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排序方式: 共有2167条查询结果,搜索用时 15 毫秒
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
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Rongrong Li Hongjie Peng Qingping Wu Xuejun Zhou Jiang He Hangjia Shen Minghui Yang Chilin Li 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(29):12227-12236
Herein, we propose the construction of a sandwich-structured host filled with continuous 2D catalysis–conduction interfaces. This MoN-C-MoN trilayer architecture causes the strong conformal adsorption of S/Li2Sx and its high-efficiency conversion on the two-sided nitride polar surfaces, which are supplied with high-flux electron transfer from the buried carbon interlayer. The 3D self-assembly of these 2D sandwich structures further reinforces the interconnection of conductive and catalytic networks. The maximized exposure of adsorptive/catalytic planes endows the MoN-C@S electrode with excellent cycling stability and high rate performance even under high S loading and low host surface area. The high conductivity of this trilayer texture does not compromise the capacity retention after the S content is increased. Such a job-synergistic mode between catalytic and conductive functions guarantees the homogeneous deposition of S/Li2Sx, and avoids thick and devitalized accumulation (electrode passivation) even after high-rate and long-term cycling. 相似文献
4.
Jin Xie Yun-Wei Song Dr. Bo-Quan Li Dr. Hong-Jie Peng Prof. Jia-Qi Huang Prof. Qiang Zhang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(49):22334-22339
Polysulfide intermediates (PSs), the liquid-phase species of active materials in lithium–sulfur (Li-S) batteries, connect the electrochemical reactions between insulative solid sulfur and lithium sulfide and are key to full exertion of the high-energy-density Li-S system. Herein, the concept of sulfur container additives is proposed for the direct modification on the PSs species. By reversible storage and release of the sulfur species, the container molecule converts small PSs into large organosulfur species. The prototype di(tri)sulfide-polyethylene glycol sulfur container is highly efficient in the reversible PS transformation to multiply affect electrochemical behaviors of sulfur cathodes in terms of liquid-species clustering, reaction kinetics, and solid deposition. The stability and capacity of Li-S cells was thereby enhanced. The sulfur container is a strategy to directly modify PSs, enlightening the precise regulation on Li-S batteries and multi-phase electrochemical systems. 相似文献
5.
Guanjia Zhu Prof. Wan Jiang Prof. Jianping Yang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(7):1488-1496
The successful commercialization of promising silicon-based anode materials has been hampered by their poor cycling stability caused by the huge volume change. Integration of the carbon matrix with silicon-based (C/Si-based) anode materials has been demonstrated to be a powerful solution to achieve satisfactory electrochemical performance. This minireview aims to outline recent developments on C/Si-based composites, with the emphasis on the importance of carbon distribution at multiple scales. In addition, the forms of the carbon framework (carbon sources and doping of heteroatoms) have been summarized. Particularly, a novel C/Si-based hybrid with carbon distributed at the atomic scale has been highlighted. 相似文献
6.
《中国化学快报》2020,31(9):2353-2357
NiS2 has become a research hotspot of anode materials for Na-ion batteries due to its high theoretical specific capacity. However, the volume effect, the dissolution of polysulfide intermediates and the low conductivity during the charge/discharge process lead to the low specific capacity and poor cycling stability. NiS2/rGO nanocomposite was prepared by a facile two-step process: GO was prepared by modified Hummers method, and then NiS2/rGO nanocomposite was synthesized by l-cys assisted hydrothermal method. NiS2/rGO nanocomposite shows excellent cycle performance and rate performance, which could be attributed to the mesoporous structure on the graphene skeleton with high conductivity. Besides, the chemical constraint of a unique SO bond on NiS2 could inhibit the dissolution of intermediates and the loss of irreversible capacity. 相似文献
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Synthesis of Mesoporous Wall‐Structured TiO2 on Reduced Graphene Oxide Nanosheets with High Rate Performance for Lithium‐Ion Batteries 下载免费PDF全文
Mengmeng Zhen Meiqing Sun Prof. Guandao Gao Prof. Lu Liu Prof. Zhen Zhou 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(14):5317-5322
Mesoporous wall‐structured TiO2 on reduced graphene oxide (RGO) nanosheets were successfully fabricated through a simple hydrothermal process without any surfactants and annealed at 400 °C for 2 h under argon. The obtained mesoporous structured TiO2–RGO composites had a high surface area (99 0307 m2 g?1) and exhibited excellent electrochemical cycling (a reversible capacity of 260 mAh g?1 at 1.2 C and 180 mAh g?1 at 5 C after 400 cycles), demonstrating it to be a promising method for the development of high‐performance Li‐ion batteries. 相似文献
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《中国化学快报》2020,31(12):3209-3212
Constructing a reliable and favorable electrode-electrolyte interface is crucial to utilize the exceptional energy storage capability in commercial lithium-ion batteries. Here, we report a facile synthesis approach for the lithium difluorophosphate (LiPO2F2) solution as an effective film-forming additive via direct adding the Li2CO3 into LiPF6 solution at 45 °C. Benefiting from the significantly reduced interface resistance (RSEI) and charge transfer impedance (Rct) of both the cathode and anode by adding the prepared LiPO2F2 solution into a baseline electrolyte, the cycling performance of the graphite||LiNi0.5Mn0.3Co0.2O2 pouch cell is remarkably improved under all-climate condition. 相似文献
10.
A New Concept for Obtaining SnO2 Fiber‐in‐Tube Nanostructures with Superior Electrochemical Properties 下载免费PDF全文
Young Jun Hong Ji‐Wook Yoon Prof. Jong‐Heun Lee Prof. Yun Chan Kang 《Chemistry (Weinheim an der Bergstrasse, Germany)》2015,21(1):371-376
Tin oxide (SnO2) nanotubes with a fiber‐in‐tube structure have been prepared by electrospinning and the mechanism of their formation has been investigated. Tin oxide‐carbon composite nanofibers with a filled structure were formed as an intermediate product, which were then transformed into SnO2 nanotubes with a fiber‐in‐tube structure during heat treatment at 500 °C. Nanofibers with a diameter of 85 nm were found to be located inside hollow nanotubes with an outer diameter of 260 nm. The prepared SnO2 nanotubes had well‐developed mesopores. The discharge capacities of the SnO2 nanotubes at the 2nd and 300th cycles at a current density of 1 A g?1 were measured as 720 and 640 mA h g?1, respectively, and the corresponding capacity retention measured from the 2nd cycle was 88 %. The discharge capacities of the SnO2 nanotubes at incrementally increased current densities of 0.5, 1.5, 3, and 5 A g?1 were 774, 711, 652, and 591 mA h g?1, respectively. The SnO2 nanotubes with a fiber‐in‐tube structure showed superior cycling and rate performances compared to those of SnO2 nanopowder. The unique structure of the SnO2 nanotubes with a fiber@void@tube configuration improves their electrochemical properties by reducing the diffusion length of the lithium ions, and also imparts greater stability during electrochemical cycling. 相似文献