Tunable Magnetism in Atomically Thin Itinerant Antiferromagnet with Room-Temperature Ferromagnetic Order.

Addressing the need for modulated spin configurations is crucial, as they serve as the foundational building blocks for next-generation spintronics, particularly in atomically thin structures and at room temperature. In this work, we realize intrinsic ferromagnetism in monolayer flakes and tunable ferro-/antiferromagnetism in (Fe0.56Co0.44)5GeTe2 antiferromagnets. Remarkably, the ferromagnetic ordering (≥1 L) and antiferromagnetic ordering (≥4 L) remain discernible up to room temperature. The TC (∼310 K) of the monolayer flakes sets a record high for known exfoliated monolayer van der Waals magnets. Within the framework of A-type antiferromagnetism, a notable odd-even layer-number effect at elevated temperatures (T = 150 K) is observed. Of particular interest is the strong ferromagnetic order in even-layer flakes at low temperatures. The intricate interplay among magnetic field strength, layer number, and temperature gives rise to a diverse array of phenomena, holding promise not only for new physics but also for practical applications.

Lattice Engineering via Transition Metal Ions for Boosting Photoluminescence Quantum Yields of Lead-Free Layered Double Perovskite Nanocrystals.

Lead-free layered double perovskite nanocrystals (NCs), i.e., Cs4M(II)M(III)2Cl12, have recently attracted increasing attention for potential optoelectronic applications due to their low toxicity, direct bandgap nature, and high structural stability. However, the low photoluminescence quantum yield (PLQY, <1%) or even no observed emissions at room temperature have severely blocked the further development of this type of lead-free halide perovskites. Herein, two new layered perovskites, Cs4CoIn2Cl12 (CCoI) and Cs4ZnIn2Cl12 (CZnI), are successfully synthesized at the nanoscale based on previously reported Cs4CuIn2Cl12 (CCuI) NCs, by tuning the M(II) site with different transition metal ions for lattice tailoring. Benefiting from the formation of more self-trapped excitons (STEs) in the distorted lattices, CCoI and CZnI NCs exhibit significantly strengthened STE emissions toward white light compared to the case of almost non-emissive CCuI NCs, by achieving PLQYs of 4.3% and 11.4% respectively. The theoretical and experimental results hint that CCoI and CZnI NCs possess much lower lattice deformation energies than that of reference CCuI NCs, which are favorable for the recombination of as-formed STEs in a radiative way. This work proposes an effective strategy of lattice engineering to boost the photoluminescent properties of lead-free layered double perovskites for their future warm white light-emitting applications.

Rational Design of Multinary Metal Chalcogenide Bi0.4Sb1.6Te3 Nanocrystals for Efficient Potassium Storage.

Multinary metal chalcogenides hold considerable promise for high-energy potassium storage due to their numerous redox reactions. However, challenges arise from issues such as volume expansion and sluggish kinetics. Here, a design featuring a layered ternary Bi0.4Sb1.6Te3 anchored on graphene layers as a composite anode, where Bi atoms act as a lattice softening agent on Sb, is presented. Benefiting from the lattice arrangement in Bi0.4Sb1.6Te3 and structure, Bi0.4Sb1.6Te3/graphene exhibits a mitigated expansion of 28% during the potassiation/depotassiation process and demonstrates facile K+ ion transfer kinetics, enabling long-term durability of 500 cycles at various high rates. Operando synchrotron diffraction patterns and spectroscopies including in situ Raman, ex situ adsorption, and X-ray photoelectron reveal multiple conversion and alloying/dealloying reactions for potassium storage at the atomic level. In addition, both theoretical calculations and electrochemical examinations elucidate the K+ migration pathways and indicate a reduction in energy barriers within Bi0.4Sb1.6Te3/graphene, thereby suggesting enhanced diffusion kinetics for K+. These findings provide insight in the design of durable high-energy multinary tellurides for potassium storage.

Electrolyte Design for In Situ Construction of Highly Zn2+ -Conductive Solid Electrolyte Interphase to Enable High-Performance Aqueous Zn-Ion Batteries under Practical Conditions.

Rechargeable aqueous Zn-ion batteries promise high capacity, low cost, high safety, and sustainability for large-scale energy storage. The Zn metal anode, however, suffers from the dendrite growth and side reactions that are mainly due to the absence of an appropriate solid electrolyte interphase (SEI) layer. Herein, the in situ formation of a dense, stable, and highly Zn2+ -conductive SEI layer (hopeite) in aqueous Zn chemistry is demonstrated, by introducing Zn(H2 PO4 )2 salt into the electrolyte. The hopeite SEI (≈140 nm thickness) enables uniform and rapid Zn-ion transport kinetics for dendrite-free Zn deposition, and restrains the side reactions via isolating active Zn from the bulk electrolyte. Under practical testing conditions with an ultrathin Zn anode (10 µm), a low negative/positive capacity ratio (≈2.3), and a lean electrolyte (9 µL mAh-1 ), the Zn/V2 O5 full cell retains 94.4% of its original capacity after 500 cycles. This work provides a simple yet practical solution to high-performance aqueous battery technology via building in situ SEI layers.

Effect of Sodium Content on the Electrochemical Performance of Li-Substituted, Manganese-Based, Sodium-Ion Layered Oxide Cathodes.

Li-substituted, manganese-based, layered oxides NaxLi0.18Mn0.66Co0.17Ni0.17O2+δ (x = 0.54, 0.66, 0.78, and 0.90) have been investigated as one kind of high-performance cathode materials for sodium ion batteries (SIBs). Phase compositions and local structures of the cathode materials with varying sodium content were elucidated by powder X-ray diffraction (PXRD) and atomic-scale high angle annular dark field scanning transmission electron microscope (HAADF-STEM), which demonstrates that a Li-O'3 phase was aroused in P2-type sodium layered oxide matrix forming a Na-P2/Li-O'3 hybrid structure. More importantly, the effect of sodium content on the preferential exposure of (102) and (104) facets and surface morphology of the cathode particles has been comprehensively studied, as well as their relationship with electrochemical performance. It reveals that, in addition to the preferential growth of (102) and (104) facets that has been proved to enhance the capacity and rate performance of the layered oxides, the smooth surface finish of the particles also plays a vital role in deciding the electrochemical performance. The layered sodium cathode material with a sodium content of 0.66 possesses sufficient exposure of (102) and (104) facets and smooth side surface, resulting in the superior capacities under various C rates (187 mAh/g at 0.2 C and 114 mAh/g at 5 C) comparing to the cathode materials with all other sodium contents. The mechanism has also been proposed in this study. These findings presented herein open up new strategies to design high performance sodium layered oxide cathode.

Improving the Electrochemical Properties of the Manganese-Based P3 Phase by Multiphasic Intergrowth.

Layered transition-metal oxides are one kind of the most promising cathode materials for sodium-ion batteries. In this study, we propose a strategy to enhance the electrochemical properties of P3-type manganese-based layered oxide cathode by introducing a small amount of layered P2 and Li-O'3 phases. Powder X-ray diffraction (PXRD) structural refinement and aberration-corrected scanning transmission electron microscopy (STEM) are performed to confirm the microstructures of different samples. PXRD refinement results show that the elevated annealing temperature leads to a partial conversion of the P3 phase to the P2 phase and the addition of lithium results in the formation of a new O'3 phase in the P3/P2-layered matrix. STEM results identify the intergrowth of P3/P2 and P3/P2/O'3 in biphasic and triphasic materials, respectively. Electron energy loss spectroscopy verifies that the alkali metal layer in the O'3 phase is occupied by the lithium ion. The intergrowth of biphasic and triphasic materials in these layered P3/P2 and P3/P2/O'3 hybrid structures brings forth a positive effect on the electrochemical properties. In particular, the formation of P3/P2/O'3-intergrown hybrid structures greatly improves the cycling stability of the P3 phase that the capacity retention of P3/P2/O'3 hybrid structures remains 78%, while capacity retention of the pure P3 phase is only 54.1% after 50 cycles at a rate of 0.2 C, and the rate performance of the P3 phase has also been enhanced.

Understanding the Enhanced Kinetics of Gradient-Chemical-Doped Lithium-Rich Cathode Material.

Although chemical doping has been extensively employed to improve the electrochemical performance of Li-rich layered oxide (LLO) cathodes for Li ion batteries, the correlation between the electrochemical kinetics and local structure and chemistry of these materials after chemical doping is still not fully understood. Herein, gradient surface Si/Sn-doped LLOs with improved kinetics are demonstrated. The atomic local structure and surface chemistry are determined using electron microscopy and spectroscopy techniques, and remarkably, the correlation of local structure-enhanced kinetics is clearly described in this work. The experimental results suggest that Si/Sn substitution decreases the TMO2 slab thickness and enlarges the interslab spacing, and the concentration gradient of Si/Sn affects the magnitude of these structural changes. The expanded interslab spacing accounts for the enhanced Li+ diffusivity and rate performance observed in Si/Sn-doped materials. The improved understanding of the local structure-enhanced kinetic relationship for doped LLOs demonstrates the potential for the design and development of other high-rate intercalated electrode materials.

Hierarchical Nanocomposite of Hollow N-Doped Carbon Spheres Decorated with Ultrathin WS2 Nanosheets for High-Performance Lithium-Ion Battery Anode.

Hierarchical nanocomposite of ultrathin WS2 nanosheets uniformly attached on the surface of hollow nitrogen-doped carbon spheres (WS2@HNCSs) were successfully fabricated via a facile synthesis strategy. When evaluated as an anode material for LIBs, the hierarchical WS2@HNCSs exhibit a high specific capacity of 801.4 mA h g(-1) at 0.1 A g(-1), excellent rate capability (545.6 mA h g(-1) at a high current density of 2 A g(-1)), and great cycling stability with a capacity retention of 95.8% after 150 cycles at 0.5 A g(-1). The Li-ion storage properties of our WS2@HNCSs nanocomposite are much better than those of the previously most reported WS2-based anode materials. The impressive electrochemical performance is attributed to the robust nanostructure and the favorable synergistic effect between the ultrathin (3-5 layers) WS2 nanosheets and the highly conductive hollow N-doped carbon spheres. The hierarchical hybrid can simultaneously facilitate fast electron/ion transfer, effectively accommodate mechanical stress from cycling, restrain agglomeration, and enable full utilization of the active materials. These characteristics make WS2@HNCSs a promising anode material for high-performance LIBs.

The Effect of Boron Doping on Structure and Electrochemical Performance of Lithium-Rich Layered Oxide Materials.

Polyanion doping shows great potential to improve electrochemical performance of Li-rich layered oxide (LLO) materials. Here, by optimizing the doping content and annealing temperature, we obtained boron-doped LLO materials Li1.2Mn0.54Ni0.13Co0.13BxO2 (x = 0.04 and 0.06) with comprehensively improved performance (94% capacity retention after 100 cycles at 60 mA/g current density and a rate capability much higher compared to that of the pristine sample) at annealing temperatures of 750 and 650 °C, respectively, which are much lower than the traditional annealing temperature of similar material systems without boron. The scenario of the complex crystallization process was captured using Cs-corrected high-angle annular dark field scanning transmission electron microscopic (HAADF-STEM) imaging techniques. The existence of layered, NiO-type, and spinel-like structures in a single particle induced by boron doping and optimization of annealing temperature is believed to contribute to the remarkable improvement of cycling stability and rate capability.