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991.
Watchareeya Kaveevivitchai Ashfia Huq Shaofei Wang Min Je Park Arumugam Manthiram 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(34)
Rechargeable batteries based on an abundant metal such as aluminum with a three‐electron transfer per atom are promising for large‐scale electrochemical energy storage. Aluminum can be handled in air, thus offering superior safety, easy fabrication, and low cost. However, the development of Al‐ion batteries has been challenging due to the difficulties in identifying suitable cathode materials. This study presents the use of a highly open framework Mo2.5 + y VO9 + z as a cathode for Al‐ion batteries. The open‐tunnel oxide allows a facile diffusion of the guest species and provides sufficient redox centers to help redistribute the charge within the local host lattice during the multivalent‐ion insertion, thus leading to good rate capability with a specific capacity among the highest reported in the literature for Al‐based batteries. This study also presents the use of Mo2.5 + y VO9 + z as a model host to develop a novel ultrafast technique for chemical insertion of Al ions into host structures. The microwave‐assisted method employing diethylene glycol and aluminum diacetate (Al(OH)(C2H3O2)2) can be performed in air in as little as 30 min, which is far superior to the traditional chemical insertion techniques involving moisture‐sensitive organometallic reagents. The Al‐inserted Al x Mo2.5 + y VO9 + z obtained by the microwave‐assisted chemical insertion can be used in Al‐based rechargeable batteries. 相似文献
992.
Sandwiched Thin‐Film Anode of Chemically Bonded Black Phosphorus/Graphene Hybrid for Lithium‐Ion Battery
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Hanwen Liu Yuqin Zou Li Tao Zhaoling Ma Dongdong Liu Peng Zhou Hongbo Liu Shuangyin Wang 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(33)
A facile vacuum filtration method is applied for the first time to construct sandwich‐structure anode. Two layers of graphene stacks sandwich a composite of black phosphorus (BP), which not only protect BP from quickly degenerating but also serve as current collector instead of copper foil. The BP composite, reduced graphene oxide coated on BP via chemical bonding, is simply synthesized by solvothermal reaction at 140 °C. The sandwiched film anode used for lithium‐ion battery exhibits reversible capacities of 1401 mAh g?1 during the 200th cycle at current density of 100 mA g?1 indicating superior cycle performance. Besides, this facile vacuum filtration method may also be available for other anode material with well dispersion in N‐methyl pyrrolidone (NMP). 相似文献
993.
Qidi Wang Chenglong Zhao Yaxiang Lu Yunming Li Yuheng Zheng Yuruo Qi Xiaohui Rong Liwei Jiang Xinguo Qi Yuanjun Shao Du Pan Baohua Li Yong‐Sheng Hu Liquan Chen 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(42)
Sodium–ion batteries (NIBs), due to the advantages of low cost and relatively high safety, have attracted widespread attention all over the world, making them a promising candidate for large‐scale energy storage systems. However, the inherent lower energy density to lithium–ion batteries is the issue that should be further investigated and optimized. Toward the grid‐level energy storage applications, designing and discovering appropriate anode materials for NIBs are of great concern. Although many efforts on the improvements and innovations are achieved, several challenges still limit the current requirements of the large‐scale application, including low energy/power densities, moderate cycle performance, and the low initial Coulombic efficiency. Advanced nanostructured strategies for anode materials can significantly improve ion or electron transport kinetic performance enhancing the electrochemical properties of battery systems. Herein, this Review intends to provide a comprehensive summary on the progress of nanostructured anode materials for NIBs, where representative examples and corresponding storage mechanisms are discussed. Meanwhile, the potential directions to obtain high‐performance anode materials of NIBs are also proposed, which provide references for the further development of advanced anode materials for NIBs. 相似文献
994.
995.
996.
Lin Mei Jiantie Xu Zengxi Wei Huakun Liu Yutao Li Jianmin Ma Shixue Dou 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(34)
With the large‐scale applications of electric vehicles in recent years, future batteries are required to be higher in power and possess higher energy densities, be more environmental friendly, and have longer cycling life, lower cost, and greater safety than current batteries. Therefore, to develop alternative electrode materials for advanced batteries is an important research direction. Recently, the Chevrel phase Mo6T8 (T = S, Se) has attracted increasing attention as electrode candidate for advanced batteries, including monovalent (e.g., lithium and sodium) and multivalent (e.g., magnesium, zinc and aluminum) ion batteries. Benefiting from its unique open crystal structure, the Chevrel phase Mo6T8 cannot only ensure rapid ion transport, but also retain the structure stability during electrochemical reactions. Although the history of the research on Mo6T8 as electrodes for advanced batteries is short, there has been significant progress on the design and fabrication of Mo6T8 for various advanced batteries as above mentioned. An overview of the recent progress on Mo6T8 electrodes applied in advanced batteries is provided, including synthesis methods and diverse structures for Mo6T8, and electrochemical mechanism and performance of Mo6T8. Additionally, a briefly conclusion on the significant progress, obvious drawbacks, emerging challenges and some perspectives on the research of Mo6T8 for advanced batteries in the near future is provided. 相似文献
997.
Large‐Scale Fabrication of Core–Shell Structured C/SnO2 Hollow Spheres as Anode Materials with Improved Lithium Storage Performance
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Yong Cheng Qian Li Chunli Wang Lianshan Sun Zheng Yi Limin Wang 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(47)
Due to the high theoretical capacity as high as 1494 mAh g?1, SnO2 is considered as a potential anode material for high‐capacity lithium–ion batteries (LIBs). Therefore, the simple but effective method focused on fabrication of SnO2 is imperative. To meet this, a facile and efficient strategy to fabricate core–shell structured C/SnO2 hollow spheres by a solvothermal method is reported. Herein, the solid and hollow structure as well as the carbon content can be controlled. Very importantly, high‐yield C/SnO2 spheres can be produced by this method, which suggest potential business applications in LIBs field. Owing to the dual buffer effect of the carbon layer and hollow structures, the core–shell structured C/SnO2 hollow spheres deliver a high reversible discharge capacity of 1007 mAh g?1 at a current density of 100 mA g?1 after 300 cycles and a superior discharge capacity of 915 mAh g?1 at 500 mA g?1 after 500 cycles. Even at a high current density of 1 and 2 A g?1, the core–shell structured C/SnO2 hollow spheres electrode still exhibits excellent discharge capacity in the long life cycles. Consideration of the superior performance and high yield, the core–shell structured C/SnO2 hollow spheres are of great interest for the next‐generation LIBs. 相似文献
998.
Fabrication of Fe3O4 Dots Embedded in 3D Honeycomb‐Like Carbon Based on Metallo–Organic Molecule with Superior Lithium Storage Performance
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Chengfei Li Liuqing Li Zhaopeng Li Weihao Zhong Zhenghui Li Xiaoqing Yang Guoqing Zhang Haiyan Zhang 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(38)
A novel metallo–organic molecule, ferrocene, is selected as building block to construct Fe3O4 dots embedded in 3D honeycomb‐like carbon (Fe3O4 dots/3DHC) by using SiO2 nanospheres as template. Unlike previously used inorganic Fe3O4 sources, ferrocene simultaneously contains organic cyclopentadienyl groups and inorganic Fe atoms, which can be converted to carbon and Fe3O4, respectively. Atomic‐scale Fe distribution in started building block leads to the formation of ultrasmall Fe3O4 dots (≈3 nm). In addition, by well controlling the feed amount of ferrocene, Fe3O4 dots/3DHC with well‐defined honeycomb‐like meso/macropore structure and ultrathin carbon wall can be obtained. Owing to unique structural features, Fe3O4 dots/3DHC presents impressive lithium storage performance. The initial discharge and reversible capacities can reach 2047 and 1280 mAh g?1 at 0.05 A g?1. With increasing the current density to 1 and 3 A g?1, remarkable capacities of 963 and 731 mAh g?1 remain. Moreover, Fe3O4 dots/3DHC also has superior cycling stability, after a long‐term charge/discharge for 200 times, a high capacity of 1082 mAh g?1 can be maintained (80% against the capacity of the 2nd cycle). 相似文献
999.
Mesoporous NiS2 Nanospheres Anode with Pseudocapacitance for High‐Rate and Long‐Life Sodium‐Ion Battery
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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
1000.
Xinghua Chang Teng Wang Zhiliang Liu Xinyao Zheng Jie Zheng Xingguo Li 《Nano Research》2017,10(6):1950-1958
We report a simple method of preparing a high performance,Sn-based anode material for lithium ion batteries (LIBs).Adding H2O2 to an aqueous solution containing Sn2+ and aniline results in simultaneous polymerization of aniline and oxidation of Sn2+ to SnO2,leading to a homogeneous composite of polyaniline and SnO2.Hydrogen thermal reduction of the above composite yields N-doped carbon with hierarchical porosity and homogeneously distributed,ultrafine Sn particles.The nanocomposite exhibits excellent performance as an anode material for lithium ion batteries,showing a high reversible specific capacity of 788 mAh·g-1 at a current density of 100 mA·g-1 after 300 cycles and very good stability up to 5,000 mA·g-1.The simple preparation method combined with the good electrochemical performance is highly promising to promote the application of Sn based anode materials. 相似文献