Boosting the Electrochemical Performance of Li- and Mn-Rich Cathodes by a Three-in-One Strategy.

There are plenty of issues need to be solved before the practical application of Li- and Mn-rich cathodes, including the detrimental voltage decay and mediocre rate capability, etc. Element doping can effectively solve the above problems, but cause the loss of capacity. The introduction of appropriate defects can compensate the capacity loss; however, it will lead to structural mismatch and stress accumulation.

Capacity Increase Investigation of CuSe Electrode by Using Electrochemical Impedance Spectroscopy.

CuSe nanoflake arrays supported by Cu foams are synthesized by a facile hydrothermal method in this study. The CuSe materials are directly used as an anode for lithium ion batteries, which show superior cycle performance with significant capacity increase. Combining with previous reports and scanning electron microscope images after cycling, the capacity increase caused by the reversible growth of a polymeric film is discussed.

Group IVA Element (Si, Ge, Sn)-Based Alloying/Dealloying Anodes as Negative Electrodes for Full-Cell Lithium-Ion Batteries.

To satisfy the increasing energy demands of portable electronics, electric vehicles, and miniaturized energy storage devices, improvements to lithium-ion batteries (LIBs) are required to provide higher energy/power densities and longer cycle lives. Group IVA element (Si, Ge, Sn)-based alloying/dealloying anodes are promising candidates for use as electrodes in next-generation LIBs owing to their extremely high gravimetric and volumetric capacities, low working voltages, and natural abundances. However, due to the violent volume changes that occur during lithium-ion insertion/extraction and the formation of an unstable solid electrolyte interface, the use of Group IVA element-based anodes in commercial LIBs is still a great challenge.

Removal of thallium from aqueous solutions using Fe-Mn binary oxides.

In this study, Fe-Mn binary oxides, which harbor the strong oxidative power of manganese dioxide and the high adsorption capacity of iron oxides, were synthesized for Tl(I) removal using a concurrent chemical oxidation and precipitation method. The adsorption of Tl onto the Fe-Mn adsorbent was fast, effective, and selective, with equilibrium sorption reaching over 95% under a broad operating pH (3-12), and high ionic strength (0.1-0.

Germanium anode with excellent lithium storage performance in a germanium/lithium-cobalt oxide lithium-ion battery.

Germanium is a highly promising anode material for lithium-ion batteries as a consequence of its large theoretical specific capacity, good electrical conductivity, and fast lithium ion diffusivity. In this work, Co3O4 nanowire array fabricated on nickel foam was designed as a nanostructured current collector for Ge anode. By limiting the voltage cutoff window in an appropriate range, the obtained Ge anode exhibits excellent lithium storage performance in half- and full-cells, which can be mainly attributed to the designed nanostructured current collector with good conductivity, enough buffering space for the volume change, and shortened ionic transport length.

Carbon-wrapped Fe3O4 nanoparticle films grown on nickel foam as binder-free anodes for high-rate and long-life lithium storage.

Carbon-wrapped Fe3O4 nanoparticle films on nickel foam were simply prepared by a hydrothermal synthesis with sucrose as a precursor of subsequent carbonization. The as-prepared samples were directly used as binder-free anodes for lithium-ion batteries which exhibited enhanced rate performance and excellent cyclability. A reversible capacity of 543 mA h g(-1) was delivered at a current density as high as 10 C after more than 2000 cycles.

Growth of nanostructured nickel sulfide films on Ni foam as high-performance cathodes for lithium ion batteries.

We report a facile and reproducible synthesis of nanostructured Ni3S2 films by a hydrothermal route with Ni foam as the precursor reactant and substrate. The synthetic mechanism was examined by investigating the dependence of the films' crystal morphologies on the hydrothermal duration, and uniform nanostructured Ni3S2 films with a porous carpet-like morphology were synthesized on the substrates. The architectures were used as cathodes for lithium ion batteries (LIBs), and their electrochemical performances were evaluated as a function of the film thickness.

Single electrospun porous NiO-ZnO hybrid nanofibers as anode materials for advanced lithium-ion batteries.

Porous NiO-ZnO hybrid nanofibers were prepared by a single-nozzle electrospinning technique combined with subsequent heating treatment. The resultant nanofibers are composed of interconnected primary nanocrystals and numerous nanopores with heterostructures between NiO and ZnO. Such characteristics of the structure can lead to excellent electrochemical performances when the nanofiber was evaluated as an anode material for lithium-ion batteries.