Strong SHG Responses in a Beryllium-Free Deep-UV-Transparent Hydroxyborate via Covalent Bond Modification

Deep-ultraviolet (deep-UV) nonlinear optical (NLO) crystals are key materials in creating tunable deep-UV lasers for frequency conversion technology. However, practical application of the sole usable crystal, KBe₂ BO₃ F₂ , has been hindered by the high toxicity of beryllium and its layering tendency in crystal growth. Herein, we report a beryllium-free deep-UV NLO material NaSr₃ (OH)(B₉ O₁₆ )[B(OH)₄ ] (NSBOH), synthesized by a covalent bond modification strategy under hydrothermal conditions. Moisture-stable NSBOH exhibits strong second-harmonic generation (SHG) at 1064 nm (3.3 × KH₂ PO₄ ) and 532 nm (0.55 × β-BaB₂ O₄ ), both amongst the largest powder SHG responses for a deep-UV borate, with good phase-matchability and a short wavelength cutoff edge (below 190 nm). NSBOH possesses a 3D covalent anionic [B₉ O₁₉ ]_∞ honeycomb-like framework with no layering. The Sr²⁺ and Na⁺ ions, residing in the cavities of the anionic framework, act as templates for the assembly and favorable alignment of NLO-active groups, resulting in an optimal balance between strong SHG activities and wide UV transparency. These merits indicate NSBOH is a very attractive candidate for deep-UV NLO applications.