Abstract
ABSTRACT
The energy‐free activation of ambient molecular oxygen (O
2
) to singlet oxygen (
1
O
2
) under neutral conditions is highly desirable for green oxidation chemistry, yet remains fundamentally limited by sluggish proton‐coupled *OOH formation and desorption. Here, we engineer an interfacial proton‐relay microenvironment between MoS
2
and CuCl that enables self‐driven O
2
‐to‐
1
O
2
conversion without external energy inputs. Electron‐deficient sulfur sites act as a proton reservoir by forming S‐H
ads
species, facilitating directional proton migration through Cu‐S‐Mo channels to activate adsorbed O
2
on electron‐rich Cu sites. This coupled electron‐proton relay accelerates *OOH hydrogenation while maintaining moderate *O2/*OOH binding, effectively suppressing O─O bond cleavage and favoring a 1O2‐dominated pathway. As a result, the system achieves quantitative pollutant removal and sustained operation for over 16 h in pilot‐scale membrane filtration. This interfacial design is broadly applicable to transition metal sulfides, offering a general strategy to overcome proton‐transfer limitations and advance autonomous catalytic platforms for sustainable oxidation and environmental remediation.