Nanoflower-like P-doped Nickel Oxide as a Catalytic Counter Electrode for Dye-Sensitized Solar Cells.

Flower-like phosphorus-doped nickel oxide (P-NiO) is proposed as a counter electrode (CE) for dye-sensitized solar cells (DSSCs). The flower-like nickel oxide essentially serves as the matrix for the CE, which is expected to promote a two-dimensional electron transport pathway. The phosphorus is intended to improve the catalytic ability by creating more active sites in the NiO for the catalysis of triiodide ions (I3-) to iodide ions (I-) on the surface of the CE. The P-NiO is controlled by a sequencing of precursor concentration, which allows the P-NiO to possess different features. The debris aggregation occurs in the P-NiO-1, while the P-NiO-0.75 leads to the incomplete flower-like nanosheets. The complete flower-like morphology can be observed in the P-NiO-0.5, P-NiO-0.25 and P-NiO-0.1 catalytic electrodes. The DSSC with the P-NiO-0.5 CE achieves a power conversion efficiency (η) of 9.05%, which is better than that of the DSSC using a Pt CE (η = 8.51%); it also performs better than that with the Pt CE, even under rear illumination and dim light conditions. The results indicate the promising potential of the P-NiO CE to replace the expensive Pt CE.

Controlling available active sites of Pt-loaded TiO2 nanotube-imprinted Ti plates for efficient dye-sensitized solar cells.

The counter electrode (CE) of dye-sensitized solar cells (DSSCs) plays an important role for transferring electrons and catalyzing the I-/I3- reduction. Active surface area of the substrate determines the reduction sites of the deposited catalyst as well as the catalytic ability of the CE. An effective method for enhancing and controlling the active surface area of metal plates is provided in this study. The Ti plates are imprinted by TiO2 nanotubes (TNT) via the technique of anodization along with the ultrasonic vibration process. The available active area of imprinted Ti plates is controlled by varying the anodization voltage to produce TNT imprints with different diameters and depths. A solar-to-electricity conversion efficiency (η) of 9.35% was obtained for the DSSC with a TNT-imprinted Ti plate as the CE substrate, while the cell with an imprint-free Ti plate shows an η of 7.81%. The enhanced η is due to the improved electrocatalytic ability of the CE by using the TNT-imprinted Ti plate as the substrate with higher active surface area.

Novel polymer gel electrolyte with organic solvents for quasi-solid-state dye-sensitized solar cells.

A cross-linked copolymer was previously synthesized from poly(oxyethylene) diamine (POE-amine) and an aromatic anhydride and cured to generate an amide-imide cross-linking structure. The copolymer containing several chemical groups such as POE, amido acids, and imide, enabled to absorb liquid electrolytes in methoxypropionitrile (MPN) for suitable uses in dye-sensitized solar cells. To establish the advantages of polymer gel electrolytes (PGE), the same copolymer was studied by using different electrolyte solvents including propylene carbonate (PC), dimethylformamide, and N-methyl-2-pyrrolidone, and shown their long-term stability. The morphology of the copolymer after absorbing liquid electrolytes in these solvents was proven the same as a 3D interconnected nanochannels, evidenced field emission-scanning electron microscopy. Among these solvents, PC was selected as the optimized PGE, which demostrated a higher power conversion efficiency (8.31%) than that of the liquid electrolyte (7.89%). In particular, the long-term stability of only a 5% decrease in the cell efficiency after 1000 h of testing was achieved. It was proven the developed copolymer as PGE was versatile for different solvents showing high efficiency and long-term durability.