Theoretical Specific Capacity Research Articles

MoC nanoparticles decorated carbon nanofibers loaded with Li2S as high-performance lithium sulfur battery cathodes

Lithium sulfur (Li-S) batteries have broad development potential in the field of electrochemical energy storage due to their high theoretical specific capacity, low cost, and environmentally friendly. However, the notorious shuttle effect of lithium polysulfides (LiPSs) during cycling process severely limits the performance improvement of Li-S batteries. In this work, carbon nanofibers (CNFs) decorated by MoC nanoparticles have been successfully established through electrospin combined with carbothermal reduction method. The effect of calcination temperature and MoC loading amount on the catalytic activity on LiPSs, as well as the electrochemical performance have been first investigated in detail. Based on the visualized adsorption and LiPSs conversion kinetics testing, the CNFs@MoC composites with 37 wt% MoC loading (CNFs@MoC-37 %) are confirmed to be the optimized sample. By using liquid-phase impregnation to load Li2S onto the CNFs@MoC-37 % composites to act as cathode, the assembled cells can achieve a reversible capacity of 941 mAh g−1 and 751 mAh g−1 at the current density of 0.1C and 1C respectively. The reversible capacity can still maintain at 550 mAh g−1 at 1C after 500 cycles, corresponding to the capacity decay rate of 0.054 % per cycle.

Free-Standing Poly(vinyl benzoquinone)/Reduced Graphene Oxide Composite Films as a Cathode for Lithium-Ion Batteries.

Quinones with a rapid reduction-oxidation rate are promising high-capacity cathodes for lithium-ion batteries. However, the high solubility of quinone molecules in polar organic electrolytes results in low cycle stability, while their low electric conductivity causes low utilization of electrode materials. In this article, a new p-benzoquinone derivative, poly(vinyl benzoquinone) (PVBQ), is designed and synthesized, and a solution-based method of preparing free-standing PVBQ/reduced graphene oxide (RGO) composite films is developed. PVBQ has a high theoretical specific capacity (400 mA h g-1) because of its low dead moiety mass. In the produced composite films, PVBQ nanoparticles are uniformly dispersed on RGO sheets, which endows the composite films with high electric conductivity and inhibits the dissolution of PVBQ through strong adsorption. As a result, the composite films show a high active material utilization, high practical specific capacity, and excellent cycling stability. PVBQ in the composite membrane containing 60.2 wt % RGO deliver 244 mA h g-1 capacity after 200 charge-discharge cycles at a current density of 300 mA g-1. At a current density of 1500 mA g-1, the reversible specific capacity is still 170 mA h g-1. This work provides a high-performance cathode material for lithium-ion batteries, and the molecular structure and electrode structure design ideas are also instructive for developing other organic electrode materials.

High‐Capacity, Long‐Life All‐Solid‐State Lithium–Selenium Batteries Enabled by Lithium Iodide Active Additive

AbstractSelenium (Se) shows promise as a cathode candidate for all‐solid‐state lithium (Li) batteries due to its impressive theoretical volumetric energy density, much higher electronic conductivity, and improved safety in comparison to those for sulfur (S). An active cathode additive, lithium iodide (LiI) is demonstrated, to address the major challenge for all‐solid‐state Li–Se batteries, namely the sluggish redox kinetics resulting from the huge solid‐state conversion barrier. The LiI additive enhances Li+ transport and provides catalytic sites for Se cathode, thus endowing the batteries with accelerated reaction kinetics and extra capacity. DFT calculation and experimental analysis clearly reveal that LiI additive efficiently accelerates the conversion between polyselenide intermediates and Li2Se. With the above advantages, the battery with LiI using Li6PS5Br electrolyte gives an outstanding capacity of 862 mAh gSe−1 beyond the theoretical specific capacity of Se and a superlong life over 1800 cycles at 1C under room temperature. This work offers a simple strategy to facilitate the kinetics of all‐solid‐state Se cathodes and paves the way for the practicality of high‐capacity and long‐life all‐solid‐state Li–Se batteries.

CoO nanocrystals dispersed in N-doped carbon networks as enhanced anode for lithium storage

CoO emerges as a promising anode material for lithium-ion batteries (LIBs) because of high theoretical specific capacity and rich resource. However, its practical application is impeded by significant volume expansion and poor electrical conductivity during the charging and discharging cycles. Herein, we construct a nanocomposite of CoO nanocrystals and N-doped carbon serving as an enhanced anode for LIBs by a facile strategy. In the nanocomposite, CoO nanocrystals with average size of 60 nm uniformly were dispersed in N-doped carbon networks. The synergy effects of CoO nanocrystals and N-doped carbon networks can extremely enhance electronic conductivity, relieve volume expansion, and effectively protect CoO nanocrystals from aggregating. Hence, the composite anode delivers large reversible capacity (1190 mAh g−1 at 0.3 A g−1 after 100 cycles), remarkable rate capability (592 mAh g−1 at 5 A g−1), and long cycling ability. This offers a simple approach for designing high-performance anodes for LIBs.

Conductive Li2S‐NbSe2 Cathode Material Capable of Bidirectional Self‐Activation for High‐Performance All‐Solid‐State Lithium Metal Batteries

AbstractAll‐solid‐state lithium metal batteries (ASSLBs) offer an alternative route to safe and high energy density power sources. Sulfur‐based cathodes with high theoretical specific capacity and low cost are crucial for advancing ASSLBs. However, the electronic insulation and sluggish kinetics of sulfide materials like Li2S severely limit battery performance. Herein, the strategy is proposed that a highly electronic conductive Li2S‐NbSe2 material enhances the electrochemical performance through bidirectional self‐activation. The chemical interaction between Li2S and NbSe2 induces NbSe2‐xSx and Li2Se derivatization, serving as the basis for activation. The carrier transport properties, chemical evolution and self‐activation mechanism of Li2S‐NbSe2 during the oxidation–reduction process are revealed. The chemical activation of NbSe2‐xSx is explored to accelerate the electrochemical processes by modifying the conductivity of sulfur species and the conversion pathways without insulating Li2S and S aggregation. Therefore, ASSLBs using Li2S‐NbSe2 as cathode active material achieve an electrode‐level energy density of 394 Wh kg−1 and a power density of 524 W kg−1 at 1 C (4.35 mA cm−2) and 25 °C. The capacity retention after 100 cycles at 0.5 C is ≈99.3% with almost no degradation. This work provides new options and insights for the rational design and development of chalcogenide cathode active materials for high‐performance ASSLBs.

Boosting the intrinsic kinetics of lithium vanadium phosphate via an electrochemically active cross-link framework

The monoclinic lithium vanadium phosphate Li3V2(PO4)3 (LVP) is considered a promising cathode for lithium-ion batteries (LIBs) due to its high working voltage (>4.0 V, vs. Li+/Li) and high theoretical specific capacity (197 mAh g−1). However, the electrochemical procedure accompanied by three-electron reactions in LVP has proven challenging due to the complexity or asymmetry of the reaction pathways, thus limiting its wide application. Herein, an electrochemically active cross-link framework of LVP, LiFe0.3Mn0.7PO4 (LFMP) and graphene are successfully synthesized by an in situ catalytic process, which enables stable cycling and high-rate capabilities up to 4.8 V (vs. Li+/Li). Graphene-like carbon can be formed in situ with VOx as the catalyst and polyvinyl alcohol as the carbon source, and LFMP also inhibits the growth of LVP particles, allowing rapid Li+ and electron transport in the cathodes. Both in situ and ex situ X-ray diffraction prove that the cross-link framework efficiently smooths the lattice mismatch and achieves highly reversible structural phase transitions. The prepared 0.9LVP·0.1LFMP is able to provide a superior rate capability of 123 mAh g−1 at 20 C. After 150 cycles, the 0.9LVP·0.1LFMP shows 97.4 % capacity retention even under a voltage of 4.8 V (vs. Li+/Li). This work develops a new strategy for the future design of high-voltage and high-power cathode materials for LIBs.

Surface-Coating Strategies of Si-Negative Electrode Materials in Lithium-Ion Batteries

Silicon (Si) is recognized as a promising candidate for next-generation lithium-ion batteries (LIBs) owing to its high theoretical specific capacity (~4200 mAh g−1), low working potential (<0.4 V vs. Li/Li+), and abundant reserves. However, several challenges, such as severe volumetric changes (>300%) during lithiation/delithiation, unstable solid–electrolyte interphase (SEI) formation, and inherently low electrical and ionic conductivity, impede its practical application. To mitigate these challenges, direct contact between the surface of the Si particle and the electrolyte must be prevented. In this review, we elucidated the surface coating strategies to enhance the electro–chemical performance of Si-based materials. We identified the impact of various coating methods and materials on the performance of Si electrodes. Furthermore, the integration of coating strategies with nanostructure design can effectively buffer Si electrode volume expansion and prevent direct contact with the electrolyte, thereby synergistically enhancing electrochemical performance. We highlight opportunities and perspectives for future research on Si-negative electrodes in LIBs, drawing on insights from previous studies.

ZnS Nanoseeds Sealed in N, P, S Co-Doped Carbon Hollow Rhombic Dodecahedra as a Superlithiophilic Host for Dendrite-Free Lithium Metal Anodes.

Lithium (Li) metal is considered ahopeful anode for next-generation Li-ion batteries thanks to its ultra-high theoretical specific capacity, extra-low theoretical density, and low negative potential. However, the uncontrolled growth of Li dendrites and volume fluctuation during plating/stripping processes severely hamper its commercial application. Herein, ZnS seeds sealed in N, P, S co-doped carbon hollow rhombic dodecahedra (ZnS@NPS-C HRD) is fabricated as a superlithiophilic host for Li metal anodes (LMAs) to solve the above problems. In addition, the Li nucleation and deposition mechanism on ZnS@NPS-C HRD is investigated by in situ optical microscopy, ex-situ X-ray diffraction, scanning electron microscopy, and theoretical calculations. Owing to the synergistic strategy of ZnS seeds-inducing nucleation and Li-limited growth, the as-prepared composite exhibits stability for 300 cycles in asymmetric cells and a long lifespan over 1100h in symmetric cells. Moreover, the ZnS@NPS-C HRD@Li|LiFePO4 full cell demonstrates a reversible capacity of 100.91mAhg-1 after 400 cycles at 1C.

Synergistic effect of oxygen defects and calabash-like hollow carbon matrix enables VO2 as high-performance cathode for zinc ion battery

Vanadium dioxide (VO2) materials exhibit significant theoretical specific capacity, which is ascribed to multi-electron transfer reactions and unique tunneled structures. However, the low electronic conductivity and sluggish reaction kinetics of VO2 have impeded its further development. Hence, in this study, we employed a synergistic strategy of defect engineering and compositing with a calabash carbon matrix to reduce Zn2+ diffusion barriers and accelerate electron transfer. The VO2 cathode provided a high specific capacity at a low rate of 303 mA h g−1 at 0.1 A g−1 after 191 cycles, along with good rate performance (168 mA h g−1 at 10 A g−1) and satisfactory long-term stability (170 mA h g−1 at 1 A g−1 after 1100 cycles). The exhaustive structural analyses indicated that oxygen vacancies accelerated the Zn2+ diffusion rate, while a uniform calabash-like hollow carbon matrix improved electronic conductivity during cycling. Moreover, ex-situ measurements demonstrated that during discharge, the composite cathode transformed to layered Zn3+x(OH)2V2O7·2H2O, which then facilitated the subsequent intercalation of Zn2+. This cooperative strategy advances the practical application of aqueous zinc ion batteries by leveraging vanadium-based electrodes.

Bimetallic ions modified 2‐methylimidazolium functionalized polypyrrole/graphene oxide for the improved supercapacitor

AbstractThin films with two‐dimensional (2D) nanostructures possess good environmental stability, thinner thickness and large surface area, which are widely used as a promising modified electrode material in the field of energy storage, supercapacitors, electrochemical sensors and biosensors. Herein, unique bimetallic ions modified polypyrrole/graphene oxide (PPy/GO) nanosheets, including Co2+‐Zr4+/(2‐MeIm)x@PPy/GO and Co2+‐Run+/(2‐MeIm)x@PPy/GO (n = 0, 4), are prepared by using 2‐methylimidazolium (2‐MeIm) as the linkers between PPy/GO and metal ions. The obtained electrodes constructed by Co2+‐Run+/(2‐MeIm)x@PPy/GO (n = 0, 4) and Co2+‐Zr4+/(2‐MeIm)x@PPy/GO exhibit improved capacitor electrochemical properties due to the reversible redox reaction, the large specific surface area and the high theoretical specific capacitance value of the metal ions compared to the unmodified PPy/GO. Especially, the specific capacitance value of Co2+‐Run+/(2‐MeIm)x@PPy/GO (n = 0, 4) electrode reaches 321.78 F g−1 at a current density of 1 A g−1 and the capacitance retention rate is achieved to 100% in the long cycle charge/discharge test after 10 000 cycles (10 A g−1). It will provide a practical experience for the design and preparation of supercapacitors based on bimetallic ions modified PPy/GO.

Reversible storage of tetraethyl ammonium cation in CFx-based cathode

Carbon fluorides (CFx) are considered as the potential cation storage materials in alkali metal-based battery systems because of the high theoretical specific capacity (865 mAh g-1 when x = 1). However, the reversibility of cathode reaction is seriously disturbed by the strong metal-fluorine interactions among the electrode products (e.g., LiF). By contrast, the relatively weak N-F bond makes the CFx-based battery system using quaternary ammonium cation (QAA+) a promising alternate, but the electrode mechanism between CFx and QAA+is little understood yet. In this work, tetraethylammonium cation (TEA+) is employed as the charge carrier using the electrolyte solution of sulfolane (SL) for CFx cathode. The CF0.56 electrode exports 710 mAh g-1 during the initial TEA+-CF reaction, and the electrode product (TEAF) can be decomposed under elevated potential that yields amorphous carbon fluoride and a reversible capacity of ∼300 mAh g-1 can be reached in the subsequent galvanostatic charge-discharge cycles. The TEAF product is non-crystallizable that exists in a sticky form on the surface of electrode, which contributes to an improved electrode structural stability while also leads to an unsatisfactory performance of the amorphous carbon fluoride with large number of superficial active sites. The electrode mechanism and the mechanical property of electrode interface are discussed in depth by in-situ Raman and electrochemical quartz crystal microbalance (EQCM) methods.

Constructing a 3D Li[sbnd]Mg alloy skeleton through mechanical rolling for high-rate Li anodes

Li is a promising anode material for lithium-ion batteries owing to its low redox potential (−3.04 V vs. standard hydrogen electrode) and exceptionally high theoretical specific capacity (3860 mAh g−1). However, considerable volume changes and uncontrolled dendrite growth reduce coulombic efficiency during charge/discharge cycles, limiting its practical application. This research introduces a straightforward method to fabricate a two-phase intertwined composite electrode featuring a LiMg phase as a three-dimensional (3D) skeleton structure aimed at high-rate Li-metal batteries. With its mixed electronic and ionic conducting networks, the 3D alloy structure offers abundant interfaces with pure Li and exhibits strong lithium affinity, enhancing Li+ diffusion throughout the electrode and enabling dendrite-free deposition. Results demonstrate a long cycle life exceeding 80 h at 30 mA cm−2 in symmetric cells. Coin- and pouch-type full cells with cathodes also show excellent rate capacity and cycling stability. The exceptional performance of this material makes it a highly desirable anode for high-rate lithium-metal batteries.

Anchored Bi with cobalt polyphthalocyanine enhances the reversibility of Bi2Te3 anode for endurable lithium-ion storage

As an intermetallic material, Bi2Te3 possesses great potential in lithium-ion batteries due to its attractive layered structure, intrinsic excellent conductivity and impressive theoretical specific capacity. However, the phase decomposition and the huge volume variation leading to rapid capacity fading hinder the further application of Bi2Te3 in lithium-ion batteries. In this study, two dimensional Bi2Te3 encapsulated in cobalt polyphthalocyanine (CoPPc) is synthesized by a facile recrystallization method, and its electrochemical properties and lithium storage mechanism are comprehensively studied. The Bi2Te3@CoPPc electrodes exhibit outstanding cycling stability with a specific capacity of 551.9 mAh g−1 at 100 mA g−1 and 628.5 mAh g−1 at 500 mA g−1 after 500 cycles, benefiting from the configured composite layered structure and the amiable interaction of Bi2Te3 and CoPPc. Our experimental and theoretic results demonstrate that the electron redistribution induced by the incorporation of CoPPc with charge accumulation around Bi2Te3 and low potential region around Co efficiently facilitates the fast lithium-ion transportation resulting in outstanding rate performance. Our explorative strategy of electron redistribution proposes a new avenue to enhance the catalysis activity and durability of alloy anodes in metal-ion batteries.

Design Unsaturated Selenium Coordinated NbSe2-x as Multifunctional Sulfur Electrocatalyst toward Fast and Durable Sulfur Reduction Reaction.

Lithium-sulfur (Li-S) battery are considered as the next generation energy storage system owing to their ultra-high theoretical specific capacity and energy density. However, the commercialization of Li-S battery is still hindered by the intrinsically low conductivity of sulfur, sluggish catalytic conversion and notorious shuttle effect of polysulfides. The implantation of defects in sulfur electrocatalyst can effectively increase its conductivity and catalytic efficiency of lithium polysulfides, but the current mainstream defective materials are limited and lack of in-depth research. Herein, a defective niobium selenide (NbSe2-x) nanosheet sulfur electrocatalyst is constructed with enriched selenium defects, which demonstrates strong interaction with sulfur species, endowing NbSe2-x with rapid and reliable sulfur reduction reaction. As a result, the Li-S cell with NbSe2-x exhibits excellent multiplicative performance in both coin cell and pouch cell, which maintains stable cycling for over 2000 cycles under 5 C, corresponding to a low-capacity fading rate of 0.024% per cycle. Ah level pouch cell is also fabricated, showing a decent energy density of 378Wh kg-1. This creative strategy not only emphasizes the importance of selenium defect engineering in Li-S batterie toward practical application, but also enlightens the material engineering to realize superior performance in related energy storage and conversion area.

Optimizing nickel-aluminium layered double hydroxides for supercapacitors: The role of 3D structural assembly

Nickel-aluminium layered double hydroxides (NiAl-LDHs) have emerged as promising electrode materials for supercapacitors (SCs) due to their inherently high specific surface area and theoretical specific capacitance, which are primarily attributed to the rapid pseudocapacitive response at the surface. However, NiAl-LDHs typically form agglomerated nanosheets, leading to a significant reduction in specific surface area, which is crucial for enhancing the number of active sites and improving the capacitive properties of the materials. To overcome this limitation, 2D nanostructures were assembled into 3D architectures by synthesizing NiAl-LDHs with distinct morphologies in a one-step hydrothermal process using an alkaline agent (NH4F). This approach resulted in the formation of 3D NiAl-LDH/HN4F structures, which exhibit a larger contact area and a greater number of redox-active sites. Consequently, the 3D NiAl-LDH/HN4F electrodes demonstrated a significantly higher specific surface area, leading to remarkable improvements in specific capacitance (1219 ± 30F g−1) and energy density (61 ± 1 Wh kg−1) compared to their 2D counterparts. This structural enhancement increases both the surface area and active site density while providing a new framework for designing high-performance LDH-based electrodes.

Design and Synthesis of D‐A Polymer as Cathode Material for Na‐Based Dual‐Ion Batteries with Excellent Cycling Performance

AbstractOrganic bipolar electrodes can undergo both n‐type and p‐type reactions for energy storage due to numerous active sites, which can usually deliver a high theoretical specific capacity. Herein, a new bipolar polymer cathode material PQPZ is designed and synthesized. The electron‐donating phenazine group undergoes a two‐electron redox reaction which can store anions, the electron‐withdrawing phenanthraquinone can store sodium‐ions through a two‐electron redox reaction. Notably, as a bipolar cathode material for sodium‐ion batteries, PQPZ exhibits a reversible specific capacity of up to 270 mAh g−1 in the voltage range of 1.0–4.0 V (vs. Na+/Na) and achieves a high energy density of 696 Wh kg−1 in a half‐cell. A capacity retention rate of 90% is obtained after 300 cycles at a current density of 0.5C. More excitingly, even after being cycled for 10000 cycles at 10C, the PQPZ electrode shows an average decay rate as low as 0.0036% per cycle, manifesting a very stable cycling performance. In addition, PQPZ also shows excellent performances when tested at −10 °C, making it promising in practical applications. Considering the bipolar character of PQPZ, symmetric batteries are also successfully constructed, fulfilling the “ready‐to‐charge” property without a pre‐activation process. The results reveal the potential application of PQPZ in practical use.

Theoretical prediction of two-dimensional metallic AM2B8 (AM = K, Rb, Cs) as anode materials for Na-ion batteries

The development of two-dimensional anode materials with superior performance is becoming a critical undertaking for the advancement of Na-ion battery technology. Using isoelectronic substitution strategies, we predicted three alkali metal borides AM2B8 (AM = K, Rb, Cs) based on the SrB8 monolayer. Ab initio molecular dynamics simulations and phonon dispersion relationship calculations demonstrated their stability. Using density functional theory, we predict the feasibility of these three new metal nanosheets as anodes for Na-ion batteries. The AM2B8 monolayer retains its metallicity after the insertion of Na ions, ensuring that the anode has good electrical conductivity. In addition, AM2B8 has a low diffusion barrier and open circuit voltage (K2B8 is 0.08 eV and 0.26 V) during charge/discharge. In the voltage range that inhibits dendrite growth, K2B8 can reach the maximum theoretical specific capacity (326 mAh/g). These results indicate that AM2B8, especially K2B8, is a promising anode material for Na-ion batteries.

Atomic Ni-catalyzed cathode and stabilized Li metal anode for high-performance Li–O2 batteries

The Li–O2 battery (LOB) has attracted growing interest, including for its great potential in next-generation energy storage systems due to its extremely high theoretical specific capacity. However, a series of challenges have seriously hindered LOB development, such as sluggish kinetics during the oxygen reduction and oxygen evolution reactions (ORR/OER) at the cathode, the formation of lithium dendrites, and undesirable corrosion at the lithium metal anode. Herein, we propose a strategy based on the ultra-low loading of atomic Ni catalysts to simultaneously boost the ORR/OER at the cathode while stabilizing the Li metal anode. The resultant LOB delivers a superior discharge capacity (>16000 mA h g−1), excellent long-term cycling stability (>200 cycles), and enhanced high rate capability (>300 cycles @ 500 mA g−1). The working mechanisms of these atomic Ni catalysts are revealed through carefully designed in situ experiments and theoretical calculations. This work provides a novel research paradigm for designing high-performance LOBs that are usable in practical applications.

Fast diffusion and stable topotactic reaction in single crystal conversion anode

Conversion electrodes typically have high theoretical specific capacity, but mostly suffer large structural changes during charge/discharge and result in poor cycling stability. The optimization of the polycrystalline materials is the mostly used strategy, however, these polycrystalline materials are intrinsically vulnerable to grain-boundary (intergranular) fracture caused by the anisotropic volume change during sodiation/desodiation, resulting in rapid impedance growth and capacity decay. Herein, we propose an alternative pathway to design single-crystal materials as potential conversion anodes. As an example, SnO2 with different crystallinities is successfully synthesized via solvothermal methods and compared to determine the implications of different crystallinity for the electrochemical properties of conversion anodes. It is demonstrated that the single-crystal SnO2 not only has faster Na+ diffusion dynamics but also maintains structural stability via topotactic reaction. Further optimization of the electron conduction and structural robustness is realized by uniformly covering a graphitic carbon shell on the surface of single-crystal SnO2 nanosheets. The modified single-crystal SnO2 exhibits a high reversible capacity of 436.2 mA h g–1 and maintains a high capacity of 257.1 mA h g-1 and remarkable capacity retention of about 98.9% after 9000 cycles at 5000 mA g-1. The deep understandings of the topotactic reaction in single crystal conversion anode in this work provide a theoretical foundation and new direction for further developing electrode materials with excellent electrochemical performance, especially high rate capabilities, and long cyclability.

Scalable Ni12P5-Coated Carbon Cloth Cathode for Lithium–Sulfur Batteries

As a better alternative to lithium-ion batteries (LIBs), lithium–sulfur batteries (LSBs) stand out because of their multi-electron redox reactions and high theoretical specific capacity (1675 mA h g−1). However, the long-term stability of LSBs and their commercialization are significantly compromised by the inherently irreversible transition of soluble lithium polysulfides (LiPS) into solid short-chain S species (Li2S2 and Li2S) and the resulting substantial density change in S. To address these issues, we used activated carbon cloth (ACC) coated with Ni12P5 as a porous, conductive, and scalable sulfur host material for LSBs. ACC has the benefit of high electrical conductivity, high surface area, and a three-dimensional (3D) porous architecture, allowing for ion transport channels and void spaces for the volume expansion of S upon lithiation. Ni12P5 accelerates the breakdown of Li2S to increase the efficiency of active materials and trap soluble polysulfides. The highly effective Ni12P5 electrocatalyst supported on ACC drastically reduced the severity of the LiPS shuttle, affected the abundance of adsorption–diffusion–conversion interfaces, and demonstrated outstanding performance. Our cells achieved near theoretical capacity (>1611 mA h g−1) during initial cycling and superior capacity retention (87%) for >250 cycles following stabilization with a 0.05% decay rate per cycle at 0.2 C.