Nitride phosphors have drawn much interest because of their outstanding thermal and chemical stability and interesting photoluminescence properties. Currently, it remains a challenge to synthesize these phosphors through a convenient chemical route. Herein we propose a general and convenient strategy based on hydrothermal-ammonolysis reaction to successfully prepare zinc germanium nitride (ZnGeN 2 ) and Mn 2+ doped ZnGeN 2 phosphors. The crystal structure, composition, morphology, luminescence and reflectance spectra, quantum efficiency, and the temperature-dependent photoluminescence behavior were studied respectively. The phase formation and crystal structure of ZnGeN 2 were confirmed from powder X-ray diffraction and Rietveld refinement. EDX analysis confirmed the actual atomic ratios of Zn/Ge and N/Ge and suggested the presence of Ge vacancy defects in the ZnGeN 2 host, which is associated with its yellow emission at 595 nm with a FWHM of 143 nm under UV light excitation. For Mn 2+ doped ZnGeN 2 phosphor, it exhibits an intense red emission due to the 4 T 1g -6 A 1g transition of Mn 2+ ions. The unusual red emission of Mn 2+ at the tetrahedral Zn 2+ sites is attributed to the strong nephelauxetic effect and crystal field between Mn 2+ and the tetrahedrally coordinated N 3À . Moreover, the PL intensity of ZnGeN 2 :Mn 2+ phosphors can be enhanced by Mg 2+ ions partially substituting for Zn 2+ ions in a certain concentration range. The optimal Mn 2+ doping concentration in the ZnGeN 2 host is 0.4 mol%. The critical energy transfer distance of this phosphor is calculated to be about 27.99 Å and the concentration quenching mechanism is proved to be the dipole-dipole interaction. With increasing temperature, the luminescence of ZnGeN 2 :Mn 2+ phosphors gradually decreases and the FWHM of the emission band broadens from 54 nm to 75 nm. The corresponding activation energy E a was reckoned to be 0.395 eV. And the nonradiative transition probability increases with the increasing temperature, finally leading to the lifetime decrease with the increase of the temperature.