Transition-metal activated phosphors are an important family of luminescent materials that can produce white light with an outstanding color rendering index and correlated color temperature for use in light-emitting diodes.

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Uniform hexagonal hematite (α-Fe(2)O(3)) nanoplates have been synthesized by a facile alcohol-thermal reaction, and a new nanostructure of α-Fe(2)O(3) has been proposed. Each nanoplate is enclosed by (0001) basal planes and {1012} side surfaces. The phase, size, shape, and growth orientation of these nanocrystals were characterized by powder X-ray diffraction and electron microscopy. The thickness and diameter of these nanocrystals could be finely tuned by the selective use of alcohol solvent with increasing carbon atom number in the linear alkyl chain. A variety of nanocrystals with systemically changeable shapes from nanoplates to nanograins have been obtained. Specific adsorption of alcohol molecules on polar (0001) facets is proposed to be the main issue to modify the growth behavior of hematite nanocrystals. The presence of distilled water and the addition of sodium acetate have also been investigated. Either of them has a great influence on the growth of hematite nanocrystals, and shape-controlled growth can be rationally achieved. In addition, the post-aging of as-grown hematite nanocrystals in alcohol and distilled water has also been described. Both vibration spectroscopy (i.e., FTIR and Raman) and electronic spectra (diffused reflectance spectra) of these nanocrystals with a continuing shape change show a highly shape-dependent nature.

A new form of TiO2 microspheres comprised of anatase/TiO2‐B ultrathin composite nanosheets has been synthesized successfully and used as Li‐ion storage electrode material. By comparison between samples obtained with different annealing temperatures, it is demonstrated that the anatase/TiO2‐B coherent interfaces may contribute additional lithium storage venues due to a favorable charge separation at the boundary between the two phases. The as‐prepared hierarchical nanostructures show capacities of 180 and 110 mAh g−1 after 1000 cycles at current densities of 3400 and 8500 mA g−1. The ultrathin nanosheet structure which provides short lithium diffusion length and high electrode/electrolyte contact area also accounts for the high capacity and long‐cycle stability.

A Li3N protection layer is fabricated on the surface of a Li anode by an in situ method to suppress the shuttle effect on the basis of anode protection. The discharge capacity is retained at 773 mA h g(-1) after 500 cycles with an average coulombic efficiency of 92.3% in the electrolyte without LiNO3, while the sulfur loading of the simple sulfur cathode was 2.5-3 mg cm(-2).

A sol-hydrothermal method has been proposed to prepare uniform and unaggregated nanocrystals of pure anatase and rutile from various acidic mediums. The phase formation, particle sizes, and morphologies varying with different acids and their concentrations at different reaction temperatures and times have been investigated using X-ray diffraction and transmission electron microscopy. The use of HCl and the effect of its concentrations on the formation of rutile phase at different temperatures for various reaction times have been described in detail. The effect of the addition of NaCl salt on particle sizes and rutile fractions has also been studied. In this work, the phase transformation from anatase to rutile in the presence of and the absence of NaCl salt has been considered both in neutral and in acidic mediums. The presence of a trace rutile in starting materials of anatase can show obvious effects on the phase transformation under hydrothermal conditions.

Currently, the main bottleneck for the widespread application of Ni-Zn batteries is their poor cycling stability as a result of the irreversibility of the Ni-based cathode and dendrite formation of the Zn anode during the charging-discharging processes. Herein, a highly rechargeable, flexible, fiber-shaped Ni-Zn battery with impressive electrochemical performance is rationally demonstrated by employing Ni-NiO heterostructured nanosheets as the cathode. Benefiting from the improved conductivity and enhanced electroactivity of the Ni-NiO heterojunction nanosheet cathode, the as-fabricated fiber-shaped Ni-NiO//Zn battery displays high capacity and admirable rate capability. More importantly, this Ni-NiO//Zn battery shows unprecedented cyclic durability both in aqueous (96.6% capacity retention after 10 000 cycles) and polymer (almost no capacity attenuation after 10 000 cycles at 22.2 A g ) electrolytes. Moreover, a peak energy density of 6.6 µWh cm , together with a remarkable power density of 20.2 mW cm , is achieved by the flexible quasi-solid-state fiber-shaped Ni-NiO//Zn battery, outperforming most reported fiber-shaped energy-storage devices. Such a novel concept of a fiber-shaped Ni-Zn battery with impressive stability will greatly enrich the flexible energy-storage technologies for future portable/wearable electronic applications.

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