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121.
122.
F~-对钛在NaBr水溶液中阳极极化行为的影响 总被引:1,自引:0,他引:1
利用电化学方法研究了F对工业纯钛(TAl)在NaBr水溶液中阳极极化行为的影响。结果发现,F加速了钛表面膜的阳极溶解速度,减缓了膜的增厚,提高了孔蚀电位,但对再钝化电位无影响。 相似文献
123.
The hydrothermal modification of Mg(OH)2 crystals in NaOH solution was investigated. The aggregated Mg(OH)2 particles with irregular shape are converted to regular Mg(OH)2 hexagonal plates after hydrothermal treatment. The prolongation of reaction time from 1-4 h or the increase of temperature from 140℃ to 200℃ can promote the formation of Mg(OH)2 plates with big particle size but small cluster size. The dispersion characteristics of the hydrothermal products are improved owing to the improvement of Mg(OH)2 crystalline degree and the in-crease of I(001)/I(101) ratio. The proper hydrothermal modification condition is as follows: solid content 0. 075 g/mL,NaOH concentration 5.0 mol/L, temperature 200℃ and time 4 h. Thermodynamic analysis indicates that the increase of MgOH^ concentration at elevated temperature or the increase of OH^- concentration in concentrated NaOH solution is favorable for the hydrothermal formation of Mg(OH)2 particles. 相似文献
124.
125.
采用密度泛函理论B3LYP法及自恰等密度PCM模型,在6-311G(d)基组条件中研究环氧乙烷在保险粉生产中参加的主要反应,系统论证环氧乙烷的去向.本文首先分析环氧乙烷于控制硫代硫酸钠含量的热力学、动力学基础及体系中各亲核试剂的反应活性,然后分析环氧乙烷各主要反应的比例关系.理论计算结果与实验结论一致,即硫代硫酸钠消耗的环氧乙烷最多(71.5%),其次是水(17.5%),甲醇(5.0%),亚硫酸氢钠(1.3%). 相似文献
126.
Jiayang Liao Xiang Lv Xi-xi Sun Junhua Li Haomin Wang Qiang Chen Hanpeng Lu Duan Wang Jian Bi Jiagang Wu 《Advanced functional materials》2023,33(34):2303637
Although the piezo-catalysis is promising for the environmental remediation and biomedicine, the piezo-catalytic properties of various piezoelectric materials are limited by low carrier concentrations and mobility, and rapid electron-hole pair recombination, and reported regulating strategies are quite complex and difficult. Herein, a new and simple strategy, integrating phase boundary engineering and defect engineering, to boost the piezo-catalytic activity of potassium sodium niobate ((K, Na)NbO3, KNN) based materials is innovatively proposed. Tur strategy is validated by exampling 0.96(K0.48Na0.52)Nb0.955Sb0.045O3-0.04(BixNa4-3x)0.5ZrO3-0.3%Fe2O3 material having phase boundary engineering and conducted the defect engineering via the high-energy sand-grinding. A high reaction rate constant k of 92.49 × 10−3 min−1 in the sand-grinding sample is obtained, which is 2.40 times than that of non-sand-grinding one and superior to those of other representative lead-free perovskite piezoelectric materials. Meanwhile, the sand-grinding sample has remarkable bactericidal properties against Escherichia coli and Staphylococcus aureus. Superior piezo-catalytic activities originate from the enhanced electron-hole pair separation and the increased carrier concentration. This study provides a novel method for improving the piezo-catalytic activities of lead-free piezoelectric materials and holds great promise for harnessing natural energy and disease treatment. 相似文献
127.
Kuan Wang Haoxiang Zhuo Jiantao Wang Fanny Poon Xueliang Sun Biwei Xiao 《Advanced functional materials》2023,33(13):2212607
Branded with low cost and a high degree of safety, with an ambitious aim of substituting lithium-ion batteries in many fields, sodium-ion batteries have received fervid attention in recent years after being dormant for decades. Layered materials are a major focus of study owing to the extensive experience already gained in lithium-ion batteries, and the pursuit of a Mn-rich composition is critical to reduce the cost while retaining the performance. This review provides a timely update of the recent progress of Mn-rich layered materials for sodium-ion batteries based on the understandings of the phase forming principles, structure transformation upon cycling and charge compensation mechanisms and discusses potential ambiguities in the pursuit of high-performance materials. 相似文献
128.
Zhuoran Lv Baixin Peng Ximeng Lv Yusha Gao Keyan Hu Wujie Dong Gengfeng Zheng Fuqiang Huang 《Advanced functional materials》2023,33(16):2214370
Alloying-type metal sulfides with high theoretical capacities are promising anodes for sodium-ion batteries, but suffer from sluggish sodiation kinetics and huge volume expansion. Introducing intercalative motifs into alloying-type metal sulfides is an efficient strategy to solve the above issues. Herein, robust intercalative In S motifs are grafted to high-capacity layered Bi2S3 to form a cation-disordered (BiIn)2S3, synergistically realizing high-rate and large-capacity sodium storage. The In S motif with strong bonding serves as a space-confinement unit to buffer the volume expansion, maintaining superior structural stability. Moreover, the grafted high-metallicity Indium increases the bonding covalency of Bi S, realizing controllable reconstruction of Bi S bond during cycling to effectively prevent the migration and aggregation of atomic Bi. The novel (BiIn)2S3 anode delivers a high capacity of 537 mAh g−1 at 0.4 C and a superior high-rate stability of 247 mAh g−1 at 40 C over 10000 cycles. Further in situ and ex situ characterizations reveal the in-depth reaction mechanism and the breakage and formation of reversible Bi S bonds. The proposed space confinement and bonding covalency enhancement strategy via grafting intercalative motifs can be conducive to developing novel high-rate and large-capacity anodes. 相似文献
129.
Mesoporous NiS2 Nanospheres Anode with Pseudocapacitance for High‐Rate and Long‐Life Sodium‐Ion Battery 下载免费PDF全文
Ruimin Sun Sijie Liu Qiulong Wei Jinzhi Sheng Shaohua Zhu Qinyou An Liqiang Mai 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(39)
It is of great importance to exploit electrode materials for sodium‐ion batteries (SIBs) with low cost, long life, and high‐rate capability. However, achieving quick charge and high power density is still a major challenge for most SIBs electrodes because of the sluggish sodiation kinetics. Herein, uniform and mesoporous NiS2 nanospheres are synthesized via a facile one‐step polyvinylpyrrolidone assisted method. By controlling the voltage window, the mesoporous NiS2 nanospheres present excellent electrochemical performance in SIBs. It delivers a high reversible specific capacity of 692 mA h g?1. The NiS2 anode also exhibits excellent high‐rate capability (253 mA h g?1 at 5 A g?1) and long‐term cycling performance (319 mA h g?1 capacity remained even after 1000 cycles at 0.5 A g?1). A dominant pseudocapacitance contribution is identified and verified by kinetics analysis. In addition, the amorphization and conversion reactions during the electrochemical process of the mesoporous NiS2 nanospheres is also investigated by in situ X‐ray diffraction. The impressive electrochemical performance reveals that the NiS2 offers great potential toward the development of next generation large scale energy storage. 相似文献
130.
High-capacity anode materials are highly desirable for sodium ion batteries.Here,a porous Sb/Sb2O3 nanocomposite is successfully synthesized by the mild oxidization of Sb nanocrystals in air.In the composite,Sb contributes good conductivity and Sb2O3 improves cycling stability,particularly within the voltage window of 0.02-1.5 V.It remains at a reversible capacity of 540 mAh·g-1 after 180 cycles at 0.66 A·g-L Even at 10 A·g-1,the reversible capacity is still preserved at 412 mAh.g-1,equivalent to 71.6% of that at 0.066 A.g-1.These results are much better than Sb nanocrystals with a similar size and structure.Expanding the voltage window to 0.02-2.5 V includes the conversion reaction between Sb2O3 and Sb into the discharge/charge profiles.This would induce a large volume change and high structure strain/stress,deteriorating the cycling stability.The identification of a proper voltage window for Sb/Sb2O3 paves the way for its development in sodium ion batteries. 相似文献