Ag@AgCl/GO was prepared by chemical coupling, in-situ deposition of supported AgCl, and photoreduction. The morphology, structure, and surface area of the prepared Ag@AgCl/GO were characterized by SEM, TEM, FT-IR, Raman spectra, and BET. The optical properties of the photocatalyst were analyzed by PL and UV-Vis DRS, respectively. The surface electrical properties and degradation stability were evaluated by zeta potential measurement and cyclic catalytic degradation experiments, and the photocatalytic mechanism was proposed in detail based on the ESR test and trapping experiment. The results showed that Ag@AgCl nanoparticles were spherical and cluster distributed on the folded structure of GO. The prepared Ag@AgCl/GO had good adsorption performance and photocatalytic degradation stability. The material showed good visible light catalytic performance; especially, the degradation rates of cationic dyes RhB and MB were significantly higher than those of anionic dyes MO and CR, and their degradation processes were in line with the quasi-first-order reaction kinetics. Holes (h+) and superoxide radicals (·O2-) were the main active species for the degradation of RhB.