Recent advances in rational design for high-performance potassium-ion batteries.

The growing global energy demand necessitates the development of renewable energy solutions to mitigate greenhouse gas emissions and air pollution. To efficiently utilize renewable yet intermittent energy sources such as solar and wind power, there is a critical need for large-scale energy storage systems (EES) with high electrochemical performance. While lithium-ion batteries (LIBs) have been successfully used for EES, the surging demand and price, coupled with limited supply of crucial metals like lithium and cobalt, raised concerns about future sustainability. In this context, potassium-ion batteries (PIBs) have emerged as promising alternatives to commercial LIBs. Leveraging the low cost of potassium resources, abundant natural reserves, and the similar chemical properties of lithium and potassium, PIBs exhibit excellent potassium ion transport kinetics in electrolytes. This review starts from the fundamental principles and structural regulation of PIBs, offering a comprehensive overview of their current research status. It covers cathode materials, anode materials, electrolytes, binders, and separators, combining insights from full battery performance, degradation mechanisms, in situ/ex situ characterization, and theoretical calculations. We anticipate that this review will inspire greater interest in the development of high-efficiency PIBs and pave the way for their future commercial applications.

Hydroxyl-Decorated Carbon Cloth with High Potassium Affinity Enables Stable Potassium Metal Anodes.

Highly anticipated potassium metal batteries possess abundant potassium reserves and high theoretical capacity but currently suffer from poor cycling stability as a result of dendritic growth and volume expansion. Here, carbon cloths modified with different functional groups treated with ethylene glycol, ethanolamine, and ethylenediamine are designed as 3D hosts, exhibiting different wettability to molten potassium. Among them, the hydroxyl-decorated carbon cloth with a high affinity for potassium can achieve molten potassium perfusion (K@EG-CC) within 3 s. By efficiently inducing the uniform deposition of metal potassium, buffing its volume expansion, and lowering local current density, the developed K@EG-CC anode alleviates the dendrite growth issue. The K@EG-CC||K@EG-CC symmetric battery can be cycled stably for 2100 h and has only a small voltage hysteresis of ≈93 mV at 0.5 mA cm-2 . Moreover, the high-voltage plateau, high energy density, and long cycle life of K metal full batteries can be realized with a low-cost KFeSO4 F@carbon nanotube cathode. This study provides a simple strategy to promote the commercial applications of potassium metal batteries.

KI-Assisted Formation of Spindle-like Prussian White Nanoparticles for High-Performance Potassium-Ion Battery Cathodes.

Prussian white (PW) is considered as a promising cathode material for potassium-ion batteries (KIBs) due to its low cost and high theoretical capacity. However, the high water content and structural defects and the strict synthesis conditions of PW lead to its unsatisfactory cycling performance and low specific capacity, hindering its practical applications. Herein, a template-engaged reduction method is proposed, using MIL-88B(Fe) as a self-template and KI as the reducing agent to prepare K-rich PW with low defects and water content. Furthermore, the hierarchical porous spindle-like morphology can be inherited from the precursor, furnishing sufficient active sites and reducing the ion diffusion path. Consequently, when applied as a KIB cathode material, spindle-like PW (K1.72Fe[Fe(CN)6]0.96·0.342H2O) manifested remarkable potassium storage properties. Notably, a full cell assembled by the spindle-like PW cathode and graphite anode exhibited a large energy density of ∼216.7 Wh kg-1, demonstrating its huge potential for energy storage systems.

Ultrathin Cobalt-Based Prussian Blue Analogue Nanosheet-Assembled Nanoboxes Interpenetrated with Carbon Nanotubes as a Fast Electron/Potassium-Ion Conductor for Superior Potassium Storage.

Rechargeable potassium-ion batteries (PIBs) are regarded as potential substitutes for industrial lithium-ion batteries in large scale energy storage systems due to the world's abundant potassium supplies. Althogh cobalt hexacyanocobaltate (CoHCC) exhibits broad potential as a PIB anode material, its performance is currently unsatisfactory. Herein, novel 5 nm scale ultrathin CoHCC nanosheet-assembled nanoboxes with interspersed carbon nanotubes (CNTs/CoHCC nanoboxes) are fabricated to realize a highly reactive PIB anode. The ultrathin CoHCC layers substantially accelerate electron conduction and provide numerous active sites, while the connected CNTs provide fast axial electron transport. Consequently, the optimized anode exhibits a remarkable discharge capacity of 580.9 mAh g-1 at 0.1 A g-1 and long-term stability with 71.3% retention over 1000 cycles. In situ and ex situ characterizations and density functional theory calculations are further employed to elucidate the K+ storage process and the reason for the enhanced performance of the CNTs/CoHCC nanoboxes.

Uniform P2-K0.6CoO2 Microcubes as a High-Energy Cathode Material for Potassium-Ion Batteries.

Layered transition-metal (TM) oxides have drawn ever-growing interest as positive electrode materials in potassium-ion batteries (PIBs). Nevertheless, the practical implementation of these positive electrode materials is seriously hampered by their inferior cyclic property and rate performance. Reported here is a self-templating strategy to prepare homogeneous P2-K0.6CoO2 (KCO) microcubes. Benefiting from the unusual microcube architecture, the interface between the electrolyte and the active material is considerably diminished. As a result, the KCO microcubes manifest boosted electrochemical properties for potassium storage including large reversible capacity (87.2 mAh g-1 under 20 mA g-1), superior rate performance, and ultralong cyclic steady (an improved capacity retention of 86.9% under 40 mA g-1 after 1000 cycles). More importantly, the fabrication approach can be effectively extended to prepare other layered TM oxide (P3-K0.5MnO2, P3-K0.5Mn0.8Fe0.2O2, P2-K0.6Co0.67Mn0.33O2, and P2-K0.6Co0.66Mn0.17Ni0.17O2) microcubes and nonlayered TM oxide (KFeO2) microcubes.

Recent Progress in Using Covalent Organic Frameworks to Stabilize Metal Anodes for Highly-Efficient Rechargeable Batteries.

Alkali metals (e.g. Li, Na, and K) and multivalent metals (e.g. Zn, Mg, Ca, and Al) have become star anodes for developing high-energy-density rechargeable batteries due to their high theoretical capacity and excellent conductivity. However, the inevitable dendrites and unstable interfaces of metal anodes pose challenges to the safety and stability of batteries. To address these issues, covalent organic frameworks (COFs), as emerging materials, have been widely investigated due to their regular porous structure, flexible molecular design, and high specific surface area. In this minireview, we summarize the research progress of COFs in stabilizing metal anodes. First, we present the research origins of metal anodes and delve into their advantages and challenges as anodes based on the physical/chemical properties of alkali and multivalent metals. Then, special attention has been paid to the application of COFs in the host design of metal anodes, artificial solid electrolyte interfaces, electrolyte additives, solid-state electrolytes, and separator modifications. Finally, a new perspective is provided for the research of metal anodes from the molecular design, pore modulation, and synthesis of COFs.

Tunable Interfacial Electric Field-Mediated Cobalt-Doped FeSe/Fe3Se4 Heterostructure for High-Efficiency Potassium Storage.

The interfacial electric field (IEF) in the heterostructure can accelerate electron transport and ion migration, thereby enhancing the electrochemical performance of potassium-ion batteries (PIBs). Nevertheless, the quantification and modulation of the IEF for high-efficiency PIB anodes currently remains a blank slate. Herein, we achieve for the first time the quantification and tuning of IEF via amorphous carbon-coated undifferentiated cobalt-doped FeSe/Fe3Se4 heterostructure (denoted UN-CoFe4Se5/C) for efficient potassium storage. Co doping can increase the IEF in FeSe/Fe3Se4, thereby improving the electron transport, promoting the potassium adsorption capacity, and lowering the diffusion barrier. As expected, the IEF magnitude in UN-CoFe4Se5/C is experimentally quantified as 62.84 mV, which is 3.65 times larger than that of amorphous carbon-coated FeSe/Fe3Se4 heterostructure (Fe4Se5/C). Benefiting from the strong IEF, UN-CoFe4Se5/C as a PIB anode exhibits superior rate capability (145.8 mAh g-1 at 10.0 A g-1) and long cycle lifespan (capacity retention of 95.1 % over 3000 cycles at 1.0 A g-1). Furthermore, this undifferentiated doping strategy can universally regulate the IEF magnitude in CoSe2/Co9Se8 and FeS2/Fe7S8 heterostructures. This work can provide fundamental insights into the design of advanced PIB electrodes.

Heat-Resistant Carbon-Coated Potassium Magnesium Hexacyanoferrate Nanoplates for High-Performance Potassium-Ion Batteries.

Metal hexacyanoferrates (HCFs) are regarded as promising cathode materials for potassium-ion batteries (PIBs) on account of their low cost and high energy density. However, the difficult-to-remove [Fe(CN)6] vacancies and crystal water lead to structural instability and capacity deterioration as well as the stereotype of poor thermostability of conventional HCFs. Herein, we report (100) face-oriented potassium magnesium hexacyanoferrate (KMgHCF) nanoplates with low [Fe(CN)6] vacancies and high crystallinity, enabling thermostability up to 550 °C, high-temperature carbon coating and crystal water elimination. The as-obtained KMgHCF/C nanoplates exhibit superior potassium storage properties, including a large reversible capacity of 84.6 mAh g-1, a high voltage plateau of 3.87 V, excellent long-term cycling performance over 15000 cycles and high rate capability at 5 A g-1. The unprecedented cycling stability of KMgHCF/C is attributed to the synergistic effect of a highly reversible two-phase reaction, low [Fe(CN)6] vacancies and no crystal water, a specially exposed steady (100) surface, and a protective carbon coating. This work provides a new material selection and modification strategy for the practical application of HCFs in PIBs.

A P2/P3 Biphasic Layered Oxide Composite as a High-Energy and Long-Cycle-Life Cathode for Potassium-Ion Batteries.

Layered transition metal oxides are extensively considered as appealing cathode candidates for potassium-ion batteries (PIBs) due to their abundant raw materials and low cost, but their further implementations are limited by slow dynamics and impoverished structural stability. Herein, a layered composite having a P2 and P3 symbiotic structure is designed and synthesized to realize PIBs with large energy density and long-term cycling stability. The unique intergrowth of P2 and P3 phases in the obtained layered oxide is plainly characterized by X-ray diffraction refinement, high-angle annular dark field and annular bright field-scanning transmission electron microscopy at atomic resolution, and Fourier transformation images. The synergistic effect of the two phases of this layered P2/P3 composite is well demonstrated in K+ intercalation/extraction process. The as-prepared layered composite can present a large discharge capacity with the remarkable energy density of 321 Wh kg-1 and also manifest excellent capacity preservation after 600 cycles of K+ uptake/removal.

Implanting CuS Quantum Dots into Carbon Nanorods for Efficient Magnesium-Ion Batteries.

Magnesium-ion batteries (MIBs) are emerging as potential next-generation energy storage systems due to high security and high theoretical energy density. Nevertheless, the development of MIBs is limited by the lack of cathode materials with high specific capacity and cyclic stability. Currently, transition metal sulfides are considered as a promising class of cathode materials for advanced MIBs. Herein, a template-based strategy is proposed to successfully fabricate metal-organic framework-derived in-situ porous carbon nanorod-encapsulated CuS quantum dots (CuS-QD@C nanorods) via a two-step method of sulfurization and cation exchange. CuS quantum dots have abundant electrochemically active sites, which facilitate the contact between the electrode and the electrolyte. In addition, the tight combination of CuS quantum dots and porous carbon nanorods increases the electronic conductivity while accelerating the transport speed of ions and electrons. With these architectural and compositional advantages, when used as a cathode material for MIBs, the CuS-QD@C nanorods exhibit remarkable performance in magnesium storage, including a high reversible capacity of 323.7 mAh g-1 at 100 mA g-1 after 100 cycles, excellent long-term cycling stability (98.5 mAh g-1 after 1000 cycles at 1.0 A g-1 ), and satisfying rate performance (111.8 mA g-1 at 1.0 A g-1 ).

Synthesis of KVPO4F/Carbon Porous Single Crystalline Nanoplates for High-Rate Potassium-Ion Batteries.

With high theoretical capacity and operating voltage, KVPO4F is a potential high energy density cathode material for potassium-ion batteries. However, its performance is usually limited by F loss, poor electronic conductivity, and unsteady electrode/electrolyte interface. Herein, a simple one-step sintering process is developed, where vanadium-oxalate-phosphite/phosphate frameworks and fluorinated polymer are used to synthesize carbon-coated KVPO4F nanoplates. It is found that the V-F-C bond generated by fluorinated-polymer-derived carbon at the interface of KVPO4F/C nanoplates diminishes the F loss, as well as enhances K-ions migration ability and the electronic conductivity of KVPO4F. The as-synthesized KVPO4F/C cathode delivers a reversible capacity of 106.5 mAh g-1 at 0.2 C, a high working voltage of 4.28 V, and a rate capability with capacity of 73.8 mAh g-1 at the ultrahigh current density of 100 C. In addition, a KVPO4F/C//soft carbon full cell exhibits a high energy density of 235.5 Wh kg-1.

Layered Oxide Cathodes Promoted by Crystal Regulation Strategies for Potassium-Ion Batteries.

Layered oxide cathodes have demonstrated great potential for potassium-ion batteries (PIBs) on account of high reversible capacity, appropriate diffusion paths, and low cost. However, their electrochemical performance in PIBs is generally worse than that in lithium-ion batteries due to large structural changes and deformations during charging and discharging. To improve their potassium storage performance, a series of strategies have been developed in recent studies. In this review, we summarize the latest advancements in layered oxide cathodes for PIBs through different crystal regulation strategies, including transition metal layer doping, potassium content optimization, oxygen partial substitution, functional morphology construction and air stability improvement. Meanwhile, the relationship between the electrochemical properties and structural evolution of these modified cathodes is also investigated. In addition, the challenges and prospects of these layered oxide cathodes in PIBs are analyzed in detail, providing constructive insights for future applications of PIBs.

Design and Experimental Study of a Tetragonal Rotor Pump Based on Wankel Geometry.

Wankel pump designs have not been fully established, with existing designs limited to bicornous rotor pumps and triangular rotor pumps. Here, on the basis of Wankel geometry, we present a tetragonal rotor pump with a three-lobe epicycloid and its conjugate envelope as chamber and rotor profile. First, the design method and basic working principle of the pump are introduced. Four groups of prototypes with different shape factors were manufactured, and their flow and pressure characteristics were experimentally studied. Numerical study showed that the flow rate irregularity of the pump is lower than that of existing Wankel pumps. Finally, the feasibility the pump for mixing applications was verified by a flow field observation experiment. The work in this paper provides a new type of rotary displacement pump design, representing an study of reverse application of a Wankel engine structure.

Research on the Machinability of Micro-Tapered Hole Group in Piezoelectric Atomizer and the Improvement Method.

A metal atomizing sheet with a group of micro-tapered holes is the core constituent of a piezoelectric atomizer. However, the diameters of large-end and small-end micro-tapered holes in industrial applications deviate from the design values by 15.25% and 15.83%, respectively, which adversely impacts the effect of atomizers. In this study, two main factors that influence the machining quality of tapered holes, the external vibration disturbance and the internal system errors inside the laser processor, were explored; consequently, the vibration model of the machining device and the laser drilling model were established, respectively. Based on the models and the experimental results, it was found that the errors in diameter caused by these two factors accounted for 20% and 67.87% of the total deviation, respectively. Finally, an improved method was proposed, where a damping system was added to the machining device, and the diameter of the initial laser spot was corrected. The measurement results of tapered holes machined by the improved method showed that the deviation of the large diameters and the small diameters from the design values declined to 4.85% and 4.83%, respectively. This study lays a foundation for the high-precision and large-scale industry of atomizing sheets, and provides a new research direction for enhancing the performance of atomizers.

A Low-Strain Phosphate Cathode for High-Rate and Ultralong Cycle-Life Potassium-Ion Batteries.

Most potassium-ion battery (PIB) cathode materials have deficient structural stability because of the huge radius of potassium ion, leading to inferior cycling performance. We report the controllable synthesis of a novel low-strain phosphate material K3 (VO)(HV2 O3 )(PO4 )2 (HPO4 ) (denoted KVP) nanorulers as an efficient cathode for PIBs. The as-synthesized KVP nanoruler cathode exhibits an initial reversible capacity of 80.6 mAh g-1 under 20 mA g-1 , with a large average working potential of 4.11 V. It also manifests an excellent rate property of 54.4 mAh g-1 under 5 A g-1 , with a high capacity preservation of 92.1 % over 2500 cycles. The outstanding potassium storage capability of KVP nanoruler cathode originates from a low-strain K+ uptake/removal mechanism, inherent semiconductor characteristic, and small K+ migration energy barrier. The high energy density and prolonged cyclic stability of KVP nanorulers//polyaniline-intercalated layered titanate full battery verifies the superiority of KVP nanoruler cathode in PIBs.

A numerical investigation on the unidirectional unsteady oscillatory wind flow over a fixed isolated downsized barchan dune.

Turbulent wind patterns over a two-dimensional isolated downsized barchan dune under the influence of sinusoidal inflow with different amplitudes and periods are simulated. The evolution rules of wind velocity over time at different positions are revealed. The flow reattachment distance and turbulence intensity distribution are also compared. The results show that wind velocities at different positions of the dune whose similar evolvement process of going from short-term fast adjustment transition to long-term stable sinusoidal fluctuation, can be reasonably estimated by the present simulation. It is found that, for the leeward toe of a dune with complex reversed flow, the balance position value of the sinusoidal wind velocity fluctuation is no longer close to the value of the steady wind velocity but shows a velocity deviation of about 0.40m/s. The flow reattachment distances under different unsteady inflows ultimately show a sinusoidal fluctuation with time, and their values are all larger than that of the steady flow. These synthetically predict that the unsteady flow has a stronger shaping effect on the leeward side of the dune body by enhancing sand transport. In addition, the predicted distribution comparison between unsteady wind velocity and turbulence intensity indicates that the unsteady wind velocity has a dominant effect on the turbulence intensity.

Calcium Signaling Is Suppressed in Magnaporthe oryzae Conidia by Bacillus cereus HS24.

Rice yield is greatly reduced owing to rice blast, a polycyclic fungal disease caused by the ascomycete Magnaporthe oryzae. Previously, Bacillus cereus HS24, isolated from a rice farm, showed a strong antimicrobial effect toward M. oryzae. To better exploit it as a biocontrol agent, HS24 was studied for the mechanism that it uses to suppress rice blast. Conidium germination in M. oryzae was significantly inhibited by HS24, whereby inhibition reached 97.8% at the concentration of 107 CFU/ml. The transcription levels of Ca2+/calmodulin-dependent protein kinase II, PMC1, and CCH1, key genes involved in the M. oryzae Ca2+ signaling pathway, were significantly decreased in HS24-treated conidia at high concentration. The treatment of M. oryzae with the corresponding Ca2+ signaling pathway inhibitors KN-93, verapamil, and cyclopiazonic acid significantly reduced conidium germination. This inhibitory effect was found to be concentration dependent, similar to the HS24 treatment. We also found that HS24 was able to decrease the intracellular free Ca2+ concentration in M. oryzae conidia significantly. The addition of exogenous Ca2+ did not diminish the inhibitory effect of HS24 on the reduction of intracellular free Ca2+ concentration and the level of conidium germination. In conclusion, B. cereus HS24 at high concentration prevents extracellular Ca2+ from entering the conidia in M. oryzae, causes a significant reduction of intracellular free Ca2+ concentration, and results in the inhibition of conidium germination.

The application of exogenous PopW increases the tolerance of Solanum lycopersicum L. to drought stress through multiple mechanisms.

Tomato is a major cultivated vegetable species of great economic importance throughout the world, but its fruit yield is severely impaired by drought stress. PopW, a harpin protein from Ralstonia solanacearum ZJ3721, plays vital roles in various plant defence responses and growth. In this study, we observed that the foliar application of PopW increased tomato drought tolerance. Our results showed that compared with water-treated plants, PopW-treated plants presented a significantly higher recovery rate and leaf relative water content under drought-stress conditions. PopW decreased the malondialdehyde content and relative electrical conductivity by 40.2% and 21%, respectively. Drought disrupts redox homeostasis through the excessive accumulation of reactive oxygen species (ROS). PopW-treated plants displayed an obvious reduction in ROS accumulation due to enhanced activities of the antioxidant enzyme catalase, superoxide dismutase and peroxidase. Moreover, PopW promoted early stomatal closure, thereby minimizing the water loss rate of plants under drought stress. Further investigation revealed that endogenous abscisic acid (ABA) levels and the transcript levels of drought-responsive genes involved in ABA signal transduction pathways increased in response to PopW. These results confirm that PopW increases drought tolerance through multiple mechanisms involving an enhanced water-retention capacity, balanced redox homeostasis, increased osmotic adjustment, reduced membrane damage and decreased stomatal aperture, suggesting that the application of exogenous PopW may be a potential method to enhance tomato drought tolerance.

A Yolk-Shell-Structured FePO4 Cathode for High-Rate and Long-Cycling Sodium-Ion Batteries.

Amorphous iron phosphate (FePO4 ) has attracted enormous attention as a promising cathode material for sodium-ion batteries (SIBs) because of its high theoretical specific capacity and superior electrochemical reversibility. Nevertheless, the low rate performance and rapid capacity decline seriously hamper its implementation in SIBs. Herein, we demonstrate a sagacious multi-step templating approach to skillfully craft amorphous FePO4 yolk-shell nanospheres with mesoporous nanoyolks supported inside the robust porous outer nanoshells. Their unique architecture and large surface area enable these amorphous FePO4 yolk-shell nanospheres to manifest remarkable sodium storage properties with high reversible capacity, outstanding rate performance, and ultralong cycle life.

Enabling Superior Electrochemical Properties for Highly Efficient Potassium Storage by Impregnating Ultrafine Sb Nanocrystals within Nanochannel-Containing Carbon Nanofibers.

Sb-based nanocomposites are attractive anode materials for batteries as they exhibit large theoretical capacity and impressive working voltage. However, tardy potassium ion diffusion characteristics, unstable Sb/electrolyte interphase, and huge volume variation pose a challenge, hindering their practical use for potassium-ion batteries (PIBs). Now, a simple robust strategy is presented for uniformly impregnating ultrasmall Sb nanocrystals within carbon nanofibers containing an array of hollow nanochannels (denoted u-Sb@CNFs), resolving the issues above and yielding high-performance PIBs. u-Sb@CNFs can be directly employed as an anode, thereby dispensing with the need for conductive additives and binders. Such a judiciously crafted u-Sb@CNF-based anode renders a set of intriguing electrochemical properties, representing large charge capacity, unprecedented cycling stability, and outstanding rate performance. A reversible capacity of 225 mAh g-1 is retained after 2000 cycles at 1 A g-1 .