Photocatalytic synthesis of H 2 O 2 , as a potential alternative to the industrial anthraquinone process, does not require additional energy input and is a nontoxic and pollution-free process, which has attracted widespread attention. Herein, we successfully anchored the SnO 2 clusters into the g-C 3 N 4 through the Sn−N bond (SnO 2 @g-C 3 N 4 ) as a highly efficient photocatalyst for visible lightdriven H 2 O 2 production. Because of the existence of the Sn−N bond, the thickness of the SnO 2 @g-C 3 N 4 material is thinner, and the lattice spacing of SnO 2 is stretched, achieving an excellent photocatalytic hydrogen peroxide production rate of 1021.15 μmol g −1 h −1 , which is 58-fold more than that of the original g-C 3 N 4 . Moreover, the turnover frequency of SnO 2 @g-C 3 N 4 (1.7 min −1 ) has a huge advantage of 57 times compared with that of the original g-C 3 N 4 . The outstanding photocatalytic activity is attributed to the lattice tensile of SnO 2 clusters in SnO 2 @g-C 3 N 4 , leading to the decreased d-band center, which can promote the OOH* to HOOH* transformation as the rate-determining step. Meanwhile, the SnO 2 @g-C 3 N 4 can improve the electron migration from bulk to the catalyst surface, as well as the electron separation, which also plays an important role in activity improvement. This work provides a promising photocatalyst for efficient visible light-driven generation of H 2 O 2 . KEYWORDS: SnO 2 cluster, g-C 3 N 4 , Visible light, H 2 O 2 production, Density functional theory