Cation-modulated aligned arrangement of [B3O7] units in an unprecedented 2∞[B3O5] layer with remarkable birefringence
摘要
Birefringence, as a crucial linear optical property of optical crystals, is pivotal for polarization modulation in birefringent crystals and phase-matching in nonlinear optical (NLO) crystals. Based on anionic group theory, the arrangement of advantageous B–O functional motifs in borate anionic frameworks can be adjusted by rational application of modification strategies, which can effectively promote the exploration of novel structures and optimization of optical properties. In this work, two novel borates containing distinct assembly modes of [B3O7] groups, Li2Rb2BaB18O30 (LRBBO) and K0.7Rb1.3BaB6O11 (KRBBO), were designed and synthesized based on the dimension reduction strategy induced by cation modification using LiB3O5 as the parent structure. Notably, KRBBO features an unprecedented 2∞[B3O5] layered structure and exhibits significantly enhanced birefringence (Δn = 0.08@546 nm) compared to both the parent compound and other compounds consisting of only [B3O7] groups. This work provides an effective strategy for designing novel short-wavelength borate optical crystals with large birefringence and enhancing the birefringence of [B3O7]-based NLO crystals to expand the deep-ultraviolet phase-matching capability.