Spacer Layer Research Articles

Structural Reconfiguration via Alternating Cation Intercalation of Chiral Hybrid Perovskites for Efficient Self-Driven X-ray Detection.

2D hybrid perovskites (HPs) have great potential for high-performance X-ray detection due to their strong radiation absorption and flexible structure. However, there remains a need to explore avenues for enhancing their detection capabilities. Optimizing the detection performance through modification of their structural properties presents a promising strategy. Herein, we explore the impact of modifying the organic spacer layer in two distinct 2D layered HPs, namely, Ruddlesden-Popper (R-MPA)2PbBr4 (R-1, R-MPA = methylphenethylammonium) and (R-MPA)EAPbBr4 (EA = ethylammonium) (R-2) with alternating cation intercalation (ACI), on their X-ray detection performance. The insertion of EA into R-2 results in a flatter inorganic skeleton, narrower spacing, and higher density compared to R-1. This structural modification effectively optimizes carrier transport and X-ray absorption in R-2, enhancing the X-ray detection performance. Notably, R-2 exhibits a polar structure with intrinsic spontaneous polarization, contributing to a bulk photovoltaic of 0.4 V. This feature enables R-2 single-crystal detectors to achieve self-driven X-ray detection with a low detection limit of 82.5 nGy s-1 under a 0 V bias. This work highlights the efficacy of the ACI strategy in structural modification and its significant effect on X-ray detection properties, providing insights for the design and optimization of new materials.

Quasi-solid-state monolithic DSSCs with optimized spacer layers and composite electrolytes for better efficiency and stability

In this study, high-performance quasi-solid-state monolithic dye-sensitized solar cells (QS-M-DSSCs) were designed using an optimized spacer layer architecture to enhance electrolyte transport and improve cell performance. Spacer layers, made from a combination of zirconium oxide (ZrO2) and titanium dioxide (TiO2), were precisely tuned to reduce mass-transport limitations. A 5.2 μm thick ZrO2/TiO2 layer provided good light reflectance and incident photon-to-current conversion efficiency compared to double layers of either material alone. Electrochemical impedance spectroscopy analysis of the m-DSSCs revealed that this architecture (photoelectrode TiO2 layer/ZrO2/TiO2 spacer layer/counter electrode catalyst layer) significantly increased recombination resistance, leading to an improvement in open-circuit voltage. As a result, acetonitrile iodide liquid-DSSCs using N719 dye achieved a high power conversion efficiency (PCE) of 8.45 %, surpassing cells with alternative spacer designs. For fully printable QS-M-DSSCs, printable gel electrolytes (PGEs) composed of polyethylene oxide and polymethyl methacrylate in 3-methoxypropionitrile (MPN) were employed. A 5 wt% PEO/PMMA composition demonstrated fast and efficient penetration of the PGEs through spacer layers. Moreover, incorporation of 4 wt% TiO2 nanoparticles into PGEs further enhanced their electrochemical properties, achieving a PCE (7.31 %) higher than cells with liquid electrolytes (6.72 %). QS-M-DSSCs demonstrated greater stability than liquid-state DSSCs.

Insight into CO2/CH4 separation by ionic liquids confined in MXene membrane from molecular level

Composite membranes incorporating ionic liquids (ILs) within MXene demonstrate promising potential for CO2 separation. However, studies on the separation of CO2/CH4 using MXene-confined ILs membranes are limited, especially in terms of understanding the mechanisms at the molecular level. In this work, the system of CO2/CH4 in MXene-confined ILs membranes was studied by molecular dynamic simulations. The number density results reveal that MXene stratifies the ILs between the layers, with higher concentrations of ILs near MXene and lower concentrations in the middle layer. Notably, MXene has a greater impact on cations distribution compared to anions. As the layer spacing of MXene expands from 1.5 to 3 nm, the interaction between MXene and IL weakens, while that between the cations and anions strengthens. The confined ILs enhance gas solubility capability but impede gas diffusion. CO2 is distributed closer to anions, while CH4 tends to be closer to cations, with the distance between CH4 and cations decreasing as the layer spacing increases. Additionally, with the increase of layer distance, the proportion of confined ILs gradually decreases, and the gas diffusion coefficient gradually increases. Furthermore, compared to 1-Ethyl-3-methylimidazolium tetrafluoroborate ([EMIM][BF4]) and 1-Ethyl-3-methylimidazolium hexafluorophosphate ([EMIM][PF6]), MXene-confined 1-Ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIM][TF2N]) is identified as the most effective for CO2/CH4 separation, owing to its superior CO2 solubility and highest diffusion selectivity.

Spatial and Temporal Bayesian Hierarchical Model Over Large Domains With Application to Holocene Sea Surface Temperature Reconstruction in the Equatorial Pacific

AbstractWe present a novel space‐time Bayesian hierarchical model (BHM) to reconstruct annual Sea Surface Temperature (SST) over a large domain based on SST at limited proxy (i.e., sediment core) locations. The model is tested in the equatorial Pacific. The BHM leverages Principal Component Analysis to identify dominant space‐time modes of contemporary variability of the SST field at the proxy locations and employs these modes in a Gaussian process framework to estimate SSTs across the entire domain. The BHM allows us to model the mean field and covariance, varying in space and time in the process layers of the hierarchy. Using the Markov Chain Monte Carlo (MCMC) method and suitable priors on the model parameters, posterior distributions of the model parameters and, consequently, posterior distributions of the SST fields and the attendant uncertainties are obtained for any desired year. The BHM is calibrated and validated in the contemporary period (1854–2014) and subsequently applied to reconstruct SST fields during the Holocene (0–10 ka). Results are consistent with prior inferences of La Niña‐like conditions during the Holocene. This modeling framework opens exciting prospects for modeling and reconstruction of other fields, such as precipitation, drought indices, and vegetation.

Secretory structures and histochemistry of roots, stem, and leaves of medicinal plant Fibraurea tinctoria Lour.

Fibraurea tinctoria Lour. (Menispermaceae) is a medicinal plant used by many local tribes in Indonesia and other countries. This species has pharmacological potential, such as antimalaria, antibacterial, antitumor, antioxidant, anticancer, antidiabetic, anti-inflammatory, and hepato-protector. However, the secretory structures and sites of secondary metabolite accumulation still need to be studied. This study aimed to explore the secretory structures and reveal the accumulation sites of the main classes of secondary metabolites in the root, stem, and leaves of F. tinctoria. Histochemical analysis using various specific reagents was performed on freehand sections of the fresh organs to detect alkaloids, phenolics, terpenoids, and lipophilic compounds. Observations of secretory structures were carried out using light microscopy. The result showed that idioblast was the predominant secretory structure in the plant organs and contained all the chemical groups investigated, while laticifer accumulated alkaloids were found only in the stem. Some secondary metabolites were localized in the xylem, intercellular space, and cuticle layer. Crystals were observed in the root, stem, and leaf of this species. These results might be helpful as guide information for extracting the particular plant parts to obtain the desired secondary metabolites. It suggested that leaves are a potential alternative source of medicinal raw material of this species, in addition to the stem. RESEARCH HIGHLIGHTS: The first study on secretory structures of Fibraurea tinctoria. Secondary metabolites in F. tinctoria organs accumulate in specialized and unspecialized structures. The idioblast is the primary secretory structure in the organs of F. tinctoria spreading over the root, stem, and leaves.

A first-principles calculations investigate the superlubricity and adhesion performance of structural superlubricity micro-components on polydimethylsiloxane surface

Adhesion and friction are crucial considerations in the design of microelectromechanical systems because they can directly influence the energy, dissipation and wear of the system. Current related studies are primarily conducted between graphite and hard materials, such as graphite, mica and gold, but lack the theoretical support of superlubricity on the surfaces of related flexible substrates, such as Polydimethylsiloxane (PDMS). Consequently, friction and wear at the flexible interface represent a significant challenge in the failure of microelectromechanical systems devices. In this paper, we use density functional theory to simulate the adhesion characteristics and friction behaviour of structural superlubricity micro-components on the surface of a flexible substrate in an atmospheric environment. The lower graphene layer of the structural superlubricity micro-components exhibits superior adhesion performance with the PDMS substrate. The increase in normal load is simulated by changing the spacing of layers. The interlayer bonding energy increases with increasing load. The transverse friction increases gradually with the increase in load, while the average friction coefficient decreases. Graphene can reach the superlubricity state on the PDMS substrate. The reliability of this phenomenon is verified by electrical performance. We also investigate the effect of tensile strain on the friction behaviour and electrical properties. These calculations should be combined with analysis of the mechanical properties to verify the reliability of the friction performance.

Composite Solid Electrolytes

The review describes composite electrolytes based on classical salt matrix phases, and also shows the possibilities of creating composites using simple or complex oxide matrices, where simple substances, salts, simple and complex oxides are used as heterogeneous dopant. The magnitude of the composite effect of electrical conductivity is discussed from the point of view of various theories of its quantitative description. The reasons for the occurrence of the composite effect are summarized. The effect of increasing ionic conductivity is due to the disorder of the surface layer in the intergranular space, amorphization or spreading of the matrix phase or the phase of heterogeneous dopant over the surface of the other phase due to the difference in surface energy, as well as the possibility of joint manifestation of these effects when using complex oxide eutectic composites with treatment above the temperature of the eutectic system.

Enhanced collection efficiency of quantum emitter mediated by extra ordinary optical transmission in a plasmonic cavity

Abstract Manipulation of light-matter interaction has played a key role in developing modern quantum optical technologies. We have designed a plasmonic cavity by placing a gold film over a dielectric layer of PMMA (spacer layer) placed on the distributed Bragg reflector (DBR) with a high reflection band between 550 to 750 nm using computational models. We then introduced periodic holes of subwavelength dimension in the gold film and a quantum emitter (QE) is placed inside the spacer layer. When QE interacts with the periodic array of nano-holes, it shows an enhanced light transmission through them due to the extraordinary optical transmission (EOT) phenomenon, which arises due to surface plasmon polariton excitations in the metallic structures. When the QE emission is coupled with these modes, EOT will help its emission to propagate into the far-field domain. We find an average Purcell enhancement of 3 times with 50% collection efficiency without using an antenna. The results have the potential to develop better single-photon coupling interfaces, quantum communication systems, and other quantum technologies.

Achieving pure-fluorescent color-tunable WOLED through long-range coupling of spatially separated electron–hole pairs

Abstract Color-tunable white organic light-emitting diode (CT-WOLED) with a wide correlated color temperature (CCT) offers numerous advantages in meeting human daily needs related to circadian rhythm. The study of CCT variation trends and the rules governing the expansion of the CCT range will help further improve the performance of such devices. This research proposes an effective strategy for achieving high-efficiency fluorescent CT-WOLEDs through long-range radiative coupling of spatially separated electron–hole pairs. After inserting a 5 nm thick DMAC-DPS layer between the donor (TAPC) and the acceptor (PO-T2T), the charge transfer excitons between TAPC and PO-T2T still exist. As the voltage increases, holes selectively undergo different photophysical processes, resulting in a wide CCT range. This demonstrates the extraordinary potential of spatially separated electron–hole pairs in regulating luminescent properties. By further introducing a bulk exciplex and the conventional red fluorescent dye DCJTB, the device’s efficiency, brightness, and CCT range have been further optimized. Additionally, significant highest occupied molecular orbital energy level difference between the hole transport layer TAPC and the spacer layer facilitates hole accumulation at the TAPC/spacer interface, thereby enhancing the long-range coupling effect. In device E, we achieved a wide CCT range of 2774 K along with a high external quantum efficiency of 9.2%. The results indicate that our proposed long-range coupling strategy not only enables a wide CCT range but also ensures broad spectral emission and high electroluminescence efficiency, providing new possibilities for the field of intelligent lighting.

Yolk-shell structured FeS0.5Se0.5@N-doped mesoporous carbon composite as high-performance lithium-ion battery anodes

Transition metal selenides/sulfides are drawing growing attention as promising electrode material for lithium-ion batteries owing to their larger layer spacing and weaker ionic bond compared to transition metal oxides, which are conducive to the intercalation/de-intercalation of Li ions. However, the intrinsic low conductivity and large volume expansion remain a major obstacle for their practical applications. In this work, with the prediction help of the theory model, we design a yolk-shell structure of single-phase ternary FeS0.5Se0.5 and nitrogen-doped mesopore carbon (YS-FeS0.5Se0.5@NMC) via an interfacial co-assembly, followed by one-step selenization and vulcanization. In the composite, single-phase ternary FeS0.5Se0.5 yolk provides more active sites and faster ion/electron transport dynamics than binary Fe2O3, while N-doped mesoporous carbon shell effectively alleviates the large volume expansion of FeS0.5Se0.5, as revealed by in-situ Raman analysis and TEM observation. Meanwhile, the spatial confinement of outer carbon shell also ensures the mechanical stability of the electrode during cycles. These merits endow the YS-FeS0.5Se0.5@NMC anode with a high reversible capacity of 1417mA h/g at 200mA h/g after 120 cycles, and an exceptional rate capability. This work offers an inspired approach for achieving high-performance energy storage electrode materials

Preparation and characterization of temperature-induced ultrasensitive SERS large-scale vertical Au nanosphere dimers

Plasmonic dimers have a very wide range of applications as a unique platform for studying the fundamental effects of plasmonics. Most dimer structures are prepared by chemical methods and direct-writing methods, such as coupling agents and lithography. These methods are often complex and expensive. Here, we prepared Au nanospheres (AuNSs) by layer-by-layer (LBL) deposition, used polymethyl methacrylate (PMMA) as a spacer layer, and then annealed the deposited AuNSs to orient the assembly and integrate them together. In this paper, suitable PMMA spin coating conditions and optimal annealing temperatures were explored, and large-scale AuNSs-PMMA-AuNSs(NSs-P-NSs) composed of vertical Au nanosphere dimers were prepared successfully. The detection limits of this substrate can reach 4 × 10−12 M/L and 4 × 10−10 M/L for Rhodamine 6 G (R6G) and Crystal Violet (CV), respectively, demonstrating excellent Raman activity. In addition, the sensitivity of detecting aspartame (APM) is 0.015625 g/L. This method is not only simple to operate but also allows the preparation of a large-scale uniform substrate with excellent detection capabilities.

Tailoring Na+ Diffusion Kinetics and Structural Stability of P2‐Layered Material by W‐Lattice Doping†

Comprehensive SummaryThe pursuit of advanced sodium‐ion batteries (SIBs) has been intensified due to the escalating demand for sustainable energy storage solutions. A W‐doped P2‐type layered cathode material, Na0.67Ni0.246W0.004Mn0.75O2 (NNWMO), has been developed to address the limitations of traditional cathode materials. Compared to the pristine Na0.67Ni0.25Mn0.75O2 (NNMO), NNWMO exhibits improved reversible capacity, excellent cycle performance, and remarkable rate performance. It can deliver an increased discharge capacity of 142.20 mAh/g at 0.1 C, with an admirable capacity retention of 80.5% after 100 cycles at high voltage. In situ XRD results demonstrate that the rivet effect related to the strong W—O bonds inhibits irreversible phase transition and enhances structural reversibility during charge/discharge processes. High‐resolution scanning transmission electron microscopy and X‐ray diffraction results confirm successful lattice doping of W6+ and increased layer spacing, contributing to favorable sodium ion diffusion kinetics. Density‐functional theory (DFT) calculation results further reveal that the smoother Na+ ion diffusion dynamics is attributed to the reduced migration energy barrier of Na+ with the insertion of W6+. This study provides valuable insights into the design of high‐performance cathode materials for next‐generation SIBs, showcasing the potential for more efficient, stable, and enduring energy storage solutions.

Quark: Real-time, High-resolution, and General Neural View Synthesis

We present a novel neural algorithm for performing high-quality, highresolution, real-time novel view synthesis. From a sparse set of input RGB images or videos streams, our network both reconstructs the 3D scene and renders novel views at 1080p resolution at 30fps on an NVIDIA A100. Our feed-forward network generalizes across a wide variety of datasets and scenes and produces state-of-the-art quality for a real-time method. Our quality approaches, and in some cases surpasses, the quality of some of the top offline methods. In order to achieve these results we use a novel combination of several key concepts, and tie them together into a cohesive and effective algorithm. We build on previous works that represent the scene using semi-transparent layers and use an iterative learned render-and-refine approach to improve those layers. Instead of flat layers, our method reconstructs layered depth maps (LDMs) that efficiently represent scenes with complex depth and occlusions. The iterative update steps are embedded in a multi-scale, UNet-style architecture to perform as much compute as possible at reduced resolution. Within each update step, to better aggregate the information from multiple input views, we use a specialized Transformer-based network component. This allows the majority of the per-input image processing to be performed in the input image space, as opposed to layer space, further increasing efficiency. Finally, due to the real-time nature of our reconstruction and rendering, we dynamically create and discard the internal 3D geometry for each frame, generating the LDM for each view. Taken together, this produces a novel and effective algorithm for view synthesis. Through extensive evaluation, we demonstrate that we achieve state-of-the-art quality at real-time rates.

Revealing the Effect of Curvature Structure in Hard Carbon Anodes for Lithium/Sodium Ion Batteries.

Heteroatom doping is the most common means to enhance the Li+/Na+ ions storage of hard carbon (HC). The explanation of the storage mechanism of heteroatom-doped HC is to increase the active site or widen the layer spacing while ignoring the effect of local bending structure induced by it. Meanwhile, the storage mechanism by the localized bending structure also lacks in-depth study. Herein, a locally curved configuration and an amorphous structure are designed by introducing different heteroatoms, respectively, and the mechanism of the two types of structures on the Li+/Na+ ions storage is explored. The density functional theory (DFT) calculation shows that the adsorption energy of Li+/Na+ ions is optimal at the appropriate curvature of 27.72 m-1. Serving as anode for lithium/sodium ion batteries in ester electrolytes, the optimized HCs demonstrate satisfied specific capacity and high-rate capability, respectively. Furthermore, the charging capacity below 1.0V of HC with suitable curvature microstructure reaches 84.8% and 90.1% of the total charge capacity, confirming that the curvature defects can better control the delithiation/desodiation process, and provide a higher energy density. This study enlightens new insights into the storage mechanisms of Li+/Na+ ions and provides guidance for better design of heteroatom-doped carbon anodes with superior performance.

Organic cation‐supported layered vanadate cathode for high‐performance aqueous zinc‐ion batteries

AbstractLayered vanadates are ideal energy storage materials due to their multielectron redox reactions and excellent cation storage capacity. However, their practical application still faces challenges, such as slow reaction kinetics and poor structural stability. In this study, we synthesized [Me2NH2]V3O7 (MNVO), a layered vanadate with expended layer spacing and enhanced pH resistance, using a one‐step simple hydrothermal gram‐scale method. Experimental analyses and density functional theory (DFT) calculations revealed supportive ionic and hydrogen bonding interactions between the thin‐layered [Me2NH2]+ cation and [V3O7]− anion layers, clarifying the energy storage mechanism of the H+/Zn2+ co‐insertion. The synergistic effect of these bonds and oxygen vacancies increased the electronic conductivity and significantly reduced the diffusion energy barrier of the insertion ions, thereby improving the rate capability of the material. In an acidic electrolyte, aqueous zinc‐ion batteries employing MNVO as the cathode exhibited a high specific capacity of 433 mAh g−1 at 0.1 A g−1. The prepared electrodes exhibited a maximum specific capacity of 237 mAh g−1 at 5 A g−1 and maintained a capacity retention of 83.5% after 10,000 cycles. This work introduces a novel approach for advancing layered cathodes, paving the way for their practical application in energy storage devices.

Metal-Hydroxide Organic Frameworks for Aqueous Nickel-Zinc Batteries.

Hydroxides exhibit a high theoretical capacity for energy storage by ion release and are often intercalated with anions to enhance the ion migration kinetics. In this study, a series of metal-hydroxide organic frameworks (MHOFs) are synthesized by intercalating aromatic organic linkers into hydroxides using I-M/Ni(OH)2 (where M = Co2+, Cu2+, Mg2+, Fe2+). The coordination environment and layer spacing (1.09 nm) of I-M/Ni(OH)2 are explored by X-ray absorption fine structure and cryo-electron microscopy. The intercalation nanostructure improves the conductivity of the hydroxides and facilitates Zn2+ migration by increasing the interlayer spacing, while enhancing the rate capability and cycling stability. Consequently, the I-Co/Ni(OH)2 material exhibites a satisfactory specific capacity of 0.35 mAh cm-2 at 3 mA cm-2 and a high peak power density of 6.78 mW cm-2. This study offers a novel perspective on the design of intercalated hydroxide and provides new insights into high-performance nickel-zinc batteres.

Short-Range Coulomb Interaction Is a Key to Switch the Utilization of Higher Triplet Excitons in Multiresonance Thermally Activated Delayed Fluorescence Doped Film.

Multiresonance thermally activated delayed fluorescence (MR-TADF) materials have attracted widespread attention due to ultrahigh definition display standards. However, many MR-TADF materials lack TADF properties in both the solution and solid states. Interestingly, the TADF characteristics appear once these MR-TADF compounds are doped in a suitable host film, but the precise mechanism involved in the host-guest interaction remains uncertain. Herein, we systematically investigated the role of host-guest interactions employing doped films (DABNA-1@mCBP and DABNA-1@DPEPO) with opposite phenomena. The results indicate that mCBP with a V-shape and enhanced rigidity could facilitate the formation of an energy spacing layer by employing short-range Coulomb energy through the MR luminescent core, which could offset the sensitivity of the stacking distance, enhancing the coupling between T1 and T2, and thus switch the reverse internal conversion and the higher T2 reverse intersystem crossing process. This work is a further development of luminescence mechanisms and an update of the host-guest interaction criteria for the targeted design of doped films.

Boosting Carrier Transport in Quasi-2D/3D Perovskite Heterojunction for High-Performance Perovskite/Organic Tandems.

Wide-bandgap (WBG) perovskites are continuously in the limelight owing to their applicability in tandem solar cells. The main bottlenecks of WBG perovskites are interfacial non-radiative recombination and carrier transport loss caused by interfacial defects and large energy-level offsets, which induce additional energy losses when WBG perovskites are stacked with organic solar cells in series because of unbalanced carrier recombination in interconnecting layer (ICL). To solve these issues, 1,3-propanediammonium iodide (PDADI) is incorporated to form Dion-Jacobson -phase quasi-2D perovskites with mixed high-n-values in WBG perovskites. PDADI simultaneously repairs the shallow/deep defects and establishes a Type-II energy-level alignment between quasi-2D/3D and 3D perovskites for rapid carrier extraction. More importantly, the short-chain diammonium cation in quasi-2D perovskite with high n-values results in a short Pb-I inorganic layer spacing, which enhances the interlayer electronic coupling and weakens the quantum-well confinement effect that restricts carrier transport. The suppressed transport loss increases the electron concentration in the ICL for balanced carrier recombination. The 0.0628 and 1.004 cm2 perovskite/organic tandems achieve remarkable efficiencies of 25.92% and 24.63%, respectively. The quasi-2D capping layer can inhibit ion migration, allowing perovskite/organic tandems to show excellent operational stability (T85 >1000h).

Insights of physicochemical structure changes of bituminous coal with acidification-assisted controlled electric pulse through SEM, XRD and FTIR

Controlled electric pulse (CEP) cracking coal effectively enhances its permeability, but a high coal breakdown voltage (BV) can result in technical difficulties. To address this problem, the method of using HCl solution to improve the electrical conductivity of coal was proposed. The effects of HCl on coal BV were investigated, and the microstructural changes in coal were analyzed through scanning electron microscopy, X-ray diffraction, and Fourier-transform infrared spectroscopy. Compared with raw coal, the BV of acidified coal decreased significantly. The crushing degree of the coal samples was clearly enhanced with an increasing HCl concentration. Some internal coal minerals were acidified and dissolved, the aromatic layer spacing (d002) increased and the layer sheet stacking height (Lc) decreased, and the crystal structure was damaged. When acidified coal was broken down, numerous internal pores and cracks appeared, active coal groups were shed, the aliphatic hydrocarbons and oxygen-containing functional group contents increased, surface activity was reduced, and the hydroxyl content was reduced, which was conducive to rapid gas desorption. Acidification effectively reduces the BV of coal and improves the cracking and permeability enhancement effect of coal by CEP action.

Carbon-Encapsulated Bimetallic Fe-W-Based Selenides with Abundant Heterogeneous Conductive Network for Superior Potassium Ion Storage.

Potassium-ion batteries (KIBs) are one of the most promising alternatives to lithium-ion batteries (LIBs) due to their high ion mobility, abundant resources, and low cost. However, the problems of low capacity and poor cycling stability of KIBs remain unsolved; therefore, it is crucial to explore alternative electrode materials suitable for reversible insertion and extraction of K+. Herein, carbon-encapsulated Fe3Se4/WSe2 microsphere material assembled from nanosheets with abundant heterogeneous interfaces and expanded interlayer spacing (denoted as FWSC) is designed as an anode material for superior potassium ion storage. The microspheres assembled from nanosheets, the outer carbon coating, and the expanded layer spacing can expose more active sites and improve the electronic conductivity and structural stability of the material. The abundant heterogeneous conductive network not only improves the conductivity of the material but also enhances the reversibility of the electrochemical reaction. As a result, the FWSC exhibits outstanding cycling stability, excellent rate performance (the capacity retention is 53% when the current density is from 0.5 to 1.0 A g-1), and stable long-term cycle performance (a capacity of 209 mAh g-1 at 1.0 A g-1 over 1000 cycles).