Vanadium-Based Cathodes for Aqueous Zinc-Ion Batteries: Mechanisms, Challenges, and Strategies.

ConspectusZinc-ion batteries (ZIBs) are highly promising for large-scale energy storage because of their safety, high energy/power density, low cost, and eco-friendliness. Vanadium-based compounds are attractive cathodes because of their versatile structures and multielectron redox processes (+5 to +3), leading to high capacity. Layered structures or 3-dimensional open tunnel frameworks allow easy movement of zinc-ions without breaking the structure apart, offering superior rate-performance. However, challenges such as dissolution and phase transformation hinder the long-term stability of vanadium-based cathodes in ZIBs. Although significant research has been dedicated to understanding the mechanisms and developing high-performance vanadium-based cathodes, uncertainties still exist regarding the critical mechanisms of energy storage and dissolution, the actual active phase and the specific optimization strategy. For example, it is unclear whether materials such as α-V2O5, VO2, and V2O3 serve as the active phase or undergo phase transformations during cycling. Additionally, the root cause of V-dissolution and the role of byproducts such as Zn3(OH)2V2O7·2H2O in ZIBs are debated.In this account, we aim to outline a clear and comprehensive roadmap for V-based cathodes in ZIBs. On the basis of our studies, we analyzed intrinsic crystal structures and their correlation with performance to guide the design of V-based materials with high-capacity and high-stability for ZIBs. Then, we revealed the underlying mechanisms of energy storage and instability, enabling more effective design and optimization of V-based cathodes. After identifying the key challenges, we proposed effective design principles to achieve high cycling performance of V-based cathodes and outlined future development directions toward their practical application. Vanadium-based compounds include [VO4] tetrahedrons, [VO5] square pyramids, and [VO6] octahedra, which are connected through a cocorner, coedge and coplane. The [VO4] tetrahedron is inactive, and the [VO5] square pyramid is unstable in aqueous solutions because water attacks the exposed vanadium, whereas stable [VO6] octahedra are desirable because of their ability to reduce from +5 to +3 with minimal structural distortion. Therefore, high-performance vanadium-based oxides in ZIBs should maintain intact [VO6] octahedra while avoiding [VO4] tetrahedra or [VO5] square pyramids. The energy storage mechanism involves H2O/H+/Zn2+ coinsertion. The existence of interlayer water in V-based cathodes significantly improves the rate and cycling performance by expanding galleries, screening Zn2+ electrostatically via solvation, reducing ion diffusion energy barriers, and increasing layer flexibility. The insertion of H+/Zn2+ and the instability of V-based cathodes lead to the formation of byproducts such as basic zinc salts (i.e., Zn4SO4(OH)6·nH2O) and dead vanadium (Zn3(OH)2V2O7·2H2O), whose reversibility strongly affects long-term stability. To increase the cycling stability of vanadium-based cathodes, strategies such as electrolyte modulation and coating have been proposed to decrease water attack on the surface of V-oxides, thereby affecting the formation of byproducts. Additionally, in situ electrochemical transformation, ion preintercalation, and ion exchange were explored to prepare intrinsically stable V-based cathodes with enhanced performance. Furthermore, future research should focus on revealing atomic-scale mechanisms through advanced in situ characterization and theoretical calculations, enhancing rate-performance by facilitating ion/electron diffusion, promoting cycling stability by developing highly stable cathodes and refining interface engineering, and scaling up vanadium-based cathodes for practical ZIB applications.

Critical Issues of Vanadium-Based Cathodes Towards Practical Aqueous Zn-Ion Batteries.

Aqueous zinc-ion batteries (ZIBs) are gaining significant attention for their numerous advantages, including high safety, high energy density, affordability, and environmental friendliness. However, the development of ZIBs has been hampered by the lack of suitable cathode materials that can store Zn2+ with high capacity and reversibility. Currently, vanadium-based materials with tunnel or layered structures are widely researched owing to their high theoretical capacity and diversified structures. However, their long-term cycling stability is unsatisfactory because of material dissolution, phase transformation, and restrictive kinetics in aqueous electrolytes, which limits their practical applications. Different from previous reviews on ZIBs, this review specifically addresses the critical issues faced by vanadium-based cathodes for practical aqueous ZIBs and proposes potential solutions. Focusing on vanadium-based cathodes, their ion storage mechanisms, the critical parameters affecting their performance, and the progress made in addressing the aforementioned problems are also summarized. Finally, future directions for the development of practical aqueous ZIB are suggested.

Enhancing Energy Conversion Efficiency and Durability of Alkaline Nickel-Zinc Batteries with Air-Breathing Cathode.

Despite their high output voltage and safety advantages, rechargeable alkaline nickel-zinc batteries face significant challenges associated with the cathodic side reaction of oxygen evolution, which results in low energy efficiency (EE) and poor stability. Herein, we propose to leverage the side oxygen evolution reaction (OER) in nickel-zinc batteries by coupling electrocatalysts for oxygen reduction reactions (ORR) in the cathode, thus constructing an air breathing cathode. Such a novel battery (Ni-ZnAB), designed in a pouch-type cell with a lean electrolyte, exhibits an outstanding EE of 85 % and a long cycle life of 100 cycles at 2 mA cm-2 , which are significantly superior to those of traditional Ni-Zn batteries (54 %, 50 cycles). Compared to Ni-Zn, the enhanced EE of Ni-ZnAB is attributed to the contribution from ORR, while the improved cycling stability is because the stability of the anode, cathode and electrolyte are also enhanced in Ni-ZnAB. Furthermore, an ultrahigh stability of 500 cycles with an average EE of 84 % at 2 mA cm-2 was achieved using a mold cell with rich electrolyte, demonstrating the strong application potential of Ni-ZnAB.

Hewettite ZnV6 O16 ⋠8H2 O with Remarkably Stable Layers and Ultralarge Interlayer Spacing for High-Performance Aqueous Zn-Ion Batteries.

Aqueous Zn-ion batteries (ZIBs) are promising candidates for grid-scale energy storage because of their intrinsic safety, low-cost and high energy-intensity. Vanadium-based materials are widely used as the cathode of ZIBs, especially A2 V6 O16 ⋅ nH2 O (AVO, A=NH4 + , Na, K). However, AVO suffers from serious dissolution, phase transformation and narrow gallery spacing (∼3 Å), leading to poor cycling stability and rate capability. Herein, we unveiled the root cause of the performance degradation in the AVO cathode and therefore developed a new high-performance cathode of ZnV6 O16 ⋅ 8H2 O (ZVO) for ZIB. Through a method of ion exchange induced phase transformation, AVO was converted to hewettite ZVO with larger gallery spacing (∼6 Å) and more stable V6 O16 layers. ZVO cathode thus constructed delivers a high capacity of 365 and 170 mAh g-1 at 0.5 and 15 A g-1 , while 86 % and 70 % of its capacity are retained at 0.5 A g-1 after 300 cycles and at 15 A g-1 after 10000 cycles, substantially better than conventional AVO.

Application of In Situ Techniques for the Characterization of NiFe-Based Oxygen Evolution Reaction (OER) Electrocatalysts.

Developing high-efficiency and affordable electrocatalysts for the sluggish oxygen evolution reaction (OER) remains a crucial bottleneck on the way to the practical applications of rechargeable energy storage technologies and water splitting for producing clean fuel (H2 ). In recent years, NiFe-based materials have proven to be excellent electrocatalysts for OER. Understanding the characteristics that affect OER activity and determining the OER mechanism are of vital importance for the development of OER electrocatalysts. Therefore, in situ characterization techniques performed under OER conditions are urgently needed to monitor the key intermediates together with identifying the OER active centers and phases. In this Minireview, recent advances regarding in situ techniques for the characterization of NiFe-based electrocatalysts are thoroughly summarized, including Raman spectroscopy, X-ray absorption spectroscopy, ambient pressure X-ray photoelectron spectroscopy, Mössbauer spectroscopy, Ultraviolet-visible spectroscopy, differential electrochemical mass spectrometry, and surface interrogation scanning electrochemical microscopy. The results from these in situ measurements not only reveal the structural transformation and the progressive oxidation of the catalytic species under OER conditions, but also disclose the crucial role of Ni and Fe during the OER. Finally, the need for developing new in situ techniques and theoretical investigations is discussed to better understand the OER mechanism and design promising OER electrocatalysts.

Advancements in Achieving High Reversibility of Zinc Anode for Alkaline Zinc-Based Batteries.

Rechargeable alkaline zinc-based batteries (ZBBs) have attracted extensive research attention due to their advantages of low cost, high specific energy, and high safety. Although the investigation of cathodes for alkaline secondary ZBBs has reached a relatively advanced stage, the exploration of zinc anodes is still in its infancy. Zinc anodes in alkaline electrolytes encounter challenges such as dendrite formation, passivation, corrosion during periods of cell inactivity, and hydrogen evolution during cycling, thereby limiting their rechargeability and storability. Drawing upon the latest research on zinc anodes, six fundamental strategies that encompass a wide range of aspects are identified and categorized, from electrode modifications and electrolytes to charge protocols. Specifically, these strategies include 3D structures, coatings, alloying, additives, separators, and charge protocols. They serve as an insight summary of the current research progress on zinc anodes. Additionally, the complementary nature of these strategies allows for flexible combinations, enabling further enhancement of the overall performance of zinc anodes. Finally, several future directions for the advancement of practical alkaline Zn anode are proposed. This comprehensive review not only consolidates the existing knowledge but also paves the way for broader research opportunities in the pursuit of high-performance alkaline zinc anodes.

Breaking the trade-off between capacity and stability in vanadium-based zinc-ion batteries.

Water in electrolytes is a double-edged sword in zinc-ion batteries (ZIBs). While it allows for proton insertion in the cathode, resulting in a significant increase in capacity compared to that of organic ZIBs, it also causes damage to electrodes, leading to performance degradation. To overcome the capacity-stability trade-off, organic solvents containing a small amount of water are proposed to mitigate the harmful effects of water while ensuring sufficient proton insertion. Remarkably, in a Zn(OTf)2 electrolyte using 8% H2O in acetonitrile as the solvent, Zn‖(NH4)0.5V2O5·0.5H2O exhibited a capacity as high as 490 mA h g-1 at a low current (0.3 A g-1), with a capacity retention of 80% even after 9000 cycles at high current (6 A g-1), simultaneously achieving the high capacity as in pure aqueous electrolytes and excellent stability as in organic electrolytes. We also found that the water content strongly impacts the kinetics and reversibility of ion insertion/extraction and zinc stripping/plating. Furthermore, compared to electrolytes with pure acetonitrile or H2O solvents, electrolytes with only 8% H2O in acetonitrile provide higher capacities at temperatures ranging from 0 to -50 °C. These discoveries enhance our understanding of the mechanisms involved in ZIBs and present a promising path toward enhancing electrolyte solutions for the creation of high-performance ZIBs.

Highly 002-Oriented Dendrite-Free Anode Achieved by Enhanced Interfacial Electrostatic Adsorption for Aqueous Zinc-Ion Batteries.

Rechargeable aqueous zinc-ion batteries (AZIBs) are gaining recognition as promising next-generation energy storage solution, due to their intrinsic safety and low cost. Nevertheless, the advancement of AZIBs is greatly limited by the abnormal growth of zinc dendrites during cycling. Electrolyte additives are effective at suppressing zinc dendrites, but there is currently no effective additive screening criterion. Herein, we propose employing the interfacial electrostatic adsorption strength of zinc ions for the initial screening of additives. Subsequently, dendrite-free plating is achieved by employing the anionic surfactant sodium dodecyl benzenesulfonate (SDBS) to enhance electrostatic adsorption. The cycled zinc anode exhibited a dense plating morphology and a high (002) orientation (I002/I101 = 22). The Zn||MnO2 full cell with SDBS exhibited a capacity retention of 85% after 1000 cycles at 1 A g-1. Furthermore, an instantaneous nucleation model and continuous nucleation model (CNM) are constructed to reveal the microscale plating/stripping dynamics under the scenarios of weak adsorption and strong adsorption. The CNM accurately explains the self-optimizing reconstruction of electrodes resulting from enhanced electrostatic adsorption. Our exploration was extended to other anionic surfactants (sodium dodecyl sulfate and disodium laureiminodipropionate), confirming the effectiveness of strong electrostatic adsorption in the screening of electrolyte additives.

Effects of curing concentration and drying time on flavor and microorganisms in dry salted Spanish mackerel.

This study investigated the quality changes of dry salted mackerel during curing and drying process and the relationship between flavor substances and microorganisms. The results showed that the thiobarbituric acid reactive substances (TBARS) values increased gradually with the increase of salt concentration and treatment time. The total volatile base nitrogen (TVB-N) values and total viable counts (TVC) values showed the same trend. Under 3% condition, the TVB-N values exceeded the standard and was not suitable for consumption. A total of 61 volatile flavor substances were identified by Gas chromatography-ion mobility spectrometry (GC-IMS), among which aldehydes contributed the most. Staphylococcus and Cobetia were the most abundant by High-throughput sequencing (HTS). There was significant correlation between TOP15 microorganisms and TOP20 flavor substances. Staphylococcus and Cobetia were positively correlated with 13 volatile flavor substances, which contributed to the formation of flavor in naturally fermented Spanish mackerel.

Characterization of non-volatile and volatile flavor profiles of Coregonus peled meat cooked by different methods.

This study investigated the effects of different cooking methods on non-volatile flavor (free amino acids, 5'-nucleotides, and organic acids, etc.) of Coregonus peled meat. The volatile flavor characteristics were also analyzed by electric nose and gas chromatography-ion migration spectrometry (GC-IMS). The results indicated that the content of flavor substances in C. peled meat varied significantly. The electronic tongue results indicated that the richness and umami aftertaste of roasting were significantly greater. The content of sweet free amino acids, 5'-nucleotides, and organic acids was also higher in roasting group. Electronic nose principal component analysis can distinguish C. peled meat cooked (the first two components accounted for 98.50% and 0.97%, respectively). A total of 36 volatile flavor compounds were identified among different groups, including 16 aldehydes, 7 olefine aldehydes, 6 alcohols, 4 ketones, and 3 furans. In general, roasting was recommended and gave more flavor substances in C. peled meat.

Atomic scale analysis of Zn2+ storage in robust tunnel frameworks.

Realizing rapid and reversible Zn2+ storage at the cathode is imperative for the advancement of aqueous Zn-ion batteries (ZIBs), which offer an excellent option for large-scale electrochemical energy storage. However, owing to limitations of the structural stability of previously investigated frameworks, the Zn2+ storage processes remain unclear, thus hindering progress towards the above goal. Herein, we present the novel application of MoVTe oxide with an M1 phase (MVT-M1) as a potential cathode material for ZIBs. MVT-M1 features broad and robust tunnels that facilitate reversible Zn2+ insertion/extraction during cycling, as well as rich redox centers (Mo, V, and Te) to aid in charge redistribution, resulting in good performances in ZIBs. The exceptional resilience of MVT-M1 to high-energy electron beams allows for direct observation of Zn2+ insertion/extraction at the atomic scale within the tunnels for the first time using high-angle annular dark field scanning transmission electron microscopy; the storage location of zinc ions within the cathode is accurately determined layer by layer from the surface to the bulk phase by employing time-of-flight secondary ion mass spectrometry. Additionally, solvent molecules (H2O and methanol) are also found inside the tunnels along with Zn2+. Due to the broader heptagonal tunnels and Te ions in the hexagonal tunnels, MVT-M1 exhibits good cycling stability, outperforming MoVTe oxide with the M2 phase (no heptagonal tunnels) and MoV oxide with the M1 phase (no Te). These findings hold significant importance in advancing our understanding of the Zn2+ storage mechanism and enable the design of novel materials specifically optimized for efficient Zn2+ storage.

Insight into the relationship between metabolite dynamic changes and microorganisms of sea urchin (S. intermedius) gonads during storage.

Sea urchin gonads have high nutritional value and degenerate rapidly during storage. Previous assessment of the freshness of sea urchin gonads was based on experience without valid biochemical indicators. Thus, the current study is to find biochemical indicators representing the freshness of sea urchin gonads. Results showed that the dominant genera of sea urchin gonads were changed from Psychromonas, Ralstonia, and Roseimarinus to Aliivibrio, Psychrilyobacter, and Photobacterium. The differential metabolites of sea urchin gonads were mainly produced through amino acids metabolism. Among them, GC-TOF-MS based differential metabolites had the greatest enrichment in the valine, leucine and isoleucine biosynthesis pathway, while LC-MS based differential metabolites had the greatest enrichment in the alanine, aspartate and glutamate metabolism pathway. The growth of dominant genus (Aliivibrio) had a great influence on the production of differential metabolites. These results will provide valuable information for accurately judging the freshness and shelf life of sea urchin gonads.

Non-Buffer Epi-AlGaN/GaN on SiC for High-Performance Depletion-Mode MIS-HEMTs Fabrication.

A systematic study of epi-AlGaN/GaN on a SiC substrate was conducted through a comprehensive analysis of material properties and device performance. In this novel epitaxial design, an AlGaN/GaN channel layer was grown directly on the AlN nucleation layer, without the conventional doped thick buffer layer. Compared to the conventional epi-structures on the SiC and Si substrates, the non-buffer epi-AlGaN/GaN structure had a better crystalline quality and surface morphology, with reliable control of growth stress. Hall measurements showed that the novel structure exhibited comparable transport properties to the conventional epi-structure on the SiC substrate, regardless of the buffer layer. Furthermore, almost unchanged carrier distribution from room temperature to 150 °C indicated excellent two-dimensional electron gas (2DEG) confinement due to the pulling effect of the conduction band from the nucleation layer as a back-barrier. High-performance depletion-mode MIS-HEMTs were demonstrated with on-resistance of 5.84 Ω·mm and an output current of 1002 mA/mm. The dynamic characteristics showed a much smaller decrease in the saturation current (only ~7%), with a quiescent drain bias of 40 V, which was strong evidence of less electron trapping owing to the high-quality non-buffer AlGaN/GaN epitaxial growth.

A Novel Atomic-Level Post-Etch-Surface-Reinforcement Process for High-Performance p-GaN Gate HEMTs Fabrication.

A novel atomic-level post-etch-surface-reinforcement (PESR) process is developed to recover the p-GaN etching induced damage region for high performance p-GaN gate HEMTs fabrication. This process is composed of a self-limited surface modification step with O2 plasma, following by an oxide removal step with BCl3 plasma. With PESR process, the AlGaN surface morphology after p-GaN etching was comparable to the as-epitaxial level by AFM characterization, and the AlGaN lattice crystallization was also recovered which was measured in a confocal Raman system. The electrical measurement further confirmed the significant improvement of AlGaN surface quality, with one-order of magnitude lower surface leakage in a metal-semiconductor (MS) Schottky-diode and 6 times lower interface density of states (Dit) in a MIS C-V characterization. The XPS analysis of Al2O3/AlGaN showed that the p-GaN etching induced F-byproduct and Ga-oxide was well removed and suppressed by PESR process. Finally, the developed PESR process was successfully integrated in p-GaN gate HEMTs fabrication, and the device performance was significantly enhanced with ~20% lower of on-resistance and ~25% less of current collapse at Vds,Q bias of 40 V, showing great potential of leverage p-GaN gate HEMTs reliability.

Carbon-encapsulated V2O3 nanorods for high-performance aqueous Zn-ion batteries.

Searching for stable cathodes is of paramount importance to the commercial development of low-cost and safe aqueous Zn-ion batteries (AZIBs). V2O3 is a good candidate for AZIB cathodes but has unsatisfied cycling stability. Herein, we solve the stability issue of a V2O3 cathode by coating a robust carbon shell. Strong evidence was provided that V2O3 was oxidized to favorable V2O5·nH2O during charging and the carbon shell could promote the oxidation of V2O3 to V2O5·nH2O. The discharge capacity was increased from ∼45 mA h g-1 to 336 mA h g-1 after V2O3 was oxidized to V2O5·nH2O, indicating a higher Zn2+-storage capability of V2O5·nH2O than V2O3. In addition, the rate-capability and long-term cycling performance are greatly enhanced after coating carbon shells on the surface of V2O3 nanorods. Therefore, the presented strategy of introducing carbon shells and fundamental insights into the favorable role of carbon shells in this study contribute to the advancement of highly stable AZIBs.

Mixed conifer-broadleaf trees on arbuscular mycorrhizal and ectomycorrhizal communities in rhizosphere soil of different plantation stands in the temperate zone, Northeast China.

In comparison with ectomycorrhizal (EM) tree species, arbuscular mycorrhizal (AM) trees have different litter quality and nitrogen cycle modes, which may affect mycorrhizal colonization and the community composition and diversity. However, available studies addressing the mycorrhizal fungal colonization rate, diversity and community composition in mixed forest stands composed of AM and EM trees are rare. In the present study, we assessed litter quality, soil physicochemical properties and correlated them with mycorrhizal community characteristics in rhizosphere soils of monoculture and mixture plantation stands of AM tree species (Fraxinus mandschurica Rupr.) and EM tree species (Larix gmelinii Rupr., Picea koraiensis Nakai) in Northeast China. We hypothesized that (1) the effect of mixture pattern on mycorrhizal colonization rate and diversity would change with tree species, (2) the effect of mixture pattern on mycorrhizal community composition would be less pronounced in comparison with that of tree species. We found that mixture did not change AMF colonization rate regardless of mixture identity, whereas mixture and tree species exerted significant effects on EMF colonization rate. For AMF community, both M-AS (Fraxinus mandschurica Rupr. and Picea koraiensis Nakai) and M-AL (Fraxinus mandschurica Rupr. and Larix gmelinii Rupr.) mixtures significantly increased Pielou index and Simpson index, whereas only M-AS significantly increased Sobs. For EMF community, mixture significantly affected examined diversity indices except for Chao1. Mixture significantly shifted AMF and EMF community, and the magnitude was tree species dependent. The dominant genera in AMF and EMF communities in plantation stands were Glomus and Tomentella, respectively. The EnvFit analysis showed that the determinant factors of EMF community are soil moisture, pH, nitrate nitrogen content, dissolved organic nitrogen content, soil organic matter content, soil organic carbon/total nitrogen and litter carbon/total nitrogen. In conclusion, mixed conifer-broadleaf trees significantly changed soil physicochemical properties, litter quality as well as mycorrhizal fungi community diversity and composition.

High Selectivity, Low Damage ICP Etching of p-GaN over AlGaN for Normally-off p-GaN HEMTs Application.

A systematic study of the selective etching of p-GaN over AlGaN was carried out using a BCl3/SF6 inductively coupled plasma (ICP) process. Compared to similar chemistry, a record high etch selectivity of 41:1 with a p-GaN etch rate of 3.4 nm/min was realized by optimizing the SF6 concentration, chamber pressure, ICP and bias power. The surface morphology after p-GaN etching was characterized by AFM for both selective and nonselective processes, showing the exposed AlGaN surface RMS values of 0.43 nm and 0.99 nm, respectively. MIS-capacitor devices fabricated on the AlGaN surface with ALD-Al2O3 as the gate dielectric after p-GaN etch showed the significant benefit of BCl3/SF6 selective etch process.

Reversible Molecular and Ionic Storage Mechanisms in High-Performance Zn0.1V2O5·nH2O Xerogel Cathode for Aqueous Zn-Ion Batteries.

The cathode is a critical component for aqueous Zn-ion batteries (ZIBs) to achieve high capacity and long stability. In this work, we demonstrate a dissolution-free, low-Zn-preinserted bilayer-structured V2O5 xerogel cathode, Zn0.1V2O5·nH2O (ZnVO), with excellent capacity and stability using a low-cost ZnSO4 electrolyte. Its discharge capacity reaches 463 mAh g-1 at 0.2 A g-1 and 240 mAh g-1 at 10 A g-1, while 93% and 88% of its capacity are retained at 0.2 A g-1 for 200 cycles and at 10 A g-1 for 20 000 cycles, respectively. We then show that the outstanding performance of ZnVO is derived from the enlarged gallery spacing by the solvent water intercalation and the water stable V2O5 bilayer structure. We further unveil via ab initio molecular dynamics that H+ is largely originated from the dissociation of the gallery water, while OH- moves out of the gallery to form Zn4(SO4)(OH)6·5H2O with ZnSO4 electrolyte on the surface of ZnVO; the intercalated Zn2+ forms aquo complex [Zn(H2O)6]2+ with the gallery water. Our theoretical analysis also suggests that the gallery water and solvent water in the electrolyte are statistically the same and functionally equivalent. Overall, this study shows the promise of ZnVO as a practical cathode for ZIBs and offers fundamental insights into the roles of gallery water, solvent water, bilayer V2O5 structure, and dual Zn2+/H+ intercalation mechanisms in achieving high capacity and long stability.

[Root architecture and fine root characteristics of Juglans mandshurica saplings in different habitats in the secondary forest on the west slope of Zhangguangcailing, China]. / å¼ å¹¿æ‰å²­è¥¿å¡æ¬¡ç”Ÿæž—ä¸åŒç”Ÿå¢ƒèƒ¡æ¡ƒæ¥¸å¹¼æ ‘æ ¹ç³»æž„åž‹åŠç»†æ ¹ç‰¹å¾.

The whole root excavation method was used to examine root configuration of Juglans mandshurica, with the age of 5-6 years in three habitats (forest edge, gap, and canopy) in a secondary forest on the western part of Zhangguangcailing Mountains. Root structure and fine root function were measured. The root topological index, average joint length, cross-sectional area ratio before and after root branching were calculated and fine root chemical compositions were analyzed. Roots of J. mandshurica at forest edge tended to be dichotomous branch (Topological index:TI=0.68), that under the canopy were herringbone-like branch (TI=0.79), and the gap was between the two (TI=0.72). The average connection length of roots among the three habitats was not significant. The cross-sectional area ratio of roots before and after root branching in three habitats was 1.06, 1.04 and 1.07, respectively, which was not affected by root diameter, in accordance with the Leonardo da Vinci rule. For the same order fine root in different habitats, its length and specific surface area gradually increased from the edge of the forest to the canopy. The N content decreased first and then increased, while the C content and C/N increased first and then decreased. From the forest edge to the gap and to the under canopy, roots tended to move from the dichotomous branch to the herringbone-like branch by reducing the overlap between the secondary branches and roots, increasing specific root length, specific surface area and changing the contents of C and N to cope with environmental change and improve nutrient absorption efficiency.

A High Capacity Bilayer Cathode for Aqueous Zn-Ion Batteries.

Aqueous Zn-ion batteries (ZIBs) are promising candidates for grid-scale energy storage because they are intrinsically safe, cost competitive, and energy intense. However, the development of ZIBs is currently challenged by the performance of cathode materials. Herein, we report on Ca0.67V8O20·3.5H2O (CaVO) nanobelts as a type of ZIB cathode with a discharge capacity of 466 mAh g-1 (equivalent to an energy density of 345.6 Wh kg-1) at 0.1 A g-1 and a capacity retention rate of 100%, 95%, and 74% at 5.0 A g-1 for 500, 1000, and 2000 cycles, respectively. Through a combined theoretical and experimental study, we reveal that the outstanding energy and power performances of CaVO are deeply rooted in its Zn2+-transport friendly, bilayer ρ-type V2O5 structure, and the structure-derived reversibility in single-phase Zn2+-intercalation/deintercalation process. We also uncover that Ca2+ as a structural stabilizer in CaVO undergoes a fast, performance-harmless ion-exchange with Zn2+ in the electrolyte and the entire Zn2+-intercalation/deintercalation process is accompanied by a counter migration of solvent water. Last, we show that a successful synthesis of CaVO depends critically on pH value of the precursor solution and the structural stability of CaVO is controlled by the co-presence of Ca2+/Zn2+ and structural water.