کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
178955 459329 2015 4 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
An alluaudite Na2 + 2xFe2 − x(SO4)3(x = 0.2) derivative phase as insertion host for lithium battery
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
An alluaudite Na2 + 2xFe2 − x(SO4)3(x = 0.2) derivative phase as insertion host for lithium battery
چکیده انگلیسی


• A completely new compound was prepared by the chemical oxidation of alluaudite Na2.4Fe1.8(SO4)3 phase.
• The electrochemical performance of Na0.89Fe1.8(SO4)3 in lithium battery application was investigated for the first time.
• A high capacity of 110 mAh g− 1 at 0.1 C (1 C = 118 mAh g− 1) was obtained.
• A good rate kinetics and reversibility was confirmed involving a high Fe3 +/Fe2 + redox potential of 3.75 V (vs. Li/Li+).

A new desodiated derivative compound, Na0.89Fe1.8(SO4)3, was prepared by the chemical oxidation of alluaudite Na2.4Fe1.8(SO4)3 phase using NOBF4 as oxidant. The structure and valency of Fe were characterized by X-ray diffraction (XRD) and 57Fe Mössbauer spectroscopy. Intercalation behavior of lithium ions in the structure of Na0.89Fe1.8(SO4)3 was gauged by electrochemical analyses and ex-situ X-ray diffraction. A high capacity of 110 mAh g− 1 at 0.1 C was obtained with a good rate kinetics within a range of 0.1–10 C(1 C = 118 mAh g− 1) involving a high Fe3 +/Fe2 + redox potential of 3.75 V (vs. Li/Li+). These results confirmed that the Na2.4− δFe1.8(SO4)3 framework was stable even after oxidation and forms a new competitive cathode for the reversible intercalation of lithium ions.

A new desodiated derivative compound of Na0.89Fe1.8(SO4)3 was introduced as a host for the insertion/de-insertion of lithium ions, and a high capacity of 110 mAh g− 1 at 0.1 C was obtained with a good rate kinetics within a range of 0.1–10 C (1 C= 118 mAh g− 1) involving a high Fe3 +/Fe2 + redox potential of 3.75 V (vs. Li/Li+).Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Electrochemistry Communications - Volume 51, February 2015, Pages 19–22
نویسندگان
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