Phosphates are ideal candidates in the search for deep
ultraviolet
(DUV) nonlinear optical (NLO) materials due to their wide DUV transmission.
However, the small optical anisotropy of the highly symmetric [PO4]3– tetrahedron hinders phase matching (PM)
in the DUV wavelength range. In this work, the polar tetrahedron [PO2(NHCONH2)2]−, which
combines the π-conjugated urea unit and the non-π-conjugated
[PO4]3– unit via covalent bonds, is proposed
as a new DUV NLO-active unit. [PO2(NHCONH2)2]− tetrahedron exhibits greatly improved
polarizability, anisotropy, and hyperpolarizability while maintaining
a large highest occupied molecular orbital–lowest unoccupied
molecular orbital gap. Accordingly, two DUV transparent alkali metal
N, N-bis(aminocarbonyl)-phosphorodiamidates [A[PO2(NHCONH2)2] (A = K, Rb)] are screened out, and their nonlinear
properties are systematically evaluated by first-principles methods.
The results show that K[PO2(NHCONH2)2] (KPOU) achieves significant enhancements in multiple properties
compared to the existing phosphate DUV NLO materials, including a
strong SHG effect (3.44 × KDP) and the largest birefringence
(0.088@532 nm) for DUV PM. Moreover, the shortest PM wavelength (λPM) of KPOU is 196 nm, making it a promising DUV NLO candidate
for practical applications. This work proposes an excellent NLO-active
unit and offers a new direction for exploring novel high-performance
DUV NLO materials.