Abstract
Electrochemical synthesis of H(2)O(2)via a two-electron oxygen reduction reaction (2e(-) ORR) has emerged as a promising alternative to the anthraquinone process. However, the strong competition from the 4e(-) pathway severely limits its activity and selectivity, especially for Pt-based catalysts. Herein, ultrathin single-crystal PtSe2 nanosheets were successfully prepared via an in situ selenization process using commercial Pt/C as a precursor, demonstrating an exclusive 2e(-) ORR pathway compared to the 4e(-) pathway of commercial Pt/C, delivering a high H2O2 selectivity over a wide pH range (>80%, up to 94.1%). Furthermore, in situ infrared spectroscopy results revealed Pt as an active center, accompanied by the key intermediate OOH* adsorption and HOOH formation.