Cyanurate anions are promising functional bulding blocks for birefringent materials. In this work, two new isocyanurates with mixed alkali cations were successfully synthesized by a hydrothermal method, namely, RbK(H2C3N3O3)(2)2H(2)O (I) and Cs3Li(H2C3N3O3)(4)3H(2)O (II). Compounds I and II are both featured with two-dimensional layers constructed by an isocyanurate six-membered ring extending along the bc plane. The characterization results show that both of these two new compounds exhibit wide band gaps (E-g similar to 5.2 eV) and giant birefringence (Delta n > 0.3) simultaneously. Moreover, theoretical calculations are performed to evaluate the relationship between microscopic structures and their anisotropic optical properties, indicating that the pi-conjugated groups make a dominant contribution to the optical anisotropy. These findings demonstrate that the combination of alkali cations and merits of pi-conjugated (iso)cyanurates would promote the study of optical integrated devices for emerging photonic technologies.

An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.

Herein, we have successfully synthesized two rubidium antimony (III) oxalates, namely, Rb2Sb(C2O4)2.5(H2O)3 and RbSb2(C2O4)F5, utilizing a low-temperature hydrothermal method. These two compounds share a similar chemical composition, consisting of Sb3+ cations with active lone pair electrons, alkali metal Rb+ ions, and planar π-conjugated C2O42- anions. However, they exhibit different symmetries, Rb2Sb(C2O4)2.5(H2O)3 is centrosymmetric (CS), while RbSb2(C2O4)F5 is noncentrosymmetric (NCS), which should be caused by the presence of F- ions. Notably, the NCS compound, RbSb2(C2O4)F5, demonstrates a moderate second-harmonic generation (SHG) response, approximately 1.3 times that of KH2PO4 (KDP), and exhibits a large birefringence of 0.09 at 546 nm. These characteristics indicate that RbSb2(C2O4)F5 holds promising potential as a nonlinear optical material for ultraviolet (UV) applications. Detailed structural analysis and theoretical calculations confirm that the excellent optical properties arise from the synergistic effects between Sb3+ cations with SCALP and planar π-conjugated [C2O4]2- groups.

Fluorine-containing borate crystal materials are particularly attractive due to their rich structural chemistry and excellent properties for optical applications. In this work, a new compound Ba3.75MgB7O14F2.5 has been synthesized through the high-temperature solution method. In the crystal structure of Ba3.75MgB7O14F2.5, the [B7O14] basic building unit and the [MgO3F3] octahedra are interconnected to create a complex three-dimensional network. The structural feature of the less commonly observed [B7O14] units is discussed, and it has been found that such units in Ba3.75MgB7O14F2.5 are most conducive to achieving large birefringence. In addition, Ba3.75MgB7O14F2.5 exhibits good thermal stability, a short ultraviolet cutoff of 203 nm, and large birefringence (0.081@546 nm), indicating its potential as a new UV birefringent crystal.

A new cesium hydroxyborate CsB3O4(OH)2, was designed and synthesized by a hydrothermal method. Remarkably, CsB3O4(OH)2 presents novel [B3O4(OH)2]∞ chains formed by [B3O4(OH)2] fundamental building blocks (FBBs). The report of less common [B3O4(OH)2] FBBs and [B3O4(OH)2]∞ chains in CsB3O4(OH)2 enriches the structural diversity of hydroxyborates. In addition, CsB3O4(OH)2 has a wide transparent window in the DUV spectral range and a large birefringence.

Transition-metal oxides (TMOs) are promising anode materials for high-performance lithium-ion batteries (LIBs) because of their abundant reserves and high theoretical capacity. However, the poor conductivity, unstable solid electrolyte interface (SEI) film, and poor cycling stability still limit their practical applications. As a novel kind of anode material, a high-entropy oxide (HEO) is a single-phase crystal structure composed of multiple metal elements, demonstrating a huge potential for energy storage applications due to the synergistic effect of various metal species. Herein, we have designed the porous spinel-phase HEO (Cr0.2Fe0.2Co0.2Ni0.2Zn0.2)3O4 synthesized at low temperature by a sol-gel method. On the one hand, the unique porous nanostructure not only promotes transport of the electrolyte but also alleviates the volume change of active materials upon cycling. On the other hand, the stabilization effect of entropy can suppress the formation of cation short-range order within the crystalline structure of HEO by a lattice distortion effect, thus guaranteeing a fast lithium-ion transport and achieving an excellent electrochemical performance. As a result, the as-prepared HEO-450 electrode delivers 1022 mAh/g after 1000 cycles at 1 A/g and 220 mAh/g at an ultrahigh current density of 30 A/g, respectively.