Exploration of renewable energy, such as solar energy, is imminent not only to cater to the escalating energy demand but also to address the uprising environmental issues due to heavy usage of non-renewable fossil fuel. The dye-sensitized solar cells (DSSCs) which are considered as the third-generation solar cells, have a huge potential to be commercialized due to their low cost, simplicity in fabrication, and promising photon-to-electrical energy conversion efficiency. Nevertheless, a high cell efficiency can only be achieved when an organic solvent is incorporated into the formulation of the electrolyte, which is prone to evaporation and leakage. As a result, DSSCs become unsuitable for long-run usage due to thermal instability in the electrolyte. The early intention of incorporating ionic liquids (ILs) into the electrolyte was to curb the abovementioned problem and to enable the DSSCs to function as a sustainable energy device. As such, this article briefly reviews how ILs have been incorporated into the electrolyte formulation and the extent of how the ILs can affect the cell efficiency in various electrolyte states. The role of the ILs in a range of electrolytes is also highlighted. This sheds light on the true purpose of introducing ILs into DSSC electrolyte, which is to enhance the ionicity of the electrolyte.

A multilinear relationship between the viscosity and interaction energies using a stepwise model-building approach was applied to generate the correlation model.

The titled Zn(II) complex was synthesized by reacting the compound (E)-2-hydroxy-N -{1-(4-methoxyphenyl)ethylidene}benzohydrazide with zinc(II) acetate dihydrate in alkaline DMSO and ethanol solution under reflux condition for 28 hours. The resulting solid was filtered and recrystallized from the mixture of ethanol and DMSO. The hydrazone Schiff base and its Zn(II) complex were characterized using 1 H, 13 C NMR, FTIR, UV-Vis spectroscopy, and single crystal X-ray diffraction analysis. Meanwhile, their antibacterial activities were examined using disc diffusion method. The spectral studies showed that the hydrazone Schiff base underwent keto-enol tautomerization, forming a bidentate ligand (N,O) towards Zn(II) ion. Surprisingly, on top of the two hydrazone Schiff base molecules which coordinated to the Zn metal center, an additional DMSO molecule was found attached to the Zn metal center in the crystal data, resulting in a 5-coordinate distorted trigonal bipyramidal Zn(II) complex. Both hydrazone Schiff base and its Zn(II) complexes were found to exhibit low antibacterial activity even when the concentrations were increased to 800 ppm.

The present paper reports the use of 31P NMR spectroscopy to predict the isomer structures of [bis{4-methoxy-phenyl-[3-(4-methoxy-phenyl)-allylidene]-amino}]-bis[triphenylphosphine]ruthenium(II), also known as bis{(di-p-anisole)-1,4-azabutadiene}-bis[triphenylphosphine]ruthenium(II), complexes. The complexation reaction was carried out under refluxing condition of (di-p-anisole)-1,4-azabutadiene (compound 1), triphenylphosphine (PPh3), and ruthenium chloride in the ratio of 2 : 2 : 1 for five hours. In addition, ruthenium(II) complexes were also characterized using FTIR and UV-Vis spectroscopy to support the formation of ruthenium(II) complexes. 31P NMR spectroscopic study on ruthenium(II) complexes suggested that there are three isomers present after the complexation reaction and all the ruthenium complexes demonstrate octahedral geometry.

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