37
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      A morphology, porosity and surface conductive layer optimized MnCo2O4 microsphere for compatible superior Li+ ion/air rechargeable battery electrode materials

      Read this article at

      ScienceOpenPublisher
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          A porosity and morphology controlled MnCo 2O 4 microsphere for superior rechargeable Li + battery electrodes.

          Abstract

          Uniform surface conductive layers with porous morphology-conserved MnCo 2O 4 microspheres are successfully synthesized, and their electrochemical performances are thoroughly investigated. It is found that the microwave-assisted hydrothermally grown MnCo 2O 4 using citric acid as the carbon source shows a maximum Li + ion lithiation/delithiation capacity of 501 mA h g −1 at 500 mA g −1 with stable capacity retention. Besides, the given microsphere compounds are effectively activated as air cathode catalysts in Li–O 2 batteries with reduced charge overpotentials and improved cycling performance. We believe that such an affordable enhanced performance results from the appropriate quasi-hollow nature of MnCo 2O 4 microspheres, which can effectively mitigate the large volume change of electrodes during Li + migration and/or enhance the surface transport of the LiO x species in Li–air batteries. Thus, the rationally designed porous media for the improved Li + electrochemical reaction highlight the importance of the 3D macropores, the high specific area and uniformly overcoated conductive layer for the promising Li + redox reaction platforms.

          Related collections

          Most cited references17

          • Record: found
          • Abstract: found
          • Article: not found

          Graphene anchored with co(3)o(4) nanoparticles as anode of lithium ion batteries with enhanced reversible capacity and cyclic performance.

          We report a facile strategy to synthesize the nanocomposite of Co(3)O(4) nanoparticles anchored on conducting graphene as an advanced anode material for high-performance lithium-ion batteries. The Co(3)O(4) nanoparticles obtained are 10-30 nm in size and homogeneously anchor on graphene sheets as spacers to keep the neighboring sheets separated. This Co(3)O(4)/graphene nanocomposite displays superior Li-battery performance with large reversible capacity, excellent cyclic performance, and good rate capability, highlighting the importance of the anchoring of nanoparticles on graphene sheets for maximum utilization of electrochemically active Co(3)O(4) nanoparticles and graphene for energy storage applications in high-performance lithium-ion batteries.
            • Record: found
            • Abstract: found
            • Article: not found

            Conversion reaction mechanisms in lithium ion batteries: study of the binary metal fluoride electrodes.

            Materials that undergo a conversion reaction with lithium (e.g., metal fluorides MF(2): M = Fe, Cu, ...) often accommodate more than one Li atom per transition-metal cation, and are promising candidates for high-capacity cathodes for lithium ion batteries. However, little is known about the mechanisms involved in the conversion process, the origins of the large polarization during electrochemical cycling, and why some materials are reversible (e.g., FeF(2)) while others are not (e.g., CuF(2)). In this study, we investigated the conversion reaction of binary metal fluorides, FeF(2) and CuF(2), using a series of local and bulk probes to better understand the mechanisms underlying their contrasting electrochemical behavior. X-ray pair-distribution-function and magnetization measurements were used to determine changes in short-range ordering, particle size and microstructure, while high-resolution transmission electron microscopy (TEM) and electron energy-loss spectroscopy (EELS) were used to measure the atomic-level structure of individual particles and map the phase distribution in the initial and fully lithiated electrodes. Both FeF(2) and CuF(2) react with lithium via a direct conversion process with no intercalation step, but there are differences in the conversion process and final phase distribution. During the reaction of Li(+) with FeF(2), small metallic iron nanoparticles (<5 nm in diameter) nucleate in close proximity to the converted LiF phase, as a result of the low diffusivity of iron. The iron nanoparticles are interconnected and form a bicontinuous network, which provides a pathway for local electron transport through the insulating LiF phase. In addition, the massive interface formed between nanoscale solid phases provides a pathway for ionic transport during the conversion process. These results offer the first experimental evidence explaining the origins of the high lithium reversibility in FeF(2). In contrast to FeF(2), no continuous Cu network was observed in the lithiated CuF(2); rather, the converted Cu segregates to large particles (5-12 nm in diameter) during the first discharge, which may be partially responsible for the lack of reversibility in the CuF(2) electrode.
              • Record: found
              • Abstract: not found
              • Article: not found

              Rechargeable Li–O2 batteries with a covalently coupled MnCo2O4–graphene hybrid as an oxygen cathode catalyst

                Author and article information

                Journal
                ICHBD9
                Dalton Transactions
                Dalton Trans.
                Royal Society of Chemistry (RSC)
                1477-9226
                1477-9234
                2016
                2016
                : 45
                : 12
                : 5064-5070
                Affiliations
                [1 ]Advanced Battery Materials Research Group
                [2 ]Korea Research Institute of Chemical Technology
                [3 ]Daejeon
                [4 ]Republic of Korea
                [5 ]School of Materials Science and Engineering and Optoelectronics Convergence Research Center
                [6 ]Chonnam National University
                [7 ]Gwangju 500-757
                [8 ]Division of Materials Science and Engineering Hanyang University
                [9 ]Seoul
                Article
                10.1039/C5DT04975J
                6e8019d7-9ab2-4c9f-a9bb-7a4c1ea6cad1
                © 2016
                History

                Comments

                Comment on this article

                Related Documents Log