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      Optimization of Von Mises Stress Distribution in Mesoporous α‐Fe 2 O 3 /C Hollow Bowls Synergistically Boosts Gravimetric/Volumetric Capacity and High‐Rate Stability in Alkali‐Ion Batteries

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          Nanostructured reduced graphene oxide/Fe2O3 composite as a high-performance anode material for lithium ion batteries.

          Reduced graphene oxide/Fe(2)O(3) composite was prepared using a facile two-step synthesis by homogeneous precipitation and subsequent reduction of the G-O with hydrazine under microwave irradiation to yield reduced graphene oxide (RG-O) platelets decorated with Fe(2)O(3) nanoparticles. As an anode material for Li-ion batteries, the RG-O/Fe(2)O(3) composite exhibited discharge and charge capacities of 1693 and 1227 mAh/g, respectively, normalized to the mass of Fe(2)O(3) in the composite (and ∼1355 and 982 mAh/g, respectively, based on the total mass of the composite), with good cycling performance and rate capability. Characterization shows that the Fe(2)O(3) nanoparticles are uniformly distributed on the surface of the RG-O platelets in the composite. The total specific capacity of RG-O/Fe(2)O(3) is higher than the sum of pure RG-O and nanoparticle Fe(2)O(3), indicating a positive synergistic effect of RG-O and Fe(2)O(3) on the improvement of electrochemical performance. The synthesis approach presents a promising route for a large-scale production of RG-O platelet/metal oxide nanoparticle composites as electrode materials for Li-ion batteries.
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            Highly elastic binders integrating polyrotaxanes for silicon microparticle anodes in lithium ion batteries

            Lithium-ion batteries with ever-increasing energy densities are needed for batteries for advanced devices and all-electric vehicles. Silicon has been highlighted as a promising anode material because of its superior specific capacity. During repeated charge-discharge cycles, silicon undergoes huge volume changes. This limits cycle life via particle pulverization and an unstable electrode-electrolyte interface, especially when the particle sizes are in the micrometer range. We show that the incorporation of 5 weight % polyrotaxane to conventional polyacrylic acid binder imparts extraordinary elasticity to the polymer network originating from the ring sliding motion of polyrotaxane. This binder combination keeps even pulverized silicon particles coalesced without disintegration, enabling stable cycle life for silicon microparticle anodes at commercial-level areal capacities.
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              Metal oxides and oxysalts as anode materials for Li ion batteries.

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                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Advanced Functional Materials
                Adv. Funct. Mater.
                Wiley
                1616-301X
                1616-3028
                August 20 2019
                August 2019
                June 20 2019
                August 2019
                : 29
                : 34
                : 1902822
                Affiliations
                [1 ]Institute for Advanced Materials and TechnologyUniversity of Science and Technology Beijing Beijing 100083 China
                [2 ]Department of Materials Science and MetallurgyUniversity of Cambridge Cambridge CB3 0FS UK
                [3 ]Department of Materials Science and EngineeringCornell University Ithaca NY 14853 USA
                [4 ]School of Material Science and EngineeringXiangtan University Hunan 411105 China
                [5 ]Collaborative Innovation Center of Steel TechnologyUniversity of Science and Technology Beijing Beijing 100083 China
                [6 ]School of Materials Science and EngineeringChina University of Geosciences Beijing Beijing 100083 China
                [7 ]John A. Paulson School of Engineering and Applied SciencesHarvard University Cambridge MA 02138 USA
                [8 ]Beijing Advanced Innovation Center for Materials Genome EngineeringUniversity of Science and Technology Beijing Beijing 100083 China
                Article
                10.1002/adfm.201902822
                abf46641-d51c-40ba-92a2-9ad2461402ff
                © 2019

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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