In this study, we investigated the role of redox potential in the ability of nano-synthesis by plasma–liquid interactions. From redox potential, a parameter featured the standard Gibbs free energy, and the equilibrium constant of a reduction reaction can be determined. Our calculation showed that the reactions of AuCl4−/Au0 with a redox potential of 1.0 V and Cu2+/Cu0 of 0.34 V have equilibrium constants of approximately 1050 and 1011, respectively. The results are significant to explain the failure in the copper nanoparticle synthesis in the process of nucleation through the Lamer theory. To compare these results to experimental data, the nanoparticles synthesized in a mixed solution of AuCl4− and Cu2+ by AC glow discharge were characterized. The experimental results showed that there were only gold nanoparticles synthesized even though the concentration of gold ions is 200 times smaller. Other results of silver and platinum nanoparticles were also agreeable to the theory. Our findings provide a prediction to explain the ability in the nano-synthesis by plasma in contact with liquid for any noble metals.
BiFeO 3 (BFO) has been widely investigated in many forms and morphologies because of its combined multiferroic and photovoltaic properties. However, direct growth of vertically aligned BFO nanorods on an underlying substrate has remained a challenge. In this work, we report template free growth of BiFeO 3 nanorod arrays on fluorine doped tin oxide coated glass substrate. This has been achieved by a two-step process, in which FeOOH nanorods are grown by chemical bath deposition and converted into BFO using bismuth (Bi) coating by physical vapour deposition (PVD). Both DC sputtering and thermal evaporation are attempted under PVD and the results suggest that Bi deposited by DC sputtering leads to well-defined BFO nanorods, which show superior performance in both multiferroic and photoelectrochemical studies. Piezoelectric force microscopy data shows the signature butterfly loop that confirms piezoelectric behaviour with a d 33 value of 8 pmV −1 in the BFO nanorods grown by DC sputtering. Further, the M-H hysteresis curve for the same samples reveals a remanent magnetization (M r ) value of 0.54 emu cc −1 and antiferromagnetic nature at room temperature. Finally, a stable photocurrent density of 0.05 mA cm −2 is achieved at 0.8 V vs Ag/AgCl under 1 Sun illumination. This work opens up new avenues for BFO in applications involving 1D nanostructures.
Nanogenerator energy harvesting technologies that transform thermal energies into electricity may help address the growing need for green power. Therefore, this research aims to increase power generation by combining waste heat with pyroelectric nanogenerators as a sustainable energy source. Under optimal conditions, an external multi-pulse electric field can be utilized to generate power using thermoelectric cycle power generation. The greatest power may be gathered by applying various pulses of the external electric field at temperature changes on the surface of the pyroelectric materials. To generate pyroelectric power, a C9 BZT sample was used, and the lowest temperature difference for accomplishing this was 20 °C, with all measurements made on a sample with a lower limit of 120 °C. The maximum generation density was 0.104 mJ/cm2°CkV for a pulse width of 10 ms and 20 pulses of a low voltage (250 V/mm) input electric field. A multi-pulse electric field with low input voltage increases the power generation performance ratio (η) with the pulse count. At the largest number of pulses, the greatest η value for 250 V/mm was 7.834. Finally, it was determined that the developed pyroelectric power generation system may be more effective if a low-voltage, multi-pulse electric field is used.
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