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In this work, ultrathin nickel films are developed for application as transparent electrodes in thermoelectric devices. The quality of the films is determined systematically by electrical, optical, and morphological characterization in a series of samples with different thickness. The thermal properties of the films show a dramatic dependence of the Seebeck coefficient on the film thickness. This dependence, with values ranging from −16 to +5 휇V K−1 for thicknesses from 10 to 2 nm, includes a change in the behavior of the thermoelectric response from n‐ to p‐type. It has also been demonstrated that the accurate estimation of the thermal conductivity in thin films is challenging due to substrate effects. In this situation, a differential measurement method based on scanning thermal microscopy is proposed, as in these conditions the measurements are less sensitive to the substrate effects. In further works, the dependence of the thermal properties of ultrathin nickel films can be exploited as a tuning parameter for the design of thermoelectric devices. [ABSTRACT FROM AUTHOR]

This work focuses on the encapsulation of two organic phase change materials (PCMs), hexadecane and octadecane, through the formation of nanocapsules of the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) obtained by oxidative polymerization in miniemulsion. The energy storage capacity of nanoparticles is studied by preparing polymer films on supporting substrates. The results indicate that the prepared systems can store and later release thermal energy in the form of latent heat efficiently, which is of vital importance to increase the efficiency of future thermoelectric devices. [ABSTRACT FROM AUTHOR]

The development of wearable technology has promoted the research of new power supply sources to feed wearable devices without the need of batteries. Wearable thermoelectric generators (wTEGs) can generate energy using the thermal gradient between the human body and the ambient temperature. The most comfortable way to adapt wTEGs to the human body is by using textiles, which are flexible and breathable. In this work, we have developed a method to coat textiles with conductive polymers by electrodeposition on fabrics previously coated with multi-walled carbon nanotubes (MWCNT). The results show that the fabrics coated with polyaniline: sulfuric acid (PANI:H2SO4) present a very low thermal stability, and the variation of the electrical conductivity under wearable stress is not suitable for their use in smart textiles. However, the fabrics coated with poly (3,4-ethylenedioxythiophene: perchlorate) (PEDOT:ClO4) and polypyrrole: perchlorate (PPy:ClO4) show a good thermal stability, positive evolution of the electrical conductivity as a function of the twist angle, bending cycles, and bending radius, demostrating their potential use in practical wearable applications to coat fabrics by electrochemical deposition. [ABSTRACT FROM AUTHOR]

In this review, we report the state-of-the-art of polymers in thermoelectricity. Classically, a number of inorganic compounds have been considered as the best thermoelectric materials. Since the prediction of the improvement of the figure of merit by means of electronic confinement in 1993, it has been improved by a factor of 3-4. In the mean time, organic materials, in particular intrinsically conducting polymers, had been considered as competitors of classical thermoelectrics, since their figure of merit has been improved several orders of magnitude in the last few years. We review here the evolution of the figure of merit or the power factor during the last years, and the best candidates to compete with inorganic materials. We also outline the best polymers to substitute classical thermoelectric materials and the advantages they present in comparison with inorganic systems. [ABSTRACT FROM AUTHOR]

Hybrid thermoelectric flexible films based on poly(3,4-ethylenedioxythiophene) (PEDOT) nanoparticles and carbon nanotubes were prepared by using layer-by-layer (LbL) assembly. The employed PEDOT nanoparticles were synthesized by oxidative miniemulsion polymerization by using iron(III) p-toluenesulfonate hexahydrate (FeTos) as an oxidant and poly(diallyldimethylammonium chloride) (PDADMAC) as stabilizer. Sodium deoxycholate (DOC) was used as a stabilizer to prepare the aqueous dispersions of the carbon nanotubes. Hybrid thermoelectric films were finally prepared with different monomer/oxidant molar ratios and different types of carbon nanotubes, aiming to maximize the power factor (PF). The use of single-wall (SWCNT), double-wall (DWCNT), and multiwall (MWCNT) carbon nanotubes was compared. The Seebeck coefficient was measured by applying a temperature difference between the ends of the film and the electrical conductivity was measured by the Van der Pauw method. The best hybrid film in this study exhibited a PF of 72 µW m−1K−2. These films are prepared from aqueous dispersions with relatively low-cost materials and, due to lightweight and flexible properties, they are potentially good candidates to recover waste heat in wearable electronic applications. [ABSTRACT FROM AUTHOR]

This work focuses on the encapsulation of two organic phase change materials (PCMs), hexadecane and octadecane, through the formation of nanocapsules of the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) obtained by oxidative polymerization in miniemulsion. The energy storage capacity of nanoparticles is studied by preparing polymer films on supporting substrates. The results indicate that the prepared systems can store and later release thermal energy in the form of latent heat efficiently, which is of vital importance to increase the efficiency of future thermoelectric devices., Competing Interests: The authors declare no conflicts of interest.

Micro- and submicrosized ZnO-polymer hybrid materials were synthesized by precipitating zinc oxide from an aqueous medium in the presence of poly(styrene-acrylic acid) latex nanoparticles, prepared by miniemulsion polymerization. Up to 10 wt % of the latex becomes incorporated into the crystals. Although the long-range order of the inorganic material is essentially not altered by the polymer, studies by photoluminescence (PL) spectroscopy and electron paramagnetic resonance (EPR) show that the latex particles influence the optical and paramagnetic properties of the hybrids, which can be correlated with changes in the defect structure. Typical PL emission spectra showed a narrow UV peak and a defect-related broad band in the green-yellow spectral region. The former emission is attributed to exciton recombination, whereas the latter seems to be related with deep-level donors. Latex acts as a quencher of the visible emission, and compared to pure ZnO, ZnO-latex hybrids show a significantly lower PL intensity in the visible range. A noticeable dynamic behavior of the PL, clearly more remarkable in the presence of latex, was observed, and it is explained in terms of photodesorption of oxygen adsorbed at surface positions. EPR provided additional information about crystal defects and species with unpaired electrons. All EPR spectra showed a single signal at g approximately 1.96, whose intensity and temperature dependence did not correlate with those of the PL visible band. These findings indicate that the green-yellow emission and the EPR signal of our samples have a different physical origins.