Nanostructured NiO film was prepared by depositing nickel hydroxide slurry on conducting glass and sintering at 500 °C to a thickness of about 1 µm. The photocurrent-voltage (IV) characteristics of the plain nanostructured NiO electrode recorded potentiostatically in a standard three-electrode setup upon UV illumination demonstrate p-type behavior, while the IV characteristics of a dye-sensitized nanostructured NiO electrode coated with erythrosin B show cathodic photocurrent under visible light illumination. The highest incident photon-to-current conversion efficiencies of tetrakis(4-carboxyphenyl)porphyrin (TPPC) and erythrosin B-coated NiO films were 0.24% and 3.44%, respectively. In sandwich solar cells with a platinized conducting glass as counter electrode exposed to light from a sun simulator (light intensity: 68 mW/cm 2 ), a short-circuit cathodic photocurrent density (I SC ) of 0.079 mA/cm 2 and an open-circuit voltage (V OC ) of 98.5 mV for TPPC-coated NiO electrode were achieved. Similarly, I SC ) 0.232 mA/cm 2 and V OC ) 82.8 mV were registered when the NiO electrode was coated with erythrosin B. The cathodic photocurrent is explained by hole injection from dye molecule to the valence band of the p-NiO electrode.
Powered by market hype, trends among youth, and enormous funds, wearable technology has propelled itself as one of the most discussed topics in the field during past few years. A number of different companies representing all throughout the world have already entered into the market with hundreds of different products like smart watches, fitness trackers, smart garments, and even different smart medical attachments.Together with the evolution of digital health care, the wearable electronics field has evolved rapidly during the past few years and is expected to be expanded even further within the first few years of the next decade. As the next stage of wearables is predicted to move toward integrated wearables, nanomaterials and nanocomposites are in the spotlight of the search for novel concepts for integration. In addition, the conversion of current devices and attachment-based wearables into integrated technology may involve a significant size reduction while retaining their functional capabilities. Nanomaterialbased wearable sensors have already marked their presence with a significant distinction while nanomaterial-based wearable actuators are still at their embryonic stage. This review looks into the contribution of nanomaterials and nanocomposites to wearable technology with a focus on wearable sensors and actuators.
A zinc phthalocyanine with tyrosine substituents (ZnPcTyr), modified for efficient far-red/near-IR performance in dye-sensitized nanostructured TiO(2) solar cells, and its reference, glycine-substituted zinc phthalocyanine (ZnPcGly), were synthesized and characterized. The compounds were studied spectroscopically, electrochemically, and photoelectrochemically. Incorporating tyrosine groups into phthalocyanine makes the dye ethanol-soluble and reduces surface aggregation as a result of steric effects. The performance of a solar cell based on ZnPcTyr is much better than that based on ZnPcGly. Addition of 3alpha,7alpha-dihydroxy-5beta-cholic acid (cheno) and 4-tert-butylpyridine (TBP) to the dye solution when preparing a dye-sensitized TiO(2) electrode diminishes significantly the surface aggregation and, therefore, improves the performance of solar cells based on these phthalocyanines. The highest monochromatic incident photo-to-current conversion efficiency (IPCE) of approximately 24% at 690 nm and an overall conversion efficiency (eta) of 0.54% were achieved for a cell based on a ZnPcTyr-sensitized TiO(2) electrode. Addition of TBP in the electrolyte decreases the IPCE and eta considerably, although it increases the open-circuit photovoltage. Time-resolved transient absorption measurements of interfacial electron-transfer kinetics in a ZnPcTyr-sensitized nanostructured TiO(2) thin film show that electron injection from the excited state of the dye into the conduction band of TiO(2) is completed in approximately 500 fs and that more than half of the injected electrons recombines with the oxidized dye molecules in approximately 300 ps. In addition to surface aggregation, the very fast electron recombination is most likely responsible for the low performance of the solar cell based on ZnPcTyr.
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