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Eco-friendly and cost-effective materials and processes to manufacture functional substrates are crucial to further advance the area of printed electronics. One potential key component in the printed electronics platform is an electrically functionalized paper, produced by simply mixing common cellulosic pulp fibers with high-performance electroactive materials. Herein, an electronic paper including nanographite has been prepared using a standardized and scalable papermaking technique. No retention aid was needed to achieve a conducting nanographite loading as high as 50 wt %. The spontaneous retention that provides the integrity and stability of the nanographite paper, likely originates partially from an observed water-stable adhesion of nanographite flakes onto the fiber surfaces. The resulting paper exhibits excellent electrical characteristics, such as an in-plane conductivity of 107 S/cm and an areal capacitance of 9.2 mF/cm(2), and was explored as the back-electrode in printed electrochromic displays. Funding Agencies|Digital Cellulose Centre, a competence center set up by the Swedish Innovation Agency VINNOVA; consortium of Swedish forest industries; Wallenberg Wood Science Center (Knut and Alice Wallenberg Foundation); VINNOVA "EPIC" projectVinnova [2017-05413]; Karl-Erik Onnesjo Foundation

Conductive elastic fabrics are desirable in wearable electronics and related applications. Highly elastic conductive polyamide/lycra knitted fabric was prepared using intrinsically conductive polymer poly (3, 4-ethylenedioxythiophene) (PEDOT) blended with polyelectrolyte poly (styrene sulfonate) (PSS) using easily scalable coating and immersion methods. The effects of these two methods of treatments on uniformity, electromechanical property, stretchability, and durability were investigated. Different grades of waterborne polyurethanes (PU) were employed in different concentrations to improve the coating and adhesion of the PEDOT:PSS on the fabric. The immersion method gave better uniform treatment, high conductivity, and durability against stretching and cyclic tension than the coating process. The surface resistance increased from ~1.7 and ~6.4 Ω/square at 0% PU to ~3.7 and ~12.6 Ω/square at 50% PU for immersion and coating methods, respectively. The treatment methods as well as the acidic PEDOT:PSS did not affect the mechanical properties of the fabric and the fabric show high strain at break of ~650% and remain conductive until break. Finally, to assess the practical applicability of the treated fabric for wearable e-textiles, the change in surface resistance was assessed by cyclically stretching 10 times at 100% strain and washing in a domestic laundry for 10 cycles. The resistance increases only by a small amount when samples were stretched cyclically at 100% strain and the samples show good durability against washing. Quality inspection and evaluation of functional or smart textile fabric surface by skin contact mechanics

Thermoelectric plastics are a class of polymer-based materials that combine the ability to directly convert heat to electricity, and vice versa, with ease of processing., Thermoelectric plastics are a class of polymer-based materials that combine the ability to directly convert heat to electricity, and vice versa, with ease of processing. Potential applications include waste heat recovery, spot cooling and miniature power sources for autonomous electronics. Recent progress has led to surging interest in organic thermoelectrics. This tutorial review discusses the current trends in the field with regard to the four main building blocks of thermoelectric plastics: (1) organic semiconductors and in particular conjugated polymers, (2) dopants and counterions, (3) insulating polymers, and (4) conductive fillers. The design and synthesis of conjugated polymers that promise to show good thermoelectric properties are explored, followed by an overview of relevant structure–property relationships. Doping of conjugated polymers is discussed and its interplay with processing as well as structure formation is elucidated. The use of insulating polymers as binders or matrices is proposed, which permit the adjustment of the rheological and mechanical properties of a thermoelectric plastic. Then, nanocomposites of conductive fillers such as carbon nanotubes, graphene and inorganic nanowires in a polymer matrix are introduced. A case study examines poly(3,4-ethylenedioxythiophene) (PEDOT) based materials, which up to now have shown the most promising thermoelectric performance. Finally, a discussion of the advantages provided by bulk architectures e.g. for wearable applications highlights the unique advantages that thermoelectric plastics promise to offer.

We systematically investigated the effect of the molecular weight of additives on the conductivity of poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) by using different concentrations and molecular weights of polyethylene glycol (PEG) and ethylene glycol (EG). The conductivity enhancement depends on both the molecular weight and concentration of PEG used. The conductivity of PEDOT:PSS was enhanced from 0.3 S cm−1 to 805 S cm−1 with 2% PEG but to only 640 S cm−1 with 6% EG. PEGs with molecular weight higher than 400 have too low mobility to impart the required screening effect, and hence, the conductivity enhancement is less. Through FTIR, XPS and AFM investigations, the mechanism for the conductivity enhancement is found to be charge screening between PEDOT and PSS followed by phase separation and reorientation of PEDOT chains leading to bigger and better connected particles. The molecular weight and concentration of PEG also affect solar cell performances even though the conductivities are the same. Due to their high conductivity and high transmittance, ITO-free organic solar cell devices fabricated using PEDOT:PSS treated with 2% PEG anodes exhibited performance almost equal to that of the ITO counterparts.