Lithium-sulfur (Li-S) batteries offer unique advantages, which include an energy density six times greater than that of current commercial lithium-ion batteries and low production cost owing to the abundance of sulfur resources [1,2]. Furthermore, the equipment for Li-S battery production is similar to that used for lithium-ion battery production. This condition offers a distinct competitive advantage to Li-S battery manufacturers in the secondary battery market [3,4]. The superior energy density and substantial commercial potential of Li-S batteries have attracted widespread attention in recent years [5]. However, several inherent flaws hinder their commercialization. These flaws include the low electrical conductivity of sulfur, which increases internal resistance and impedes reaction kinetics, and the shuttle effect due to polysulfide dissolution, which reduces sulfur utilization efficiency [6,7].

A common strategy for resolving these flaws involves compositing sulfur with carbon materials to improve conductivity and incorporating polar metallic components to enhance adsorption and catalytic activity. This strategy mitigates the shuttle effect and accelerates electrochemical reaction kinetics [8–12]. However, these methods do not fully resolve the dissolution and shuttling effect of polysulfides. Wang et al. altered the dissolution–precipitation mechanism by covalently bonding sulfur to the main chain of polyacrylonitrile (PAN) to form sulfurized polyacrylonitrile (SPAN). This modification effectively prevents polysulfide formation and significantly improves battery performance [13]. Although SPAN effectively addresses the dissolution and shuttling effects of polysulfides, the scarcity of bonding sites on the PAN molecular chain, along with the need for additional conductive agents, binders, and current collectors, further reduces active material loading capacity [14–16]. Consequently, the actual loading capacity of SPAN rarely exceeds 40 wt% [17]. In our previous work, SeS_x was incorporated into the lotus-root-like pores of SPAN to obtain a standalone cathode with a loading capacity of 53 wt% [18]. During discharge, the insoluble products from the nucleophilic reaction of SeS_x with carbonate electrolytes form a solid electrolyte interface on the surface of the porous structure. This interface protects the extended solid–solid reaction pathway of S₈ to Li₂S. However, the low conductivity of the solid discharge product, Li₂S, exacerbates sulfur accumulation within the battery, which in turn impedes the transfer of electrons and ions to internal sulfur atoms [19–22]. Moreover, high energy barriers prevent the nucleation and decomposition of solid Li₂S. This effect impedes the overall reaction kinetics [23]. These challenges become more pronounced as the surface loading of active materials increases. To advance the commercialization of Li-SPAN batteries, it is crucial to develop innovative electrocatalysts that enhance the kinetics of redox reactions. Integrating these electrocatalysts with SPAN cathode materials effectively anchors polysulfides and substantially lowers the reaction barriers for converting S₈ to Li₂S, thereby accelerating the redox kinetics along this solid-solid reaction pathway. This strategy is expected to improve the efficiency of battery charge-discharge cycles significantly and extend its operational lifespan [24,25]

In this study, a heterostructure with an embedded electric field is proposed. This contraption features graded porous structures and in situ encapsulation of the cathode solid electrolyte interface (CEI) to enhance active material loading and improve electrochemical reaction kinetics. A self-supporting SeSPAN film integrated with FeS₂/CoS₂ heterostructure nanocages (denoted as FeS₂/CoS₂@SeSPAN/CNTs) was synthesized via a simple casting method. First, a casting method was employed to create the PAN film. Following this, Fe-ZIF-67 was grown on the PAN framework through a hydrothermal process, and it was subsequently converted into a CoS₂/FeS₂@SeSPAN/CNTs via heat treatment. This unique structure provides numerous FeS₂/CoS₂ heterojunction interfaces, which facilitate electron transfer and increase chemical reactivity. The embedded electric field generated by these heterojunctions further improves reaction kinetics by accelerating the migration of lithium ions and polysulfides across the interface. The well-distributed, uniformly sized FeS₂/CoS₂ nanoparticles, characterized by a high specific surface area, act as excellent repositories for active materials and promote the formation of a CEI on their surfaces. The porous nanocage structure effectively mitigates volume expansion, while the externally connected membrane structure reduces electron transport distances, which in turn improves overall reaction kinetics. Consequently, FeS₂/CoS₂@SeSPAN/CNTs achieves an active material loading capacity of 61 wt% and delivers an impressive specific capacity of 602 mAh/g over 200 cycles at 0.2 C. Notably, the capacity retention was 97.9% after 800 cycles at 1 C. Energy level analysis and density functional theory (DFT) calculations provide insights into the influence of the FeS₂/CoS₂ heterostructure on polysulfide adsorption and interfacial electron transfer. The heterostructure facilitates the rational design of bimetallic sulfides for SPAN cathodes in Li-SPAN batteries.

The CoS₂/FeS₂@SeSPAN/CNTs film with a heterostructure was successfully synthesized via a combination of casting, hydrothermal reaction, and heat treatment processes (Fig. 1a). First, PAN was mixed with CNTs to prepare a PAN precursor film with enhanced conductivity via the casting method. The film (~30 µm thick) formed a structurally intact three-dimensional conductive network (Fig. 1b). Subsequently, the PAN precursor film was immersed in a solution containing 2-Mim, Fe(NO₃)₃·9H₂O, and Co(NO₃)₂·6H₂O for the hydrothermal reaction, which promoted the formation of Fe-ZIF-67 nanoparticles on the film scaffold. Finally, the Fe-ZIF-67@PAN film underwent heat treatment in an argon atmosphere with the addition of SeS_x to form the CoS₂/FeS₂@SeSPAN/CNTs film. The binding of selenium with metals is not discussed in detail, as the primary purpose of adding trace amounts of selenium is to utilize the insoluble products formed from the reaction between SeS_x and the electrolyte. These insolubles facilitate the formation of the CEI layer, which prevents direct contact between the electrolyte and the active material [18,26,27]. After heat treatment, the film thickness remained relatively unchanged, and the interconnected network structure remained intact without collapse. CoS₂/FeS₂ nanoparticles exhibiting the characteristic rhombic dodecahedral ZIF-67 morphology were observed on the scaffold (Fig. 1c), with particle diameters under 100 nm. Element mapping results confirmed the presence of Co, Fe, and S within the framework (Fig. S1 in Supporting information). High-resolution transmission electron microscopy images revealed the interface between CoS₂/FeS₂ nanoparticles and the SeSPAN membrane. This observation indicated strong bonding between the components (Fig. 1d). Distinct crystal and carbon lattice fringes were observed in the CoS₂/FeS₂ heterostructure, with lattice fringes corresponding to the (111) crystal planes of CoS₂ and FeS₂. These planes exhibited interplanar spacings of 0.17 nm and 0.22 nm, respectively. The lattice fringes of CoS₂ and FeS₂ interweave and extend continuously, indicating a strong coupling between the two materials at the interface, further suggesting the formation of a stable heterostructure. The selected area electron diffraction pattern exhibited diffraction rings corresponding to the (111) and (200) planes of CoS₂ and the (101) and (220) planes of FeS₂. This result confirmed the excellent crystallinity of the sample. High-angle annular dark-field scanning electron microscopy (HAADF-STEM) and elemental mapping confirmed a uniform distribution of Fe, Co, and S elements. This finding validated the successful preparation of the heterostructure nanoparticles (Fig. 1e). The complete overlap of these elements indicated a uniform distribution at the interface. The presence of crystalline S and Se elements within the nanoparticles confirmed the incorporation of SeS_x. Elemental analysis results revealed that the active material content was up to 61 wt% (Table S1 in Supporting information). Thermogravimetric analysis (TGA) was used to analyze the volatilization of elemental SeS_x between 200 ℃ and 600 ℃, allowing for a rough estimation of the elemental SeS_x loading. The results indicate that the elemental SeS_x loading is highest in CoS₂/FeS₂@SeSeSPAN/CNTs, at approximately 23% (Fig. S2 in Supporting information). The high active material loading capacity demonstrated that the hierarchical porous structure provided ample storage and reaction space for active materials. This condition effectively mitigated volume expansion during the charge-discharge cycles.

X-ray diffraction (XRD) analysis was utilized to characterize the crystalline structure of the samples (Fig. 2a). CoS₂@SeSPAN/CNTs and FeS₂@SeSPAN/CNTs exhibited characteristic diffraction peaks corresponding to the monometallic sulfides CoS₂ and FeS₂. This observation confirmed the successful synthesis of the sulfides. The XRD spectrum of CoS₂/FeS₂@SeSPAN/CNTs exhibited standard peaks for both CoS₂ and FeS₂, which included (111) and (200) for CoS₂, as well as (101), (200), and (220) for FeS₂. This observation provided indirect evidence of the CoS₂/FeS₂ heterostructure. Raman spectroscopy (Fig. 2b) and FT-IR spectroscopy (Fig. 2c) further elucidated the composite structure of the CoS₂/FeS₂@SeSPAN/CNTs samples. Tables S2 and S3 (Supporting information) present detailed peak information for the CoS₂/FeS₂@SeSPAN/CNTs samples. Characteristic peaks corresponding to C–S and S–S bonds indicated that the sulfurization process of PAN and the formation of the six-membered carbon ring framework were unaffected by the incorporation of CoS₂ and FeS₂.

X-ray photoelectron spectroscopy (XPS) confirmed the presence of Co, Fe, C, S and Se in the CoS₂/FeS₂@SeSPAN/CNTs composite (Fig. S3 in Supporting information). Characteristic peaks for pyrrolic and pyridinic nitrogen were observed in the N 1s spectrum. These components enhanced both electron and ion conductivity, which facilitated the adsorption of solid polysulfides. This effect prevented the agglomeration of solid polysulfides encapsulated within the CoS₂/FeS₂ dodecahedral structure and maintained the overall reaction kinetics [25,28]. High-resolution Co 2p spectra exhibited peaks at 779.0 eV and 794.3 eV, attributed to Co²⁺, with additional peaks at 782.6 eV and 801.0 eV attributed to Co³⁺ (Fig. 2d). The Co peaks in CoS₂/FeS₂@SeSPAN/CNTs exhibited a slight positive shift compared with those in pure CoS₂@SeSPAN/CNTs. The shift in the Co 2p peak can be attributed to the formation of the CoS₂/FeS₂ heterostructure. In the heterostructure, the interaction between Co and Fe alters the local electronic environment of Co, resulting in a positive shift of the Co 2p peak. This shift typically indicates a change in the electronic density of Co, which is likely due to the stable formation of the CoS₂ and FeS₂ heterostructure, affecting the electron affinity and lattice strain of Co. This change in electronic density serves as direct evidence for the formation of the heterostructure, highlighting the strong interaction between CoS₂ and FeS₂ [29]. High-resolution Fe 2p spectroscopy further supports this conclusion (Fig. 2e). The main peaks of Fe 2p_3/2 and Fe 2p_1/2 appear at approximately 710 eV and 724 eV, respectively, indicating that Fe primarily exists in the forms of Fe²⁺ and Fe³⁺. Compared to the pure FeS₂@SeSPAN/CNTs sample, the Fe 2p peaks in CoS₂/FeS₂@SeSPAN/CNTs shift slightly to higher binding energies, providing further evidence of the interaction between Fe and CoS₂/FeS₂, thereby strengthening the indirect evidence for the formation of the heterostructure. In the high-resolution S 2p spectrum, all three samples exhibited S–S, C–S, and C–S–S bonds, while CoS₂/FeS₂@SeSPAN/CNTs exhibited a high proportion of C–S–S bonds (Fig. 2f). This observation indicated that the formation of long-chain sulfur within SeSPAN was promoted. The XPS spectra of Se 3d exhibited peaks at 53.9 eV (Se 3d_5/2) and 56.3 eV (Se 3d_3/2), which are characteristic of Se in a covalent SeS_x environment. No low-binding energy peaks, typically associated with metal selenides such as CoSe or FeSe (around 53 eV), were observed. This absence suggests that selenium in the material remains primarily in its covalently bonded SeS_x state, without forming metal selenides with Co or Fe. These findings confirm that Se does not interact with the metal components to form metal selenide phases in the synthesized materials.

Nitrogen adsorption–desorption methods were utilized to assess the surface area and porosity of CoS₂/FeS₂@SeSPAN/CNTs films before and after heat treatment (Figs. 2g and h). The Fe-ZIF-67@PAN films initially exhibited a pore volume of 0.062 cm³/g and a surface area of 20.3 m²/g. After heat treatment at 450 ℃, the pore volume of CoS₂/FeS₂@SeSPAN/CNTs films increased to 0.306 cm³/g, and the surface area expanded to 43.3 m²/g. The films exhibited a distinct hierarchical porous structure with pore sizes ranging from 2 nm to 30 nm. The films also exhibited notable flexibility and electrolyte wettability, with an electrolyte contact angle of ~40.1° and a wettability time of 5.7 s. These observations highlighted their potential in self-supporting cathode applications for Li-SPAN batteries (Fig. 2i and Fig. S4 in Supporting information).

Performance of CoS₂/FeS₂@SeSPAN/CNTs. Enhancing the capacity for polysulfide adsorption at the phase interface is essential for maximizing active material reactivity and increasing electrochemical reaction efficiency. Static adsorption experiments were performed with Li₂S₆ solutions to evaluate the polysulfide adsorption capacity of CoS₂, FeS₂, and CoS₂/FeS₂. Optical photographs of the post-experiment samples revealed notable changes in color (Fig. 3a). The solutions containing FeS₂ and CoS₂/FeS₂ turned colorless within 12 h, while those with only CoS₂ exhibited a lighter hue. This observation indicated superior polysulfide adsorption capacity for CoS₂/FeS₂. UV–vis absorption spectroscopy confirmed the effective fixation of polysulfides by the CoS₂/FeS₂ heterostructure. This suitable fixation effect promoted effective contact and sustained electrochemical reactions. XPS analysis revealed negative shifts in the Co and Fe peaks after the adsorption of Li₂S₆. This observation indicated electron acquisition from polysulfide anions through Lewis acid-base interactions (Fig. 3b and Fig. S5 in Supporting information). This finding demonstrated the significant role of the heterostructure in enhancing electrochemical performance by facilitating robust interactions with polysulfides [30,31]. Notably, during the initial reaction stages, the FeS₂ component served as the primary binding site for long-chain polysulfides, which subsequently migrated to CoS₂ for catalytic conversion. This process enhanced the interaction between FeS₂ and CoS₂, which in turn facilitated the formation of an electric field that sustained the catalytic processes. To evaluate electrocatalytic activity, CV tests were conducted on CoS₂, FeS₂, and CoS₂/FeS₂ electrodes using Li₂S₆ electrolyte (Fig. 3c). The CV tests revealed two pairs of redox peaks in the CoS₂/FeS₂ symmetric cell: One pair corresponded to the conversion from S₈ to Li₂S_n (4 ≤ n ≤ 8), and the other corresponded to the conversion from Li₂S_n to Li₂S [32]. The CoS₂/FeS₂ electrodes exhibited significantly increased current densities in redox reactions, which indicated superior bidirectional catalytic activity due to enhanced electron transfer efficiency and reduced energy barriers. The Li₂S deposition capacity of CoS₂/FeS₂ reached 150.3 mAh/g, which was notably higher than that of CoS₂ at 38.7 mAh/g and that of FeS₂ at 132.1 mAh/g (Fig. 3d). These findings demonstrated the effective combination of the catalytic capabilities of CoS₂ with the adsorption capabilities of FeS₂ in the heterostructure. Tafel plot tests indicated that CoS₂/FeS₂ exhibited the highest exchange current density at 0.501 mA/cm², which surpassed that of FeS₂ at 0.210 mA/cm² and that of CoS₂ at 0.433 mA/cm². This observation demonstrated the ability of the heterostructure to accelerate charge transfer processes (Fig. 3e). The decomposition and oxidation behavior of Li₂S was evaluated via three-electrode linear sweep voltammetry (LSV) using 0.1 mol/L Li₂S in methanol as the electrolyte, along with a platinum counter electrode and an AgCl/Ag reference electrode (Fig. 3f). The CoS₂/FeS₂ electrode exhibited a lower onset voltage (−0.51 V) and a stronger current response compared with the CoS₂ (−0.49 V) and FeS₂ (−0.40 V) electrodes. This observation indicated reduced energy barriers for the conversion of Li₂S to long-chain polysulfides. The Tafel slope for the CoS₂/FeS₂ electrode (35.6 mV/dec) was lower than that for the other electrodes, which confirmed the exceptional adsorption and catalytic activity of CoS₂/FeS₂ owing to its porous heterostructure (Fig. 3g). This analysis demonstrated the unique capabilities of the heterostructure in enhancing electrochemical performance.

The porous heterostructure of CoS₂/FeS₂ functions as a nano-reactor in batteries, which accommodates active materials and facilitates electron transfer. To further investigate CoS₂/FeS₂ performance enhancement in SeSPAN cathodes, a series of electrochemical experiments were conducted for comparison with single-component systems. The cycle stability of CoS₂@SeSPAN/CNTs, FeS₂@SeSPAN/CNTs, and CoS₂/FeS₂@SeSPAN/CNTs was evaluated at 0.2 C (Fig. 4a). CoS₂/FeS₂@SeSPAN/CNTs achieved a peak stable capacity of 602.3 mAh/g after a brief activation period. The activation behavior is primarily attributed to the interaction between the C and N sites within the SeSPAN framework and lithium ions, leading to the formation of irreversible covalent bonds. These bonds effectively enhance the conductivity of the electrode. The reduced activation cycle time indicates that CoS₂/FeS₂@SeSPAN/CNTs offers significant advantages in improving reaction kinetics. In contrast, CoS₂@SeSPAN/CNTs and FeS₂@SeSPAN/CNTs required ~50 cycles to reach activation. The charge-discharge curves of the electrode after activation indicated notable advantages for CoS₂/FeS₂@SeSPAN/CNTs in both capacity and voltage polarization (Fig. 4b). The single discharge plateau observed in the charge–discharge curves and CV curves indicated that the active materials encapsulated within the dodecahedral structure exhibited a solid-solid discharge mode similar to that of SPAN, without generating soluble polysulfides. This observation also indicated the gradual conversion of solid S₈ to Li₂S (Fig. 4c). This characterization demonstrated the superior functionality of the CoS₂/FeS₂ heterostructure and highlighted its potential in enhancing the electrochemical performance of Li-S batteries. The CoS₂/FeS₂@SeSPAN/CNTs electrodes exhibited higher peak current densities and lower polarization compared with the CoS₂@SeSPAN/CNTs and FeS₂@SeSPAN/CNTs electrodes. The anodic peaks of the electrodes shifted positively to higher potentials, while the cathodic peaks shifted negatively to lower potentials. This finding confirmed enhanced reaction kinetics attributed to the intrinsic electric field and staged catalytic conversion. The Inductively Coupled Plasma (ICP) analysis revealed that the total Fe and Co content in CoS₂/FeS₂@SeSPAN/CNTs is 0.9 wt%. In the charge-discharge and CV curves, no significant involvement of CoS₂ and FeS₂ in lithium-ion insertion/extraction reactions was observed. This indicates that while CoS₂ and FeS₂ may participate in a small degree of lithium-ion insertion/extraction, their contribution to the overall capacity is minimal. The CoS₂/FeS₂ heterostructure primarily enhances the battery performance by facilitating polysulfide conversion and adsorption, rather than directly contributing to the capacity. Rate capability tests (Fig. 4d and Fig. S6 in Supporting information) demonstrated the superior charge–discharge performance of CoS₂/FeS₂@SeSPAN/CNTs across various rates, particularly excelling from 0.1 C to 2 C with high recovery rates. Compared with CoS₂@SeSPAN/CNTs and FeS₂@SeSPAN/CNTs, CoS₂/FeS₂@SeSPAN/CNTs exhibited more stable capacities and less capacity fade during high-rate tests. The electrochemical impedance spectroscopy (EIS) results show that the initial electrode impedance is characterized by a curve that does not form a complete semicircle, indicating poor charge transfer resistance (R_ct) in the initial stage (Fig. S7 in Supporting information) [17,18]. After 100 charge-discharge cycles, EIS of each electrode curve exhibited a complete semicircle corresponding to R_ct and CEI layer resistance (R_CEI), confirming that the slow, irreversible insertion of Li⁺ into the C and N sites of the SPAN framework improves conductivity, thereby reducing R_ct (Figs. 4e and f). Additionally, the CEI layer remains stable during cycling. EIS analysis and equivalent circuit fitting results indicate that the CoS₂/FeS₂@SeSPAN/CNTs electrode demonstrates the lowest R_ct and R_CEI, highlighting its excellent electrochemical performance (Table S4 in Supporting information). Furthermore, the R_ct at 1.0 V during discharge (20 Ω) is lower than at 3.0 V during charge (53 Ω), which is closely related to the interconversion between Li₂S and elemental sulfur or SeSPAN, as well as the formation and rupture of covalent bonds between Li⁺ and the SeSPAN framework. Long-term cyclic stability assessment is crucial for confirming side reactions in Li-SPAN batteries. Cyclic performance tests were conducted on CoS₂/FeS₂@SeSPAN/CNTs at 1 C to investigate whether the electrolyte reacted nucleophilically with sulfur molecules or formed soluble polysulfides under high current density (Fig. 4g). At 1 C, the CoS₂/FeS₂@SeSPAN/CNTs electrodes maintained a capacity retention rate of 97.9% after 800 cycles, with only a 0.003% capacity fade per cycle and a coulombic efficiency near 100%. The stable cycling curves indicated that the CEI layer effectively prevented direct contact between the carbonate electrolyte and the sulfur molecules encapsulated within the CoS₂/FeS₂ structure to avoid performance degradation due to nucleophilic reactions. The significant capacity reduction observed in the second cycle was attributed to the formation of the CEI layer and the irreversible lithiation of carbon and nitrogen within SeSPAN [19,33]. These observations indicated that the Li-SPAN battery, supported by an intrinsic electric field and enhanced adsorptive catalytic actions, exhibited superior active material loading and electrochemical performance, as well as exceptional redox kinetics compared with the batteries from previous studies (Fig. 4h, Fig. S8 and Table S5 in Supporting information) [14,17,34–38]. The comprehensive analyses demonstrated the potential of the CoS₂/FeS₂ heterostructure in advancing Li-SPAN battery technology.

The exceptional performance of CoS₂/FeS₂@SeSPAN/CNTs was further investigated via DFT calculations to analyze its electronic properties and catalytic capabilities at the atomic level. The configurations of CoS₂, FeS₂, and CoS₂/FeS₂ were examined. Partial density of states (PDOS) analysis revealed no energy gap near the Fermi level. This observation indicated intrinsic conductivity (Fig. 5a). The p-band center of the CoS₂/FeS₂ heterostructure was higher (−0.73 eV) than that of FeS₂ (−0.80 eV) and CoS₂ (−0.97 eV). This observation indicated enhanced interactions with polysulfides. Meanwhile, the d-band center of the CoS₂/FeS₂ heterostructure (−1.32 eV) was situated between those of FeS₂ (−1.24 eV) and CoS₂ (−1.43 eV). This unique electronic configuration indicated optimal electronic properties, which facilitated charge transfer and enhanced catalytic activity for efficient polysulfide conversion. Figs. 5b and c, Figs. S9 and S10 (Supporting information) show the adsorption energies and configurations for various polysulfide intermediates for CoS₂, FeS₂, and CoS₂/FeS₂. FeS₂ demonstrated the strongest adsorption energy, while CoS₂/FeS₂ exhibited a suitable amount of adsorption energy, which facilitated the desorption of long-chain polysulfides from the substrate. Differential charge density maps indicated a positive correlation between binding energy and electron density. This finding demonstrated the advanced electronic structure of the CoS₂/FeS₂ heterostructure (Fig. 5d and Fig. S10). High electron density was observed between Li and S atoms in the transition metal sulfides, where S atoms formed stable covalent bonds with Co and Fe atoms. Cross-sectional charge accumulation diagrams revealed the presence of an intrinsic electric field, which facilitated the adsorption of solid polysulfides and the migration of Li⁺ (Fig. 5e). Gibbs free energy simulations were conducted to explore the conversion from S₈ to longer-chain polysulfides (Li₂S₈, Li₂S₆, Li₂S₄) and final products (Li₂S₂, Li₂S). Fig. 5f shows the optimized configurations of reaction intermediates and their corresponding free energy curves. CoS₂/FeS₂ exhibited a high exothermic effect and low positive Gibbs free energy barriers in subsequent endothermic reactions. This observation indicated thermodynamically favorable conditions for predominant solid-state reactions. Figs. 5g-i and Fig. S11 (Supporting information) show the decomposition energy barriers for Li₂S on the surfaces of CoS₂ (0.73 eV), FeS₂ (0.81 eV), and CoS₂/FeS₂ (0.63 eV). The comprehensive comparison of electronic structures, polysulfide adsorption capacities, and energy barriers demonstrated that the CoS₂/FeS₂ heterostructure enhanced electronic structure and adsorption capabilities, reduced reaction barriers, and significantly improved electrochemical reaction kinetics. These findings provide theoretical support for the superior electrochemical performance of the CoS₂/FeS₂ heterostructure, which demonstrates its advanced capabilities in enhancing Li-SPAN battery technology.

Detailed studies were conducted to comprehensively understand the morphology and chemical composition of the CoS₂/FeS₂@SeSPAN/CNTs cathode after extensive cycling. After 100 cycles, the cathode surface exhibited increased roughness and was covered by a thick polymer layer, indicative of the microscopic characteristics of the CEI layer (Fig. S12 in Supporting information). True-color confocal and atomic force microscopy revealed significant contrast variations on the membrane surface, which indicated the formation of a CEI layer ~30 nm thick (Fig. 6a). Further characterization of the surface chemistry of the film via XPS etching demonstrated that the outer and sub-surface layers were enriched with C–O and C=O bonds, which was consistent with the decomposition of carbonate electrolytes into organic compounds. Additionally, the XPS spectra indicated the presence of inorganic products, such as Li₂O, LiF, and Li_xPF_y, resulting from the decomposition of FEC and LiPF₆. This observation confirmed the formation of a composite CEI layer consisting of both organic and inorganic materials on the cathode surface (Fig. 6b, Figs. S13 and S14 in Supporting information). Contour maps of C, F, and Li (Figs. 6c-f and Fig. S15 in Supporting information) further indicated that the outer layer of the CEI predominantly comprised carbon-rich organic compounds, while the inner layer predominantly comprised inorganics, mainly LiF and Li_xPF_y. Furthermore, the consistent presence of Li and S throughout the etching process confirmed the gradual formation of the CEI layer along the dendritic framework of the SeSPAN membrane, and the CEI layer ultimately covered the entire membrane surface. These findings are in agreement with previous studies, which indicate that the formation of the CEI layer involves electrolyte decomposition, followed by the formation of both organic and inorganic layers, along with nucleophilic reactions between S^2- and carbonate electrolytes. When the carbonate electrolyte enters the pores and reacts with SeS_x, a nucleophilic reaction occurs, producing insoluble solid products that block the pores and prevent further contact between the electrolyte and SeS_x. The inorganic species produced from electrolyte decomposition subsequently nucleate on these products, thereby accelerating the formation of the CEI layer. With the protection of the CEI, the additional SeS_x in the electrode pores can undergo complete charge-discharge cycles, ensuring high utilization of active material. This design not only optimizes the overall battery performance but also ensures the efficient utilization of active materials [26,33].

The porous structure of the CoS₂/FeS₂@SeSPAN/CNTs membrane provided numerous attachment sites for active materials. This effect significantly enhanced active material loading capacity. The CEI layer effectively prevented direct contact between the active materials and the electrolyte, which, in turn, prevented the depletion of the additional active materials. Moreover, the enhanced conductivity of the CoS₂/FeS₂ heterostructure significantly improves the overall conductivity of the electrode, reducing internal resistance and mitigating early-cycle capacity loss. The intrinsic electric field within the heterostructure facilitates the transport of lithium ions and polysulfides, preventing the formation of dead sulfur and enhancing the utilization of active materials (Fig. 6g). Owing to the synergistic effects of the CEI and the heterostructure, CoS₂/FeS₂@SeSPAN/CNTs exhibited exceptional electrochemical performance, which demonstrated its substantial potential in industrial applications.

In conclusion, this study presents a novel flexible CoS₂/FeS₂@SeSPAN/CNTs composite film cathode developed through a combination of straightforward casting technique and hydrothermal reactions. The cathode exhibited remarkable electrochemical performance and substantial potential for industrial applications. The unique graded porous structure of the cathode effectively increased the storage sites for active materials. The cathode achieved a loading capacity of 61 wt%, which significantly exceeded the typical 40 wt% reported in previous studies. Experimental results and DFT calculations indicated that the CoS₂/FeS₂ heterointerface significantly enhanced the adsorption and catalytic conversion of polysulfides. The intrinsic electric field at the interface enhanced the migration efficiency of lithium ions. This effect significantly improved the electrochemical reaction kinetics. The synergistic effect of the CoS₂/FeS₂ heterojunction, coupled with a protective CEI, significantly facilitated the utilization efficiency of active materials. Notably, even after 800 cycles at 1 C, the battery retained 97.9% of its capacity. This observation demonstrated the exceptional long-cycle performance of the Li-SPAN battery. This work presents a novel solution for the development of high-energy-density, long-cycle-life Li-S batteries, specifically suitable for future high-performance energy storage applications and wearable technologies.