Anode For Sodium-ion Batteries Research Articles

External ligand-free nickel-catalyzed synthesis of polypyrazines towards stable, high-capacity and low-potential sodium ion storage

Sodium ion batteries (SIBs) have been regarded as a promising alternative to lithium-ion battery owing to low cost and good sustainability, but its competitiveness in energy storage is still limited largely by the development of suitable electrode materials. Traditional inorganic anode materials for SIBs face the problems of sluggish electrochemical kinetics and large volume strain due to the insertion/extraction of large size Na+. By comparison, organic anodes have the advantages of abundance resources, renewability, and designability, but suffer from the lack of stable electrode materials with both high specific capacity and low redox potential. Here, a class of pyrazine rings-rich organic polymers (polypyrazines) were designed and synthesized through external ligand-free nickel-catalyzed carbon–carbon coupling reactions. Among them, poly(2,6-pyrazine) shows the lowest synthetic cost, the highest porosity and the best conductivity. Consequently, as the anode of SIBs, poly(2,6-pyrazine) delivers a low redox potential (about 1 V, vs Na+/Na), high-specific-capacity (617.2 mA h/g at 0.1 A/g), excellent rate-capability (300 mA h/g at 10 A/g) and long-term cycling stability (81 % after 1000 cycles at 1.0 A/g). The low preparation cost and outstanding electrochemical performance of poly(2,6-pyrazine) make it a promising anode candidate for further boosting the energy density of SIBs.

Elimination of hydrogen bonds in cellulose enables high-performance disordered carbon anode in sodium-ion batteries

Pre-oxidation remains an advantageous method to regulate the cross-linking structure of cellulose to prepare an increasingly disordered hard carbon applied in sodium-ion batteries. However, it is ambiguous how the introduction of oxygen affects the changes in the molecular structure of cellulose as well as the micro-structure of hard carbon. We herein systematically investigate the effect of air pre-oxidation on the crystallinity and cross-linking structure of cellulose macro-molecules by controlling the degree of oxidation. The findings indicate that the introduction of air can break the hydrogen bonding network of cellulose in advance and release a large number of reactive hydroxyl groups on the surface to be oxidized to form ether and ester cross-linking bonds. Ether bonds can transversely cross-link and extend the carbon layer and the bent carbon layers enclose a well-developed connective pore structure. Additionally, the breakage of oxygen-containing functional groups leads to the escape of large amounts of oxygen-containing gases to etch out more open pore structures with large pore sizes. Benefiting from these advantages, the prepared hard carbon possesses a specific capacity of 335 mAh·g‒1 and 89% of initial coulombic efficiency at 30 mA·g‒1 by pre-oxidating at 300°C for 12 h.

Construction of Microporous Structure in Hard Carbon via Adjustable Zn Salt Templates for High-Performance Sodium-Ion Batteries

Template method is an effective strategy for the construction of microporous structure in hard carbons. However, the introduction of templates will inevitably affect the original structure of hard carbon, making it necessary to develop an adjustable template for the high sodium storage property of Sodium-ion battery anodes. Herein, we propose an effective strategy of developing size-controlled ZnO microcrystal in precursor carbon by zinc salts templates and promoting the formation of numerous closed pores during subsequent pyrolysis. All of the obtained hard carbons exhibit high specific capacities of over 340 mAh/g, and initial Coulomb efficiencies of over 90%. Besides, the information of closed pore structure in hard carbon, accompanying with the diffusive behavior of Na+ and the in-situ Raman spectroscopy reveal a strong link between the increased plateau and the closed pore volume, providing a compelling insight for the mechanism of Na+ storage in hard carbon. The optimal sample exhibits the highest closed pore volume, which performs a remarkable specific capacity of 374 mAh/g and a high initial Coulombic efficiency of 92.4%. Furthermore, all zinc salt-derived hard carbon exhibit analogous microstructures and electrochemical behaviors, demonstrating the universality of utilizing both inorganic and organic zinc salts as templates for adjusting the microporous structure of hard carbon. These findings provide a systematic approach to enhance the reversible capacity and maintain high initial Coulombic efficiency for sodium-ion battery anodes.

Sulfuric acid treatment to control the microcrystalline structure of starch-based hard carbon for sodium storage

By treating starch with different concentrations of sulfuric acid, we investigated the effect of cross-linked starch-based hard carbon on the performance of sodium-ion batteries (SIBs) at various concentrations. After treatment, the optimal sample exhibits a spherical microstructure, which can provide effective active sites and enhance structural stability, thereby achieving high capacity and long cycle life for SIB electrodes. In subsequent electrochemical tests, after 100 cycles at low current density of 0.1 A g−1, the capacity of H40 remains of 306 mA h g−1. And under the high current density of 1 A g−1, the capacity of H40 can still maintain of 228 mA h g−1, exhibiting a high capacity retention rate of 89 %, which is higher than other samples. This study provides a promising approach for the large-scale production of biomass-derived carbonaceous SIBs anodes.

Innovative Multielement Modification of Pitch-Derived Two-Dimensional Carbon Nanosheets as Anodes for Superior Performance Sodium-Ion Batteries.

The development of advanced anode materials for sodium-ion batteries (SIBs) using pitch-based carbon materials has the advantages of low cost, high electrical conductivity and easy structural modification. In this research, various well-established modification techniques for petroleum pitch are integrated, including the use of recrystallized NaCl as molten salt template, pretreatment and high-temperature carbonization under a pure oxygen atmosphere, and the introduction of heteroatoms (N and S) by hydrothermal methods. The resulting two-dimensional carbon nanosheets with multielement modification exhibit enhanced Na+ storage properties, thereby bringing higher cycling stability and superior rate performance. Due to its specific structure and chemical composition, NS-P-OPDC exhibited a high reversible capacity of 406.77 mAh g-1 at a current density of 100 mA g-1 and a superior rate performance of 193.20 mAh g-1 at a current density of 3 A g-1 after being applied to the anode of SIB half-cell. Especially, a capacity retention of 97.7% was still achieved after 4000 cycles. Meanwhile, the full-cell assembled by Na3V2(PO4)3 (NVP) cathode and NS-P-OPDC anode could provide a reversible capacity of 235.30 mAh g-1 at a current density of 300 mA g-1. This application proves to advance petroleum pitch-based high-performance electrodes toward greater efficiency in electrochemical energy storage.

Biomass-derived hard carbon material for high-capacity sodium-ion battery anode through structure regulation

Economical and environmentally friendly hard carbon materials are attractive options for high-performance sodium-ion battery anode materials. Biomass-derived hard carbon materials have good economic benefits and environmentally friendliness as anode materials for sodium-ion batteries. In this work, we propose a new hard carbon material prepared from agricultural waste olive shells through a simple and environmentally friendly process. The effects of high-temperature treatments and pre-carbonization strategies on the pore structure and graphitization degree of the hard carbon materials were investigated. Combined with electrochemical performance tests, the influence of structural changes on the sodium storage properties of the olive shell-derived hard carbon was revealed. Under the optimized conditions of carbonization temperature and pre-carbonization strategy, the OSHC-Air electrode exhibits excellent sodium storage capacity with 87 % capacity remaining after 1000 cycles at 1000 mA g−1. The assembled PB//OSHC-Air sodium-ion full cell exhibits a high capacity of 216 mAh g−1. Our research provides a potential candidate for commercial anode materials for high-capacity sodium-ion batteries.

Free-standing medium-entropy porous needle-like FeCoCuNi phosphide nanowires-formed flower clusters/carbon fiber anode with high capacity and long durability for sodium-ion batteries

The drastic volume expansion and slow sodium-ion kinetics hinder the practical application of phosphides with high specific capacity and low discharge voltage in sodium-ion batteries (SIBs). Herein, we introduced entropy configuration into nanostructures and prepared a novel free-standing, three-dimensional, porous needle-like medium-entropy Fe, Co, Cu, Ni phosphide (ME-FCCNP) nanowires-formed flower clusters/carbon fiber cloth (CFC) anode (ME-FCCNP@CFC) for SIBs. The distorted lattices caused by medium-entropy configuration provide abundant sites for sodium-ion reactions and improve the electron transfer rate. The medium-entropy effects improve the mechanical stability, while the three-dimensional networks and porous needle-like nanowires provide sufficient space for the volume expansion. These combined properties enable the ME-FCCNP@CFC electrode to exhibit a high-rate capability of 170.8 mAh g−1 at 5.0 A g−1 and deliver a specific capacity of 325.8 mAh g−1 after 2000 cycles at 2.0 A g−1, far surpassing most of reported transition-metal phosphides. Moreover, the Na3V2(PO4)3 || ME-FCCNP@CFC full cell showcases a high-energy density of 256.8 Wh kg−1 and a long cycling life (267.8 mAh g−1 at 2.0 A g−1 with a capacity retention of 83.2 % after 1000 cycles). These results provide significantly promising implications for the anode design of SIBs by employing self-supporting and medium-entropy structures.

Understanding the Relationship of Closed Pore Structure in Biomass- derived Hard Carbon with Cellulose Regulating Strategy.

Recycling waste biomass to pyrolytic carbon has become a development direction of sodium-ion batteries (SIBs)anodes. However, it remains a challenge to precisely control the composition and structure of biomass to modify the properties of derived carbon. Herein, a strategy of hydrolyzing cellulose in phellem with sulfuric acid is proposed, which can promote cellulose fracture, reduce the graphitization and increase the content of closed pores in hard carbon. Accordingly, after the regulation of closed pore structure, the reversible capacity increased from 207 to 330 mAh g-1 at 20mA g-1, realizing an increase of ≈130 mAh g-1 in the plateau region and the initial Coulombic efficiency (ICE) is enhanced from 78% to 90%. When applied in full cell with O3-Na[Ni1/3Fe1/3Mn1/3]O2, it showed an energy density of 247Wh kg-1. This strategy has certain universality, and it provides the feasibility to use low-value cellulose-containing biomass to fabricate high-performance hard carbon materials.

N, S-Codoped 3D Carbon Protected Nanoporous MnS With Record High Sodium Ion Storage Performance for Potential Industry Applications.

With a high theoretical capacity, the MnS anode, however, exhibits a rather complex sodium diffusion kinetics and poor mechanical stability that hinder its application in sodium-ion batteries (SIBs). In this work, a simple, economical, and scalable strategy is developed to inherently coat nanoporous MnS with a 3D N, S co-doped thin carbon layer by using commercially available MnCO3 as precursors. Specifically, the strategy involves a two-step annealing process, which converts the MnCO3 microparticles into nanoporous Mn2O3 and MnS step by step. The 3D N, S codoped carbon layer is in situ formed during the second annealing process by first coating the nanoporous Mn2O3 with a polyaniline layer. Due to the inherent 3D carbon protection and the strong electronic interaction between N, S dopants and MnS, the N, S codoped carbon protected MnS obtained at 900 °C (NS-C@MnS-900) anode displays a high specific capacity of 845mAhg-1 at 0.1Ag-1, which is higher than all reported MnS-based SIB anodes. It also shows an outstanding cyclability and rate performance, maintaining a stable capacity of ≈493mAhg-1 after 1300 cycles at 10Ag-1, which is also the best according to knowledge. These exceptional electrochemical performances and the scalable/simple/low-cost synthesis make the NS-C@MnS-900 attractive for industry application.

Electrolyte-Salts Regulated Hydrogen-Bonding Configuration and Interphase Formation Achieving Highly Stable Anode for Rechargeable Aqueous Sodium-Ion Batteries.

Hydrogen evolution reactions that cause the alkalization of aqueous electrolytes generally frustrate the structural stability and cycling performance of NaTi2(PO4)3/C anode material for rechargeable aqueous sodium-ion batteries (ASIBs). Herein, a novel highly concentrated electrolyte with a large hydrogen-evolution overpotential and hydroxide-capture ability is rationally established by incorporating a bifunctional Mg(Ac)2 additive into a concentrated NaAc aqueous solution. The highly concentrated electrolyte salts (4m NaAc+3m Mg(Ac)2) favor regulation on hydrogen-bonding configurations and kinetically shift the hydrogen evolution potential to a lower value of -1.37 V (vs Ag/AgCl). The Mg(Ac)2 additive plays particular roles in spontaneously capturing hydroxide ions generated during hydrogen evolution reactions on anode surfaces and simultaneously forming a protective Mg(OH)2-like interphase. As a result, the unique electrolyte significantly improves the structural stability and cycling performance of NaTi2(PO4)3/C anode (94.8% capacity retention after 100 cycles at 100 mA·g-1). The effect of salt concentration on hydrogen bonding configurations of aqueous electrolytes is investigated with Raman spectroscopy and FTIR spectroscopy. The interphase is identified by coupling EDS mapping, X-ray photoelectron spectroscopy, and X-ray diffraction. This work provides a new strategy for improving the cycling stability of aqueous sodium-ion batteries.

Electrolyte Reconfiguration by Cation/Anion Cross-coordination for Highly Reversible and Facile Sodium Storage.

Hard carbon (HC) materials are promising anodes for sodium-ion batteries (SIBs) owing to low cost, high specific capacity and low working potential. However, the poor compatibility of the electrolyte with HC leads to low initial coulombic efficiency (ICE) and sluggish Na+ transport kinetics. Here, we propose an electrolyte reconfiguration strategy based on the hard and soft acid and base (HSAB) theory by introducing methyltriphenylphosphonium bromide (MTPPB). MTPPB can realize a spontaneous cross-coordination solvation structure with NaPF6 by selective affinity, synchronously optimizing the interfacial chemistry and sodium storage process. The advantages of the chemical π-π bridging of MTPP+-HC and interaction of MTPP+-PF6- contribute to preferential and oriented reduction of PF6-, forming a low-resistance supramolecular SEI. Additionally, Na+-Br- coordination weakens the Na+-solvent interactions, facilitating Na+ de-solvation kinetics. Consequently, the HC||Na cell achieves a superior ICE of 96.6%, desirable rate capability under 25 °C and invisible capacity decay after 500 cycles at 1 C under -20 °C. The Na4Fe3(PO4)2P2O7||HC pouch battery displays a high ICE of 90.3% and a 15% increment of energy density under 25 °C. This work provides a guidance through electrolyte reconfiguration engineering for designing practical HC-based SIBs with high energy/power density and long-life span in the extended operating-temperature range.

Biomass derived 3D N, P co-doped porous carbon incorporated with Ni-Cu bimetallic phosphide: Synergistic effect of Ni-Cu boosting Na+ storage performance

Transition metal phosphides (TMPs) as promising anode materials for sodium-ion batteries (SIBs) due to their amazing properties such as high theoretical specific capacity, various bond types and good electrical conductivity. However, TMPs are still facing poor cycling stability and unsatisfactory specific capacity, which restrict their practical application. Herein, NixCu3-xP incorporated in biomass derived 3D N, P co-doped porous carbon (NixCu3-xP-NPC) is constructed as SIB anode and the electrochemical behaviors with various Ni/Cu ratios are explored. The synergistic effect of Ni-Cu in NixCu3-xP is approved by the resulting investigation, and density functional theory (DFT) calculation further confirmed its important influence in enhancing electronic conductivity and boosting Na+ storage. Evidently, the optimum synergistic effect was observed when Ni0.15Cu2.85P/NPC is utilized for SIB anode. It exhibits a reversible specific capacity of 663 mAh g−1 after 200 cycles at 0.2 A g−1, long cycling stability (467 mAh g−1 after 1000 cycles at 1.0 A g−1), and excellent rate capability (432 mAh g−1 at 2.0 A g−1). The ex-situ X-ray diffraction and ex-situ X-ray photoelectron spectroscopy verify the combined conversion mechanism of Ni and Cu during sodiation/desodiation processes, which is greatly favorable for high specific capacity and cycling stability.

Abnormal Gas Generation during First Discharge Process of Sodium Ion Battery.

In recent years, sodium-ion batteries (SIBs) have attracted a lot of attention and are considered an ideal alternative to lithium-ion batteries (LIBs). The hard carbon (HC) anode in SIBs presents a unique challenge for studying the formation process of the solid electrolyte interphase (SEI) during initial cycling, owing to its distinctive porous structure. This study employs a combination of ultrasonic scanning techniques and differential electrochemical mass spectrometry to conduct an in-depth analysis of the two-dimensional distribution and composition of gases during the formation process. The findings reveal distinct gas evolution behaviors in SIBs compared to LIBs during formation. Notably, significant gas evolution is observed during the discharge phase of the formation cycle in SIBs, with higher discharge rates leading to increased gas evolution rates. This phenomenon is likely attributed to the adsorption of CO2 gas by the abundant pores in HC, followed by desorption during discharge. Furthermore, the study demonstrates that the addition of 5A molecular sieves, which competitively adsorb gases, effectively reduces gas adsorption on the anode during formation, thereby significantly enhancing battery performance. This research elucidates the gas adsorption and desorption behavior at the battery interface, providing new insights into the SEI formation process in SIBs.

Abnormal Gas Generation during First Discharge Process of Sodium Ion Battery

AbstractIn recent years, sodium‐ion batteries (SIBs) have attracted a lot of attention and are considered an ideal alternative to lithium‐ion batteries (LIBs). The hard carbon (HC) anode in SIBs presents a unique challenge for studying the formation process of the solid electrolyte interphase (SEI) during initial cycling, owing to its distinctive porous structure. This study employs a combination of ultrasonic scanning techniques and differential electrochemical mass spectrometry to conduct an in‐depth analysis of the two‐dimensional distribution and composition of gases during the formation process. The findings reveal distinct gas evolution behaviors in SIBs compared to LIBs during formation. Notably, significant gas evolution is observed during the discharge phase of the formation cycle in SIBs, with higher discharge rates leading to increased gas evolution rates. This phenomenon is likely attributed to the adsorption of CO2 gas by the abundant pores in HC, followed by desorption during discharge. Furthermore, the study demonstrates that the addition of 5A molecular sieves, which competitively adsorb gases, effectively reduces gas adsorption on the anode during formation, thereby significantly enhancing battery performance. This research elucidates the gas adsorption and desorption behavior at the battery interface, providing new insights into the SEI formation process in SIBs.

CVD-Synthesized Titanium Carbide Nanoflowers as High-Performance Anodes for Sodium-Ion Batteries.

Sodium-ion batteries (SIBs) have emerged as promising candidates for energy storage applications due to the abundance and low cost of sodium. However, the larger radius of sodium ions limits their diffusion kinetics within electrode materials and contributes to electrode volume expansion. Here, we successfully synthesized porous titanium carbide (TiC) nanoflowers through chemical vapor deposition (CVD). The TiC nanoflowers exhibit exceptional electrochemical performance as SIB anodes, with their porous structure enhancing the conductivity, mechanical stability, and Na-ion diffusion. The TiC nanoflowers demonstrate a high reversible specific capacity of 73.5 mAh g-1 at 1 A g-1 after 2500 cycles, corresponding to an impressive capacity retention of 80.81%. Additionally, we developed a full sodium-ion cell utilizing TiC nanoflowers as the anode and Na3V2(PO4)3 as the cathode, which demonstrates a substantial reversible capacity and outstanding cycling stability. Our work presents a promising strategy for synthesizing nanostructured TiC materials as anode electrodes for SIBs.

Cu2-xSe@MXene (Ti3C2Tx) 2D layered heterostructure as an anode for high-performance sodium-ion batteries

With a notable focus on developing efficient sodium storage electrode materials, sodium-ion batteries (SIBs) have been identified as a promising contender in the pursuit of high-performing substitutes for lithium-ion batteries. Among varying sodium storage anode materials for SIBs, nonstoichiometric Cu2-xSe exhibits significant promise. This material stands out due to its ultrahigh electrical conductivity and theoretical sodium storage capacity. However, the practical implementation of Cu2-xSe-based anodes in SIBs is significantly impeded by their sluggish electrochemical reaction kinetics and severe pulverization during the repeated charge–discharge cycles. In the current research, we introduce a novel and straightforward methodology for the synthesis of a heterostructured SIBs anode material (Cu2-xSe@Ti3C2Tx), by coupling Cu2-xSe nanoparticles with two-dimensional (2D) layered MXene (Ti3C2Tx). The 2D layered Ti3C2Tx can provide abundant fast Na+ transport pathways, which effectively promote the ion transport kinetics in the composite anode. Moreover, the pulverization of Cu2-xSe can be effectively mitigated due to the interlamellar spatial confinement of the 2D layered MXene matrix. Consequently, the electrochemical performances of the Cu2-xSe-based anode are significantly improved. Concretely, the Cu2-xSe@Ti3C2Tx anodes demonstrate remarkable rate performance (248mAh g−1 at 10.0 A/g), along with commendable cycling stability, exhibiting a capacity retention of 92 % at 5.0 A/g after 750 cycles. A comprehensive assessment of the Cu2-xSe@Ti3C2Tx anode has been conducted by assembling a full SIB alongside a Na3V2(PO4)3 cathode. This comprehensive study underscores the significant potential of Cu2-xSe-based composite materials, positioning it as a promising candidate for future advancements in SIB technology.

An Oriented Diffusion Strategy to Configure All-Region Ultrahigh-Density Metal Single Atoms for High-Capacity Sodium Storage.

Single-atom metals (SAMs), despite being promising for high-utilization catalysis, biomedicine, and energy storage, usually suffer from limited catalytic performance caused by low metal loading. Herein, via an oriented diffusion strategy, all-region ultrahigh-loading (18.9wt.%) Sn-SAMs over carbon nanorings matrix (Sn-SAMs@CNR) are initially achieved based on the transformation of a g-C3N4@SnO2@polydopamine ring-like nested structure. The formation process of Sn-SAMs involves a critical conversion from oxygen-coordination (SnO2) to nitrogen-coordination (Sn-N4) and simultaneous anti-Osterwalder ripening promoted under spatial confinement. Notably, the g-C3N4-derived N-containing gaseous intermediates dynamically drive the oriented diffusion (inside-out diffusion) of Sn-SAMs across the carbon nanorings, realizing an all-region ultrahigh loading of SAMs throughout the carbon matrix. This strategy is also applied to other metal materials (Fe, Co, Ni, Cu, and Sb), and features excellent universality. When applied as the anode for sodium-ion batteries, experimental analyses and theoretical calculations demonstrate that high-loading Sn-N4 active sites significantly optimize electron density distribution and improve reaction kinetics. Consequently, Sn-SAMs@CNR exhibits outstanding durability of 364mAhg-1 even after 5000 cycles with an impressively low (0.00068%) capacity decay per cycle. This work opens up a universally new avenue for all-region ultrahigh loading of SAMs to carbon matrix for high-performance energy storage.

Towards More Sustainable Schiff Base Carboxylate Anodes for Sodium-Ion Batteries.

Bismine sodium salt (BSNa), a Schiff base with two sodium carboxylates, has shown promising electrochemical performance as an anode material. However, its synthesis involves toxic reagents and generates impurities, requiring significant solvent use for purification. This study introduces a novel synthetic method using sodium hydroxide as the sole reagent, which acts as both a base and Na source in the ion exchange step. With this procedure, we reduce the amounts of chemicals, diminish toxicity, improve the purity of the target compound, and use less solvent while maintaining comparable electrochemical performance. Additionally, the procedure is carried out under anhydrous conditions that avoid the undesirable hydrolysis of the imine linkages. In a previous report, the processing of the composite electrode was not established. In this article, we address this issue; the electrochemical performance, specifically the rate capability, is enhanced by processing the electrodes in laminate form rather than powder. As alternative to N-methyl-2-pyrrolidone (NMP), a common but disadvantageous solvent in laminate processing, other solvents were explored by testing acetone (DMK), methylisopropylketone (MIPK), and a DMK-NMP mixture. The remarkable electrochemical performance (specific capacity of 260-280 mAh/g, and capacity retentions higher than 84% at 1C (260 mA/g) remained consistent across these solvents. Furthermore, we investigated replacing copper with aluminum as the current collector to reduce costs and increase the energy density of the battery. While aluminum performed comparably to copper at low specific currents C/10 (26 mA/g), it showed a significant shift in the redox process potentials at higher specific currents.

High-Capacity Anode for Sodium-Ion Batteries Using Hard Carbons Derived from Polyurea-Cross-Linked Silica Xerogel Powders

High-Capacity Anode for Sodium-Ion Batteries Using Hard Carbons Derived from Polyurea-Cross-Linked Silica Xerogel Powders

Three-Dimensional Flexible SnO2@Hard Carbon@MoS2@Soft Carbon Fiber Film Anode toward Ultrafast and Stable Sodium Storage.

Developing flexible electrodes for the application in sodium-ion batteries (SIBs) has received great attention and has been still challenging due to their merits of additive-free, lightweight, and high energy density. In this work, a free-standing 3D flexible SIB anode with the composition of SnO2@hard carbon@MoS2@soft carbon is designed and successfully synthesized. This electrode combines the energy storage advantages and hybrid sodium storage mechanisms of each material, manifested in the enhanced flexibility, specific capacity, conductivity, rate, cycling performances, etc. Based on the synergistic effects, it exhibits much higher specific capacity than SnO2 carbon nanofibers, as well as more excellent cycling performance (250 mA h g-1 after 500 cycles at 1 A g-1) than MoS2 nanospheres (32 mA h g-1). In addition, relevant kinetic mechanisms are also expounded with the aid of theoretical calculation. This work provides a feasible and advantageous strategy for constructing high-performance and flexible energy storage electrodes based on hybrid mechanisms and synergistic effects.