F127 assisted fabrication of Ge/r GO/CNTs nanocomposites with three-dimensional network structure for efficient lithium storage

To solve the volume expansion and poor electrical conductivity of germanium-based anode materials,Ge/rGO/CNTs nanocomposites with three-dimensional network structure are fabricated through the dispersion of polyethylene-polypropylene glycol(F127)and reduction of hydrogen.An interesting phenomenon is discovered that F127 can break GeO_(2)polycrystalline microparticles into 100 nm nanoparticles by only physical interaction,which promotes the uniform dispersion of GeO_(2)in a carbon network structure composed of graphene(rGO)and carbon nanotubes(CNTs).As evaluated as anode material of Lithium-ion batteries,Ge/rGO/CNTs nanocomposites exhibit excellent lithium storage performance.The initial specific capacity is high to 1549.7 mAh/g at 0.2 A/g,and the reversible capacity still retains972.4 mAh/g after 100 cycles.The improved lithium storage performance is attributed to that Ge nanoparticles can effectively slow down the volume expansion during charge and discharge processes,and threedimensional carbon networks can improve electrical conductivity and accelerate lithium-ion transfer of anode materials.

Grain boundary optimization induced substantial squareness enhancement and high performance in iron-rich Sm-Co-Fe-Cu-Zr magnets

Increasing iron content has been witnessed an essential method to improve the remanence of 2:17-type Sm-Co-Fe-Cu-Zr magnets,however,the inferior squareness factor accompanied with the increased iron content turns into a neck sticking problem.In this work,the grain boundary optimization induced substantial squareness enhancement from 63.4%to 91.4%,and consequently an excellent maximum energy product of 32.63 MGOe have been achieved in iron-rich Sm-Co-Fe-Cu-Zr magnets via tuning solution process.It is clearly revealed that the grain boundary(GB)phases as well as the micro-twins’density in grain interiors can be controlled and interprets the enhancement mechanism of squareness.

Magnetic properties of melt-spun ribbons(Sm1-xZrx)(Fe0.92Ti0.08)10 with ThMn12 structure and their hydrides

The structure and magnetic hysteresis properties of the cast Sm1-xZrx(Fe0.92Ti0.08)10(x = 0-0.3)alloys and melt-spun ribbons prepared from them were studied.In the cast alloy with x>0.2, a considerable amount of the eutectic phase is found in the SEM micrographs.Analysis of the temperature dependences of the magnetic susceptibility and XRD patterns allows amorphous state in the as-spun ribbons with x>0.2 to be determined.The specific magnetization measured in a field of 17 kOe and remanence decrease with increasing annealing temperature from 800 to 900 ℃ and weakly depend on Zr concentration.The maximal value of coercivity Hc = 4.7 kOe is obtained on the ribbons with x = 0.2 after annealing at 850℃ for 10 min.After additional hydrogenation of the ribbons,both the coercivity and remanence increase by 54% and 7%,respectively.

Morphology evolution of SmCox permanent magnetic nanoparticles

Sm-Co nanoparticles (NPs) are promising candidates for preparing superstable magnets and exchange-coupled nanocomposite magnets with unprecedented magnetic properties.However,the morphology evolution of the NPs remains unclear.Here,single crystalline SmCox(x=4.07,4.79,6.94,and 8.61) NPs with dimensions below the critical size of a single magnetic domain were synthesized.These NPs consist of Sm_(2)Co_(7),SmCo_(5),and Sm2Co17phases with divergent typical morphologies.An evolution model for the different morphological characteristics was proposed based on phase-structure changes and surface-energy calculations using the density functional theory.The results show that these SmCo_(4.79) NPs can be well aligned along the easy magnetization axis and exhibit an ultrahigh coercivity of 5.7 T,thus enabling to advance the control of NP morphology and to facilitate their use in superstable or nanocomposite magnets.

Electron structures and non-linear optical properties of tert butyl-nitro-phthalocyanines

The electron structures and the non-linear optical properties of phthalocyanines and asymmetrically substituted phthalocyanines are studied with the AM1 method. The results show that the fertbutyl-nitro-phthalocyanines have much higher second order non-linear optical coefficients .