Tetrathiotetracene thin film morphology and electrical properties

The electrical properties of organic thin films are determined by their chemical constituents and the morphology of the films deposited. In this paper the morphology of vacuum sublimed (7∙10-6 mbar) tetrathiotetracene (TTT) thin films is shown to be strongly affected by the thermal deposition temperature (222-350 K) and rate of deposition. Mostly needle-like morphologies are identified by scanning electron microscopy. Optimal TTT purity (a pre-requisite for device preparation via subsequent oxidation) is evidenced by their initially low electrical conductivity. Altering the TTT morphology, by variation of the evaporation parameters, strongly affects this base electrical conductivity. Four probe conductivity measurements and charge extraction by linear increasing voltage methods are used to characterize film electrical properties. In-plane conductivity of up to 7.03∙10-5 S/cm is achieved for pure TTT thin films. Subsequent aerial oxidation resulted in a 3.4-fold increase in electrical conductivity

Nanocrystalline CaWO4_4 and ZnWO4_4 tungstates for hybrid organic-inorganic X-ray detectors

Hybrid materials combining an organic matrix and high-Z nanomaterials show potential for applications in radiation detection, allowing unprecedented device architectures and functionality. Herein, novel hybrid organic–inorganic systems were produced using a mixture of tungstate (CaWO$_4$ or ZnWO$_4$) nanoparticles with a P3HT:PCBM blend. The nano-tungstates with a crystallite size of 43 nm for CaWO$_4$ and 30 nm for ZnWO$_4$ were synthesized by the hydrothermal method. Their structure and morphology were characterized by X-ray diffraction and scanning electron microscopy. The hybrid systems were used to fabricate direct conversion X-ray detectors able to operate with zero bias voltage. The detector performance was tested in a wide energy range using monochromatic synchrotron radiation. The addition of nanoparticles with high-Z elements improved the detector response to X-ray radiation compared with that of a pure organic P3HT:PCBM bulk heterojunction cell. The high dynamic range of our detector allows for recording X-ray absorption spectra, including the fine X-ray absorption structure located beyond the absorption edge. The obtained results suggest that nanocrystalline tungstates are promising candidates for application in direct organic–inorganic X-ray detectors

Bio-Inspired Macromolecular Ordering of Elastomers for Enhanced Contact Electrification and Triboelectric Energy Harvesting

Abstract Triboelectrification of polymers enables mechanical energy harvesting in triboelectric generators, droplet generators, and ferroelectrets. Herein, triboelectric polymers, inspired by the ordering in spider‐silk, with strongly enhanced contact electrification are presented. The ordering in polyether block amide (PEBA) is induced by the addition of inorganic goethite (α‐FeOOH) nanowires that form H‐bonds with the elastomeric matrix. The addition of as little as 0.1 vol% of α‐FeOOH into PEBA increases the surface charge by more than order of magnitude (from 0.069 to 0.93 nC cm–2). The H‐bonds between α‐FeOOH and PEBA promote the formation of inclusions with higher degree of macromolecular ordering, analogous to the structure of spider silk. The formation of these inclusions is proven via nanoindentation hardness measurements and correlated with H‐bond‐induced chemical changes by Fourier transform infrared spectroscopy and direct scanning calorimetry. Theoretical studies reveal that the irregularity in hardness provides stress accumulation on the polymer surface during contact‐separation. Subsequent molecular dynamic studies demonstrate that stress accumulation promotes the mass‐transfer mechanism of contact electrification. The proposed macromolecular structure design provides a new paradigm for developing materials for applications in mechanical energy harvesting