Sulfur Host For Lithium-sulfur Batteries Research Articles

Sub-nanometer cobalt clusters embedded carbon networks to promote the kinetics of polysulfide conversion

The sluggish oxidation-reduction kinetics of sulfur and the shuttle effect of polysulfides are the bottlenecks restricting the practical application of lithium-sulfur batteries. In this study, subnanometer cobalt clusters were embedded into the cross-linked network of carbon sheets framework as high-efficiency sulfur host materials to promote the kinetics of polysulfides conversion for lithium-sulfur batteries. In such composite structure, the carbon network provides a rapid electron transfer pathway for interfacial electrochemical reaction. Co and N atoms can chemisorb polysulfides by forming Co-S and Li-N bonds with polysulfides, and catalyze the conversion of polysulfides. Such structure exhibits excellent rate performance and cycle stability during the cycle of lithium-sulfur battery. The capacity decay rate per cycle is only 0.061% for 500 cycles at 1 C, and the capacity retention rate is 69.4%. The composite structure developed in this work is a promising and high-efficiency sulfur host for lithium-sulfur batteries.

Ce-Doped Three-Dimensional Ni/Fe LDH Composite as a Sulfur Host for Lithium-Sulfur Batteries.

Lithium-sulfur batteries (LSBs) have become the most promising choice in the new generation of energy storage/conversion equipment due to their high theoretical capacity of 1675 mAh g-1 and theoretical energy density of 2600 Wh kg-1. Nevertheless, the continuous shuttling of lithium polysulfides (LiPSs) restricts the commercial application of LSBs. The appearance of layered double hydroxides (LDH) plays a certain role in the anchoring of LiPSs, but its unsatisfactory electronic conductivity and poor active sites hinder its realization as a sulfur host for high-performance LSBs. In this paper, metal organic framework-derived and Ce ion-doped LDH (Ce-Ni/Fe LDH) with a hollow capsule configuration is designed rationally. The hollow structure of Ce-Ni/Fe LDH contains a sufficient amount of sulfur. Fe, Ni, and Ce metal ions effectively trap LiPSs; speed up the conversion of LiPSs; and firmly anchor LiPSs, thus effectively inhibiting the shuttle of LiPSs. The electrochemical testing results demonstrate that a lithium-sulfur battery with capsule-type S@Ce-Ni/Fe LDH delivers the initial discharge capacities of 1207 mAh g-1 at 0.1 C and 1056 mAh g-1 at 0.2 C, respectively. Even at 1 C, a lithium-sulfur battery with S@Ce-Ni/Fe LDH can also cycle 1000 times. This work provides new ideas to enhance the electrochemical properties of LSBs by constructing a hollow capsule configuration.

Graphene/Heterojunction Composite Prepared by Carbon Thermal Reduction as a Sulfur Host for Lithium-Sulfur Batteries.

An interlayer nanocomposite (CC@rGO) consisting of a graphene heterojunction with CoO and Co9S8 was prepared using a simple and low-cost hydrothermal calcination method, which was tested as a cathode sulfur carrier for lithium-sulfur batteries. The CC@rGO composite comprises a spherical heterostructure uniformly distributed between graphene sheet layers, preventing stacking the graphene sheet layer. After the introduction of cobalt heterojunction on a graphene substrate, the Co element content increases the reactive sites of the composite and improves its electrochemical properties to some extent. The composite exhibited good cycling performance with an initial discharge capacity of 847.51 mAh/g at 0.5 C and a capacity decay rate of 0.0448% after 500 cycles, which also kept 452.91 mAh/g at 1 C and in the rate test from 3 C back to 0.1 C maintained 993.27 mAh/g. This article provides insight into the design of cathode materials for lithium-sulfur batteries.

Bimetal-Organic Framework Nanoboxes Enable Accelerated Redox Kinetics and Polysulfide Trapping for Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries are considered as promising candidates for next-generation energy storage systems in view of the high theoretical energy density and low cost of sulfur resources. The suppression of polysulfide diffusion and promotion of redox kinetics are the main challenges for Li-S batteries. Herein, we design and prepare a novel type of ZnCo-based bimetallic metal-organic framework nanoboxes (ZnCo-MOF NBs) to serve as a multifunctional sulfur host for Li-S batteries. The hollow architecture of ZnCo-MOF NBs can ensure fast charge transfer, improved sulfur utilization, and effective confinement of lithium polysulfides (LiPSs). The atomically dispersed Co-O4 sites in ZnCo-MOF NBs can firmly capture LiPSs and electrocatalytically accelerate their conversion kinetics. Benefiting from the multiple structural advantages, the ZnCo-MOF/S cathode shows high reversible capacity, impressive rate performance, and superior cycling stability for 300 cycles.

CoSe2 nanoparticles-decorated carbon nanofibers as a hierarchical self-supported sulfur host for high-energy lithium-sulfur batteries

Lithium-sulfur (Li-S) batteries have gained widespread attention owing to their high theoretical energy density and low cost. However, the commercial application of these batteries is hindered by the severe shuttle effect and slow redox reaction kinetics of polysulfides. In this study, a hierarchically porous membrane consisting of CoSe2 nanoparticle-decorated carbon nanofibers containing carbon nanotubes (CoSe2@CNF/CNT) is constructed as a self-supported sulfur host for Li-S batteries. The hierarchical conductive network of CNFs/CNTs with N-doped porous carbon facilitates electron/ion transport and provides sufficient space to mitigate the volume expansion of lithium polysulfides (LiPSs). Moreover, the modified CoSe2 nanoparticles serve as both chemical trappers and electrocatalysts, chemically anchoring LiPSs and accelerating the redox kinetics to inhibit the shuttle effect. As a result, an initial specific discharge capacity of 1098.8 mA h g−1 is achieved at 1 C. Importantly, the cathode exhibits superior cycling stability with a capacity decay rate as low as 0.06% over 500 cycles. This work offers a feasible approach to designing multi-functional sulfur hosts for high-energy-density Li-S batteries.

Tubular C3N4 Nanotubes as Metal-Free Sulfur Hosts toward Stable Lithium–Sulfur Batteries

Lithium–sulfur batteries (LSBs) with high energy density have the potential to replace current commercial lithium-ion batteries. However, the shuttle effect and the low conversion kinetics of lithium polysulfide (LiPS) remain the main challenges in the development of LSBs. In this study, a metal-free and simple-to-prepare carbon nitride with a high surface area and tubular morphology (CN-nt) is used as the sulfur host for LSBs. Due to its unique nanostructure and rich active sites, it not only effectively disperses the active sulfur material and anchors soluble polysulfide species, but it also promotes the nucleation process of Li2S, thus achieving fast and sustainable Li-S redox reactions. Experimental results show that the obtained S@CN-nt electrodes exhibit a high sulfur utilization of 1296.2 mAh g−1 at 0.1 C and a significant rate capability of 689.4 mAh g−1 at the high current rate of 3C. More importantly, the capacity retention reaches 87.7% after 500 cycles. This simple strategy of engineering unique carbon-based nanostructured hosts can inspire new ideas for developing cost-effective and metal-free host materials for sulfur-based batteries.

Electrospun CuCoN0.6 coating necklace-like N-doped carbon nanofibers for high performance lithium-sulfur batteries

Freestanding electrodes with high energy density and cycle stability have attracted attention on the development of lithium-sulfur (Li-S) batteries. However, both severe shuttle effect and sluggish conversion kinetics hinder their practical applications. Herein, we employed the electrospinning and subsequent nitridation processes to prepare a necklace-like structure of CuCoN0.6 nanoparticles anchored on N-doped carbon nanofibers (CuCoN0.6/NC) as freestanding sulfur host for Li-S batteries. Such bimetallic nitride boosts chemical adsorption and catalytic activity throughout detailed theoretical calculation and experimental electrochemical characterization. The three-dimensional conductive necklace-like framework could provide abundant cavities for realizing high sulfur utilization and alleviating the volume variation, as well as fast lithium-ions diffusion and electron transfer. The Li-S cell with the S@CuCoN0.6/NC cathode delivers a stable cycling performance with a capacity attenuation rate of 0.076% per cycle after 150cycles at 2.0C and an exceptional capacity retention of 657 mAh g−1 even at a high sulfur loading of 6.8 mg cm−2 over 100cycles. The facile and scalable method can help promote the widespread application of fabrics.

Hollow carbon dual-decorated with MnO2 shielding layer and carbon nanotube as a sulfur host for Li-S batteries

The shuttle effect of polysulfides and sluggish reaction kinetics have been the main obstacles for the practical applications of lithium-sulfur (Li-S) batteries. Herein, we report a rationally designed sulfur cathode (DLHC/S@MnO2-ACNT) based on double-layered hollow carbon sphere (DLHC) decorated with manganese dioxide (MnO2) shielding layer and carbon nanotube conductive network (ACNT). The Ultramicrotome technique demonstrates that S and MnO2 nanosheets are mainly located into the interlayer of the DLHC. In the elaborate nanostructured protocol, the interlayer MnO2 nanosheets catalyze the conversion of polysulfides and the surface MnO2 nanosheets effectively adsorb polysulfides to suppress the shuttle effect. Additionally, the ACNT conductive network facilitates electrons/ions transport. Benefiting from the hierarchical confinement, Li-S batteries with DLHC/S@MnO2-ACNT composite cathodes exhibit a high reversible capacity of 1051 mAh g−1 at 0.5 C and a remarkable cycling stability over 500 cycles at 1 C. Even at a high sulfur loading of 4 mg cm−2, the cell delivers a superior areal capacity of 4.47 mAh cm−2. This work provides a new route to the design of hierarchical confinement sulfur hosts for high-performance Li-S batteries.

Encapsulation of sulfur inside micro-nano carbon/molybdenum carbide by in-situ chemical transformation for high-performance Li-S batteries

AbstractIn lithium-sulfur (Li-S) batteries, the electrochemical properties of the sulfur cathode are determined by the sulfur host, and this controls the shuttle effect and the kinetics, two of the major problems in these batteries. We confined the S in hollow thin-wall C/Mo2C particles smaller than 7 nm across that clustered together to form micrometer-size particles. The conducting network of C/Mo2C shells facilitates lithium-ion and electron transport while acting as a barrier to the outward diffusion of polysulfides. They also improve the redox kinetics because of the catalytic conversion of polysulfides to sulfur. As a result of these features the material achieved a high reversible capacity of 1 210 mAh g−1 at 0.5 C with a low capacity fade rate of 0.127% per cycle over 300 cycles and a high rate performance (780 mAh g−1 at 3.0 C). It is expected that this work will help in the design of sulfur hosts for Li-S batteries with a high rate performance and high cycling stability.

Bio-mass derived hierarchically porous and high surface area carbon as an efficient sulfur host for lithium-sulfur batteries

Lithium–sulfur (Li-S) batteries are attractive candidates for electric vehicles and grid storage applications due to their high energy density than Li-ion batteries. Development of high energy Li-S batteries employing eco-friendly, and bio-waste derived materials will further increase the sustainability of the energy storage devices. Herein, we utilize porous carbon derived from waste watermelon rind for Li-S battery application. The porous carbon with hierarchal architecture, and functional heteroatoms can efficiently infiltrate the sulfur cathode and overcomes the major challenges in the Li-S battery, namely (i) poor electronic conductivity of sulfur cathode, and (ii) dissolution of long-chain polysulfides. The Li-S cell with a sulfur-infiltrated porous carbon delivered a high initial discharge capacity of 1176 mAh g−1 at 0.5C rate with a low capacity fading rate of 0.057% over 500 cycles. The strong carbon framework can accommodate the volume changes during the sulfur conversion reaction, and the unoccupied pores in porous carbon can function as polysulfide reservoir to efficiently trap polysulfide migration to achieve a high stability. The highly inter-connected hierarchical pores further facilitated a faster electronic and ionic transport to achieve a high rate performance, higher than pristine sulfur cathode. These results demonstrate the potential to develop high-performance energy storage devices using eco-friendly and renewable materials for electric vehicles and other energy storage systems.

Layered double hydroxides used as the sulfur hosts for lithium-sulfur batteries and the influence of metal composition on their performance

Layered double hydroxides used as the sulfur hosts for lithium-sulfur batteries and the influence of metal composition on their performance

Hierarchical carbon hollow nanospheres coupled with ultra-small molybdenum carbide as sulfiphilic sulfur hosts for lithium-sulfur batteries.

Lithium-sulfur (Li-S) batteries are an attractive candidate to replace the current state-of-the-art lithium-ion batteries due to their promising theoretical capacity of 1675 mA h g-1 and energy density of 2500 W h kg-1. However, the lithium polysulfide (LiPS) shuttle effect and the slow sulfur redox kinetics seriously decrease the utilization of sulfur and deteriorate battery performance. Here, hierarchical carbon hollow nanospheres containing intimately coupled molybdenum carbide nanocrystals were synthesized as a sulfiphilic sulfur host. The sufficient interior void space accommodates the sulfur and physically confines LiPSs, while the in situ introduced molybdenum carbide nanoparticles can chemically immobilize LiPSs and catalytically accelerate their redox transformations. As a result, the Li-S batteries with this synergistic effect achieve an excellent rate capability of 566 mA h g-1 at 2C and a long cycle stability over 300 cycles at 1C.

Sulfur-deficient MoS2-carbon hollow nanospheres for synergistic trapping and electrocatalytic conversion of polysulfides.

Lithium-sulfur battery is one of the most promising candidates for next-generation energy storage systems, but the serious shuttle effect and sluggish reaction kinetics of polysulfides impair its practical applications. Herein, sulfur-deficient MoS2/carbon hollow nanospheres (MoS2-CHNs) are firstly synthesized by a NaCl-template pyrolysis and employed as sulfur host for lithium-sulfur batteries. TEM analysis reveals that carbon hollow nanospheres existing in the composite are the backbones that help to immobilize the ultrathin MoS2 nanosheets and ensure their large specific surface area. The MoS2 nanosheets consist of 5-10 layers of MoS2 with rich sulfur vacancies. The first principle calculation demonstrates that sulfur vacancy led to an intensively enhanced binding energy (-4.70eV) towards Li2S6 compared to the pristine MoS2 (-1.57eV). It suppressed the shuttle effect efficiently. The catalytic experiments reveal that MoS2-CHNs have a superior ability for the nucleation of Li2S and bidirectional electrocatalytic capability for the conversion of polysulfide. The large storage space inside MoS2-CHNs can work as a reservoir for intermediate polysulfides to substantially reduce the concentration overpotential. Due to this advantageous structural design of MoS2-CHNs electrode, its reversible capacity remains 1139 mAh g-1 after 100 cycles at 0.2C, and 600 mAh g-1 after 500 cycles at 5C with a sulfur loading of 5mgcm-2. Even though the sulfur loading increases to 10mgcm-2, the Li-S battery delivers a stable capacity of 978 mAh g-1 after 50 cycles at 0.2C. So the MoS2-CHNs demonstrate a promising application for high-energy Li-S batteries.

Porosity vs carbon shell number: Key factor actually affecting the performance of multi-shelled hollow carbon nanospheres in Li-S batteries

• The pores in the carbon shells of HCNs play a key role in the Li + diffusion and Li 2 S x confinement. • Simply increasing the shell number in HCNs can not effectively confine the leakage of Li 2 S x from the S cathode. • Porous 1S-HCNs endow the S cathode with better cycling stability and rate capability than the oligoporous 2S-HCNs and 3S-HCNs do. • After 700 cycles, a capacity of 759 mAh g -1 with 63% retention is achieved for the S@1S-HCNs cathode at 0.2 C. As a type of sulfur host for lithium-sulfur batteries (LSBs), hollow carbon nanospheres (HCNs) are of particular interest due to their high electrical conductivity, available cavities, and unique morphology. However, there is a lack of in-depth study about the pivotal factors affecting their performance in LSBs. Herein, a series of multi-shelled HCNs have been prepared by a template-free method and the corresponding sulfur cathodes have been systematically investigated. A positive dependence of electrochemical properties on the specific surface area and pore volume of HCNs is confirmed. In case of low porosity of carbon shell, increasing the shell numbers in HCNs could not accelerate the Li + diffusion and restrict the dissolution of lithium polysulfide in the S@HCNs cathode. As a result, the highly porous 1S-HCNs endow the sulfur cathode with better cycling stability and rate performance than the oligoporous 2S-HCNs and 3S-HCNs do. This work may not only provide a useful reference in the design of novel sulfur hosts but also shed a light on the understanding of the complicated mechanism behind the sulfur redox reactions.

Kinetic Acceleration of Lithium Polysulfide Conversion via a Copper-Iridium Alloying Catalytic Strategy in Li-S Batteries.

To solve the shuttle effect of soluble lithium polysulfides (LiPSs), a porous N-doped carbon-supported copper-iridium alloy catalyst composite (CuIr/NC) has been synthesized and served as a modified cathode sulfur host for lithium-sulfur batteries (LSBs). The metal-organic framework-derived calcined carbon frameworks build efficient conductive channels for fast ion/electron transport. Furthermore, alloying noble metals Ir with thiophilic metal Cu provides abundant active sites to effectively capture LiPSs and accelerate the catalytic conversion process, originating from modulating the surface electronic structure of the metal Cu by introducing Ir atoms to affect the 3d-orbital distribution. All of the above are strongly supported by a range of characterization studies and density functional theory calculations. Benefiting from the above advantages, the LSBs generally show satisfactory cycling performance. Apart from exhibiting a terrific initial specific capacity of 1288 mA h g-1 at 0.2 C, they can also keep long-term cycling stability under a high current density up to 5 C together with a slow specific capacity decay ratio (0.033%) per cycle after 1000 cycles. In addition, it is worth mentioning that a high areal capacity (4.7 mA h cm-2) with a low E/S ratio (6.2 μL mg-1) could still be accomplished at higher sulfur loading (4.3 mg cm-2).

Rational design of ultrathin Mo2C/C nanosheets decorated on mesoporous hollow carbon spheres as a multifunctional sulfur host for advanced Li-S batteries

Developing sulfur hosts with reasonable structure and effective catalyst is essential for lithium-sulfur (Li-S) batteries. Herein, a novel multifunctional sulfur host composed of hollow carbon spheres with mesoporous channels (MHCS) coupled with few ultrathin Mo2C/C nanosheets embedded with Mo2C nanocrystals ([email protected]2C/C) has been prepared via one-pot self-assembly and in-situ grown strategies. The Mo2C/C nanosheets with heterostructure can shorten the electron/ion transport path, and ultra-small Mo2C nanocrystals with abundant active sites contribute to enhancing chemical adsorption towards polysulfides and propel their conversion. Meanwhile, the MHCS facilitates physical adsorption towards polysulfides, effective sulfur/electrolyte permeation, fast electron/ion transportation, and sufficient buffering for volume change. Given these, the multifunctional [email protected]2C/C-S cathode demonstrates an initial specific capacity of 1316.8 mAh g−1 at 0.1 C and outstanding cycling stability with an average capacity decay rate of 0.045 % for 500 cycles at 0.5 C. Moreover, [email protected]2C/C-S cathode with high areal sulfur loading of 4.5 mg cm−2 can deliver a high initial discharge specific capacity of 797.4 mAh g−1, and a reversible capacity of 542.7 mAh g−1 after 500 cycles at 0.5 C. It is expected this work could provide a new perspective to the rational design of sulfur hosts for Li-S batteries with enhanced performance.

A hollow Co0.12Ni1.88S2/NiO heterostructure that synergistically facilitates lithium polysulfide adsorption and conversion for lithium-sulfur batteries

• An ingenious Co 0.12 Ni 1.88 S 2 /NiO heterostructure with a hollow and semi-open architecture was engineered in situ , which synergistically enhanced lithium polysulfide adsorption and conversion for lithium-sulfur batteries. • The considerable electrochemical impedance variation was observed via in situ EIS measurements, which was proved to be related to the content of soluble LiPSs in the electrolyte. • The mechanisms of the strong affinities between Co 0.12 Ni 1.88 S 2 /NiO and lithium polysulfides, and the catalytic effect were further investigated by theoretical calculations. The significant capacity deterioration and inadequate cycling lifespan that are mainly caused by the undesirable “shuttle effect” and torpid redox kinetics have encumbered the development of practically applicable lithium-sulfur (Li-S) battery technology. Modifying sulfur cathodes with lithium polysulfide (LiPS) adsorptive and electrocatalytic host materials is a promising approach to resolving these issues. Herein, a Co 0.12 Ni 1.88 S 2 /NiO heterostructure, which has multiple merits, is designed and serves as a sulfur host to improve the electrochemical performance of Li-S batteries. Possessing strong LiPS adsorbability and excellent electrocatalytic activity, the heterostructural Co 0.12 Ni 1.88 S 2 /NiO exhibits favorable synergistic effects, which effectively facilitate the anchoring and converting of diffused LiPSs. As a result, the corresponding cell delivers rapid redox kinetics and higher sulfur utilization. An impressive initial discharge capacity of 1424.8 mAh g −1 and a reversible capacity near 1056.7 mAh g −1 at 1 C over 1000 cycles are achieved with an average Coulombic efficiency of 98.8%. Benefiting from the unique nanoarchitecture and superior catalytic efficiency, only a very small amount of Co 0.12 Ni 1.88 S 2 /NiO (∼7 wt% in the cathode) is used as the sulfur host. The rational design of Co 0.12 Ni 1.88 S 2 /NiO in this work will hopefully offer inspiration for exploring advanced heterostructure materials for Li-S batteries and other electrochemical devices. Heterostructural Co 0.12 Ni 1.88 S 2 /NiO was engineered as a sulfur host for lithium-sulfur batteries. The catalytic effect and strong LiPS adsorbability synergistically promoted redox kinetics and LiPS conversion, which significantly improved the sulfur utilization during the charging and discharging processes.

Metal Ion Cutting-Assisted Synthesis of Defect-Rich MoS2 Nanosheets for High-Rate and Ultrastable Li2S Catalytic Deposition.

Active metal ions often show a strong cutting effect on the chemical bonds during high-temperature thermal processes. Herein, a one-pot metal ion cutting-assisted method was adopted to design defect-rich MoS2-x nanosheet (NS)/ZnS nanoparticle (NP) heterojunction composites on carbon nanofiber skeletons (CNF@MoS2-x/ZnS) via a simple Ar-ambience annealing. Results show that Zn2+ ions capture S2- ions from MoS2 and form into ZnS NPs, and the MoS2 NSs lose S2- ions and become MoS2-x ones. As sulfur hosts for lithium-sulfur batteries (LSBs), the CNF@MoS2-x/ZnS-S cathodes deliver a high reversible capacity of 1233 mA h g-1 at 0.1 C and keep 944 mA h g-1 at 3 C. Moreover, the cathodes also show an extremely low decay rate of 0.012% for 900 cycles at 2 C. Series of analysis indicate that the MoS2-x NSs significantly improve the chemisorption and catalyze the kinetic process of redox reactions of lithium polysulfides, and the heterojunctions between MoS2-x NSs and ZnS NPs further accelerate the transport of electrons and the diffusion of Li+ ions. Besides, the CNF@MoS2-x/ZnS-S LSBs also show an ultralow self-discharge rate of 1.1% in voltage. This research would give some new insights for the design of defect-rich electrode materials for high-performance energy storage devices.

The Fig-Like hierarchical Double-Shelled hollow TiN particles as sulfur host for Lithium-Sulfur batteries

Lithium-sulfur battery(LSB)’s commercial manufacturing has been mainly retarded by the “shuttle effect” and low electrical conductivity of polysulfides (LiPSs). Designing a cathode with hollow and hierarchically porous structures was expected to solve the above problems. Herein, a kind of TiN particles with the hierarchical hollow double-shelled structures was synthesized and applied to cathodes of LSB. The Fig-like hollow TiO2 particles (FHTiO2s) were firstly synthesized by the hard-template method. Subsequently, the Fig-like hierarchical hollow double-shelled TiN particles (FHTiNs) were synthesized by the template-free sequential transformation and separation approach (STSA). It was verified that the heating temperature and time were key parameters. Special Fig-like double-shell hollow structures could greatly increase the loading of S, and the excellent initial capacity of FHTiNs cathodes was up to 1159 mAh/g. On the one hand, the Fig-like framework in internal cavity and double-shell structures could promote the ultrahigh specific surface area, and the adsorption to LiPSs was improved by increasing active sites; On the other hand, the shuttle effect of LiPSs was weakened by the fig-like framework and double-shell structures, which slowed down the massive dissolution of sulfur in the electrolyte. As a result, the pleasant rate performance of FHTiNs cathodes was up to 400 mAh/g at 5C. This novel structures and synthesis method provided a new strategy for the designing of LSB cathodes.

Bamboo-shaped Co@NCNTs as superior sulfur host for Li-S batteries

Functional and active carbon material is of great concern in facilitating the performance of lithium-sulfur (Li-S) battery. In this work, we develop a bamboo-like nitrogen-doped carbon nanotubes (Co@NCNTs-2) with low cobalt metal content, which acts as not only the host matrix for sulfur loading but also an efficient catalyst for the adsorption and conversion of lithium polysulfides (LiPSs). The characterization results show that the Co particles are mainly encapsulated inside the Co@NCNTs-2, and the N species are mainly distributed on the outer surface of Co@NCNTs-2. The Co particles are the growth sites of carbon nanotubes and are wrapped by carbon to form Co@NCNTs-2. It is confirmed that the uniform graphitized structure contributes to charge transfer, while the enriched N species assist the trap and catalytic conversion of the polysulfides, thus helping to restrain the shuttle effect. As a result, the resultant Co@NCNTs-2-S cathode presents high reversible capacity at different current densities and exhibits superior cycling stability for 300 cycles at 0.5 C.