New insights into tunnel-type NaxMnO2-yFy with high performance and excellent cycling stability: the impact of F-doping.

Developing sustainable batteries based on abundant elements such as sodium and manganese is very attractive. Thus, sodium-manganese oxides can be employed as electrodes for sodium-ion batteries. Herein, an NaxMnO2-yFy electrode material is investigated and optimized. Galvanostatic cycling and diffusion coefficient calculations have been employed. It is found that tailoring the stoichiometry using the sodium/manganese ratio and fluorine content in the synthesis can improve the electrochemical performance and achieve high capacity and superb cycling stability. An anion-doping strategy (F-doping) can significantly improve electrode stability, and greatly raise the maximum specific capacity from ca. 70 mA h g-1 for an F-free sample to ca. 120 mA h g-1 for an F-doped sample at a slow rate (10 mA g-1 of current intensity). The reversible capacity of the F-doped sample is stable for many cycles (around 40-45 mA h g-1 at 500 mA g-1 for 1000 cycles).

The Magnesium Insertion Effects into P2-Type Na2/3 Ni1/3 Mn2/3 O2.

A Mg-cell with P2-Na2/3 Ni1/3 Mn2/3 O2 layered oxide cathode provides novel reaction mechanism not observed in Na-cells. The sodium/vacancy ordering and Jahn-Teller effects are suppressed with the insertion of magnesium ion. The Mg-cell exhibits different features when operating between 4.5 and 0.15 V and 3.9 and 0.15 V versus Mg2+ /Mg. To analyze the structural and chemical changes during Mg insertion, the cathode is first charged to obtain the Na1/3 Ni1/3 Mn2/3 O2 compound, which is formally accompanied by an oxidation from Ni2+ to Ni3+ . As structure models Mg1/6 Na1/3 Ni1/3 Mn2/3 O2 and Mg1/12 Na1/2 Ni1/3 Mn2/3 O2 are utilized with a large 2 3 a $2\sqrt 3 a$ × 2 3 a $2\sqrt 3 a$ supercell. On discharge, the Mg-cell exhibits a multistep profile which reaches ≈100 mA h g-1 with the valence change from Ni3+ to Ni2+ . Such profile is quite different from its sodium counterpart (230 mA h g-1 ) which exhibits the sodium/vacancy ordering and deleterious presence of Mn3+ . Depending on how the two interlayer spacings are filled by Na and Mg the "staged," "intermediated," and "average" models are analyzed for Mgy Na8 Ni8 Mn16 O48 supercell. This fact suggests differences in the cell performance when Mg is used as counter electrode providing some tips to improve the structure engineering on cathode materials.

Review and New Perspectives on Non-Layered Manganese Compounds as Electrode Material for Sodium-Ion Batteries.

After more than 30 years of delay compared to lithium-ion batteries, sodium analogs are now emerging in the market. This is a result of the concerns regarding sustainability and production costs of the former, as well as issues related to safety and toxicity. Electrode materials for the new sodium-ion batteries may contain available and sustainable elements such as sodium itself, as well as iron or manganese, while eliminating the common cobalt cathode compounds and copper anode current collectors for lithium-ion batteries. The multiple oxidation states, abundance, and availability of manganese favor its use, as it was shown early on for primary batteries. Regarding structural considerations, an extraordinarily successful group of cathode materials are layered oxides of sodium, and transition metals, with manganese being the major component. However, other technologies point towards Prussian blue analogs, NASICON-related phosphates, and fluorophosphates. The role of manganese in these structural families and other oxide or halide compounds has until now not been fully explored. In this direction, the present review paper deals with the different Mn-containing solids with a non-layered structure already evaluated. The study aims to systematize the current knowledge on this topic and highlight new possibilities for further study, such as the concept of entatic state applied to electrodes.

New perspectives on the multianion approach to adapt electrode materials for lithium and post-lithium batteries.

Developing new and sustainable batteries is essential for modern society. Both cationic doping (e.g. transition metals) and anionic doping (F-, O2-, S2-, PO43-, etc.) can be employed to improve the electrochemical behaviour of electrode materials. Herein, the anion-doping, or multianion approach, is comprehensively reviewed and investigated. It is observed that the optimized compositions of some electrode materials can involve metastable or transient states. Going beyond the inductive effect, we propose that the simultaneous use of several kinds of anions in the framework of the same host material could create a sort of energized state in the electrode material, and this could be interpreted within the "entatic state" principle which is used in coordination chemistry, catalysis, and bioinorganic chemistry. In this new hypothesis, the coordination of a cation by several anions with different properties can modify the local structure and it could enhance the electrochemical performance; this could be particularly useful for the future post-lithium batteries. The multianion approach can also be applied to electrolytes and interfaces. Finally, new theoretical calculations on multianion-based materials (carbonophosphates, thiocarbonates and Mg8Mn16O32-zFz) are reported here, highlighting the need for further research in the coordination sphere of metal-ligand systems for tuning battery properties.

Olivine-Type MgMn0.5 Zn0.5 SiO4 Cathode for Mg-Batteries: Experimental Studies and First Principles Calculations.

Magnesium driven reaction in olivine-type MgMn0.5 Zn0.5 SiO4 structure is subject of study by experimental tests and density functional theory (DFT) calculations. The partial replacement of Mn in Oh sites by other divalent metal such as Zn to get MgMn0.5 Zn0.5 SiO4 cathode is successfully developed by a simple sol-gel method. Its comparison with the well-known MgMnSiO4 olivine-type structure with (Mg)M1 (Mn)M2 SiO4 cations distribution serves as the basis of this study to understand the structure, and the magnesium extraction/insertion properties of novel olivine-type (Mg)M1 (Mn0.5 Zn0.5 )M2 SiO4 composition. This work foresees to extend the study to others divalent elements in olivine-type (Mg)M1 (Mn0.5 M0.5 )M2 SiO4 structure with M = Fe, Ca, Mg, and Ni by DFT calculations. The obtained results indicate that the energy density can be attuned between 520 and 440 W h kg-1 based on two properties of atomic weight and redox chemistry. The presented results commit to open new paths toward development of cathodes materials for Mg batteries.

Advancing towards a Practical Magnesium Ion Battery.

A post-lithium battery era is envisaged, and it is urgent to find new and sustainable systems for energy storage. Multivalent metals, such as magnesium, are very promising to replace lithium, but the low mobility of magnesium ion and the lack of suitable electrolytes are serious concerns. This review mainly discusses the advantages and shortcomings of the new rechargeable magnesium batteries, the future directions and the possibility of using solid electrolytes. Special emphasis is put on the diversity of structures, and on the theoretical calculations about voltage and structures. A critical issue is to select the combination of the positive and negative electrode materials to achieve an optimum battery voltage. The theoretical calculations of the structure, intercalation voltage and diffusion path can be very useful for evaluating the materials and for comparison with the experimental results of the magnesium batteries which are not hassle-free.

Magnesium Deintercalation From the Spinel-Type MgMn2-y Fey O4 (0.4≤y≤2.0) by Acid-Treatment and Electrochemistry.

Rechargeable magnesium batteries attract lots of attention because of their high safety and low cost compared to lithium batteries, and it is needed to develop more efficient electrode materials. Although MgMn2 O4 is a promising material for the positive electrode in Mg rechargeable batteries, it usually exhibits poor cyclability. To improve the electrochemical behavior, we have prepared nanoparticles of MgMn2-y Fey O4 . The XRD results have confirmed that when Mn3+ (Jahn-Teller ion) ions are replaced by Fe3+ (non-Jahn-Teller ion), the resulting MgMn2-y Fey O4 is a cubic phase. The structure and theoretical voltage are theoretically calculated by using the DFT method. The obtained samples have been chemically treated in acid solution for partial demagnesiation, and it is observed that the presence of iron inhibits the deinsertion of Mg through disproportionation and favors the exchange reaction. The electrochemical behavior in non-aqueous magnesium cells has been explored.

Testing the reversible insertion of magnesium in a cation-deficient manganese oxy-spinel through a concentration cell.

Magnesium-ion batteries could be competitive with lithium-ion batteries, but the reversible intercalation of magnesium in the framework of the host material needs to be verified. A concentration cell was built by using electrodes with different concentrations of magnesium ions in the cubic spinel MgxMn2O4. For this purpose, firstly cations were partially extracted from MgMn2O4 by acid-treatment. This concentration cell was used to test the reversible intercalation of magnesium and the effect of the cationic vacancies. The theoretical results of the percolation energy can explain the lower polarization experimentally observed in the voltage curve of the acid-treated sample. The reversible capacity (ca. 115 mA h g-1) is preserved after charge-discharge cycling.

Increasing Energy Density with Capacity Preservation by Aluminum Substitution in Sodium Vanadium Phosphate.

Highly Al-substituted C-coated Na3V2-xAlx(PO4)3 compounds with a sodium superionic conductor structure are synthesized by a single and easily scalable sol-gel route. The effect of the experimental conditions is examined. Their structural, chemical, and morphological features are described. The first-principles method is used to determine the theoretical voltage vs Na content profile during Na extraction. The electrochemical Na extraction is characterized by the presence of two plateaus. The first one at ca. 3.4 V is assigned to the V4+/V3+ redox pair and shows good cyclability. The second plateau at ca. 3.9-4.0 V can be assigned to the V5+/V4+ pair, as evidenced by X-ray photoelectron spectroscopy. This second plateau is less reversible during further discharge.

Use of XRD and SEM/EDX to predict age and sex from fire-affected dental remains.

In fire scenarios, the application and accuracy of traditional odontological methods are often limited. Crystalline studies and elemental profiling have been evaluated for their applicability in determining biological profiles (age and sex) from human dentition, particularly fire- and heat-affected dental remains. Thirty-seven teeth were paired according to tooth type and donor age/sex for the analysis of crown and root surfaces pre- and post-incineration using X-ray diffraction (XRD) and scanning electron microscopy (SEM/EDX). In unburned crowns, carbon (C) content showed a positive correlation with age, whereas phosphorus (P) and calcium (Ca) contents showed a negative correlation with age. In unburned roots, C, P and Ca contents also showed significant changes that were opposite of those observed in the crowns. In relation to sex, females exhibited a higher C ratio than males, whereas males showed significantly higher levels of oxygen (O), P and Ca in unburned roots. Incineration resulted in an increase in the crystallite size that correlated with increasing temperature. No differences in hydroxyapatite (HA) crystallite size were found between age groups; however, unburned teeth from females exhibited a larger crystallite size than did those from males. The challenges of using XRD with a 3D sample were overcome to allow analysis of whole teeth in a nondestructive manner. Further studies may be useful in helping predict the temperature of a fire.

On the Mechanism of Magnesium Storage in Micro- and Nano-Particulate Tin Battery Electrodes.

This study reports on the electrochemical alloying-dealloying properties of Mg2Sn intermetallic compounds. 119Sn Mössbauer spectra of β-Sn powder, thermally alloyed cubic-Mg2Sn, and an intermediate MgSn nominal composition are used as references. The discharge of a Mg/micro-Sn half-cell led to significant changes in the spectra line shape, which is explained by a multiphase mechanism involving the coexistence of c-Mg2Sn, distorted Mg2−δSn, and Mg-doped β-Sn. Capacities and capacity retention were improved by using nanoparticulate tin electrodes. This material reduces significantly the diffusion lengths for magnesium and contains surface SnO and SnO2, which are partially electroactive. The half-cell potentials were suitable to be combined versus the MgMn2O4 cathodes. Energy density and cycling properties of the resulting full Mg-ion cells are also scrutinized.

Electrochemical in battery polymerization of poly(alkylenedioxythiophene) over lithium iron phosphate for high-performance cathodes.

A molecular wiring concept was induced in LiFePO4 cathodes by in battery polymerization methods. This was performed by the addition of alkylthiophene monomers over the LiFePO4-based cathode during the first charging step in lithium test cells. The driving force for the in battery polymerization of the monomers was supplied by the oxidizing current and by the physical contact of monomers with delithiated Li1-xFePO4 formed during the charging of the battery. The resulting molecularly engineered cathodes give higher initial capacity, superior rate capability and improved cyclability compared to the pristine LiFePO4 compound. Further to observe changes in the oxidation state of iron, Mössbauer spectroscopy was employed and the results were correlated with those of impedance spectroscopy, which reveal a significant increase in conductivity during charging. The presented methods provide simple yet effective routes for manufacturing efficient cathode materials at room temperature, without the need of additional oxidizing compounds to carry out the polymerization process and to rival high temperature based carbon coatings.

Lithium storage mechanisms and effect of partial cobalt substitution in manganese carbonate electrodes.

A promising group of inorganic salts recently emerged for the negative electrode of advanced lithium-ion batteries. Manganese carbonate combines low weight and significant lithium storage properties. Electron paramagnetic resonance (EPR) and magnetic measurements are used to study the environment of manganese ions during cycling in lithium test cells. To observe reversible lithium storage into manganese carbonate, preparation by a reverse micelles method is used. The resulting nanostructuration favors a capacitive lithium storage mechanism in manganese carbonate with good rate performance. Partial substitution of cobalt by manganese improves cycling efficiency at high rates.

Synthesis and electrochemical reaction with lithium of mesoporous iron oxalate nanoribbons.

Mesoporous FeC 2O 4 was prepared by dehydration of bulk monoclinic- and micellar orthorhombic FeC 2O 4.2H 2O precursors at 200 degrees C. The micellar material shows nanoribbon shaped particles, which are preserved after dehydration. These solids are used as high-capacity lithium storage materials with improved rate performance. The mesoporous nanoribbons exhibit higher capacities close to 700 mA h/g after 50 cycles at 2C (C = 1 Li h (-1) mol (-1)) rate between 0 and 2 V.