Photocatalytic technology based on carbon nitride offers a sustainable and clean approach for hydrogen peroxide (H2O2) production, but the yield is severely limited by the sluggish hot carriers due to the weak internal electric field. In this study, we devised a novel approach by fragmenting graphitic carbon nitride into smaller pieces (CN‐NH4), followed by subjecting it to a directed healing process to create multiple order‐disorder interfaces (CN‐NH4‐NaK). The resulting junctions in CN‐NH4‐NaK significantly boosted charge dynamics and facilitated more spatially and orderly separated redox centers. As a result, CN‐NH4‐NaK demonstrated outstanding photosynthesis of H2O2 via both two‐step single‐electron and one‐step double‐electron oxygen reduction pathways, achieving a remarkable yield of 16675 μmol h–1 g–1, excellent selectivity (> 91%), and a prominent solar‐to‐chemical conversion efficiency exceeding 2.3%. These remarkable results surpassed pristine C3N4 by 158 times and outperformed previously reported C3N4‐based photocatalysts. This work represents a significant advancement in catalyst design and modification technology, inspiring the development of more efficient metal‐free photocatalysts for the synthesis of highly valued fuels.This article is protected by copyright. All rights reserved