Bimetallic CuSbSe2 : A Potential Anode Material for Sodium and Lithium-Ion Batteries with High-Rate Capability and Long-Term Stability.

Bimetallic transition metal chalcogenides (TMCs) materials have emerged as attractive anodes for lithium-ion batteries (LIBs) and sodium-ion batteries (SIBs) because of the high intrinsic electronic conductivity, rich redox sites and unique reaction mechanism. In this work, we report the synthesis and electrochemical properties of a novel bimetallic TMCs material CuSbSe2 . The as-prepared anode delivers a high reversible capacity of 545.6  mA h g-1 for SIBs and 592.6  mA h g-1 for LIBs at a current density of 0.2 A g-1 , and an excellent rate capability of 425.9  mA h g-1 at 20 A g-1 for SIBs and 226.0  mA h g-1 at 10 A g-1 for LIBs without any common-used surface modification or carbonaceous compositing. In addition, ex situ X-ray diffraction (XRD) and High-resolution transmission electron microscopy (HRTEM) reveal a combined conversion-alloying reaction mechanism of LIBs and NIBs. Our findings suggest bimetallic CuSbSe2 could be a potential anode material for both SIBs and LIBs.

NeDSeM: Neutrosophy Domain-Based Segmentation Method for Malignant Melanoma Images.

Skin lesion segmentation is the first and indispensable step of malignant melanoma recognition and diagnosis. At present, most of the existing skin lesions segmentation techniques often used traditional methods like optimum thresholding, etc., and deep learning methods like U-net, etc. However, the edges of skin lesions in malignant melanoma images are gradually changed in color, and this change is nonlinear. The existing methods can not effectively distinguish banded edges between lesion areas and healthy skin areas well. Aiming at the uncertainty and fuzziness of banded edges, the neutrosophic set theory is used in this paper which is better than fuzzy theory to deal with banded edge segmentation. Therefore, we proposed a neutrosophy domain-based segmentation method that contains six steps. Firstly, an image is converted into three channels and the pixel matrix of each channel is obtained. Secondly, the pixel matrixes are converted into Neutrosophic Set domain by using the neutrosophic set conversion method to express the uncertainty and fuzziness of banded edges of malignant melanoma images. Thirdly, a new Neutrosophic Entropy model is proposed to combine the three memberships according to some rules by using the transformations in the neutrosophic space to comprehensively express three memberships and highlight the banded edges of the images. Fourthly, the feature augment method is established by the difference of three components. Fifthly, the dilation is used on the neutrosophic entropy matrixes to fill in the noise region. Finally, the image that is represented by transformed matrix is segmented by the Hierarchical Gaussian Mixture Model clustering method to obtain the banded edge of the image. Qualitative and quantitative experiments are performed on malignant melanoma image dataset to evaluate the performance of the NeDSeM method. Compared with some state-of-the-art methods, our method has achieved good results in terms of performance and accuracy.

Effects of Structure and Magnetism on the Electrochemistry of the Layered Li1+x(Ni0.5Mn0.5)1-xO2 Cathode Material.

We have synthesized a series of Li1+x(Ni0.5Mn0.5)1-xO2 (LNMO) materials to study the influence of excess lithium ions on the structure and electrochemical behaviors of nickel-manganese-based layered compounds. The increasing content of Li+ ions in the transition-metal (TM) layer leads to the departure of the follower-like clusters to Ni-rich and Mn-rich clusters. The Ni2+ ions in the Li layer couple with adjacent transition-metal ions via strong 180° exchange interactions and moderate the local structure, which leads to magnetic clusters with finite size. Electrochemical performance shows that appropriate Ni2+ ions could improve the cycle stability without decreasing the rate capability. Among them, Li1.1Ni0.45Mn0.45O2 shows a rate capability of 76 mAh g-1 at 1000 mA g-1 and a lifespan of 300 cycles at 200 mA g-1. This work shows that structure moderation has an essential impact on its electrochemical performance. Besides this, the crystal and magnetic combined methods we use could offer a better way of studying cathode materials.

Dual Roles of Li3 N as an Electrode Additive for Li-Excess Layered Cathode Materials: A Li-Ion Sacrificial Salt and Electrode-Stabilizing Agent.

Li2 CO3 -passivated Li3 N with high stability is prepared by aging Li3 N powder in dry air, and is then used as an electrode additive for a Li(Li0.18 Ni0.15 Co0.15 Mn0.52 )O2 (LLMO) cathode material. The material shows a large irreversible capacity of 800 mA h g-1 during the first charge, with the formation of a Li2 N intermediate product. Acting as a Li+ sacrificial salt for a LLMO(+)/graphite(-) Li-ion battery, 2 wt % Li3 N results in a 10 % increase in discharge capacity. The Li2 N intermediate product reacts with the electrolyte, forming a uniform and regular surface film on the cathode. Moreover, chemical bonding between LLMO and N improves the electrode stability, resulting in excellent electrochemical performance.

Li+ /Mg2+ Hybrid-Ion Batteries with Long Cycle Life and High Rate Capability Employing MoS2 Nano Flowers as the Cathode Material.

The demand for large-scale and safe energy storage is increasing rapidly due to the strong push for smartphones and electric vehicles. As a result, Li+ /Mg2+ hybrid-ion batteries (LMIBs) combining a dendrite-free deposition of Mg anode and Li+ intercalation cathode have attracted considerable attention. Here, a LMIB with hydrothermal-prepared MoS2 nano flowers as cathode material was prepared. The battery showed remarkable electrochemical properties with a large discharge capacity (243 mAh g-1 at the 0.1 C rate), excellent rate capability (108 mAh g-1 at the 5 C rate), and long cycle life (87.2 % capacity retention after 2300 cycles). Electrochemical analysis showed that the reactions occurring in the battery cell involved Mg stripping/plating at the anode side and Li+ intercalation at the cathode side with a small contribution from Mg2+ adsorption. The excellent electrochemical performance and extremely safe cell system show promise for its use in practical applications.

Lithium-Rich Layered Oxide Li1.18 Ni0.15 Co0.15 Mn0.52 O2 as the Cathode Material for Hybrid Sodium-Ion Batteries.

Li-rich layered oxide Li1.18 Ni0.15 Co0.15 Mn0.52 O2 (LNCM) is, for the first time, examined as the positive electrode for hybrid sodium-ion battery and its Na(+) storage properties are comprehensively studied in terms of galvanostatic charge-discharge curves, cyclic voltammetry and rate capability. LNCM in the proposed sodium-ion battery demonstrates good rate capability whose discharge capacity reaches about 90 mA h g(-1) at 10 C rate and excellent cycle stability with specific capacity of about 105 mA h g(-1) for 200 cycles at 5 C rate. Moreover, ex situ ICP-OES suggests interesting mixed-ions migration processes: In the initial two cycles, only Li(+) can intercalate into the LNCM cathode, whereas both Li(+) and Na(+) work together as the electrochemical cycles increase. Also the structural evolution of LNCM is examined in terms of ex situ XRD pattern at the end of various charge-discharge scans. The strong insight obtained from this study could be beneficial to the design of new layered cathode materials for future rechargeable sodium-ion batteries.

Yolk-shell-structured Si@TiN nanoparticles for high-performance lithium-ion batteries.

The huge volume expansion of over 300%, dreadful electrical conductivity and labile solid electrolyte interphase (SEI) are the principal reasons of the sluggish development of Si anodes for lithium-ion batteries (LIBs). Therefore, we propose, for the first time, that titanium nitride (TiN) be utilized as a coating layer to fabricate yolk-shell-structured Si@TiN nanoparticles. The design of the yolk-shell structure can reserve excrescent space for the volume expansion of Si electrodes, which helps to mitigate volumetric changes. Moreover, the TiN protecting layer is beneficial to the formation of a stable and flimsy SEI film, avoiding the excessive consumption of electrolytes. Finally, the ultrahigh conductivity (4 × 104 S cm-1) as well as the high mechanical modulus of TiN can significantly promote charge transfer and avoid the crushing of the SEI film caused by excessive local stress during reduplicative Li deposition/stripping. Accordingly, the Si@TiN composites show excellent electrochemical properties and suppressed volume expansion compared with pure silicon nanoparticles (Si NPs). Here, these yolk-shell-structured Si@TiN nanoparticles exhibit improved rate performance and excellent long cycling stability with 2047 mA h g-1 at 1000 mA g-1 after 180 cycles. This paradigm may provide a feasible engineering protocol to push the properties of Si anodes for next-generation LIBs.

NaV6O15 microflowers as a stable cathode material for high-performance aqueous zinc-ion batteries.

Reversible aqueous zinc-ion batteries (ZIBs) have great potential for large-scale energy storage owing to their low cost and safety. However, the lack of long-lifetime positive materials severely restricts the development of ZIBs. Herein, we report NaV6O15 microflowers as a cathode material for ZIBs with excellent electrochemical performance, including a high specific capacity of ∼300 mA h g-1 at 100 mA g-1 and 141 mA h g-1 maintained after 2000 cycles at 5 A g-1 with a capacity retention of ∼107%. The high diffusion coefficient and stable tunneled structure of NaV6O15 facilitate Zn2+ intercalation/extraction and long-term cycle stability.

Preparation and electrochemical performance of VO2(A) hollow spheres as a cathode for aqueous zinc ion batteries.

Rechargeable aqueous zinc ion batteries (ZIBs), owing to their low-cost zinc metal, high safety and nontoxic aqueous electrolyte, have the potential to accelerate the development of large-scale energy storage applications. However, the desired development is significantly restricted by cathode materials, which are hampered by the intense charge repulsion of bivalent Zn2+. Herein, the as-prepared VO2(A) hollow spheres via a feasible hydrothermal reaction exhibit superior zinc ion storage performance, large reversible capacity of 357 mA h g-1 at 0.1 A g-1, high rate capability of 165 mA h g-1 at 10 A g-1 and good cycling stability with a capacity retention of 76% over 500 cycles at 5 A g-1. Our study not only provides the possibility of the practical application of ZIBs, but also brings a new prospect of designing high-performance cathode materials.

VS4 Nanoparticles Anchored on Graphene Sheets as a High-Rate and Stable Electrode Material for Sodium Ion Batteries.

The size and conductivity of the electrode materials play a significant role in the kinetics of sodium-ion batteries. Various characterizations reveal that size-controllable VS4 nanoparticles can be successfully anchored on the surface of graphene sheets (GSs) by a simple cationic-surfactant-assisted hydrothermal method. When used as an electrode material for sodium-ion batteries, these VS4 @GS nanocomposites show large specific capacity (349.1 mAh g-1 after 100 cycles), excellent long-term stability (84 % capacity retention after 1200 cycles), and high rate capability (188.1 mAh g-1 at 4000 mA g-1 ). A large proportion of the capacity was contributed by capacitive processes. This remarkable electrochemical performance was attributed to synergistic interactions between nanosized VS4 particles and a highly conductive graphene network, which provided short diffusion pathways for Na+ ions and large contact areas between the electrolyte and electrode, resulting in considerably improved electrochemical kinetic properties.

Ultrathin TiO2-B nanowires as an anode material for Mg-ion batteries based on a surface Mg storage mechanism.

Ultrathin TiO2-B nanowires with a naked (-110) surface were prepared by a hydrothermal process and used as the anode material for Mg-ion batteries. The material delivered a reversible Mg2+ ion capacity of 110 mA h g-1 at the 0.1C rate. Excellent cycling stability was achieved with a small capacity-fading rate of 0.08% per cycle. In addition, a discharge capacity of 34 mA h g-1 was obtained at the 50C rate, demonstrating the material's excellent high rate capability. First-principles calculations showed that Mg2+ ions hardly penetrated into the TiO2-B lattice because of a very large Mg2+ ion diffusion barrier of 0.63 eV. Instead, the Mg2+ ions were stored at the 4-coordinated vacancies of TiO2-B nanowire (-110) surfaces. The adsorbed Mg2+ ions were bonded with unpaired surface oxygen atoms. Meanwhile, a small amount of electrons were transferred from the O-2p state to the Ti-3d state.

Multi-Functional Surface Engineering for Li-Excess Layered Cathode Material Targeting Excellent Electrochemical and Thermal Safety Properties.

The Li(Li(0.18)Ni(0.15)Co(0.15)Mn(0.52))O2 cathode material is modified by a Li4M5O12-like heterostructure and a BiOF surface layer. The interfacial heterostructure triggers the layered-to-Li4M5O12 transformation of the material which is different from the layered-to-LiMn2O4 transformation of the pristine Li(Li(0.18)Ni(0.15)Co(0.15)Mn(0.52))O2. This Li4M5O12-like transformation helps the material to keep high working voltage, long cycle life and excellent rate capability. Mass spectrometry, in situ X-ray diffraction and transmission electron microscope show that the Li4M5O12-like phase prohibits oxygen release from the material bulk at elevated temperatures. In addition, the BiOF coating layer protects the material from harmful side reactions with the electrolyte. These advantages significantly improve the electrochemical performance of Li(Li(0.18)Ni(0.15)Co(0.15)Mn(0.52))O2. The material shows a discharge capacity of 292 mAh g(-1) at 0.2 C with capacity retention of 92% after 100 cycles. Moreover, a high discharge capacity of 78 mAh g(-1) could be obtained at 25 C. The exothermic temperature of the fully charged electrode is elevated from 203 to 261 °C with 50% reduction of the total thermal release, highlighting excellent thermal safety of the material.