Na2FeF4 as a stable cathode material for Na-ion batteries

Author:

Yan Qi12,Xu Huan13,Hoang Khang4ORCID,Zhou Xiaolong1,Kidkhunthod Pinit5ORCID,Lightfoot Philip6,Yao Wenjiao17,Tang Yongbing138ORCID

Affiliation:

1. Advanced Energy Storage Technology Research Center, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China

2. Nano Science and Technology Institute, University of Science and Technology of China, Suzhou 215123, China

3. School of Chemical Sciences, University of Chinese Academy of Sciences, Shenzhen 518055, China

4. Center for Computationally Assisted Science and Technology and Department of Physics, North Dakota State University, Fargo, North Dakota 58108, USA

5. Synchrotron Light Research Institute, Nakhon Ratchasima 30000, Thailand

6. School of Chemistry and EaStChem, University of St Andrews, St Andrews, Fife KY16 9ST, United Kingdom

7. Shenzhen Key Laboratory of Energy Materials for Carbon Neutrality, Shenzhen 518055, China

8. Key Laboratory of Advanced Materials Processing & Mold, Ministry of Education, Zhengzhou University, Zhengzhou 450002, China

Abstract

In the search of cathode materials for Na-ion batteries, iron-based compounds have attracted much attention due to the abundant resource, easy access, and environmental friendliness of iron. Herein, we report the synthesis, structure, and electrochemistry of a previously unknown compound in the Na–Fe–F system, formulated as Na2FeF4. It is prepared by an easy and mild hydrothermal reaction with oxalate as a Fe2+ protector. Based on the single crystal x-ray diffraction analysis, it crystallizes in space group Pmcb with a =  3.255 (3) Å, b =  5.591(7) Å, and c =  9.557(1) Å. The crystal structure features edge-sharing FeF6 octahedra to form [FeF4] chains with Na+ ions located between chains. In electrochemical investigations, it is demonstrated that the material can deliver a reversible capacity of ∼90 mAh g−1 for 300 cycles in the window of 1.5–4.3 V with redox reactions at ∼3.0 V (vs Na+/Na). Such an activity originates from the Fe3+/Fe2+ redox couple, confirmed by x-ray absorption spectra and first-principles calculations.

Funder

the National Science Foundation of China

Shenzhen International Collaboration Research Project

Shenzhen Science and Technology Planning Project

Science and Technology Planning Project of Guangdong Province

NSFC/RGC Joint Research Scheme

Publisher

AIP Publishing

Subject

Physics and Astronomy (miscellaneous)

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