4.6 Article

Nanocrystalline FeF3 and MF2 (M = Fe, Co, and Mn) from metal trifluoroacetates and their Li(Na)-ion storage properties

期刊

JOURNAL OF MATERIALS CHEMISTRY A
卷 5, 期 16, 页码 7383-7393

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7ta00862g

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资金

  1. Swiss Federal Commission for Technology and Innovation (CTI) through the CTI Swiss Competence Centers for Energy Research (SCCER)
  2. Swiss Federal Commission for Technology and Innovation (CTI) through the CTI Swiss Competence Centers for Energy Research (CTI) [14698.2 PFIW-IW]
  3. Swiss Federal Commission for Technology and Innovation (CTI) through the CTI Swiss Competence Centers for Energy Research (Heat and Electricity Storage)
  4. Competence Center for Energy and Mobility (CCEM, Project SLIB)
  5. Swiss National Science Foundation (SNF Ambizione project) [ZENP2_154287]
  6. Belenos Clean Power Holding LTD

向作者/读者索取更多资源

With demands placed on batteries constantly increasing, new positive electrode materials with higher energy density, satisfactory power density, and long-term cycling capabilities, composed of highly abundant elements with low-cost, are desired. One such low-cost cathodic material is iron(III) fluoride - FeF3. Its theoretical capacity for single-electron reduction, accompanied by the insertion of Li+ ions, is 237 mA h g(-1). Herein we present a new synthesis for nanocrystalline FeF3 using inexpensive iron trifluoroacetate as a molecular single-source precursor. We also report an adaptation of this simple chemistry to several transition metal difluorides (M = Fe, Co, and Mn). With FeF3, a high capacity of 220 mA h g(-1) was attained at a moderate current density of 100 mA g(-1) (similar to 0.5 C). In addition to high capacity, we see the evidence for high rate-capability. Capacities of up to 155 mA h g(-1) were observed with 1-minute (10 A g(-1)) charge-discharge ramps, and at least 88% of this capacity was retained after 100 cycles. When tested as a sodium cathode, FeF3 exhibits capacities of up to 160 mA h g(-1) at a current rate of 200 mA h g(-1).

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