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Organic–inorganic halide perovskite solar cells (PSCs) have reached certified efficiencies of over 23 % with expensive organic hole‐transporting materials. However, the use of an inorganic hole‐transport layer (HTL) remains crucial as it would reduce cost combined with higher mobility and stability. In this direction, the application of Cu2O as the top layer in PSCs is still complicated owing to the difficulty of solution processing. Herein, a solution‐processing method is reported for preparing Cu2O nanocubes as a p‐type HTL in regular structure (n‐i‐p) PSCs. The controlled synthesis of Cu2O nanocubes in a size range of 60–80 nm is achieved without using any surfactants, which are usually toxic and tricky to remove. The new structure of these Cu2O nanocubes enhances the carrier mobility with preferable energy alignment to the perovskite layer and superb stability. The PSCs based on these Cu2O nanocubes HTMs could achieve an efficiency exceeding 17 % with high stability, whereas organic P3HT‐based PSCs display an efficiency of 15.59 % with a poorer running stability. This indicates that Cu2O nanocubes are a promising HTM for efficient and stable PSCs.

Synergism between oxygen and sulfur donors allows highly variable thioether side chains to be built into the matrices of Zr(iv)–carboxylate networks, boosting the functionality and stability of this promising class of porous solids.

Anticorrosive coatings are extensively investigated as a potential solution to prevent or at least retard metal corrosion occurrence. However, the actual breakthrough is still hampered by the risk of barrier properties loss because of the local failure of the coating. Self-healing coatings can effectively repair microcracks, but outstanding self-healing behavior is always accompanied by poor self-cleaning ability. Herein, we report a series of poly­(dimethylsiloxane) (PDMS) modified with a terephthalic aldehyde (TA)-polyurea (PDMS-TA-PUa) copolymer with a double reversible dynamic bond crosslinking network structure. The PDMS-TA-PUa coating exhibits fast and re-recycled self-healing behavior that heals cracks within 40–50 min at room temperature. The fast self-healing property is attributed to the dynamic nature of the imine bonds and hydrogen bonds in polymer networks. The PDMS-TA-PUa coating also shows great self-cleaning and anticorrosive ability, due to high hydrophobic, low surface energy, and high corrosion potential. Our work gives an insight into the design and preparation of multifunctional coating material with excellent anticorrosion performance, fast self-healing, and self-cleaning properties.

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