Metal corrosion can potentially cause catastrophic engineering accidents threatening personal safety; thus, coating protection is a tremendously valuable anti-corrosion initiative. Recently, biphenylene, a novel two-dimensional (2D) graphene-based material, has achieved a remarkable synthetic breakthrough; the anti-corrosion properties of biphenylene, with its specific pore structure, are predicted to be beneficial in applications of metal corrosion resistance. In this study, the anti-corrosion mechanism of biphenylene is deciphered utilizing first principles and molecular dynamics. The results suggest that biphenylene with tetragonal, hexagonal, and octagonal carbon rings supplies adequate sites for stable O atom adsorption. The charge transfer amounts of +0.477 and +0.420 e facilitate the formation of a compact oxygen-rich layer on the material surface to acquire outstanding anti-corrosion properties. The moderate wettability of biphenylene prevents the water-based solution from encroaching on the biphenylene coating and substrate. In addition, the intensive binding between biphenylene and the aluminum substrate strengthens the integration of the two heterogeneous structures with −413.7 and 415.5 eV, which guarantees the durable application of biphenylene coating.

High entropy alloys (HEA) applied to oxygen evolution reactions in electrocatalysis.

The SrCoO_3−δ system has broad application potential due to its diverse crystal structures, oxidation stoichiometric ratio, and significant electrical and magnetic properties.

Freshwater is a scarce and vulnerable resource that has never encountered such an extensive focus on a nearly worldwide scale as it does today. Recently, it has been found that desalination powered by two-dimensional (2D) carbon materials as separation membranes has significantly reduced the operational costs and complexity but presents heavy requirements for the structural stability and separation properties of the membrane materials. Here, we combined carbon materials with promising adsorption properties and zeolites characterized by a regular pore structure to obtain a zeolite-like structured carbon membrane Zeo-C and investigated the suitability of the Zeo-C membrane for seawater desalination based on the computational-simulation-driven approach. The results of molecular dynamics (MD) simulations and density functional theory (DFT) calculations revealed that the periodic pore distribution conferred favorable structural stability and mechanical strength to the Zeo-C desalination membrane. The rejection rate of Na⁺ and Cl⁻ is ensured at 100% under a pressure of 40–70 MPa, and that of Na⁺ could reach 97.85% even though the pressure increases to 80 MPa, exhibiting superior desalination properties. The porous nature of the zeolite-like structure and the low free energy potential barrier are conducive for reliable adsorption and homogeneous diffusion of salt ions, which facilitates the acquisition of desirable water molecule permeability and salt ion selectivity. In particular, the interlinked delocalized π-network imparts inherent metallicity to Zeo-C for self-cleaning in response to electrical stimulation, thereby extending the lifetime of the desalination membrane. These studies have greatly encouraged theoretical innovations and serve as a guiding reference for desalination materials.