air. Our work highlights the advantages of integrating strong electron acceptors with donor fluorination to boost the performance and stability of n-type OECTs.

To model complex biological tissue in vitro, a specific layout for the position and numbers of each cell type isnecessary. Establishing such a layout requires manual cell placement in three dimensions (3D) with micrometricprecision, which is complicated and time-consuming. Moreover, 3D printed materials used in compartmentalizedmicrofluidic models are opaque or autofluorescent, hindering parallel optical readout and forcing serial charac-terization methods, such as patch-clamp probing. To address these limitations, we introduce a multi-level co-culture model realized using a parallel cell seeding strategy of human neurons and astrocytes on 3D structuresprinted with a commercially available non-autofluorescent resin at micrometer resolution. Using a two-stepstrategy based on probabilistic cell seeding, we demonstrate a human neuronal monoculture that forms net-works on the 3D printed structure and can establish cell-projection contacts with an astrocytic-neuronal co-cultureseeded on the glass substrate. The transparent and non-autofluorescent printed platform allows fluorescence-based immunocytochemistry and calcium imaging. This approach provides facile multi-level compartmentaliza-tion of different cell types and routes for pre-designed cell projection contacts, instrumental in studying complextissue, such as the human brain.

Organic ionic/electronic conductors (OMIECs) offer a promising alternative to metals and inorganic semiconductors for direct interfacing between human-made electronics and biological tissues. A device that takes advantage of the mixed ionic/electronic conductivity of OMIEC materials is the organic electrochemical transistor (OECT). High-density OECTs are typically fabricated using costly cleanroom-based lithography and complex lift-off processes. To simplify the fabrication of OECTs, we propose laser direct writing of conjugated polymers using a commercial two-photon polymerization 3D printer. Ultrafast laser direct writing allows single-digit micrometer resolution and high-speed processing, thereby enabling a cost-effective and simple fabrication process.