Anode For Potassium-ion Batteries Research Articles

A needle-like covalent organic framework with highly accessible phenazine and π-conjugated structure for potassium storage and its reaction mechanism

Covalent organic frameworks (COFs) with features of light elements, tailored functional groups, and designable structures are regarded as promising candidates for future potassium ion batteries (PIBs), while the low electronic conductivity and intricate reaction mechanism restrict their practical application. Herein, a needle-like COF material, marked as CPT, was synthesized by an acid-catalyzed condensation reaction between cyclohexanehexone and 2,3,7,8-phenazine tetramine. It was constructed by interconnected phenazine with π-conjugated structures, displaying the advantages of rich electron delocalization, thin sheet thickness, and low dissolution in electrolytes. When applied as the anode of PIBs, the CPT anode delivered a high reversible capacity of 305 mAh g−1 at 0.1 A g−1 over 200 cycles. Besides, it also exhibited promising potential for “high-temperature” application potential by retaining a capacity of 400 mAh g−1 at 0.1 A g−1 after 100 cycles at 45 °C. Full cells with CPT anode and potassiathed organic cathode displayed good cycling and rate performances. Furthermore, the step-wise K-storage mechanism was jointly determined by in-situ characterization techniques and theoretical calculations. This study not only presents a molecular engineering approach for designing organic materials but also provides novel insights into the underlying mechanism governing potassium storage.

Construction of foam-like carbon microspheres with controllable pseudo-graphitic domains: Synergistic enhancement of K-ion adsorption/intercalation storage

Hard carbon shows promise as a potassium-ion battery (PIB) anode, but its high capacity and rate property are limited by insufficient active sites and poor kinetics. Creating a porous channel structure offers an effective route, but such design often disrupts the development of intercalation sites critical for low-voltage plateau capacity, and may reduce the energy density of full cells. Herein, a staged pyrolysis strategy was developed to tailor foam-like carbon microspheres (FCMs) with controllable pseudo-graphitic domains by exploiting polymer with the temperature difference in pyrolysis. Such tactics perfectly retains abundant pseudo-graphitic domains and creates rich defect/pore structures, ensuring efficient K+ low-voltage intercalation and benefiting fast K+ transport. The optimized electrode exhibits balanced adsorption/intercalation capacity, delivering a large reversible capacity (386.7 mAh g−1 at 0.1C), outstanding rate performance (223.1 mAh g−1 at 4C) and excellent capacity retention (79.2 % over 2000 cycles at 4C). Additionally, the FCM-2//PTCDA full cell submits a high energy density of 198 Wh kg−1 and superb rate property/stability compared to same-type full cells. Tracked K-storage behavior confirmed the “adsorption–intercalation” mechanism and kinetic studies clarified that exact balance of defect, mesopore and pseudo-graphitic phase was crucial for the synergistic enhancement of adsorption/intercalation kinetics. This work opens up a unique method to tune the microstructure of hard carbon and offers design principles for developing practical anodes with synergistic storage behavior suitable for PIBs.

Oxygen-containing groups assist in enhancing Li+/K+ storage: Balancing adsorption and intercalation mechanisms

Porous carbon nanosheets were prepared using a high-temperature solid-phase method and subsequently modified through oxidative acid treatment to introduce oxygen-containing groups. The application and performance of these nanosheets as anodes in lithium-ion and potassium-ion batteries were investigated. The results indicated that the oxidative acid treatment successfully enhanced the porous carbon nanosheets' capacity for storing Li+/K+. Electrochemical analysis revealed that the oxygen-containing groups balanced intercalation and surface storage behaviors, optimizing the nanosheets' storage performance. These modified porous carbon nanosheets (termed SN@PCNs) demonstrated significantly boosted reversible Li+ and K+ storage capacities, achieving 1038.1 mAh⋅g−1 and 371.7 mAh⋅g−1 at 0.1 A g−1, respectively, while maintaining capacities of 443.3 mAh⋅g−1 for Li+ and 153.9 mAh⋅g−1 for K+ at 5.0 A g−1. Furthermore, the study emphasized the significance of a balanced surface capacitance and solid-phase diffusion storage mechanism in attaining high storage capacity and cycle stability. Moderate oxidation and the introduction of oxygen-containing groups were identified as crucial factors in optimizing performance. Additionally, potassium adsorption storage exhibited an advantage over lithium adsorption storage, and the impact of oxygen-containing groups on potassium storage performance was even more pronounced.

Biomass-Derived Carbon With Large Interlayer Spacing for Anode of Potassium Ion Batteries.

Potassium-ion batteries (PIBs) are emerging as powerful candidate for grid-oriented energy storage owing to their potentially low cost. Carbon is considered the promising anode for PIBs on the basis of its high conductivity and abundant sources. The biggest challenge confronted by carbon anodes lies in insufficient cycle life as well as rate capability, resulting from the limited interlayer spacing of the sp2-hybrid carbon incompatible with the large-radius potassium. Herein, a biomass-derived carbon with a large interlayer spacing of 0.44nm is fabricated via a zinc-assisted pyrolysis synthesis. The unique structure endows the carbon with superior capacity, rate capability, and cycle durability. The large interlayer spacing of carbons can promote fast potassium diffusion and alleviate the volume expansion during potassiation, conferring those rate capabilities and cycleability. The interconnected network structure is also able to shorten both the transport distances of electrons and ions. The demonstration exemplifies an advanced carbon for anodes of PIBs for energy storage applications.

A versatile opened hollow carbon sphere with highly loaded antimony alloy for ultra-stable potassium-ion storage

Carbon materials meet the stringent practical requirements for anodes for potassium-ion batteries (PIBs) due to their abundance and chemical stability. The major issue of carbon-based anodes is the low specific capacity and poor cyclic stability. Equally importantly, scalable synthesis approaches for electrodes are highly desired for the future application in large-scale energy storage systems. Herein, we developed a novel composite of Sb encapsulated in N/P co-doped opened hollow carbon spheres (N/POHCs) with high Sb loading through a simple carbonization and subsequent impregnation process. Beneficial from the virtue of abundant pyridinic-N−P bonding and opened hollow spherical structure advantages, N/POHCs exhibit much lower diffusion barrier than that of pure carbon, prominent Sb carrier capability, as well as the extraordinary resistance to volume expansion. The resulting Sb@N/POHCs composite delivers a high specific capacity of 533.3 mAh g−1 at 0.1 A g−1 with an initial Coulombic efficiency of 83 %, and can maintain a specific capacity of 345 mAh g−1 at 1 A g−1 after 4000 cycles. This work provides rational structure design with universal carrier capability of active materials to achieve high-capacity and long cycle life anode for advanced PIBs accompanied by the potential for large-scale production.

Cationic and Anionic Dual Redox Activity of MoS2 for Electrochemical Potassium Storage.

MoS2 is regarded as one of the most promising potassium-ion battery (PIB) anodes. Despite the great progress to enhance its electrochemical performance, understanding of the electrochemical mechanism to store K-ions in MoS2 remains unclear. This work reports that the K storage process in MoS2 follows a complex reaction pathway involving the conversion reactions of Mo and S, showing both cationic redox activity of Mo and anionic redox activity of S. The presence of dual redox activity, characterized in-depth through synchrotron X-ray absorption, X-ray photoelectron, Raman, and UV-vis spectroscopies, reveals that the irreversible Mo oxidation during the depotassiation process directs the reaction pathway toward S oxidation, which leads to the occurrence of K-S electrochemistry in the (de)potassiation process. Moreover, the dual reaction pathway can be adjusted by controlling the discharge depth at different cycling stages of MoS2, realizing a long-term stable cycle life of MoS2 as a PIB anode.

Recent Advances in Developing High-Performance Anode for Potassium-Ion Batteries based on Nitrogen-Doped Carbon Materials.

Owing to the low potential (vs K/K+), good cycling stability, and sustainability, carbon-based materials stand out as one of the optimal anode materials for potassium-ion batteries (PIBs). However, achieving high-rate performance and excellent capacity with the current carbon-based materials is challenging because of the sluggish reaction kinetics and the low capacity of carbon-based anodes. The doping of nitrogen proves to be an effective way to improve the rate performance and capacity of carbon-based materials as PIB anode. However, a review article is lacking in systematically summarizing the features and functions of nitrogen doping types. In this sense, it is necessary to provide a fundamental understanding of doped nitrogen types in nitrogen-doped(N-doped) carbon materials. The types, functions, and applications of nitrogen-doped carbon-based materials are overviewed in this review. Then, the recent advances in the synthesis, properties, and applications of N-doped carbon as both active and modification materials for PIBs anode are summarized. Finally, doped nitrogen's main features and functions are concluded, and critical perspectives for future research in this field are outlined.

Revealing Asymmetric Phase Transformation of the BiVO4 Anodes for Potassium-Ion Batteries by In Situ Transmission Electron Microscopy.

Potassium-ion batteries (PIBs) have emerged as a promising alternative to lithium-ion batteries (LIBs), thanks to the cost-effectiveness of potassium resources and a favorable redox potential of approximately -2.936 V. The monoclinic BiVO4, known for its layered structure, shows noteworthy electrochemical properties when utilized as an anode material for both LIBs and sodium-ion batteries. However, the fundamental electrochemical reaction mechanisms of the BiVO4 anode during the potassium insertion/extraction processes remain unclear. Here, we constructed a BiVO4 anode PIB inside the transmission electron microscope (TEM) to explore the real-time potassiation/depotassiation behaviors of BiVO4 during electrochemical cycling. Utilizing the state-of-art in situ TEM technique, the BiVO4 nanorods are found to undergo an asymmetric phase transformation for the first time, where the pristine BiVO4 material is transformed into an amorphous KxBiVO4 phase after the first cycle. More interestingly, the anode materials near and far from the potassium source exhibit opposite volume-changing trends under the same voltage potential. Also, this phenomenon should be attributed to the mass flow of the unstable K-Bi alloy under the electric field. Our findings provide significant insights into the electrochemical mechanism of BiVO4 nanorods during the potassiation/depotassiation process, with the hope of assistance in designing anodes for high-performance PIBs.

Heteroatom doped graphitic carbon nanotubes as freestanding anodes for advanced potassium-ion batteries

Owing to its higher earth element reserve and similar chemical properties to lithium, potassium ion batteries (PIBs) have been regarded as a potential alternative to lithium-ion batteries. And considering the relatively larger ionic radius of potassium, available electrode materials need to be equipped with enough space for volume expansion during charge-discharge cycles, thus graphitic carbon nanomaterials with adjustable layer spacing gradually come into researcher's version. Here with copper nanowires serving as growth template and organic polyvinyl pyrrolidone (PVP) providing carbon source, freestanding and ultra-light graphitic carbon nanotube (GCNT) aerogels were simply assembled and annealed, which were directly used as anodes of PIBs. Annealing parameters (temperature and atmosphere) were adapted to regulate the lattice order and interlayer spacing of GCNTs, and N, O heteroatoms derived from PVP were directly doped into the carbon lattice during thermal annealing, to optimize and enhance the cycle capacity and rate performance of GCNT anodes. The electrochemical potassium storage mechanism of GCNTs was also quantitatively analyzed. Most of the potassium ions are reversibly stored by squeezing into and escaping from the carbon lattice, and simultaneously oxygen-containing functional groups with different chemical states also offer active redox sites and dedicate partial capacity. Therefore, our assembled GCNTs with large lumen are expected to sandwich-like load with active substances efficiently, further constructing next-generation PIBs with excellent performance.

The potassium storage performance of carbon nanosheets derived from heavy oils

As by-products of petroleum refining, heavy oils are characterized by a high carbon content, low cost and great variability, making them competitive precursors for the anodes of potassium ion batteries (PIBs). However, the relationship between heavy oil composition and potassium storage performance remains unclear. Using heavy oils containing distinct chemical groups as the carbon source, namely fluid catalytic cracking slurry (FCCS), petroleum asphalt (PA) and deoiled asphalt (DOA), three carbon nanosheets (CNS) were prepared through a molten salt method, and used as the anodes for PIBs. The composition of the heavy oil determines the lamellar thicknesses, sp3-C/sp2-C ratio and defect concentration, thereby affecting the potassium storage performance. The high content of aromatic hydrocarbons and moderate amount of heavy component moieties in FCCS produce carbon nanosheets (CNS-FCCS) that have a smaller layer thickness, larger interlayer spacing (0.372 nm), and increased number of folds than in CNS derived from the other three precursors. These features give it faster charge/ion transfer, more potassium storage sites and better reaction kinetics. CNS-FCCS has a remarkable K+ storage capacity (248.7 mAh g−1 after 100 cycles at 0.1 A g−1), long cycle lifespan (190.8 mAh g−1 after 800 cycles at 1.0 A g−1) and excellent rate capability, ranking it among the best materials for this application. This work sheds light on the influence of heavy oil composition on carbon structure and electrochemical performance, and provides guidance for the design and development of advanced heavy oil-derived carbon electrodes for PIBs.

MXene-based materials composite with phytic acid for potassium-ion battery anodes

MXenes, with their metallic conductivity and complex surface chemistry, are emerging as promising newcomers in the field of energy storage materials. In this work, we present innovative iterations of MXene synthesised by phytic acid selective etching and self-assembly, denoted P-MXene, with phytic acid adhered tightly to the surface and increased the interlayer spacing of the MXene, which was beneficial to the embedment/desorption of K+, and etched more active sites. When used as an anode material for potassium ion batteries, P-MXene exhibits superior specific capacity of 135 mAh*g−1, long-term cycling stability capacity of 128.8 mAh*g−1 and higher rate performance (the final capacity of 110.0 mAh*g−1). This transformative development not only establishes a new paradigm for MXene derivatives, but also paves the way for the exploration of high-performance MXene-based energy storage materials.

Electrochemical behavior and reaction mechanism of nano-BiOBr/rGO composite micro flower with strong interface coupling as potassium-ion battery anodes

To explore the potential of bismuth oxybromide (BiOBr) as anodes for high-performance potassium (K)-ion batteries and understand its potassium storage mechanism, a novel nano-BiOBr/reduced graphene oxide (rGO) composite micro flower (labelled as SI-coupled nano-BiOBr/rGO micro flower), where nano-BiOBr slices are firmly anchored on rGO by strong interface coupling, is constructed. Unique microstructure accompanied by C-Bi bonds at the interface between BiOBr and rGO endows it with abundant high-speed charge transfer channels and excellent structural stability. As a result, it exhibits an excellent rate performance (a high reversible capacity of 278 mAh/g at 5 A/g) and a remarkable long-term cycling stability maintaining 95.4 % after 1000 cycles at 2.5 A/g. Furthermore, it is also found that SI-coupled nano-BiOBr/rGO micro flower anode undergoes intercalation, conversion, and alloying (BiOBr → KzBiOBr → Bi → KBi2 → K3Bi2 → K3Bi) at the initial discharge process, and the subsequent charge process is only reversible dealloying and conversion reaction (K3Bi → K3Bi2 → KBi2 → Bi → BiOxBry). This work not only demonstrates the large potential of BiOBr as high-performance K-ion battery anodes, but also elucidates for the first time its K storage mechanism.

Encapsulation of Sn Sub‐Nanoclusters in Multichannel Carbon Matrix for High‐Performance Potassium‐Ion Batteries

AbstractSub‐nanoclusters with ultra‐small particle sizes are particularly significant to create advanced energy storage materials. Herein, Sn sub‐nanoclusters encapsulated in nitrogen‐doped multichannel carbon matrix (denoted as Sn‐SCs@MCNF) are designed by a facile and controllable route as flexible anode for high‐performance potassium ion batteries (PIBs). The uniformly dispersed Sn sub‐nanoclusters in multichannel carbon matrix can be precisely identified, which ensure us to clarify the size influence on the electrochemical performance. The sub‐nanoscale effect of Sn‐SCs@MCNF restrains electrode pulverization and enhances the K+ diffusion kinetics, leading to the superior cycling stability and rate performance. As freestanding anode in PIBs, Sn‐SCs@MCNF manifests superior K+ storage properties, such as exceptional cycling stability ( around 331 mAh g−1 after 150 cycles at 100 mA g−1) and rate capability. Especially, the Sn‐SCs@MCNF||KFe[Fe(CN)6] full cell demonstrates impressive reversible capacity of around 167 mAh g−1 at 0.4 A g−1 even after 200 cycles. Theoretical calculations clarify that the ultrafine Sn sub‐nanoclusters are beneficial for electron transfer and contribute to the lower energy barriers of the intermediates, thereby resulting in promising electrochemical performance. Comprehensive investigation for the intrinsic K+ storage process of Sn‐SCs@MCNF is revealed by in situ analysis. This work provides vital guidance to design sub‐nanoscale functional materials for high‐performance energy‐storage devices.

Encapsulation of Sn Sub-Nanoclusters in Multichannel Carbon Matrix for High-Performance Potassium-Ion Batteries.

Sub-nanoclusters with ultra-small particle sizes are particularly significant to create advanced energy storage materials. Herein, Sn sub-nanoclusters encapsulated in nitrogen-doped multichannel carbon matrix (denoted as Sn-SCs@MCNF) are designed by a facile and controllable route as flexible anode for high-performance potassium ion batteries (PIBs). The uniformly dispersed Sn sub-nanoclusters in multichannel carbon matrix can be precisely identified, which ensure us to clarify the size influence on the electrochemical performance. The sub-nanoscale effect of Sn-SCs@MCNF restrains electrode pulverization and enhances the K+ diffusion kinetics, leading to the superior cycling stability and rate performance. As freestanding anode in PIBs, Sn-SCs@MCNF manifests superior K+ storage properties, such as exceptional cycling stability ( around 331 mAh g-1 after 150 cycles at 100 mA g-1) and rate capability. Especially, the Sn-SCs@MCNF||KFe[Fe(CN)6] full cell demonstrates impressive reversible capacity of around 167 mAh g-1 at 0.4 A g-1 even after 200 cycles. Theoretical calculations clarify that the ultrafine Sn sub-nanoclusters are beneficial for electron transfer and contribute to the lower energy barriers of the intermediates, thereby resulting in promising electrochemical performance. Comprehensive investigation for the intrinsic K+ storage process of Sn-SCs@MCNF is revealed by in situ analysis. This work provides vital guidance to design sub-nanoscale functional materials for high-performance energy-storage devices.

Boosting the potassium storage property of spongia-like copper phosphide anode via nano-in-micro construction

Metal phosphides (MPs) show great promise as anode material in potassium-ion batteries (PIBs) owing to their cost-effectiveness and high theoretical capacity. Despite that, MPs anode usually manifests inferior poor cyclability as a result of dramatic volume fluctuation during discharge–charge cycling. Herein, a scalable salt template-assisted spray-drying method is developed to fabricate the porous carbon microspheres wrapped CuP2 nanoparticles (p-CuP2/C) with a nano-in-micro structure. The combination of the CuP2 nanoparticles, large meso-porous carbon microspheres can simultaneously offer plenty of reactive sites, promote electrolyte penetration, and maintain structural integrity. Additionally, the proposed synthesis strategy is suit for the industrial manufacture. As an anode for PIBs, the p-CuP2/C anode presents a high reversible capacity (494 mAh/g at 0.05 A/g), excellent cycling stability (a capacity degradation rate of 0.04 % per cycle during 2000 cycles at 2 A/g), and superior rate capability (244 mAh/g at 2 A/g). More impressively, pairing with a potassium Prussian blue cathode, the potassium-ion coin cell shows an excellent cycling lifespan with 87.1 % capacity retention after 200 cycles at a current density of 0.1 A/g, the assembled pouch cell also maintains stable cycling at 0.3 A/g over 80 cycles. This research could offer a facile approach to develop other advanced anodes with industrial practicability for alkali ion batteries.

Microwave plasma conversion of food waste using carbon foam: Production of heteroatom-doped graphene and combustible gas

The mass production of food waste (FW) has a terrible impact on the environment, but with proper treatment, FW can be transformed into a new resource. Currently, thermal conversion (especially incineration) has been the most common and efficient means of handling FW, but it also entails negative impacts, such as high carbon emissions and lower added value. In this study, a new high-efficiency thermal conversion process is proposed that uses carbon foams to induce the formation of microwave plasma (MP), which generates very high final temperatures to enable the direct conversion of FW into combustible gases and high-value-added heteroatom-doped microwave plasma graphene (HMPG) in 5–20 s. This work investigated the optimal carbonization temperature of the melamine sponge (carbon foam precursor) and the effect of microwave plasma reaction duration on the distribution of the gas products and the properties of HMPG, and HMPG was characterized in detail by Raman spectroscopy, X-ray diffraction, scanning electron microscope, etc. Ultimately, HMPG was tested in potassium ion battery anodes for evaluation of its energy storage potential, and the results showed that the capacities were able to reach ∼270 mAh g−1 at 50 mA g−1 after 60 cycles.

A High-Rate and Ultrastable Re2Te5/MXene Anode for Potassium Storage Enabled by Amorphous/Crystalline Heterointerface Engineering.

The pursuit of anode materials capable of rapid and reversible potassium storage performance is a challenging yet fascinating target. Herein, a heterointerface engineering strategy is proposed to prepare a novel superstructure composed of amorphous/crystalline Re2Te5 anchored on MXene substrate (A/C-Re2Te5/MXene) as an advanced anode for potassium-ion batteries (KIBs). The A/C-Re2Te5/MXene anode exhibits outstanding reversible capacity (350.4 mAh g-1 after 200 cycles at 0.2 A g-1), excellent rate capability (162.5 mAh g-1 at 20 A g-1), remarkable long-term cycling capability (186.1 mAh g-1 at 5 A g-1 over 5000 cycles), and reliable operation in flexible full KIBs, outperforming state-of-the-art metal chalcogenides-based devices. Experimental and theoretical investigations attribute this high performance to the synergistic effect of the A/C-Re2Te5 with a built-in electric field and the elastic MXene, enabling improved pseudocapacitive contribution, accelerated charge transfer behavior, and high K+ ion adsorption/diffusion ability. Meanwhile, a combination of intercalation and conversion reactions mechanism is observed within A/C-Re2Te5/MXene. This work offers a new approach for developing metal tellurides- and MXene-based anodes for achieving stable cyclability and fast-charging KIBs.

Carbon coating engineering enhances the stability of graphite anode in potassium ion batteries

Graphite forms reversible potassium-graphite intercalation compounds electrochemically. Graphite anode possesses a high reversible specific capacity (279 mAh g−1) and an optimal low potential platform, rendering it an ideal anode material for potassium-ion batteries. However, the intercalation of K+ ions in graphite causes a bulk volume expansion of up to 61%, resulting in irreversible damage to the structure of graphite, which leads to inferior cycling stability. In this paper, surface-oxidized graphite (OG) with reduced particle size and increased defect densities was obtained by mechanical ball milling and chemical oxidation. Composites of soft carbon-coated OG (OG@PC) were prepared by soft carbon coating. The soft carbon coating can alleviate the bulk expansion caused by K+ intercalation/deintercalation in OG, thus slowing down the destruction of the crystalline structure of graphite after multiple charging/discharging cycles. OG@PC exhibits increased reversible specific capacity from 267 mAh g−1 to 314 mAh g−1 compared with pristine graphite at a current density of 0.05 A g−1. Moreover, at a high current density of 0.5 A g−1, a reversible specific capacity of 213 mAh g−1 was achieved after 200 cycles. This work investigates simple surface carbon coating strategies to improve the cycling stability of a graphite anode of potassium-ion batteries.

A Bandgap-Tuned Tetragonal Perovskite as Zero-Strain Anode for Potassium-Ion Batteries.

PIBs are emerging as a promising energy storage system due to high abundance of potassium resources and theoretical energy density, however, progress of PIBs is severely hindered by structural instability and poor cycling of anode material during continual insertion and extraction of larger-sized K+. Hence, developing anode material with structural stability and stable cycling remains a great challenge. Herein, bandgap-tuned Mo-doped and carbon-coated lead titanate (CMPTO) with zero-strain K+ storage is presented as ultra-stable PIBs anode. Mo doping introduces narrowed bandgap and optimized crystal lattice for enhanced intrinsic electron and ion transfer. Demonstrated by in situ XRD characterizations, the crystal structure stays stable with unchanged peak positions, fully revealing zero-strain characteristic of CMPTO anode during potassium storage for stable cyclic capability. Ultimately, CMPTO anode achieved ultra-stable cycling performance of 7000 cycles at 500 mA g-1 with high capacity retention of 90% and considerable specific capacity of 130.9 mAh g-1 after 600 cycles at 100 mA g-1; with relatively large density, CMPTO realized eminent volumetric capacity of 1111.09 mAh cm-3 and ultra-long cycling life of 10000 cycles at 7041 mA cm-3. This work introduces a promisingly new route into developing anode materials with ultra-stable performance for PIBs.

In-situ doped and activated N, S co-doped porous carbon derived from organic salt for application in high-performance potassium-ion batteries

Owing to its abundance in nature and low cost, potassium has attracted considerable attention as a substitute for lithium in the manufacture of secondary-ion batteries. However, developing amorphous carbon materials that show fast K+ ion kinetics for application in high-performance potassium-ion battery (PIB) anodes remains challenging. In this study, we designed and synthesized a 3-D hierarchical nitrogen and sulfur co-doped porous carbon electrode via in-situ doping and activation using acesulfame potassium. Owing to its prominent structural advantages, the as-prepared N, S co-doped electrode showed a high reversible capacity (459.8 mAh g−1 at 0.05 A g−1) and long-term cycle stability (205 mAh g−1 after 1000 cycles at 0.5 A g−1). Further, the results of ex-situ Raman spectroscopy and X-ray photoelectron spectroscopy verified the advantages of N and S co-doping with respect to K+ ion intercalation and adsorption/desorption properties within the carbon matrix. Therefore, our findings enhance understanding regarding the advantages of the dual-doped system with respect to K+ ion storage and highlight an efficient strategy for developing high-performance and durable carbon anode materials for PIBs.