The phonon, infrared, and Raman spectroscopic properties of zirconium tungsten phosphate, Zr 2 (WO 4 )(PO 4 ) 2 (space group Pbcn, IT No. 60; Z = 4), have been extensively investigated using density functional perturbation theory (DFPT) calculations with the Perdew, Burke, and Ernzerhof exchange−correlation functional revised for solids (PBEsol) and validated by experimental characterization of Zr 2 (WO 4 )(PO 4 ) 2 prepared by hydrothermal synthesis. Using DFPT-simulated infrared, Raman, and phonon density-of-state spectra combined with Fourier transform infrared and Raman measurements, new comprehensive and extensive assignments have been made for the spectra of Zr 2 (WO 4 )(PO 4 ) 2 , resulting in the characterization of its 29 and 34 most intense IR-and Raman-active modes, respectively. DFPT results also reveal that ν 1 (PO 4 ) symmetric stretching and ν 3 (PO 4 ) antisymmetric stretching bands have been interchanged in previous Raman experimental assignments. Negative thermal expansion in Zr 2 (WO 4 )(PO 4 ) 2 appears to have very limited impact on the spectral properties of this compound. This work shows the high accuracy of the PBEsol exchange−correlation functional for studying the spectroscopic properties of crystalline materials using first-principles methods.