7
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Realizing a High‐Performance Na‐Storage Cathode by Tailoring Ultrasmall Na 2FePO 4F Nanoparticles with Facilitated Reaction Kinetics

      research-article

      Read this article at

      Bookmark
          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

          In this paper, the synthesis of ultrasmall Na 2FePO 4F nanoparticles (≈3.8 nm) delicately embedded in porous N‐doped carbon nanofibers (denoted as Na 2FePO 4F@C) by electrospinning is reported. The as‐prepared Na 2FePO 4F@C fiber film tightly adherent on aluminum foil features great flexibility and is directly used as binder‐free cathode for sodium‐ion batteries, exhibiting admirable electrochemical performance with high reversible capacity (117.8 mAh g −1 at 0.1 C), outstanding rate capability (46.4 mAh g −1 at 20 C), and unprecedentedly high cyclic stability (85% capacity retention after 2000 cycles). The reaction kinetics and mechanism are explored by a combination study of cyclic voltammetry, ex situ structure/valence analyses, and first‐principles computations, revealing the highly reversible phase transformation of Na 2Fe IIPO 4F ↔ NaFe IIIPO 4F, the facilitated Na + diffusion dynamics with low energy barriers, and the desirable pseudocapacitive behavior for fast charge storage. Pouch‐type Na‐ion full batteries are also assembled employing the Na 2FePO 4F@C nanofibers cathode and the carbon nanofibers anode, demonstrating a promising energy density of 135.8 Wh kg −1 and a high capacity retention of 84.5% over 200 cycles. The distinctive network architecture of ultrafine active materials encapsulated into interlinked carbon nanofibers offers an ideal platform for enhancing the electrochemical reactivity, electronic/ionic transmittability, and structural stability of Na‐storage electrodes.

          Related collections

          Most cited references10

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          Array of nanosheets render ultrafast and high-capacity Na-ion storage by tunable pseudocapacitance

          Sodium-ion batteries are a potentially low-cost and safe alternative to the prevailing lithium-ion battery technology. However, it is a great challenge to achieve fast charging and high power density for most sodium-ion electrodes because of the sluggish sodiation kinetics. Here we demonstrate a high-capacity and high-rate sodium-ion anode based on ultrathin layered tin(II) sulfide nanostructures, in which a maximized extrinsic pseudocapacitance contribution is identified and verified by kinetics analysis. The graphene foam supported tin(II) sulfide nanoarray anode delivers a high reversible capacity of ∼1,100 mAh g−1 at 30 mA g−1 and ∼420 mAh g−1 at 30 A g−1, which even outperforms its lithium-ion storage performance. The surface-dominated redox reaction rendered by our tailored ultrathin tin(II) sulfide nanostructures may also work in other layered materials for high-performance sodium-ion storage.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Carbon nanosheet frameworks derived from peat moss as high performance sodium ion battery anodes.

            We demonstrate that peat moss, a wild plant that covers 3% of the earth's surface, serves as an ideal precursor to create sodium ion battery (NIB) anodes with some of the most attractive electrochemical properties ever reported for carbonaceous materials. By inheriting the unique cellular structure of peat moss leaves, the resultant materials are composed of three-dimensional macroporous interconnected networks of carbon nanosheets (as thin as 60 nm). The peat moss tissue is highly cross-linked, being rich in lignin and hemicellulose, suppressing the nucleation of equilibrium graphite even at 1100 °C. Rather, the carbons form highly ordered pseudographitic arrays with substantially larger intergraphene spacing (0.388 nm) than graphite (c/2 = 0.3354 nm). XRD analysis demonstrates that this allows for significant Na intercalation to occur even below 0.2 V vs Na/Na(+). By also incorporating a mild (300 °C) air activation step, we introduce hierarchical micro- and mesoporosity that tremendously improves the high rate performance through facile electrolyte access and further reduced Na ion diffusion distances. The optimized structures (carbonization at 1100 °C + activation) result in a stable cycling capacity of 298 mAh g(-1) (after 10 cycles, 50 mA g(-1)), with ∼150 mAh g(-1) of charge accumulating between 0.1 and 0.001 V with negligible voltage hysteresis in that region, nearly 100% cycling Coulombic efficiency, and superb cycling retention and high rate capacity (255 mAh g(-1) at the 210th cycle, stable capacity of 203 mAh g(-1) at 500 mA g(-1)).
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              A multifunctional 3.5 V iron-based phosphate cathode for rechargeable batteries.

              In the search for new positive-electrode materials for lithium-ion batteries, recent research has focused on nanostructured lithium transition-metal phosphates that exhibit desirable properties such as high energy storage capacity combined with electrochemical stability. Only one member of this class--the olivine LiFePO(4) (ref. 3)--has risen to prominence so far, owing to its other characteristics, which include low cost, low environmental impact and safety. These are critical for large-capacity systems such as plug-in hybrid electric vehicles. Nonetheless, olivine has some inherent shortcomings, including one-dimensional lithium-ion transport and a two-phase redox reaction that together limit the mobility of the phase boundary. Thus, nanocrystallites are key to enable fast rate behaviour. It has also been suggested that the long-term economic viability of large-scale Li-ion energy storage systems could be ultimately limited by global lithium reserves, although this remains speculative at present. (Current proven world reserves should be sufficient for the hybrid electric vehicle market, although plug-in hybrid electric vehicle and electric vehicle expansion would put considerable strain on resources and hence cost effectiveness.) Here, we report on a sodium/lithium iron phosphate, A(2)FePO(4)F (A=Na, Li), that could serve as a cathode in either Li-ion or Na-ion cells. Furthermore, it possesses facile two-dimensional pathways for Li+ transport, and the structural changes on reduction-oxidation are minimal. This results in a volume change of only 3.7% that--unlike the olivine--contributes to the absence of distinct two-phase behaviour during redox, and a reversible capacity that is 85% of theoretical.
                Bookmark

                Author and article information

                Contributors
                liuyc@ustb.edu.cn
                fanlizhen@ustb.edu.cn
                Journal
                Adv Sci (Weinh)
                Adv Sci (Weinh)
                10.1002/(ISSN)2198-3844
                ADVS
                Advanced Science
                John Wiley and Sons Inc. (Hoboken )
                2198-3844
                07 May 2019
                03 July 2019
                : 6
                : 13 ( doiID: 10.1002/advs.v6.13 )
                : 1900649
                Affiliations
                [ 1 ] Beijing Advanced Innovation Center for Materials Genome Engineering Institute for Advanced Materials and Technology University of Science and Technology Beijing Beijing 100083 China
                [ 2 ] College of Chemistry and Environmental Science Hebei University Baoding 071002 China
                [ 3 ] Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education) Nankai University Tianjin 300071 China
                [ 4 ] School of Electrical Engineering and Automation Tianjin Polytechnic University Tianjin 300387 China
                Author notes
                Author information
                https://orcid.org/0000-0002-6176-7278
                https://orcid.org/0000-0003-1998-9309
                https://orcid.org/0000-0003-2270-4458
                Article
                ADVS1124
                10.1002/advs.201900649
                6662290
                2cf1c641-b823-4d95-a7b5-a2006e46119c
                © 2019 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 March 2019
                Page count
                Figures: 7, Tables: 0, Pages: 10, Words: 6508
                Funding
                Funded by: National Natural Science Foundation of China
                Award ID: 21805007
                Award ID: 51532002
                Award ID: 21805066
                Funded by: Young Elite Scientists Sponsorship Program by CAST
                Award ID: 2018QNRC001
                Funded by: National Key Research and Development Program of China
                Award ID: 2018YFB0104300
                Funded by: Beijing Natural Science Foundation
                Award ID: L172023
                Award ID: L182019
                Funded by: Advanced Talents Incubation Program of the Hebei University
                Award ID: 801260201156
                Funded by: China Postdoctoral Science Foundation
                Award ID: 2018M640244
                Funded by: 111 Project
                Award ID: B12015
                Categories
                Full Paper
                Full Papers
                Custom metadata
                2.0
                advs1124
                July 3, 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.6.2 mode:remove_FC converted:29.07.2019

                binder‐free cathodes,carbon nanofibers,reaction kinetics and mechanism,sodium‐ion batteries,ultrasmall na2fepo4f nanoparticles

                Comments

                Comment on this article