In this study, a thermal conductivity of 0.22 W·m−1·K−1 was obtained for pristine epoxy (EP), and the impact of a hybrid filler composed of two-dimensional (2D) flake-like boron nitride (BN) and zero-dimensional (0D) spherical micro-sized aluminum oxide (Al2O3) on the thermal conductivity of epoxy resin was investigated. With 80 wt.% hybrid Al2O3–BN filler contents, the thermal conductivity of the EP composite reached 1.72 W·m−1·K−1, increasing approximately 7.8-fold with respect to the pure epoxy matrix. Furthermore, different important properties for the application were analyzed, such as Fourier-transform infrared (FTIR) spectra, viscosity, morphology, coefficient of thermal expansion (CTE), glass transition temperature (Tg), decomposition temperature (Td), dielectric properties, and thermal infrared images. The obtained thermal performance is suitable for specific electronic applications such as flip-chip underfill packaging.
In this work, the Fe electrodeposition and nucleation and growth mechanisms onto a glassy carbon electrode from a choline chloride-based deep eutectic solvent (DES) were studied using electrochemical techniques and surface characterization techniques (SEM, EDS, and XPS). The current density transients were characterized by the strong effect of the induction-time during the Fe electrodeposition process. A model comprising 3D nucleation and diffusion-controlled growth that considers the induction-time offset was proposed and validated to analyze and explain the Fe nucleation and growth mechanism on the glassy carbon electrode. Kinetic parameters of Fe nucleation and diffusion-controlled growth such as the nucleation rate, A, the number density of active sites, N 0 , the diffusion coefficient, D, as well as induction-time were determined. Iron electrodeposit follows an electrochemical aggregative growth mechanism and was constituted by particles of Fe(0) and a mixture of FeO, Fe 2 O 3 and Fe(OH) 3 .
This research has successfully synthesized highly flexible and conductive nanohybrid electrode films. Nanodispersion and stabilization of silver nanoparticles (AgNPs) were achieved via non-covalent adsorption and with an organic polymeric dispersant and inorganic carbon-based nanomaterials—nano-carbon black (CB), carbon nanotubes (CNT), and graphene oxide (GO). The new polymeric dispersant—polyisobutylene-b-poly(oxyethylene)-b-polyisobutylene (PIB-POE-PIB) triblock copolymer—could stabilize AgNPs. Simultaneously, this stabilization was conducted through the addition of mixed organic/inorganic dispersants based on zero- (0D), one- (1D), and two-dimensional (2D) nanomaterials, namely CB, CNT, and GO. Furthermore, the dispersion solution was evenly coated/mixed onto polymeric substrates, and the products were heated. As a result, highly conductive thin-film materials (with a surface electrical resistance of approximately 10−2 Ω/sq) were eventually acquired. The results indicated that 2D carbon-based nanomaterials (GO) could stabilize AgNPs more effectively during their reductNion and, hence, generate particles with the smallest sizes, as the COO− functional groups of GO are evenly distributed. The optimal AgNPs/PIB-POE-PIB/GO ratio was 20:20:1. Furthermore, the flexible electrode layers were successfully manufactured and applied in wearable electronic sensors to generate electrocardiograms (ECGs). ECGs were, thereafter, successfully obtained.
In this work, the leaching of the active material electrodes of spent alkaline batteries was carried out using a deep eutectic solvent formed by acetylcholine chloride-urea as leaching medium. From the leaching liquors of the cathode or the cathode/anode mix, the electrochemical formation of Mn or Mn-Zn alloy, onto a glassy carbon electrode, was respectively performed by means of cyclic voltammetry and chronoamperometry techniques. The analysis of the potentiostatic current density transients was done using of models that involve the three-dimensional nucleation and diffusion controlled growth of a) bimetallic phases [Díaz-Morales et al. J. Solid. State Electrochem. 17 (2013) 345–351], in the case of the Mn-Zn alloy and b) metallic nuclei, for Mn electrodeposition [Scharifker and Mostany, J. Electroanal. Chem., 177 (1984) 13–23]. From scanning electron microscopy and EDX, it was verified that the nuclei formed were composed of Mn, or the Mn-Zn alloy depending on the leaching liquors used.
The avoidance and mitigation of energy wastage have attracted increasing attention in the context of global warming and climate change. With advances in materials science, diverse multifunctional materials with high thermal conductivity have shown excellent energy-saving potential. In this study, a hybrid film exhibiting high thermal conductivity with excellent stretchability and washability was prepared. First, a simple surface modification of boron nitride (BN) was performed to realize a modified boron nitride (BNOH) filler. Next, an organic dispersant was synthesized to enhance the dispersion of BNOH and graphene nanoplatelets (GNPs) in the proposed composite. Subsequently, a simple procedure was used to combine the dispersed GNPs and BNOH fillers with thermoplastic polyurethane (TPU) to fabricate a hybrid structure. The hybrid films composed of BNOH−GNP/TPU with a dispersant exhibited a high thermal conductivity of 12.62 W m −1 K −1 at a low filler loading of 20 wt.%. This hybrid film afforded excellent stretchability and washability, as indicated by the very small thermal-conductivity reduction to only 12.23 W m −1 K −1 after 100 cycles of fatigue testing and to 12.01 W m −1 K −1 after 10 washing cycles. Furthermore, the cooling and hydrophobicity properties of the hybrid film were enhanced when compared with neat TPU. Overall, our approach demonstrates a simple and novel strategy to break the passive effect of traditional commercial cooling clothing by combining a high-thermal-conductivity film with an active cooling source to amplify the cooling effect and develop wearable cooled smart clothes with great commercial potential.
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