Facile preparation of a water-based antireflective SiO2 film with high transmittance for perovskite solar cells.

The synthesis of anti-reflective (AR) films has been increasingly focused on environmental friendliness and cost efficiency in order to realize green and sustainable development. Herein, a novel strategy for preparing a nanoporous SiO2 AR film with high transmittance by a sol-gel process is proposed based on a sodium silicate aqueous solution. Sodium ions in the as-prepared SiO2 AR film can be effectively removed by a facile washing process, and thus its refractive index can be regulated. Moreover, the pH value of the sol has a huge effect on the structure and properties of the SiO2 AR film. As a result, the AR film exhibited a high transmittance increase of 4.10% at 550 nm and an average transmittance increase by 3.51% in the wavelength range of 380-1100 nm compared with blank glass. In addition, the obtained water-based SiO2 AR film exhibited hydrophilicity and the water contact angle (WCA) can be regulated from 61° to 8.4°. When the AR film was applied to the upper surface of perovskite solar cells, the photoelectric conversion efficiency (PCE) revealed an improvement of 1.44% compared with the PCE of perovskite solar cells without the AR film. Therefore, this work can provide a facile and effective method to prepare water-based antireflective films with high transmittance for solar cells.

Enhanced Thermochromic Performance of VO2 Nanoparticles by Quenching Process.

Vanadium dioxide (VO2) has been a promising energy-saving material due to its reversible metal-insulator transition (MIT) performance. However, the application of VO2 films has been seriously restricted due to the intrinsic low solar-energy modulation ability (ΔTsol) and low luminous transmittance (Tlum) of VO2. In order to solve the problems, the surface structure of VO2 particles was regulated by the quenching process and the VO2 dispersed films were fabricated by spin coating. Characterizations showed that the VO2 particles quenched in deionized water or ethanolreserved VO2(M) phase structure and they were accompanied by surface lattice distortion compared to the pristine VO2. Such distortion structure contributed to less aggregation and highly individual dispersion of the quenched particles in nanocomposite films. The corresponding film of VO2 quenched in water exhibited much higher ΔTsol with an increment of 42.5% from 8.8% of the original VO2 film, because of the significant localized surface plasmon resonance (LSPR) effect. The film fabricated from the VO2 quenched in ethanol presented enhanced thermochromic properties with 15.2% of ΔTsol and 62.5% of Tlum. It was found that the excellent Tlum resulted from the highly uniform dispersion state of the quenched VO2 nanoparticles. In summary, the study provided a facile way to fabricate well-dispersed VO2 nanocomposite films and to facilitate the industrialization development of VO2 thermochromic films in the smart window field.

Enhanced Performance of Carbon-Selenide Composite with La0.9Ce0.1NiO3 Perovskite Oxide for Outstanding Counter Electrodes in Platinum-Free Dye-Sensitized Solar Cells.

For large-scale applications, dye-sensitized solar cells (DSSCs) require the replacement of the scarce platinum (Pt)-based counter electrode (CE) with efficient and cheap alternatives. In this respect, low-cost perovskite oxides (ABO3) have been introduced as promising additives to composite-based CEs in Pt-free DSSCs. Herein, we synthesized composites from La0.9Ce0.1NiO3 (L) perovskite oxide and functionalized-multiwall-carbon-nanotubes wrapped in selenides derived from metal-organic-frameworks (f-MWCNT-ZnSe-CoSe2, "F"). L and F were then mixed with carbon black (CB) in different mass ratios to prepare L@CB, F@CB, and L@F@CB composites. The electrochemical analysis revealed that the L@F@CB composite with a mass ratio of 1.5:3:1.5 exhibits better electrocatalytic activity than Pt. In addition, the related DSSC reached a better PCE of 7.49% compared to its Pt-based counterpart (7.09%). This improved performance is the result of the increase in the oxygen vacancy by L due to the replacement of La with Ce in its structure, leading to more active sites in the L@F@CB composites. Moreover, the F@CB composite favors the contribution to the high electrical conductivity of the hybrid carbon nanotube-carbon black, which also offers good stability to the L@F@CB CE by not showing any obvious change in morphology and peak-to-peak separation even after 100 cyclic voltammetry cycles. Consequently, the corresponding L@F@CB-based device achieved enhanced stability. Our work demonstrates that L@F@CB composites with a low cost are excellent alternatives to Pt CE in DSSCs.

Mesoporous ZnO nanorods array with a controllable area density for enhanced photocatalytic properties.

Usually, a ZnO nanorods array exhibits a relatively small effective surface area due to its smooth surface and large area density (the number of ZnO nanorods per unit area). In this work, a mesoporous ZnO nanorods array with a small area density and a large effective surface area was successfully synthesized on the surface of fluorine-doped tin dioxide (FTO) glass using a facile solution process, with ethylene glycol (EG) and water serving as the mixed solvent and cadmium ions serving as an additives. The area density, aspect ratio and specific surface area of mesoporous ZnO nanorods array can be controlled by adjusting the concentration of cadmium ions in the EG-H2O mixed solution. The obtained ZnO nanorods array was applied as the photocatalyst for the photodegradation of methylene blue (MB) and showed a good catalytic performance that was dependent on the area density, rather than the specific surface area. This may be because a smaller area density of nanorods array can facilitate the diffusion of MB molecules and thus provide a larger effective surface area for MB adsorption, despite a large difference in their specific surface area. Therefore, this work can provide a guidance for synthesizing nanostructures with good photocatalytic activity on the devices.