Novel copper oxide–multiwalled carbon nanotube hybrid nanostructured composites showed a high Seebeck coefficient (∼700 μV K⁻¹) and power factor (∼4 μW m⁻¹ K⁻²), exceeding the values reported for the state-of-the-art counterparts.

This work is devoted to the development of epoxy-encapsulated zinc oxide-multiwalled carbon nanotubes (ZnO–MWCNT) hybrid nanostructured composites and the investigation of their thermoelectric performance in relation to the content of MWCNTs in the composite. For the preparation of nanocomposites, self-assembling Zn nanostructured networks were coated with a layer of dispersed MWCNTs and subjected to thermal oxidation. The resulting ZnO–MWCNT hybrid nanostructured networks were encapsulated in commercially available epoxy adhesive. It was found that encapsulation of ZnO–MWCNT hybrid networks in epoxy adhesive resulted in a simultaneous decrease in their electrical resistance by a factor of 20–60 and an increase in the Seebeck coefficient by a factor of 3–15, depending on the MWCNT content. As a result, the thermoelectric power factor of the epoxy-encapsulated ZnO–MWCNTs hybrid networks exceeded that of non-encapsulated networks by more than 3–4 orders of magnitude. This effect was attributed to the ZnO–epoxy interface’s unique properties and to the MWCNTs’ contribution. The processes underlying such a significant improvement of the properties of ZnO–MWCNT hybrid nanostructured networks after encapsulation in epoxy adhesive are discussed. In addition, a two-leg thermoelectric generator composed of epoxy-encapsulated ZnO–MWCNT hybrid nanocomposite as n-type leg and polydimethylsiloxane-encapsulated CuO–MWCNT hybrid nanocomposite as p-type leg characterized at room temperatures showed better performance at temperature difference 30 °C compared with the similar devices, thus proving the potential of the developed nanocomposites for applications in domestic waste heat conversion devices.

This work presents advanced binder-free self-assembling Zn nanowire anodes synthesized by an easy-to-handle one-step low-pressure physical vapor deposition method. The morphology and structure of zinc nanowire networks are controlled and altered by the substrate temperature during deposition. Electrochemical performance of two types of Zn nanowire network samples of different morphology is studied in alkaline and mildly acidic aqueous electrolytes using cyclic voltammetry and electrochemical impedance spectroscopy techniques and compared to that of Zn foil electrodes. It is found that the morphology and structure of the Zn nanowire electrodes are directly related to their electrochemical performance and can be tuned for the type and concentration of the electrolyte to reach optimal electrochemical performance. The resulting binder-free self-assembled Zn nanowire anodes significantly outperform traditional Zn-based electrodes in both mild acidic and alkaline electrolytes, showing an areal capacitance of ~3.3 F/cm² and 3.5 F/cm² for acidic and alkaline electrolytes, respectively, and stability up to 1000 h of cycling in mild acidic electrolytes. These findings provide a pathway to fabricate and optimize binder-free zinc anodes for a variety of efficient and long-lasting aqueous zinc-based batteries and supercapacitors.

We examine the influence of colloidal Au and Ag nanoparticles (NP) on hydrothermally grown ZnO nanorods (NR). Individual 60 nm diameter NP and small NP assemblies without formation of large aggregates were deposited on poly-L-lysine covered NR films using the dip-coating method. The evaluation of morphological and optical properties of the obtained ZnO-metal hybrids was done using scanning electron microscopy, photoluminescence (PL) and diffuse reflection spectroscopy. The presence of Au NP selectively suppressed the PL components near 560 nm wavelength associated with ZnO surface defects, whereas equally sized Ag NP resulted in a much smaller change of PL signal, barely above the noise level. The presented results may be useful for tuning the optical properties of hybrid materials in development of sensor or photovoltaic devices.