Search

Polyaniline (PANI) has long been explored as a promising organic cathode for Li-ion batteries. However, its poor electrochemical utilization and cycling instability cast doubt on its potential for practical applications. In this work, we revisit the electrochemical performance of PANI in nonaqueous electrolytes, and reveal an unprecedented reversible capacity of 197.2 mAh g−1 (244.8 F g−1) when cycled in a wide potential range of 1.5 to 4.4 V vs. Li+/Li. This ultra-high capacity derives from 70% -NH- transformed to =NH+- during deep charging/discharging process. This material also demonstrates a high average coulombic efficiency of 98%, an excellent rate performance with 73.5 mAh g−1 at 1800 mA g−1, and retains 76% of initial value after 100 cycles, which are among the best reported values for PANI electrodes in battery applications. [ABSTRACT FROM AUTHOR]

While biochar and manure can provide considerable benefits to soil properties, how these amendments may alter soil microbial activity and decomposition processes remains unknown. In a split‐split‐split‐plot experiment, we amended a sandy loam soil with three rates of manure (whole plot; 0, 3, 9 Mg ha−1) and biochar (split‐plot; 0, 2.5, 10 Mg ha−1), and installed three species of wood stakes (split‐split‐split plot; triploid poplar, Populus tomentosa Carr.; trembling aspen, Populus tremuloides Michx.; and loblolly pine, Pinus taeda L.) on the soil surface and in the mineral soil (split‐split plot) to serve as a substrate for microbial degradation. Wood stakes were sampled 3 years after installation to assess decomposition rates (mass loss), and changes in wood carbon (C) and nitrogen (N). In addition, soil extracellular enzyme activities at the 0–20 cm depth were examined. Biochar alone, especially 10 Mg ha−1, increased wood stake decomposition and moisture content on the soil surface and in the mineral soil. Manure at the rate of 9 Mg ha−1 increased soil N‐acetyl‐β‐D‐glucosaminidase, α‐glucosidase, and aryl sulfatase activities by 91%, 17%, and 48% respectively. Because of the synergistic benefits of biochar and manure, we suggest that, in this climatic regime and soil texture, 10 Mg ha−1 biochar can be used for soil C sequestration and soil quality improvement, and 9 Mg ha−1 manure can be used in combination with biochar to build soil organic matter in plantations. [ABSTRACT FROM AUTHOR]

Reconstructing a well-supported phylogenetic relationship among species is a prerequisite for biological and evolutionary researches. Chondrichthyes (sharks, rays, skates and chimaeras) serves as an important clade of highly commercial, ecological, evolutionary, and conservation significance. Yet the genome-scale data of chondrichthyans are lacking, which largely restrict phylogeny, evolution, and conservation investigations of these species. Recently reported 1105 orthologous exon markers generated for ray-finned fishes are powerful tools for phylogenomics inferences. Given the relatively close relationship between cartilaginous and ray-finned fish species, we purposed to verify whether these 1105 genomic exon markers generated for ray-finned fishes were applicable for chondrichthyan phylogenomics. In this study, we collected publically available 10 genomes and 30 transcriptomes of chondrichthyans to conduct the phylogenomics analysis. Phylogenomics analyses based on the 1105 genomic exon markers and the Benchmarking Universal Single-Copy Orthologs (BUSCO) approach were performed to reconstruct phylogenetic relationships of investigated chondrichthyans. We also attempted to apply these exon markers for phylogeny of 26 jawed fish species. Our results revealed well-supported and almost identical phylogenetic relationships of chondrichthyans, confirming the applicability of genomic exon markers of ray-finned fishes in chondrichthyan phylogeny. Moreover, phylogenomics analyses of 26 jawed fish species further confirmed the application of these genomic exon markers in both cartilaginous and lobe-finned fish phylogeny. Our results highlighted the wide-ranging utility of genomic markers of ray-finned fishes in phylogenetic inference of cartilaginous and lobe-finned fish species and provided substantial and background information for the evolutionary biology and conservation of chondrichthyans and related fish species. [ABSTRACT FROM AUTHOR]

Biochar and manure can be used for sustainable land management. However, little is known about how soil amendments might affect surface and belowground microbial processes and subsequent wood decomposition. In a split‐split‐split plot design, we amended soil with two rates of manure (whole plot; 0 and 9 Mg ha−1) and biochar (split plot; 0 and 10 Mg ha−1). Wood stakes of three species (hybrid poplar, triploid Populus tomentosa Carr.; aspen, Populus tremuloides Michx.; and pine, Pinus taeda L.) were placed in two positions (horizontally on the soil surface, and inserted vertically in the mineral soil), which served as a substrate for fungal growth. In 3 years, the decomposition rate (density loss), moisture content, and fungal community (via high‐throughput sequencing methods) of stakes were evaluated. Results indicated that biochar and/or manure increased the wood stake decomposition rates, moisture content, and operational taxonomic unit abundance. However, the richness and diversity of fungi were dependent on wood stake position (surface > mineral), species (pine > the two Populus), and sample dates. This study highlights that soil amendment with biochar and/or manure can alter the fungal community, which in turn can enhance an important soil process (i.e., decomposition). [ABSTRACT FROM AUTHOR]

This paper investigates group consensus for linear multi-agent systems with nonidentical dynamics. A novel adaptive event-triggered communication scheme is presented by using the stochastic sampling information, the event-triggered matrices and time-varying event-triggered parameters are introduced into event-triggered condition, where event-triggered parameters can be adjusted with the system dynamics evolving. The group consensus protocol is designed based on the neighboring agents information at event-triggered instants, then a new stochastic sampled-data dependent error model is constructed, some group consensus criteria in mean-square can be derived and the feedback matrices can also be obtained. Finally, two numerical examples are provided to illustrate the validity of the theoretical results. [ABSTRACT FROM AUTHOR]

Doctors' diagnosis preferences are different, which makes them adopt different assumptions in medical decision making. Taking the diagnosis of thyroid nodules as an example, this study compares three assumptions, namely deletion, imputation based on the distribution (distribution), and benign by default (benign). For deletion, which is the most used assumption, the clinical reports with missing features would be deleted. For distribution, the missing features would be replaced with a distribution of features with respective probabilities. Besides the two assumptions, certain doctors have also stated that they leave benign features unrecorded because they think that such benign features are irrelevant to the final diagnosis. Under the benign assumption, the missing features would be replaced with benign features. The three assumptions are tested comparatively. Moreover, the belief rule base (BRB) is used to construct the diagnostic model under the three assumptions since it is essentially a white-box approach that can provide good interpretability and direct access to doctors and patients. A total of 3766 clinical reports on thyroid nodule diagnosis were collected from ten radiologists over a seven-year period. Case study results validate that the benign by default assumption has produced the optimal results, although different doctors could present varied tendencies towards different assumptions. Guidance and suggestions for doctors' practical work have been made based on the study results to improve work efficiency and diagnostic accuracy. [ABSTRACT FROM AUTHOR]

In this paper, we focus on parametric interval-valued full implication algorithms. The interval-valued full implication algorithms based on a class of interval-valued t-norms with parameters are proposed. Meanwhile, the [ a , b ] -type interval-valued full implication algorithms based on a class of interval-valued t-norms with parameters are introduced. Furthermore, the solutions of these algorithms are given. Finally, the proposed algorithms are applied to pattern recognition. [ABSTRACT FROM AUTHOR]

Artificial interfaces can alleviate the side reactions and the formation of the metallic (e.g., Li, Na, and Zn) dendrites. However, the traditional ones always breakdown during the repeated plating/stripping and fail to regulate the electrodeposition behaviors of the electrodes. Herein, a self‐healable ion regulator (SIR) is designed as a desolvation shield to protect the Zn electrodes and guide the Zn electrodeposition. Benefiting from the intermolecular hydrogen bonds, SIR shows a superb capability to in situ repair the plating/stripping‐induced cracks. Besides, the results of theoretical calculations and electrochemical characterizations show that the coating reduces water molecules in the solvated sheath of hydrated Zn2+ and restrains the random Zn2+ diffusion on the Zn surface. Even with a coating layer of only 360 nm, the SIR‐modified Zn electrode exhibits excellent long‐term stability for >3500 h at 2 mAh cm−2 and >950 h at an ultrahigh areal capacity of 20 mAh cm−2. [ABSTRACT FROM AUTHOR]

Artificial interfaces can alleviate the side reactions and the formation of the metallic (e.g., Li, Na, and Zn) dendrites. However, the traditional ones always breakdown during the repeated plating/stripping and fail to regulate the electrodeposition behaviors of the electrodes. Herein, a self‐healable ion regulator (SIR) is designed as a desolvation shield to protect the Zn electrodes and guide the Zn electrodeposition. Benefiting from the intermolecular hydrogen bonds, SIR shows a superb capability to in situ repair the plating/stripping‐induced cracks. Besides, the results of theoretical calculations and electrochemical characterizations show that the coating reduces water molecules in the solvated sheath of hydrated Zn2+ and restrains the random Zn2+ diffusion on the Zn surface. Even with a coating layer of only 360 nm, the SIR‐modified Zn electrode exhibits excellent long‐term stability for >3500 h at 2 mAh cm−2 and >950 h at an ultrahigh areal capacity of 20 mAh cm−2. [ABSTRACT FROM AUTHOR]

The construction of ratiometric fluorescent MOF sensors with integrated self-calibration and dual-channel detection can efficiently overcome the deficiencies of single-signal sensing. In this regard, the rational design of structurally functionalized MOFs is paramount for enhancing their performance in ratiometric fluorescent sensors. Lately, the concept of MOF-on-MOF design has garnered notable interest as a potential strategy for regulating the structural parameters of MOFs by integrating two or more distinct MOF types. Great efforts have been dedicated to exploring new MOF-on-MOF hybrids and developing their applications in diverse fields. Even so, these materials are still in the stage of advancement in the sensing field. Herein, a Zr-based metal-organic framework anchored on a rare-earth metal-organic framework (UiO-66(OH) 2 @Y-TCPP) was prepared for the ratiometric fluorescence detection toward Al (III) and pH. In this probe, the UiO-66(OH) 2 featured hydroxyl active sites for Al (III), leading to a significant enhancement in fluorescence intensity upon the addition of Al (III), while the signal emitted by the red-emitting Y-TCPP, serving as the reference, remained constant. UiO-66(OH) 2 @Y-TCPP exhibited excellent selectivity for Al (III) sensing with a wider linear range of 0.1–1000 μM, and a lower detection limit of 0.06 μM. This probe has also been utilized for the quantitative determination of Al (III) in hydrotalcite chewable tablets with satisfactory results. In addition, the probe realized ratiometric pH sensing in the range of 7–13 using UiO-66(OH) 2 as an interior reference. The paper-based probe strip was developed for visual pH sensing. By installing color recognition and processing software on a smartphone, real-time and convenient pH sensing could be achieved. This is the first ratiometric fluorescent sensor for Al (III) and pH detection based on a MOF-on-MOF composite probe, which yields two different response modes. The detection results of Al (III) in hydrotalcite chewable tables and smartphone imaging for pH test paper demonstrate the practicability of the probe. This work opens up a new outlook on constructing a multi-functional application platform with substantial potential for employment in environmental and biological analysis tasks. [Display omitted] • A novel fluorescent sensor based on MOF-on-MOF structure was designed. • UiO-66(OH) 2 @ Y-TCPP can achieve ratio fluorescence detection towards Al (III) and pH with two different response modes. • UiO-66(OH) 2 @ Y-TCPP has been successfully utilized to determinate Al (III) in hydrotalcite chewable tablets. • Smartphone-combined probe-immobilized test strips are proposed for pH detection. [ABSTRACT FROM AUTHOR]

[Display omitted] • A dual-emission fluorescent MOF has been synthesized based on the introduction of Eu3+ ions, into aluminum metal − organic frameworks. • The dual-emission Eu/Al-MOF is used to design the sensor for the quantitative detection of histidine and water by changing the independent fluorescence signals. • The Eu/Al-MOF has been successfully applied to the detection of histidine in urine samples. • The solid-state fluorescence of Eu/Al-MOF proves instrumental in visualizing and identifying fingerprints. Ratiometric fluorescent sensors possess inherent self-calibration features that enable the mitigation of interference from factors unrelated to the analysis. This characteristic results in heightened sensitivity and more pronounced visual detection during qualitative and quantitative analytical processes. A ratiometric fluorescence probe Eu/Al-MOF has been successfully prepared via Eu3+ doped aluminum metal − organic frameworks. Upon introducing histidine, the fluorescence intensity of Eu3+ showed a noteworthy increase, whereas the intensity originating from the ligand decreased owing to enhancing energy transfer from the ligand to Eu3+ ions in the probe. Eu/Al-MOF could detect histidine over a wider linear range of 0.1–400 μM and a lower detection limit of 0.04 μM. Besides, in the presence of water in organic solvents, the excited state of Eu3+ in the probe could be coupled with the O-H oscillation of water molecules, and the excited state energy from Eu3+ would be transferred to the water molecules so that only the fluorescence intensity of Eu3+ gradually decreased. Thus, the proportional detection of trace water could be realized. In ethanol and DMF, the detection range for water was 0.1–20 % and 0.5–20 %, respectively. Moreover, it was found that Eu/Al-MOF could efficiently achieve the visualization identification of fingerprints, providing the possibilities for applying the nano-sensor as a promising multifunctional fluorescence probe. [ABSTRACT FROM AUTHOR]

Data classification is an important and challenging issue encountered in many practical applications. The classifier based on Evidential Reasoning Rule (ER Rule) can well handle the uncertainty in classification and obtain competitive accuracy. However, there are many parameters to be optimized, and the computation cost of the usually adopted optimization strategy is relatively high. This fact weakens the application advantage of ER Rule classifier. To address this challenge, an asynchronous optimization approach is proposed. In the original ER Rule classifier, feature referential values and evidence weights are optimized synchronously; while in the proposed method, these two types of parameters are optimized separately based on their essential impacts on the classification results. For the optimization of feature referential values, the objective function measures the quality of belief matrix, which is the critical strategy to improve the computational efficiency. Three types of feasible objective functions are constructed. After obtaining optimal referential values, evidence weights are optimized based on the actual classification effect, and the required iterations decrease. Various experiments on 14 publicly available datasets verify the computational efficiency and classification performance of the proposed method. • The low computational efficiency of ER Rule-based classifier is addressed by optimizing its parameters asynchronously. • The objective function of feature referential values optimization measures the quality of belief matrix. • The effectiveness of the proposed method is validated by theoretical analysis and various experiments. [ABSTRACT FROM AUTHOR]

[Display omitted] • The V 2 O 5 films and devices exhibit multicolor electrochromic performances. • The calcination temperature is key factor for the successful preparation of V 2 O 5. • The V 2 O 5 film shows transmittance modulation in the visible and near infrared bands. • The V 2 O 5 films prepared at 400℃ have high cycling stability and reproducibility. V 2 O 5 films were facilely fabricated on indium tin oxide glasses by spin coating vanadyl oxalate precursor sols and subsequent calcination. The as-prepared V 2 O 5 films and devices exhibit multicolor electrochromic performances: yellow, green and blue. Calcination temperature, precursor concentration and applied power were found to largely affect the electrochromic properties of the V 2 O 5 films. The calcination temperature is key factor for the successful preparation of vanadium oxide films with electrochromic properties. V 2 O 5 film could be synthesized by calcining above 300 ℃ for 1 h. With the increase of temperature, the morphology of the film changes from flat plane to wrinkle and crack to rice-like nanoparticles and to nanoplate. The transmittance modulation in the near-infrared region is relatively high, and the maximum light modulation can reach to 48.3%. Cyclic voltammetry tests indicate that the as-prepared V 2 O 5 films have high cycling stability. After 1000 cycles, the V 2 O 5 films prepared at 400 ℃ still have excellent electrochromic properties. The coloration efficiency value is ca. 29.6 cm2/C at a wavelength of 890 nm and the exact coloring/bleaching times of the V 2 O 5 device are 12 s/18 s, respectively. The study provided a simple and low-cost method to fabricate V 2 O 5 films and their devices. [ABSTRACT FROM AUTHOR]

In order to improve the electrochemical properties of nano Si-carbon composites, a binder-free Si-CNTs composite with good dispersion of Si nanoparticles were prepared by ionic liquids self-assembly method. [Display omitted] • A binder-free Si-CNTs composites were prepared by ILs assisted self-assembly method. • The as-prepared Si-CNTs composites show ball-like structure, and the SiNPs are dispersed in the carbon nanotubes self-assembly uniformly. • The carbon nanotubes could be self-assembled into a 3D structure through electrostatic gravitational force of ILs, and the heteroatoms of ILs could dope in the carbon skeleton during annealing. • ILs plays an important role in the dispersion of SiNPs in Si-CNTs system. • Si30%-CNTs exhibit excellent cycle performance and rate capability. Binder-free nano silicon/carbon nanotube composites anodes were synthesized by electrostatic self-assembly of ionic liquids (ILs) and annealing process. The addition of [Emim]Tf 2 N ILs successfully improved the dispersion of silicon nanoparticles (SiNPs) in the carbon nanotubes (CNTs). And the carbon nanotubes could be self-assembled into a 3D structure network through electrostatic gravitational force. Moreover, the wettability of electrode also be improved due to the heteroatoms of [Emim]Tf 2 N ILs doped in the CNTs during annealing. By integrating these advantages, the Si30%-CNTs anodes exhibit a high initial reversible discharge capacity of 2580.3 mAh g−1 at a current density of 0.4 A g−1. Even at a much higher current density of 10 A g−1, the Si30%-CNTs anodes can still deliver a high reversible discharge capacity of 871.1 mAh g−1. The outstanding performances compared to traditional coating method are assigned to that the ionic liquids self-assembly method improves the dispersion of SiNPs. [ABSTRACT FROM AUTHOR]

Flat peach is one of the famous and characteristic table fruits in Xinjiang, China, and has attracted an increasing favorite because of its high nutrition and superior flavor. To evaluate the sensory properties and nutritional value of flat peach, functional components, antioxidant capacity, and aromatic compounds of five flat peach cultivars were measured by using high-performance liquid chromatography (HPLC) and headspace solid-phase microextraction coupled with gas chromatography-mass spectrometry (HS-SPME-GC-MS). The results indicated that sucrose, malic acid, and chlorogenic acid were the dominant sugars, organic acids, and phenolic compounds in flat peaches, respectively. The antioxidant activity ranged from 62 to 505.46 μmol TEs 100 g−1 FW. In addition, multivariate data analysis was used to discern differences in volatile compounds among different flat peach varieties, and 11 key aroma components were identified in combination with OAV analysis. These key aroma compounds interacted to present distinct green, fruity, floral, milk-like, sweet, and peach-like attributes and could be used as characteristic markers to distinguish the aroma of flat peach from other fruits. These results will provide a comprehensive chemical characterization of the edible quality, nutritional composition, and sensory properties of the five flat peach cultivars. • The functional components and aroma characteristics of flat peaches were comprehensively analyzed firstly. • QY had a higher level of polyphenol content and exhibited better antioxidant capacity than other four flat peach cultivars. • The key aroma compounds of five flat peach cultivars were successfully identified. • All tested flat peach cultivars grown in Xinjiang presented similar characteristic aromas. [ABSTRACT FROM AUTHOR]

Despite its merits of high specific capacity and intrinsic safety for aqueous zinc‐ion batteries (AZIBs), Zn metal as anode suffers from dendritic growth and severe corrosion during battery operation. Here, an electrolyte surfactant of succinimide (SI) that occupies the compact region of the electrical double layer (EDL) at the Zn/electrolyte interface, which protects the Zn surface from the parasitic corrosion in aqueous electrolytes is reported. More importantly, both theoretical calculation and electrochemical analysis demonstrate that the occupation of SI at the EDL can restrict the self‐diffusion of Zn adatoms and tune interfacial reaction kinetics during Zn deposition, thereby promoting small and dense nuclei rather than large Zn dendrites. Accordingly, SI surfactants enable a high Coulombic efficiency of 99.95% and a long cumulative plated capacity over 6800 mAh cm−2 at 20 mA cm−2 for 10 mAh cm−2. Moreover, the feasibility of SI is also demonstrated on a long‐term cycling stability in Zn‐VS2 batteries. [ABSTRACT FROM AUTHOR]

Stable solid electrolyte interphase (SEI) with high Li+‐ion conductivity is desperately desired for lithium (Li) metal anodes. However, it remains challenging to build a robust SEI rationally for the Li‐metal anodes in carbonate electrolytes. Herein, a heterogeneous nitride‐rich SEI that consists of organic nitrides on the surface and inorganic nitrides inside by stepwise‐reduction electrolyte design is constructed. The heterogeneous structure endows SEI with the capability to capture and distribute Li+ on the surface and facilitate internal Li+ transportation, leading to the redistributed Li+ flux and uniform Li electrodeposition. With the newly‐formulated carbonate electrolyte, Li||Cu cells deliver a high Coulombic efficiency of 98.0% after 300 cycles at 0.5 mA cm‐2 and 0.5 mAh cm‐2. Meanwhile, superb cycling stability is also determined with full Li‐metal cells using LiNi1/3Mn1/3Co1/3O2 and high‐loading LiFePO4 (12.0 mg cm−2) cathodes. This study provides a promising strategy to regulate the SEI components and stabilize the Li anodes by rational electrolyte design. [ABSTRACT FROM AUTHOR]

Electrochemical hydrogen storage can realize reversible hydrogen absorption and desorption at room temperature and pressure, which has attracted extensive attention recently. A nanosheet-like reduced graphene oxide (rGO)-porous carbon composite with N-doping defect is prepared via a facile annealing, followed by hydrothermal and freeze-drying process. After N-doping, the porous carbon materials exhibit rich pore structure, and high pyridine nitrogen and pyrrolic nitrogen content. Adding them into the graphene self-assembly process, the aggregation tendency of graphene sheets can be reduced, the composite shows a free-standing 3D porous structure. Benefit from the synthetic effect between the rGO conductive network, the hierarchical porous structure, and the doping of N atoms, the rGO-N800 delivers a high hydrogen storage capacity of 266.3 mAh g−1 at 200 mA g−1 after 100 cycles. Moreover, the reversible capacities of the composite can reach 288.4, and 267.1 mAh g−1 at 1000 mA g−1 and 2000 mA g−1, respectively. The outstanding electrochemical performance of the composite demonstrates a promising direction for design carbon-based hydrogen storage materials. A nanosheet-like 3D free-standing reduced graphene oxide/porous-carbon composite with N- doping defect was prepared via a facile annealing, followed by hydrothermal and freeze-drying process for improving electrochemical hydrogen storage performance of porous carbon materials. [Display omitted] • The rGO/N-doping porous carbon electrode was prepared via an annealing, combined with hydrothermal and freeze-drying. • The as-prepared composites show nanosheet-like 3D structure, the N-doping porous carbon anchored on the surface of rGO. • Effects of different annealing conditions on doping N content and forms were investigated. • Benefit from the synthetic effect of rGO and N-doping defects, rGO-N800 shows an excellent hydrogen storage performance. [ABSTRACT FROM AUTHOR]

Poor interfacial contacts of Li mental/solid‐state electrolytes (SSEs) cause high impedance and induce lithium dendrite growth, which hinders the practical viability of solid‐state batteries (SSBs). Optimizing the surface chemistry of SSEs has been widely adopted for improving the Li/SSE interfacial contact. Their surface's microstructure, another critical factor influencing the actual performance of SSBs, however, has seldom been paid attention to; and the corresponding mechanism remains unclear. Addressing this issue, the authors herein propose a "surface microstructure optimization" strategy that can significantly enhance the Li/SSE interfacial contact, and in the meantime, quantify the correlations between SSB's performance and SSE's surface roughness regarding the interfacial resistance, current focusing, critical current density (CCD), and lithium deposition. Based on these fundamental understandings, a low‐surface‐roughness SSE is developed, which shows extremely small interfacial impedance (1.7 Ω cm2) and ultra‐long stable cycling life (4500 h at 0.2 mA cm−2). This work not only comprehensively demonstrates the fundamental relationship between the surface microstructure of SSEs and their battery performance but also presents a new insight into the modulation of surface kinetics of ceramic SSEs toward achieving dendrite‐free SSBs. [ABSTRACT FROM AUTHOR]

• Zn 2 GeO 4 nanorods were anchored on nickel foam as a binder free anode for SIBs. • Zn 2 GeO 4 @NF anode shows 3D interlinked porous network structure. • The Zn 2 GeO 4 @NF showed excellent electrochemical sodium storage performances. Large-scale energy storage and scarcity of lithium bring exploration interest of high-performance anode materials for sodium-ion batteries (SIBs). Herein, Zn 2 GeO 4 nanorods was anchored directly on nickel foam to form a free standing, binder free anode for SIBs, though a facile hydrothermal method. Benefiting from composite effect of nanorod network structure, conductive network and mechanical stability, the Zn 2 GeO 4 @NF reaches an initial discharge capacity of 882.0 mAh/g and maintains a capacity of 435.6 mAh/g after 400 cycles at 0.1A/g. At a higher current density (2 A/g) Zn 2 GeO 4 @NF also delivers a reversible discharge capacity of 239.7 mAh/g, which is higher than that for the Zn 2 GeO 4 particles. [ABSTRACT FROM AUTHOR]

[Display omitted] A three-dimensional LiCl/Li-Al hybrid protective layer is constructed on the lithium metal anode surface, which can effectively facilitate homogeneous Li+ flux distribution and induce even Li nucleation, leading to excellent dendrite inhibition ability and durable interface stability. • Li metal anode surface is modified by a simple salt solution pre-treatment strategy. • A 3D LiCl/Li-Al hybrid interface layers is in-situ constructed on Li metal surface. • The hybrid layer adjusts homogenous ions environment to induce stable Li deposition. • The quasi-solid-state lithium metal batteries deliver excellent cycle stability. The quasi-solid-state metal battery stands out as a promising candidate for the advancement of scalable, safe, and high-performance battery technologies. However, a major challenge remains in the form of short circuits arising from dendrite penetration, a consequence of uneven lithium deposition at the solid electrolyte/lithium anode interface. To address this issue, an in-situ constructed three-dimensional LiCl/Li-Al hybrid protective layer was implemented to inhibit the growth of dendrites. The enhanced interfacial dynamics were meticulously elucidated through a synergistic analysis of simulation and experimental results, highlighting the facilitation of Li+ flux distribution and uniform mass transfers introduced by the lithiophilic Li-Al alloy component. As a result, the modified Li anode enables stable Li stripping/plating cycling at a high current density of 1.0 mA·cm−2 and over 500 h at 0.2 mA·cm−2 for 0.2 mAh·cm−2 in the quasi-solid-state symmetric batteries. Additionally, the full cell with a LiFePO 4 cathode maintains a high discharge capacity of 136.2 mAh/g after 400 cycles at 0.5C with a capacity retention of approximately 90 %. These findings demonstrate the application potential of Li anodes with a surface treatment for quasi-solid-state lithium metal battery applications. [ABSTRACT FROM AUTHOR]

Herein, nanosized fumed silica (FS) with poor electrical conductivity is used as an "electron inhibitor" between Li metal and garnet solid electrolyte (SE) to prevent lithium dendrite growth. The FS demonstrated its effectiveness in preventing the fast lithium dendrite propagation during the long-term lithium stripping and plating processes, leading to an enhanced battery performance. We believe this study could help shed light on such electron inhibitors in constructing all-solid-state batteries (ASSBs) with superior cycling performance. [ABSTRACT FROM AUTHOR]

The effects of CO2-water-rock interactions on the injectivity and safety of CO2 geological storage have drawn wide attention. The geochemical reaction mechanisms in carbonate formations after CO2 injection are still controversial. To better understand the transformation of injected CO2 in carbonates and the involved geochemical reactions, we first conducted autoclave experiments reproducing the in-situ conditions of the Lianglitage Formation, Yingshan Formation, and Qiulitage Formation at the Tazhong Uplift in the Tarim Basin. We then established a batch model using TOUGHREACT-ECO2H, validated with the experimental results, to simulate the long-term CO2-water-rock interactions. It was found that the initial mineral compositions and water chemistry have important effects on the CO2-water-rock interactions in carbonate formations. The experiment results show that the dissolution of calcite and dolomite dominates in the early reaction period. However, we still observed some secondary minerals, such as ankerite, montmorillonite, calcite, and dolomite. The CO2-water-rock reactions can be more dramatic when the contents of calcite and dolomite in carbonates are closer. Moreover, the long-term simulation results show that calcite, magnesite, and hematite are the main formed secondary minerals, whereas dolomite is the major dissolved mineral. This study is helpful for a better understanding of the CO2 mineral trapping mechanism in carbonate formations. [ABSTRACT FROM AUTHOR]

In conifers, somatic embryogenesis is uniquely initiated from immature embryos in a narrow time window, which is considerably hindered by the difficulty to induce embryogenic tissue (ET) from other tissues, including mature somatic embryos. In this study, the embryogenic ability of newly induced ET and DNA methylation levels was detected, and whole-transcriptome sequencing analyses were carried out. The results showed that ultra-low temperature treatment significantly enhanced ET induction from mature somatic embryos, with the induction rate from 0.4% to 15.5%, but the underlying mechanisms remain unclear. The newly induced ET showed higher capability in generating mature embryos than the original ET. DNA methylation levels fluctuated during the ET induction process. Here, WGCNA analysis revealed that OPT4, TIP1-1, Chi I, GASA5, GST, LAX3, WRKY7, MYBS3, LRR-RLK, PBL7, and WIN1 genes are involved in stress response and auxin signal transduction. Through co-expression analysis, lncRNAs MSTRG.505746.1, MSTRG.1070680.1, and MSTRG.33602.1 might bind to pre-novel_miR_339 to promote the expression of WRKY7 genes for stress response; LAX3 could be protected by lncRNAs MSTRG.1070680.1 and MSTRG.33602.1 via serving as sponges for novel_miR_495 to initiate auxin signal transduction; lncRNAs MSTRG.505746.1, MSTRG.1070680.1, and MSTRG.33602.1 might serve as sponges for novel_miR_527 to enhance the expression of Chi I for early somatic embryo development. This study provides new insight into the area of stress-enhanced early somatic embryogenesis in conifers, which is also attributable to practical applications. [ABSTRACT FROM AUTHOR]

Keywords: interfacial wettability; lithium metal batteries; solid-state batteries; surface microstructure EN interfacial wettability lithium metal batteries solid-state batteries surface microstructure 1 1 1 06/06/23 20230602 NES 230602 B Lithium Metal Anodes b In article number 2300165, Xiaowei Wang, Jiafeng Zhang, Ji Liang, and co-workers present an innovative "surface microstructure optimization" approach to improve the interface contact between solid-state electrolytes and lithium metal anodes. Interfacial wettability, lithium metal batteries, solid-state batteries, surface microstructure Revealing the Influence of Surface Microstructure on Li Wettability and Interfacial Ionic Transportation for Garnet-Type Electrolytes (Adv. [Extracted from the article]

The spinel LiNi 0.5 Mn 1.5 O 4 (LNMO) material is considered as a promising cathode in high-voltage lithium-ion batteries due to its advantageous voltage and capacity. Previous results indicate that the electrodes constructed by LNMO with the same compositions while differing in the crystallite geometries always exhibit various electrochemical performances. Here, to probe the relationships between the crystalline geometry of the obtained cathodes and their electrochemical properties, we synthesized different facet-exposed LNMOs with the same compositions using a template method. We demonstrate that the crystallite geometries of the hydroxide precursors can be tuned easily via varying the synthesize parameters, while the tuned precursors can be employed as the templates during the final product preparation. LNMOs enclosed by single {111} facets (LNMO-OH) and both {110} and {100} facets (LNMO-HP) are obtained and employed to elucidate the particle geometry-dependent electrochemical properties. Despite better rate capabilities exhibited for LNMO-HP because of the higher lithium diffusion coefficients along these crystal orientations, inferior cycling performance is released compared with its LNMO-OH counterpart. These insights can provide informative guidance in particle geometry-dependent material construction, thus helpful in realizing high-performance LNMO cathode. • Different facet-exposed LNMOs with the same compositions were synthesized. • The crystallite geometries of the hydroxide precursors can be tuned easily via varying the synthesize parameters. • Facet-exposed LNMOs exhibit various electrochemical properties. • Working mechanism of different LNMOs was investigated. [ABSTRACT FROM AUTHOR]

A novel porous structure MnO-SiO x @C composite has been designed and prepared as an anode material for lithium-ion batteries through scalable spray pyrolysis and a subsequent annealing process. XRD, SEM, TEM, Raman, and BET measurements indicate that the MnO-SiO x @C composite displays a spherical mesoporous structure with SiO x particles, embedded in the porous MnO structure combined with carbon coated on the surfaces. The enhanced electrochemical performance can be attributed to the mutual segregation of the heterogeneous oxides of MnO and SiO x during delithiation and the buffer composition region at the origin of uniform carbon layers and abundant nanopores. In addition, the new phase Mn 2 SiO 4 , which is formed in the MnO-SiO x @C composite after 800 ºC, can act as the joint between MnO and SiO x to restrain the strain force originating from the volume change during the charge and discharge process. As a result, the obtained MnO-SiO x @C composite exhibits significantly enhanced electrochemical performance in terms of high Coulombic efficiency, excellent rate capability and good cyclability. • Porous MnO-SiO x @C microspheres was prepared by spray drying method. • MnO-SiO x @C samples show enhanced cycle stability and rate performance. • The Mn 2 SiO 4 phase played key role in improvement the structure stabilities. [ABSTRACT FROM AUTHOR]

[Display omitted] • A novel PDDA/GO dual-layer coating strategy to effectively improve the performance of NCM811 is proposed in this paper. • NCM811 particles can be well-encapsulated in the resultant dual-layer by a simple electrostatic adsorption method. • The PDDA/GO coating depresses the LiF component, enables a homogeneous organic-enriched CEI film with fast Li diffusion and effective corrosion protection on cathodes. • NCM811-PDDA/GO cathodes exhibit a 77% capacity retention after 500 cycles at the current density of 50 mA g−1, against 28% for pristine NCM811. Cathode-electrolyte interphases (CEIs) are determinative to the electrochemical performance of lithium-ion batteries, especially those with Ni-rich cathodes. Herein, we employed the simple electrostatic adsorption (SEA) method to generate a homogenous polydimethyldiallyl ammonium chloride/ graphene oxide (PDDA/GO) dual-layer coating on the surface of a model single-crystalline Ni-rich cathode, LiNi 0.8 Co 0.1 Mn 0.1 O 2 (NCM811), and thus modified the CEIs in both compositions and microstructures. The PDDA/GO coating depresses the LiF component, enables a homogeneous organic-enriched CEI film with fast Li diffusion and effective corrosion protection on cathodes. Together with the mechanical confinement on cathodes, these characters of modified CEIs benefit the electrochemical stability effectively. For instance, NCM811-PDDA/GO cathodes exhibit a 77% capacity retention after 500 cycles at the current density of 50 mA g−1, against 28% for pristine NCM811. This study provides new insights in correlating the coating and CEIs, which effectively guide the development of Ni-rich cathodes for high performance. Such a simple strategy to form a homogeneous coating can also be extended into other electrode materials easily. [ABSTRACT FROM AUTHOR]