Encapsulation of Highly Dispersed Au NPs by Strong Metal–Support Interactions in Porous Titania Nanoplates for Efficient Electrosynthesis of H₂O₂

Abstract Tuning the electrocatalytic selectivity and long‐term stability for industrially significant, yet reactively unfavorable products, remains a challenge in oxygen reduction. Herein, the Au/TiO₂ catalysts with strong metal–support interactions (SMSI) are designed and synthesized through an in situ auto‐reduction of Au‐modified Ti‐MOF. Highly dispersed ultra‐low loading of Au NPs strongly capsulated in porous TiO₂ substrate, together with conductive carbon derivated from MOFs, enables Au/TiO₂ electrocatalysts to achieve excellent H₂O₂ electrosynthesis through the two‐electron oxygen reduction reaction (2e ORR). Au(1.0)/TiO₂ (0.52 wt% Au loading) exhibited a high selectivity of 90%, a remarkable Faradaic efficiency of 98%, and 72.2 mg L⁻¹ h⁻¹ H₂O₂ production. Highly dispersed Au NPs promote active site exposure, while the conductive carbon and the porous superstructure enhance mass diffusion. Notably, the SMSI between Au NPs and TiO₂ substrate leads to superb stability (over 168 h) of the electrocatalysts, as it ensures continuous electronic interactions. Experimental characterizations and density functional theory (DFT) simulations further revealed that the SMSI effect medicates the activation of the *OOH intermediate formation and the d‐band center, which are conductive to 2e ORR. Moreover, this strategy provides a potential way toward high‐performance electrocatalysts in flow system devices for continuously purifying sewage and chemical bleaching in extreme environments.