Effects of Cr Doping on Spinel LiMnO Morphology and Electrochemical Performance.

LiMnO, a significant cathode material for lithium-ion batteries, has garnered considerable attention due to its low cost and environmental friendliness. However, its widespread application is constrained by its rapid capacity degradation and short cycle life at elevated temperatures. To enhance the electrochemical performance of LiMnO, we employed a liquid-phase co-precipitation and calcination method to incorporate Cr into the LiMnO cathode material, successfully synthesizing a series of LiCrMnO (x = 0~0.

Effects of Ti Doping on the Structural Stability and Electrochemical Performance of Layered P2-NaMnO Cathodes for Sodium-Ion Batteries.

The P2-NaMnO cathode material has long been constrained by phase transitions induced by the Jahn-Teller (J-T) effect during charge-discharge cycles, leading to suboptimal electrochemical performance. In this study, we employed a liquid phase co-precipitation method to incorporate Ti during the precursor MnO synthesis, followed by calcination to obtain NaTiMnO materials. We investigated the effects of Ti doping on the structure, morphology, Mn concentration, and Na diffusion coefficients of NaTiMnO.

Multiple Polarization States in Hf ZrO Thin Films by Ferroelectric and Antiferroelectric Coupling.

HfO-based multi-bit ferroelectric memory combines non-volatility, speed, and energy efficiency, rendering it a promising technology for massive data storage and processing. However, some challenges remain, notably polarization variation, high operation voltage, and poor endurance performance. Here we show Hf ZrO (x = 0.

MnCoO spinel activates peroxymonosulfate for highly effective bisphenol A degradation with ultralow catalyst and persulfate usage.

Persulfates-based advanced oxidation processes are highly efficient in degrading refractory organic contaminants in wastewater. However, their practical application is often limited by the extensive consumption of catalysts and oxidants. Therefore, constructing catalysts with abundant and efficient reaction interfaces is essential for improving the efficiency of persulfate activation.

Deciphering the atomistic mechanism underlying highly tunable piezoelectric properties in perovskite ferroelectrics via transition metal doping.

Piezoelectricity, a fundamental property of perovskite ferroelectrics, endows the materials at the heart of electromechanical systems spanning from macro to micro/nano scales. Defect engineering strategies, particularly involving heterovalent trace impurities and derived vacancies, hold great potential for adjusting piezoelectric performance. Despite the prevalent use of defect engineering for modification, a comprehensive understanding of the specific features that positively impact material properties is still lacking, this knowledge gap impedes the advancement of a universally applicable defect selection and design strategy.

Preparation of TiCl from Ilmenite Concentrates via Carbothermal Reduction and Boiling Chlorination for Different Carbon Proportions.

Low-temperature boiling chlorination is the most common approach used to achieve a clean preparation of TiCl from ilmenite concentrates with high contents of calcium and magnesium impurities. However, this process did not systematically investigate the impact of the Ti/C ratio of the raw materials on the chlorination efficiency of Ti, Ca, and Mg elements. Thus, the influence of the carbon allocation proportion on the carbothermal reduction and boiling chlorination process of ilmenite concentrates with high contents of calcium and magnesium impurities was investigated in this study.

Palladium-assisted NO storage and release on CeZrO for passive NO adsorber in diesel exhaust aftertreatment.

Understanding Pd effects on NO storage and release is crucial for designing passive NO adsorber (PNA) to control NO emissions during diesel cold-starts. Herein, we report two oxidation states of Pd species on CeZrO regulated by metal-support interaction. Pd (0 < δ < 2) in Pd/CeZrO exhibits a high affinity for O adsorption, which promotes the oxidation of adsorbed NO to nitrates at 100 °C.

Crystal Form-Dependent MnS for Diabetic Wound Healing: Performance and Mechanistic Insights.

In pharmaceuticals, the structural and functional alterations induced by biotransformation are well-documented. Many pharmaceuticals exist in various crystal forms, which govern their transformation and significantly impact their activity. However, in the field of inorganic nanomedicine, there is a paucity of research focusing on the influence of crystal form-dependent "metabolism" (transformation) on their activity and biomechanism.

Development and application of a nitrogen oxides analyzer based on the cavity attenuated phase shift technique.

Nitrogen oxides (NO) are crucial in tropospheric photochemical ozone (O) production and oxidation capacity. Currently, the widely used NO measurement technique is chemiluminescence (CL) (CL-NO), which tends to overestimate NO due to atmospheric oxidation products of NO (i.e.

High-Performance Tunable Near-Infrared Emitters of Cr-Activated Garnet Phosphor Enabled by Chemical Unit Co-Substitution.

The escalating demand for portable near-infrared (NIR) light sources has posed a formidable challenge to the development of NIR phosphors characterized by high efficiency and exceptional thermal stability. Taking inspiration from the chemical unit co-substitution strategy, high-performance tunable (Lu Ca)(Ga Ge)O:6%Cr (x = 0-3) phosphors are designed with an emission center from 704 to 780 nm and a broadest full width at half maximum (FWHM) of up to 172 nm by introducing Ca and Ge ions into the garnet structure. In particular, LuGaO:6%Cr demonstrates an anti-thermal quenching phenomenon (I = 113.

Facet-Dependent Evolution of Active Components on Spinel CoO for Electrochemical Ammonia Synthesis.

Spinel cobalt oxides (CoO) have emerged as a promising class of catalysts for the electrochemical nitrate reduction reaction (eNORR) to ammonia, offering advantages such as low cost, high activity, and selectivity. However, the specific role of crystallographic facets in determining the catalysts' performance remains elusive, impeding the development of efficient catalysts. In this study, we have synthesized various CoO nanostructures with exposed facets of {100}, {111}, {110}, and {112}, aiming to investigate the dependence of the eNORR activity on the crystallographic facets.

Crystal Field Engineering Inducing Transformation from Narrow Band of Eu to Broadband of Eu.

The complete transformation from narrow peak emission of Eu to broadband emission of Eu was first realized in LaSrAlSiO:Eu series solutions relying on crystal field engineering and adjustment of synthesis parameters. The original red phosphor LaSrAlO:0.03Eupeaks at 703 nm originated from → transition of Eu under 395 nm excitation.

Unraveling Mechanism for Microstructure Engineering toward High-Capacity Nickel-Rich Cathode Materials.

Microstructural engineering on nickel-rich layered oxide (NRLO) cathode materials is considered a promising approach to increase both the capacity and lifespan of lithium-ion batteries by introducing high valence-state elements. However, rational regulation on NRLO microstructures based on a deep understanding of its capacity enhancement mechanism remains challenging. Herein for the first time, it is demonstrated that an increase of 14 mAh g in reversible capacity at the first cycle can be achieved via tailoring the micro and nano structure of NRLO through introducing tungsten.

Sulfur vacancy-rich bismuth sulfide nanowire derived from CAU-17 for radioactive iodine capture in complex environments: Performance and intrinsic mechanisms.

Effective capture and immobilization of volatile radioiodine from the off-gas of post-treatment plants is crucial for nuclear safety and public health, considering its long half-life, high toxicity, and environmental mobility. Herein, sulfur vacancy-rich Vs-BiS@C nanocomposites were systematically synthesized via a one-step solvothermal vulcanization of CAU-17 precursor. Batch adsorption experiments demonstrated that the as-synthesized materials exhibited superior iodine adsorption capacity (1505.

Electric-field-assisted proton coupling enhanced oxygen evolution reaction.

The discovery of Mn-Ca complex in photosystem II stimulates research of manganese-based catalysts for oxygen evolution reaction (OER). However, conventional chemical strategies face challenges in regulating the four electron-proton processes of OER. Herein, we investigate alpha-manganese dioxide (α-MnO) with typical Mn-O-Mn-HO motifs as a model for adjusting proton coupling.

Preparation of Solid Superacid SO/ZrO and SO/ZrO-MO (M=Ce, Co, Mn, and Zn) and Its Application in Toluene Nitration.

The nitration reaction of aromatic compounds is one of the extensively studied chemical reactions that result in the manufacturing of various industrial products applied in pharmaceuticals, dyes, perfumes, and explosives. A series of modified sulfated zirconia (SZ) catalysts SO/ZrO-MO (M=Ce, Co, Mn, Zn, and M/SZ) doped with different metal elements by a coprecipitation method were investigated in the toluene nitration reaction. Various characterization techniques (X-ray diffraction, Brunauer-Emmett-Teller, thermogravimetric analysis, X-ray photoelectron spectroscopy, and temperature-programmed desorption of ammonia) indicated that doping metal elements in SZ led to excellent catalytic properties, increasing the specific surface area of the catalyst and facilitating the formation of a stable tetragonal zirconia phase.

Two-dimensional materials by large-scale computations and chemical exfoliation of layered solids.

MXenes are a family of two-dimensional (2D) materials typically formed by etching the A element from a parent MAX phase. Computational screening for other 3D precursors suitable for such exfoliation is challenging because of the intricate chemical processes involved. We present a theoretical approach for predicting 2D materials formed through chemical exfoliation under acidic conditions by identifying 3D materials amenable for selective etching.

A Highly-Fluorinated Lithium Borate Main Salt Empowering Stable Lithium Metal Batteries.

Traditional lithium salts are difficult to meet practical application demand of lithium metal batteries (LMBs) under high voltages and temperatures. LiPF, as the most commonly used lithium salt, still suffers from notorious moisture sensitivity and inferior thermal stability under those conditions. Here, we synthesize a lithium salt of lithium perfluoropinacolatoborate (LiFPB) comprising highly-fluorinated and borate functional groups to address the above issues.

Tuning the Interface Stability of Nickel-Rich NCM Cathode Against Aggressive Structural Collapse via the Synergistic Effect of Additives.

Nickel-rich layered oxides are envisaged as one of the most promising alternative cathode materials for lithium-ion batteries, considering their capabilities to achieve ultrahigh energy density at an affordable cost. Nonetheless, with increasing Ni content in the cathodes comes a severe extent of Ni redox side reactions on the interface, leading to fast capacity decay and structural stability fading over extended cycles. Herein, dual additives of bis(vinylsulfonyl)methane (BVM) and lithium difluorophosphate (LiDFP) are adopted to synergistically generate the F-, P-, and S-rich passivation layer on the cathode, and the Ni activity and dissolution at high voltage are restricted.

Rh/InGaNO nanoarchitecture for light-driven methane reforming with carbon dioxide toward syngas.

Light-driven dry reforming of methane toward syngas presents a proper solution for alleviating climate change and for the sustainable supply of transportation fuels and chemicals. Herein, Rh/InGaNO nanowires supported by silicon wafer are explored as an ideal platform for loading Rh nanoparticles, thus assembling a new nanoarchitecture for this grand topic. In combination with the remarkable photo-thermal synergy, the O atoms in Rh/InGaNO can significantly lower the apparent activation energy of dry reforming of methane from 2.

A rechargeable calcium-oxygen battery that operates at room temperature.

Calcium-oxygen (Ca-O) batteries can theoretically afford high capacity by the reduction of O to calcium oxide compounds (CaO) at low cost. Yet, a rechargeable Ca-O battery that operates at room temperature has not been achieved because the CaO/O chemistry typically involves inert discharge products and few electrolytes can accommodate both a highly reductive Ca metal anode and O. Here we report a Ca-O battery that is rechargeable for 700 cycles at room temperature.