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As high-capacity anode materials, spinel NiFe2O4 aroused extensive attention due to its natural abundance and safe working voltage. For widespread commercialization, some drawbacks, such as rapid capacity fading and poor reversibility due to large volume variation and inferior conductivity, urgently require amelioration. In this work, NiFe2O4/NiO composites with a dual-network structure were fabricated by a simple dealloying method. Benefiting from the dual-network structure and composed of nanosheet networks and ligament-pore networks, this material provides sufficient space for volume expansion and is able to boost the rapid transfer of electrons and Li ions. As a result, the material exhibits excellent electrochemical performance, retaining 756.9 mAh g−1 at 200 mA g−1 after cycling for 100 cycles and retaining 641.1 mAh g−1 after 1000 cycles at 500 mA g−1. This work provides a facile way to prepare a novel dual-network structured spinel oxide material, which can promote the development of oxide anodes and also dealloying techniques in broad fields. [ABSTRACT FROM AUTHOR]

Metal oxide anode materials are affected by severe volume expansion and cracking in the charging/discharging process, resulting in low capacity and poor cycle stability, which limits their application in lithium-ion batteries (LIBs). Herein, a new strategy is uncovered for a preparing spinel-structured, multi-component transition metal oxide, (Ni,Co,Mn)Fe2O4−x, with oxygen vacancies as an LIB anode material. The as-fabricated material presented excellent reversible capacity and cycling stability, delivering a discharge capacity of 1240.2 mAh g−1 at 100 mA g−1 for 200 cycles and then at 300 mA g−1 for 300 additional cycles. It presented extremely long cycle stability even at 2 A g−1, revealing 650.5 mAh g−1 after 1200 cycles. The good lithium storage capacity can be ascribed to the entropy stabilization effect, the multi-cation synergistic effect, abundant oxygen vacancies and the spinel structure. This study provides a new opportunity to fabricate and optimize conversion-type anodes for LIBs with satisfactory electrochemical performance. [ABSTRACT FROM AUTHOR]

Today, the development of new self-supporting electrode materials with high porosity and excellent degradation properties is of great importance for the removal of dye pollutants. Herein, this work synthesized nanoporous nickel@nickel oxide (np-Ni@NiO) electrode containing an amorphous alloy in the middle interlayer. The nanoporous structure endowed the electrode with more active sites and facilitated the ion/electron transport. The electrochemical active surface area was about 185.5 cm2. The electrochemical degradation of rhodamine B (RhB) using a np-Ni@NiO electrode was systematically investigated. The effects of technology paraments (NaCl concentration, the applied potential and pH) on electro-catalytic degradation were explored. An RhB removal rate of 99.68% was achieved in 30 s at optimized conditions, which was attributed to the unique bicontinuous ligament/pore structure and more active sites on the surface, as well as lower charge transfer resistance. In addition, the degradation mechanism of RhB in electrochemical oxidation was proposed, according to active species capture tests and EPR measurements. [ABSTRACT FROM AUTHOR]

Designing a novel photocatalytic composite for the efficient degradation of organic dyes remains a serious challenge. Herein, the multi-layered Co3O4@NP-CuO photocatalyst with unique features, i.e., the self-supporting, hierarchical porous network as well as the construction of heterojunction between Co3O4 and CuO, are synthesized by dealloying-electrodeposition and subsequent thermal treatment techniques. It is found that the interwoven ultrathin Co3O4 nanopetals evenly grow on the nanoporous CuO network (Co3O4@NP-CuO). The three-dimensional (3D) hierarchical porous structure for the catalyst provides more surface area to act as active sites and facilitates the absorption of visible light in the photodegradation reaction. Compared with the commercial CuO and Co3O4 powders, the newly designed Co3O4@NP-CuO composite exhibits superior photodegradation performance for RhB. The enhanced performance is mainly due to the construction of heterojunction of Co3O4/CuO, greatly promoting the efficient carrier separation for photocatalysis. Furthermore, the possible photocatalytic mechanism is analyzed in detail. This work provides a promising strategy for the fabrication of a new controllable heterojunction to improve photocatalytic activity. [ABSTRACT FROM AUTHOR]

To solve the problem of insufficient node positioning accuracy in wireless sensor networks, an algorithm based on improved particle swarm optimization by membrane computing (IPSO-MC) was proposed. Kent mapping was used to initialize the population and domain particles were introduced to improve the global optimization of the particle swarm. The weight factor and nonlinear extreme value perturbation were used to improve the local optimization ability of the particle swarm, and the Levy flight mechanism was used to optimize the individual position. Finally, the optimal solution of the particle swarm algorithm was obtained by the evolutionary rules of the membrane computing. Simulation experiments show that compared with the chicken flock algorithm, the improved particle swarm algorithm and the membrane computing, the proposed algorithm improves 3.24%, 5.12% and 8.15% in the comparison of reference node ratio indicators, and the increase in the number of nodes indicators by 2.26%, 7.82% and 9.81%, and the comparison of communication radius indicators increased by 2.15%, 5.5% and 7.5%, respectively. This indicates that the algorithm has a good effect in node localization. [ABSTRACT FROM AUTHOR]