Boosted sodium ion storage performance in MnO_(2):Understanding the bond angle-mediated orbital overlap in MnO_(6)units for fast charge transfer

Symmetric six oxygen-coordinated Mn structural units(MnO6)in MnO2 with small Mn–O orbital overlap hamper electron transfer rates during energy storage.Herein,we report a novel bond angle modulation strategy to manipulate Mn–O orbital overlap in MnO2 through the construction of Mn vacancies(MnO2-VMn),aiming at expediting electron transfer,and thus enhancing energy storage performance.Both experimental and theoretical results disclose that the amplification of Mn–O–Mn bond angles exclusively augments the Mn(dx2-y2)-O(py)orbital overlap and triggers the electron redistribution in MnO2-VMn,inducing an augmented Mn dx2-y2 electron occupation.This heightened presence of active electrons in the Mn dx2-y2 orbital paves the way for accelerating electron transfer and ion transfer in MnO2-VMn.Notably,MnO2-VMn delivers an improved specific capacitance of 425 F g−1 at 1 A g−1 and a superior rate capacity of 265 F g−1 at 20 A g−1.Furthermore,an asymmetric supercapacitor(MnO2-VMn//AC ASC)was fabricated,exhibiting a high energy density of 64.3 Wh kg−1 at a power density of 1000 W kg−1.Furthermore,theoretical insights uncover the profound implications of metal–oxygen–metal bond angle regulation on interatomic orbital overlap modulation.These revelations illuminate pathways for the design of advanced energy storage materials.

Dynamic route guidance algorithm based onartificial immune system

To improve the performance of the K-shortest paths search in intelligent traffic guidance systems, this paper proposes an optimal search algorithm based on the intelligent optimization search theory and the metaphor mechanism of vertebrate immune systems. This algorithm, applied to the urban traffic network model established by the node-expanding method, can expediently realize K-shortest paths search in the urban traffic guidance systems. Because of the immune memory and global parallel search ability from artificial immune systems, K shortest paths can be found without any repeat, which indicates evidently the superiority of the algorithm to the conventional ones. Not only does it perform a better parallelism, the algorithm also prevents premature phenomenon that often occurs in genetic algorithms. Thus, it is especially suitable for real-time requirement of the traffic guidance system and other engineering optimal applications. A case study verifies the efficiency and the practicability of the algorithm aforementioned.

Shape-controlled Synthesis of Porous SnO_2 Nanostructures via Morphologically Conserved Transformation from SnC_2O_4 Precursor Approach

Porous SnO_2 nanostructures with controlled shapes were synthesized by a facile morphologically conserved transformation from Sn C_2O_4 precursor approach. Well-defined Sn C_2O_4 nanostructures can be obtained through a solution-based precipitation process at ambient conditions without any surfactant. The formation mechanism of such microstructures was tentatively proposed on the basis of intrinsic crystal structure and the reaction conditions. We found that the morphologies of precursor were well maintained while numerous pores were formed during the annealing process. The combined techniques of X-ray diffraction, nitrogen absorption–desorption, field emission scanning electron microscopy, and(high-resolution) transmission electron microscopy were used to characterize the as-prepared SnO_2 products. Moreover, cyclic voltammetry(CV) study shows that the shape of CV presents a current response like roughly rectangular mirror images with respect to the zero-current line without obvious redox peaks, which indicating an ideal capacitive behavior of the SnO_2 electrodes. The photoluminescence(PL) spectrum study suggests that the as-obtained porous SnO_2 nanostructures might have a large number of defects, vacancies of oxygen, and local lattice disorder at the interface, interior and exterior surfaces.

氮杂芴酮聚合物的酸掺杂和碘离子响应特性

4,5-二氮杂芴酮具有热稳定性高、可掺杂和低LUMO能级等特点,是潜在的聚合物半导体结构单元.基于4,5-二氮杂芴酮的上述特点,本文设计合成了一种含4,5-二氮杂芴酮的给受体型聚合物,并对其掺杂特性开展了研究.实验结果显示,聚合物可以被甲磺酸进行两次掺杂,并伴随着最大吸收峰的红移和溶液颜色变化.酸掺杂后聚合物还可以被碘离子进行第三次掺杂.电导测试显示掺杂前后聚合物电导率发生了明显的变化,上述结果显示4,5-二氮杂芴酮结构单元在可多次掺杂聚合物半导体方面的应用.