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Despite the growing demand for hydrogen peroxide it is almost exclusively manufactured by the energy-intensive anthraquinone process. Alternatively, H 2 O 2 can be produced electrochemically via the two-electron oxygen reduction reaction, although the performance of the state-of-the-art electrocatalysts is insufficient to meet the demands for industrialization. Interestingly, guided by first-principles calculations, we found that the catalytic properties of the Co–N 4 moiety can be tailored by fine-tuning its surrounding atomic configuration to resemble the structure-dependent catalytic properties of metalloenzymes. Using this principle, we designed and synthesized a single-atom electrocatalyst that comprises an optimized Co–N 4 moiety incorporated in nitrogen-doped graphene for H 2 O 2 production and exhibits a kinetic current density of 2.8 mA cm −2 (at 0.65 V versus the reversible hydrogen electrode) and a mass activity of 155 A g −1 (at 0.65 V versus the reversible hydrogen electrode) with negligible activity loss over 110 hours. Producing H 2 O 2 electrochemically currently use electrocatalysts that are insufficient to meet the demands for industrialization. A single-atom electrocatalyst with an optimized Co–N4 moiety incorporated in nitrogen-doped graphene is shown to exhibit enhanced performance for H 2 O 2 production.

Uniform nanoparticles have shown to hold great potential in many different fields. As a result, many resources have been devoted to the search for a general synthesis of uniform nanoparticles, which has led to the proliferation of solution-based methods. However, some of these techniques are inherently difficult to scale up and are unable to meet future industry needs. Additionally, since the synthesis temperature of these methods can only go as high as the evaporation point of the solvent, they are not compatible with the high temperatures required to obtain certain desired properties such as high crystallinity. Recently, solventless methods have gained considerable attention since they are relatively fast and require no expensive or toxic solvents. Inorganic salt powder can be used as separation medium to prevent aggregation and sintering by keeping the as-prepared nanoparticles or precursor materials physically separated. This review surveys the use of inorganic salts in solventless techniques for the annealing or direct synthesis of uniform nanoparticles. Graphical abstract Fine inorganic salt powder can be used as separation medium to prevent aggregation and sintering by keeping the as-prepared nanoparticles or precursor materials physically separated. The primary advantages of this strategy are its simplicity and the ability to easily scale-up. Additionally, this strategy can use a wider temperature window compared to solution-based syntheses. Lastly, the inorganic salt powder can be separated and reused by washing the final nanomaterials. This review surveys the use of inorganic salts in solventless techniques for the annealing or direct synthesis of uniform nanoparticles.

Despite the growing demand for hydrogen peroxide it is almost exclusively manufactured by the energy-intensive anthraquinone process. Alternatively, H O can be produced electrochemically via the two-electron oxygen reduction reaction, although the performance of the state-of-the-art electrocatalysts is insufficient to meet the demands for industrialization. Interestingly, guided by first-principles calculations, we found that the catalytic properties of the Co-N moiety can be tailored by fine-tuning its surrounding atomic configuration to resemble the structure-dependent catalytic properties of metalloenzymes. Using this principle, we designed and synthesized a single-atom electrocatalyst that comprises an optimized Co-N moiety incorporated in nitrogen-doped graphene for H O production and exhibits a kinetic current density of 2.8 mA cm (at 0.65 V versus the reversible hydrogen electrode) and a mass activity of 155 A g (at 0.65 V versus the reversible hydrogen electrode) with negligible activity loss over 110 hours.