Heterogeneous Deposition Research Articles

Highly crystalline nanorods pyrene-based covalent organic framework artificial solid electrolyte interface accelerated interface Li+ regulation on lithium anode

The detrimental effects of heterogeneous Li deposition and aeolotropic Li dendrite propagation critically hamper its serviceability of Li metal batteries. The exploitation of neutral multifunctional porous polymer artificial SEI is imperative to modulate interfacial ionic transfer behavior. Herein, we propose a strategy based on dual-functional nanorod-shaped covalent organic frameworks (COF) to accelerate Li+ diffusion and mitigate lithium dendrite growth by creating an artificial solid electrolyte interface (SEI) layer. As anticipated, the immobilized high-polarity –OH and −CN- groups, along with the porous channel facilitates, facilitate uniform Li+ flux distribution and rapid Li+ migration. Additionally, the highly conjugated nature of the pyrene moiety not only enhances the plane π-π stacking crystallinity of TFDH-COF, but contributes positively to Li+ and repelling TFSI−. The combination of comprehensive ex-situ/in-situ characterizations and DFT calculations have unraveled the underlying mechanisms on the reductive Li mitigation energy barrier and enhancive Li+ transfer ability. In contrast with bare Li, the resultant TFDH-COF@Li electrode demonstrates the elevated reversibility of Li+ utilization, slight polarization, dendrite-free interface and prolonged cyclic performance in Li|Cu, Li|Li, and Li-based full cells operated at rigorous current densities. Those unswerving evidences enlighten the feasibility of engineering the neutrality COF layer to get rid of adverse disordered Li proliferation.

Heterostructure Mo2C/α-MoO3/G catalyst based heterogeneous catalysis/deposition mechanism for high-performance Li-S battery

Lithium-sulfur batteries (LSBs) have been recognized as a promising energy device due to their outstanding theoretical energy density and abundant resources. However, the commercial application remains obstruction by the sluggish redox kinetics and serious shuttle effect of polysulfides. Herein, a heterostructural Mo2C/α-MoO3/graphene (Mo2C/α-MoO3/G) catalyst based on a heterogeneous catalysis/deposition mechanism is proposed to address these issues. The prepared Mo2C/α-MoO3/G catalyst is feature with high-activity facet, fast electron delocalization and build-in electric field, which drastically promotes the redox kinetics of polysulfides on the surface of crystal phase. Simultaneously, the heterostructural Mo2C/α-MoO3/G catalyst is capable of capturing polysulfides effectively and eliciting the heterogeneous deposition of Li2S on the surface of amorphous phase, of which guarantee the efficient catalytic characteristic during the charge/discharge processes. In addition, the shuttle effect is restricted with a lower shuttle factor (∼0.02). Therefore, the assembled LSBs based Mo2C/α-MoO3/G catalyst modifying separator exhibits an impressive specific capacity of 1311.4 mAh g−1 at 0.2 C and excellent rate capability of 580.3 mAh g−1 at 4 C. More importantly, it demonstrated satisfied cycling stability even at a high sulfur loading mass (4.2 mgS cm−2) and lean electrolyte conditions (9.3 μL gS-1). This work reveals a novel paradigm for optimizing the kinetics behaviors to achieve the commercialization of LSBs.

Stabilizing water and regulating interfacial electrostatic interaction with economical supporting salt for stable Zn metal anode

Developing rechargeable aqueous Zn batteries for large-scale energy storage is impeded by inadequate reversibility and stability of the Zn anode, primarily caused by parasitic reactions and heterogeneous deposition. This study proposes an economical electrolyte strategy to address these Zn-related issues. The addition of a supporting salt enhances the thermodynamic stability of water, reduces the number of highly reactive water molecules, and modulates the interfacial electrostatic interaction. This approach effectively suppresses hydrogen evolution reaction and uncontrolled deposition. Remarkably, the rationally proportioned electrolyte allows a high average Coulombic efficiency of 99.93% for 1000 cycles in a Zn||Cu battery and a prolonged lifespan exceeding 4800 h in Zn||Zn cells. The knock-on effect is that Zn||MnO2 pouch cells deliver stable cycling performance, demonstrating the viability of this approach for practical applications.

Stabilization Strategies of Lithium Metal Anode Toward Dendrite-Free Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries are considered as a most promising rechargeable lithium metal batteries because of their high energy density and low cost. However, the Li-S batteries mainly suffer the capacity decay issue caused by the shutting effect of lithium polysulfides and the safety issues arising from the Li dendrites formation. This review outlines the current issues of Li-S batteries. Furthermore, we comprehensively summarized the challenges encountered by Li anode in Li-S batteries, such as the heterogeneous deposition of the Li anode, the unstable solid electrolyte interface (SEI) layer, and volume expansion. Moreover, research progresses in the stabilization strategies of Li anodes (physical approaches, optimization of electrolyte, surface protection layer, and design of current collector) is discussed in detail. Lastly, the remaining challenges and future research directions of Li metal anode stabilization in Li-S batteries are also present.

Anode-Free Li Metal Batteries: Feasibility Analysis and Practical Strategy.

Energy storage devices are striving to achieve high energy density, long lifespan, and enhanced safety. In view of the current popular lithiated cathode, anode-free lithium metal batteries (AFLMBs) will deliver the theoretical maximum energy density among all the battery chemistries. However, AFLMBs face challenges such as low plating-stripping efficiency, significant volume change, and severe Li-dendrite growth, which negatively impact their lifespan and safety. This study provides an overview and analysis of recent progress in electrode structure, characterization, performance, and practical challenges of AFLMBs. The deposition behavior of lithium is categorized into two stages: heterogeneous and homogeneous interface deposition. The feasibility and practical application value of AFLMBs are critically evaluated. Additionally, key test models, evaluation parameters, and advanced characterization techniques are discussed. Importantly, practical strategies of different battery components in AFLMBs, including current collector, interface layer, solid-state electrolyte, liquid-state electrolyte, cathode, and cycling protocol, are presented to address the challenges posed by the two types of deposition processes, lithium loss, crosstalk effect and volume change. Finally, the application prospects of AFLMBs are envisioned, with a focus on overcoming the current limitations and unlocking their full potential as high-performance energy storage solutions.

Spatial heterogeneity: Necessary and feasible for revealing soil trace elements pollution, sources, risks, and their links

The source diversity and health risk of trace elements (TEs) in soil make it necessary to reveal the relationship between pollution, source, and risk. However, neglect of spatial heterogeneity restricts the reliability of existing identification methods. In this study, spatial heterogeneity is proposed as a necessary and feasible factor for accurately dissecting the pollution-source-risk link of soil TEs. A comprehensive framework is developed by integrating positive matrix factorization, Geodetector, and risk evaluation tools, and successfully applied in a mining-intensive city in northern China. Overall, the TEs are derived from natural background (28.5 %), atmospheric deposition (25.6 %), coal mining (21.8 %), and metal industry (24.1 %). The formation mechanism of heterogeneity for high-variance TEs (Se, Hg, Cd) is first systematically deciphered by revealing the heterogeneous source-sink relationship. Specifically, Se is dominated (76.5 %) by heterogeneous coal mining (q=0.187), Hg is determined (92.6 %) by the heterogeneity of metal mining (q=0.183) and smelting (q=0.363), and Cd is caused (50.9 %) by heterogeneous atmospheric deposition (q>0.254) co-influenced by the terrains and soil properties. Highly heterogeneous sources are also noteworthy for their potential to pose extreme risks (THI=1.122) in local areas. This study highlights the necessity of integrating spatial heterogeneity in pollution and risk assessment of soil TEs.

Effect of Fe2O3 on CeO2 films in the photocatalytic evaluation towards the degradation of brilliant green and oxytetracycline

This paper presents a photochemical synthesis method for producing pure CeO2 deposits and CeO2 deposits loaded with varying proportions of Fe2O3. The deposits were calcined at 950 °C and characterized structurally, compositionally, and morphologically using XRD, XPS, SEM, FT-IR, and Raman spectroscopy techniques. Cerianite and hematite phases were identified in CeO2/Fe2O3 samples, indicating heterogeneous surface deposits. Photocatalytic testing under UV–Vis illumination for 5 h demonstrated promising results. For the degradation of bright green dye, efficiencies of 78.9 % and 90.1 % were achieved for pure CeO2 and CeO2 samples loaded with 1.0 mol% Fe2O3, respectively. Similarly, for oxytetracycline drug degradation, performance rates of 35.3 % and 67.0 % were observed for CeO2 and CeO2 samples loaded with 1.0 mol% Fe2O3, respectively. Recyclability tests showed a gradual decline in photocatalytic performance over successive cycles due to by-product accumulation contaminating the catalyst.

Differential association of abdominal, liver, and epicardial adiposity with anthropometry, diabetes, and cardiac remodeling in Asians.

Heterogenous deposition and homeostasis roles of physiologic and ectopic adipose tissues underscore the impact of fat compartmentalization on cardiometabolic risk. We aimed to characterize the distribution of abdominal visceral adipose tissue (VAT), subcutaneous adipose tissue (SAT), epicardial adipose tissue (EAT), and liver fat on magnetic resonance imaging (MRI), and evaluate their associations with anthropometric indices and adverse cardiac remodeling. In this cross-sectional observational study, 149 Asian adults (57.0 ± 12.8 years; 65% males) with at least one cardiometabolic risk factor underwent multiparametric fat and cardiovascular MRI. Anthropometric indices included body mass index (BMI), waist circumference (WC), waist-hip ratio (WHR), and bioimpedance body fat mass (BFM). Associations between fat depots and anthropometric measures as well as cardiac remodeling features were examined as a single cohort and stratified by type 2 diabetes mellitus (T2DM) status. VAT and SAT had opposing associations with liver fat and EAT. Therefore the VAT/SAT ratio was explored as an integrated marker of visceral adiposity. VAT/SAT was positively associated with EAT (β=0.35, P<0.001) and liver fat (β=0.32, P=0.003) independent of confounders. Of the anthropometric measurements assessed, only WHR was independently associated with VAT/SAT (β=0.17, P=0.021). Individuals with T2DM had higher VAT and lower SAT compared to those without T2DM, translating to a significantly higher VAT/SAT ratio. EAT volume was independently associated with adverse features of cardiac remodeling: increased left ventricular (LV) mass (β=0.24, P=0.005), larger myocyte volume (β=0.26, P=0.001), increased myocardial fibrosis (β=0.19, P=0.023), higher concentricity (β=0.18, P=0.035), and elevated wall stress (β=-0.18, P=0.023). Multiparametric MRI revealed abdominal VAT and SAT have differential associations with anthropometric indices and ectopic fats in a single cohort of Asians at risk of cardiometabolic disease. People with T2DM have expanded VAT and diminished SAT, endorsing the VAT/SAT ratio beyond usual anthropometric measurements as a marker for multiorgan visceral fat composition. Among the fat depots examined, EAT is uniquely associated with adverse cardiac remodeling, suggesting its distinctive cardiometabolic properties and implications.

A comprehensive transformation-thermomechanical model on deformation history in directed energy deposition of high-speed steel

ABSTRACT Phase transformation is a crucial factor that determines the quality and deformation of components in laser-directed energy deposition (L-DED). Owing to the limitations of in situ observation methods, there is a lack of effective means to study the complete phase transformation and their impacts on deformation during the deposition process. In this study, multilayer heterogeneous deposition was investigated with the high-carbon high-speed steel by modelling the coupled phase transformation-thermomechanical physics. The methodology was proposed to identify the specific phase transformations by iteratively comparing the whole deformation history between digital image correlation (DIC) measurements and simulations. Besides the thermo-mechanical coupling effect and basic volumetric phase transformation, carbon partitioning between precipitated carbides and matrix was manifested, which also resulted in a rise of the Ms point by 208.4 °C and a reduction of the transformation rate by 73.2%. Additionally, an increase of 13.8% in energy absorption could be attributed to the surface oxidation of the deposited layer. The model predictions exhibited good consistency with the DIC in-situ measurement data, indicating that the deformation history contained sufficient information on the phase transformations. Based on the proposed transformation-thermomechanical coupling model, it helps to understand the complete phase transformation during deposition.

Advancing Tau PET Quantification in Alzheimer Disease with Machine Learning: Introducing THETA, a Novel Tau Summary Measure.

Alzheimer disease (AD) exhibits spatially heterogeneous 3- or 4-repeat tau deposition across participants. Our overall goal was to develop an automated method to quantify the heterogeneous burden of tau deposition into a single number that would be clinically useful. Methods: We used tau PET scans from 3 independent cohorts: the Mayo Clinic Study of Aging and Alzheimer's Disease Research Center (Mayo, n = 1,290), the Alzheimer's Disease Neuroimaging Initiative (ADNI, n = 831), and the Open Access Series of Imaging Studies (OASIS-3, n = 430). A machine learning binary classification model was trained on Mayo data and validated on ADNI and OASIS-3 with the goal of predicting visual tau positivity (as determined by 3 raters following Food and Drug Administration criteria for 18F-flortaucipir). The machine learning model used region-specific SUV ratios scaled to cerebellar crus uptake. We estimated feature contributions based on an artificial intelligence-explainable method (Shapley additive explanations) and formulated a global tau summary measure, Tau Heterogeneity Evaluation in Alzheimer's Disease (THETA) score, using SUV ratios and Shapley additive explanations for each participant. We compared the performance of THETA with that of commonly used meta-regions of interest (ROIs) using the Mini-Mental State Examination, the Clinical Dementia Rating-Sum of Boxes, clinical diagnosis, and histopathologic staging. Results: The model achieved a balanced accuracy of 95% on the Mayo test set and at least 87% on the validation sets. It classified tau-positive and -negative participants with an AUC of 1.00, 0.96, and 0.94 on the Mayo, ADNI, and OASIS-3 cohorts, respectively. Across all cohorts, THETA showed a better correlation with the Mini-Mental State Examination and the Clinical Dementia Rating-Sum of Boxes (ρ ≥ 0.45, P < 0.05) than did meta-ROIs (ρ < 0.44, P < 0.05) and discriminated between participants who were cognitively unimpaired and those who had mild cognitive impairment with an effect size of 10.09, compared with an effect size of 3.08 for meta-ROIs. Conclusion: Our proposed approach identifies positive tau PET scans and provides a quantitative summary measure, THETA, that effectively captures heterogeneous tau deposition observed in AD. The application of THETA for quantifying tau PET in AD exhibits great potential.

Freestanding Films of Reduced Graphene Oxide Fully Decorated with Prussian Blue Nanoparticles for Hydrogen Peroxide Sensing.

Developing thin, freestanding electrodes that work simultaneously as a current collector and electroactive material is pivotal to integrating portable and wearable chemical sensors. Herein, we have synthesized graphene/Prussian blue (PB) electrodes for hydrogen peroxide detection (H2O2) using a two-step method. First, an reduced graphene oxide/PAni/Fe2O3 freestanding film is prepared using a doctor blade technique, followed by the electrochemical deposition of PB nanoparticles over the films. The iron oxide nanoparticles work as the iron source for the heterogeneous electrochemical deposition of the nanoparticles in a ferricyanide solution. The size of the PB cubes electrodeposited over the graphene-based electrodes was controlled by the number of voltammetric cycles. For H2O2 sensing, the PB10 electrode achieved the lowest detection and quantification limits, 2.00 and 7.00 μM, respectively. The findings herein evidence the balance between the structure of the graphene/PB-based electrodes with the electrochemical performance for H2O2 detection and pave the path for developing new freestanding electrodes for chemical sensors.

Assessment of the Applicability of a Constant-Head Borehole Permeameter Test to River Levees

Abstract The Guelph Permeameter (GP) test, one of the constant-head borehole permeameter tests, is a potential tool for studying the heterogeneous alluvial deposits in the foundation of river levees. However, the applicability in the targeted environment and adequacy of the information obtained by the tests are still unclear. Experiments are conducted in a model ground and in the field to verify the applicability of the GP test concerning underseepage through river levees. Discussions focus on the effects of the groundwater table, seepage behavior during the test, and the representative volume of soil tested. It is noted that for sandy and silty soils, reasonable estimations of the hydraulic conductivity can be made by applying the Reynolds’ solution, but the estimation of the hydraulic conductivity in clayey soil is affected by the macropores in the soil. The GP tests performed in this study have representative volumes on the order of a few to tens of centimeters so that heterogeneity can be investigated at the meter scale. In summary, the GP test is a useful tool for evaluating the underseepage through river levees.

In-situ fabrication of martensitic stainless steel via heterogeneous double-wire arc-directed energy deposition

ABSTRACT In recent years, there has been a growing focus on additive manufacturing of martensitic stainless steel with exceptional performance. This study introduces a new pathway to fabricate martensitic stainless steel through heterogeneous double-wire arc-directed energy deposition (DED). ER316L and ER70-G are used as raw materials, melting together and forming a common molten pool. A steel block with a chemical composition of Fe-11.38Cr-7.52Ni-1.44Mo-1.54Mn-0.497Si (wt.%) is successfully manufactured. The microstructure, mechanical properties and corrosion resistance of the martensitic stainless steel are investigated. The results indicate that the microstructure of the steel consists of martensite and austenite, achieving satisfactory microhardness (381.38 ± 11.94 HV), tensile strength (1172.1 ± 25.7 MPa), ductility (11.3 ± 1.3%), toughness (146.3 ± 8.0 J) and corrosion resistance (0.865 μA/cm2). This work demonstrates great potential of fabricating martensitic stainless steel using heterogeneous double-wire arc DED, providing a new choice to manufacture martensitic stainless steel and potentially other alloys.

Organic nano carbon source inducing 3D silica nanoparticles-graphene nanosheet layer on Cu current collector for high-performance anode-free lithium metal batteries

Anode-free lithium metal batteries (AFLBs) have attracted considerable attention due to their high theoretical specific capacity and absence of Li. However, the heterogeneous Li deposition and stripping on the lithiophobic Cu collector hamper AFLBs in practice. To achieve a uniform and reversible Li deposition, a carbon-based layer on the Cu collector has attracted intense interest due to its high conductivity. However, the 2D single-component carbon-based interface is inadequate lithiophilic for obtaining the homogeneous Li deposition and preventing the lithium dendrite from piercing the separator. Herein, we present a 3D embedded lithiophilic SiO2 nanoparticles-graphene nanosheet matrix (SiO2@G-M) on the Cu collector by organic nano carbon source. In this structure, the lithiophilic SiO2 nanoparticles as active points promote the homogeneous lithium nucleation and the 3D graphene nanosheet matrix offers homogenous electron distribution and voids to prevent the piercing. Finally, SiO2@G-M/Li cell shows a high coulombic efficiency of 98.62 % after 100 cycles at a high current density of 2 mA cm−2 with an areal capacity of 1 mAh cm−2.

High-Power and Large-Area Anodes for Safe Lithium-Metal Batteries.

The lithium deposited via the complex electrochemical heterogeneous lithium deposition reaction (LDR) process on a lithium foil-based anode (LFA) forms a high-aspect-ratio shape whenever the reaction kinetics reach its limit, threatening battery safety. Thereby, a research strategy that boosts the LDR kinetics is needed to construct a high-power and safe lithium metal anode. In this study, the kinetic limitations of the LDR process on LFA are elucidated through operando and ex situ observations using in-depth electrochemical analyses. In addition, ultra-thin (≈0.5µm) and high modulus (≥19GPa) double-walled carbon nanotube (DWNT) membranes with different surface properties are designed to catalyze high-safety LDRs. The oxygen-functionalized DWNT membranes introduced on the LFA top surface simultaneously induce multitudinous lithium nuclei, leading to film-like lithium deposition even at a high current density of 20mAcm-2. More importantly, the layer-by-layer assembly of the oxygen-functionalized and pristine DWNT membranes results in different surface energies between the top and bottom surfaces, enabling selective surface LDRs underneath the high-modulus bilayer membranes. The protective LDR on the bilayer-covered LFA guarantees an invulnerable cycling process in large-area pouch cells at high current densities for more than 1000 cycles, demonstrating the practicability of LFA in a conventional liquid electrolyte system.

Dual-functional Separators Regulating Ion Transport Enabled by 3D-Reinforced Polyimide Microspheres Protective Layer for Dendrite-Free and High-Temperature Lithium Metal Batteries.

High-energy-density lithium metal batteries (LMBs) are confronted with crucial concerns of security and a short cycle lifespan caused by the uncontrollable formation of lithium (Li) dendrites. The poor thermal stability and heterogeneous Li deposition of conventional polyolefin separators often cause battery short circuiting and thermal runaway in LMBs. Herein, a novel dual-functional PE composite separator (PI-COOH/PE) coated by carboxyl polyimide (PI) microspheres is fabricated by an etching-acidification method. The three-dimensional (3D) high-temp PI microsphere with rich carboxyl groups on the surface improve the security of LMBs at extremely high temperatures and facilitate the formation of a stable and uniform SEI layer, which contributes to accelerating the Li+ transport and stabilizing the formation of the SEI layer. Consequently, the Li symmetric cell assembled with the (PI-COOH)/PE separator exhibits stable overpotential over 3000 h, and the corresponding Li//NCM811 full cells also show a high-level discharge capacity of 146.6 mAh g-1 at 5 C. Meanwhile, it also demonstrates outstanding cycling stability and thermal safety, which can survive continuously over 160 min at 140 °C (vs 21 min for PE). The above results indicate the (PI-COOH)/PE separator constructed by a low-cost and industrial-friendly strategy simultaneously addresses high-temperature stability and dendrite resistance.

Poly(vinylidene fluoride)-based composite membranes with continuous metal–organic framework layer for high-performance separators of lithium-ion batteries

Lithium-ion batteries (LIBs) play a critical role in modern portable electronic devices, electric vehicles, and wearable electronics. However, the formation of lithium dendrites during cycling results in serious capacity loss and safety risks owing to the heterogeneous transport and deposition of Li+. In this work, we present a poly(vinylidene fluoride) (PVDF)-based composite membrane with a continuous metal–organic framework (MOF) layer as high-performance separators in LIBs. The PVDF membranes with uniform pore structures are prepared by using superspreading strategy, facilitating the growth of continuous and controllable MOF layer inside the membranes via a simple interfacial synthesis. The as prepared PVDF-MOF composite membranes display uniform and continuous subnanochannels with connected opened metal sites (OMS), which can generate a homogeneous transport of Li+. Taking advantages of the low impedance (∼2 Ω), high ionic conductivity (0.61 mS cm−1), and high stripping peak current (0.89 mA cm−2), the PVDF-MOF composite separators efficiently prevent the uneven deposition and the generation of lithium dendrites. Moreover, the PVDF-MOF-based LIBs showed a high capacity retention rate of 81.0 % after 250 cycles. This strategy paves a new avenue for MOF-based composite separator in LIBs.

Efficacy of topical gabapentin in women with primary macular amyloidosis: A side-by-side triple-blinded randomized clinical trial.

Primary cutaneous macular amyloidosis (PCMA) is a chronic pruritic cutaneous disease characterized by heterogeneous extracellular deposition of amyloid protein in the skin. This study aimed to evaluate the efficacy of topical 6% gabapentin cream for the treatment of patients with PCMA. In this triple-blind clinical trial, a total of 34 patients, who were diagnosed with PCMA, treated using two different strategies of topical gabapentin as the active group and vehicle cream as the control group. Pruritus score reduction in both groups was statistically significant compared with the baseline value (p < 0.001). There was a significant pigmentation score reduction in intervention group compared with control group after 1 month of the study (p < 0.001). The differences of pigmentation score changes between the groups were not significant at month 2 (p = 0.52) and month 3 (p = 0.22). The results of this study suggest that topical gabapentin cream may be effective as a topical agent in the treatment of pruritus associated with PCMA without any significant adverse effects. It is recommended to perform similar studies with a larger sample size and longer duration in both sexes.

CHEMICAL REMOVAL OF IRON SULFIDE DEPOSIT IN PIPES FROM OIL AND SOUR GAS PRODUCTION

Hydrogen sulfide (H2S) and carbon dioxide (CO2) present in oil and natural gas cause mild steel corrosion, potentially resulting in formation of corrosion product layers on the internal surfaces of tubulars. In field experiences relating to the research reported herein, this has led to restrictions on the flow of water produced from a three-phase horizontal separator. This paper demonstrates a specific case of chemical removal of relatively hard, dark, and adherent heterogeneous deposits on the internal surface of the pipe. The phases involved in this process are iron sulfide, iron oxides and calcium carbonate existing as scales/corrosion products. To evaluate their dissolution, laboratory tests were conducted using hydrochloric acid (HCl) with additions of chlorine in the form of calcium hypochlorite [Ca(ClO)2]. Appropriate safety measures were taken employed, considering hazards associated with chlorine and toxicity of hydrogen sulfide. The treatment regime had 87 % effectiveness for scale removal in combination with propargyl alcohol (2-propyn-1-ol) as a corrosion inhibitor.

Using a cyclocarbon additive as a cyclone separator to achieve fast lithiation and delithiation without dendrite growth in lithium-ion batteries.

Carbon materials are widely used for reversible lithium uptake in the anode of lithium-ion batteries. Nevertheless, the challenge of uncontrollable dendrite deposition during fast charge-discharge cycles remains a grand hurdle. Various strategies have been explored to prevent detrimental heterogeneous dendrite metal deposits, such as interface engineering and electrolyte modification, but they often compromise the reverse diffusion freedom of Li+ ions during discharging and are incompatible with the most mainstream use of graphite as an anode material. Here, we propose the incorporation of a novel carbon allotrope of cyclocarbon as a potential additive in the anode. In contrast to conventional carbon materials, density functional theory calculations reveal that cyclocarbon has a much higher affinity for Li atoms than Li+ ions, even surpassing the inherent cohesion of Li atoms, due to the charge transfer from the 2s orbital of Li atoms to the unique in-plane π orbital of cyclocarbon. Furthermore, ab initio molecular dynamics simulations show that Li+ ions can shuttle freely back and forth across cyclocarbon, whereas the lithiation process for Li atoms occurs rapidly within picoseconds. The delithiation of Li atoms within cyclocarbon follows a voltage-gated mechanism that is effectively controlled by an external electric field of 3 V nm-1. Remarkably, cyclocarbon exhibits potential compatibility with commercialized graphite electrodes via the π-π interaction and also can be extended to sodium-ion and potassium-ion batteries. These distinct compatibility, scalability and electrochemical properties of cyclocarbon provide a new avenue to realize both safety and ultrafast rechargeable performance of ion batteries.