A facile ultra-rapid solution method was developed to fabricate ZnO nanosheets with tunable BET surface area and rich oxygen-vacancy defects. The addition of 1 mol L-1 Na2SO4 led to an increase of BET surface area of ZnO nanosheets from 6.7 to 34.5 m(2)/g, through an electrostatic-controlled growth and self-assembly mechanism. Detailed analysis based on Raman scattering, room-temperature photoluminescence, X-ray photoelectron spectroscopy and electron spin resonance revealed that the as-prepared ZnO nanosheets were rich in oxygen-vacancies. Increased BET surface area led to a further increase of surface oxygen-vacancy concentration. The rich oxygen-vacancies promoted the visible-light absorption of the ZnO nanosheets, leading to high photocurrent responses and photocatalytic activities towards the degradation of rhodamine B (apparent rate constants, k = 0.0179 min(-1)) under visible-light illumination (lambda > 420 nm), about 13 and 11 times higher, respectively than that of ZnO nanoparticles with few oxygen defects. In addition, the high-surface-area ZnO nanosheets could be effectively hybridized with Ag3PO4 nanoparticles, resulting in a further enhancement of the visible-light photocatalytic performance (k = 0.0421 min(-1)). This increase in performance was attributed to the increased visible-light absorption as well as the energy level matching, the latter leading to efficient charge transfer between oxygen-vacancy-rich ZnO nanosheet and Ag3PO4, suggesting a synergistic effect of surface oxygen vacancies and Ag3PO4 coupling. (C) 2016 Elsevier B.V. All rights reserved.