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Chemical doping of organic semiconductors is an essential enabler for applications in electronic and energy-conversion devices such as thermoelectrics. Here, Lewis-paired complexes are advanced as high-performance dopants that address all the principal drawbacks of conventional dopants in terms of limited electrical conductivity, thermal stability, and generality. The study focuses on the Lewis acid B(C 6 F 5 ) 3 (BCF) and 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F 4 TCNQ) bearing Lewis-basic -CN groups. Due to its high electron affinity, BCF:F 4 TCNQ dopes an exceptionally wide range of organic semiconductors, over 20 of which are investigated. Complex activation and microstructure control lead to conductivities for poly(3-hexylthiophene) (P3HT) exceeding 300 and 900 S cm -1 for isotropic and chain-oriented films, respectively, resulting in a 10 to 50 times larger thermoelectric power factor compared to those obtained with neat dopants. Moreover, BCF:F 4 TCNQ-doped P3HT exhibits a 3-fold higher thermal dedoping activation energy compared to that obtained with neat dopants and at least a factor of 10 better operational stability., Competing Interests: The authors declare no competing financial interest., (© 2024 The Authors. Published by American Chemical Society.)

In order for organic thermoelectrics to successfully establish their own niche as energy-harvesting materials, they must reach several crucial milestones, including high performance, long-term stability, and scalability. Performance and stability are currently being actively studied, whereas demonstrations of large-scale compatibility are far more limited and for carbon nanotubes (CNTs) are still missing. The scalability challenge includes material-related economic considerations as well as the availability of fast deposition methods that produce large-scale films that simultaneously satisfy the thickness constraints required for thermoelectric modules. Here we report on true solutions of CNTs that form gels upon air exposure, which can then be dried into micron-thick films. The CNT ink can be extruded using a slot-shaped nozzle into a continuous film (more than half a meter in the present paper) and patterned into alternating n- and p-type components, which are then folded to obtain the finished thermoelectric module. Starting from a given n-type film, differentiation between the n and p components is achieved by a simple postprocessing step that involves a partial oxidation reaction and neutralization of the dopant. The presented method allows the thermoelectric legs to seamlessly interconnect along the continuous film, thus avoiding the need for metal electrodes, and, most importantly, it is compatible with large-scale printing processes. The resulting thermoelectric legs retain 80% of their power factor after 100 days in air and about 30% after 300 days. Using the proposed methodology, we fabricate two thermoelectric modules of 4 and 10 legs that can produce maximum power outputs of 1 and 2.4 μW, respectively, at a temperature difference Δ T of 46 K., Competing Interests: The authors declare the following competing financial interest(s): A patent on this work has been filed., (© 2024 The Authors. Published by American Chemical Society.)

The low endogenous regenerative capacity of the heart, added to the prevalence of cardiovascular diseases, triggered the advent of cardiac tissue engineering in the last decades. The myocardial niche plays a critical role in directing the function and fate of cardiomyocytes; therefore, engineering a biomimetic scaffold holds excellent promise. We produced an electroconductive cardiac patch of bacterial nanocellulose (BC) with polypyrrole nanoparticles (Ppy NPs) to mimic the natural myocardial microenvironment. BC offers a 3D interconnected fiber structure with high flexibility, which is ideal for hosting Ppy nanoparticles. BC-Ppy composites were produced by decorating the network of BC fibers (65 ± 12 nm) with conductive Ppy nanoparticles (83 ± 8 nm). Ppy NPs effectively augment the conductivity, surface roughness, and thickness of BC composites despite reducing scaffolds' transparency. BC-Ppy composites were flexible (up to 10 mM Ppy), maintained their intricate 3D extracellular matrix-like mesh structure in all Ppy concentrations tested, and displayed electrical conductivities in the range of native cardiac tissue. Furthermore, these materials exhibit tensile strength, surface roughness, and wettability values appropriate for their final use as cardiac patches. In vitro experiments with cardiac fibroblasts and H9c2 cells confirmed the exceptional biocompatibility of BC-Ppy composites. BC-Ppy scaffolds improved cell viability and attachment, promoting a desirable cardiomyoblast morphology. Biochemical analyses revealed that H9c2 cells showed different cardiomyocyte phenotypes and distinct levels of maturity depending on the amount of Ppy in the substrate used. Specifically, the employment of BC-Ppy composites drives partial H9c2 differentiation toward a cardiomyocyte-like phenotype. The scaffolds increase the expression of functional cardiac markers in H9c2 cells, indicative of a higher differentiation efficiency, which is not observed with plain BC. Our results highlight the remarkable potential use of BC-Ppy scaffolds as a cardiac patch in tissue regenerative therapies.

Electronic doping in organic materials has remained an elusive concept for several decades. It drew considerable attention in the early days in the quest for organic materials with high electrical conductivity, paving the way for the pioneering work on pristine organic semiconductors (OSCs) and their eventual use in a plethora of applications. Despite this early trend, however, recent strides in the field of organic electronics have been made hand in hand with the development and use of dopants to the point that are now ubiquitous. Here, we give an overview of all important advances in the area of doping of organic semiconductors and their applications. We first review the relevant literature with particular focus on the physical processes involved, discussing established mechanisms but also newly proposed theories. We then continue with a comprehensive summary of the most widely studied dopants to date, placing particular emphasis on the chemical strategies toward the synthesis of molecules with improved functionality. The processing routes toward doped organic films and the important doping-processing-nanostructure relationships, are also discussed. We conclude the review by highlighting how doping can enhance the operating characteristics of various organic devices.

This work documents an all-in-one custom setup that allows us to measure the in-plane Seebeck coefficients and electrical conductivities of anisotropic thin film samples close to room temperature. Both pairs, S ∥ and σ ∥ and S ⊥ and σ ⊥ , can be measured using four contacts on the same sample, reducing measurement time and minimizing potential sources of error due to aggregating data from several distinct samples. The setup allows us to measure the electrical conductivity of isotropic samples using the well-known van der Pauw method. For samples with in-plane anisotropy, the two components σ ∥ and σ ⊥ can be extracted from the same type of measurements by performing additional calculations. Using the same contacts, the Seebeck coefficient along one direction is measured using a differential steady-state method. After rotating the sample by 90°, the orthogonal Seebeck component can be measured. In order to show the generality of the method, we measure different types of samples, from metal references to oriented doped conjugated polymers.

Here we show that molecular doping of polymer thermoelectrics increases the electrical conductivity while reducing the thermal conductivity. A high-throughput methodology based on annealing and doping gradients within individual films is employed to self-consistently analyze and correlate electrical and thermal characteristics for the equivalent of >100 samples. We focus on the benchmark material system poly(2,5-bis(3-alkylthiophen-2-yl)thieno[3,2- b ]thiophene) (PBTTT) doped with molecular acceptor 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4TCNQ). The thermal conductivity of neat PBTTT films is dominated by the degree of crystallinity, with thermal percolation observed for annealing temperatures >170 °C. Upon doping the samples with a relatively low amount of F4TCNQ (anion content <1 mol %), the thermal conductivity exhibits a two-fold reduction without compromising the crystalline quality, which resembles the effect of alloy scattering observed in several inorganic systems. The analysis of the relation between thermal and electrical conductivities shows that thermal transport is dominated by a doping-induced reduced lattice contribution., Competing Interests: The authors declare no competing financial interest., (Copyright © 2020 American Chemical Society.)

Two doping mechanisms are known for the well-studied materials poly(3-hexylthiophene) (P3HT) and poly(2,5-bis(3-alkylthiophen-2-yl)thieno[3,2- b ]thiophene) (PBTTT), namely, integer charge transfer (ICT) and charge transfer complex (CTC) formation. Yet, there is poor understanding of the effect of doping mechanism on thermal stability and the thermoelectric properties. In this work, we present a method to finely adjust the ICT to CTC ratio. Using it, we characterize electrical and thermal conductivities as well as the Seebeck coefficient and the long-term stability under thermal stress of P3HT and PBTTT of different ICT/CTC ratios. We establish that doping through the CTC results in more stable, yet lower conductivity samples compared to ICT doped films. Importantly, moderate CTC fractions of ∼33% are found to improve the long-term stability without a significant sacrifice in electrical conductivity. Through visible and IR spectroscopies, polarized optical microscopy, and grazing-incidence wide-angle X-ray scattering, we find that the CTC dopant molecule access sites within the polymer network are less prone to dedoping upon thermal exposure., Competing Interests: The authors declare no competing financial interest., (Copyright © 2020 American Chemical Society.)

Waste heat to electricity conversion using thermoelectric generators is emerging as a key technology in the forthcoming energy scenario. Carbon-based composites could unleash the as yet untapped potential of thermoelectricity by combining the low cost, easy processability, and low thermal conductivity of biopolymers with the mechanical strength and good electrical properties of carbon nanotubes (CNTs). Here we use bacteria in environmentally friendly aqueous media to grow large area bacterial nanocellulose (BC) films with an embedded highly dispersed CNT network. The thick films (≈10 μm) exhibit tuneable transparency and colour, as well as low thermal and high electrical conductivity. Moreover, they are fully bendable, can conformally wrap around heat sources and are stable above 500 K, which expands the range of potential uses compared to typical conducting polymers and composites. The high porosity of the material facilitates effective n-type doping, enabling the fabrication of a thermoelectric module from farmed thermoelectric paper. Because of vertical phase separation of the CNTs in the BC composite, the grown films at the same time serve as both the active layer and separating layer, insulating each thermoelectric leg from the adjacent ones. Last but not least, the BC can be enzymatically decomposed, completely reclaiming the embedded CNTs.