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Durability under UV illumination remains a big challenge of TiO 2 -based superhydrophobic coatings, with the photocatalytic effect causing degradation of low-surface-energy material over time, resulting in the surfaces losing their hydrophobicity. We report surfaces made from tolylene-2,4diisocyanate (TDI)/TiO 2 hybrid networks that demonstrate superhydrophobicity and superior UV durability. Structural and morphological studies reveal that the TDI/TiO 2 hybrid networks are composed of TiO 2 nanoparticles interconnected with TDI bridges and then encapsulated by a TDI layer. Through controlling the fraction of TDI in the synthesis process, the thickness of the TDI encapsulation layer around the TDI/TiO 2 hybrid networks can be varied. When the weight ratio of TDI/TiO 2 is 5:1, the superhydrophobicity of the hybrid network surface remains almost unchanged after a month of continuous UV illumination. This hybrid network surface can also clean methylene blue solution through the synergistic effects of cation adsorption and photocatalysis, holding promising potential for applications toward reducing cation pollutions in both liquid and air environments.

Mesoporous silica nanoparticle hybrids have been synthesized and explored to cast as an antireflective coating onto the glass substrate of non-fullerene organic solar cells (OSCs) to enhance the light absorption and efficiency (from 15.4% to 16.2%).

Nanoscale morphology has been established as one of the controlling factors in the device performance of bulk heterojunction polymer solar cells. We report in this work morphology changes in both lateral and vertical directions in PffBT4T-2OD:PC71BM solar cells, as well as their effects on device performance. Thermal annealing was found to increase the crystallinity of PffBT4T-2OD and domain size of PC71BM clusters without any observable impact on vertical component redistribution, whilst methanol rinsing reduces the crystallinity of PffBT4T-2OD, encourages the migration of PC71BM towards the mixed polymer-rich phase as well as towards the film surface on both PEDOT:PSS and TiO2 substrates. The polymer-rich surface region in vacuum-and thermal annealing-treated conventional devices obstructs electron injection towards the cathode, and reduces the maximum achievable device efficiency, whilst this polymer-rich surface region is beneficial in the inverted devices. However, although a PC71BM-rich region will locate at the cathode or anode interface upon methanol rinsing treatment in conventional and inverted devices respectively, holes can still be effectively injected from both sides the device to ensure effective charge transport, as supported by a number of optoelectronic property investigations.