Atomic-level tuning of Co–N–C catalyst for high-performance electrochemical H2O2 production

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.