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        Unveiling the sodium intercalation properties in Na<sub>1.86</sub>□<sub>0.14</sub>Fe<sub>3</sub>(PO<sub>4</sub>)<sub>3</sub>

        Essehli, R.,Ben Yahia, H.,Maher, K.,Sougrati, M.T.,Abouimrane, A.,Park, J.-B.,Sun, Y.-K.,Al-Maadeed, M.A.,Belharouak, I. Elsevier Sequoia 2016 Journal of Power Sources Vol. No.

        <P><B>Abstract</B></P> <P>The new compound Na<SUB>1.86</SUB>□<SUB>0.14</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> was successfully synthesized via hydrothermal synthesis and its crystal structure was determined using powder X-ray diffraction data. Na<SUB>1.86</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> was also characterized by operando XRD and Mössbauer spectroscopy, cyclic voltammetry, and galvanostatic cycling. Na<SUB>1.86</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> crystallizes with the alluaudite-type structure with the eight coordinated Na1 and Na2 sodium atoms located within the channels. The combination of the Rietveld- and Mössbauer-analyses confirms that the sodium vacancies in the Na1 site are linked to a partial oxidation of Fe<SUP>2+</SUP> during synthesis. The electrochemical tests indicated that Na<SUB>1.86</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> is a 3 V sodium intercalating cathode. At the current densities of 5, 10, and 20 mA g<SUP>−1</SUP>, the material delivers the specific capacities of 109, 97, and 80 mA h g<SUP>−1</SUP>, respectively. After 100 charge and discharge cycles, Na<SUB>1.86</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> exhibited good sodium removal and uptake behavior although no optimizations of particle size, morphology, and carbon coating were performed.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Na<SUB>1.86</SUB>□<SUB>0.14</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> was synthesized via hydrothermal synthesis method. </LI> <LI> Na<SUB>1.86</SUB>□<SUB>0.14</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> crystallizes with the Alluaudite-type structure. </LI> <LI> Operando in situ XRD and Mössbauer spectroscopy studies were carried on. </LI> <LI> The crystal structure of Na<SUB>1.86</SUB>□<SUB>0.14</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> is stable during cycling. </LI> <LI> Na<SUB>1.86</SUB>□<SUB>0.14</SUB>Fe<SUB>3</SUB>(PO<SUB>4</SUB>)<SUB>3</SUB> is a promising 3 V cathode material for sodium ion batteries. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>Na1.86□0.14Fe3(PO4)3 was synthesized via hydrothermal synthesis method. Na1.86Fe3(PO4)3 crystallizes with the alluaudite-type structure. Na1.86Fe3(PO4)3 is a 3 V sodium intercalating cathode. At the current densities of 5, 10, and 20 mA g<SUP>−1</SUP>, the material delivers the specific capacities of 109, 97, and 80 mA h g<SUP>−1</SUP>, respectively. After 100 charge and discharge cycles, Na1.86Fe3(PO4)3 exhibited good sodium removal and uptake behavior with a stable crystal structure.</P> <P>[DISPLAY OMISSION]</P>

      • Alluaudite Na<sub>2</sub>Co<sub>2</sub>Fe(PO<sub>4</sub>)<sub>3</sub> as an electroactive material for sodium ion batteries

        Essehli, R.,Belharouak, I.,Ben Yahia, H.,Maher, K.,Abouimrane, A.,Orayech, B.,Calder, S.,Zhou, X. L.,Zhou, Z.,Sun, Y-K. The Royal Society of Chemistry 2015 Dalton Transactions Vol.44 No.17

        <P>The electroactive orthophosphate Na<SUB>2</SUB>Co<SUB>2</SUB>Fe(PO<SUB>4</SUB>)<SUB>3</SUB> was synthesized using a solid state reaction. Its crystal structure was solved using the combination of powder X-ray- and neutron-diffraction data. This material crystallizes according to the alluaudite structure (S.G. <I>C</I>2/<I>c</I>). The structure consists of edge sharing [MO<SUB>6</SUB>] octahedra (M = Fe, Co) resulting in chains parallel to [−101]. These chains are linked together <I>via</I> the [PO<SUB>4</SUB>] tetrahedra to form two distinct tunnels in which sodium cations are located. The electrochemical properties of Na<SUB>2</SUB>Co<SUB>2</SUB>Fe(PO<SUB>4</SUB>)<SUB>3</SUB> were evaluated by galvanostatic charge–discharge cycling. During the first discharge to 0.03 V, Na<SUB>2</SUB>Co<SUB>2</SUB>Fe(PO<SUB>4</SUB>)<SUB>3</SUB> delivers a specific capacity of 604 mA h g<SUP>−1</SUP>. This capacity is equivalent to the reaction of more than seven sodium ions per formula unit. Hence, this is a strong indication of a conversion-type reaction with the formation of metallic Fe and Co. The subsequent charge and discharge involved the reaction of fewer Na ions as expected for a conversion reaction. When discharged to 0.9 V, the material intercalated only one Na<SUP>+</SUP>-ion leading to the formation of a new phase Na<SUB>3</SUB>Co<SUB>2</SUB>Fe(PO<SUB>4</SUB>)<SUB>3</SUB>. This phase could then be cycled reversibly with an average voltage of 3.6 V <I>vs.</I> Na<SUP>+</SUP>/Na and a capacity of 110 mA h g<SUP>−1</SUP>. This result is in good agreement with the theoretical capacity expected from the extraction/insertion of two sodium atoms in Na<SUB>3</SUB>Co<SUB>2</SUB>Fe(PO<SUB>4</SUB>)<SUB>3</SUB>.</P> <P>Graphic Abstract</P><P>Na<SUB>2</SUB>Co<SUB>2</SUB>Fe(PO<SUB>4</SUB>)<SUB>3</SUB> crystallizes with the alluaudite-type structure (S.G. <I>C</I>2/<I>c</I>) and plays a dual anode/cathode behavior in sodium ion batteries. <IMG SRC='http://pubs.rsc.org/services/images/RSCpubs.ePlatform.Service.FreeContent.ImageService.svc/ImageService/image/GA?id=c5dt00971e'> </P>

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