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Harvesting ambient mechanical energy at the nanometric scale holds great promise for powering small electronics and achieving self-powered electronic devices. The current review is focused on kinetic energy harvesters, particularly on flexible piezoelectric nanogenerators (p-NGs) based on barium titanate (BaTiO 3 ) nanomaterials. p-NGs based on nanotubes, nanowires, nanofibres, nanoplatelets, nanocubes or nanoparticles of BaTiO 3 fabricated in vertical or lateral orientation, as well as mixed composite structures, are overviewed here. The achievable power output level is shown to depend on the fabrication method, processing parameters and potential application conditions. Therefore, the most widely studied aspects, such as influence of geometry/orientation, BaTiO 3 content, poling process and other factors in the output performance of p-NGs, are discussed. The current standing of BaTiO 3 -based p-NGs as possible candidates for various applications is summarized, and the issues that need to be addressed for realization of practical piezoelectric energy harvesting devices are discussed.

The current development of clean and high efficiency energy sources such as solar or wind energy sources has to be supported by the design and fabrication of energy storage systems. Electrochemical capacitors (or supercapacitors (SCs)) are promising devices for energy storage thanks to their highly efficient power management and possible small size. However, in comparison to commercial batteries, SCs do not have very high energy densities that significantly limit their applications. The value of energy density directly depends on the capacitance of full SCs and their cell voltage. Thus, an increase of SCs electrode specific capacitance together with the use of the wide potential window electrolyte can result in high performance SCs. Conductive polymer polyaniline (PANI) as well as carbonaceous materials graphene (G) or reduced graphene oxide (RGO) have been widely studied for usage in electrodes of SCs. Although pristine PANI electrodes have shown low cycling stability and graphene sheets can have low specific capacitance due to agglomeration during their preparation without a spacer, their synergetic effect can lead to high electrochemical properties of G/PANI composites. This review points out the best results for G/PANI composite in comparison to that of pristine PANI or graphene (or RGO). Various factors, such as the ratio between graphene and PANI, oxidants, time, and the temperature of chemical oxidative polymerization, which have been determined to influence the morphology, capacitance, cycling stability, etc. of the composite electrode materials measured in three-electrode system are discussed. Consequently, we provide an in-depth summary on diverse promising approaches of significant breakthroughs in recent years and provide strategies to choose suitable electrodes based on PANI and graphene.

Thanks to the advanced technologies for energy generation such as solar cells and thermo- or piezo-generators the amount of electricity transformed from light, heat or mechanical pressure sources can be significantly enhanced. However, there is still a demand for effective storage devices to conserve electrical energy which addresses the wide range of large stationary applications from electric vehicles to small portable devices. Among the large variety of energy-storage systems available today, electrochemical energy sources and, in particular, supercapacitors (SC), are rather promising in terms of cost, scaling, power management, life cycle and safety. Therefore, this review surveys recent achievements in the development of SC based on composites of such carbon-derived materials as graphene (G) and reduced graphene oxide (rGO) with carbon nanotubes (CNT). Various factors influencing the specific capacitance are discussed, while specific energy and power as well as cycling stability of SC with G/rGO-CNT composite electrode materials are overviewed.

If piezoelectric micro-devices based on K 0.5 Na 0.5 NbO 3 (KNN) thin films are to achieve commercialization, it is critical to optimize the films' performance using low-cost scalable processing conditions. Here, sol-gel derived KNN thin films are deposited using 0.2 and 0.4 M precursor solutions with 5% solely potassium excess and 20% alkali (both potassium and sodium) excess on platinized sapphire substrates with reduced thermal expansion mismatch in relation to KNN. Being then rapid thermal annealed at 750 °C for 5 min, the films revealed an identical thickness of ~340 nm but different properties. An average grain size of ~100 nm and nearly stoichiometric KNN films are obtained when using 5% potassium excess solution, while 20% alkali excess solutions give the grain size of 500-600 nm and (Na + K)/Nb ratio of 1.07-1.08 in the prepared films. Moreover, the 5% potassium excess solution films have a perovskite structure without clear preferential orientation, whereas a (100) texture appears for 20% alkali excess solutions, being particularly strong for the 0.4 M solution concentration. As a result of the grain size and (100) texturing competition, the highest room-temperature dielectric permittivity and lowest dissipation factor measured in the parallel-plate-capacitor geometry were obtained for KNN films using 0.2 M precursor solutions with 20% alkali excess. These films were also shown to possess more quadratic-like and less coercive local piezoelectric loops, compared to those from 5% potassium excess solution. Furthermore, KNN films with large (100)-textured grains prepared from 0.4 M precursor solution with 20% alkali excess were found to possess superior local piezoresponse attributed to multiscale domain microstructures.