Noise-like mode-locked Yb-doped fiber laser in a linear cavity based on SnS2 nanosheets as a saturable absorber.

In this study, a high-energy noise-like mode-locked Yb-doped fiber laser in a linear cavity was achieved with SnS2-polyvinyl alcohol film as the saturable absorber. In addition, the nonlinear saturable absorption characteristics of the SnS2 were investigated experimentally. The saturation intensity and modulation depth were about 6.01 MW/cm2 and 8.68%, respectively. Under pump power of 422 mW, stable noise-like mode-locked operation with a maximum output power and largest single pulse energy of 9.50 mW and 18.1 nJ, respectively, was obtained. To the best of our knowledge, this study is the first to observe and experimentally investigate noise-like operation in a linear laser cavity. Our study may provide some valuable design guidelines for noise-like operation and create new directions for advanced photonic devices based on SnS2.

Intrinsic Grain Boundary Structure and Enhanced Defect States in Air-Sensitive Polycrystalline 1T'-WTe2 Monolayer.

Monolayer WTe2 has attracted significant attention for its unconventional superconductivity and topological edge states. However, its air sensitivity poses challenges for studying intrinsic defect structures. This study addresses this issue using a custom-built inert gas interconnected system, and investigate the intrinsic grain boundary (GB) structures of monolayer polycrystalline 1T' WTe2 grown by nucleation-controlled chemical vapor deposition (CVD) method. These findings reveal that GBs in this system are predominantly governed by W-Te rhombi with saturated coordination, resulting in three specific GB prototypes without dislocation cores. The GBs exhibit anisotropic orientations influenced by kinks formed from these fundamental units, which in turn affect the distribution of grains in various shapes within polycrystalline flakes. Scanning tunneling microscopy/spectroscopy (STM/S) analysis further reveals metallic states along the intrinsic 120° twin grain boundary (TGB), consistent with computed band structures. This systematic exploration of GBs in air-sensitive 1T' WTe2 monolayers provides valuable insights into emerging GB-related phenomena.

High-Voltage Long-Cycling All-Solid-State Lithium Batteries with High-Valent-Element-Doped Halide Electrolytes.

All-solid-state batteries (ASSBs) have garnered considerable attention as promising candidates for next-generation energy storage systems due to their potentially simultaneously enhanced safety capacities and improved energy densities. However, the solid future still calls for materials with high ionic conductivity, electrochemical stability, and favorable interfacial compatibility. In this study, we present a series of halide solid-state electrolytes (SSEs) utilizing a doping strategy with highly valent elements, demonstrating an outstanding combination of enhanced ionic conductivity and oxidation stability. Among these, Li2.6In0.8Ta0.2Cl6 emerges as the standout performer, displaying a superionic conductivity of up to 4.47 mS cm-1 at 30 °C, along with a low activation energy barrier of 0.321 eV for Li+ migration. Additionally, it showcases an extensive oxidation onset of up to 5.13 V (vs Li+/Li), enabling high-voltage ASSBs with promising cycling performance. Particularly noteworthy are the ASSBs employing LiCoO2 cathode materials, which exhibit an extended cyclability of over 1400 cycles, with 70% capacity retention under 4.6 V (vs Li+/Li), and a capacity of up to 135 mA h g-1 at a 4 C rate, with the loading of active materials at 7.52 mg cm-2. This study demonstrates a feasible approach to designing desirable SSEs for energy-dense, highly stable ASSBs.

Continuously tunable ferroelectric domain width down to the single-atomic limit in bismuth tellurite.

Emerging functionalities in two-dimensional materials, such as ferromagnetism, superconductivity and ferroelectricity, open new avenues for promising nanoelectronic applications. Here, we report the discovery of intrinsic in-plane room-temperature ferroelectricity in two-dimensional Bi2TeO5 grown by chemical vapor deposition, where spontaneous polarization originates from Bi column displacements. We found an intercalated buffer layer consist of mixed Bi/Te column as 180° domain wall which enables facile polarized domain engineering, including continuously tunable domain width by pinning different concentration of buffer layers, and even ferroelectric-antiferroelectric phase transition when the polarization unit is pinned down to single atomic column. More interestingly, the intercalated Bi/Te buffer layer can interconvert to polarized Bi columns which end up with series terraced domain walls and unusual fan-shaped ferroelectric domain. The buffer layer induced size and shape tunable ferroelectric domain in two-dimensional Bi2TeO5 offer insights into the manipulation of functionalities in van der Waals materials for future nanoelectronics.

Direct Visualization of Large-Scale Intrinsic Atomic Lattice Structure and Its Collective Anisotropy in Air-Sensitive Monolayer 1T'- WTe2.

Probing large-scale intrinsic structure of air-sensitive 2D materials with atomic resolution is so far challenging due to their rapid oxidization and contamination. Here, by keeping the whole experiment including growth, transfer, and characterizations in an interconnected atmosphere-control environment, the large-scale intact lattice structure of air-sensitive monolayer 1T'-WTe2 is directly visualized by atom-resolved scanning transmission electron microscopy. Benefit from the large-scale atomic mapping, collective lattice distortions are further unveiled due to the presence of anisotropic rippling, which propagates perpendicular to only one of the preferential lattice planes in the same WTe2 monolayer. Such anisotropic lattice rippling modulates the intrinsic point defect (Te vacancy) distribution, in which they aggregate at the constrictive inner side of the undulating structure, presumably due to the ripple-induced asymmetric strain as elaborated by density functional theory. The results pave the way for atomic characterizations and defect engineering of air-sensitive 2D layered materials.

Lithium-Rich Anti-perovskite Li2OHBr-Based Polymer Electrolytes Enabling an Improved Interfacial Stability with a Three-Dimensional-Structured Lithium Metal Anode in All-Solid-State Batteries.

All-solid-state lithium-metal batteries, with their high energy density and high-level safety, are promising next-generation energy storage devices. Their current performance is however compromised by lithium dendrite formation. Although using 3D-structured metal-based electrode materials as hosts to store lithium metal has the potential to suppress the lithium dendrite growth by providing a high surface area with lithiophilic sites, their rigid and ragged interface with solid-state electrolytes is detrimental to the battery performance. Herein, we show that Li2OHBr-containing poly(ethylene oxide) (PEO) polymer electrolytes can be used as a flexible solid-state electrolyte to mitigate the interfacial issues of 3D-structured metal-based electrodes and suppress the lithium dendrite formation. The presence of Li2OHBr in a PEO matrix can simultaneously improve the mechanical strength and lithium ion conductivity of the polymer electrolyte. It is confirmed that Li2OHBr does not only induce the PEO transformation of a crystalline phase to an amorphous phase but also serves as an anti-perovskite superionic conductor providing additional lithium ion transport pathways and hence improves the lithium ion conductivity. The good interfacial contact and high lithium ion conductivity provide sufficient lithium deposition sites and uniform lithium ion flux to regulate the lithium deposition without the formation of lithium dendrites. Consequently, the Li2OHBr-containing PEO polymer electrolyte in a lithium-metal battery with a 3D-structured lithium/copper mesh composite anode is able to improve the cycle stability and rate performance. The results of this study provide the experimental proof of the beneficial effects of the Li2OHBr-containing PEO polymer electrolyte on the 3D-structured lithium metal anode.