Perspective on cycling stability of lithium-iron manganese phosphate for lithium-ion batteries

Lithium-iron manganese phosphates(LiFex Mn_(1-x)PO_(4),0.1<x<0.9)have the merits of high safety and high working voltage.However,they also face the challenges of insufficient conductivity and poor cycling stability.Some progress has been achieved to solve these problems.Herein,we firstly summarized the influence of different electrolyte systems on the electrochemical performance of LiFexMn_(1-x)PO_(4),and then discussed the effect of element doping,lastly studied the influences of conductive layer coating and morphology control on the cycling stability.Finally,the prospects and challenges of developing high-cycling LiFexMn_(1-x)PO_(4) were proposed.

Lead and Cadmium Adsorption onto Iron Oxides and Manganese Oxides in the Natural Surface Coatings Collected on Natural Substances in the Songhua River of China

Natural surface coatings collected from natural substances （NSCsNS） were employed to study the roles of the main chemical components （iron oxides, manganese oxides, and other components） in controlling the adsorption of lead（Pb） and cadmium（Cd） in aquatic environments. The selective chemical extraction followed by the adsorption of Pb and Cd experiments and statistical analysis, were used to investigate the adsorption property of each component. Hydroxylamine hydrochloride was used to remove manganese oxides selectively, and sodium dithionite was used to extract iron oxides and manganese oxides. The result indicated that iron oxides and manganese oxides played an important role in the adsorption of Pb and Cd on NSCsNS, and the relative contribution was about two-thirds. The contribution of manganese oxides was the greatest, with a lesser role indicated for other components. The adsorption ability of manganese oxides for Pb and Cd was greater than that of iron oxides or other components for Pb and Cd. The Pb adsorption observed in each component was greater than Cd adsorption.

Spatio-temporal succession of iron and manganese microbial community in biological filter layer

This paper studied the structure and dynamic change of microbial communities in bio-reactor for treating ground water which contained high concentration of iron and manganese.In this study,polymerase chain reaction(PCR) denaturing gradient gel electrophoresis(DGGE) was used to evaluate the bacterial diversity.Different samples in spatio-temporal of bacterial community suceession in sands were analyzed,and the removal of iron and manganese were discussed.The results showed that a significant change in the community structure was observed during running time and the bio-reactor which designed by ourselves:the removal rate of iron and manganese could achieve 88.93%.The mass of microrganisms was decreasing,and the type of micro-organisms tended to stable with the increase of operating time.Besides,the change of mass and types of micro-organisms in sands was related to temperature.Along the depth of filter layer,the mass and types of micro-organisms were gradually decreasing.Further,pseudomonas were found to be the main microbiology by recycling the band sequencing and phylogenetic analysis.And with time increasing the mass and kind of bacteria were growing from less to more,finally to be stable.

An amorphous manganese iron oxide hollow nanocube cathode for aqueous zinc ion batteries

Aqueous zinc ion batteries(ZIBs) are attracting considerable attentions for practical energy storage because of their low cost and high safety.Nevertheless,the traditional manganese oxide cathode materials suffer from the low intrinsic electronic conductivity,sluggish ions diffusion kinetics,and structural collapse,hindering their large-scale application.Herein,we successfully developed a latent amorphous Mn_(1.8)Fe_(1.2)O_(4) hollow nanocube(a-H-MnFeO) cathode material derived from Prussian blue analogue precursor.The amorphous nature endows the cathode with lower diffusion barrier and narrower band gap compared with crystalline counterpart,resulting in the superior Zn^(2+) ions and electrons transport kinetics.Hollow structure can furnish abundant surface sites and suppress the structural collapse during the repeated charge/discharge processes.By virtue of the multiple advantageous features,the a-H-MnFeO cathode exhibits exceptional electrochemical performance,in terms of high capacity,excellent rate capability,and prolonged cycle life.This strategy will pave the way for the structural design of emerging cathode materials.

Ore petrography of low-grade siliceous manganese ores from the Bonai-Keonjhar belt, Orissa, India: The influence of mineral-fabric on their beneficiation

Low grade siliceous manganese ores from the iron ore group of the Bonai-Keonjhar belt, Orissa, India are found mostly in shear zones. The ore characteristics of siliceous manganese ore samples from three differ- ent mines, viz. the Shankar (Barbil OMC lease hold area), the Sone-Patuli (Patmunda, OMM lease hold area), and the Musaghar (Roida, OMDC lease hold area), were studied. These siliceous manganese ores are of three types, respectively: (i) spongy-granular; (ii) massive-mosaic; and (iii) hard-mylonitized. The spongy-gran- ular type contains granular, saccharoidal quartz and the major manganese mineral present is pyrolusite. The second type contains well crystallized quartz and cryptomelane, while the third has cherty, fine grained quartz (mylonite) along with romanechite. All three ores were subjected to physical beneficiation under similar conditions. Both gravity and magnetic separation techniques were employed. The mineral-fabric of the ores has been correlated to the extent of their beneficiation using these physical techniques. Of these three ores only the spongy-granular type responded well to upgrading. The feed with 22% Mn content could be upgraded to 44% with a 28% yield and a 49% recovery. The good response to beneficiation of the spongy- granular sample could be due to the large euhedral crystals of pyrolusite and the friable nature of the sac- charoidal quartz. This study reveals the influence of mineral-fabric on beneficiation of low grade ore, siliceous Mn ore in particular.

Variations between rice cultivars in iron and manganese plaque on roots and the relation with plant cadmium uptake

To understand certain mechanisms causing variations between rice cultivars with regard to cadmium uptake and tolerance, pot soil experiments were conducted with two rice cultivars of different genotypes under different soil Cd levels. The relationships between plant Cd uptake and iron/manganese （Fe/Mn） plaque formation on roots were investigated. The results showed that rice cultivars differed markedly in Cd uptake and tolerance. Under soil Cd treatments, Cd concentrations and accumulations in the cultivar Shanyou 63 （the genotype indica） were significantly higher than those in the cultivar Wuyunjing 7 （the genotype japonica） （P 〈 0.01, or P 〈 0.05）, and Shanyou 63 was more sensitive to Cd toxicity than Wuyunjing 7. The differences between the rice cultivars were the largest at relatively low soil Cd level （i.e., 10 mg/kg）. Fe concentrations in dithionite-citrate-bicarbonate root extracts of Shanyou 63 were generally lower than that of Wuyunjing 7, and the difference was the most significant under the treatment of 10 mg Cd/kg soil. The results indicated that the formation of iron plaque on rice roots could act as a barrier to soil Cd toxicity, and may be a ＂buffer＂ or a ＂reservoir＂ which could reduce Cd uptake into rice roots. And the plaque may contribute, to some extent, to the genotypic differences of rice cultivars in Cd uptake and tolerance.

Investigation on Fe,Mn,Zn,Cu,Pb and Cd fractions in the natural surface coating samples and surficial sediments in the Songhua River,China

Natural surface coating samples （NSCSs） from the surface of shingles and surficial sediments （SSs） in the Songhua River, China were employed to investigate the relationship between NSCSs and SSs in fractions of heavy metals （Fe, Mn, Zn, Cu, Pb, and Cd） using the modified sequential extraction procedure （MSEP）. The results show that the differences between NSCSs and SSs in Fe fi＇actions were insignificant and Fe was dominantly present as residual phase （76.22% for NSCSs and 80.88% for SSs） and Fe-oxides phase （20.33% for NSCSs and 16.15% for SSs）. Significant variation of Mn distribution patterns between NSCSs and SSs was observed with Mn in NSCSs mainly present in Mn-oxides phase （48.27%） and that in SSs present as residual phase （45.44%）. Zn, Cu, Pb and Cd were found dominantly in residual fractions （〉48%）, and next in solid oxides/hydroxides for Zn, Pb and Cd and in easily oxidizable solids/compounds form for Cu, respectively. The heavy metal distribution patterns implied that Fe/Mn oxides both in NSCSs and SSs were more important sinks for binding and adsorption of Zn, Pb and Cd than organic matter （OM）, and inversely, higher affinity of Cu to OM than Fe/Mn oxides in NSCSs and SSs was obtained. Meanwhile, it was found that the distributions of heavy metals in NSCSs and SSs were similar to each other and the pseudo-total concentrations of Zn, Cu, Pb and Cd in NSCSs were greater than those in SSs, highlighting the more importance for NSCSs than SSs in controlling behaviours of heavy metals in aquatic environments.

Adsorptive removal of iron and manganese ions from aqueous solutions with microporous chitosan/polyethylene glycol blend membrane

Microporous chitosan （CS） membranes were directly prepared by extraction of poly（ethylene glycol） （PEG） from CS/PEG blend membrane and were examined for iron and manganese ions removal from aqueous solutions. The different variables affecting the adsorption capacity of the membranes such as contact time, pH of the sorption medium, and initial metal ion concentration in the feed solution were investigated on a batch adsorption basis. The affinity of CS/PEG blend membrane to adsorb Fe（II） ions is higher than that of Mn（II） ions, with adsorption equilibrium achieved after 60 min for Fe（II） and Mn（II） ions. By increasing CS]PEG ratio in the blend membrane the adsorption capacity of metal ions increased. Among all parameters, pH has the most significant effect on the adsorption capacity, particularly in the range of 2.9-5.9. The increase in CS/PEG ratio was found to enhance the adsorption capacity of the membranes. The effects of initial concentration of metal ions on the extent of metal ions removal were investigated in detail. The experimental data were better fitted to Freundlich equation than Langmuir. In addition, it was found that the iron and manganese ions adsorbed on the membranes can be effectively desorbed in 0.1 mol/L HCl solution （up to 98% desorption efficiency） and the blend membranes can be reused almost without loss of the adsorption capacity for iron and manganese ions.

Immobilization biological activated carbon used in advanced drinking water treatment

Bacteria separated from a mature filter bed of groundwater treatment plants were incubated in a culture media containing iron and manganese. A consortium of 5 strains of bacteria removing iron and manganese were obtained by repeated enrichment culturing. It was shown from the experiments of effect factors that ironmanganese removal bacteria in the euhure media containing both Fe and Mn grew better than in that containing only Fe, however, they were unable to grow in the culture media containing only Mn. When comparing the bacteria biomass in the case ofp （DO） ：2.8 mg/L andp （DO） ：9. 0 mg/L, no significant difference was found. The engineering bacteria removing the organic and the bacteria removing iron and manganese were simuhaneously inoculated into activated carbon reactor to treat the effluent of distribution network. The experimental results showed that by using IBAC （ Immobilization Biological Activated Carbon） treatment, the removal efficiency of iron, manganese and permanganate index was more than 98% , 96% and 55% , respectively. After the influent with turbidity of 1.5 NTU, color of 25 degree and oflbnsive odor was treated, the turbidity and color of effluence were less than 0.5 NTU and 15 degree, respectively, and it was odorless. It is determined that the cooperation function of engineering bacteria and activated carbon achieved advanced drinking water treatment.

Syntheses，Structures and Properties of Some New Composition Perovskite Compounds：Sr0．6Bi0．4FeO2．7，Sr1－xBixFeO3－y and Ba1．5Pt0．5Mn2O6

New composition perovskite-type compounds with formula Sr0.6Bi0.4FeO2.7,Sr1-xBixFeO3-y(x=0.1 to 0. 9 in interveral of 0.1),and Ba1.5Pt0.5Mn2O6 have been synthsized and structurally characterized.The crystal structure of Sr0.6Bi0.4FeO2.7has been determined by X-ray single crystal diffraction,and the data of neutron powder diffraction collected at both room temperature and elevated temperature(380℃).The compound Sr0.6Bi0.4FeO2.7 crystallizes in the cubic space group of Pm3m with Z=1,a=3.9330(6) at room temperature,a=3.9498(6)A at 380℃.The magnetic structure from the neutron powder diffraction data collected at room temperature is consistent with a simple G-type antiferromagnetism and has a magnetic moment of 4.98 μB per Fe atom.The structures of Sr1-xBixFeO3-y with x other than 0.4 were also refined from the X-ray powder diffraction data.The data were consistent with a tetragonal cell when x=0.1,a rhombohedral cell when x= 0.9,and a cubic cell for x=0.2～0.8.From single crystal X-ray diffraction data,Ba1.5Pt0.5Mn2O6 crystallizes in hexagonal space group of P63mc with a= 5.7722 (6),c=4.4504(9),V=128.42(2),Z=1.The Sr(1-x)BixFeO(3-y)are found to be a good electronic and ionic conductor.

Modification of LiMn_(0.6)Fe_(0.4)PO_(4)lithium-ion battery cathode materials with a fluorine-doped carbon coating

In this study,glucose and NH4F were utilized as sources of carbon and fluorine,respectively,for the synthesis of LiMn_(0.6)Fe_(0.4)PO_(4)(LMFP)nanoscales.These nanoscales were subsequently modified with varying levels of fluorine-doped carbon through co-precipitation and mechanical ball milling processes.The LMFP,incorporating carbon and varying levels of fluoride ions,exhibit higher specific discharge capacities at 0.2 Cand electrochemical characteristics compared to the original LMFP coated solely with carbon.The inclusion of fluorine-doped carbon in the composite material creates numerous pathways for expeditious electron transfer.Moreover,the partial formation of metal fluoride at the interface between the surface of LMFP and the layer of carbon coating doped with fluorine enhances the reduction in the charge-transfer resistance.The modified ferromanganese phosphate cathode material reveals an outstanding discharge capacity displaying a reversible discharge specific capacity value of 131.73 mA h g^(−1)at 10C and 154.6 mA h g^(−1)at 0.2C,due to its unique structure.