Expansion counteraction effect assisted vanadate with rich oxygen vacancies as a high cycling stability cathode for aqueous zinc-ion batteries.

In this study, a novel tunnel structure vanadate NaVO (NaVO) cathode for aqueous zinc ion batteries (AZIBs) is facilely fabricated by thermal decomposition of polyoxovanadate containing NH ions. The NaVO cathode is characterized by abundant oxygen vacancies and nanometer dimensions. These attributes can offer extra reaction sites and suppress structural collapse during circulation.

Confining Liquid Electrolytes in a Nitrogen-Rich Nanoporous Carbon Sponge for Superior Lithium-Ion Conduction.

Solid-state Li-ion batteries are recognized as highly promising energy storage devices due to their ability to overcome issues related to the inferior cycle life and potential risks of traditional liquid Li-ion batteries. However, developing solid-state electrolytes with fast Li-ion conductivity continues to be a major challenge. In this study, we present a family of quasi-solid-state electrolytes (QSSEs) synthesized by confining liquid electrolytes within a N-rich porous carbon sponge, exhibiting superior Li-ion conduction for solid-state battery applications.

A Superior Ionic Conducting Plastic Crystal Near Room Temperature with Electrical Bistability and Magnetic Transition.

Multifunctional ionic plastic crystals (IPCs) are a class of unique materials that exhibit a wide range of advanced applications. In this work, we proposed a strategy for the design of multifunctional, superior ion-conducting IPCs with bistability in both magnetic and electric properties, moreover, we successfully prepared and thoroughly characterized such an IPC, [PMPyr][Ni(mnt)] (1; PMPyr=N-propyl-N-methylpyrrolidinium, and mnt=maleonitriledithiolate). Plastic crystal 1 exhibits superior ion conduction near room temperature, and its ion conductivity reaches the order of 10 S cm at 373 K.

Multifunctional chiral metal hydrogen-bonded organic frameworks constructed from lanthanide ions with a trigonal prismatic coordination environment.

Two pairs of chiral enantiomers D/L-Dy(PMP)·2HO (D-1/L-1) and D/L-Yb(PMP)·2HO (D-2/L-2) were synthesized by the introduction of enantiomerically pure D/L-PMP (PMP = (phosphonomethyl)proline) ligands into lanthanide coordination chemistry. The chiral characteristics of these products were confirmed by single crystal X-ray diffraction, second harmonic generation (SHG) measurements and circular dichroism (CD) spectroscopy. These complexes are composed of 1D chains constructed from lanthanide ions with a trigonal prismatic coordination geometry and PMP ligands.

Spin and dielectric transitions promoted by dimerization of anionic radical stacks and volume-conserving motion of cations in an ion-pair compound.

Demonstrating the mechanism of a structural phase transition (SPT) is significantly important for guiding the precise design of new phase transition materials. Herein, an ion-pair compound [DPIm][Ni(mnt)] (1, DPIm = 1,3-dipropylimidazolium and mnt = maleonitriledithiolate) has been obtained and thoroughly characterized through microanalysis, spectral, and thermal analysis techniques. The [Ni(mnt)] anions form columnar stacks, featuring one-dimensional (1D) = ½ spin chains.

Confined Polyethylene Glycol Anchored in Kaolinite as High Ionic Conductivity Solid-State Electrolyte for Lithium Batteries.

Solid-state electrolytes (SSEs) have garnered significant attention as critical materials for enabling safer, energy-dense, and reversible electrochemical energy storage in batteries. Among the various types of solid electrolytes developed, composite polymer electrolytes (CPEs) have stood out as some of the most promising candidates due to their well-rounded performance. In this study, we choose polyethylene glycol (PEG) as the covalent grafting intercalant and lithium perchlorate as carrier source to prepare a fast lithium ion conductor, K-PEG-Li doped with clay-based active filler as a CPE.

Correction: Single molecule magnet features in luminescent lanthanide coordination polymers with heptacoordinate Dy/Yb(III) ions as nodes.

Correction for 'Single molecule magnet features in luminescent lanthanide coordination polymers with heptacoordinate Dy/Yb(III) ions as nodes' by Xiang-Tao Dong , , 2023, , 12686-12694, https://doi.org/10.1039/D3DT02106H.

Prussian blue analogue derived from leather waste as a bifunctional catalyst in zinc-air batteries.

A Prussian blue analogue was synthesized using biomass leather waste as a precursor by doping with Co ions. This material, demonstrates good performance in both the oxygen reduction reaction and oxygen evolution reaction, and exhibits excellent charge-discharge performance and stability in zinc-air batteries.

Polymorph transformation in a mixed-stacking nickel-dithiolene complex with the derivative of 4,4'-bipyridinium.

In this study, two polymorphs of the [1,1'-dibutyl-4,4'-bipyridinium][Ni(mnt)] salt () were synthesized. The dark-green polymorph (designated as 1-g) was prepared under ambient conditions by the rapid precipitation method in aqueous solutions. Subsequently, the red polymorph (labeled as 1-r) was obtained by subjecting 1-g to ultrasonication in MeOH at room temperature.

Mixed-Dimensional (2D/3D/3D) Heterostructured Vanadium Oxide with Rich Oxygen Vacancies for Aqueous Zinc Ion Batteries with High Capacity and Long Cycling Life.

Heterostructure engineering and oxygen vacancy engineering are the most promising modification strategies to reinforce the Zn ion storage of vanadium oxides. Herein, a rare mixed-dimensional material (), composed of VO (2D), VO (3D), and VO (3D) heterostructures, rich in oxygen vacancies, was synthesized via thermal decomposition of layered ammonium vanadate. The cathode provides an exceptional discharge capacity (411 mA h g at 0.

Thermotropic Structure Phase Transitions and Two Types of Thermochromic Behaviors in a Bromoargentate Cluster [Pr-dabco]AgBr.

Organic-inorganic silver halide hybrids show abundant phase transitions and thermochromism. However, it is very rare that silver halides exhibit thermochromism related to thermotropic structure phase transition. Herein, a bromoargentate hybrid, [Pr-dabco]AgBr () (Pr-dabco = 1-propyl-1,4-diazabicyclo-[2.

Supramolecular crystals of Mn(15-crown-5)(MnCl)(DMF) with dielectric phase transition, high quantum yield and phase transition-induced luminescence enhancement behavior.

The supramolecular crystals, Mn(15-crown-5)(MnCl)(DMF), (1; 15-crown-5 = 1,4,7,10,13-pentaoxacyclopentadecane), were synthesized a self-assembly strategy under ambient conditions. Comprehensive characterization of the crystals involved microanalysis for C, H, and N elements, thermogravimetric (TG) analysis, differential scanning calorimetry (DSC) and single-crystal X-ray diffraction techniques. The results reveal that 1 undergoes a two-step thermotropic and isostructural phase transition at around 217 K and 351 K upon heating.

Acidified Nitrogen Self-Doped Porous Carbon with Superprotonic Conduction for Applications in Solid-State Proton Battery.

Solid proton electrolytes play a crucial role in various electrochemical energy storage and conversion devices. However, the development of fast proton conducting solid proton electrolytes at ambient conditions remains a significant challenge. In this study, a novel acidified nitrogen self-doped porous carbon material is presented that demonstrates exceptional superprotonic conduction for applications in solid-state proton battery.

Single molecule magnet features in luminescent lanthanide coordination polymers with heptacoordinate Dy/Yb(III) ions as nodes.

Two sets of 1D/2D lanthanide coordination polymers with formulas of Ln(oqa)·2HO [Hoqa = 2-(4-oxoquinolin-1(4)-yl) acetic acid, Ln = Dy (1), Yb (2)] and Ln(oaa)(HCOO)(HO) [Hoaa = 2-(9-oxoacridin-10(9)-yl) acetic acid, Ln = Dy (3), Yb (4)] have been synthesized and their physical properties were investigated. All four complexes are constructed from seven-coordinate lanthanide ions and corresponding organic linkers. The lanthanide ions in 1 and 2 adopt a pentagonal bipyramid coordination geometry, whereas the coordination geometry of lanthanide ions in 3 and 4 can be described as a capped octahedron.

Organic-inorganic haloargentate hybrids of [Me-dabco]AgX (X = I or Br) with halide ions manipulating the crystal structure, phase transition, and dielectric behavior.

Two haloargentate hybrids, [Me-dabco]AgX (Me-dabco = 1-methyl-1,4-diazabicyclo-[2.2.2]octan-1-ium, X = I (1) or Br (2)), with the same formula but different structures have been synthesized by a slow evaporation method and characterized by microanalysis, infrared spectroscopy, thermogravimetric, and powder X-ray diffraction techniques.

Thermochromism of rapid responses to temperature changes mechanochromism in a Ni-dithiolene complex salt.

A thermochromic or mechanochromic material can switch between at least two stable states in response to changes in temperature or static pressure/strain. In this study, we investigated a Ni-dithiolene dianion salt, 1,1'-diheptyl-4,4'-bipyridinium bis(maleonitriledithiolato)nickelate (1), and found that its cations and anions stack alternately to form a uniform mixed stack. These mixed stacks then combine to form a molecular solid through Coulomb and van der Waals interactions.

Phase transition and ionic conduction enhancement induced by co-doping of LiI and MnI in a one-dimensional lead iodide perovskite.

Herein, we demonstrated the unique advantage of a mechanochemical reaction to prepare a salt with hard and soft acid and base ions concurrently by solution synthesis owing to the soft acid preferring to combine with the soft base and . We prepared BuNLiMnPbI ( = 0.011-0.

A {CuI} chain hybrid with two-step phase transition, switchable dielectrics, thermochromism and piezochromism.

Stimuli-responsive smart materials have applications in a range of technologies. Herein, we present a hybrid (1), built from MeEtN organic cations and {CuI} inorganic chains with Cu⋯Cu metal⋯metal interactions. The two-step phase transition undergone in 1 on the first heating and the phase transition at a lower temperature show symmetry-broken features, leading to switchable dielectrics; the one at a higher temperature displays isomorphic characteristics.

Two Organic-Inorganic Manganese(II) Halide Hybrids Showing Compelling Photo- and Mechanoluminescence as well as Rewritable Anticounterfeiting Printing.

Two organic-inorganic manganese(II) halide hybrids (OIMHs) with formulas of [(TEA)(TMA)]MnCl () and [(TPA)(TMA)](MnCl) () (TEA = tetraethylammonium, TMA = tetramethylammonium, and TPA = tetrapropylammonium) were synthesized by a mixed-ligand strategy. Both compounds crystallize in the acentric space group and are composed of isolated [MnCl] tetrahedral units separated by two types of organic cations. They show high thermal stability and emit strong green light with different emission bandwidths, quantum yields, and high-temperature photostability.

MOF-Polymer Mixed Matrix Membranes as Chemical Protective Layers for Solid-Phase Detoxification of Toxic Organophosphates.

Zirconium-based metal-organic frameworks (Zr-MOFs) have been demonstrated as potent catalysts for the hydrolytic detoxification of organophosphorus nerve agents and their simulants. However, the practical implementation of these Zr-MOFs is limited by the poor processability of their powdered form and the necessity of water media buffered by a volatile liquid base in the catalytic reaction. Herein, we demonstrate the efficient solid-state hydrolysis of a nerve agent simulant (dimethyl-4-nitrophenyl phosphate, DMNP) catalyzed by Zr-MOF-based mixed matrix membranes.

Dielectrics and possible ferroelectricity in diol/glycerol covalently grafted kaolinites.

Kaolinite possesses a structure with asymmetrically layered 1 : 1 dioctahedral aluminum silicate, and this structural property provides a useful platform for creating new cost-efficient functional materials that require noncentrosymmetric crystal packing. In this study, we prepared three covalently grafted kaolinites of propanediol (PD)/butanediol (BD)/glycerol (GL) by forming Al-O-C bonds between the OH groups of PD/BD/GL and the surface of kaolinite (K). Three covalently grafted kaolinites (K-PD, K-BD and K-GL) were characterized by X-ray diffraction, infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy and microanalysis for C, H and N elements.

Two-step thermotropic phase transition and dielectric relaxation in 1D supramolecular lead iodide perovskite [NH@18-crown ether]PbI.

The supramolecular lead iodide perovskite crystals, {[NH(18-crown-6)]PbI} (1), (18-crown-6 = 1,4,7,10,13,16-hexaoxacyclooctadecane), was successfully achieved by a facile solvent evaporation strategy using a DMF solution containing equal molar quantities of PbI, NHI and 18-crown-6. The supramolecular perovskite was characterized by microanalysis for C, H and N elements, thermogravimetric (TG) analysis, differential scanning calorimetry (DSC), powder X-ray diffraction (PXRD) and single crystal X-ray diffraction techniques. DSC measurements demonstrated that 1 experiences a two-step thermotropic phase transition around 333 K and 383 K, respectively.

Inorganic Chain Mediated Excitonic Properties in One-Dimensional Lead Halide Hybrid Perovskites.

Semiconductors that emit intrinsic white light are considered next-generation lighting sources. Herein, the broadband emission of one-dimensional (1D) lead halide perovskites, TMAPbBrI ( = 0, 1, 1.5, 2, 3; TMA = tetramethylammonium), is systematically investigated.