A facile two‐step strategy involving a polyol method and subsequent thermal annealing treatment is successfully developed for the large‐scale preparation of ZnCo2O4 various hierarchical micro/nanostructures (twin mcrospheres and microcubes) without surfactant assistance. To the best of our knowledge, this is the first report on the synthesis of ZnCo2O4 mesoporous twin microspheres and microcubes. More significantly, based on the effect of the reaction time on the morphology evolution of the precursor, a brand‐new crystal growth mechanism, multistep splitting then in situ dissolution recrystallization accompanied by morphology and phase change, is first proposed to understand the formation of the 3D twin microshperes, providing new research opportunity for investigating the formation of novel micro/nanostructures. When evaluated as anode materials for lithium‐ion batteries (LIBs), ZnCo2O4 hierarchical microstructures exhibit superior capacity retention, excellent cycling stability at the 5 A g−1 rate for 2000 cycles. Surprisingly, the ZnCo2O4 twin microspheres show an exceptionally high rate capability up to the 10 A g−1 rate. It should be noted that such super‐high rate performance and cycling stability at such high charge/discharge rates are significantly higher than most work previously reported on ZnCo2O4 micro/nanostructures and ZnCo2O4‐based heterostructures. The ZnCo2O4 3D hierarchical micro/nanostructures demonstrate the great potential as negative electrode materials for high‐performance LIBs.

Despite the desirable advancement in synthesizing transition-metal phosphides (TMPs)-based hybrid structures, most methods depend on foreign-template-based multistep procedures for tailoring the specific structure. Herein, a self-template and recrystallization-self-assembly strategy for the one-step synthesis of core-shell-like cobalt phosphide (CoP) nanoparticles embedded into nitrogen and phosphorus codoped porous carbon sheets (CoP⊂NPPCS), is first proposed. Relying on the unusual coordination ability of melamine with metal ions and the cooperative hydrogen bonding of melamine and phytic acid to form a 2D network, a self-synthesized single precursor can be attained. Importantly, this approach can be easily expanded to synthesize other TMPs⊂NPPCS. Due to the unique compositional and structural characteristics, these CoP⊂NPPCSs manifest outstanding electrochemical performances as anode materials for both lithium- and potassium-ion batteries. The unusual hybrid architecture, the high specific surface area, and porous features make the CoP⊂NPPCS attractive for other potential applications, such as supercapacitors and electrocatalysis.

The effects of long chain branching on the nucleation density enhancements and morphological evolution for polylactide (PLA) materials during shear-induced isothermal crystallization process were thoroughly investigated by using rotational rheometer and polarized optical microscopy (POM). Shear-induced nucleation density enhancements for the long chain branched PLA (LCB PLA) were studied on the basis of the determination of the critical shear rate, for which the stretch of the longest chains of the linear component is expected. The results of shear-induced isothermal crystallization kinetics show that the crystallization process under shear is greatly enhanced compared to the quiescent conditions and the crystallization kinetics is accelerated with the increases in shear rate and/or shear time. LCB PLA crystallizes much faster than linear PLA under the same shear condition. A saturation effect of shear time on crystallization kinetics is observed for both linear PLA and LCB PLA. In-situ POM observations demonstrate that LCB PLA not only possesses higher nucleation density under the identical shear time and a constant lower value of spherulitic growth rate compared with that of linear PLA but also forms the shish-kebab structure after sheared for sufficient time. The quantitative evaluation of the shear-induced nucleation densities from rheological measurements is based on the space-filling model by using the Avrami equation, and the obtained nucleation density values are well consistent with that estimated from POM observations. A saturation of nucleation density under shear can be reached for both linear PLA and LCB PLA. The saturated nucleation density values are higher than that under the quiescent condition by a factor of over 3 orders of magnitude, and the saturated nucleation density value for LCB PLA is more than that for linear PLA by a factor of 1 order of magnitude under the same shear condition. The enhancement of nucleation ability and the morphological evolution from the spherulitic to shish-kebab structures induced by shear flow can be ascribed to the broadened and complex relaxation behaviors of LCB PLA.

A facile method is presented for the large-scale preparation of rationally designed mesocrystalline MnO@carbon core-shell nanowires with a jointed appearance. The nanostructures have a unique arrangement of internally encapsulated highly oriented and interconnected MnO nanorods and graphitized carbon layers forming an external coating. Based on a comparison and analysis of the crystal structures of MnOOH, Mn2 O3 , and MnO@C, we propose a sequential topotactic transformation of the corresponding precursors to the products. Very interestingly, the individual mesoporous single-crystalline MnO nanorods are strongly interconnected and maintain the same crystallographic orientation, which is a typical feature of mesocrystals. When tested for their applicability to Li-ion batteries (LIB), the MnO@carbon core-shell nanowires showed excellent capacity retention, superior cycling performance, and high rate capability. Specifically, the MnO@carbon core-shell nanostructures could deliver reversible capacities as high as 801 mA h g(-1) at a high current density of 500 mA g(-1) , with excellent electrochemical stability after testing over 200 cycles, indicating their potential application in LIBs. The remarkable electrochemical performance can mainly be attributed to the highly uniform carbon layer around the MnO nanowires, which is not only effective in buffering the structural strain and volume variations of anodes during repeated electrochemical reactions, but also greatly enhances the conductivity of the electrode material. Our results confirm the feasibility of using these rationally designed composite materials for practical applications. The present strategy is simple but very effective, and appears to be sufficiently versatile to be extended to other high-capacity electrode materials with large volume variations and low electrical conductivities.

Low-cost controlled strategies for the synthesis of mesoporous nickel oxide materials are highly desirable owing to its significant applications for power storage and other fields. In this contribution, we develop a novel hydrothermal route to synthesize a-Ni(OH) 2 , in which urea has not only been utilized to produce hydroxyl anions, but also to organize ultrathin nanowires/nanosheets into a network-like hierarchical assemblage. The morphological evolution process of this organized product has been investigated by examining different reaction intermediates during the synthesis. The growth and thus final assemblage of a-Ni(OH) 2 can be finely tuned by selecting preparative parameters such as the molar ratio of starting chemicals. Based on the topotactic transformation from a-Ni(OH) 2 , various mesoporous NiO hierarchical microspheres from ultrathin nanowires/nanosheets self-assembly have been prepared via thermal decomposition in an air atmosphere. The electrochemical performances of the typical nickel oxide products are evaluated. It is demonstrated that tuning of the surface texture and the pore size of the NiO products is very significant for electrochemical capacitor and water treatment applications. The mesoporous NiO network-like hierarchical microspheres exhibit excellent cyclic performance with nearly 100% capacity retention at a current density of 10 A g À1 in a testing range of 2000 cycles. Moreover, the mesoporous NiO network-like hierarchical microspheres have excellent ability to remove organic pollutants from wastewater by their wonderful surface adsorption ability.

The relentless pursuit of new electrode materials for lithium ion batteries (LIBs) has been conducted for decades. Structures with either porous or nanostructure configurations have been confirmed as advantageous candidates for energy storage/conversion applications. The integration of the two features into one structure can provide another chance to improve the electroactivities. Recently, single-phased mixed metal oxides (MMOs) containing different metal cations, in particular, have confirmed high electrochemical activities because of their complex chemical composition, interfacial effects, and the synergic effects of the multiple metal species. In this review, we will focus on recent research advances of MMOs with porous architectures as anode materials in the matter of structural arrangement and compositional manipulation. Moreover, the application of self-supported MMO-based porous structures as LIB anodes is also explained herein. More importantly, investigations on the synthetic system and formation mechanism of porous MMOs will be highlighted. Some future trends for the innovative design of new electrode materials are also discussed in this review. The challenges and prospects will draw many researchers' attention.

Bimodal architecture and rheological and foaming properties for gamma-irradiated long-chain branched polylactides3

An easy procedure was applied to prepare high-melt-strength polylactide (PLA) that involves γ-radiation-induced free-radical reactions to introduce a long-chain branched structure onto a linear PLA precursor with addition of a trifunctional monomer, trimethylolpropane triacrylate (TMPTA). The results from size-exclusion chromatography coupled with multiangle laser light scattering (SEC-MALLS) detection indicate that the resultant long-chain branched PLA (LCB PLA) samples have an increased molecular mass and an elevated branching degree with increasing amount of TMPTA incorporated during the irradiation process. Various rheological plots including viscosity, storage modulus, loss tangent, Cole−Cole plots, and weighted relaxation spectra were used to distinguish the improved melt strength for LCB PLA samples. The effect of LCB structure on elongational rheological properties was further investigated. The LCB PLA samples exhibited an enhancement of strainhardening under elongational flow. The enhanced melt strength substantially improved the foaming performance of the LCB PLA samples.