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Benefiting from the planar π-conjugated (HxC3N3O3)x−3 (x = 0–3) groups, cyanurate crystals have recently become a research hotspot in birefringent materials. Herein, by combining the (HxC3N3O3)x−3 (x = 0–3) group with the (CN3H6)+ cationic group, two metal-free cyanurates, GU(H2C3N3O3) (I) and GU3(H2C3N3O3)3(H3C3N3O3) (II), were obtained by the hydrothermal method. These compounds have wide band gaps (∼5 eV) and a large birefringence (∼0.40@400 nm), demonstrating their potential to be ultraviolet birefringent crystals. Moreover, first-principles calculations indicate that their large birefringence values originated from the synergistic effect of the (CN3H6)+ cations and (HxC3N3O3)x−3 (x = 0–3) groups. These findings provide a new design strategy for exploring low-cost UV birefringent crystals with a large birefringence. [ABSTRACT FROM AUTHOR]

• Single crystal structure of a novel ultraviolet NLO tourmaline was solved. • Sellmeier equations were obtained by fitting the measured refractive indices. • Phase matching range of the title crystal is obtained from the Sellmeier equations. • The linear and NLO properties were investigated by the experimental and theory calculation. Transparent tourmaline NaAl 9 (BO 3) 3 Si 6 O 21 OH is first reported by combining experimental and theory calculation methods, which exhibits potential ultraviolet nonlinear optical properties. [Display omitted] Tourmaline, as an important mineral, has received intensive interest, since it is not only a valuable gemstone, but also is a piezoelectric or pyroelectric material, due to the polar structural configuration. However, its nonlinear optical (NLO) properties were not explored so far, because a transparent crystal with high transmittance is scarce, being essential to optical functional materials. Here, we report a novel ultraviolet (UV) NLO tourmaline crystal with chemical composition NaAl 9 (BO 3) 3 Si 6 O 21 OH for the first time by combining first-principles analysis and experimental measurements. It exhibits a short UV absorption edge, considerable second harmonic generation effect and moderate birefringence, thereby facilitating its phase-matching coherent beam output in the range from visible to UV regions. [ABSTRACT FROM AUTHOR]

Commercial infrared (IR) nonlinear optical (NLO) materials are mainly from chalcopyrite‐type AMQ2 (A = Ag, Zn, M = Ga, Ge, Q = S, Se, P) crystals such as AgGaS2 (AGS), AgGaSe2 (AGSe), and ZnGeP2 (ZGP), in which the basic NLO‐active groups are MQ4 tetrahedral units. However, the small anisotropic character of them critical for small birefringence hinders the practical applications in the available IR wavelength range. In this study, a novel strategy for modulating birefringence is proposed using a cation regulation‐driven compressed hypertetrahedral layer approach and a family of AAg2MS4 (A = Na, K, Rb; M = P, As) IR NLO crystals are successfully obtained. Remarkably, the title compounds increase the birefringence to 0.12–0.15, about three times larger than that of AGS (0.04), while they can maintain large bandgaps and strong NLO effects. In addition, they exhibit congruent‐melting properties, beneficial for bulk single crystal growth. The work offers a firsthand access for designing and fabricating high‐performance IR NLO materials. [ABSTRACT FROM AUTHOR]

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]