Hydroxyl‐Bonded Co Single Atom Site on Boroncarbonitride Surface Realizes Nonsacrificial H2O2 Synthesis in the Near‐Infrared Region

Abstract

AbstractPhotocatalytic synthesis of hydrogen peroxide (H2O2) from O2 and H2O under near‐infrared light is a sustainable renewable energy production strategy, but challenging reaction. The bottleneck of this reaction lies in the regulation of O2 reduction path by photocatalyst. Herein, the center of the one‐step two‐electron reduction (OSR) pathway of O2 for H2O2 evolution via the formation of the hydroxyl‐bonded Co single‐atom sites on boroncarbonitride surface (BCN‐OH2/Co1) is constructed. The experimental and theoretical prediction results confirm that the hydroxyl group on the surface and the electronic band structure of BCN‐OH2/Co1 are the key factor in regulating the O2 reduction pathway. In addition, the hydroxyl‐bonded Co single‐atom sites can further enrich O2 molecules with more electrons, which can avoid the one‐electron reduction of O2 to •O2−, thus promoting the direct two‐electron activation hydrogenation of O2. Consequently, BCN‐OH2/Co1 exhibits a high H2O2 evolution apparent quantum efficiency of 0.8% at 850 nm, better than most of the previously reported photocatalysts. This study reveals an important reaction pathway for the generation of H2O2, emphasizing that precise control of the active site structure of the photocatalyst is essential for achieving efficient conversion of solar‐to‐chemical.