Chirality-induced spin selectivity (CISS), the effect of helical molecules acting as room temperature hard magnets that confer spin polarization to electrical current, is an intriguing effect with potential applications in nanospintronics. In this scenario, molecules that are paramagnetic as well as helical would introduce a new degree of freedom in the same nano-scale device that has not been explored so far. Here, in order to investigate this idea, we propose the preparation of self-assembled monolayers (SAMs) based on a helical lanthanide binding tag peptide (LnLBTC) on a ferromagnetic substrate. We confirmed room temperature spin filtering of LnLBTC SAMs by well-established electrochemical approach and by direct local spin transport measurements in solid state devices. The latter were studied by a common liquid-metal drop electron transport system, easily implemented for spin dependent measurements. Electrochemistry shows an averaged spin polarization (SP) of ~5% in presence of a saturation magnetic field (H = 350 mT) while local measurements performed in solid state showed a SP of ~50 20% thanks to the reduction of the contribution of pure electron transport in non-covered areas. Calculations showed that conduction electrons interact strongly with the coordinated lanthanide ion, meaning a fixed chirality-based spin filtering can coexist with a spin filtering that is dependent on the polarization of the magnetic metal ion. This opens the door to all-organic single-molecule memristive devices.
Energy harvesting through residual heat is considered one of the most promising ways to power wearable devices. In this work, thermoelectric textiles were prepared by coating the fabrics, first with multiple-wall carbon nanotubes (MWCNTs) by using the layer-by-layer technique and second with poly(3,4-ethylenedioxythiophene) (PEDOT) deposited by electrochemical polymerization. Sodium deoxycholate and poly(diallyldimethylammonium chloride) were used as stabilizers to prepare the aqueous dispersions of MWCNTs. The electrochemical deposition of PEDOT on the MWCNTcoated fabric was carried out in a three-electrode electrochemical cell. The polymerization of PEDOT on the fabric increased the electrical conductivity by ten orders of magnitude (through the plane), establishing an excellent path for electric transport across the fabrics. In addition, the fibers showed a Seebeck coefficient of 14.3 μV K −1 , which is characteristic of highly doped PEDOT. As a proof of concept, several thermoelectric modules were made with different elements based on the coated acrylic and cotton fabrics. The best generator made of 30 thermoelectric elements using acrylic fabrics exhibited an output power of 0.9 μW with a temperature difference of 31 K.
Transition metal chalcogenophosphates of general formula MPX3 have attracted recent interest in the field of 2D materials due to the possibility of tuning their properties when reaching the 2D limit....
We describe the first meltable iron-based zeolitic imidazolate framework (ZIF), denoted MUV-24. This material, elusive from direct synthesis, is obtained from the thermal treatment of [Fe 3 (im) 6 (Him) 2 ], which yields Fe(im) 2 upon loss of the neutral imidazole molecules. Different crystalline phase transformations are observed upon further heating, until the material melts at 482 °C. Vitrification upon cooling of the liquid phase gives rise to the first Fe-metal−organic framework glass. X-ray total scattering experiments show that the tetrahedral environment of the crystalline solids is maintained in the glass, whereas nanoindentation measurements reveal an increase in Young's modulus, in agreement with stiffening upon vitrification.
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