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1.
《Mendeleev Communications》2022,32(2):226-227
We report a nickel tetrathiooxalate (NiTTO) coordination polymer as a cathode material for potassium batteries. In a potential range of 1.3–3.6 V vs. K+/K, the specific capacity of the material is 209 mA h g?1 at a current density of 0.1 A g?1, which roughly corresponds to the two-electron reduction of polymer repeating units. The charge–discharge mechanisms of NiTTO in potassium cells were examined using operando Raman spectroscopy. 相似文献
2.
Metal-sulfur batteries are a promising next-generation energy storage technology, offering high theoretical energy densities with low cost and good sustainability. An active area of research is the development of electrolytes that address unwanted migration of sulfur and intermediate species known as polysulfides during operation of metal-sulfur batteries, a phenomenon that leads to low energy efficiency and short life-spans. A particular class of electrolytes, gel polymer electrolytes, are especially attractive for their ability to repel polysulfides on the basis of structure, electrostatics, and other polymer properties. Herein, within the context of magnesium- and lithium-sulfur batteries, we investigate the impact of gel polymer electrolyte cation solvation capacity, a property related to network dielectric constant and chemistry, on sulfur/polysulfide-polymer interactions, an understudied property-performance relationship. Polymers with lower cation solvation capacity are found to permanently absorb less polysulfide active material, which increases sulfur utilization for Li−S batteries and significantly increases charge efficiency and life-span for Li−S and Mg−S batteries. 相似文献
3.
Yuejun Ding 《中国物理 B》2022,31(6):68201-068201
Na-ion batteries (NIBs) are regarding as the optimum complement for Li-ion batteries along with the rapid development of stationary energy storage systems. In order to meet the commercial demands of cathodes for NIBs, O3-type Cu containing layered oxide Na0.90Cu0.22Fe0.30Mn0.48O2 with good comprehensive performance and low-cost element components is very promising for the practical use. However, only part of the Cu3+/Cu2+ redox couple participated in the redox reaction, thus impairing the specific capacity of the cathode materials. Herein, Mg2+-doped O3-Na0.90Mg0.08Cu0.22Fe0.30Mn0.40O2 layered oxide without Mn3+ was synthesized successfully, which exhibited improved reversible specific capacity of 118 mAh/g in the voltage range of 2.4-4.0 V at 0.2 C, corresponding to the intercalation/deintercalation of 0.47 Na+ (0.1 more than that of Na0.90Cu0.22Fe0.30Mn0.48O2). This work demonstrates an important strategy to obtain advanced layered oxide cathodes for NIBs. 相似文献
4.
5.
《Operations Research Letters》2022,50(3):274-280
The minimum k-enclosing ball problem seeks the ball with smallest radius that contains at least k of m given points. This problem is NP-hard. We present a branch-and-bound algorithm on the tree of the subsets of k points to solve this problem. Our method is able to solve the problem exactly in a short amount of time for small and medium sized datasets. 相似文献
6.
双金属有机骨架及其衍生物一方面具有单金属有机骨架孔道丰富、比表面积大、结构可调、活性位点丰富等特点,另一方面具有双组分与多孔结构之间的协同效应,因而受到了研究人员的密切关注,在储能、催化、分离、传感器、医药、气体存储等领域广泛应用。和单金属MOFs类似,双金属MOFs的导电性不佳、结构易坍塌,这极大地限制了其在电化学储能中的应用。通过对双金属MOFs进行热处理,易得到分布均匀的多孔碳@双金属氧化物/硫化物/磷化物/硒化物等衍生物,不仅保持了独特的多孔结构,而且提高了材料的导电性和结构稳定性,有利于在电化学储能中的应用。因此,本文从双金属MOFs中的主要金属离子入手,综述了双金属MOFs及其衍生物用于超级电容器、锂离子电池、钠离子电池、金属空气电池等电化学储能器件的最新应用进展。在此基础上,总结了双金属MOFs在电化学储能应用中的优势,并对其制备、作用机理和后处理研究提出了建议。 相似文献
7.
Thiacalixarene-supported Co32nanoclusters encapsulated in polyacrylonitrile nanofibers(Co32@PAN-NFs) by electrospinning have been utilized as precursors to fabricate N-doped CoO@Co9S8 carbon nanofibers(CoO@Co9S8@CNFs) for superior Li-ion storage. The S-rich Co32 clusters capped by organic sheets afforded the well dispersed cobalt oxide/sulfide nanoparticles embedded in carbon nanofiber composites by direct calcination. The N-doped CoO@Co9S8@CNFs nanocomposites have been utilized as anode materials for lithium ion battery with the reversible capabilities being of 1051.8, 967.6, 894.7, 782.7, 669.5 and 525.4 mA·h/g at 0.1, 0.2, 0.5, 1, 2 and 3 A/g, respectively. The CoO@Co9S8@CNFs also showed a relatively high stable capacity of 551.7 mA·h/g at the current density of 1 A/g after 200 cycles of rate experiments. The as-obtained N-doped CoO@Co9S8@CNFs nanocomposites exhibited superior reversible capacity, rate performance, Coulomb efficiency(74.5% vs. 63.9%) and cyclic stability comparing with the CoO@Co9S8@C derived from simple annealing of Co32 templates. 相似文献
8.
The carbon composite materials have been a research hotspot in the fields of catalysis, energy conversion and so on, because of their features of large structure and morphology variety, good chemical and electrochemical stability, and high electronic conductivity, large specific surface area and rich active sites. This paper summarizes some research progress of carbon composite materials, including assembly methodologies, their structure regulation, properties, and related applications. Moreover, the current challenges and the prospects of these materials are also discussed. 相似文献
9.
Dr. Deepak Gupta Dr. Alae E. Lakraychi Dr. Buddha D. Boruah Simon De Kreijger Dr. Ludovic Troian-Gautier Prof. Benjamin Elias Prof. Michael De Volder Prof. Alexandru Vlad 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(42):e202201220
Controlling redox activity of judiciously appended redox units on a photo-sensitive molecular core is an effective strategy for visible light energy harvesting and storage. The first example of a photosensitizer - electron donor coordination compound in which the photoinduced electron transfer step is used for light to electrical energy conversion and storage is reported. A photo-responsive Ru-diimine module conjugated with redox-active catechol groups in [Ru(II)(phenanthroline-5,6-diolate)3]4− photosensitizer can mediate photoinduced catechol to dione oxidation in the presence of a sacrificial electron acceptor or at the surface of an electrode. Under potentiostatic condition, visible light triggered current density enhancement confirmed the light harvesting ability of this photosensitizer. Upon implementation in galvanostatic charge-discharge of a Li battery configuration, the storage capacity was found to be increased by 100 %, under 470 nm illumination with output power of 4.0 mW/cm−2. This proof-of-concept molecular system marks an important milestone towards a new generation of molecular photo-rechargeable materials. 相似文献
10.
Electrochemical hydrogen storage in porous carbon materials is emerging as a cost-effective hydrogen storage and transport technology with competitive power and energy densities. The merits of electrochemical hydrogen storage using porous conductive carbon-based electrodes are reviewed. The employment of acidic electrolytes in such storage systems is compared with alkaline electrolytes. The recent innovations of a proton battery for smaller-scale electricity storage, and a proton flow reactor system for larger (grid)-scale storage and bulk export of hydrogen produced from renewable energy, are briefly described. It is argued that such systems, along with variants proposed by others, all of which rely on electrochemical hydrogen storage in porous carbons, can contribute to the search for energy storage technologies essential for the transition to a zero-emission global economy. 相似文献