Urgent needs for second life using and recycling design of wasted electric vehicles (EVs) lithium-ion battery: a scientometric analysis.

Currently, lithium-ion batteries are increasingly widely used and generate waste due to the rapid development of the EV industry. Meanwhile, how to reuse "second life" and recycle "extracting of valuable metals" of these wasted EVBs has been a hot research topic. The 4810 relevant articles from SCI and SSCI Scopus databases were obtained. Scientometric analysis about second life using and recycling methodologies of wasted EVBs was conducted by VOSviewer, Pajek, and Netdraw. According to analytical results, the research of second life using and recycling mythologies has been growing and the expected achievement will continue to increase. China, Germany, the USA, Italy, and the UK are the most active countries in this field. Tsinghua University in China, "Fraunhofer ISI, Karlsruhe" in Germany, and "Polytechnic di Torino" in Italy are the most productive single and collaborative institutions. The journals SAE technical papers and World Electric Vehicle Journal have the highest publication and citations than other journals. Chinese author "Li Y" has the highest number of 36 publications, and his papers were cited 589 times by other authors. By analyzing the co-occurrence and keywords, energy analysis, second life (stationary using, small industry), and treatment methods, (hydrometallurgy and pyrometallurgical, electrochemical, bio-metallurgical) were the hot research topics. The S-curve from the article indicates hydrometallurgical and bio-metallurgical methods are attached with great potential in the near future. Further, different treatment methodologies are observed especially advanced techniques in hydrometallurgical, and spent medium bioleaching techniques in bio-metallurgical are good, economically cheap, has low CO2 emission, environmentally friendly, and has high recovery rate. Finally, this research provides information on second life use and top recycling methodology opportunities for future research direction for researchers and decision-makers who are interested in this research.

The Influence of Reduced Graphene Oxide on the Texture and Chemistry of N,S-Doped Porous Carbon. Implications for Electrocatalytic and Energy Storage Applications.

In this work, we study the influence of reduced graphene oxide (rGO) on the morphology and chemistry of highly porous N,S-doped carbon cryogels. Simultaneously, we propose an easily upscalable route to prepare such carbons by adding graphene oxide (GO) in as-received suspended form to the aqueous solution of the ι-carrageenan and urea precursors. First, 1.25-5 wt% GO was incorporated into the dual-doped polymer matrix. The CO2, CO, and H2O emitted during the thermal treatments resulted in the multifaceted modification of the textural and chemical properties of the porous carbon. This facilitated the formation of micropores through self-activation and resulted in a substantial increase in the apparent surface area (up to 1780 m2/g) and pore volume (up to 1.72 cm3/g). However, adding 5 wt% GO led to overactivation. The incorporated rGO has an ordering effect on the carbon matrix. The evolving oxidative species influence the surface chemistry in a complex way, but sufficient N and S atoms (ca. 4 and >1 at%, respectively) were preserved in addition to the large number of developing defects. Despite the complexity of the textural and chemical changes, rGO increased the electrical conductivity monotonically. In alkaline oxygen reduction reaction (ORR) tests, the sample with 1.25 wt% GO exhibited a 4e- mechanism and reasonable stability, but a higher rGO content gradually compromised the performance of the electrodes. The sample containing 5 wt% GO was the most sensitive under oxidative conditions, but after stabilization it exhibited the highest gravimetric capacitance. In Li-ion battery tests, the coulombic efficiency of all the samples was consistently above 98%, indicating the high potential of these carbons for efficient Li-ion insertion and reinsertion during the charge-discharge process, thereby providing a promising alternative for graphite-based anodes. The cell from the 1.25 wt% GO sample showed an initial discharge capacity of 313 mAh/g, 95.1% capacity retention, and 99.3% coulombic efficiency after 50 charge-discharge cycles.

Post-restoration grassland management overrides the effects of restoration methods in propagule-rich landscapes.

Grassland restoration is gaining momentum worldwide to tackle the loss of biodiversity and associated ecosystem services. Restoration methods and their effects on ecological community reassembly have been extensively studied across various grassland types, while the importance of post-restoration management has so far received less attention. Grassland management is an important surrogate for natural disturbances, with which most ancient grasslands have coevolved. Thus, without the reintroduction of management-related disturbance, restoration targets are unlikely to be achieved in restored grasslands. In this study, we aimed to explore how 20 yr of management by mowing once a year or light cattle grazing affects restoration success in Palearctic meadow-steppe grasslands restored by either sowing native grasses (sown sites), applying Medicago sativa as a nurse plant (Medicago sites), or allowing spontaneous succession (spontaneous sites). We found that, following mowing, sown sites maintained long-lasting establishment limitation, while Medicago sites experienced a delay in succession. These limitations resulted in low total and target species richness, low functional redundancy, and distinct species and functional composition compared to reference data from ancient grasslands. Spontaneous sites that were mowed reached a more advanced successional stage, although they did not reach reference levels regarding most vegetation descriptors. Sown and Medicago sites that were grazed had higher total and target species richness than those that were mowed, and showed restoration success similar to that of spontaneous sites, on which grazing had only moderate further positive effects. Grazed sites, irrespective of the restoration method, were uniformly species rich, functionally diverse, and functionally redundant, and thus became important biodiverse habitats with considerable resilience. We conclude that an optimally chosen post-restoration management may have an impact on long-term community reassembly comparable to the choice of restoration method. Restoration planners may, therefore, need to put more emphasis on future management than on the initial restoration method. However, our findings also imply that if local constraints, such as potentially high invasive propagule pressure, necessitate the application of restoration methods that could also hinder the establishment of target species, the long-term recovery of the grassland can still be ensured by wisely chosen post-restoration management.

Space-Charge Effects at the Li7La3Zr2O12/Poly(ethylene oxide) Interface.

Composites consisting of garnet-type Li7La3Zr2O12 (LLZO) ceramic particles dispersed in a solid polymer electrolyte based on poly(ethylene oxide) (PEO) have recently been investigated as a possible electrolyte material in all solid state Li ion batteries. The interface between the two materials, that is, LLZO/PEO, is of special interest for the transport of lithium ions in the composite. For obtaining the desired high ionic conductivity, Li+ ions have to pass easily across this interface. However, previous research found that the interface is highly resistive. Here, we further investigate the interface between Al-substituted LLZO and PEO-LiClO4 electrolytes in the frame of a theoretical description, which is based on space-charge layers. By theoretical calculations supported by experiments, we find that the interface is highly resistive. From the results, we have deduced that the highest contribution to this resistance comes from a high activation energy and not from electrostatic repulsion of lithium.

Structural and Computational Assessment of the Influence of Wet-Chemical Post-Processing of the Al-Substituted Cubic Li7La3Zr2O12.

Li7La3Zr2O12 (LLZO) and related compounds are considered as promising candidates for future all-solid-state Li-ion battery applications. Still, the processing of those materials into thin membranes with the right stoichiometry and crystal structure is difficult and laborious. The sensitivity of the Li-ion conductive garnets against moisture and the associated Li+/H+ cation exchange makes their processing even more difficult. Formulation of suitable polymer/ceramic hybrid solid state electrolytes could be a prosperous way to reach the future large scale production of solid state Li-ion batteries. In fact, solvent mediated and/or slurry based wet-processing of the LLZO, e.g., tape-casting, could result in irreversible Li-ion loss of the pristine material due to Li+/H+ cation exchange. The concomitant structural changes and loss in functionality in terms of Li-ion conductivity are the results of the above process. Therefore, in the present work a systematic study on the chemical stability and structural retention of Al-substituted LLZO in different solvents is reported. It was found that Li+/H+ exchange in LLZO occurs upon solvent immersion, and its magnitude is dependent on the availability of -OH functional groups of the solvent molecules. As a result, a larger degree of Li+/H+ exchange causes higher increase of the lattice parameter of the LLZO, determined by synchrotron diffraction analyses. The expansion of the cubic unit cell was ascertained, when Li+ was replaced by H+ in the host lattice, by ab initio computational studies. The application of the most common solvent as dispersion medium, i.e., high purity water, causes the most significant Li+/H+ exchange and, therefore, structural change, while acetonitrile was proven to be the best suitable solvent for wet postprocessing of LLZO. Finally, computational calculations suggested that the Li+/H+ exchange could result in diminished ionic, i.e., mixed Li+-H+, conductivity due to the insertion of protons with lower mobility than that of Li-ions.

Screening Precursor-Solvent Combinations for Li4Ti5O12 Energy Storage Material Using Flame Spray Pyrolysis.

The development and industrial application of advanced lithium based energy-storage materials are directly related to the innovative production techniques and the usage of inexpensive precursor materials. Flame spray pyrolysis (FSP) is a promising technique that overcomes the challenges in the production processes such as scalability, process control, material versatility, and cost. In the present study, phase pure anode material Li4Ti5O12 (LTO) was designed using FSP via extensive systematic screening of lithium and titanium precursors dissolved in five different organic solvents. The effect of precursor and solvent parameters such as chemical reactivity, boiling point, and combustion enthalpy on the particle formation either via gas-to-particle (evaporation/nucleation/growth) or via droplet-to-particle (precipitation/incomplete evaporation) is discussed. The presence of carboxylic acid in the precursor solution resulted in pure (>95 mass %) and homogeneous LTO nanoparticles of size 4-9 nm, attributed to two reasons: (1) stabilization of water sensitive metal alkoxides precursor and (2) formation of volatile carboxylates from lithium nitrate evidenced by attenuated total reflection Fourier transform infrared spectroscopy and single droplet combustion experiments. In contrast, the absence of carboxylic acids resulted in larger inhomogeneous crystalline titanium dioxide (TiO2) particles with significant reduction of LTO content as low as ∼34 mass %. In-depth particle characterization was performed using X-ray diffraction with Rietveld refinement, thermogravimetric analysis coupled with differential scanning calorimetry and mass spectrometry, gas adsorption, and vibrational spectroscopy. High-resolution transmission electron microscopy of the LTO product revealed excellent quality of the particles obtained at high temperature. In addition, high rate capability and efficient charge reversibility of LTO nanoparticles demonstrate the vast potential of inexpensive gas-phase synthesis for energy-storage materials.

Hydrothermal synthesis and humidity sensing property of ZnO nanostructures and ZnO-In(OH)3 nanocomposites.

Prism- and raspberry-like ZnO nanoparticles and ZnO-In(OH)(3) nanocomposites were prepared by template free hydrothermal method. XRD investigations and microscopic studies showed that pill-like In(OH)(3) particles with body-centered cubic crystal structure formed on the surface of ZnO nanoparticles resulting in increased specific surface area. TEM-EDX mapping images demonstrated that not only nanocomposite formation took place in the course of the synthesis, but zinc ions were also built into the crystal lattice of the In(OH)(3). However, only undoped In(OH)(3) was found on the surface of the pill-like particle aggregates by XPS analyses. The raspberry- and prism-like ZnO particles exhibit strong visible emission with a maximum at 585 and 595 nm, respectively, whose intensity significantly increase due to nanocomposite formation. Photoelectric investigations revealed that photocurrent intensity decreased with increasing indium ion concentration during UV light excitation, which was explained by increase in visible fluorescence emission. QCM measurements showed that morphology of ZnO and concentration of In(OH)(3) had an influence on the water vapor sensing properties.

Hydrophobization of bovine serum albumin with cationic surfactants with different hydrophobic chain length.

The interaction between bovine serum albumin (BSA) and cationic surfactants with different chain length was investigated. The hydrodynamic diameters, electrokinetic potentials, as well as the fluorescence emission properties of the protein-surfactant complexes with different hydrophobic character were studied. Dynamic light scattering was applied to determine how the size and electrokinetic potential of the protein aggregates changes due to surfactant loading. It was found that by increasing the chain length of the surfactant the required amount of the surfactant for total aggregation of the system is decreased dramatically, which means that in the course on the aggregation process hydrophobic effects should be considered and it was further proved with fluorescence emission intensity measurements. By changing the pH of the protein solution the contribution of the electrostatic interactions to the aggregation processes was studied. It was showed that both hydrophobic and electrostatic interactions are present in the protein-cationic surfactant interaction.