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.

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%.

Effective low-grade waste heat harvesting and its conversion into electric energy by the means of thermoelectrochemical cells (TECs) are a strong theme in the field of renewable energy investigation. Despite considerable scientific research, TECs have not yet been practically applied due to the high cost of electrode materials and low effectiveness levels. A large hypothetical Seebeck coefficient allow the harvest of the low-grade waste heat and, particularly, to use TECs for collecting human body heat. This paper demonstrates the investigation of estimated hypothetical Seebeck coefficient dependency on KOH electrolyte concentration for TECs with hollow nanostructured Ni/NiO microsphere electrodes. It proposes a thermoelectrochemical cell with power density of 1.72 W·m⁻² and describes the chemistry of electrodes and near-electrode space. Also, the paper demonstrates a decrease in charge transfer resistance from 3.5 to 0.52 Ω and a decrease in capacitive behavior with increasing electrolyte concentration due to diffusion effects.

Thermoelectrochemical cells are a promising scientific direction in the field of renewable energy development and a way to increase the efficiency of various exothermic technological processes. In this work, the output parameters of the thermoelectrochemical cell based on nickel electrodes at alkaline electrolyte have been investigated. The measurements were carried out by the potentiodynamic method in thermostated cells with a salt bridge. The main indicators of the thermocells efficiency (open-circuit voltage, short-circuit current, output power and filling factor) have been measured and calculated for electrolyte concentrations from 0.1 M, to 3 M and at temperature gradient from 5 to 30 K. It was shown, that the volt-ampere characteristics have a nonlinear view and the deflection point strongly depended on the electrolyte concentration. The best fill factor value within the studied system is 40%. The machanism of non-linear voltage-current curve was supposed. It has been shown, that the potential difference in the cell depends on two opposite processes: the main potential-forming reaction (Ni²⁺↔Ni³⁺+e⁻) and the side NiOOH decomposition reaction. Presumably the side reaction is realized by the accumulation of a certain potential on the electrode and it depends on the electrolyte concentration.