Influence of structural and chemical properties on electron transport in mesoporous ZnO-based dye-sensitized solar cell

Ionics - Two chemical bath deposition (CBD) solutions were prepared at two different temperatures of 60 and 80 °C for dye-sensitized solar cell (DSSC) application. The deposition time...     

Influence of anthocyanin co-pigment on electron transport and performance in black rice dye-sensitized solar cell

This work reports the novel contribution of chlorophyll b as natural anthocyanin co-pigment in unpurified black rice extract for improved electron transport and performance of natural dye-sensitized solar cell. The dyes are extracted as prominent photosensitizers by considering the concentration, the dye electronic structure, the extraction, and immersion time. The anthocyanin dye containing 1.92 mM cyanidin-3-O-glucoside structure has been extracted without purification. Interestingly, 0.33 mM chlorophyll b is found as a natural co-sensitizer in unpurified anthocyanin. The role of chlorophyll b supporting the electron transfer of anthocyanin dye will be investigated for improved cell performance. Both purified and unpurified dyes are compared in the same anthocyanin concentration. The combined Tauc plot and voltametric method will be conducted to show the interfacial electronic band edges of TiO₂-dye-electrolyte. Electrochemical impedance spectroscopy method will investigate electron transfer dynamic in both cell systems. As a result, chlorophyll b has dominantly acted as two intermediate states in boosting electron injection and dye regeneration to improve cell efficiency from 1.31 to 2.17 % due to the narrower LUMO–TiO₂ conduction band gap and the narrower HOMO-iodide (I ^?) potential gap, respectively. According to the electron transport, the co-sensitizer contributes to the smaller transport resistance (R _t?=?21.9 Ω), the higher chemical diffusion coefficient (D_n?=?1.696?×?10^?3 cm²/s), the higher chemical capacitance (C_μ?=?14.32 μF), and the faster electron transport (τ_d?=?39.88 μs).     

Biomolecule-Assisted Synthesis of Hierarchical Multilayered Boehmite and Alumina Nanosheets for Enhanced Molybdenum Adsorption

The effective utilization of various biomolecules for creating a series of mesoporous boehmite (γ-AlOOH) and gamma-alumina (γ-Al₂O₃) nanosheets with unique hierarchical multilayered structures is demonstrated. The nature and concentration of the biomolecules strongly influence the degree of the crystallinity, the morphology, and the textural properties of the resulting γ-AlOOH and γ-Al₂O₃ nanosheets, allowing for easy tuning. The hierarchical γ-AlOOH and γ-Al₂O₃ multilayered nanosheets synthesized by using biomolecules exhibit enhanced crystallinity, improved particle separation, and well-defined multilayered structures compared to those obtained without biomolecules. More impressively, these γ-AlOOH and γ-Al₂O₃ nanosheets possess high surface areas up to 425 and 371 m² g⁻¹, respectively, due to their mesoporous nature and hierarchical multilayered structure. When employed for molybdenum adsorption toward medical radioisotope production, the hierarchical γ-Al₂O₃ multilayered nanosheets exhibit Mo adsorption capacities of 33.1–40.8 mg g⁻¹. The Mo adsorption performance of these materials is influenced by the synergistic combination of the crystallinity, the surface area, and the pore volume. It is expected that the proposed biomolecule-assisted strategy may be expanded for the creation of other 3D mesoporous oxides in the future.