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Abstract Background Cryptolaemus montrouzieri (Coccinellidae) is widely utilized as biological control agents in modern agriculture. A comprehensive understanding of its food preference can help guide mass rearing and safety management during field application of pest control. Although some studies have paid attentions to the impacts of prey shift on C. montrouzieri, little is known regarding the role of post-transcriptional regulations in its acclimation to unnatural preys. Results We performed a genome-wide investigation on alternative splicing dynamics in C. montrouzieri in response to the predation transition from natural prey to unnatural ones. When feeding on undesired diets, 402–764 genes were differentially alternative spliced in C. montrouzieri. It is noteworthy that the majority of these genes (> 87%) were not differentially expressed, and these differentially spliced genes regulated distinct biological processes from differentially expressed genes, such as organ development and morphogenesis, locomotory behavior, and homeostasis processes. These suggested the functionally nonredendant role of alternative splicing in modulating physiological and metabolic responses of C. montrouzieri to the shift to undesired preys. In addition, the individuals feeding on aphids were subject to a lower level of changes in splicing than other alternative diets, which might be because of the similar chemical and microbial compositions. Our study further suggested a putative coupling of alternative splicing and nonsense-mediated decay (AS-NMD), which may play an important role in fine-tuning the protein repertoire of C. montrouzieri, and promoting its acclimation to predation changes. Conclusion These findings highlight the key role of alternative splicing in modulating the acclimation of ladybirds to prey shift and provide new genetic clues for the future application of ladybirds in biocontrol.

Abstract Ingenious design and fabrication of advanced carbon‐based sulfur cathodes are extremely important to the development of high‐energy lithium‐sulfur batteries, which hold promise as the next‐generation power source. Herein, for the first time, we report a novel versatile hyphae‐mediated biological assembly technology to achieve scale production of hyphae carbon fibers (HCFs) derivatives, in which different components including carbon, metal compounds, and semiconductors can be homogeneously assembled with HCFs to form composite networks. The mechanism of biological adsorption assembly is also proposed. As a representative, reduced graphene oxides (rGOs) decorated with hollow carbon spheres (HCSs) successfully co‐assemble with HCFs to form HCSs@rGOs/HCFs hosts for sulfur cathodes. In this unique architecture, not only large accommodation space for sulfur but also restrained volume expansion and fast charge transport paths are realized. Meanwhile, multiscale physical barriers plus chemisorption sites are simultaneously established to anchor soluble lithium polysulfides. Accordingly, the designed HCSs@rGOs/HCFs‐S cathodes deliver a high capacity (1189 mA h g−1 at 0.1 C) and good high‐rate capability (686 mA h g−1 at 5 C). Our work provides a new approach for the preparation of high‐performance carbon‐based electrodes for energy storage devices.

Metal-ion (Li-, Na-, Zn-, K-, Mg-, and Al-ion) batteries (MIBs) play an important role in realizing the goals of “emission peak and carbon neutralization” because of their green production techniques, lower pollution, high voltage, and large energy density. Carbon-based materials are indispensable for developing MIBs and are widely adopted as active or auxiliary materials in the anodes and cathodes. For example, carbon-based materials, including graphite, Si/C and hard carbon, have been used as anode materials for Li- and Na-ion batteries. Carbon can also be used as a conductive coating for cathodes, such as in LiFePO4/C, to achieve better performance. In addition, as new high-valence MIBs (Zn-, Al-, and Mg-ion) have emerged, a growing number of novel carbon-based materials have been utilized to construct high-performance MIBs. Herein, we discuss the recent development trends in advanced carbon-based materials for MIBs. The impact of the structure properties of advanced carbon-based materials on energy storage is addressed, and a perspective on their development is also proposed.

Artificial coastal protection forests are difficult to manage because of nutrient stress in harsh environment. To explore the effects of salt and phosphorus stress on the seed germination and seedling growth of Casuarina equisetifolia and Acacia confusa, we respectively watered the seeds and seedlings of the two kinds of plants with the solutions of NaCl (salt) and KH2PO4 (phosphorus) in different concentrations, and then determined their growth indicators, respectively. The results were as follows: (1) High salt concentration solutions significantly inhibited seed germination and had a certain effect on the growth of seedlings, however, the effects of salt stress on seed gemination and growth were different. The salt tolerance of Acacia confusa seed germination was higher than that of Casuarina equisetifolia. The biggest relative salt damage rate of Acacia confusa was 23.03% and that of Casuarina equisetifolia was 89.15%. As the concentration of NaCl increased, the germination rate, germination potential, germination index and vitality index of Casuarina equisetifolia and Acacia confusa seeds decreased. And the maximums of the four germination indexes of Casuarina equisetifolia seed were 38.70%, 34.67%, 18.70 and 0.055, and of Acacia confusa seeds were 76.67%, 62.22%, 48.46 and 6.11, respectively. (2) The height and root length of the plants decreased with the increase of salt concentration. The plant heights of Casuarina equisetifolia and Acacia confusa were 12.29 to 6.01 mm and 48.27 to 17.33 mm, and the root lengths were 8.57 to 1.45 mm and 33.41 to 5.88 mm, respectively. The biomass of root, stem and leaf as well as root shoot ratio of Acacia confusa gradually decreased with the increase of salt concentration, but the differences between the treatments of Casuarina equisetifolia were not obvious. 0.6% and 0.4% salt stress were the thresholds for seed germination and seedling growth of the two plants, respectively. (3)The seed and seedling of Acacia confusa were more tolerant to low-phosphorus environment than Casuarina equisetifolia, and there was a difference in the optimum phosphorus concentration between the two. When the phosphorus concentration was 0.1 mmol·L-1, the seed germination rate(49.33%), germination index (23.12%) and vitality index(0.093) of Casuarina equisetifolia, as well as the biomass of root, stem and leaf, all reached the maximum. In the 5 mmol·L-1 treatment, the maximums of germination rate(81.11%), germination potential(62.22%), gemination index(38.23), vitality index(5.07), plant height (54.48 mm) and root length (37.16 mm) of Acacia confusa seeds all appeared, while their germination was inhibited in the treatment of 10 mmol·L-1. Therefore, when sowing the seed of coastal defense forest or planting its seedling, the sowing or planting mode must be selected according to the soil salt and phosphorus contents.

Abstract For pursuing the ambitious goals in the burgeoning electric vehicles, portable electronic devices, and energy storage sectors, Li‐ion batteries (LIBs) are considered as one of the most promising electrochemical power sources because of their high energy density and moderate cost. Particularly, the improvement of battery materials and recycling of spent LIBs are receiving great attention since the sustainable approaches for the synthesis, modification, and recycling of battery materials are the crucial factors to the successful large‐scale implementation of LIBs. In this regard, supercritical carbon dioxide (SC‐CO2), which possesses many merits, such as environmentally friendly, low‐cost, individual chemical environment, and especially its unique physical properties, has been employed as solvent and reaction medium in the synthesis and modification of diverse functional materials. In this review, we mainly aim at compiling the applications of SC‐CO2 technology in the synthesis and modification of electrode materials as well as the recycling of LIBs. First, the unique properties and principles of SC‐CO2 technology are highlighted. Second, the latest progresses of the electrode materials design and recycling with the assistance of SC‐CO2 technique are summarized. Finally, the challenges, future directions, and perspectives on the design and development of battery materials and battery recycling by SC‐CO2 technology are proposed.

Dwarfed stature is a desired agronomic trait for pomegranate (Punica granatum L.), with its advantages such as lower cost and increased yield. A comprehensive understanding of regulatory mechanisms underlying the growth repression would provide a genetic foundation to molecular-assisted dwarfing cultivation of pomegranate. Our previous study induced dwarfed pomegranate seedlings via exogenous application of plant growth retardants (PGRs) and highlighted the important roles of differential expression of plant growth-related genes in eliciting the dwarfed phenotype of pomegranate. Alternative polyadenylation (APA) is an important post-transcriptional mechanism and has been demonstrated to act as a key regulator in plant growth and development. However, no attention has been paid to the role of APA in PGR-induced dwarfing in pomegranate. In this study, we characterized and compared APA-mediated regulation events underlying PGR-induced treatments and normal growth condition. Genome-wide alterations in the usage of poly(A) sites were elicited by PGR treatments, and these changes were involved in modulating the growth and development of pomegranate seedlings. Importantly, ample specificities were observed in APA dynamics among the different PGR treatments, which mirrors their distinct nature. Despite the asynchrony between APA events and differential gene expression, APA was found to regulate transcriptome via influencing microRNA (miRNA)-mediated mRNA cleavage or translation inhibition. A global preference for lengthening of 3’ untranslated regions (3’ UTRs) was observed under PGR treatments, which was likely to host more miRNA target sites in 3’ UTRs and thus suppress the expression of the corresponding genes, especially those associated with developmental growth, lateral root branching, and maintenance of shoot apical meristem. Together, these results highlighted the key role of APA-mediated regulations in fine-tuning the PGR-induced dwarfed stature of pomegranate, which provides new insights into the genetic basis underlying the growth and development of pomegranate.

Abstract Sulfide solid state electrolyte (SSE) possesses high ionic conductivity and great processability but suffers from narrow electrochemical window. Conversion sulfide cathode FeS2 has higher specific capacity and moderate redox potential, making it appropriate toward sulfide SSE. However, the complex reaction pathway and capacity fading mechanism in FeS2 are rarely studied, especially in all‐solid‐state lithium battery (ASSLB). Herein, argyrodite sulfide SSE is paired with FeS2 to investigate the electrochemical reaction pathways and the capacity fade mechanism. Instead of single conversion reaction, an anionic redox driven reaction of FeS2 is revealed. The oxidization of Li2S vanishes and large quantity of inactive Li2S accumulates to cause the interfacial deterioration, along with the stress concentration during cycling, which leads to the rapid capacity fade of FeS2. Finally, a simple strategy of slurry‐coated composite electrode with highly conductive network is proposed to direct the uniform deposition of Li2S and alleviate the stress concentration.

Plant regeneration through somatic embryogenesis provides a solution for maintaining and genetically improving crop or fruit varieties with desirable agronomic traits. For the fruit tree pomegranate (Punica granatum L.), despite some successful applications, the existing somatic embryogenesis protocols are limited by low availability of explants and susceptibility to browning. To address these problems, in this study, we developed an effective system for induction of high-vigor pomegranate somatic embryos derived from stem explants. The usage of stem explants breaks through the difficulty in obtaining material, thus making our system suitable for widespread commercial production. To enhance the performance of our system, we identified the optimal explants, subculture cycles and combination of basal media and plant growth regulators for each step. The results showed that inoculating stem explants onto a Murashige and Skoog (MS) medium supplemented with 1.0 mg/L 6-benzylaminopurine (6-BA) and 1.0 mg/L 1-naphthaleneacetic acid (NAA) achieved the best induction rate and growth status of pomegranate calli (induction rate = ~72%), and MS medium containing 0.5 mg/L 6-BA and 1.0 mg/L NAA was the optimal condition for the induction of embryogenic calli and somatic embryos (induction rate = ~74% and 79%, respectively). The optimal subculture period for embryogenic calli was found to be 30–35 days. Strong roots were then induced in the developed somatic embryo seedlings, which survived and grew well after transplantation to the natural environment, indicating the good vitality of the induced pomegranate somatic embryos. Together, our system provides a solution to mass somatic embryo induction and plant regeneration of pomegranate and lays a foundation for future genetic transformation and bioengineering improvement of pomegranate with favorable agronomic traits.

Abstract Lithium‐sulfur batteries (Li‐S batteries) have been regarded as one of the most promising technologies to change the status quo of lithium‐ion battery and realize large‐scale energy storage applications. Nevertheless, the process of launching Li‐S batteries from lab to market is seriously hindered by their inherent shortages (for example, shuttled lithium polysulfides (LiPSs), and sluggish redox kinetics), which greatly restrict sulfur utilization and the battery cycle life. In this regard, Co‐based materials are effective to suppress the shuttle effect through anchoring soluble LiPSs and enhancing reaction kinetics. It is of great significance for the development of advanced catalytic materials to clarify the research progress of Co‐based materials in design strategy, modification mechanism and electrochemical properties. Considering this, we conduct a comprehensive review of recent progress with Co‐based materials utilized in Li‐S batteries. Specifically, the state‐of‐the‐art principles, challenges, and build strategies of Li‐S batteries are systematically summarized. Meanwhile, the chemical and catalytic interactions between the Co‐based materials and LiPSs, as well as energy storage performance of Co‐based materials are thoroughly discussed. Finally, we prospect the future opportunities and challenges for the practical application for advanced Li‐S batteries.

Abstract Li has garnered enormous attention for next‐generation Li metal batteries owing to its remarkable theoretical capacity. Unfortunately, as an anode, Li suffers from serious safety issues and fast capacity fading due to the formation of Li dendrites, which hinders the practical application of Li anode. Herein, a LiAlO2‐PVDF composite modification layer is fabricated on the surface of Li metal to enhance its stability and electrochemical performance. Benefitting from the synergetic effects of high Li+ conductivity, high Li+ transference number, excellent mechanical properties, superior chemical durability, and compactness of the modification layer, the LiAlO2‐PVDF@Li electrode delivers an ultra‐long lifespan and a high capacity retention rate in the LiAlO2‐PVDF@Li│LiFePO4 full cell. The proposed strategy provides a new alternative anode for Li metal batteries with high performance and scalable production.

Abstract Lithium (Li) metal is considered as one of the most promising anode materials for next‐generation high‐energy‐density storage systems. However, the practical application of Li metal anode is hindered by interfacial instability and air instability due to the highly reactivity of Li metal. Unstable interface in Li metal batteries (LMBs) directly dictates Li dendrite growth, “dead Li” and low Coulombic efficiency, resulting in inferior electrochemical performance of LMBs and even safety issues. In addition, its sensitivity to ambient air leads to the severe corrosion of Li metal anode, high requirements of production and storage, and increased manufacturing cost. Plenty of efforts in recent years have overcome many bottlenecks in these fields and hastened the practical applications of high‐energy‐density LMBs. In this review, we focus on emerging methods of these two aspects to fulfill a stable and low cost electrode. In this perspective, design artificial solid electrolyte interphase (SEI) layers, construct three‐dimensional conductive current collectors, optimize electrolytes, employ solid‐state electrolytes, and modify separators are summarized to be propitious to ameliorate interfacial stability. Meanwhile, ex situ/in situ formed protective layers are highlighted in favor of heightening air stability. Finally, several possible directions for the future research on advanced Li metal anode are addressed.

Abstract Metal‐organic frameworks (MOFs) are of quite a significance in the field of inorganic‐organic hybrid crystals. Especially, MOFs have attracted increasing attention in recent years due to their large specific surface area, desirable electrical conductivity, controllable porosity, tunable geometric structure, and excellent thermal/chemical stability. Some recent studies have shown that carbon materials prepared by MOFs as precursors can retain the privileged structure of MOFs, such as large specific surface area and porous structure and, in contrast, realize in situ doping with heteroatoms (eg, N, S, P, and B). Moreover, by selecting appropriate MOF precursors, the composition and morphology of the carbon products can be easily adjusted. These remarkable structural advantages enable the great potential of MOF‐derived carbon as high‐performance energy materials, which to date have been applied in the fields of energy storage and conversion systems. In this review, we summarize the latest advances in MOF‐derived carbon materials for energy storage applications. We first introduce the compositions, structures, and synthesis methods of MOF‐derived carbon materials, and then discuss their applications and potentials in energy storage systems, including rechargeable lithium/sodium‐ion batteries, lithium‐sulfur batteries, supercapacitors, and so forth, in detail. Finally, we put forward our own perspectives on the future development of MOF‐derived carbon materials.

High-rate electrode materials are the key to fast-charging batteries that can store large quantities of charge in minutes or even seconds. Here the authors introduce adaptive carbon layer to oxygen defective Ti2Nb10O29 forming composite electrodes that deliver impressive rate performance and stability.

Developing high-quality solid-state electrolytes is important for producing next-generation safe and stable solid-state lithium-ion batteries. Herein, a three-dimensional highly porous polymer electrolyte based on poly (vinylidenefluoride-hexafluoropropylene) (PVDF-HFP) with Li6.4La3Zr1.4Ta0.6O12 (LLZTO) nanoparticle fillers (PVDF-HFP-LLZTO) is prepared using the electrospinning technique. The PVDF-HFP-LLZTO gel polymer electrolyte possesses a high ionic conductivity of 9.44 × 10–4 S cm−1 and a Li-ion transference number of 0.66, which can be ascribed that the 3D hierarchical nanostructure with abundant porosity promotes the liquid electrolyte uptake and wetting, and LLZTO nanoparticles fillers decrease the crystallinity of PVDF-HFP. Thus, the solid-state lithium battery with LiFePO4 cathode, PVDF-HFP-LLZTO electrolyte, and Li metal anode exhibits enhanced electrochemical performance with improved cycling stability.

This paper studies the trajectory tracking control of a space robot system (SRS) in the presence of the lumped uncertainties with no prior knowledge of their upper bound. Although some related control methods have been proposed, most of them have either not been applied to SRSs or lack rigorous stability proof. Therefore, it is still a challenge to achieve high accuracy and rigorous theoretical proof for tracking control of SRSs. This paper proposes a new integrated neural network- based control scheme for the trajectory tracking of a SRS actuated by control moment gyros (CMGs). A new adaptive non-singular terminal sliding mode (ANTSM) control method is developed based on an improved radial basis function neural network (RBFNN). In the control method, a new weight update law is proposed to learn the upper bound of the lumped uncertainties. With the advantages of RBFNN and ANTSM, the controller has high control accuracy, fast learning speed and finite-time convergence. Different from most on-ground robotic manipulator controllers, a kinematic controller with position and attitude control laws is also designed for the satellite platform to remain stable. The stability of the closed-loop system is proved by the Lyapunov method with a high mathematical standard. Comparative simulation results demonstrate the effectiveness of the proposed control scheme with preferable performance and robustness.

The F-box family exists in a wide variety of plants and plays an extremely important role in plant growth, development and stress responses. However, systematic studies of F-box family have not been reported in populus trichocarpa. In the present study, 245 PtrFBX proteins in total were identified, and a phylogenetic tree was constructed on the basis of their C-terminal conserved domains, which was divided into 16 groups (A–P). F-box proteins were located in 19 chromosomes and six scaffolds, and segmental duplication was main force for the evolution of the F-box family in poplar. Collinearity analysis was conducted between poplar and other species including Arabidopsis thaliana, Glycine max, Anemone vitifolia Buch, Oryza sativa and Zea mays, which indicated that poplar has a relatively close relationship with G. max. The promoter regions of PtrFBX genes mainly contain two kinds of cis-elements, including hormone-responsive elements and stress-related elements. Transcriptome analysis indicated that there were 82 differentially expressed PtrFBX genes (DEGs), among which 64 DEGs were in the roots, 17 in the leaves and 26 in the stems. In addition, a co-expression network analysis of four representative PtrFBX genes indicated that their co-expression gene sets were mainly involved in abiotic stress responses and complex physiological processes. Using bioinformatic methods, we explored the structure, evolution and expression pattern of F-box genes in poplar, which provided clues to the molecular function of F-box family members and the screening of salt-tolerant PtrFBX genes.

Abstract An elastic and safe electrolyte is demanded for flexible batteries. Herein, a stretchable solid electrolyte comprised of crosslinked elastic polymer matrix, poly(vinylidene fluoride‐hexafluoropropylene) (PVDF‐HFP), and flameproof triethyl phosphate (TEP) is fabricated, which exhibits ultrahigh elongation of 450%, nonflammability and ionic conductivity above 1 mS cm−1. In addition, in order to improve the interface compatibility between the electrolyte and Li anode and stabilize the solid‐electrolyte interphase (SEI), a protecting layer containing poly(ethylene oxide) (PEO) is designed to effectively prevent the anode from reacting with TEP and optimize the chemical composition in SEI, leading to a tougher and more stable SEI on the anode. The LiFePO4/Li cells employing this double‐layer electrolyte exhibit an 85.0% capacity retention after 300 cycles at 1 C. Moreover, a flexible battery based on this solid electrolyte is fabricated, which can work in stretched, folded, and twisted conditions. This design of a stretchable double‐layer solid electrolyte provides a new concept for safe and flexible solid‐state batteries.

Abstract Rational design of hybrid carbon host with high electrical conductivity and strong adsorption toward soluble lithium polysulfides is the main challenge for achieving high-performance lithium–sulfur batteries (LSBs). Herein, novel binder-free Ni@N-doped carbon nanospheres (N-CNSs) films as sulfur host are firstly synthesized via a facile combined hydrothermal-atomic layer deposition method. The cross-linked multilayer N-CNSs films can effectively enhance the electrical conductivity of electrode and provide physical blocking “dams” toward the soluble long-chain polysulfides. Moreover, the doped N heteroatoms and superficial NiO layer on Ni layer can work synergistically to suppress the shuttle of lithium polysulfides by effective chemical interaction/adsorption. In virtue of the unique composite architecture and reinforced dual physical and chemical adsorption to the soluble polysulfides, the obtained Ni@N-CNSs/S electrode is demonstrated with enhanced rate performance (816 mAh g−1 at 2 C) and excellent long cycling life (87% after 200 cycles at 0.1 C), much better than N-CNSs/S electrode and other carbon/S counterparts. Our proposed design strategy offers a promising prospect for construction of advanced sulfur cathodes for applications in LSBs and other energy storage systems.

Abstract Controllable synthesis of highly active micro/nanostructured metal electrocatalysts for oxygen evolution reaction (OER) is a particularly significant and challenging target. Herein, we report a 3D porous sponge-like Ni material, prepared by a facile hydrothermal method and consisting of cross-linked micro/nanofibers, as an integrated binder-free OER electrocatalyst. To further enhance the electrocatalytic performance, an N-doping strategy is applied to obtain N-doped sponge Ni (N-SN) for the first time, via NH3 annealing. Due to the combination of the unique conductive sponge structure and N doping, the as-obtained N-SN material shows improved conductivity and a higher number of active sites, resulting in enhanced OER performance and excellent stability. Remarkably, N-SN exhibits a low overpotential of 365 mV at 100 mA cm−2 and an extremely small Tafel slope of 33 mV dec−1, as well as superior long-term stability, outperforming unmodified sponge Ni. Importantly, the combination of X-ray photoelectron spectroscopy and near-edge X-ray adsorption fine structure analyses shows that γ-NiOOH is the surface-active phase for OER. Therefore, the combination of conductive sponge structure and N-doping modification opens a new avenue for fabricating new types of high-performance electrodes with application in electrochemical energy conversion devices.

Abstract For efficient electrolysis of water for hydrogen generation or other value-added chemicals, it is highly relevant to develop low-temperature synthesis of low-cost and high-efficiency metal sulfide electrocatalysts on a large scale. Herein, we construct a new core–branch array and binder-free electrode by growing Ni3S2 nanoflake branches on an atomic-layer-deposited (ALD) TiO2 skeleton. Through induced growth on the ALD-TiO2 backbone, cross-linked Ni3S2 nanoflake branches with exposed {$$\bar{2}10$$ 2¯10 } high-index facets are uniformly anchored to the preformed TiO2 core forming an integrated electrocatalyst. Such a core–branch array structure possesses large active surface area, uniform porous structure, and rich active sites of the exposed {$$\bar{2}10$$ 2¯10 } high-index facet in the Ni3S2 nanoflake. Accordingly, the TiO2@Ni3S2 core/branch arrays exhibit remarkable electrocatalytic activities in an alkaline medium, with lower overpotentials for both oxygen evolution reaction (220 mV at 10 mA cm−2) and hydrogen evolution reaction (112 mV at 10 mA cm−2), which are better than those of other Ni3S2 counterparts. Stable overall water splitting based on this bifunctional electrolyzer is also demonstrated.

Electrode materials are key factors for supercapacitors to endow them with excellent electrochemical properties. Here, a novel hybrid structure of a CoSe/Co3O4-CNTs binder free composite electrode on nickel foam was prepared via a facile flame method, followed by an electrodeposition process. Benefitting from the synergetic effects of the multicomponent (with low resistances of 1.542 Ω cm2 and a moderate mesoporous size of 3.12 nm) and the enlarged specific surface area of the composite material (77.4 m2 g−1), the CoSe/Co3O4-CNTs composite electrode delivers a high specific capacitance of 2906 F g−1 at 5 mV s−1 with an excellent rate stability. The fabricated CoSe/Co3O4-CNTs/NF//AC ASC exhibits a high energy density of 43.4 Wh kg−1 at 0.8 kW kg−1 and a long cycle life (92.7% capacitance retention after 10,000 cycles).

High levels of toxic organic pollutants commonly detected during domestic/industrial wastewater treatment have been attracting research attention globally because they seriously threaten human health. Sulfate-radical-based advanced oxidation processes (SR-AOPs) have been successfully used in wastewater treatment, such as that containing antibiotics, pesticides, and persistent organic pollutants, for refractory contaminant degradation. This review summarizes activation methods, including physical, chemical, and other coupling approaches, for efficient generation of sulfate radicals and evaluates their applications and economic feasibility. The degradation behavior as well as the efficiency of the generated sulfate radicals of typical domestic and industrial wastewater treatment is investigated. The categories and characteristics of the intermediates are also evaluated. The role of sulfate radicals, their kinetic characteristics, and possible mechanisms for organic elimination are assessed. In the last section, current difficulties and future perspectives of SR-AOPs for wastewater treatment are summarized.

This study statistically reported the current state of sludge treatment/disposal in China from the aspects of sources, technical routes, geographical distribution, and development by using observational data after 1978. By the end of 2019, 5476 municipal wastewater treatment plants were operating in China, leading to an annual sludge productivity of 39.04 million tons (80% water content). Overall, 29.3% of the sludge in China was disposed via land application, followed by incineration (26.7%) and sanitary landfills (20.1%). Incineration, compost, thermal hydrolysis and anerobic digestion were the mainstream technologies for sludge treatment in China, with capacities of 27,122, 11,250, 8342 and 6944 t/d in 2019, respectively. Incineration and drying were preferentially constructed in East China. In contrast, sludge compost was most frequently used in Northeast China (46.5%), East China (22.4%) and Central China (12.8%), while anaerobic digestion in East China, North China and Central China. The capacities of sludge facilities exhibited a sharp increase in 2009–2019, with an overall greenhouse gas emissions in China in 2019 reached 108.18 × 108 kg CO2-equivaient emissions, and the four main technical routes contributed as: incineration (45.11%) > sanitary landfills (23.04%) > land utilization (17.64%) > building materials (14.21%). Challenges and existing problems of sludge disposal in China, including high CO2 emissions, unbalanced regional development, low stabilization and land utilization levels, were discussed. Finally, suggestions regarding potential technical and administrative measures in China, and sustainable sludge management for developing countries, were also given.

The notorious lithium dendrite growth, causing the safety concern, hinders the practical application of high-capacity Li metal anodes for rechargeable batteries. Here, a robust and highly ionic conductive solid electrolyte interphase (SEI) layer to protect Li metal anode is in-situ constructed by introducing trace additive of tetrapotassium heptaiodobismuthate (K4BiI7) into electrolyte. The K4BiI7-added electrolyte enables Li metal anode to display a stable cycling for over 600 cycles at 1.0 mA cm−2/1.0 mAh cm−2 and over 400 cycles at 5.0 mA cm−2/5.0 mAh cm−2. In situ optical microscopy observations also conform the suppression of Li dendrites at high current density. Moreover, the in-situ SEI layer modified Li anode exhibits an average Coulombic efficiency of 99.57% and less Li dendrite growth. The Li-S full sells with the modified electrolyte also show improved electrochemical performance. This research provides a cost-efficient method to achieve a highly ionic conductive and stable SEI layer toward advanced Li metal anodes.

Developing cost-effective advanced carbon anode is critical for innovation of sodium ion batteries. Herein, we develop a powerful combined method for rational synthesis of free-standing binder-free carbon nanospheres arrays via chemical bath plus hydrothermal process. Impressively, carbon spheres with diameters of 150–250 nm are randomly interconnected with each other forming highly porous arrays. Positive advantages including large porosity, high surface and strong mechanical stability are combined in the carbon nanospheres arrays. The obtained carbon nanospheres arrays are tested as anode material for sodium ion batteries (SIBs) and deliver a high reversible capacity of 102 mAh g−1 and keep a capacity retention of 95% after 100 cycles at a current density of 0.25 A g−1 and good rate performance (65 mAh g−1 at a high current density of 2 A g−1). The good electrochemical performance is attributed to the stable porous nanosphere structure with fast ion/electron transfer characteristics.

Improving the utilization efficiency of active materials and suppressing the dissolution of lithium polysulfides into the electrolyte are very critical for development of high-performance lithium-sulfur batteries. Herein, a novel strategy is proposed to construct a three-dimensional (3D) N-doped carbon nanotubes (CNTs) networks to support lithium polysulfides (3D-NCNT-Li2S6) as a binder-free cathode for high-performance lithium-sulfur batteries. The 3D N-doped CNTs networks not only provide a conductive porous 3D architecture for facilitating fast ion and electron transport but also create void spaces and porous channels for accommodating active sulfur. In addition, lithium polysulfides can be effectively confined among the networks through the chemical bond between Li and N. Owing to the synergetic effect of the physical and chemical confinement for the polysulfides dissolution, the 3D-NCNT-Li2S6 cathodes exhibit enhanced charge capacity and cyclic stability with lower polarization and faster redox reaction kinetics. With an initial discharge capacity of 924.8 mAh g−1 at 1 C, the discharge capacity can still maintain 525.1 mAh g−1 after 200 cycles, which is better than that of its counterparts.

In the original publication Figure S4 is an ancillary image to compare the specific surface areas of TiO2/Ni3S2 and Ni3S2 samples was incorrectly published.

Amorphous carbon is considered as a prospective and serviceable anode for the storage of sodium. In this contribution, we illuminate the transformation rule of defect/void ratio and the restrictive relation between specific capacity and rate capability. Inspired by this mechanism, ratio of plateau/slope capacity is regulated via temperature-control pyrolysis. Moreover, pore-forming reaction is induced to create defects, open up the isolated voids, and build fast ion channels to further enhance the capacity and rate ability. Numerous fast ion channels, high ion-electron conductivity, and abundant defects lead the designed porous hard carbon/Co3O4 anode to realize a high specific capacity, prolonged circulation ability, and enhanced capacity at high rates. This research deepens the comprehension of sodium storage behavior and proposes a fabrication approach to achieve high performance carbonaceous anodes for sodium-ion batteries.

Sodium ion batteries are a promising alternative to lithium ion technology, however their sluggish sodiation kinetics currently hinder performance. Here the authors fabricate ultrathin layered tin(II) sulfide nanostructures displaying a pseudocapacitance contribution for high capacity sodium ion anodes.

Abstract Exploring advanced high‐rate anodes is of great importance for the development of next‐generation high‐power lithium‐ion batteries (LIBs). Here, novel carbon nanotubes (CNTs)/Li4Ti5O12 (LTO) core/shell arrays on carbon cloth (CC) as integrated high‐quality anode are constructed via a facile combined chemical vapor deposition–atomic layer deposition (ALD) method. ALD‐synthesized LTO is strongly anchored on the CNTs' skeleton forming core/shell structures with diameters of 70–80 nm the combined advantages including highly conductive network, large surface area, and strong adhesion are obtained in the CC‐LTO@CNTs core/shell arrays. The electrochemical performance of the CC‐CNTs/LTO electrode is completely studied as the anode of LIBs and it shows noticeable high‐rate capability (a capacity of 169 mA h g−1 at 1 C and 112 mA h g−1 at 20 C), as well as a stable cycle life with a capacity retention of 86% after 5000 cycles at 10 C, which is much better than the CC‐LTO counterpart. Meanwhile, excellent cycling stability is also demonstrated for the full cell with LiFePO4 cathode and CC‐CNTs/LTO anode (87% capacity retention after 1500 cycles at 10 C). These positive features suggest their promising application in high‐power energy storage areas.

Abstract Designing ever more efficient and cost‐effective bifunctional electrocatalysts for oxygen/hydrogen evolution reactions (OER/HER) is greatly vital and challenging. Here, a new type of binder‐free hollow TiO2@Co9S8 core–branch arrays is developed as highly active OER and HER electrocatalysts for stable overall water splitting. Hollow core–branch arrays of TiO2@Co9S8 are readily realized by the rational combination of crosslinked Co9S8 nanoflakes on TiO2 core via a facile and powerful sulfurization strategy. Arising from larger active surface area, richer/shorter transfer channels for ions/electrons, and reinforced structural stability, the as‐obtained TiO2@Co9S8 core–branch arrays show noticeable exceptional electrocatalytic performance, with low overpotentials of 240 and 139 mV at 10 mA cm−2 as well as low Tafel slopes of 55 and 65 mV Dec−1 for OER and HER in alkaline medium, respectively. Impressively, the electrolysis cell based on the TiO2@Co9S8 arrays as both cathode and anode exhibits a remarkably low water splitting voltage of 1.56 V at 10 mA cm−2 and long‐term durability with no decay after 10 d. The versatile fabrication protocol and smart branch‐core design provide a new way to construct other advanced metal sulfides for energy conversion and storage.

Rational design/fabrication of integrated porous metal oxide arrays is critical for the construction of advanced electrochemical devices. Herein, we report self-supported CuO/C core/shell nanowire arrays prepared by the combination of electro-deposition and chemical vapor deposition methods. CuO/C nanowires with diameters of ~400 nm grow quasi-vertically to the substrates forming three-dimensional arrays architecture. A thin carbon shell is uniformly coated on the CuO nanowire cores. As an anode of lithium ion batteries, the resultant CuO/C nanowire arrays are demonstrated to have high specific capacity (672 mAh·g−1 at 0.2 C) and good cycle stability (425 mAh·g−1 at 1 C up to 150 cycles). The core/shell arrays structure plays positive roles in the enhancement of Li ion storage due to fast ion/electron transfer path, good strain accommodation and sufficient contact between electrolyte and active materials.