Browse
Submit Data
Databases
API
Help

Dataset Information

30 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

SnS₂@C Hollow Nanospheres with Robust Structural Stability as High-Performance Anodes for Sodium Ion Batteries.

ABSTRACT: Constructing unique and highly stable structures with plenty of electroactive sites in sodium storage materials is a key factor for achieving improved electrochemical properties through favorable sodium ion diffusion kinetics. An SnS₂@carbon hollow nanospheres (SnS₂@C) has been designed and fabricated via a facile solvothermal route, followed by an annealing treatment. The SnS₂@C hybrid possesses an ideal hollow structure, rich active sites, a large electrode/electrolyte interface, a shortened ion transport pathway, and, importantly, a buffer space for volume change, generated from the repeated insertion/extraction of sodium ions. These merits lead to the significant reinforcement of structural integrity during electrochemical reactions and the improvement in sodium storage properties, with a high specific reversible capacity of 626.8 mAh g^-1 after 200 cycles at a current density of 0.2 A g^-1 and superior high-rate performance (304.4 mAh g^-1 at 5 A g^-1).

SUBMITTER: Li S

PROVIDER: S-EPMC7770728 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Crab Shell-Derived SnS2/C and FeS2/C Carbon Composites as Anodes for High-Performance Sodium-Ion Batteries.

Project description:The demand for energy storage devices has increased significantly, and the sustainable development of lithium-ion batteries is limited by scarce lithium resources. Therefore, alternative sodium-ion batteries which are rich in resource may become more competitive in the future market. In this work, we synthesized low-cost SnS2/C and FeS2/C anode materials of sodium-ion batteries which used waste crab shells as biomass carbon precursor. The SnS2 nanosheet and FeS2 nanosphere structures are deposited on the crab shell-derived carbon through simple hydrothermal reaction. Due to the coexistence of transition metal dichalcogenides (TMDs) and crab-derived biomass carbon, the anode material has excellent cycle stability and rate performance. SnS2/C and FeS2/C deliver capacities of 535.4 and 479 mA h g-1 at the current density of 0.1 A g-1, respectively. This study explored an effective and economical strategy to use biomass and TMDs to construct high-performance sodium-ion batteries.

| S-EPMC10018519 | biostudies-literature

MOF-Derived CoSe2@N-Doped Carbon Matrix Confined in Hollow Mesoporous Carbon Nanospheres as High-Performance Anodes for Potassium-Ion Batteries.

Project description:In this work, a novel vacuum-assisted strategy is proposed to homogenously form Metal-organic frameworks within hollow mesoporous carbon nanospheres (HMCSs) via a solid-state reaction. The method is applied to synthesize an ultrafine CoSe2 nanocrystal@N-doped carbon matrix confined within HMCSs (denoted as CoSe2@NC/HMCS) for use as advanced anodes in high-performance potassium-ion batteries (KIBs). The approach involves a solvent-free thermal treatment to form a Co-based zeolitic imidazolate framework (ZIF-67) within the HMCS templates under vacuum conditions and the subsequent selenization. Thermal treatment under vacuum facilitates the infiltration of the cobalt precursor and organic linker into the HMCS and simultaneously transforms them into stable ZIF-67 particles without any solvents. During the subsequent selenization process, the "dual confinement system", composed of both the N-doped carbon matrix derived from the organic linker and the small-sized pores of HMCS, can effectively suppress the overgrowth of CoSe2 nanocrystals. Thus, the resulting uniquely structured composite exhibits a stable cycling performance (442 mAh g-1 at 0.1 A g-1 after 120 cycles) and excellent rate capability (263 mAh g-1 at 2.0 A g-1) as the anode material for KIBs.

| S-EPMC8187686 | biostudies-literature

Heteroatom Doped-Carbon Nanospheres as Anodes in Lithium Ion Batteries.

Project description:Long cycle performance is a crucial requirement in energy storage devices. New formulations and/or improvement of "conventional" materials have been investigated in order to achieve this target. Here we explore the performance of a novel type of carbon nanospheres (CNSs) with three heteroatom co-doped (nitrogen, phosphorous and sulfur) and high specific surface area as anode materials for lithium ion batteries. The CNSs were obtained from carbonization of highly-crosslinked organo (phosphazene) nanospheres (OPZs) of 300 nm diameter. The OPZs were synthesized via a single and facile step of polycondensation reaction between hexachlorocyclotriphosphazene (HCCP) and 4,4'-sulphonyldiphenol (BPS). The X-ray Photoelectron Spectroscopy (XPS) analysis showed a high heteroatom-doping content in the structure of CNSs while the textural evaluation from the N₂ sorption isotherms revealed the presence of micro- and mesopores and a high specific surface area of 875 m²/g. The CNSs anode showed remarkable stability and coulombic efficiency in a long charge-discharge cycling up to 1000 cycles at 1C rate, delivering about 130 mA·h·g-1. This study represents a step toward smart engineering of inexpensive materials with practical applications for energy devices.

| S-EPMC5456559 | biostudies-literature

SnS/C nanocomposites for high-performance sodium ion battery anodes.

Project description:Sodium-ion batteries have been considered as one of the most promising types of batteries, beyond lithium-ion batteries, for large-scale energy storage applications. However, their deployment hinges on the development of new anode materials, since it has been shown that many important anode materials employed in lithium ion batteries, such as graphite and silicon, are inadequate for sodium-ion batteries. We have simply prepared novel SnS/C nanocomposites through a top-down approach as anode materials for sodium-ion batteries. Their electrochemical performance has been significantly improved when compared to bare SnS, especially in terms of cycling stability and rate capabilities. SnS/C nanocomposites exhibit excellent capacity retention, at various current rates, and deliver capacities as high as 400 mA h g-1 even at the high current density of 800 mA g-1 (2C). Ex situ transmission electron microscopy, X-ray diffraction and operando X-ray absorption near edge structure studies have been performed in order to unravel the reaction mechanism of the SnS/C nanocomposites.

| S-EPMC9081785 | biostudies-literature

Rational Design of Layered SnS2 on Ultralight Graphene Fiber Fabrics as Binder-Free Anodes for Enhanced Practical Capacity of Sodium-Ion Batteries.

Project description:Generally, the practical capacity of an electrode should include the weight of non-active components such as current collector, polymer binder, and conductive additives, which were as high as 70 wt% in current reported works, seriously limiting the practical capacity. This work pioneered the usage of ultralight reduced graphene fiber (rGF) fabrics as conductive scaffolds, aiming to reduce the weight of non-active components and enhance the practical capacity. Ultrathin SnS2 nanosheets/rGF hybrids were prepared and used as binder-free electrodes of sodium-ion batteries (SIBs). The interfused graphene fibers endow the electrode a porous, continuous, and conductive network. The in situ phase transformation from SnO2 to SnS2 could preserve the strong interfacial interactions between SnS2 and graphene. Benefitting from these, the designed binder-free electrode delivers a high specific capacity of 500 mAh g-1 after 500 cycles at a current rate of 0.5 A g-1 with almost 100% Coulombic efficiency. Furthermore, the weight percentage of SnS2 in the whole electrode could reach up to 67.2 wt%, much higher than that of common electrode configurations using Cu foil, Al foil, or carbon cloth, significantly highlighting the ultralight characters and advantages of the rGF fabrics for using as binder-free electrodes of SIBs.

| S-EPMC7770950 | biostudies-literature

Nano Hard Carbon Anodes for Sodium-Ion Batteries.

Project description:A hindrance to the practical use of sodium-ion batteries is the lack of adequate anode materials. By utilizing the co-intercalation reaction, graphite, which is the most common anode material of lithium-ion batteries, was used for storing sodium ion. However, its performance, such as reversible capacity and coulombic efficiency, remains unsatisfactory for practical needs. Therefore, to overcome these drawbacks, a new carbon material was synthesized so that co-intercalation could occur efficiently. This carbon material has the same morphology as carbon black; that is, it has a wide pathway due to a turbostratic structure, and a short pathway due to small primary particles that allows the co-intercalation reaction to occur efficiently. Additionally, due to the numerous voids present in the inner amorphous structure, the sodium storage capacity was greatly increased. Furthermore, owing to the coarse co-intercalation reaction due to the surface pore structure, the formation of solid-electrolyte interphase was greatly suppressed and the first cycle coulombic efficiency reached 80%. This study shows that the carbon material alone can be used to design good electrode materials for sodium-ion batteries without the use of next-generation materials.

| S-EPMC6567009 | biostudies-literature

Porous Amorphous Silicon Hollow Nanoboxes Coated with Reduced Graphene Oxide as Stable Anodes for Sodium-Ion Batteries.

Project description:Amorphous silicon (a-Si), due to its satisfactory theoretical capacity, moderate discharge potential, and abundant reserves, is treated as one of the most prospective materials for the anode of sodium-ion batteries (SIBs). However, the slow Na+ diffusion kinetics, poor electrical conductivity, and rupture-prone structures of a-Si restrict its further development. In this work, a composite (a-Si@rGO) consisting of porous amorphous silicon hollow nanoboxes (a-Si HNBs) and reduced graphene oxide (rGO) is prepared. The a-Si HNBs are synthesized through "sodiothermic reduction" of silica hollow nanoboxes at a relatively low temperature, and the rGO is covered on the surface of the a-Si HNBs by electrostatic interaction. The as-synthesized composite anode applying in SIBs exhibits a high initial discharge capacity of 681.6 mAh g-1 at 100 mA g-1, great stability over 2000 cycles at 800 mA g-1, and superior rate performance (261.2, 176.8, 130.3, 98.4, and 73.3 mAh g-1 at 100, 400, 800, 1500, and 3000 mA g-1, respectively). The excellent electrochemical properties are ascribed to synergistic action of the porous hollow nanostructure of a-Si and the rGO coating. This research not only offers an innovative synthetic means for the development of a-Si in various fields but also provides a practicable idea for the design of other alloy-type anodes.

| S-EPMC9434769 | biostudies-literature

Fast Energy Storage of SnS2 Anode Nanoconfined in Hollow Porous Carbon Nanofibers for Lithium-Ion Batteries.

Project description:The development of conversion-typed anodes with ultrafast charging and large energy storage is quite challenging due to the sluggish ions/electrons transfer kinetics in bulk materials and fracture of the active materials. Herein, the design of porous carbon nanofibers/SnS2 composite (SnS2 @N-HPCNFs) for high-rate energy storage, where the ultrathin SnS2 nanosheets are nanoconfined in N-doped carbon nanofibers with tunable void spaces, is reported. The highly interconnected carbon nanofibers in three-dimensional (3D) architecture provide a fast electron transfer pathway and alleviate the volume expansion of SnS2 , while their hierarchical porous structure facilitates rapid ion diffusion. Specifically, the anode delivers a remarkable specific capacity of 1935.50 mAh g-1 at 0.1 C and excellent rate capability up to 30 C with a specific capacity of 289.60 mAh g-1 . Meanwhile, at a high rate of 20 C, the electrode displays a high capacity retention of 84% after 3000 cycles and a long cycle life of 10 000 cycles. This work provides a deep insight into the construction of electrodes with high ionic/electronic conductivity for fast-charging energy storage devices.

| S-EPMC10811495 | biostudies-literature

In-situ Grown SnO2 Nanospheres on Reduced GO Nanosheets as Advanced Anodes for Lithium-ion Batteries.

Project description:Nanostructured tin dioxide (SnO2) has emerged as a promising anode material for lithium-ion batteries (LIBs) due to its high theoretical capacity (1494?mA?h?g-1) and excellent stability. Unfortunately, the rapid capacity fading and poor electrical conductivity of bulk SnO2 material restrict its practical application. Here, SnO2 nanospheres/reduced graphene oxide nanosheets (SRG) are fabricated through in-situ growth of carbon-coated SnO2 using template-based approach. The nanosheet structure with the external layer of about several nanometers thickness can not only accommodate the volume change of Sn lattice during cycling but also enhance the electrical conductivity effectively. Benefited from such design, the SRG composites could deliver an initial discharge capacity of 1212.3?mA?h?g-1 at 0.1?A?g-1, outstanding cycling performance of 1335.6?mA?h?g-1 after 500 cycles at 1?A?g-1, and superior rate capability of 502.1?mA?h?g-1 at 5?A?g-1 after 10 cycles. Finally, it is believed that this method could provide a versatile and effective process to prepare other metal-oxide/reduced graphene oxide (rGO) 2D nanocomposites.

| S-EPMC6587327 | biostudies-literature

TiO2 Hollow Spheres With Flower-Like SnO2 Shell as Anodes for Lithium-Ion Batteries.

Project description:SnO2 is a promising anode material for lithium-ion batteries due to its high theoretical specific capacity and low operation voltage. However, its poor cycling performance hinders its commercial application. In order to improve the cycling stability of SnO2 electrodes, novel flower-like SnO2/TiO2 hollow spheres were prepared by facile hydrothermal method using carbon spheres as templates. Their flower-like shell and mesoporous structure highlighted a large specific surface area and excellent ion migration performance. Their TiO2 hollow sphere matrix and 2D SnO2 nano-flakes ensured good cycle stability. The electrochemical measurements indicated that novel flower-like SnO2/TiO2 hollow spheres delivered a high specific capacity, low irreversible capacity loss and superior rate performance. After 1,000 cycles at current densities of 200 mA g-1, the capacity of the flower-like SnO2/TiO2 hollow spheres was still maintained at 720 mAh g-1. Their rate capacity reached 486 mAh g-1 when the current densities gradually increase to 2,000 mA g-1.

| S-EPMC8692286 | biostudies-literature