Solid‐state polymer electrolytes (SPEs) with flexibility, easy processability, and low cost have been regarded as promising alternatives for conventional liquid electrolytes in next‐generation ...high‐safety lithium metal batteries. However, SPEs generally suffer poor strength to block Li dendrite growth during the charge/discharge process, which severely limits their wide practical applications. Here, a rational design of 3D cross‐linked network asymmetric SPE modified with a metal–organic framework (MOF) layer on one side is proposed and prepared through an in‐situ polymerization process. In such unique asymmetric SPEs, the nanoscale MOF layer acts as a shield that effectively suppresses the growth of Li dendrites and regulates the uniform Li+ transport, and the polymer electrolyte can be scattered in the whole cell to endow the smooth transmission of Li+. As a result, the asymmetric SPE exhibits high ionic conductivity, wide electrochemical window, high thermal stability and safety, which endows the Li/Li symmetrical cell with outstanding cyclic stability (operate well over 800 h at a current density of 0.1 mA cm−2 for the capacity of 0.1 mAh cm−2).
Asymmetric solid‐state polymer electrolytes (SPEs) modified with an ultrathin metal–organic framework (MOF) layer on one side is constructed via an in situ polymerization process. The nanoscale MOF layer acts as a shield that suppresses the growth of Li dendrites and regulates uniform Li+ transport. Consequently, the lithium metal batteries based on such SPEs exhibit long cycle stability and high safety.
The No Hair theorem in classical general relativity predicts that rotating black holes are specified by the Kerr metric, which is uniquely identified by the mass and spin. However, as a pioneering ...study beyond general relativity, the rotating hairy black hole has been proposed, which encompasses the Kerr black hole as a special case. In these black holes, there are extra hair which could appear due to the additional surrounding sources such as dark matter or dark energy. In this work, we study the phenomenology of the rotating hairy black hole in terms of gravitational perturbations. In particular, the superradiance and the quasinormal modes. Using the matching-asymptotic method, we derive the amplification factor and the superradiance conditions. We also calculate the quasinormal modes using the continued fraction method. The results are in very good agreement with previous studies in the Kerr limit. We also show how the amplification and quasinormal modes will shift in response to variations in the hairy parameters, black hole spin, and quantum numbers.
Rechargeable magnesium batteries (RMBs), which have attracted tremendous attention in large‐scale energy storage applications beyond lithium ion batteries, have many advantages such as high ...volumetric capacity, low cost, and environmental friendliness. However, the strong polarization effect, slow kinetic de‐intercalation of Mg2+ ions, and the incompatibility between electrodes and electrolytes limit their commercial application. Thus, developing stable and high‐efficiency electrode materials and optimization of electrolytes are key to promoting the practical application of RMBs. In this review, a summary and discussion are provided regarding the recent progress in the development of the key materials for RMBs, including cathodes, anodes, and electrolytes. The cathode materials including intercalation type cathodes and conversion type cathodes are classified and introduced in detail by the reaction mechanism, the effects of structure on the kinetics of Mg2+ ion migration are clarified; the modification and interface issues of Mg anode materials are comprehensively stated, and the potential development prospects of RMB electrolytes are systematically analyzed. In addition, the main opportunities and challenges in this field are briefly elaborated and discussed. Finally, this review will provide a framework for the key materials for RMBs as a reference for future research.
This review comprehensively summarizes and discusses the recent progress in the key materials for rechargeable magnesium batteries (RMBs) including cathodes, anodes, and electrolytes. The challenges and opportunities in this field are systematically analyzed. This work will provide valuable references for achieving the high specific capacity and long‐lifespan RMBs in the near future.
Solid‐state lithium (Li) batteries using solid electrolytes and Li anodes are highly desirable because of their high energy densities and intrinsic safety. However, low ambient‐temperature ...conductivity and poor interface compatibility of solid electrolytes as well as Li dendrite formation cause large polarization and poor cycling stability. Herein, a high transference number intercalated composite solid electrolyte (CSE) is prepared by the combination of a solution‐casting and hot‐pressing method using layered lithium montmorillonite, poly(ethylene carbonate), lithium bis(fluorosulfonyl)imide, high‐voltage fluoroethylene carbonate additive, and poly(tetrafluoroethylene) binder. The electrolyte presents high ionic conductivity (3.5 × 10−4 S cm−1), a wide electrochemical window (4.6 V vs Li+/Li), and high ionic transference number (0.83) at 25 °C. In addition, a 3D Li anode is also fabricated via a facile thermal infusion strategy. The synergistic effect of high transference number intercalated electrolyte and 3D Li anode is more favorable to suppress Li dendrites in a working battery. The solid‐state batteries based on LiFePO4 (Al2O3 @ LiNi0.5Co0.2Mn0.3O2), CSE, and 3D Li deliver admirable cycling stability with discharge capacity 145.9 mAh g−1 (150.7 mAh g−1) and capacity retention 91.9% after 200 cycles at 0.5 C (92.0% after 100 cycles at 0.2 C) at 25 °C. This work affords a splendid strategy for high‐performance solid‐state battery.
The intercalated composite solid electrolyte presents a large ionic conductivity and high ionic transference number. The synergistic effect of the high transference number intercalated electrolytes and 3D lithium anode effectively suppresses lithium dendrites. The assembled batteries deliver a high cycling performance, demonstrating a promising strategy for ambient‐temperature solid‐state lithium metal batteries.
The construction of bifunctional electrode materials for hydrogen evolution reaction (HER) and lithium‐ion batteries (LIBs) has been a hot topic of research. Herein, metal–organic frameworks (MOFs) ...derived micro‐/nanostructured Ni2P/Ni hybrids with a porous carbon coating (denoted as Ni2P/Ni@C) are prepared using a feasible pyrolysis–phosphidation strategy. On the one hand, the optimal Ni2P/Ni@C catalyst exhibits superior HER performance with a low overpotential of 149 mV versus a reversible hydrogen electrode (RHE) at 10 mA cm−2 and excellent durability. The density functional theory computations verify that the strong synergistic effect between Ni2P and Ni could optimize the electronic structure, thus rendering the enhanced electrocatalytic performance. On the other hand, the Ni2P/Ni@C electrode displays a reversible capacity of 597 mAh g−1 after 1000 cycles at 1000 mA g−1 and improved rate capability as an anode for LIBs, owing to the well‐organized micro‐/nanostructure and conductive Ni core. In addition, the electrochemical reaction mechanism of the Ni2P/Ni@C electrode upon lithiation/delithiation is investigated in detail via ex situ X‐ray powder diffraction and X‐ray photoelectron spectroscopy methods. It is expected that the facile and controllable approach can be extended to fabricate other MOF‐based metal phosphides/metal hybrids for electrochemical energy storage and conversion systems.
Metal‐organic framework derived micro/nano‐structured Ni2P/Ni hybrids with a porous carbon coating are successfully prepared. As hydrogen evolution reaction catalysts, both experimental and computational results verify that the strong synergistic effect between Ni2P and Ni renders an enhanced electrocatalytic performance. As anode for Li‐ion batteries, the well‐organized micro/nano‐structure and the conductive Ni core jointly promote the electrochemical reaction kinetics.
The pursuit of high reversible capacity and long cycle life for rechargeable batteries has gained extensive attention in recent years, and the development of applicable electrode materials is the key ...point. Herein, thanks to the preintercalation of lithium ions, a stable and highly conductive nanostructure of V2C MXene is successfully fabricated via a facile self‐discharge mechanism, which provides open spaces for rapid ion diffusion and guarantees fast electron transport. Taking the prelithiated V2C as electrode, an outstanding initial coulombic efficiency of 80% and an impressive capacity retention of ≈98% after 5000 charge/discharge cycles are achieved for lithium‐ion batteries. Especially, it demonstrates a fascinating reversible capacity of up to 230.3 mA h g−1 at 0.02 A g−1 and a long cycling life of 82% capacity retention over 480 cycles in the hybrid magnesium/lithium‐ion batteries. In addition, the Mg2+ and Li+ ions cointercalation mechanism of the prelithiated V2C is elucidated through ex situ X‐ray diffraction and X‐ray photoelectron spectroscopy characterizations. This work not only offers an effective approach to compensate the large initial lithium loss of high‐capacity anode materials but also opens up a new and viable avenue to develop promising hybrid Mg/Li‐storage materials with eminent electrochemical performance.
Prelithiated V2C MXene with a stable and highly conductive nanostructure is prepared through a facile self‐discharge mechanism. The preintercalation of Li+ enables improved initial coulombic efficiency and enhances cycling performance in Li‐ion batteries; exceptional rate capability and unprecedentedly long cycling life are also achieved for Mg2+/Li+ cointercalation chemistry.
Li metal is one of the most promising anode materials for high energy density batteries. However, uncontrollable Li dendrite growth and infinite volume change during the charge/discharge process lead ...to safety issues and capacity decay. Herein, a carbonized metal–organic framework (MOF) nanorod arrays modified carbon cloth (NRA‐CC) is developed for uniform Li plating/stripping. The carbonized MOF NRAs effectively convert the CC from lithiophobic to lithiophilic, decreasing the polarization and ensuring homogenous Li nucleation. The 3D interconnected hierarchal CC provides adequate Li nucleation sites for reducing the local current density to avoid Li dendrite growth, and broadens internal space for buffering the volume change during Li plating/stripping. These characteristics afford a stable cycling of the NRA‐CC electrode with ultrahigh Coulombic efficiencies of 96.7% after 1000 h cycling at 2 mA cm−2 and a prolonged lifespan of 200 h in the symmetrical cell under ultrahigh areal capacity (12 mAh cm−2) and current (12 mA cm−2). The solid‐state batteries assembled with the composite Li anode, high‐voltage cathode (LiNi0.5Co0.2Mn0.3O2), and composite solid‐state electrolyte also deliver excellent cyclic and rate performance at 25 °C. This work sheds fresh insights on the design principles of a dendrite‐free Li metal anode for safe solid‐state Li metal batteries.
Dendrite‐free Li anodes can be achieved through a carbonized Co‐based zeolitic imidazolate framework nanorod arrays modified carbon cloth (NRA‐CC). Owing to the synergistic effect of the interconnected carbon cloth and lithiophilic Co–N–C NRAs, NRA‐CC can regulate the Li plating/stripping behavior and withstand high areal capacity and current density. The composite Li anode is successfully applied in solid‐state Li metal batteries.
Pretreatment is widely used before drying of agro-products to inactivate enzymes, enhance drying process and improve quality of dried products. In current work, the influence of various pretreatments ...on drying characteristics and quality attributes of fruits and vegetables is summarized. They include chemical solution (hyperosmotic, alkali, sulfite and acid, etc.) and gas (sulfur dioxide, carbon dioxide and ozone) treatments, thermal blanching (hot water, steam, super heated steam impingement, ohmic and microwave heating, etc), and non-thermal process (ultrasound, freezing, pulsed electric field, and high hydrostatic pressure, etc). Chemical pretreatments effectively enhance drying kinetics, meanwhile, it causes soluble nutrients losing, trigger food safety issues by chemical residual. Conventional hot water blanching has significant effect on inactivating various undesirable enzymatic reactions, destroying microorganisms, and softening the texture, as well as facilitating drying rate. However, it induces undesirable quality of products, e.g., loss of texture, soluble nutrients, pigment and aroma. Novel blanching treatments, such as high-humidity hot air impingement blanching, microwave and ohmic heat blanching can reduce the nutrition loss and are more efficient. Non-thermal technologies can be a better alternative to thermal blanching to overcome these drawbacks, and more fundamental researches are needed for better design and scale up.
LINKED CONTENT
This article is linked to Toyoda et al papers. To view these articles, visit https://doi.org/10.1111/apt.17088 and https://doi.org/10.1111/apt.17139
Globally, liver cancer, which is one of the major cancers worldwide, has attracted the growing attention of technological researchers for its high mortality and limited treatment options. Hydrogels ...are soft 3D network materials containing a large number of hydrophilic monomers. By adding moieties such as nitrobenzyl groups to the network structure of a cross‐linked nanocomposite hydrogel, the click reaction improves drug‐release efficiency in vivo, which improves the survival rate and prolongs the survival time of liver cancer patients. The application of a nanocomposite hydrogel drug delivery system can not only enrich the drug concentration at the tumor site for a long time but also effectively prevents the distant metastasis of residual tumor cells. At present, a large number of researches have been working toward the construction of responsive nanocomposite hydrogel drug delivery systems, but there are few comprehensive articles to systematically summarize these discoveries. Here, this systematic review summarizes the synthesis methods and related applications of nanocomposite responsive hydrogels with actions to external or internal physiological stimuli. With different physical or chemical stimuli, the structural unit rearrangement and the controlled release of drugs can be used for responsive drug delivery in different states.
Cross‐linked hydrophilic polymer chains that can form gels are widely utilized for biomedical applications, such as drug delivery. Various studies have also demonstrated the effects of particle size and surface morphology on drug release from particles in liver cancer therapy. Mechanistic understandings of responsive hydrogels in responsive stimuli are provided, by which better clinical choices may be approached.
