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Cristobalite‐type boron phosphate BPO4, an important nonlinear‐optical (NLO) crystal, exhibits nearly the largest bandgap (Eg ≈ 9.3 eV) and a significant second‐harmonic‐generation (SHG) effect (d36 ≈ 0.7 pm V−1) in the deep‐ultraviolet (DUV, < 200 nm) spectral region. However, its conventional tetrahedral framework structure tends to have low structural anisotropy, resulting in a severe deficiency of birefringence (Δn < 0.01), which fails to achieve DUV birefringent phase matching. In this work, the local anisotropy of tetrahedral structures are proposed to enlarge by constructing van der Waals (vdW) anisotropic motifs under synthetic chemical conditions, which can effectively convert unattainable extreme external forces into internal stresses in chemical bond structures. Depending on unique hierarchical vdW assemblies, enormous tetrahedral distortions can be achieved by stable in‐plane or in‐line bond matching between rigid tetrahedral primitives. First‐principles calculations demonstrate that the birefringence of 2D layered and 1D chained BPO4 achieved by vdW engineering are scaled from Δn < 0.01 to 0.07–0.13, with the shortest birefringent phase‐matched wavelengths down to DUV 189–154 nm. The finding is of seminal importance for the design of vdW NLO crystals in structural chemistry and would provide opportunities to explore unique vdW DUV NLO materials under extreme synthetic conditions. [ABSTRACT FROM AUTHOR]

Van‐der‐Waals (vdW) deep‐ultraviolet (DUV) nonlinear‐optical (NLO) materials hold great potential to extend DUV NLO applications to two dimensions, but they are rare in nature. In this study, we propose a design principle to realize vdW DUV NLO materials via structural evolution from the non‐vdW (BO3)‐(BeO3F) layers in KBe2BO3F2 (KBBF) to the vdW (BO3)‐(BeO4H) layers in berborite Be2BO5H3 (BBH) and the vdW (BO4)‐(BeO4) layers in beryllium metaborate BeB2O4 (BEBO). Based on first‐principles calculations, the fundamental NLO properties of BBH and BEBO demonstrate that a balanced DUV NLO performance can be achieved in these two systems. Importantly, BBH, a layered material existing in nature, can achieve an available DUV phase‐matched output with strong second harmonic generation (SHG) for 177.3/193.7 nm DUV lasers, which is almost identical to that of KBBF. Remarkably, BEBO shows an excellent DUV SHG capacity and an even shorter phase‐matching wavelength than KBBF. Therefore, the newly discovered vdW BBH and BEBO, once verified by experiments, could provide an ideal platform to study DUV NLO effects in three dimensions and two dimensions. [ABSTRACT FROM AUTHOR]

The first alkaline‐earth metal tin(II) phosphate, BaSn2(PO4)2, has been discovered, which consists of layered structures constructed from strictly alternating [SnO3]4− and [PO4]3− moieties. This compound is expected to have a large birefringence with Δn≈0.071 at 1064 nm, owing to the presence of stereochemically active lone pair metal cations. [ABSTRACT FROM AUTHOR]

In this work, we propose a strategy to design new deep‐ultraviolet (deep‐UV) nonlinear optical (NLO) materials through the combination of borate and phosphate NLO material genome. Accordingly, a series of borophosphates are predicted with very large energy bandgaps, strong second harmonic generation (SHG) effects, and moderate birefringence in the deep‐UV region. In particular, two novel fluoride borophosphates, PBO3F2 and PB3O6F2, are able to achieve the deep‐UV SHG laser output with shorter phase‐matching wavelengths (≈155 and 137 nm) than that of KBe2BO3F2 (KBBF, ≈161 nm). Further calculations show that these two structures are dynamically and thermodynamically stable, thus triggering possible synthesis, growth, and applications of them. The results attest that the proposed strategy is instructive and pave a comprehensive road map for us to discover new NLO crystals, especially in the borophosphate catalog with excellent deep‐UV phase‐matching capabilities beyond KBBF. [ABSTRACT FROM AUTHOR]

The first alkaline‐earth metal tin(II) phosphate, BaSn2(PO4)2, has been discovered, which consists of layered structures constructed from strictly alternating [SnO3]4− and [PO4]3− moieties. This compound is expected to have a large birefringence with Δn≈0.071 at 1064 nm, owing to the presence of stereochemically active lone pair metal cations. [ABSTRACT FROM AUTHOR]