Bioinspired CoMn-Diatomic Superoxide Dismutase Nanozymes for High-Performance, Selective, and Long-Lasting H 2 O 2 Production

The practical deployment of electrochemical hydrogen peroxide (H2O2) production is severely hampered by the corrosive superoxide radicals (O2•−) generated at industrial current densities via a one-electron-transfer process, which rapidly degrade active sites and catalysts, consequently deteriorating long-term stability. Inspired by the natural manganese superoxide dismutase (Mn-SOD) enzyme, we designed a biomimetic CoMn-diatomic catalyst (CoMn-DACs), where the Co−N4 sites primarily drive the two-electron oxygen reduction reaction (2e− ORR) for the selective H2O2 production, while the adjacent Mn−N4 sites function as SOD-mimetic nanozymes, efficiently reversely converting O2•− radicals into H2O2, thus bypassing the destructive reaction pathway. Combined operando spectroscopy and density functional theory calculations reveal the dual functions of Mn sites in facilitating O2•− conversion and optimizing the *OOH adsorption energy on Co centers via the Co−Mn orbital coupling, which induces electronic structure redistribution and moderates the interaction between Co sites and oxygen intermediates toward highly selective and stable H2O2 production. Correspondingly, bioinspired CoMn-DACs achieve 99.3% H2O2 selectivity with an onset potential of 0.83 V (vs. RHE) and a maximum H2O2 production rate of 6.35 mM mgcat−1, surpassing the state-of-the-art catalyst, while maintaining 83.0−85.1% FE during 200 h continuous operation at 200 mA cm−2. A techno-economic analysis confirms the practical viability of this system, projecting a low H2O2 production cost of US$0.371 kg−1 when operated directly with ambient air, significantly outperforming the conventional anthraquinone process (US$1.50 kg−1). This work achieves durable electrosynthesis by emulating natural radical defense mechanisms, enabling enhanced stability and selectivity in energy-efficient H2O2 production.