Thermo-electrochemical cells (also known as thermocells, TECs) represent a promising technology for harvesting and exploiting low-grade waste heat (<100–150 °C) ubiquitous in the modern environment. Based on temperature-dependent redox reactions and ion diffusion, emerging liquid-state thermocells convert waste heat energy into electrical energy, generating power at low costs, with minimal material consumption and negligible carbon footprint. Recent developments in thermocell performances are reviewed in this article with specific focus on new redox couples, electrolyte optimisation towards enhancing power output and operating temperature regime and the use of carbon and other nanomaterials for producing electrodes with high surface area for increasing current density and device performance. The highest values of output power and cell potentials have been achieved for the redox ferri/ferrocyanide system and Co^2+/3+, with great opportunities for further development in both aqueous and non-aqueous solvents. New thermoelectric applications in the field include wearable and portable electronic devices in the health and performance-monitoring sectors; using body heat as a continuous energy source, thermoelectrics are being employed for long-term, continuous powering of these devices. Energy storage in the form of micro supercapacitors and in lithium ion batteries is another emerging application. Current thermocells still face challenges of low power density, conversion efficiency and stability issues. For waste-heat conversion (WHC) to partially replace fossil fuels as an alternative energy source, power generation needs to be commercially viable and cost-effective. Achieving greater power density and operations at higher temperatures will require extensive research and significant developments in the field.

In this study, we report the effect of intercalation of dimethyl sulfoxide (DMSO) and urea molecules into the interlayer space of Ti₃C₂T_x MXene on the dielectric properties of poly(vinylidene fluoride) (PVDF)/MXene polymer nanocomposites. MXenes were obtained by a simple hydrothermal method using Ti₃AlC₂ and a mixture of HCl and KF, and they were then intercalated with DMSO and urea molecules to improve the exfoliation of the layers. Then, nanocomposites based on a PVDF matrix loading of 5–30 wt.% MXene were fabricated by hot pressing. The powders and nanocomposites obtained were characterized by using XRD, FTIR, and SEM. The dielectric properties of the nanocomposites were studied by impedance spectroscopy in the frequency range of 10²–10⁶ Hz. As a result, the intercalation of MXene with urea molecules made it possible to increase the permittivity from 22 to 27 and to slightly decrease the dielectric loss tangent at a filler loading of 25 wt.% and a frequency of 1 kHz. The intercalation of MXene with DMSO molecules made it possible to achieve an increase in the permittivity up to 30 at a MXene loading of 25 wt.%, but the dielectric loss tangent was increased to 0.11. A discussion of the possible mechanisms of MXene intercalation influence on the dielectric properties of PVDF/Ti₃C₂T_x MXene nanocomposites is presented.

New three-phase composites, destined for application as dielectrics in the manufacturing of passive elements of flexible electronics, and based on polymer (PVDF) matrix filled with powdered ceramics of the hollandite-like (KFTO(H)) structure (5.0; 7.5; 15; 30 vol.%) and carbon (MWCNT) additive (0.5; 1.0; 1.5 wt.% regarding the KFTO(H) amount), were obtained and studied by XRD, FTIR and SEM methods. Chemical composition and stoichiometric formula of the ceramic material synthesized by the sol–gel method were confirmed with the XRF analysis data. The influence of the ceramic and carbon fillers on the electrical properties of the obtained composites was investigated using impedance spectroscopy. The optimal combination of permittivity and dielectric loss values at 1 kHz (77.6 and 0.104, respectively) was found for the compositions containing K_1.6Fe_1.6Ti_6.4O₁₆ (30 vol.%) and MWCNTs (1.0 wt.% regarding the amount of ceramic filler).

An important direction in the development of energy saving policy is harvesting and conversion into electricity of low-grade waste heat. The present paper is devoted to the improvement of the efficiency of thermo-electrochemical cells based on carbon fiber electrodes and potassium ferri-/ferrocyanide redox electrolyte. The influence of the carbon fiber electrode surface modification (magnetron deposition of silver and titanium or infiltration implantation of nanoscale titanium oxide) on the output power and parameters of the impedance equivalent scheme of a thermo-electrochemical cell has been studied. Two kinds of cell designs (a conventional electrochemical cell with a salt bridge and a coin cell-type body) were investigated. It was found that the nature of the surface modification of electrodes can change the internal resistance of the cell by three orders of magnitude. The dependence of the equivalent scheme parameters and output power density of the thermoelectric cell on the type of electrode materials was presented. It was observed that the maximum power for carbon fiber modified with titanium metal and titanium oxide was 25.2 mW/m² and the efficiency was 1.37%.