Functional thin films provide many opportunities for advanced glazing systems. This can be achieved by adding additional functionalities such as self-cleaning or power generation, or alternately by providing energy demand reduction through the management or modulation of solar heat gain or blackbody radiation using spectrally selective films or chromogenic materials. Self-cleaning materials have been generating increasing interest for the past two decades. They may be based on hydrophobic or hydrophilic systems and are often inspired by nature, for example hydrophobic systems based on mimicking the lotus leaf. These materials help to maintain the aesthetic properties of the building, help to maintain a comfortable working environment and in the case of photocatalytic materials, may provide external pollutant remediation. Power generation through window coatings is a relatively new idea and is based around the use of semi-transparent solar cells as windows. In this fashion, energy can be generated whilst also absorbing some solar heat. There is also the possibility, in the case of dye sensitized solar cells, to tune the coloration of the window that provides unheralded external aesthetic possibilities. Materials and coatings for energy demand reduction is highly desirable in an increasingly energy intensive world. We discuss new developments with low emissivity coatings as the need to replace scarce indium becomes more apparent. We go on to discuss thermochromic systems based on vanadium dioxide films. Such systems are dynamic in nature and present a more sophisticated and potentially more beneficial approach to reducing energy demand than static systems such as low emissivity and solar control coatings. The ability to be able to tune some of the material parameters in order to optimize the film performance for a given climate provides exciting opportunities for future technologies. In this article, we review recent progress and challenges in these areas and provide a perspective for future trends and developments.

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Titanium dioxide thin films were deposited using a Tween ® surfactant modified non-aqueous sol-gel method onto fluorine doped tin oxide glass substrates. The surfactant concentration and type in the sols was varied as well as the number of deposited layers. The as deposited thin films were annealed at 500 °C for 15 min before characterisation and photocatalytic testing with resazurin intelligent ink. The films were characterised using scanning electron microscopy, atomic force microscopy, X-ray diffraction, Raman spectroscopy and UV-Vis spectroscopy. Photocatalytic activity of the films was evaluated using a resazurin dye-ink test and the hydrophilicity of the films was analysed by water-contact angles measurements. Characterisation and photocatalytic testing has shown that the addition of surfactant in varying types and concentrations had a significant effect on the resulting thin film microstructure, such as changing the average particle size from 130 to 25 nm, and increasing the average root mean square roughness from 11 to 350 nm. Such structural changes have resulted in an enhanced photocatalytic performance for the thin films, with an observed reduction in dye half-life from 16.5 to three minutes.

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Highly uniformed, surfactant free and vertically oriented titanium-di-oxide (TiO2) nanorods were grown on pre-treated fluorine doped tin oxide (FTO) using hydrothermal method through titanium tetra butoxide (Ti(OBu)4) as titanium source. Three different temperatures 130 °C, 150 °C and 180 °C were followed to grow the nanorods at a fixed reaction time of 4 h. The prepared TiO2 nanorods were annealed at the temperatures of 550 °C and 600 °C for 3 h. X-ray diffraction (XRD) analysis shows that obtained nanorods exhibit pure rutile phase. From scanning electron microscopy (SEM) analysis, it was found that increasing temperature led to decreasing the diameter of the nanorods. In addition to these, formation of hierarchical type TiO2 nanorods was also observed at 130 °C. UV-visible spectra analysis was carried out to find the influence of diameter of the nanorods on its optical properties. The plausible mechanism of the growth process is also discussed.

Cu2SnSe3 nanoparticles are synthesised using oleylamine as both a solvent and capping agent and spray coated to form dye‐sensitised solar cell (DSSC) counter electrodes (CEs) using earth‐abundant elements. The film requires annealing at only 400 °C in nitrogen, which is a lower temperature than previous reports of both Cu2SnSe3and Cu2ZnSnSe4 films, also avoiding the use of Se gas. The composition and phase of the material is confirmed to be kesterite Cu2SnSe3. DSSCs using Cu2SnSe3 CEs give a power conversion efficiency of 4.87%, compared to 5.35% when using Pt. Electrochemical impedance spectroscopy indicates that the performance of the Cu2SnSe3 CE is enhanced under illumination, leading to a drop in the charge transfer resistance. This illumination‐induced enhancement of the catalytic activity provides a novel mechanism for the enhancement of CE performance in DSSCs. Photo‐excitation of the nanostructured Cu2SnSe3 counter electrode provides a higher overpotential for electrolyte reduction, giving improved catalytic performance.