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Advanced high-energy-density sodium-ion batteries (SIBs) are inseparable from cathode materials with high specific capacities. Layered manganese-rich oxides (Na x MnO 2 , 0.6 ≤ x ≤1) are promising cathode materials owing to their ease of intercalation and extraction of a considerable amount of sodium ions. However, lattice interactions, especially electrostatic repulsive forces and anisotropic stresses, are usually caused by deep desodiatin/sodiation process, resulting in intragranular cracks and capacity degradation in SIBs. Here, boron ions are introduced into the layered structure to build up B─O─Mn bonds. The regulated electronic structure in Na 0.637 B 0.038 MnO 2 (B-NMO) materials inhibits the deformation of MnO 6 octahedra, which finally achieves a gentle structural transition during the deep sodiation process. B-NMO electrode exhibits a high capacity (141 mAh g -1 ) at 1 C with a capacity retention of 81% after 100 cycles. Therefore, anchoring boron to manganese-rich materials inhibits the detrimental structural evolution of deep sodiation and can be used to obtain excellent cathode materials for SIBs., (© 2023 Wiley‐VCH GmbH.)

The deployment of lithium metal anode in solid-state batteries with polymer electrolytes has been recognized as a promising approach to achieving high-energy-density technologies. However, the practical application of the polymer electrolytes is currently constrained by various challenges, including low ionic conductivity, inadequate electrochemical window, and poor interface stability. To address these issues, a novel eutectic-based polymer electrolyte consisting of succinonitrile (SN) and poly (ethylene glycol) methyl ether acrylate (PEGMEA) is developed. The research results demonstrate that the interactions between SN and PEGMEA promote the dissociation of the lithium difluoro(oxalato) borate (LiDFOB) salt and increase the concentration of free Li + . The well-designed eutectic-based PAN 1.2 -SPE (PEGMEA: SN=1: 1.2 mass ratio) exhibits high ionic conductivity of 1.30 mS cm -1 at 30 °C and superior interface stability with Li anode. The Li/Li symmetric cell based on PAN 1.2 -SPE enables long-term plating/stripping at 0.3 and 0.5 mA cm -2 , and the Li/LiFePO 4 cell achieves superior long-term cycling stability (capacity retention of 80.3 % after 1500 cycles). Moreover, Li/LiFePO 4 and Li/LiNi 0.6 Co 0.2 Mn 0.2 O 2 pouch cells employing PAN 1.2 -SPE demonstrate excellent cycling and safety characteristics. This study presents a new pathway for designing high-performance polymer electrolytes and promotes the practical application of high-stable lithium metal batteries., (© 2023 Wiley-VCH GmbH.)

Due to the scarce of lithium resources, potassium-ion batteries (PIBs) have attracted extensive attention due to their similar electrochemical properties to lithium-ion batteries (LIBs) and more abundant potassium resources. Even though there is considerable progress in SbBi alloy anode for LIBs and PIBs, most studies are focused on the morphology/structure tuning, while the inherent physical features of alloy composition's effect on the electrochemical performance are rarely investigated. Herein, combined the nanonization, carbon compounding, and alloying with composition regulation, the anode of nitrogen-doped carbon-coated Sb x Bi 1-x (Sb x Bi 1-x @NC) with a series of tuned chemical compositions is designed as an ideal model. The density functional theory (DFT) calculation and experimental investigation results show that the K + diffusion barrier is lower and the path is easier to carry out when element Bi dominates the potassiation reaction, which is also the reason for better circulation. The optimized Sb 0.25 Bi 0.75 @NC shows an excellent cycling performance with a reversible specific capacity of 301.9 mA h g -1 after 500 cycles at 0.1 A g -1 . Meanwhile, the charge-discharge mechanism is intuitively invetigated and analyzed by in situ X-ray diffraction (XRD) and transmission electron microscopy (TEM) in detail. Such an alloy-type anode synthesis approach and in situ observation method provide an adjustable strategy for the designing and investigating of PIB anodes., (© 2023 Wiley-VCH GmbH.)

Secondary batteries have been widespread in the daily life causing an ever-growing demand for long-cycle lifespan and high-energy alkali-ion batteries. As an essential constituent part, electrode materials with superior electrochemical properties play a vital role in the battery systems. Here, an outstanding electrode of yolk-shell ZnS@C nanorods is developed, introducing considerable void space via a self-sacrificial template method. Such carbon encapsulated nanorods moderate integral electronic conductivity, thus ensuring rapid alkali-ions/electrons transporting. Furthermore, the porous structure of these nanorods endows enough void space to mitigate volume stress caused by the insertion/extraction of alkali-ions. Due to the unique structure, these yolk-shell ZnS@C nanorods achieve superior rate performance and cycling performance (740 mAh g -1 at 1.0 A g -1 after 540 cycles) for lithium-ion batteries. As a potassium-ion batteries anode, they achieve an ultra-long lifespan delivering 211.1 mAh g -1 at 1.0 A g -1 after 5700 cycles. The kinetic analysis reveals that these ZnS@C nanorods with considerable pseudocapacitive contribution benefit the fast lithiation/delithiation. Detailed transmission electron microscopy (TEM) and X-ray diffraction (XRD) analyses indicate that such yolk-shell ZnS@C anode is a typical reversible conversion reaction mechanism accomplished by alloying processes. This rational design strategy opens a window for the development of superior energy storage materials., (© 2022 The Authors. Advanced Science published by Wiley-VCH GmbH.)

Solid-state lithium metal batteries (SLMBs) are attracting enormous attention due to their enhanced safety and high theoretical energy density. However, the alkali lithium with high reducibility can react with the solid-state electrolytes resulting in the inferior cycle lifespan. Herein, inspired by the idea of interface design, the 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl) imide as an initiator to generate an artificial protective layer in polymer electrolyte is selected. Time-of-flight secondary ion mass spectrometry and X-ray photoelectron spectroscopy reveal the stable solid electrolyte interface (SEI) is in situ formed between the electrolyte/Li interface. Scanning electron microscopy (SEM) images demonstrate that the constructed SEI can promote homogeneous Li deposition. As a result, the Li/Li symmetrical cells enable stable cycle ultralong-term for over 4500 h. Moreover, the as-prepared LiFePO 4 /Li SLMBs exhibit an impressive ultra-long cycle lifespan over 1300 cycles at 1 C, as well as 1600 cycles at 0.5 C with a capacity retention ratio over 80%. This work offers an effective strategy for the construction of the stable electrolyte/Li interface, paving the way for the rapid development of long lifespan SLMBs., (© 2022 The Authors. Advanced Science published by Wiley-VCH GmbH.)

Lithium-sulfur (Li-S) batteries have been considered as one of the most promising electrochemical energy storage systems because of their high energy density. However, a series of issues severely limit the practical performances of Li-S batteries such as low conductivity, significant volume change, and shuttle effect. The hollow carbon spheres with huge voids and high electrical conductivity are promising as sulfur hosts. Unfortunately, the nonpolar nature of carbon materials cannot prevent the shuttle effect effectively. In this case, the atomic cobalt is introduced to a nitrogen-doped hollow carbon sphere (ACo@HCS) through polymerization and controlled pyrolysis. The atomic cobalt dopants not only act as active sites to restrict the shuttle effect, but also can promote the kinetics of the sulfur redox reactions. ACo@HCS acting as sulfur host exhibits a high discharge capacity (1003 mAh g -1 ) at a 1.0 C rate after 500 cycles, and the corresponding decay rate is as low as 0.002% per cycle. This exciting work paves a new way to design high-performance Li-S batteries., (© 2022 Wiley-VCH GmbH.)

For the past few years, a new generation of energy storage systems with large theoretical specific capacity has been urgently needed because of the rapid development of society. Lithium-sulfur (Li-S) batteries are regarded as one of the most promising candidates for novel battery systems, since their resurgence at the end of the 20th century Li-S batteries have attracted ever more attention, attributed to their notably high theoretical energy density of 2600 W h kg -1 , which is almost five times larger than that of commercial lithium-ion batteries (LIBs). One of the determining factors in Li-S batteries is how to design/prepare the sulfur cathode. For the sulfur host, the major technical challenge is avoiding the shuttling effect that is caused by soluble polysulfides during the reaction. In past decades, though the sulfur cathode has developed greatly, there are still some enormous challenges to be conquered, such as low utilization of S, rapid decay of capacity, and poor cycle life. This article spotlights the recent progress and foremost findings in improving the performance of Li-S batteries by employing multifunctional metal phosphides as host materials. The current state of development of the sulfur electrode of Li-S batteries is summarized by emphasizing the relationship between the essential properties of metal phosphide-based hybrid nanomaterials, the chemical reaction with lithium polysulfides and the latter's influence on electrochemical performance. Finally, trends in the development and practical application of Li-S batteries are also pointed out., (© 2021 Wiley-VCH GmbH.)

Most P2-type layered oxides exhibit a large volume change when they are charged into high voltage, and it further leads to bad structural stability. In fact, high voltage is not the reason which causes the irreversible phase transition. There are two internal factors which affect structural evolution: the amount and distribution of Na ions retained in the lattice. Hereon, a series of layered oxides Na 2/3 Mn x Ni x-1/3 Co 4/3-2x O 2 (1/3≤x≤2/3) were synthesized. It is observed that different components have different structural evolutions during the charge/discharge processes, and further researches find that the distribution of Na ions in layers is the main factor. By controlling the distribution of Na ions, the phase transition process can be well controlled. As the referential component, P2-Na 2/3 Mn 1/2 Ni 1/6 Co 1/3 O 2 cathode with uniform distribution of Na ions is cycled at the voltage window of 1.5-4.5 V, which exhibits a volume change as low as 1.9 %. Such a low strain is beneficial for cycling stability. The current work provides a new and effective route to regulate the structural evolution of the promising P2-type layered cathode for sodium ion batteries., (© 2021 Wiley-VCH GmbH.)

As concerns about the safety of lithium-ions batteries (LIBs) increases, aqueous zinc-ion batteries (ZIBs) with a lower cost, higher safety, and higher co-efficiency have attracted more and more interest. However, finding suitable cathode materials is still an urgent problem in ZIBs. In recent years, a lot of significant works have been reported, including manganese-based cathodes, vanadium-based cathodes, Prussian blue analog-based materials, and sustainable quinone cathodes. In this review, some typical cathode materials are introduced. The detailed storage mechanisms and methods for improving the reaction kinetics of the zinc ions are summarized. Finally, the issues, challenges, and the research directions are provided., (© 2020 Wiley-VCH GmbH.)

Sodium-ion batteries (SIBs) have attracted much attention due to their abundance, easy accessibility, and low cost. All of these advantages make them potential candidates for large-scale energy storage. The P2-type layered transition-metal oxides (Na x TMO 2 ; TM=Mn, Co, Ni, Ti, Fe, V, Cr, and a mixture of multiple elements) exhibit good Na + ion conductivity and structural stability, which make them an excellent choice for the cathode materials of SIBs. Herein, the structural evolution, anionic redox reaction, some challenges, and recent progress of Na x TMO 2 cathodes for SIBs are reviewed and summarized. Moreover, a detailed understanding of the relationship of chemical components, structures, phase compositions, and electrochemical performance is presented. This Review aims to provide a reference for the development of P2-type layered transition-metal oxide cathode materials for SIBs., (© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Conventional lithium-ion batteries, with flammable organic liquid electrolytes, have serious safety problems, which greatly limit their application. All-solid-state batteries (ASSBs) have received extensive attention from large-scale energy-storage fields, such as electric vehicles (EVs) and intelligent power grids, due to their benefits in safety, energy density, and thermostability. As the key component of ASSBs, solid electrolytes determine the properties of ASSBs. In past decades, various kinds of solid electrolytes, such as polymers and inorganic electrolytes, have been explored. Among these candidates, organic-inorganic composite solid electrolytes (CSEs) that integrate the advantages of these two different electrolytes have been regarded as promising electrolytes for high-performance ASSBs, and extensive studies have been carried out. Herein, recent progress in organic-inorganic CSEs is summarized in terms of the inorganic component, electrochemical performance, effects of the inorganic ceramic nanostructure, and ionic conducting mechanism. Finally, the main challenges and perspectives of organic-inorganic CSEs are highlighted for future development., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Lithium-sulfur batteries (LSBs) are considered as one of the best candidates for novel rechargeable batteries due to their high energy densities and abundant required materials. However, the poor conductivity and large volume expansion of sulfur and the "shuttle effect" of lithium polysulfides (LPSs) have significantly hindered the development and successful commercialization of LSBs. Bean-like B,N codoped carbon nanotubes loaded with Co nanoparticles (Co@BNTs), which can act as advanced sulfur hosts for the novel LSB cathode, are fabricated. Uniform graphitic nanotubes improve the conductivity of the electrode and load more electroactive sulfur and buffer volume expansion during the electrochemical reaction. In addition, loaded Co nanoparticles and codoped B,N sites can significantly suppress the "shuttle effect" of LPSs with strong chemical interaction. It is established that the Co nanoparticles and codoped B,N can provide more active sites to catalyze the redox reaction of sulfur cathode. This stable Co@BNTs-S cathode displays an exceptional electrochemical performance (1160 mA h g -1 after 200 cycles at 0.1 C) and outstanding stable cycle performance (1008 mA h g -1 after 400 cycles at 1.0 C with an extremely low attenuation rate of 0.038% per cycle)., (© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

As anode materials for high-performance Li-ion batteries, peapod-like Ge-based composites, including Ge, a Li-inactive conducting Cu 3 Ge, and a porous carbon matrix are synthesized simply by annealing CuGeO 3 @dopamine in a H 2 /Ar atmosphere. The introduction of the carbon layer and inactive alloying phase Cu 3 Ge not only enhances the electrical conductivity of the Ge anode, but also reduces the volume change of Ge during the cell cycle as a buffer. In particular, the anode of this peapod-like Cu 3 Ge/Ge@C shows an excellent long cycle life as well as outstanding capacity performance, with a discharge specific capacity up to 934 mA h g -1 after 500 cycles., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Lithium-sulfur (Li-S) batteries have attracted much attention in the field of electrochemical energy storage due to their high energy density and low cost. However, the "shuttle effect" of the sulfur cathode, resulting in poor cyclic performance, is a big barrier for the development of Li-S batteries. Herein, a novel sulfur cathode integrating sulfur, flexible carbon cloth, and metal-organic framework (MOF)-derived N-doped carbon nanoarrays with embedded CoP (CC@CoP/C) is designed. These unique flexible nanoarrays with embedded polar CoP nanoparticles not only offer enough voids for volume expansion to maintain the structural stability during the electrochemical process, but also promote the physical encapsulation and chemical entrapment of all sulfur species. Such designed CC@CoP/C cathodes with synergistic confinement (physical adsorption and chemical interactions) for soluble intermediate lithium polysulfides possess high sulfur loadings (as high as 4.17 mg cm -2 ) and exhibit large specific capacities at different C-rates. Specially, an outstanding long-term cycling performance can be reached. For example, an ultralow decay of 0.016% per cycle during the whole 600 cycles at a high current density of 2C is displayed. The current work provides a promising design strategy for high-energy-density Li-S batteries., (© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Amorphous nanoparticles of ZnO and TiO 2 embedded in carbon nanocages (AZT⊂CNCs) were successfully synthesized through a simple annealing process of TiO 2 -coated zeolitic imidazolate framework-8 (ZIF-8). In the current anode of AZT⊂CNCs, tiny ZnO and TiO 2 nanoparticles were uniformly distributed in the carbon matrix (carbon nanocages), which could effectively buffer the volume expansion of electroactive ZnO and provide excellent electric conductivity. After fully investigating the electrochemical performance of the AZT⊂CNCs samples obtained with different additive amounts of tetrabutyl orthotitanate (TBOT) for TiO 2 coating, it has been found that AZT-30 (0.1 g ZIF-8 with 30 mL TBOT) shows the best cycle stability (510 mA h g -1 after 350 cycles at 200 mA g -1 ) and a superior rate capability (610 mA h g -1 after 3500 cycles at 2 A g -1 ). The greatly enhanced Li-ion storage performance could be ascribed to the fact that the introduction of amorphous TiO 2 could activate the reversible lithiation/delithiation reaction of ZnO during the charge/discharge process., (© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

An anode of self-supported FeP@C nanotube arrays on carbon fabric (CF) is successfully fabricated via a facile template-based deposition and phosphorization route: first, well-aligned FeOOH nanotube arrays are simply obtained via a solution deposition and in situ etching route with hydrothermally crystallized (Co,Ni)(CO 3 ) 0.5 OH nanowire arrays as the template; subsequently, these uniform FeOOH nanotube arrays are transformed into robust carbon-coated Fe 3 O 4 (Fe 3 O 4 @C) nanotube arrays via glucose adsorption and annealing treatments; and finally FeP@C nanotube arrays on CF are achieved through the facile phosphorization of the oxide-based arrays. As an anode for lithium-ion batteries (LIBs), these FeP@C nanotube arrays exhibit superior rate capability (reversible capacities of 945, 871, 815, 762, 717, and 657 mA h g -1 at 0.1, 0.2, 0.4, 0.8, 1.3, and 2.2 A g -1 , respectively, corresponding to area specific capacities of 1.73, 1.59, 1.49, 1.39, 1.31, 1.20 mA h cm -2 at 0.18, 0.37, 0.732, 1.46, 2.38, and 4.03 mA cm -2 , respectively) and a stable long-cycling performance (a high specific capacity of 718 mA h g -1 after 670 cycles at 0.5 A g -1 , corresponding to an area capacity of 1.31 mA h cm -2 at 0.92 mA cm -2 )., (© 2018 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The sulfur cathode, as a new generation of lithium-ion battery cathode material, has a high theoretical energy density of about 2500 Wh kg -1 . However, the low conductivity of sulfur and the "shuttle effect", widely presenting in the lithiation/de-lithiation process, seriously hinder its practical application. Here, we report a new nanoconfined oxidation route (first complete oxidation of metal sulfide and subsequently partial oxidation of the generated S from sulfide) for S cathode encapsulated with MnO 2 nanosheets and N-doped carbon hollow spheres. This nanoconfined oxidation route can successfully confine the sulfur particles in the interior of the carbon shell, and the rationally introduced nonpolar carbon and polar MnO 2 can both reduce the dissolution of polysulfide during the charge-discharge process. The obtained well-defined S-MnO 2 @C cathode exhibits high specific capacity with excellent cycling performance and superior rate capability., (© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Three polyacetylenes were isolated and purified from Platycodon grandiflorum A. DC for the first time by high-speed counter-current chromatography using a two-phase solvent system composed of hexane/ethyl acetate/methanol/water (1:31:1:31, v/v/v/v) and high-performance liquid chromatography with an Agilent ZORBAX® SB-C18 column (4.6 mm × 150 mm, 5 μm). After separation by high-speed counter-current chromatography and high-performance liquid chromatography, we obtained 3.5 mg of platetyolin A, 4.1 mg of platetyolin B, and 18.1 mg of lobetyolin with purities of 97.2, 96.7, and 96.9%, respectively. The purity of each compound was assessed by high-performance liquid chromatography and the chemical structures were evaluated by high-resolution electrospray ionization time-of-flight mass spectrometry and one- and two-dimensional NMR spectroscopy. Among the isolated compounds, platetyolin A and platetyolin B are newly reported compounds., (© 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

Accelerated solvent extraction (ASE) was applied to the extraction of saikosaponin a, saikosaponin c and saikosaponin d from the roots of Bupleurum falcatum. Main extraction parameters such as the extraction solvents, extraction temperature and static extraction time were investigated and optimized. The optimized procedure employed 70% methanol as extraction solvent, 120 degrees C of extraction temperature, 10 min of static extraction time, 60% of flush volume and the extraction recoveries of the three compounds were near to 100% with one extraction cycle. The extracted samples were analyzed by HPLC with UV detector. The HPLC conditions were as follows: Hypersil ODS2 (4.6 mmx250 mm, 5 microm) column, acetonitrile and water as mobile phase, flow rate of 1.0 mL/min, UV detection wavelength of 204 nm and injection volume of 20 microL. Compared with the traditional methods including heat-reflux extraction and ultrasonic-assisted extraction, the proposed ASE method was more efficient and faster to be operated. The results indicated that ASE was an alternative method for extracting saikosaponins from the roots of B. falcatum.

Supercritical fluid extraction (SFE) was used to extract saikosaponins a, c and d from the root of Bupleurum falcatum. An orthogonal array design L(9)(3)(4) was employed as a chemometric method for the optimization of the SFE conditions. The effects of four factors including pressure (30-40 MPa), temperature (40-50 degrees C), ethanol concentration (60-100%) and time (2.5-3.5 h) on the yields of saikosaponins were investigated by a preparative SFE system in the SFE mode. Under the optimized conditions, namely 35 MPa of pressure, 45 degrees C of temperature, 80% of ethanol concentration and 3.0 h of time, the yields of saikosaponin c, saikosaponin a, saikosaponin d, total saikosaponins and SFE extract were 0.16, 0.12, 0.96, 1.24 and 16.48 mg/g, respectively. Determinations of the saikosaponins were performed by HPLC.