A polymer-based textile thermoelectric generator for wearable energy harvesting

Conducting polymers offer new opportunities to design soft, conformable and light-weight thermoelectric textile generators that can be unobtrusively integrated into garments or upholstery. Using the widely available conducting polymer:polyelectrolyte complex poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) as the p-type material, we have prepared an electrically conducting sewing thread, which we then embroidered into thick wool fabrics to form out-of-plane thermoelectric textile generators. The influence of device design is discussed in detail, and we show that the performance of e-textile devices can be accurately predicted and optimized using modeling developed for conventional thermoelectric systems, provided that the electrical and thermal contact resistances are included in the model. Finally, we demonstrate a thermoelectric textile device that can generate a, for polymer-based devices, unprecedented power of 1.2 μW at a temperature gradient ΔT of 65 K, and over 0.2 μW at a more modest ΔT of 30 K

Machine-Washable Conductive Silk Yarns with a Composite Coating of Ag Nanowires and PEDOT:PSS

Electrically conducting fibers and yarns are critical components of future wearable electronic textile (e-textile) devices such as sensors, antennae, information processors, and energy harvesters. To achieve reliable wearable devices, the development of robust yarns with a high conductivity and excellent washability is urgently needed. In the present study, highly conductive and machine-washable silk yarns were developed utilizing a Ag nanowire and PEDOT:PSS composite coating. Ag nanowires were coated on the silk yarn via a dip-coating process followed by coating with the conjugated polymer:polyelectrolyte complex PEDOT:PSS. The PEDOT:PSS covered the Ag nanowire layers while electrostatically binding to the silk, which significantly improved the robustness of the yarn as compared with the Ag nanowire-coated reference yarns. The fabricated conductive silk yarns had an excellent bulk conductivity of up to ∼320 S/cm, which is largely retained even after several cycles of machine washing. To demonstrate that these yarns can be incorporated into e-textiles, the conductive yarns were used to construct an all-textile out-of-plane thermoelectric device and a Joule heating element in a woven heating fabric

Thermally Activated in Situ Doping Enables Solid-State Processing of Conducting Polymers

Free-standing bulk structures encompassing highly doped conjugated polymers are currently heavily explored for wearable electronics as thermoelectric elements, conducting fibers, and a plethora of sensory devices. One-step manufacturing of such bulk structures is challenging because the interaction of dopants with conjugated polymers results in poor solution and solid-state processability, whereas doping of thick conjugated polymer structures after processing suffers from diffusion-limited transport of the dopant. Here, we introduce the concept of thermally activated latent dopants for in situ bulk doping of conjugated polymers. Latent dopants allow for noninteractive coprocessing of dopants and polymers, while thermal activation eliminates any thickness-dependent diffusion and activation limitations. Two latent acid dopants were synthesized in the form of thermal acid generators based on aryl sulfonic acids and an o-nitrobenzyl capping moiety. First, we show that these acid dopant precursors can be coprocessed noninteractively with three different polythiophenes. Second, the polymer films were doped in situ through thermal activation of the dopants. Ultimately, we demonstrate that solid-state processing with a latent acid dopant can be readily carried out and that it is possible to dope more than 100 μm-thick polymer films through thermal activation of the latent dopant

Sequential doping of solid chunks of a conjugated polymer for body-heat-powered thermoelectric modules

Sequential doping of 1 mm3 sized cubes of regio-regular poly(3-hexylthiophene) (P3HT) with 2,3,5,6-tetrafluoro-tetracyanoquinodimethane is found to result in a doping gradient. The dopant ingresses into the solid material and after two weeks of sequential doping yields a 250 μm thick doped surface layer, while the interior of the cubes remains undoped. The doping gradient is mapped with energy dispersive x-ray spectroscopy (EDX), which is used to estimate a diffusion coefficient of 1 7 10-10 cm2 s-1 at room temperature. The cubes, prepared by pressing at 150 \ub0C, feature alignment of polymer chains along the flow direction, which yields an electrical conductivity of 2.2 S cm-1 in the same direction. A 4-leg thermoelectric module was fabricated with slabs of pressed and doped P3HT, which generated a power of 0.22 μW for a temperature gradient of 10.2 \ub0C generated by body heat

Læreruddannelsen som udviklingslaboratorium: - interaktioner, relationer og spændingsfelter på lærerstuderendes vej ind i lærerfaget

Artiklen diskuterer muligheder og udfordringer for deltagelse og tilblivelse som lærerstuderende på 1. årgang, baseret på empirisk materiale fra “Ind i lærerfaget”, som er ét af en række projekter i “Læreruddannelsen som udviklingslaboratorium”(LULAB). Det bliver en pointe, der fremskrives i artiklens analyser, at projektet ikke kan forstås uden at forstå det som et LULAB-projekt med bott om-up eksperimenterende indsatser i professionelt samarbejde. Baseret på analyserne kondenseres en række interaktioner og relationer, der opleves som afgørende af aktørerne: oplevelse af sammenhæng på fl ere planer, udstrakt praktik på 1. årgang giver både muligheder og udfordringer, relationen mellem læreruddanner og lærerstuderende, herunder positionering af lærerstuderende som medudviklere, at studerende opleves at tage ansvar, og at forankring ikke bare må ses som et format, der rulles ud, de nye aktører skal også opleve mening. Der peges således både på positive mulighedsrum i relation til læreruddannelsen som professionsrett et uddannelse, men også på udfordringer og spændinger

Energy harvesting textiles for a rainy day: woven piezoelectrics based on melt-spun PVDF microfibres with a conducting core

Recent advances in ubiquitous low-power electronics call for the development of light-weight and flexible energy sources. The textile format is highly attractive for unobtrusive harvesting of energy from e.g., biomechanical movements. Here, we report the manufacture and characterisation of fully textile piezoelectric generators that can operate under wet conditions. We use a weaving loom to realise textile bands with yarns of melt-spun piezoelectric microfibres, that consist of a conducting core surrounded by β-phase poly(vinylidene fluoride) (PVDF), in the warp direction. The core-sheath constitution of the piezoelectric microfibres results in a—for electronic textiles—unique architecture. The inner electrode is fully shielded from the outer electrode (made up of conducting yarns that are integrated in the weft direction) which prevents shorting under wet conditions. As a result, and in contrast to other energy harvesting textiles, we are able to demonstrate piezoelectric fabrics that do not only continue to function when in contact with water, but show enhanced performance. The piezoelectric bands generate an output of several volts at strains below one percent. We show that integration into the shoulder strap of a laptop case permits the continuous generation of four microwatts of power during a brisk walk. This promising performance, combined with the fact that our solution uses scalable materials and well-established industrial manufacturing methods, opens up the possibility to develop wearable electronics that are powered by piezoelectric textiles