Investigations on Tunnel-Structure MnO2 for Utilization as a High-Voltage and Long-Life Cathode Material in Aqueous Ammonium-Ion and Hybrid-Ion Batteries.

Recently, nonmetal NH4 + ions have attracted extensive attention for use as charge carries in the field of energy storage due to their abundant resources, environmental friendliness, and low cost. However, the development of aqueous ammonium-ion batteries (AAIBs) is constrained by the absence of high-voltage and long-life materials. Herein, different tunnel-structure MnO2 materials (α-, ß-, and γ-MnO2) are utilized as cathodes for AAIBs and hybrid-ion batteries and compared, and α-MnO2 is demonstrated to exhibit the most remarkable electrochemical performance. The α-MnO2 cathode material delivers the highest discharge capacity of 219 mAh g-1 at a current density of 0.1 A g-1 and the best cyclability with a capacity retention of 95.4% after 10 000 cycles at 1.0 A g-1. Moreover, aqueous ammonium-ion and hybrid-ion (ammonium/sodium ions) full batteries are successfully constructed using α-MnO2 cathodes. This work provides a novel direction for the development of aqueous energy storage for practical applications.

High Voltage Ga-Doped P2-Type Na2/3 Ni0.2 Mn0.8 O2 Cathode for Sodium-Ion Batteries.

Ni/Mn-based oxide cathode materials have drawn great attention due to their high discharge voltage and large capacity, but structural instability at high potential causes rapid capacity decay. How to moderate the capacity loss while maintaining the advantages of high discharge voltage remains challenging. Herein, the replacement of Mn ions by Ga ions is proposed in the P2-Na2/3 Ni0.2 Mn0.8 O2 cathode for improving their cycling performances without sacrificing the high discharge voltage. With the introduction of Ga ions, the relative movement between the transition metal ions is restricted and more Na ions are retained in the lattice at high voltage, leading to an enhanced redox activity of Ni ions, validated by ex situ synchrotron X-ray absorption spectrum and X-ray photoelectron spectroscopy. Additionally, the P2-O2 phase transition is replaced by a P2-OP4 phase transition with a smaller volume change, reducing the lattice strain in the c-axis direction, as detected by operando/ex situ X-ray diffraction. Consequently, the Na2/3 Ni0.21 Mn0.74 Ga0.05 O2 electrode exhibits a high discharge voltage close to that of the undoped materials, while increasing voltage retention from 79% to 93% after 50 cycles. This work offers a new avenue for designing high-energy density Ni/Mn-based oxide cathodes for sodium-ion batteries.

Effects of the construction of fertile and cultivated soil layer on soil fertility and maize yield in Albic soil.

We examined the effects of fertile soil layer construction technology on soil fertility and maize yield with a 3-year field experiment in Albic soil in Fujin, Heilongjiang Province. There were five treatments, including conventional tillage (T15, without organic matter return) and fertile soil layer construction methods [deep tillage (0-35 cm) with straw return, T35+S; deep tillage with organic manure, T35+M; deep tillage with straw and organic manure return, T35+S+M; deep tillage with straw, organic manure return and chemical fertilizer, T35+S+M+F]. The results showed that: 1) compared with the T15 treatment, maize yield was significantly increased by 15.4%-50.9% under fertile layer construction treatments. 2) There was no significant difference of soil pH among all treatments in the first two years, but fertile soil layer construction treatments significantly increased soil pH of topsoil (0-15 cm soil layer) in the third year. The pH of subsoil (15-35 cm soil layer) significantly increased under T35+S+M+F, T35+S+M, and T35+M treatments, while no significant difference was observed for T35+S treatment, compared with T15 treatment. 3) The fertile soil layer construction treatments could improve the nutrient contents of the topsoil and subsoil layer, especially in the subsoil layer, with the contents of organic matter, total nitrogen, available phosphorus, alkali-hydrolyzed nitrogen and available potassium being increased by 3.2%-46.6%, 9.1%-51.8%, 17.5%-130.1%, 4.4%-62.8%, 22.2%-68.7% under the subsoil layer, respectively. The fertility richness indices were increased in the subsoil layer, and nutrient contents of the subsoil layer were close to those of topsoil layer, indicating that 0-35 cm fertile soil layer had been constructed. 4) Soil organic matter contents in the 0-35 cm layer were increased by 8.8%-23.2% and 13.2%-30.1% in the second and third years of fertile soil layer construction, respectively. Soil organic carbon storage was also gradually increased under fertile soil layer construction treatments. 5) The carbon conversion rate of organic matter was 9.3%-20.9% under T35+S treatment, and 10.6%-24.6% under T35+M, T35+S+M, and T35+S+M+F treatments. The carbon sequestration rate was 815.7-3066.4 kg·hm-2·a-1 in fertile soil layer construction treatments. The carbon sequestration rate of T35+S treatment increased with experimental periods, and soil carbon content under T35+M, T35+S+M and T35+S+M+F treatments reached saturation point in the experimental second year. Construction of fertile soil layers could improve the fertility of topsoil and subsoil and maize yield. In term of economic benefits, combination application of maize straw, organic material and chemical fertilizer within 0-35 cm soil, cooperating with conservation tillage, is recommended for the Albic soil fertility improvement.

Coupling regeneration strategy of lithium-ion electrode materials turned with naphthalenedisulfonic acid.

The resource exhaustion and environmental assessment driven by sustainable development make recycle of spent LIBs urgent to be achieved. However, the conventional recycling processes are quite complicated in terms of the tedious steps and secondary contamination. In this paper, hydrosoluble naphthalenedisulfonic acid is firstly proposed to selectively extract valuable metals (Co and Li) for the regeneration of battery materials. Lithium is selectively recovered as lithium enriched solution with a high yield of 99%, while 96.6% cobalt remains in a complex-precipitate benefited from the high acidity and coordination role of naphthalenedisulfonic acid. The leaching of Li fits well with the logarithmic rate law model with an activation energy of 32.42 kJ/mol. Additionally, the regenerated lithium-ion battery active materials (Co3O4 anode and LiCoO2 cathode) prepared from the cobalt complex-precipitate and lithium-enriched solution exhibit excellent discharged-charged performances and rate capability. This feasible strategy assisted by multifunctional naphthalenedisulfonic acid may offer an alternative option for the simultaneous recovery of Li and Co and the rational resource utilization of spent lithium-ion batteries.

Carbon Dots Evoked Li Ion Dynamics for Solid State Battery.

Solid composite electrolyte-based Li battery is viewed as one of the most competitive system for the next generation batteries; however, it is still restricted by sluggish ion diffusion. Fast ion transport is a characteristic of the polyethylene oxide (PEO) amorphous phase, and the mobility of Li+ is restrained by the coordination interaction within PEO and Li+ . Herein, the design of applying functionalized carbon dots (CDs) with abundant surface features as fillers is proposed. High ionic conductivity is achieved in the CD-based composite electrolytes resulting from enhanced ion migration ability of polymer segments and mobility of Li+ . Specially, the optimum effect with nitrogen and sulfur co-doped carbon dots (NS-CD) is a consequence of strong interaction between edge-nitrogen/sulfur in NS-CD and Li+ . Solid-state nuclear magnetic resonance results confirm that more mobile Li+ is generated. Moreover, it is observed that lithium dendrite is suppressed compared to PEO electrolyte associated with reinforced mechanical properties and high transference number. The corresponding all-solid-state batteries, with the cathode of LiFePO4 or high voltage NCM523, exhibit long cycling life and excellent rate performances. It is a novel strategy to achieve high ionic conductivity composite electrolyte with uniform lithium deposition and provides a new direction to the mechanism of fast Li+ movement.

Compact-Nanobox Engineering of Transition Metal Oxides with Enhanced Initial Coulombic Efficiency for Lithium-Ion Battery Anodes.

A novel strategy is proposed to construct a compact-nanobox (CNB) structure composed of irregular nanograins (average diameter ≈ 10 nm), aiming to confine the electrode-electrolyte contact area and enhance initial Coulombic efficiency (ICE) of transition metal oxide (TMO) anodes. To demonstrate the validity of this attempt, CoO-CNB is taken as an example which is synthesized via a carbothermic reduction method. Benefiting from the compact configuration, electrolyte can only contact the outer surface of the nanobox, keeping the inner CoO nanograins untouched. Therefore, the solid electrolyte interphase (SEI) formation is reduced. Furthermore, the internal cavity leaves enough room for volume variation upon lithiation and delithiation, resulting in superior mechanical stability of the CNB structure and less generation of fresh SEI. Consequently, the SEI remains stable and spatially confined without degradation, and hence, the CoO-CNB electrode delivers an enhanced ICE of 82.2%, which is among the highest values reported for TMO-based anodes in lithium-ion batteries. In addition, the CoO-CNB electrode also demonstrates excellent cyclability with a reversible capacity of 811.6 mA h g-1 (90.4% capacity retention after 100 cycles). These findings open up a new way to design high-ICE electrodes and boost the practical application of TMO anodes.

Graphitic carbon-wrapped NiO embedded three dimensional nitrogen doped aligned carbon nanotube arrays with long cycle life for lithium ion batteries.

In this work, a three-dimensional nitrogen doped aligned carbon nanotube array (NACNTs)@NiO@graphitic carbon composite was fabricated by an effective strategy involving nebulized ethanol assisted infiltration, In this structure, the NiO nanoparticles were wrapped by graphitic carbon layers and NiO@graphitic carbon core-shell nanoparticles adhered strictly to the surface of NACNTs to form a highly ordered 3D structure. When this composite was used as an anode for lithium ion batteries, the well-ordered pore of its NACNTs can facilitate the electrolyte to penetrate and improve electronic conductivity. At the same time, the graphitic layers can promote the stability of a solid electrolyte interface film. Therefore, the NACNTs@NiO@graphitic carbon composite containing 68.1 wt% NiO delivers excellent capacity retention of 91.6% after 200 cycles at 0.2C.

N-glycan profiles in H9N2 avian influenza viruses from chicken eggs and human embryonic lung fibroblast cells.

N-glycosylation can affect the host specificity, virulence and infectivity of influenza A viruses (IAVs). In this study, the distribution and evolution of N-glycosylation sites in the hemagglutinin (HA) and neuraminidase (NA) of H9N2 virus were explored using phylogenetic analysis. Then, one strain of the H9N2 subtypes was proliferated in the embryonated chicken eggs (ECE) and human embryonic lung fibroblast cells (MRC-5) system. The proliferated viral N-glycan profiles were analyzed by a glycomic method that combined the lectin microarray and MALDI-TOF/TOF-MS. As a result, HA and NA of H9N2 viruses prossess six and five highly conserved N-glycosylation sites, respectively. Sixteen lectins (e.g., MAL-II, SNA and UEA-I) had increased expression levels of the glycan structures in the MRC-5 compared with the ECE system; however, 6 lectins (e.g., PHA-E, PSA and DSA) had contrasting results. Eleven glycans from the ECE system and 13 glycans from the MRC-5 system were identified. Our results showed that the Fucα-1,6GlcNAc(core fucose) structure was increased, and pentaantennary N-glycans were only observed in the ECE system. The SAα2-3/6Gal structures were highly expressed and Fucα1-2Galß1-4GlcNAc structures were only observed in the MRC-5 system. We conclude that the existing SAα2-3/6Gal sialoglycans make the offspring of the H9N2 virus prefer entially attach to each other, which decreases the virulence. Alterations in the glycosylation sites for the evolution and role of IAVs have been widely described; however, little is known about the exact glycan structures for the same influenza strain from different hosts. Our findings may provide a novel way for further discussing the molecular mechanism of the viral transmission and virulence associated with viral glycosylation in avian and human hosts as well as vital information for designing a vaccine against influenza and other human viruses.

LifePo4 Coated Homogeneously with 3D Carbon Nanotube Conductive Networks for Enhanced Electrochemical Performance.

LiFePO4 (LFP) microparticles coated homogeneously with three-dimensional (3D) carbon nanotube (CNT) conductive networks were successfully prepared via a simple and effective ball milling method by controlling Polyvinylidene fluoride (PVDF) content in cathode electrode slurry. Scanning electron microscopy (SEM) demonstrated that the electrical bridge between the LFP could be well modulated by varying the amount of the CNTs and PVDF. The LFP/CNTs composite with 3 wt% CNTs and 5 wt% PVDF, in which CNTs are embedded in the microspheres homogeneously, possesses the best 3D CNT conductive networks and exhibits the best electrochemical property with high capacity retention of 95.72% at 0.25 C after 50 cycles. Essentially, in comparison with those samples without CNT networks, this CNT network structure can greatly enhance the electrical conductivity, thus markedly improving the electrochemical performance. (LFP) microparticles coated homogeneously with three-dimensional (3D) carbon nanotube (CNT) conductive networks were successfully prepared via a simple and effective ball milling method by controlling Polyvinylidene fluoride (PVDF) content in cathode electrode slurry. Scanning electron microscopy (SEM) demonstrated that the electrical bridge between the LFP could be well modulated by varying the amount of the CNTs and PVDF. The LFP/CNTs composite with 3 wt% CNTs and 5 wt% PVDF, in which CNTs are embedded in the microspheres homogeneously, possesses the best 3D CNT conductive networks and exhibits the best electrochemical property with high capacity retention of 95.72% at 0.25 C after 50 cycles. Essentially, in comparison with those samples without CNT networks, this CNT network structure can greatly enhance the electrical conductivity, thus markedly improving the electrochemical performance.

Alignment and structural control of nitrogen-doped carbon nanotubes by utilizing precursor concentration effect.

Nitrogen-doped carbon nanotubes (NCNTs) were prepared using a simple ultrasonic spray pyrolysis method. The precursor concentration effect was examined to effectively control alignment, open tip and diameter of the NCNTs by changing xylene/cyclohexylamine ratio. The structure and morphology of the resultant NCNTs were characterized by scanning electron microscopy, transmission electron microscopy and x-ray photoelectron spectroscopy. The degree of alignment and the diameter of the NCNTs increased as the xylene/cyclohexylamine precursor mixture was changed from 0 to 35% cyclohexylamine. This precursor composition also caused a large number of open-ended nanotubes to form with graphite layers inside the cavities of the NCNTs. However, further increase cyclohexylamine content in the precursor reduced the degree of alignment and diameter of the NCNTs. We demonstrate control over the NCNT alignment and diameter, along with the formation of open-ended nanotube tips, and propose a growth mechanism to understand how these properties are interlinked.