The Gd2O2S:Tb scintillation ceramics is extensively used for neutron radiography and industrial non-destructive testing due to its bright green emission, high intrinsic conversion efficiency and high thermal neutron capture cross-section. However, the existence of Gd2O3 secondary phase in Gd2O2S ceramics will affect the scintillation property. In this work, The Gd2O2S:Tb precursors were synthesized in water-bath with H2SO4 and Gd2O3 as starting materials. The molar ratio of H2SO4 to Gd2O3 defined as n was adjusted to synthesize the precursors. The influence of n values on the properties of the precursors and powders was studied. The chemical composition of the precursors changes with the increase of n values, which can be described as 2Gd2O3), and Gd2(SO4)3• 8H2O (n=3). After being calcined and reduced, all the powders exhibit a pure Gd2O2S phase. The morphology of the Gd2O2S:Tb powders is closely related to the phase composition of the precursor. The increase of the XEL intensity shows two stages with the increase of n values, corresponding to the phase transition of the precursor respectively. The Gd2O2S:Tb scintillation ceramics were fabricated by vacuum pre-sintering and HIP post-treatment. The ceramics fabricated from the powders prepared with different n values achieved high relative density and XEL intensity except the ceramics fabricated from the powders prepared with the n= 2, 2.25, 2.5. The increase of n value is beneficial to the removal of the Gd2O3 secondary phase from the FESEM morphologies of the Gd2O2S:Tb ceramics. This work provides ideas for eliminating the secondary phase in Gd2O2S:Tb scintillation ceramics.