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The electrochemical synthesis of hydrogen peroxide (H2O2) provides a greener and more efficient method compared with classic catalysts containing toxic metals. Herein, we used first-principles density functional theory (DFT) calculations to investigate 174 different single-atom catalysts with graphyne substrates, and conducted a three-step screening strategy to identify the optimal noble metal-free single atom catalyst. It is found that a single Ni atom loaded on γ-graphyne with carbon vacancies (Ni@V-γ-GY) displayed remarkable thermodynamic stability, excellent selectivity, and high activity with an ultralow overpotential of 0.03 V. Furthermore, based on ab-initio molecular dynamic and DFT calculations under the H2O solvent, it was revealed that the catalytic performance for H2O2 synthesis in aqueous phase was much better than that in gas phase condition, shedding light on the hydrogen bond network being beneficial to accelerate the transfer of protons for H2O2 synthesis.

A novel noninterpenetrated tetranuclear cobalt(II)-based metal-organic framework, (NH4)2·[Co4(μ3-OH)2(ina)2(pip)3]·4EtOH·H2O (simplified as NbU-10·S), constructed by mix linkers was synthesized by a hydrothermal method. Interestingly, the presence of a hydrophobic benzene ring in the organic linker makes NbU-10·S exhibit high stability in high temperature and even in aqueous solution over a wide pH range of about 4-13. Magnetic studies showed that the tetranuclear cobalt(II) units in NbU-10·S show dominant antiferromangetic properties. However, in the absence of Lewis basic functional sites and open metal sites in the material, NbU-10 still displays high C2H2/CO2 and C2H2/C2H4 selectivity in ideal adsorbed solution theory calculations and dynamic breakthrough experiments. Moreover, density functional theory calculations were performed to identify the adsorption characteristics of different gas molecules.