co-workers reported a one-step method to obtain the uniform tannic acid-Fe (TA-Fe) films (11.9 ± 1.2 nm) by changing the pH value of solution. [2] Similar to the assembly of TA-Fe films, 18 different metal ions have been selected to design and prepare MPNs multifunctional capsules. [3] Additionally, a large variety of superstructures based on the polyphenol surface functionalization have been obtained through cross-linking interaction. [4] Such studies show that a design based on coordination bond between polyphenols and various metal ions can provide a platform to prepare multifunctional materials. However, the requirements of synthesis of MPNs are a wet environment, [2] which restricts their widespread applications of monomers with no or poor solubility in solvents. [5] The development of a solvent-free method to prepare MPNs films with tunable properties is an urgent requirement. Mechanochemistry, a green and sustainable technology, [6] is now emerging as an environmentally friendly alternative to conventional solution-based approach in the fields of porous carbon materials, [7] organic reactions, [8] nanomaterials, [9] and metal-organic complexes. [10] Dai and co-workers synthesized
The development of functional metal-phenolic networks (MPNs) films by a simple and green strategy on metallic plane substrates for surface modification is a big challenge. Herein, tribochemistry, as an effective and robust method to prepare MPNs films with versatile applications and controllable thickness (≈1.5 nm to 2.2 µm) by surface coordination complexation derived from tannic acid (TA) and metal oxides or ions (M) on plane substrates, is reported. The mechanism of the formation of TA-M films is investigated in detail, showing that films are constructed by two-layer structures. At the bottom of films, the chelation of TA active moieties and M is triggered by friction, facilitating the coating growth and reducing the friction coefficient.There is a downward trend in the concentration of M with the thickness of films increasing, which is attributed to the diffusion of metal ions. As a result, the dominant structure of films changes into the hydrogen bonding or π-π stacking interaction among oligomers derived from coupling of the TA active moieties. Such facile surface modification strategy can broaden in situ mechanochemical synthesis of functional layers and open a promising route for the design of patterning, antifouling, and controlled release coatings.