CsAlB3O6Cl: the rational construction of a KBBF-type structure with aligned 2∞[AlB3O6Cl] layers via introducing unprecedented [AlO3Cl] tetrahedra.

The first chloroaluminoborate, CsAlB3O6Cl, with innovative AlO3Cl tetrahedra and a perfect planar arrangement of [B3O6] groups, was structurally designed and synthesized via chlorination of [AlO4] tetrahedra. Simultaneously, the smooth introduction of the [AlO3Cl] group into borates initiates the development of a chloroaluminoborate and greatly enriches the structural chemistry of aluminoborates.

Structure-Prediction-Oriented Synthesis of Thiophosphates as Promising Infrared Nonlinear Optical Materials.

Oriented synthesis of functional materials is a focus of attention in material science. As one of the most important function materials, infrared nonlinear optical materials with large second harmonic generation effects and broad optical bandgap are in urgent need. In this work, directed by the theoretical structure prediction, the first series of non-centrosymmetric (NCS) alkali-alkaline earth metal [PS4]-based thiophosphates LiCaPS4 (Ama2), NaCaPS4 (P21), KCaPS4 (Pna21), RbCaPS4 (Pna21), CsCaPS4 (Pna21) were successfully synthesized. Comprehensive characterizations reveal that ACaPS4 could be regarded as promising IR NLO materials, exhibiting wide bandgap (3.77-3.86 eV), moderate birefringence (0.027-0.064 at 1064 nm), high laser-induced damage threshold (LIDT, ~10 × AGS), and suitable phase-matching second harmonic generation responses (0.4-0.6 × AGS). Structure-properties analyses illustrate that the Ca-S bonds show non-ignorable covalent feature, and [PS4] together with [CaSn] units play dominant roles to determine the bandgap and SHG response. This work indicates that Li-, Na- and K- analogs may be promising infrared nonlinear optical material candidates, and this is the first successful case of "prediction to synthesis" involving infrared (IR) nonlinear optical (NLO) crystals in the thiophosphate system and may provide a new avenue to the design and oriented synthesis of high-performance function materials in the future.

Wide band gap selenide infrared nonlinear optical materials AIIMg6Ga6Se16 with strong SHG responses and high laser-induced damage thresholds.

Infrared (IR) nonlinear optical (NLO) materials with strong NLO response, wide band gap and high laser-induced damage threshold (LIDT) are highly expected in current laser technologies. Herein, by introducing double alkaline-earth metal (AEM) atoms, three wide band gap selenide IR NLO materials AIIMg6Ga6Se16 (AII = Ca, Sr, Ba) with excellent linear and NLO optical properties have been rationally designed and fabricated. AIIMg6Ga6Se16 (AII = Ca, Sr, Ba) are composed of unique [AIISe6] triangular prisms, [MgSe6] octahedra and [GaSe4] tetrahedra. The introduction of double AEMs effectively broadens the band gaps of selenide-based IR NLO materials. Among them, CaMg6Ga6Se16, achieving the best balance between the second-harmonic generation response (∼1.5 × AgGaS2), wide band gap (2.71 eV), high LIDT (∼9 × AgGaS2), and moderate birefringence of 0.052 @ 1064 nm, is a promising NLO candidate for high power IR laser. Theoretical calculations indicate that the NLO responses and band gaps among the three compounds are mainly determined by the NLO-active [GaSe4] units. The results enrich the chemical diversity of chalcogenides, and give some insight into the design of new functional materials based on the rare [AIISe6] prismatic units.

Recent advances in rational structure design for nonlinear optical crystals: leveraging advantageous templates.

Nonlinear optical (NLO) crystals that can expand the spectral range of laser outputs have attracted significant attention for their optoelectronic applications. The research progress from the discovery of new single crystal structures to the realization of final device applications involves many key steps and is very time consuming and challenging. Consequently, exploring efficient design strategies to shorten the research period and accelerate the rational design of novel NLO materials has become imperative to address the pressing demand for advanced materials. The recent shift in paradigm toward exploring new NLO crystals involves significant progress from extensive "trial and error" methodologies to strategic approaches. This review proposes the concept of rational structure design for nonlinear optical crystals leveraging advantageous templates. It further discusses their optical characteristics, promising applications as second-order NLO materials, and the relationship between their structure and performance, and highlights urgent issues that need to be addressed in the field of NLO crystals in the future. The review aims to provide ideas and driving impetus to encourage researchers to achieve new breakthroughs in the next generation of NLO materials.

Two Hydroxyfluorooxoborates Achieving Deep-Ultraviolet Cutoff Edges and Moderate Birefringence by Assembling Multi-Anionic Groups.

Assembling multi-anionic groups is conducive to utilizing respective advantage to achieve the enhancement of optical performance. Two new hydroxyfluorooxoborates, Ama2-Rb2B3O3F4(OH) and K8Cs2B15O14(OH)7F20 ⋅ H2O with [B3O3F4(OH)] six-membered rings were synthesized for the first time. The title compounds exhibit short ultraviolet cutoff edges (<200 nm) and K8Cs2B15O14(OH)7F20 ⋅ H2O possesses a moderate experimental refractive index difference of 0.051@546 nm.

Where do the Fluorine Atoms Go in Inorganic-Oxide Fluorinations? A Fluorooxoborate Illustration under Terahertz Light.

The substitution of fluorine atoms for oxygen atoms/hydroxyl groups has emerged as a promising strategy to enhance the physical and chemical properties of oxides/hydroxides in fluorine chemistry. However, distinguishing fluorine from oxygen/hydroxyl in the reaction products poses a significant challenge in existing characterization methods. In this study, we illustrate that terahertz (THz) spectroscopy provides a powerful tool for addressing this challenge. To this end, we investigated two fluorination reactions of boric acid, utilizing MHF2 (M=Na, C(NH2)3) as fluorine reagents. Through an interplay between THz spectroscopy and solid-state density functional theory, we have conclusively demonstrated that fluorine atoms exclusively bind with the sp3-boron but not with the sp2-boron in the reaction products of Na[B(OH)3][B3O3F2(OH)2] (NaBOFH) and [C(NH2)3]2B3O3F4OH (GBF2). Based on this evidence, we have proposed a reaction pathway for the fluorinations under investigation, a process previously hindered due to structural ambiguity. This work represents a step forward in gaining a deeper understanding of the precise structures and reaction mechanisms involved in the fluorination of oxides/hydroxides, illuminated by the insights provided by THz spectroscopy.

New antimony fluorooxoborates with strong birefringence and unprecedented structural characterisation.

Fluorooxoborates constitute a rich source of optical crystals due to their structural diversity and excellent performance. Antimony fluorooxoborates with stereochemically active lone pairs of electrons still have not been found, although the first antimony borate was discovered several years ago. In this study, we have achieved the successful synthesis of the first antimony(III) fluorooxoborate with an unprecedented [B2O4F]∞ chain, namely SbB2O4F. Remarkably, SbB2O4F shows strong birefringence (0.171@1064 nm) and short UV cutoff edges (about 220 nm) according to calculations. The birefringence of SbB2O4F mainly originates from the highly distorted [SbO4] groups.

AIB3 IIC2 IIIQ6 VIXVII: A Thioborate Halide Family for Developing Wide Bandgap Infrared Nonlinear Materials by Coupling Planar [BS3] and Polycations.

Developing high-performance infrared (IR) nonlinear optical (NLO) materials is urgent but challenging due to the competition between NLO coefficient and bandgap in one compound. Herein, by coupling NLO-active [BS3] planar units and halide-centered polycations, six new metal thioborate halides ABa3B2S6X (A = Rb, Cs; X = Cl, Br, I) composed of zero-dimensional [XBamRbn/Csn] polycations and [BS3] units, belonging to a new A I B 3 II C 2 III Q 6 VI X VII ${\mathrm{A}}^{\mathrm{I}}{\mathrm{B}}_{3}^{\mathrm{II}}{\mathrm{C}}_{2}^{\mathrm{III}}{\mathrm{Q}}_{6}^{\mathrm{VI}}{\mathrm{X}}^{\mathrm{VII}}$ family, are rationally designed and fabricated. The compounds show an interesting structural transition from Pbcn (ABa3B2S6Cl) to Cmc21 (ABa3B2S6Br and ABa3B2S6I) driven by the clamping effect of polycationic frameworks. ABa3B2S6Br and ABa3B2S6I are the first series metal thioborate halide IR NLO materials, and the introduction of [BS3] unit effectively widens the bandgap of planar unit-constructed chalcogenides. ABa3B2S6Br and ABa3B2S6I, exhibiting wide bandgaps (3.55-3.60 eV), high laser-induced damage thresholds (≈ 6 × AgGaS2), and strong SHG effects (0.5-0.6 × AgGaS2) with phase-matching behaviors, are the promising IR NLO candidates for high-power laser applications. The results enrich the chemical and structural diversity of boron chemistry and give some insights into the design of new IR NLO materials with planar units.

PbTeB4O9: a lead tellurium borate with unprecedented fundamental building block [B4O10] and large birefringence.

Herein, the first lead tellurium borate, PbTeB4O9, with an unprecedented fundamental building block [B4O10] was successfully synthesized. The near-parallel alignment of [B4O10] groups and [TeO3] polyhedra resulted in a high birefringence (0.099@1064 nm). The structure-property relationship was discussed by using the first-principles calculations.

Fluorination Strategy Towards Symmetry Breaking of Boron-centered Tetrahedron for Poly-fluorinated Optical Crystals.

Borate crystals can be chemically and functionally modified by the fluorination strategy, which encourages the identification of emerging fluorooxoborates with a structure and set of characteristics not seen in any other oxide parents. However, the bulk of fluorooxoborates have been found accidentally, rational methods of synthesis are required, particularly for the infrequently occurring poly-fluorinated components. Herein, we reported the use of bifluoride salts as a potent source of fluorine to prepare fluorooxoborates that contain rarely tri-fluorinated [BF3 X] (X=O and CH3 ) tetrahedra and eleven compounds were found. We identified the optical properties of the organofluorinated group [CH3 BF3 ] and their potential for nonlinear optics for the first time. Among these, two non-centrosymmetric components hold potential for the production of 266 nm harmonic coherent light for nonlinear optics, and more crucially, have the benefit of growing large size single crystals. Our study establishes experimental conditions for the coexistence of the diverse functional groups, enabling the production of poly-fluorinated optical crystals.

Cd8(BO3)4SiO4: Metal Cation Inducing the Formation of Isolated [BO3] and [SiO4] Units in Borate Silicate.

The first compound of cadmium-borate silicate Cd8(BO3)4SiO4, crystallizing in space group P42/n (no. 86), has been successfully synthesized by the conventional high-temperature solution method and melts congruently. The zero-dimensional anionic groups of Cd8(BO3)4SiO4 are isolated [BO3] triangles and isolated [SiO4] tetrahedra which are filled in the framework formed by [CdO6] polyhedra. It has a moderate birefringence (Δn = 0.053 at 546 nm), which is measured by experiment and evaluated by first-principles calculations; meanwhile, the source of birefringence is revealed through the response electronic distribution anisotropy method. The UV-vis-NIR diffuse reflectance spectrum indicates that Cd8(BO3)4SiO4 possesses a wide optical transparency range, with a UV cutoff edge at about 254 nm. This work enriches the structure chemistry of borate silicates, and we discussed the possible methods for the exploration and synthesis of novel optical crystals possessing zero-dimensional anionic groups in the borate silicate system.

(C(NH2)3)2(I2O5F)(IO3)(H2O) and C(NH2)3IO2F2: Two Guanidine Fluorooxoiodates with Wide Band Gap and Large Birefringence.

Enhancing anisotropy through an effective synergistic arrangement of anionic and cationic groups is crucial for improving the birefringence optical properties of materials. In this work, by transforming I-O into I-F through the fluorination strategy, two metal-free guanidine fluorooxoiodates (C(NH2)3)2(I2O5F)(IO3)(H2O) and C(NH2)3IO2F2 and one guanidine iodate C(NH2)3IO3 were successfully synthesized using the hydrothermal method. An unprecedented dimer [I2O5F] formed by [IO3F] and [IO3] in (C(NH2)3)2(I2O5F)(IO3)(H2O) was found, which greatly enriches the structural diversity of fluorooxoiodates. All three compounds feature a relatively large birefringence (Δn = 0.068, 0.110 and 0.075 at 546 nm) and a short ultraviolet cutoff edge. The theoretical calculation was carried out to understand the electronic structures and linear optical properties.

[RbSr3X][(BS3)2] (X = Cl, Br): two salt-inclusion thioborates with large birefringence and structure transformation from centrosymmetric to asymmetric.

[RbSr3X][(BS3)2] (X = Cl, Br), two salt-inclusion chalcogenides with planar [BS3] as anionic units, were obtained. Structure analysis indicates that the size effect of halogens may adjust the arrangement between the [BS3] units and further lead to the CS-to-NCS structure transformation. Experimental characterizations reveal that they have wide bandgaps (3.64-3.70 eV), large birefringence (0.136-0.144) and high LIDT (12-14 × AgGaS2). This work indicates that the thioborate family is a rich source to explore structure chemistry and promising infrared functional materials.

Breaking the Inherent Interarrangement of [B3O6] Clusters for Nonlinear Optics with Orbital Hybridization Enhancement.

The [B3O6] group as a prime functional unit provides borates with intrinsic properties that are modified by coordination to cations. Inherent [B3O6] cluster structures in borates exclusively made of them have a near-plane configuration, with more than 90% of them having a maximum dihedral angle of zero and the remaining ones being less than 13°. Although such an inherent configuration can produce considerable birefringence for good phase-matching ability, this is not conducive to obtaining high conversion efficiency and beam quality due to the walk-off effects in the nonlinear optical process. In this article, two new borate halides Ca2B3O6X (X = Cl and Br) were reported, in which the confinement effects of distorted halogen-centered secondary building blocks compress the existence space of [B3O6] primitives, resulting in the nonparallel arrangement between [B3O6] clusters in this series. Both compounds show large second harmonic generation effects, and more importantly, the broken inherent interarrangement of [B3O6] clusters makes them a moderate birefringence and small walk-off angle. Their moderate birefringence is due to the large angular alignment between [B3O6] clusters, resulting from the orbital hybridization between the Ca s and the O p orbitals of the terminal O atoms on [B3O6] clusters. Our model supports this viewpoint and offers guidelines for rearranging [B3O6] clusters' arrangements in borates.

Hydroxyfluorooxoborate (NH4)[C(NH2)3][B3O3F4(OH)] for exploring the effects of cation substitution on structure and optical properties.

Cation substitution is a straightforward but effective technique for improving the structure and properties; however, controlling directed substitution still poses significant difficulties. Herein, a metal-free hydroxyfluorooxoborate (NH4)[C(NH2)3][B3O3F4(OH)] has been synthesized using the strategy of heterologous substitution based on the template of A2[B3O3F4(OH)]. Tunable structure and optical properties have been achieved via varied A-site cation substitution. The intrinsic mechanism for this tunability was established by crystallography and theoretical research.

Zn2 HgP2 S8 : A Wide Bandgap Hg-Based Infrared Nonlinear Optical Material with Large Second-Harmonic Generation Response.

Hg-based chalcogenides, as good candidates for the exploration of high-performance infrared (IR) nonlinear optical (NLO) materials, usually exhibit strong NLO effects, but narrow bandgaps. Herein, an unprecedented wide bandgap Hg-based IR NLO material Zn2 HgP2 S8 (ZHPS) with diamond-like structure is rationally designed and fabricated by a tetrahedron re-organization strategy with the aid of structure and property predictions. ZHPS exhibits a wide bandgap of 3.37 eV, which is the largest one among the reported Hg-based chalcogenide IR NLO materials and first breaks the 3.0 eV bandgap "wall" in this system, resulting in a high laser-induced damage threshold (LIDT) of ≈2.2 × AgGaS2 (AGS). Meanwhile, it shows a large NLO response (1.1 × AGS), achieving a good balance between bandgap (≥3.0 eV) and NLO effect (≥1 × AGS) for an excellent IR NLO material. DFT calculations uncover that, compared to normal [HgS4 ]n , highly distorted [HgS4 ]d tetrahedral units are conducive to generating wide bandgap, and the wide bandgap in ZHPS can be attributed to the strong s-p hybridization between Hg─S bonding in distorted [HgS4 ]d , which gives some insights into the design of Hg-based chalcogenides with excellent properties based on distorted [HgS4 ]d tetrahedra.

Improved Birefringence Activated by Tetrahedra Decorated with a Single Linear Unit.

Performance enhancement induced by structural modification has long been the target in materials science fields. Direct evidence to witness the effectivity of one strategy is challenging and necessary. In this work, a tetrahedra-decoration strategy was proposed to improve the birefringent performance sharply, namely decorating the tetrahedra with a single linear [S2 ] unit. The strategy was verified by comprehensive characterization of two thiogermanates K2 BaGeS4 and K2 BaGeS5 , which crystallize in the same space group, have similar unit cells and the same units arrangements. Theoretical characterization verified that the [GeS5 ] group has much larger polarization anisotropy than [GeS4 ], further demonstrated that the linear [S2 ] led to the sharp birefringence enlargement of K2 BaGeS5 (0.19 vs 0.03 of K2 BaGeS4 ). This work provides a new guiding thought to improve the birefringence performance.

Stereochemically Active Tin(II)-Induced Enhancement of Birefringence in SnII SnIV (PO4 )2 and SrSn(PO4 )PO2 (OH)2.

Two new tin(II) phosphates, SnII SnIV (PO4 )2 and SrSn(PO4 )PO2 (OH)2 , were synthesized by the high-temperature solution method and hydrothermal method, respectively. Theoretical study indicates that by introducing tin(II) with stereochemical activity lone pairs (SCALP) in metal phosphates, the birefringence was enhanced, 0.048@1064 nm for SnII SnIV (PO4 )2 and 0.080@1064 nm for SrSn(PO4 )PO2 (OH)2 .

Two Ultraviolet Optical Crystals K6B12O19F4 and K12B28O48: The Effects of Metal Cations Size and the F Ions on the Structure.

Borates and fluorooxoborates are advanced optical materials with great potential applications in the ultraviolet (UV) and deep ultraviolet (DUV) regions. Herein, two new UV optical crystals K6B12O19F4 and K12B28O48 were synthesized. Among them, K6B12O19F4 has a rare disorder of BO3 and BO4 units, which is the first time this disordered type has been found in fluorooxoborates. In this paper, the properties of K6B12O19F4 and K12B28O48 were tested and calculated, and their crystal structures and structural evolution were carefully analyzed. In addition, the effects of metal cations size and F ions on the crystal structure were analyzed. This research enriches the structural chemistry of borates and fluorooxoborates, and provides experience for the design of new UV optical crystals.